| geneid | 23263 |
|---|---|
| ensemblid | ENSG00000126217.22 |
| hgncid | 14576 |
| symbol | MCF2L |
| name | MCF.2 cell line derived transforming sequence like |
| refseq_nuc | NM_001112732.3 |
| refseq_prot | NP_001106203.2 |
| ensembl_nuc | ENST00000535094.7 |
| ensembl_prot | ENSP00000440374.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 112969214 |
| end | 113099742 |
| strand | + |
| ver | v1.2 |
| region | chr13:112969214-113099742 |
| region5000 | chr13:112964214-113104742 |
| regionname0 | MCF2L_chr13_112969214_113099742 |
| regionname5000 | MCF2L_chr13_112964214_113104742 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1125 | 106 | 29 | 34 | 17 | 8 | 16 | 9 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0002 | 0/0 | 1125 | 6 | 0 | 4 | 2 | 0 | 0 | 2 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0003 | 0/0 | 1125 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0004 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0005 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3378 | 51 | 16 | 17 | 4 | 4 | 8 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0002 | 0/0 | 3378 | 12 | 3 | 6 | 0 | 0 | 3 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0003 | 0/0 | 3378 | 11 | 0 | 1 | 7 | 2 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0004 | 0/0 | 3378 | 10 | 2 | 3 | 1 | 2 | 2 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0005 | 0/0 | 3378 | 9 | 2 | 4 | 3 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0006 | 0/0 | 3378 | 5 | 1 | 2 | 1 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0007 | 0/0 | 3378 | 5 | 0 | 3 | 2 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0008 | 0/0 | 3378 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0009 | 0/0 | 3378 | 2 | 0 | 2 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0010 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0011 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0012 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0013 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0014 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0015 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0016 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| c0017 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3050 | 51 | 8 | 22 | 9 | 5 | 7 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0002 | 0/0 | 3050 | 15 | 1 | 4 | 8 | 0 | 2 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0003 | 0/0 | 3051 | 6 | 3 | 2 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0004 | 0/0 | 3051 | 6 | 1 | 5 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0005 | 0/0 | 3051 | 5 | 1 | 0 | 0 | 2 | 2 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0006 | 0/1 | 3050 | 4 | 0 | 1 | 0 | 1 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0007 | 0/0 | 3051 | 3 | 2 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0008 | 0/0 | 3050 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0009 | 0/0 | 3050 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0010 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0011 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0012 | 0/0 | 3051 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0013 | 1/0 | 3050 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0014 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0015 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0016 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0017 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0018 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0019 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0020 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0021 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0022 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0023 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0024 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0025 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0026 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0027 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0028 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0029 | 0/0 | 3050 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0030 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0031 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| t0032 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3378 | 51 | 16 | 17 | 4 | 4 | 8 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002 | 0/0 | 3378 | 12 | 3 | 6 | 0 | 0 | 3 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0003 | 0/0 | 3378 | 11 | 0 | 1 | 7 | 2 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0004 | 0/0 | 3378 | 10 | 2 | 3 | 1 | 2 | 2 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0005 | 0/0 | 3378 | 9 | 2 | 4 | 3 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0006 | 0/0 | 3378 | 5 | 1 | 2 | 1 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0008 | 0/0 | 3378 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0010 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0012 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0013 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0015 | 0/0 | 3378 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0016 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0002c0007 | 0/0 | 3378 | 5 | 0 | 3 | 2 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0002c0017 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0003c0009 | 0/0 | 3378 | 2 | 0 | 2 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0004c0011 | 0/0 | 3378 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0005c0014 | 0/0 | 3378 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6427 | 26 | 5 | 12 | 1 | 3 | 5 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0002 | 0/0 | 6427 | 3 | 0 | 1 | 1 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0003 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0004 | 0/0 | 6428 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0005 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0006 | 0/1 | 6427 | 4 | 0 | 1 | 0 | 1 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0007 | 0/0 | 6428 | 3 | 2 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0008 | 0/0 | 6427 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0012 | 0/0 | 6428 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0013 | 1/0 | 6427 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0014 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0017 | 0/0 | 6428 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0018 | 0/0 | 6427 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0019 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0022 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0023 | 0/0 | 6428 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0026 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0001t0028 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0001 | 0/0 | 6427 | 4 | 1 | 3 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0002 | 0/0 | 6427 | 2 | 1 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0003 | 0/0 | 6428 | 2 | 0 | 2 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0005 | 0/0 | 6428 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0015 | 0/0 | 6428 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0016 | 0/0 | 6428 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0002t0027 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0003t0001 | 0/0 | 6427 | 4 | 0 | 0 | 1 | 2 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0003t0002 | 0/0 | 6427 | 6 | 0 | 1 | 5 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0003t0020 | 0/0 | 6427 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0004t0001 | 0/0 | 6427 | 3 | 2 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0004t0003 | 0/0 | 6428 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0004t0004 | 0/0 | 6428 | 3 | 0 | 3 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0004t0005 | 0/0 | 6428 | 3 | 0 | 0 | 0 | 2 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0005t0001 | 0/0 | 6427 | 6 | 0 | 3 | 3 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0005t0025 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0005t0029 | 0/0 | 6427 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0005t0032 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0006t0002 | 0/0 | 6427 | 3 | 0 | 1 | 1 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0006t0009 | 0/0 | 6427 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0006t0030 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0008t0003 | 0/0 | 6428 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0008t0004 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0010t0021 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0012t0031 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0013t0001 | 0/0 | 6427 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0015t0001 | 0/0 | 6427 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0001c0016t0004 | 0/0 | 6428 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0002c0007t0001 | 0/0 | 6427 | 5 | 0 | 3 | 2 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0002c0017t0001 | 0/0 | 6427 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0003c0009t0010 | 0/0 | 6428 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0003c0009t0011 | 0/0 | 6428 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0004c0011t0002 | 0/0 | 6427 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| a0005c0014t0024 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | copy fasta | chr13 | 112964214 | 113104742 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0006g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0013g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0014g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0017g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0018g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0019g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0022g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0023g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0001t0028g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0015g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0016g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0002t0027g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0003t0020g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0005g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0004t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0025g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0029g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0005t0032g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0006t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0006t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0006t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0006t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0008t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0008t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0008t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0010t0021g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0012t0031g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0013t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0015t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0001c0016t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0002c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0002c0007t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0002c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0002c0007t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0002c0007t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0002c0017t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0003c0009t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0003c0009t0011g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0004c0011t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| a0005c0014t0024g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0010 | EUR | FIN | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG00544 | hp1 | a0001 | c0013 | t0001 | g0067 | EAS | CHS | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG00544 | hp2 | a0001 | c0001 | t0018 | g0077 | EAS | CHS | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01109 | hp1 | a0001 | c0004 | t0004 | g0046 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0035 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01175 | hp2 | a0001 | c0016 | t0004 | g0085 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01243 | hp1 | a0003 | c0009 | t0011 | g0101 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0079 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01257 | hp2 | a0001 | c0004 | t0004 | g0097 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01258 | hp1 | a0001 | c0005 | t0001 | g0080 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01346 | hp1 | a0002 | c0017 | t0001 | g0109 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01358 | hp2 | a0002 | c0007 | t0001 | g0112 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01361 | hp1 | a0001 | c0005 | t0001 | g0081 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01496 | hp1 | a0001 | c0001 | t0023 | g0018 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01515 | hp1 | a0001 | c0004 | t0005 | g0012 | EUR | IBS | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0073 | EUR | IBS | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01517 | hp1 | a0001 | c0004 | t0005 | g0011 | EUR | IBS | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0092 | EUR | IBS | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0025 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01891 | hp2 | a0005 | c0014 | t0024 | g0100 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01978 | hp2 | a0002 | c0007 | t0001 | g0074 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01993 | hp1 | a0001 | c0006 | t0009 | g0028 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0078 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02074 | hp1 | a0001 | c0003 | t0002 | g0047 | EAS | KHV | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02074 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | KHV | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02129 | hp1 | a0001 | c0005 | t0001 | g0020 | EAS | KHV | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02129 | hp2 | a0001 | c0003 | t0020 | g0089 | EAS | KHV | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02135 | hp1 | a0001 | c0005 | t0001 | g0088 | EAS | KHV | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02135 | hp2 | a0001 | c0005 | t0001 | g0068 | EAS | KHV | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02145 | hp1 | a0001 | c0001 | t0026 | g0034 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02145 | hp2 | a0001 | c0012 | t0031 | g0021 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02273 | hp1 | a0002 | c0007 | t0001 | g0114 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02273 | hp2 | a0001 | c0006 | t0002 | g0029 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02293 | hp1 | a0001 | c0004 | t0004 | g0084 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02293 | hp2 | a0001 | c0005 | t0029 | g0091 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02300 | hp1 | a0003 | c0009 | t0010 | g0115 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | GWD | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02572 | hp2 | a0001 | c0005 | t0032 | g0106 | AFR | GWD | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02602 | hp1 | a0001 | c0004 | t0005 | g0095 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0053 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02622 | hp1 | a0001 | c0002 | t0027 | g0065 | AFR | GWD | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02622 | hp2 | a0001 | c0008 | t0004 | g0083 | AFR | GWD | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02738 | hp1 | a0001 | c0006 | t0002 | g0043 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02738 | hp2 | a0001 | c0001 | t0017 | g0059 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | GWD | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0104 | AFR | GWD | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03098 | hp1 | a0001 | c0005 | t0025 | g0016 | AFR | MSL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | MSL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03209 | hp2 | a0001 | c0006 | t0030 | g0096 | AFR | MSL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0060 | SAS | PJL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0056 | SAS | STU | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03688 | hp2 | a0001 | c0002 | t0015 | g0007 | SAS | STU | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03834 | hp2 | a0001 | c0004 | t0003 | g0009 | SAS | BEB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG04115 | hp1 | a0001 | c0015 | t0001 | g0013 | SAS | STU | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG04115 | hp2 | a0001 | c0002 | t0016 | g0054 | SAS | STU | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | YRI | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | YRI | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0111 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0102 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19005 | hp2 | a0001 | c0006 | t0002 | g0110 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19066 | hp1 | a0002 | c0007 | t0001 | g0072 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19081 | hp1 | a0001 | c0003 | t0002 | g0042 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19081 | hp2 | a0002 | c0007 | t0001 | g0076 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19085 | hp1 | a0004 | c0011 | t0002 | g0090 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0107 | AFR | YRI | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA19240 | hp2 | a0001 | c0008 | t0003 | g0044 | AFR | YRI | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02109 | hp2 | a0001 | c0008 | t0003 | g0039 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02486 | hp2 | a0001 | c0010 | t0021 | g0015 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02559 | hp1 | a0001 | c0001 | t0028 | g0098 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0103 | AFR | MSL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | MSL | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | USA | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | USA | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0027 | REF | REF | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0105 | REF | REF | MCF2L_chr13_112964214_113104742 | MCF2L | chr13 | 112964214 | 113104742 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113075100
|
C | T | 1 | a0003 | 2 | HG01243.hp1 HG02300.hp1 |
missense_variant | MODERATE | c.1219C>T | p.Arg407Trp | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/30 | 1385/6427 | 1219/3378 | 407/1125 | chr13 | 113075100 | ||
| chr13:113077058
|
G | A | 1 | a0004 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.1507G>A | p.Val503Met | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/30 | 1673/6427 | 1507/3378 | 503/1125 | chr13 | 113077058 | ||
| chr13:113094558
|
G | A | 1 | a0002 | 6 | HG01346.hp1 HG01358.hp2 HG01978.hp2 others(3): Show |
missense_variant | MODERATE | c.2998G>A | p.Gly1000Arg | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/30 | 3164/6427 | 2998/3378 | 1000/1125 | chr13 | 113094558 | ||
| chr13:113096580
|
G | C | 1 | a0005 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.3219G>C | p.Glu1073Asp | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 29/30 | 3385/6427 | 3219/3378 | 1073/1125 | chr13 | 113096580 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113024705
|
G | A | 1 | a0001c0010 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.225G>A | p.Glu75Glu | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/30 | 391/6427 | 225/3378 | 75/1125 | chr13 | 113024705 | ||
| chr13:113066162
|
C | T | 2 | a0001c0003a0002c0017 | 12 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(9): Show |
synonymous_variant | LOW | c.873C>T | p.Thr291Thr | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/30 | 1039/6427 | 873/3378 | 291/1125 | chr13 | 113066162 | ||
| chr13:113074467
|
G | A | 3 | a0001c0003a0001c0006a0004c0011 | 17 | HG01515.hp2 HG01517.hp2 HG01993.hp1 others(14): Show |
synonymous_variant | LOW | c.1020G>A | p.Ala340Ala | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/30 | 1186/6427 | 1020/3378 | 340/1125 | chr13 | 113074467 | ||
| chr13:113074497
|
C | T | 1 | a0001c0008 | 3 | HG02109.hp2 HG02622.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.1050C>T | p.Ile350Ile | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/30 | 1216/6427 | 1050/3378 | 350/1125 | chr13 | 113074497 | ||
| chr13:113078677
|
T | C | 1 | a0001c0012 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1746T>C | p.Ser582Ser | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/30 | 1912/6427 | 1746/3378 | 582/1125 | chr13 | 113078677 | ||
| chr13:113078695
|
C | T | 2 | a0001c0004a0001c0016 | 11 | HG01109.hp1 HG01175.hp2 HG01257.hp2 others(8): Show |
synonymous_variant | LOW | c.1764C>T | p.Arg588Arg | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/30 | 1930/6427 | 1764/3378 | 588/1125 | chr13 | 113078695 | ||
| chr13:113082453
|
A | G | 1 | a0001c0015 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1902A>G | p.Pro634Pro | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/30 | 2068/6427 | 1902/3378 | 634/1125 | chr13 | 113082453 | ||
| chr13:113084912
|
T | C | 2 | a0001c0005a0003c0009 | 11 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
synonymous_variant | LOW | c.2082T>C | p.Tyr694Tyr | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 19/30 | 2248/6427 | 2082/3378 | 694/1125 | chr13 | 113084912 | ||
| chr13:113086177
|
G | A | 1 | a0001c0013 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.2301G>A | p.Ala767Ala | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/30 | 2467/6427 | 2301/3378 | 767/1125 | chr13 | 113086177 | ||
| chr13:113087276
|
G | A | 2 | a0001c0002a0001c0008 | 15 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
synonymous_variant | LOW | c.2415G>A | p.Ser805Ser | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 22/30 | 2581/6427 | 2415/3378 | 805/1125 | chr13 | 113087276 | ||
| chr13:113096787
|
G | A | 1 | a0001c0016 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.3306G>A | p.Gly1102Gly | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 3472/6427 | 3306/3378 | 1102/1125 | chr13 | 113096787 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:112969338
|
G | A | 1 | a0001c0006t0009 | 1 | HG01993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/30 | 42 | chr13 | 112969338 | |||||
| chr13:113096891
|
T | A | 3 | a0001c0001t0012a0003c0009t0010a0003c0009t0011 | 3 | HG01243.hp1 HG02300.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*32T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 32 | chr13 | 113096891 | |||||
| chr13:113096961
|
C | G | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*102C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 102 | chr13 | 113096961 | |||||
| chr13:113097027
|
G | A | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(22): Show | 81 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*168G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 168 | chr13 | 113097027 | |||||
| chr13:113097096
|
C | A | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*237C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 237 | chr13 | 113097096 | |||||
| chr13:113097156
|
T | C | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*297T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 297 | chr13 | 113097156 | |||||
| chr13:113097462
|
G | C | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | 112 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*603G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 603 | chr13 | 113097462 | |||||
| chr13:113097473
|
C | T | 1 | a0001c0005t0032 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*614C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 614 | chr13 | 113097473 | |||||
| chr13:113097661
|
C | CA | 25 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(22): Show | 33 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*810dupA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 811 | INFO_REALIGN_3_PRIME | chr13 | 113097661 | ||||
| chr13:113097743
|
A | T | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(16): Show | 25 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*884A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 884 | chr13 | 113097743 | |||||
| chr13:113097804
|
C | A | 1 | a0001c0001t0018 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 945 | chr13 | 113097804 | |||||
| chr13:113097863
|
C | T | 1 | a0001c0001t0017 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 1004 | chr13 | 113097863 | |||||
| chr13:113098259
|
G | A | 2 | a0001c0001t0006a0001c0001t0019 | 5 | HG00323.hp1 HG01243.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1400G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 1400 | chr13 | 113098259 | |||||
| chr13:113098517
|
A | G | 9 | a0001c0001t0005a0001c0001t0012a0001c0001t0017others(6): Show | 11 | HG01515.hp1 HG01517.hp1 HG02300.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1658A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 1658 | chr13 | 113098517 | |||||
| chr13:113098587
|
A | G | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1728A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 1728 | chr13 | 113098587 | |||||
| chr13:113098850
|
T | C | 13 | a0001c0001t0005a0001c0001t0007a0001c0001t0012others(10): Show | 17 | HG01109.hp2 HG01496.hp1 HG01515.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1991T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 1991 | chr13 | 113098850 | |||||
| chr13:113098925
|
T | C | 22 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(19): Show | 32 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2066T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2066 | chr13 | 113098925 | |||||
| chr13:113099001
|
G | A | 13 | a0001c0001t0005a0001c0001t0007a0001c0001t0012others(10): Show | 17 | HG01109.hp2 HG01496.hp1 HG01515.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2142G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2142 | chr13 | 113099001 | |||||
| chr13:113099137
|
G | A | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 91 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2278G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2278 | chr13 | 113099137 | |||||
| chr13:113099215
|
C | T | 13 | a0001c0001t0002a0001c0001t0007a0001c0001t0014others(10): Show | 25 | HG00733.hp1 HG01109.hp2 HG01256.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2356C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2356 | chr13 | 113099215 | |||||
| chr13:113099234
|
G | A | 1 | a0001c0002t0027 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2375 | chr13 | 113099234 | |||||
| chr13:113099247
|
G | C | 1 | a0001c0002t0027 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2388G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2388 | chr13 | 113099247 | |||||
| chr13:113099468
|
C | T | 1 | a0001c0001t0019 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2609C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2609 | chr13 | 113099468 | |||||
| chr13:113099531
|
G | A | 1 | a0001c0002t0015 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2672G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2672 | chr13 | 113099531 | |||||
| chr13:113099562
|
T | C | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | 115 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2703T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 30/30 | 2703 | chr13 | 113099562 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:112970048
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0014g0001 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79+590T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970048 | ||||||
| chr13:112970177
|
G | A | 1 | a0001c0002t0002g0003 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.79+719G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970177 | ||||||
| chr13:112970332
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+874G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970332 | ||||||
| chr13:112970391
|
A | G | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+933A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970391 | ||||||
| chr13:112970625
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1167G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970625 | ||||||
| chr13:112970702
|
G | A | 1 | a0001c0002t0003g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.79+1244G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970702 | ||||||
| chr13:112970708
|
G | A | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+1250G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112970708 | ||||||
| chr13:112971053
|
A | G | 22 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(19): Show | 22 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+1595A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971053 | ||||||
| chr13:112971055
|
A | G | 3 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.79+1597A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971055 | ||||||
| chr13:112971082
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.79+1624A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971082 | ||||||
| chr13:112971265
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.79+1807G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971265 | ||||||
| chr13:112971400
|
G | A | 2 | a0001c0001t0001g0082a0001c0008t0004g0083 | 2 | HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.79+1942G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971400 | ||||||
| chr13:112971722
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.79+2264C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971722 | ||||||
| chr13:112971725
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.79+2267T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971725 | ||||||
| chr13:112971839
|
T | G | 3 | a0001c0001t0007g0017a0001c0001t0023g0018a0001c0005t0025g0016 | 3 | HG01496.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79+2381T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971839 | ||||||
| chr13:112971966
|
C | T | 2 | a0001c0003t0002g0078a0001c0004t0001g0102 | 2 | HG01993.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.79+2508C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112971966 | ||||||
| chr13:112972263
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+2805G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972263 | ||||||
| chr13:112972282
|
G | A | 1 | a0001c0001t0022g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+2824G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972282 | ||||||
| chr13:112972334
|
G | C | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.79+2876G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972334 | ||||||
| chr13:112972359
|
G | GTGGA | 9 | a0001c0001t0001g0075a0001c0001t0004g0070a0001c0001t0018g0077others(6): Show | 9 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+2931_79+2934dup others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972359 | |||||
| chr13:112972359
|
GTGGA | G | 3 | a0001c0001t0001g0038a0001c0001t0014g0001a0001c0008t0003g0039 | 3 | HG01070.hp2 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.79+2931_79+2934del others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972359 | |||||
| chr13:112972359
|
GTGGATGG others(1): Show |
G | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 50 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.79+2927_79+2934del others(8): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972359 | |||||
| chr13:112972369
|
G | T | 2 | a0001c0001t0007g0017a0001c0001t0023g0018 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79+2911G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972369 | ||||||
| chr13:112972622
|
A | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+3164A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972622 | ||||||
| chr13:112972798
|
T | TGGATGGA others(932): Show |
17 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(14): Show | 17 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+3343_79+3344ins others(939): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(936): Show |
2 | a0001c0001t0001g0041a0001c0002t0001g0040 | 2 | HG01175.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.79+3343_79+3344ins others(943): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(924): Show |
1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+3343_79+3344ins others(931): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(932): Show |
31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(28): Show | 31 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.79+3343_79+3344ins others(939): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(936): Show |
47 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.79+3343_79+3344ins others(943): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(936): Show |
1 | a0001c0008t0003g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.79+3343_79+3344ins others(943): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(936): Show |
15 | a0001c0001t0001g0113a0001c0001t0002g0116a0001c0001t0006g0108others(12): Show | 15 | HG01109.hp2 HG01243.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+3343_79+3344ins others(943): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972798
|
T | TGGATGGA others(1045): Show |
1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+3343_79+3344ins others(1052): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112972798 | |||||
| chr13:112972845
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.79+3387A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972845 | ||||||
| chr13:112972955
|
G | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+3497G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112972955 | ||||||
| chr13:112973208
|
G | C | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+3750G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973208 | ||||||
| chr13:112973246
|
T | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+3788T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973246 | ||||||
| chr13:112973448
|
T | G | 22 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(19): Show | 22 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+3990T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973448 | ||||||
| chr13:112973576
|
A | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+4118A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973576 | ||||||
| chr13:112973588
|
C | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4130C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973588 | ||||||
| chr13:112973611
|
G | A | 1 | a0001c0003t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.79+4153G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973611 | ||||||
| chr13:112973707
|
G | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+4249G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973707 | ||||||
| chr13:112973734
|
G | A | 1 | a0001c0001t0003g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79+4276G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973734 | ||||||
| chr13:112973756
|
C | A | 22 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(19): Show | 22 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+4298C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973756 | ||||||
| chr13:112973955
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(42): Show | 45 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.79+4497C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973955 | ||||||
| chr13:112973993
|
G | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+4535G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112973993 | ||||||
| chr13:112974007
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+4549C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974007 | ||||||
| chr13:112974331
|
G | A | 2 | a0001c0004t0004g0084a0001c0016t0004g0085 | 2 | HG01175.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.79+4873G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974331 | ||||||
| chr13:112974334
|
G | A | 17 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(14): Show | 17 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+4876G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974334 | ||||||
| chr13:112974382
|
G | C | 7 | a0001c0001t0001g0087a0001c0003t0001g0086a0001c0003t0001g0092others(4): Show | 7 | HG00733.hp2 HG01517.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4924G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974382 | ||||||
| chr13:112974400
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0014g0001 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79+4942G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974400 | ||||||
| chr13:112974439
|
A | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+4981A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974439 | ||||||
| chr13:112974693
|
C | T | 1 | a0001c0004t0004g0097 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.79+5235C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974693 | ||||||
| chr13:112974731
|
A | G | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+5273A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974731 | ||||||
| chr13:112974891
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79+5433T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974891 | ||||||
| chr13:112974954
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+5496G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112974954 | ||||||
| chr13:112975021
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+5563C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975021 | ||||||
| chr13:112975031
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.79+5573C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975031 | ||||||
| chr13:112975076
|
T | C | 1 | a0001c0006t0002g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.79+5618T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975076 | ||||||
| chr13:112975204
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.79+5746A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975204 | ||||||
| chr13:112975376
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+5918G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975376 | ||||||
| chr13:112975407
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(52): Show | 55 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.79+5949A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975407 | ||||||
| chr13:112975488
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.79+6030A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975488 | ||||||
| chr13:112975793
|
C | T | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79+6335C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975793 | ||||||
| chr13:112975859
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.79+6401C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975859 | ||||||
| chr13:112975869
|
T | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.79+6411T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975869 | ||||||
| chr13:112975927
|
GGCCT | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.79+6470_79+6473del others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975927 | ||||||
| chr13:112975928
|
G | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+6470G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112975928 | ||||||
| chr13:112976071
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+6613C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976071 | ||||||
| chr13:112976083
|
C | G | 2 | a0001c0005t0001g0068a0001c0013t0001g0067 | 2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.79+6625C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976083 | ||||||
| chr13:112976094
|
G | A | 2 | a0001c0001t0004g0070a0001c0002t0001g0071 | 2 | HG01168.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.79+6636G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976094 | ||||||
| chr13:112976103
|
G | A | 3 | a0001c0001t0007g0017a0001c0001t0023g0018a0001c0005t0025g0016 | 3 | HG01496.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79+6645G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976103 | ||||||
| chr13:112976139
|
C | T | 19 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(16): Show | 19 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+6681C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976139 | ||||||
| chr13:112976142
|
GT | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.79+6695delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112976142 | |||||
| chr13:112976142
|
GTT | G | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+6694_79+6695del others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112976142 | |||||
| chr13:112976174
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+6716G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976174 | ||||||
| chr13:112976176
|
ATG | A | 3 | a0001c0001t0018g0077a0001c0005t0001g0068a0001c0013t0001g0067 | 3 | HG00544.hp1 HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.79+6731_79+6732del others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112976176 | |||||
| chr13:112976187
|
T | TGC | 4 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0002t0001g0036others(1): Show | 4 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+6730_79+6731ins others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112976187 | |||||
| chr13:112976189
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+6731T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976189 | ||||||
| chr13:112976191
|
C | CGT | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+6750_79+6751dup others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112976191 | |||||
| chr13:112976193
|
T | C | 3 | a0001c0001t0018g0077a0001c0005t0001g0068a0001c0013t0001g0067 | 3 | HG00544.hp1 HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.79+6735T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976193 | ||||||
| chr13:112976470
|
C | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+7012C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976470 | ||||||
| chr13:112976564
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+7106C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976564 | ||||||
| chr13:112976585
|
C | T | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.79+7127C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976585 | ||||||
| chr13:112976671
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.79+7213G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976671 | ||||||
| chr13:112976829
|
T | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 80 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.79+7371T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976829 | ||||||
| chr13:112976894
|
C | T | 2 | a0001c0004t0001g0103a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.79+7436C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976894 | ||||||
| chr13:112976924
|
T | C | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+7466T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976924 | ||||||
| chr13:112976931
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.79+7473G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112976931 | ||||||
| chr13:112977017
|
T | C | 1 | a0001c0002t0002g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.79+7559T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977017 | ||||||
| chr13:112977112
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+7654C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977112 | ||||||
| chr13:112977316
|
C | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+7858C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977316 | ||||||
| chr13:112977447
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+7989T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977447 | ||||||
| chr13:112977466
|
A | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.79+8008A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977466 | ||||||
| chr13:112977786
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+8328G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977786 | ||||||
| chr13:112977795
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+8337G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977795 | ||||||
| chr13:112977892
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+8434G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977892 | ||||||
| chr13:112977963
|
A | G | 17 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(14): Show | 17 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+8505A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112977963 | ||||||
| chr13:112978130
|
A | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 28 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+8672A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112978130 | ||||||
| chr13:112978306
|
C | G | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+8848C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112978306 | ||||||
| chr13:112978879
|
C | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+9421C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112978879 | ||||||
| chr13:112978990
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.79+9532G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112978990 | ||||||
| chr13:112979107
|
T | A | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+9649T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979107 | ||||||
| chr13:112979265
|
G | A | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+9807G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979265 | ||||||
| chr13:112979277
|
G | A | 1 | a0001c0003t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.79+9819G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979277 | ||||||
| chr13:112979287
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+9829G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979287 | ||||||
| chr13:112979429
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+9971G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979429 | ||||||
| chr13:112979482
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.79+10024G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979482 | ||||||
| chr13:112979556
|
G | T | 1 | a0001c0001t0008g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.79+10098G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979556 | ||||||
| chr13:112979580
|
C | T | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79+10122C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979580 | ||||||
| chr13:112979694
|
A | G | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+10236A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979694 | ||||||
| chr13:112979777
|
G | C | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+10319G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112979777 | ||||||
| chr13:112980047
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+10589G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980047 | ||||||
| chr13:112980095
|
G | A | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+10637G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980095 | ||||||
| chr13:112980196
|
G | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(46): Show | 49 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.79+10738G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980196 | ||||||
| chr13:112980481
|
G | A | 2 | a0001c0005t0001g0068a0001c0013t0001g0067 | 2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.79+11023G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980481 | ||||||
| chr13:112980588
|
A | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+11130A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980588 | ||||||
| chr13:112980623
|
A | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.79+11165A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980623 | ||||||
| chr13:112980628
|
G | GCCGCCTT others(10): Show |
55 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(52): Show | 55 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.79+11195_79+11211d others(19): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112980628 | |||||
| chr13:112980628
|
G | GCCGCCTT others(27): Show |
35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(32): Show | 35 | HG00323.hp1 HG00733.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.79+11178_79+11211d others(36): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112980628 | |||||
| chr13:112980628
|
G | GCCGCCTT others(44): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0002t0003g0023 | 3 | HG01069.hp1 HG01071.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.79+11211_79+11212i others(53): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112980628 | |||||
| chr13:112980636
|
C | CCCCTTTC others(27): Show |
1 | a0001c0005t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79+11211_79+11212i others(36): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112980636 | |||||
| chr13:112980737
|
C | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+11279C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980737 | ||||||
| chr13:112980817
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.79+11359G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980817 | ||||||
| chr13:112980890
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+11432C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112980890 | ||||||
| chr13:112981031
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+11573G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981031 | ||||||
| chr13:112981058
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0041others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.79+11600G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981058 | ||||||
| chr13:112981089
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+11631C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981089 | ||||||
| chr13:112981095
|
G | A | 1 | a0001c0002t0015g0007 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.79+11637G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981095 | ||||||
| chr13:112981103
|
C | G | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.79+11645C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981103 | ||||||
| chr13:112981341
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+11883C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981341 | ||||||
| chr13:112981409
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+11951G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981409 | ||||||
| chr13:112981493
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+12035G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981493 | ||||||
| chr13:112981552
|
G | A | 1 | a0001c0001t0006g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.79+12094G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981552 | ||||||
| chr13:112981557
|
C | T | 2 | a0001c0001t0007g0035a0001c0001t0026g0034 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.79+12099C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981557 | ||||||
| chr13:112981640
|
G | A | 2 | a0001c0001t0007g0035a0001c0001t0026g0034 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.79+12182G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981640 | ||||||
| chr13:112981649
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.79+12191C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981649 | ||||||
| chr13:112981685
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+12227G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981685 | ||||||
| chr13:112981747
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+12289C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981747 | ||||||
| chr13:112981748
|
G | A | 2 | a0001c0001t0007g0035a0001c0001t0026g0034 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.79+12290G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981748 | ||||||
| chr13:112981818
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79+12360G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981818 | ||||||
| chr13:112981842
|
C | T | 22 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(19): Show | 22 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+12384C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112981842 | ||||||
| chr13:112982060
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+12602G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982060 | ||||||
| chr13:112982179
|
G | T | 1 | a0001c0003t0002g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.79+12721G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982179 | ||||||
| chr13:112982190
|
G | A | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+12732G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982190 | ||||||
| chr13:112982331
|
C | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 78 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.79+12873C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982331 | ||||||
| chr13:112982695
|
T | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 27 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+13237T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982695 | ||||||
| chr13:112982695
|
T | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0041others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.79+13237T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982695 | ||||||
| chr13:112982696
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.79+13238T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982696 | ||||||
| chr13:112982877
|
A | G | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+13419A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112982877 | ||||||
| chr13:112983347
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+13889G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983347 | ||||||
| chr13:112983450
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.79+13992T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983450 | ||||||
| chr13:112983520
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+14062C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983520 | ||||||
| chr13:112983547
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+14089G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983547 | ||||||
| chr13:112983570
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+14112G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983570 | ||||||
| chr13:112983632
|
C | G | 7 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098others(4): Show | 7 | HG01109.hp2 HG02074.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+14174C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983632 | ||||||
| chr13:112983809
|
T | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+14351T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983809 | ||||||
| chr13:112983872
|
A | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+14414A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983872 | ||||||
| chr13:112983952
|
C | T | 1 | a0001c0001t0007g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+14494C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112983952 | ||||||
| chr13:112984135
|
G | A | 8 | a0001c0001t0002g0048a0001c0001t0004g0070a0001c0001t0018g0077others(5): Show | 8 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+14677G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984135 | ||||||
| chr13:112984258
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.79+14800T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984258 | ||||||
| chr13:112984395
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+14937T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984395 | ||||||
| chr13:112984463
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+15005T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984463 | ||||||
| chr13:112984609
|
A | C | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+15151A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984609 | ||||||
| chr13:112984702
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0014g0001 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79+15244G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984702 | ||||||
| chr13:112984785
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+15327A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984785 | ||||||
| chr13:112984819
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.79+15361A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984819 | ||||||
| chr13:112984861
|
G | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+15403G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984861 | ||||||
| chr13:112984893
|
T | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.79+15435T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984893 | ||||||
| chr13:112984921
|
A | G | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.79+15463A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984921 | ||||||
| chr13:112984956
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.79+15498G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112984956 | ||||||
| chr13:112985068
|
C | T | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+15610C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985068 | ||||||
| chr13:112985148
|
G | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+15690G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985148 | ||||||
| chr13:112985222
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+15764G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985222 | ||||||
| chr13:112985301
|
A | C | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+15843A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985301 | ||||||
| chr13:112985354
|
C | T | 1 | a0001c0003t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.79+15896C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985354 | ||||||
| chr13:112985357
|
G | A | 22 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(19): Show | 22 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+15899G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985357 | ||||||
| chr13:112985383
|
A | G | 1 | a0002c0007t0001g0114 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.79+15925A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985383 | ||||||
| chr13:112985418
|
G | A | 1 | a0001c0001t0018g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.79+15960G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985418 | ||||||
| chr13:112985548
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(49): Show | 52 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.79+16090G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985548 | ||||||
| chr13:112985555
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+16097A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985555 | ||||||
| chr13:112985558
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.79+16100A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985558 | ||||||
| chr13:112985750
|
A | C | 7 | a0001c0001t0001g0087a0001c0003t0001g0086a0001c0003t0001g0092others(4): Show | 7 | HG00733.hp2 HG01517.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+16292A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985750 | ||||||
| chr13:112985923
|
G | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+16465G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985923 | ||||||
| chr13:112985979
|
G | A | 19 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(16): Show | 19 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+16521G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112985979 | ||||||
| chr13:112986034
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.79+16576C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986034 | ||||||
| chr13:112986070
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79+16612G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986070 | ||||||
| chr13:112986087
|
C | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+16629C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986087 | ||||||
| chr13:112986121
|
TCGCCCCT others(115): Show |
T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+16667_79+16788d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112986121 | |||||
| chr13:112986123
|
G | A | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79+16665G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986123 | ||||||
| chr13:112986364
|
T | TCA | 5 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0075others(2): Show | 5 | HG01978.hp1 HG01993.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+16908_79+16909d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112986364 | |||||
| chr13:112986407
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0005g0062 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.79+16949C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986407 | ||||||
| chr13:112986416
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+16958T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986416 | ||||||
| chr13:112986512
|
G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.79+17054G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986512 | ||||||
| chr13:112986739
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79+17281A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986739 | ||||||
| chr13:112986828
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.79+17370A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986828 | ||||||
| chr13:112986852
|
TG | T | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+17395delG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986852 | ||||||
| chr13:112986893
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+17435C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112986893 | ||||||
| chr13:112987031
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.79+17573C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987031 | ||||||
| chr13:112987109
|
T | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+17651T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987109 | ||||||
| chr13:112987170
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0002g0048a0001c0001t0004g0070others(8): Show | 11 | HG00544.hp2 HG00733.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+17712C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987170 | ||||||
| chr13:112987300
|
C | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.79+17842C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987300 | ||||||
| chr13:112987311
|
C | CATGCAGC others(18): Show |
97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+17854_79+17855i others(27): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112987311 | |||||
| chr13:112987340
|
G | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+17882G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987340 | ||||||
| chr13:112987497
|
C | T | 2 | a0001c0001t0001g0022a0001c0002t0003g0023 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.79+18039C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987497 | ||||||
| chr13:112987586
|
G | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+18128G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987586 | ||||||
| chr13:112987590
|
T | C | 1 | a0001c0001t0006g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.79+18132T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987590 | ||||||
| chr13:112987787
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.79+18329G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987787 | ||||||
| chr13:112987821
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.79+18363G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987821 | ||||||
| chr13:112987829
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+18371A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987829 | ||||||
| chr13:112987854
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(5): Show | 8 | HG00323.hp1 HG01256.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+18396G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112987854 | ||||||
| chr13:112988159
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79+18701G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988159 | ||||||
| chr13:112988445
|
C | T | 2 | a0001c0001t0023g0018a0001c0003t0002g0064 | 2 | HG01496.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.79+18987C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988445 | ||||||
| chr13:112988458
|
G | C | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+19000G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988458 | ||||||
| chr13:112988482
|
A | G | 3 | a0001c0003t0002g0019a0001c0005t0001g0020a0001c0005t0025g0016 | 3 | HG02074.hp2 HG02129.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+19024A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988482 | ||||||
| chr13:112988490
|
T | TCCTGAGC others(30): Show |
1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.79+19086_79+19122d others(39): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112988490 | |||||
| chr13:112988490
|
TCCTGAGC others(30): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.79+19086_79+19122d others(39): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112988490 | |||||
| chr13:112988556
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19098C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988556 | ||||||
| chr13:112988585
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.79+19127C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988585 | ||||||
| chr13:112988743
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.79+19285G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988743 | ||||||
| chr13:112988806
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+19348C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988806 | ||||||
| chr13:112988847
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19389G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988847 | ||||||
| chr13:112988850
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19392C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988850 | ||||||
| chr13:112988851
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.79+19393A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988851 | ||||||
| chr13:112988869
|
G | A | 3 | a0001c0003t0002g0019a0001c0005t0001g0020a0001c0005t0025g0016 | 3 | HG02074.hp2 HG02129.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+19411G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988869 | ||||||
| chr13:112988870
|
G | C | 3 | a0001c0003t0002g0019a0001c0005t0001g0020a0001c0005t0025g0016 | 3 | HG02074.hp2 HG02129.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+19412G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988870 | ||||||
| chr13:112988876
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19418G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988876 | ||||||
| chr13:112988884
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.79+19426G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988884 | ||||||
| chr13:112988887
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19429C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988887 | ||||||
| chr13:112988906
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19448A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988906 | ||||||
| chr13:112988907
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19449C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988907 | ||||||
| chr13:112988925
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.79+19467G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988925 | ||||||
| chr13:112988950
|
GCTATCAC others(30): Show |
G | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19496_79+19532d others(39): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112988950 | |||||
| chr13:112988954
|
T | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(25): Show | 28 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+19496T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988954 | ||||||
| chr13:112988961
|
T | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(25): Show | 28 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+19503T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988961 | ||||||
| chr13:112988968
|
T | C | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+19510T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988968 | ||||||
| chr13:112988980
|
G | A | 25 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+19522G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988980 | ||||||
| chr13:112988981
|
G | C | 25 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+19523G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988981 | ||||||
| chr13:112988987
|
A | G | 28 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(25): Show | 28 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+19529A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988987 | ||||||
| chr13:112988991
|
C | T | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19533C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988991 | ||||||
| chr13:112988995
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19537A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988995 | ||||||
| chr13:112988998
|
C | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19540C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988998 | ||||||
| chr13:112988998
|
C | T | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19540C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112988998 | ||||||
| chr13:112989016
|
GACATGGA others(28): Show |
G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19559_79+19593d others(37): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989016 | ||||||
| chr13:112989017
|
A | G | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19559A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989017 | ||||||
| chr13:112989018
|
C | G | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19560C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989018 | ||||||
| chr13:112989024
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19566G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989024 | ||||||
| chr13:112989028
|
C | T | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19570C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989028 | ||||||
| chr13:112989032
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19574G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989032 | ||||||
| chr13:112989035
|
C | T | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19577C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989035 | ||||||
| chr13:112989036
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19578A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989036 | ||||||
| chr13:112989053
|
GAC | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19597_79+19598d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112989053 | |||||
| chr13:112989054
|
A | G | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19596A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989054 | ||||||
| chr13:112989055
|
C | G | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19597C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989055 | ||||||
| chr13:112989061
|
G | A | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19603G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989061 | ||||||
| chr13:112989065
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19607C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989065 | ||||||
| chr13:112989069
|
G | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+19611G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989069 | ||||||
| chr13:112989072
|
C | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19614C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989072 | ||||||
| chr13:112989072
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19614C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989072 | ||||||
| chr13:112989072
|
CGAGTCCT others(30): Show |
C | 3 | a0001c0003t0002g0019a0001c0005t0001g0020a0001c0005t0025g0016 | 3 | HG02074.hp2 HG02129.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+19744_79+19780d others(39): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112989072 | |||||
| chr13:112989091
|
G | A | 25 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+19633G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989091 | ||||||
| chr13:112989092
|
G | C | 25 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+19634G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989092 | ||||||
| chr13:112989098
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19640G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989098 | ||||||
| chr13:112989105
|
C | T | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19647C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989105 | ||||||
| chr13:112989106
|
A | G | 25 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+19648A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989106 | ||||||
| chr13:112989109
|
G | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+19651G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989109 | ||||||
| chr13:112989128
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19670G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989128 | ||||||
| chr13:112989128
|
G | C | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19670G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989128 | ||||||
| chr13:112989129
|
G | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19671G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989129 | ||||||
| chr13:112989142
|
C | T | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19684C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989142 | ||||||
| chr13:112989143
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19685A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989143 | ||||||
| chr13:112989146
|
G | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19688G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989146 | ||||||
| chr13:112989165
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.79+19707G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989165 | ||||||
| chr13:112989165
|
G | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19707G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989165 | ||||||
| chr13:112989166
|
G | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19708G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989166 | ||||||
| chr13:112989179
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0063others(25): Show | 28 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+19721C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989179 | ||||||
| chr13:112989180
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.79+19722A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989180 | ||||||
| chr13:112989183
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19725G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989183 | ||||||
| chr13:112989183
|
G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.79+19725G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989183 | ||||||
| chr13:112989202
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19744G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989202 | ||||||
| chr13:112989202
|
G | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0063others(25): Show | 28 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.79+19744G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989202 | ||||||
| chr13:112989203
|
G | C | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19745G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989203 | ||||||
| chr13:112989217
|
A | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19759A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989217 | ||||||
| chr13:112989220
|
G | A | 26 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(23): Show | 26 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.79+19762G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989220 | ||||||
| chr13:112989220
|
G | C | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19762G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989220 | ||||||
| chr13:112989239
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.79+19781A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989239 | ||||||
| chr13:112989246
|
G | A | 2 | a0001c0001t0007g0035a0001c0001t0026g0034 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.79+19788G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989246 | ||||||
| chr13:112989254
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19796G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989254 | ||||||
| chr13:112989257
|
C | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19799C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989257 | ||||||
| chr13:112989257
|
C | G | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19799C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989257 | ||||||
| chr13:112989276
|
A | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19818A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989276 | ||||||
| chr13:112989277
|
C | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19819C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989277 | ||||||
| chr13:112989291
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19833G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989291 | ||||||
| chr13:112989294
|
C | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19836C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989294 | ||||||
| chr13:112989313
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+19855G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989313 | ||||||
| chr13:112989314
|
G | A | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.79+19856G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989314 | ||||||
| chr13:112989314
|
G | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19856G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989314 | ||||||
| chr13:112989320
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.79+19862A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989320 | ||||||
| chr13:112989327
|
C | T | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.79+19869C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989327 | ||||||
| chr13:112989350
|
A | G | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19892A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989350 | ||||||
| chr13:112989351
|
C | G | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19893C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989351 | ||||||
| chr13:112989357
|
G | A | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19899G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989357 | ||||||
| chr13:112989368
|
A | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+19910A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989368 | ||||||
| chr13:112989369
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+19911G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989369 | ||||||
| chr13:112989383
|
C | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19925C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989383 | ||||||
| chr13:112989387
|
G | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+19929G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989387 | ||||||
| chr13:112989388
|
G | C | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+19930G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989388 | ||||||
| chr13:112989394
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+19936G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989394 | ||||||
| chr13:112989396
|
T | C | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19938T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989396 | ||||||
| chr13:112989406
|
G | A | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+19948G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989406 | ||||||
| chr13:112989424
|
A | G | 30 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(27): Show | 30 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.79+19966A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989424 | ||||||
| chr13:112989425
|
C | G | 30 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(27): Show | 30 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.79+19967C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989425 | ||||||
| chr13:112989439
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19981G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989439 | ||||||
| chr13:112989442
|
C | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+19984C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989442 | ||||||
| chr13:112989442
|
CGAGTCCT others(67): Show |
C | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(43): Show | 46 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.79+20003_79+20076d others(76): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112989442 | |||||
| chr13:112989443
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(24): Show | 27 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+19985G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989443 | ||||||
| chr13:112989460
|
GACATGGA others(102): Show |
G | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+20003_79+20111d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989460 | ||||||
| chr13:112989461
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+20003A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989461 | ||||||
| chr13:112989462
|
C | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+20004C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989462 | ||||||
| chr13:112989470
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0041others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+20012C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989470 | ||||||
| chr13:112989476
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+20018G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989476 | ||||||
| chr13:112989478
|
C | T | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+20020C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989478 | ||||||
| chr13:112989479
|
C | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+20021C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989479 | ||||||
| chr13:112989480
|
G | A | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+20022G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989480 | ||||||
| chr13:112989498
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+20040G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989498 | ||||||
| chr13:112989499
|
G | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.79+20041G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989499 | ||||||
| chr13:112989505
|
G | A | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+20047G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989505 | ||||||
| chr13:112989513
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0041others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+20055A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989513 | ||||||
| chr13:112989516
|
G | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0041others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+20058G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989516 | ||||||
| chr13:112989517
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+20059G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989517 | ||||||
| chr13:112989535
|
G | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+20077G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989535 | ||||||
| chr13:112989536
|
G | C | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+20078G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989536 | ||||||
| chr13:112989536
|
GATGGAGC others(30): Show |
G | 26 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0075others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+20092_79+20128d others(39): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112989536 | |||||
| chr13:112989541
|
A | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.79+20083A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989541 | ||||||
| chr13:112989550
|
A | G | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.79+20092A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989550 | ||||||
| chr13:112989552
|
T | C | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.79+20094T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989552 | ||||||
| chr13:112989553
|
G | C | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.79+20095G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989553 | ||||||
| chr13:112989572
|
A | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+20114A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989572 | ||||||
| chr13:112989573
|
C | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+20115C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989573 | ||||||
| chr13:112989579
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0041others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.79+20121G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989579 | ||||||
| chr13:112989653
|
ACTACCAC others(30): Show |
A | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.79+20225_79+20261d others(39): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112989653 | |||||
| chr13:112989661
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+20203A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989661 | ||||||
| chr13:112989697
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+20239C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989697 | ||||||
| chr13:112989698
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.79+20240A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989698 | ||||||
| chr13:112989945
|
G | A | 2 | a0001c0001t0001g0022a0001c0002t0003g0023 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.79+20487G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989945 | ||||||
| chr13:112989959
|
T | A | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.79+20501T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112989959 | ||||||
| chr13:112990183
|
G | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 20 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.79+20725G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990183 | ||||||
| chr13:112990227
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+20769G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990227 | ||||||
| chr13:112990263
|
A | T | 1 | a0001c0008t0004g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.79+20805A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990263 | ||||||
| chr13:112990487
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+21029C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990487 | ||||||
| chr13:112990515
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+21057G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990515 | ||||||
| chr13:112990755
|
C | T | 1 | a0001c0001t0007g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+21297C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990755 | ||||||
| chr13:112990768
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.79+21310C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990768 | ||||||
| chr13:112990857
|
AAGG | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+21402_79+21404d others(5): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112990857 | |||||
| chr13:112990868
|
G | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+21410G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112990868 | ||||||
| chr13:112991162
|
C | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.79+21704C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991162 | ||||||
| chr13:112991204
|
C | G | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.79+21746C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991204 | ||||||
| chr13:112991318
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+21860T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991318 | ||||||
| chr13:112991408
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.79+21950G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991408 | ||||||
| chr13:112991440
|
G | T | 1 | a0001c0002t0005g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.79+21982G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991440 | ||||||
| chr13:112991459
|
A | T | 2 | a0001c0001t0001g0058a0001c0001t0017g0059 | 2 | HG02738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.79+22001A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991459 | ||||||
| chr13:112991718
|
T | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+22260T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991718 | ||||||
| chr13:112991734
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.79+22276G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991734 | ||||||
| chr13:112991776
|
C | T | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.79+22318C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112991776 | ||||||
| chr13:112992315
|
G | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-22448G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992315 | ||||||
| chr13:112992442
|
A | G | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-22321A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992442 | ||||||
| chr13:112992530
|
G | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.80-22233G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992530 | ||||||
| chr13:112992682
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.80-22081A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992682 | ||||||
| chr13:112992724
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80-22039G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992724 | ||||||
| chr13:112992873
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-21890G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992873 | ||||||
| chr13:112992876
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.80-21887A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112992876 | ||||||
| chr13:112993007
|
G | A | 20 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(17): Show | 20 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.80-21756G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112993007 | ||||||
| chr13:112993041
|
G | A | 1 | a0001c0001t0007g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-21722G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112993041 | ||||||
| chr13:112993233
|
C | T | 1 | a0001c0001t0006g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-21530C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112993233 | ||||||
| chr13:112993650
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-21113G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112993650 | ||||||
| chr13:112993729
|
G | A | 1 | a0001c0001t0007g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-21034G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112993729 | ||||||
| chr13:112993884
|
G | T | 1 | a0001c0005t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.80-20879G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112993884 | ||||||
| chr13:112993932
|
TA | T | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-20827delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112993932 | |||||
| chr13:112994026
|
C | T | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.80-20737C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994026 | ||||||
| chr13:112994086
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-20677C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994086 | ||||||
| chr13:112994090
|
G | T | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.80-20673G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994090 | ||||||
| chr13:112994156
|
C | A | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-20607C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994156 | ||||||
| chr13:112994166
|
G | A | 1 | a0001c0003t0002g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80-20597G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994166 | ||||||
| chr13:112994207
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.80-20556G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994207 | ||||||
| chr13:112994209
|
G | A | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-20554G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994209 | ||||||
| chr13:112994212
|
A | G | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.80-20551A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994212 | ||||||
| chr13:112994237
|
A | G | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 52 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.80-20526A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994237 | ||||||
| chr13:112994278
|
C | T | 24 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0045others(21): Show | 24 | HG00323.hp2 HG00544.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-20485C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994278 | ||||||
| chr13:112994292
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80-20471G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994292 | ||||||
| chr13:112994428
|
C | G | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.80-20335C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994428 | ||||||
| chr13:112994435
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 24 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-20328G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994435 | ||||||
| chr13:112994455
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.80-20308G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994455 | ||||||
| chr13:112994714
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-20049C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994714 | ||||||
| chr13:112994722
|
G | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 26 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.80-20041G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994722 | ||||||
| chr13:112994921
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-19842C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994921 | ||||||
| chr13:112994951
|
G | A | 1 | a0001c0002t0015g0007 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.80-19812G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112994951 | ||||||
| chr13:112995170
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-19593G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995170 | ||||||
| chr13:112995180
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-19583C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995180 | ||||||
| chr13:112995276
|
C | T | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.80-19487C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995276 | ||||||
| chr13:112995438
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-19325C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995438 | ||||||
| chr13:112995468
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.80-19295G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995468 | ||||||
| chr13:112995521
|
A | G | 5 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098others(2): Show | 5 | HG01109.hp2 HG02074.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-19242A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995521 | ||||||
| chr13:112995543
|
G | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80-19220G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995543 | ||||||
| chr13:112995672
|
T | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 53 | HG00323.hp1 HG00733.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.80-19091T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995672 | ||||||
| chr13:112995732
|
A | G | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-19031A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995732 | ||||||
| chr13:112995854
|
A | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-18909A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995854 | ||||||
| chr13:112995864
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-18899G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112995864 | ||||||
| chr13:112996103
|
C | T | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-18660C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996103 | ||||||
| chr13:112996108
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-18655G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996108 | ||||||
| chr13:112996419
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.80-18344G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996419 | ||||||
| chr13:112996431
|
C | T | 1 | a0001c0004t0004g0097 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.80-18332C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996431 | ||||||
| chr13:112996564
|
T | C | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-18199T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996564 | ||||||
| chr13:112996636
|
G | T | 1 | a0001c0001t0022g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-18127G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996636 | ||||||
| chr13:112996650
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.80-18113C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996650 | ||||||
| chr13:112996658
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.80-18105T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996658 | ||||||
| chr13:112996801
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0049 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.80-17962G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996801 | ||||||
| chr13:112996806
|
G | A | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-17957G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996806 | ||||||
| chr13:112996818
|
T | C | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.80-17945T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996818 | ||||||
| chr13:112996846
|
A | G | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0094others(18): Show | 21 | HG00733.hp2 HG01175.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.80-17917A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996846 | ||||||
| chr13:112996962
|
G | A | 3 | a0001c0001t0001g0082a0001c0002t0001g0036a0001c0008t0004g0083 | 3 | HG02622.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.80-17801G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112996962 | ||||||
| chr13:112997031
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-17732C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997031 | ||||||
| chr13:112997079
|
G | A | 1 | a0002c0007t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.80-17684G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997079 | ||||||
| chr13:112997126
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.80-17637G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997126 | ||||||
| chr13:112997167
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.80-17596A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997167 | ||||||
| chr13:112997657
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0023g0018 | 2 | HG01070.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.80-17106C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997657 | ||||||
| chr13:112997743
|
T | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-17020T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997743 | ||||||
| chr13:112997755
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0023g0018 | 2 | HG01070.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.80-17008C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997755 | ||||||
| chr13:112997796
|
C | T | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-16967C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997796 | ||||||
| chr13:112997831
|
C | T | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-16932C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997831 | ||||||
| chr13:112997982
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-16781C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112997982 | ||||||
| chr13:112998006
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0026g0034a0001c0001t0028g0098 | 3 | HG01109.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.80-16757G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998006 | ||||||
| chr13:112998055
|
G | A | 7 | a0001c0001t0001g0087a0001c0003t0001g0086a0001c0003t0001g0092others(4): Show | 7 | HG00733.hp2 HG01517.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-16708G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998055 | ||||||
| chr13:112998120
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-16643G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998120 | ||||||
| chr13:112998338
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-16425G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998338 | ||||||
| chr13:112998504
|
G | A | 2 | a0001c0001t0007g0035a0001c0001t0026g0034 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.80-16259G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998504 | ||||||
| chr13:112998726
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-16037G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998726 | ||||||
| chr13:112998917
|
C | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-15846C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112998917 | ||||||
| chr13:112999205
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-15558G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999205 | ||||||
| chr13:112999265
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.80-15498A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999265 | ||||||
| chr13:112999532
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.80-15231A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999532 | ||||||
| chr13:112999559
|
C | G | 3 | a0001c0001t0023g0018a0001c0003t0002g0019a0001c0005t0001g0020 | 3 | HG01496.hp1 HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-15204C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999559 | ||||||
| chr13:112999597
|
G | C | 6 | a0001c0001t0001g0082a0001c0001t0023g0018a0001c0002t0001g0036others(3): Show | 6 | HG01496.hp1 HG02074.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-15166G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999597 | ||||||
| chr13:112999659
|
G | A | 2 | a0001c0001t0007g0035a0001c0001t0026g0034 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.80-15104G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999659 | ||||||
| chr13:112999889
|
C | G | 3 | a0001c0001t0023g0018a0001c0003t0002g0019a0001c0005t0001g0020 | 3 | HG01496.hp1 HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-14874C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999889 | ||||||
| chr13:112999930
|
TGGGAATG others(58): Show |
T | 16 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0002t0002g0093others(13): Show | 16 | HG01175.hp2 HG01243.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-14820_80-14756d others(67): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112999930 | |||||
| chr13:112999943
|
A | G | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-14820A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999943 | ||||||
| chr13:112999949
|
GGGCCCCA others(58): Show |
G | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-14786_80-14722d others(67): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 112999949 | |||||
| chr13:112999986
|
C | T | 1 | a0001c0004t0004g0097 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.80-14777C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 112999986 | ||||||
| chr13:113000008
|
G | A | 3 | a0001c0003t0002g0019a0001c0004t0001g0025a0001c0005t0001g0020 | 3 | HG01891.hp1 HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-14755G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000008 | ||||||
| chr13:113000010
|
CG | C | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-14751delG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113000010 | |||||
| chr13:113000011
|
G | A | 1 | a0001c0001t0007g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-14752G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000011 | ||||||
| chr13:113000012
|
G | T | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-14751G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000012 | ||||||
| chr13:113000014
|
AG | A | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-14747delG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113000014 | |||||
| chr13:113000023
|
A | G | 2 | a0001c0001t0007g0035a0001c0001t0028g0098 | 2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.80-14740A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000023 | ||||||
| chr13:113000025
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(28): Show | 31 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.80-14738T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000025 | ||||||
| chr13:113000204
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0007g0017a0001c0002t0001g0036others(1): Show | 4 | HG02622.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-14559A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000204 | ||||||
| chr13:113000211
|
C | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 28 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-14552C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000211 | ||||||
| chr13:113000695
|
A | G | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-14068A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000695 | ||||||
| chr13:113000707
|
C | T | 3 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.80-14056C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000707 | ||||||
| chr13:113000752
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-14011C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000752 | ||||||
| chr13:113000802
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80-13961G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113000802 | ||||||
| chr13:113000910
|
G | GTGGGTGT others(34): Show |
19 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0002t0002g0093others(16): Show | 19 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.80-13826_80-13825i others(43): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113000910 | |||||
| chr13:113001154
|
C | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-13609C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001154 | ||||||
| chr13:113001247
|
G | A | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.80-13516G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001247 | ||||||
| chr13:113001322
|
A | G | 18 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0002t0002g0093others(15): Show | 18 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-13441A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001322 | ||||||
| chr13:113001590
|
G | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-13173G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001590 | ||||||
| chr13:113001650
|
C | A | 1 | a0001c0006t0002g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.80-13113C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001650 | ||||||
| chr13:113001735
|
C | T | 3 | a0001c0001t0023g0018a0001c0003t0002g0019a0001c0005t0001g0020 | 3 | HG01496.hp1 HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-13028C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001735 | ||||||
| chr13:113001803
|
C | T | 1 | a0001c0003t0002g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.80-12960C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001803 | ||||||
| chr13:113001857
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-12906C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001857 | ||||||
| chr13:113001902
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 57 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.80-12861C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001902 | ||||||
| chr13:113001979
|
C | T | 2 | a0001c0004t0001g0103a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80-12784C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001979 | ||||||
| chr13:113001995
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80-12768G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113001995 | ||||||
| chr13:113002017
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-12746G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113002017 | ||||||
| chr13:113002057
|
G | C | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80-12706G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113002057 | ||||||
| chr13:113002196
|
C | A | 1 | a0001c0001t0003g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-12567C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113002196 | ||||||
| chr13:113002208
|
G | A | 1 | a0001c0001t0003g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-12555G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113002208 | ||||||
| chr13:113002428
|
C | T | 16 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0002t0002g0093others(13): Show | 16 | HG01175.hp2 HG01257.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-12335C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113002428 | ||||||
| chr13:113003004
|
T | TA | 4 | a0001c0001t0001g0038a0001c0002t0005g0060a0001c0003t0002g0019others(1): Show | 4 | HG01070.hp2 HG02074.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-11741dupA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113003004 | |||||
| chr13:113003004
|
TA | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 44 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.80-11741delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113003004 | |||||
| chr13:113003004
|
TAA | T | 5 | a0001c0001t0001g0006a0001c0001t0006g0010a0001c0001t0006g0027others(2): Show | 5 | HG00323.hp1 HG01496.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-11742_80-11741d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113003004 | |||||
| chr13:113003074
|
G | C | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-11689G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003074 | ||||||
| chr13:113003181
|
A | G | 10 | a0001c0001t0001g0082a0001c0001t0007g0017a0001c0001t0007g0035others(7): Show | 10 | HG01109.hp2 HG01496.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-11582A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003181 | ||||||
| chr13:113003251
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0005g0062 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.80-11512G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003251 | ||||||
| chr13:113003288
|
C | G | 2 | a0001c0001t0006g0056a0001c0002t0001g0069 | 2 | HG01168.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.80-11475C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003288 | ||||||
| chr13:113003553
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(55): Show | 58 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.80-11210T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003553 | ||||||
| chr13:113003745
|
G | A | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.80-11018G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003745 | ||||||
| chr13:113003978
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0007g0035a0001c0001t0028g0098 | 3 | HG01070.hp2 HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.80-10785G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113003978 | ||||||
| chr13:113004035
|
G | A | 3 | a0001c0003t0002g0064a0001c0003t0020g0089a0001c0005t0001g0088 | 3 | HG02129.hp2 HG02135.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.80-10728G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004035 | ||||||
| chr13:113004365
|
G | A | 2 | a0001c0004t0001g0103a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80-10398G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004365 | ||||||
| chr13:113004418
|
T | C | 27 | a0001c0001t0001g0082a0001c0001t0001g0094a0001c0001t0003g0099others(24): Show | 27 | HG00544.hp1 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.80-10345T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004418 | ||||||
| chr13:113004419
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-10344G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004419 | ||||||
| chr13:113004452
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0007g0035a0001c0001t0028g0098 | 3 | HG01070.hp2 HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.80-10311C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004452 | ||||||
| chr13:113004540
|
G | T | 1 | a0001c0002t0005g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.80-10223G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004540 | ||||||
| chr13:113004770
|
T | C | 1 | a0001c0006t0002g0029 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.80-9993T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004770 | ||||||
| chr13:113004794
|
G | A | 21 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0001t0023g0018others(18): Show | 21 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.80-9969G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004794 | ||||||
| chr13:113004821
|
C | A | 1 | a0001c0001t0022g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-9942C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113004821 | ||||||
| chr13:113005187
|
G | A | 2 | a0001c0004t0001g0103a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80-9576G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005187 | ||||||
| chr13:113005268
|
A | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(23): Show | 26 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.80-9495A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005268 | ||||||
| chr13:113005297
|
T | C | 2 | a0001c0003t0002g0019a0001c0005t0001g0020 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.80-9466T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005297 | ||||||
| chr13:113005371
|
G | A | 1 | a0001c0006t0002g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.80-9392G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005371 | ||||||
| chr13:113005392
|
G | A | 22 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0001t0007g0035others(19): Show | 22 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-9371G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005392 | ||||||
| chr13:113005435
|
T | C | 1 | a0001c0008t0004g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80-9328T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005435 | ||||||
| chr13:113005478
|
G | A | 2 | a0001c0001t0028g0098a0001c0006t0030g0096 | 2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.80-9285G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005478 | ||||||
| chr13:113005658
|
G | A | 3 | a0001c0001t0007g0035a0001c0001t0023g0018a0001c0005t0001g0020 | 3 | HG01109.hp2 HG01496.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.80-9105G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005658 | ||||||
| chr13:113005732
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80-9031C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005732 | ||||||
| chr13:113005839
|
C | T | 4 | a0001c0001t0007g0035a0001c0001t0023g0018a0001c0003t0002g0019others(1): Show | 4 | HG01109.hp2 HG01496.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8924C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005839 | ||||||
| chr13:113005840
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-8923G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113005840 | ||||||
| chr13:113006060
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.80-8703G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006060 | ||||||
| chr13:113006134
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-8629C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006134 | ||||||
| chr13:113006323
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-8440G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006323 | ||||||
| chr13:113006357
|
C | T | 4 | a0001c0001t0001g0082a0001c0002t0001g0036a0001c0005t0025g0016others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8406C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006357 | ||||||
| chr13:113006506
|
C | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-8257C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006506 | ||||||
| chr13:113006746
|
G | A | 4 | a0001c0001t0001g0082a0001c0002t0001g0036a0001c0005t0025g0016others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8017G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006746 | ||||||
| chr13:113006959
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0005g0062others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-7804G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113006959 | ||||||
| chr13:113007085
|
C | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 48 | HG00323.hp1 HG00544.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.80-7678C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007085 | ||||||
| chr13:113007301
|
G | A | 1 | a0001c0005t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.80-7462G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007301 | ||||||
| chr13:113007313
|
C | A | 1 | a0001c0004t0004g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.80-7450C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007313 | ||||||
| chr13:113007394
|
C | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-7369C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007394 | ||||||
| chr13:113007401
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-7362G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007401 | ||||||
| chr13:113007472
|
G | A | 2 | a0001c0001t0007g0026a0001c0001t0007g0035 | 2 | HG01109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80-7291G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007472 | ||||||
| chr13:113007622
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80-7141C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007622 | ||||||
| chr13:113007863
|
C | T | 12 | a0001c0001t0001g0094a0001c0001t0002g0116a0001c0001t0003g0099others(9): Show | 12 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-6900C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007863 | ||||||
| chr13:113007888
|
G | GT | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.80-6870dupT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113007888 | |||||
| chr13:113007916
|
CT | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 76 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.80-6829delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113007916 | |||||
| chr13:113007916
|
CTT | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0037others(28): Show | 31 | HG01069.hp2 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.80-6830_80-6829del others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113007916 | |||||
| chr13:113007981
|
A | G | 1 | a0001c0004t0003g0009 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.80-6782A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113007981 | ||||||
| chr13:113008037
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.80-6726T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008037 | ||||||
| chr13:113008142
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.80-6621C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008142 | ||||||
| chr13:113008186
|
G | A | 11 | a0001c0001t0003g0099a0001c0001t0006g0108a0001c0001t0007g0017others(8): Show | 11 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-6577G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008186 | ||||||
| chr13:113008213
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-6550C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008213 | ||||||
| chr13:113008257
|
A | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-6506A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008257 | ||||||
| chr13:113008367
|
C | CT | 26 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.80-6395dupT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113008367 | |||||
| chr13:113008368
|
T | C | 1 | a0001c0002t0027g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80-6395T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008368 | ||||||
| chr13:113008630
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(57): Show | 60 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.80-6133A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008630 | ||||||
| chr13:113008694
|
C | T | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80-6069C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008694 | ||||||
| chr13:113008817
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(61): Show | 64 | HG00323.hp2 HG00733.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.80-5946G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008817 | ||||||
| chr13:113008919
|
TGGGCGAG others(56): Show |
T | 2 | a0001c0001t0023g0018a0001c0002t0027g0065 | 2 | HG01496.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.80-5823_80-5761del others(63): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113008919 | |||||
| chr13:113008940
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-5823G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008940 | ||||||
| chr13:113008946
|
C | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-5817C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008946 | ||||||
| chr13:113008958
|
C | T | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.80-5805C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113008958 | ||||||
| chr13:113009007
|
G | C | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-5756G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009007 | ||||||
| chr13:113009195
|
C | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.80-5568C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009195 | ||||||
| chr13:113009213
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.80-5550T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009213 | ||||||
| chr13:113009582
|
A | C | 62 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0045others(59): Show | 62 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.80-5181A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009582 | ||||||
| chr13:113009583
|
T | TC | 101 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.80-5176dupC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113009583 | |||||
| chr13:113009645
|
G | A | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80-5118G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009645 | ||||||
| chr13:113009706
|
G | A | 13 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-5057G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009706 | ||||||
| chr13:113009910
|
A | T | 46 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.80-4853A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113009910 | ||||||
| chr13:113010113
|
A | C | 3 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0010t0021g0015 | 3 | HG01496.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-4650A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010113 | ||||||
| chr13:113010114
|
T | C | 3 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0010t0021g0015 | 3 | HG01496.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-4649T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010114 | ||||||
| chr13:113010115
|
A | AC | 12 | a0001c0001t0001g0024a0001c0001t0018g0077a0001c0001t0023g0018others(9): Show | 12 | HG00544.hp1 HG00544.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-4640dupC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113010115 | |||||
| chr13:113010128
|
G | A | 43 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0045others(40): Show | 43 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.80-4635G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010128 | ||||||
| chr13:113010133
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.80-4630A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010133 | ||||||
| chr13:113010156
|
C | T | 8 | a0001c0001t0001g0024a0001c0002t0027g0065a0001c0004t0001g0102others(5): Show | 8 | HG01175.hp2 HG01257.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-4607C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010156 | ||||||
| chr13:113010171
|
G | A | 3 | a0002c0007t0001g0072a0002c0007t0001g0074a0002c0007t0001g0076 | 3 | HG01978.hp2 NA19066.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.80-4592G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010171 | ||||||
| chr13:113010223
|
A | G | 54 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.80-4540A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010223 | ||||||
| chr13:113010256
|
G | C | 54 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.80-4507G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010256 | ||||||
| chr13:113010443
|
G | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0037others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.80-4320G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010443 | ||||||
| chr13:113010628
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.80-4135C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010628 | ||||||
| chr13:113010646
|
G | A | 13 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-4117G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010646 | ||||||
| chr13:113010691
|
G | A | 9 | a0001c0001t0001g0075a0001c0001t0002g0116a0001c0001t0004g0070others(6): Show | 9 | HG00733.hp1 HG01168.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-4072G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010691 | ||||||
| chr13:113010701
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0002g0008others(3): Show | 6 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-4062C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113010701 | ||||||
| chr13:113011120
|
G | C | 2 | a0001c0002t0001g0036a0001c0008t0004g0083 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.80-3643G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011120 | ||||||
| chr13:113011260
|
G | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3503G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011260 | ||||||
| chr13:113011359
|
G | C | 10 | a0001c0001t0001g0075a0001c0001t0002g0116a0001c0001t0004g0070others(7): Show | 10 | HG00733.hp1 HG01168.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-3404G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011359 | ||||||
| chr13:113011441
|
T | C | 60 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.80-3322T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011441 | ||||||
| chr13:113011468
|
A | G | 61 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 61 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80-3295A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011468 | ||||||
| chr13:113011534
|
T | C | 40 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.80-3229T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011534 | ||||||
| chr13:113011564
|
C | T | 3 | a0001c0004t0004g0084a0001c0004t0004g0097a0001c0016t0004g0085 | 3 | HG01175.hp2 HG01257.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.80-3199C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011564 | ||||||
| chr13:113011626
|
G | GGTGTGGA others(13): Show |
2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-3120_80-3101dup others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011626 | |||||
| chr13:113011630
|
T | TGGACGGT others(157): Show |
3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-3118_80-3117ins others(164): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011630 | |||||
| chr13:113011630
|
T | TGGACGGT others(239): Show |
7 | a0001c0001t0003g0099a0001c0001t0006g0108a0001c0001t0019g0107others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-3118_80-3117ins others(246): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011630 | |||||
| chr13:113011630
|
T | TGGACGGT others(280): Show |
5 | a0001c0001t0001g0094a0001c0003t0001g0086a0001c0005t0001g0079others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-3118_80-3117ins others(287): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011630 | |||||
| chr13:113011631
|
GGACGGTG others(34): Show |
G | 40 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.80-3117_80-3077del others(41): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011631 | |||||
| chr13:113011646
|
A | G | 17 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-3117A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011646 | ||||||
| chr13:113011664
|
T | C | 17 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-3099T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011664 | ||||||
| chr13:113011672
|
A | G | 17 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-3091A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011672 | ||||||
| chr13:113011687
|
G | GGTGTGGA others(198): Show |
1 | a0001c0001t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.80-3011_80-3010ins others(205): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011687 | |||||
| chr13:113011728
|
G | GGTGTGGA others(239): Show |
1 | a0001c0002t0002g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.80-3011_80-3010ins others(246): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011728 | |||||
| chr13:113011753
|
A | C | 17 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-3010A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011753 | ||||||
| chr13:113011787
|
T | C | 57 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.80-2976T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011787 | ||||||
| chr13:113011828
|
T | C | 8 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0018g0077others(5): Show | 8 | HG00544.hp2 HG01109.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-2935T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011828 | ||||||
| chr13:113011836
|
G | A | 1 | a0002c0007t0001g0114 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.80-2927G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011836 | ||||||
| chr13:113011852
|
G | A | 2 | a0001c0006t0002g0029a0001c0006t0009g0028 | 2 | HG01993.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.80-2911G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011852 | ||||||
| chr13:113011869
|
T | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-2894T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011869 | ||||||
| chr13:113011892
|
G | A | 2 | a0001c0002t0001g0036a0001c0008t0004g0083 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.80-2871G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011892 | ||||||
| chr13:113011912
|
T | C | 3 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0010t0021g0015 | 3 | HG01496.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-2851T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011912 | ||||||
| chr13:113011921
|
C | CGGTGGAC others(484): Show |
1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-2823_80-2822ins others(491): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011921 | |||||
| chr13:113011921
|
C | CGGTGGAC others(441): Show |
1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-2823_80-2822ins others(448): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011921 | |||||
| chr13:113011921
|
C | CGGTGGAC others(443): Show |
1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-2823_80-2822ins others(450): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011921 | |||||
| chr13:113011933
|
GGTGTGGA others(401): Show |
G | 32 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(29): Show | 32 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.80-2822_80-2415del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011933 | |||||
| chr13:113011933
|
GGTGTGGA others(647): Show |
G | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0002t0005g0060others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-2822_80-2169del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113011933 | |||||
| chr13:113011941
|
T | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2822T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011941 | ||||||
| chr13:113011949
|
AGGCGGTG others(156): Show |
A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2813_80-2651del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011949 | ||||||
| chr13:113011962
|
G | A | 1 | a0001c0002t0015g0007 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.80-2801G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113011962 | ||||||
| chr13:113012002
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0005g0062 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.80-2761C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012002 | ||||||
| chr13:113012015
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.80-2748G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012015 | ||||||
| chr13:113012054
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80-2709G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012054 | ||||||
| chr13:113012055
|
C | A | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-2708C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012055 | ||||||
| chr13:113012109
|
G | C | 1 | a0001c0004t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.80-2654G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012109 | ||||||
| chr13:113012113
|
A | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2650A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012113 | ||||||
| chr13:113012114
|
G | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2649G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012114 | ||||||
| chr13:113012118
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2645G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012118 | ||||||
| chr13:113012121
|
T | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2642T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012121 | ||||||
| chr13:113012137
|
A | G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2626A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012137 | ||||||
| chr13:113012152
|
C | T | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80-2611C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012152 | ||||||
| chr13:113012178
|
A | G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2585A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012178 | ||||||
| chr13:113012186
|
T | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2577T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012186 | ||||||
| chr13:113012194
|
AGGCGGTG others(115): Show |
A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2568_80-2447del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012194 | ||||||
| chr13:113012213
|
C | T | 3 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0010t0021g0015 | 3 | HG01496.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-2550C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012213 | ||||||
| chr13:113012317
|
A | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2446A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012317 | ||||||
| chr13:113012318
|
G | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2445G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012318 | ||||||
| chr13:113012322
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2441G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012322 | ||||||
| chr13:113012325
|
T | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2438T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012325 | ||||||
| chr13:113012325
|
T | TGGACGGT others(34): Show |
1 | a0001c0001t0008g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.80-2361_80-2321dup others(41): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012325 | |||||
| chr13:113012341
|
A | G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2422A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012341 | ||||||
| chr13:113012349
|
C | T | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80-2414C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012349 | ||||||
| chr13:113012350
|
GGTGGACA others(239): Show |
G | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.80-2381_80-2136del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012350 | |||||
| chr13:113012382
|
A | G | 33 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(30): Show | 33 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.80-2381A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012382 | ||||||
| chr13:113012417
|
A | G | 3 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0010t0021g0015 | 3 | HG01496.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-2346A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012417 | ||||||
| chr13:113012423
|
A | G | 33 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(30): Show | 33 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.80-2340A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012423 | ||||||
| chr13:113012432
|
G | T | 14 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-2331G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012432 | ||||||
| chr13:113012432
|
GGTGGACA others(157): Show |
G | 32 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(29): Show | 32 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.80-2320_80-2157del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012432 | |||||
| chr13:113012443
|
C | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2320C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012443 | ||||||
| chr13:113012444
|
A | G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2319A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012444 | ||||||
| chr13:113012445
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2318G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012445 | ||||||
| chr13:113012452
|
T | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2311T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012452 | ||||||
| chr13:113012461
|
GGTGGTGT others(116): Show |
G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2300_80-2178del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012461 | |||||
| chr13:113012587
|
A | G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-2176A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012587 | ||||||
| chr13:113012596
|
T | G | 28 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.80-2167T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012596 | ||||||
| chr13:113012658
|
G | A | 14 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-2105G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012658 | ||||||
| chr13:113012669
|
GGTGTGGA others(54): Show |
G | 29 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0052others(26): Show | 29 | HG00323.hp2 HG00544.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.80-2074_80-2014del others(61): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012669 | |||||
| chr13:113012687
|
TGCAGTGT others(13): Show |
T | 11 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 11 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2074_80-2055del others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012687 | |||||
| chr13:113012711
|
G | A | 11 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 11 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2052G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012711 | ||||||
| chr13:113012714
|
T | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 11 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2049T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012714 | ||||||
| chr13:113012730
|
A | G | 11 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050others(8): Show | 11 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2033A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012730 | ||||||
| chr13:113012730
|
AGTGTGGA others(157): Show |
A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-1917_80-1754del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012730 | |||||
| chr13:113012738
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-2025C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012738 | ||||||
| chr13:113012771
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.80-1992G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012771 | ||||||
| chr13:113012791
|
TGATGCGG others(75): Show |
T | 3 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0010t0021g0015 | 3 | HG01496.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80-1890_80-1809del others(82): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012791 | |||||
| chr13:113012796
|
C | CGGACGGT others(279): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80-1891_80-1890ins others(286): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012796 | |||||
| chr13:113012796
|
C | CGGACGGT others(279): Show |
13 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(10): Show | 13 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-1891_80-1890ins others(286): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012796 | |||||
| chr13:113012832
|
TGATGCGG others(34): Show |
T | 37 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(34): Show | 37 | HG00323.hp2 HG00544.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.80-1890_80-1850del others(41): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012832 | |||||
| chr13:113012873
|
A | T | 19 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(16): Show | 19 | HG00544.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-1890A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012873 | ||||||
| chr13:113012873
|
AGATGCGG others(34): Show |
A | 1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.80-1794_80-1754del others(41): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113012873 | |||||
| chr13:113012961
|
G | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0063others(5): Show | 8 | HG00733.hp1 HG01069.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-1802G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012961 | ||||||
| chr13:113012964
|
C | T | 1 | a0001c0005t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.80-1799C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113012964 | ||||||
| chr13:113013012
|
C | A | 1 | a0001c0004t0004g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.80-1751C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113013012 | ||||||
| chr13:113013076
|
G | A | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80-1687G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113013076 | ||||||
| chr13:113013168
|
CAGAGAGG others(14): Show |
C | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.80-1592_80-1572del others(21): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | 113013168 | |||||
| chr13:113013418
|
G | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0037others(59): Show | 62 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.80-1345G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113013418 | ||||||
| chr13:113013506
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-1257C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113013506 | ||||||
| chr13:113013657
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-1106G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113013657 | ||||||
| chr13:113013966
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.80-797A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113013966 | ||||||
| chr13:113014038
|
G | C | 15 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.80-725G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113014038 | ||||||
| chr13:113014478
|
C | A | 2 | a0001c0006t0030g0096a0001c0008t0003g0039 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.80-285C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113014478 | ||||||
| chr13:113014747
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0006g0027 | 2 | HG02486.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80-16T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 1/29 | chr13 | 113014747 | ||||||
| chr13:113014897
|
G | A | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.163+51G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113014897 | ||||||
| chr13:113014905
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+59C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113014905 | ||||||
| chr13:113014959
|
G | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+113G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113014959 | ||||||
| chr13:113015350
|
T | C | 60 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.163+504T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015350 | ||||||
| chr13:113015466
|
G | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.163+620G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015466 | ||||||
| chr13:113015472
|
G | A | 40 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.163+626G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015472 | ||||||
| chr13:113015519
|
C | T | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.163+673C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015519 | ||||||
| chr13:113015521
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163+675G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015521 | ||||||
| chr13:113015560
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(14): Show | 17 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+714G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015560 | ||||||
| chr13:113015935
|
C | T | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.163+1089C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113015935 | ||||||
| chr13:113016040
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(17): Show | 20 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.163+1194C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016040 | ||||||
| chr13:113016303
|
C | G | 4 | a0001c0003t0002g0019a0001c0003t0002g0064a0001c0003t0020g0089others(1): Show | 4 | HG02074.hp2 HG02129.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+1457C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016303 | ||||||
| chr13:113016333
|
G | A | 39 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(36): Show | 39 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.163+1487G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016333 | ||||||
| chr13:113016559
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163+1713G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016559 | ||||||
| chr13:113016587
|
G | C | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+1741G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016587 | ||||||
| chr13:113016588
|
A | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(69): Show | 72 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.163+1742A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016588 | ||||||
| chr13:113016629
|
GC | G | 40 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.163+1788delC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113016629 | |||||
| chr13:113016634
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.163+1788C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016634 | ||||||
| chr13:113016656
|
C | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.163+1810C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016656 | ||||||
| chr13:113016711
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.163+1865C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016711 | ||||||
| chr13:113016734
|
C | T | 1 | a0001c0013t0001g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163+1888C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016734 | ||||||
| chr13:113016762
|
G | T | 1 | a0001c0001t0008g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.163+1916G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016762 | ||||||
| chr13:113016875
|
G | A | 1 | a0001c0008t0003g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+2029G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016875 | ||||||
| chr13:113016952
|
T | G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.163+2106T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113016952 | ||||||
| chr13:113017007
|
T | C | 1 | a0001c0004t0004g0097 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163+2161T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113017007 | ||||||
| chr13:113017030
|
C | G | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+2184C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113017030 | ||||||
| chr13:113017050
|
A | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0038others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.163+2204A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113017050 | ||||||
| chr13:113017158
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.163+2312C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113017158 | ||||||
| chr13:113017911
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(71): Show | 74 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.163+3065T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113017911 | ||||||
| chr13:113017917
|
C | T | 1 | a0001c0001t0004g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163+3071C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113017917 | ||||||
| chr13:113018038
|
A | C | 14 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0001t0003g0099others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.163+3192A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018038 | ||||||
| chr13:113018063
|
A | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+3217A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018063 | ||||||
| chr13:113018163
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.163+3317C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018163 | ||||||
| chr13:113018221
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+3375C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018221 | ||||||
| chr13:113018232
|
C | A | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+3386C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018232 | ||||||
| chr13:113018393
|
C | T | 57 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.163+3547C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018393 | ||||||
| chr13:113018508
|
T | C | 40 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.163+3662T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018508 | ||||||
| chr13:113018580
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.163+3734G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018580 | ||||||
| chr13:113018648
|
A | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+3802A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018648 | ||||||
| chr13:113018689
|
G | A | 40 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.163+3843G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113018689 | ||||||
| chr13:113019086
|
C | T | 58 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.163+4240C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019086 | ||||||
| chr13:113019274
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+4428A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019274 | ||||||
| chr13:113019299
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(64): Show | 67 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.163+4453G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019299 | ||||||
| chr13:113019349
|
A | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.163+4503A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019349 | ||||||
| chr13:113019381
|
G | A | 58 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.163+4535G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019381 | ||||||
| chr13:113019428
|
C | T | 58 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.163+4582C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019428 | ||||||
| chr13:113019631
|
T | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.163+4785T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019631 | ||||||
| chr13:113019638
|
A | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+4792A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019638 | ||||||
| chr13:113019685
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0005g0062 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.163+4839G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019685 | ||||||
| chr13:113019770
|
G | A | 2 | a0001c0006t0030g0096a0001c0008t0003g0039 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.164-4874G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113019770 | ||||||
| chr13:113020245
|
G | A | 57 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.164-4399G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020245 | ||||||
| chr13:113020262
|
C | T | 57 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.164-4382C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020262 | ||||||
| chr13:113020316
|
G | A | 57 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.164-4328G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020316 | ||||||
| chr13:113020378
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-4266G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020378 | ||||||
| chr13:113020466
|
C | T | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.164-4178C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020466 | ||||||
| chr13:113020523
|
C | T | 1 | a0001c0001t0008g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.164-4121C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020523 | ||||||
| chr13:113020524
|
G | A | 1 | a0001c0008t0003g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-4120G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020524 | ||||||
| chr13:113020750
|
C | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.164-3894C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020750 | ||||||
| chr13:113020780
|
CTGTGTGT others(9): Show |
C | 13 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-3852_164-3837d others(18): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113020780 | |||||
| chr13:113020796
|
A | C | 4 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-3848A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020796 | ||||||
| chr13:113020820
|
C | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.164-3824C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020820 | ||||||
| chr13:113020821
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.164-3823G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020821 | ||||||
| chr13:113020836
|
T | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(47): Show | 50 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.164-3808T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020836 | ||||||
| chr13:113020868
|
ATGTGTGT others(11): Show |
A | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3770_164-3753d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113020868 | |||||
| chr13:113020924
|
A | AGC | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.164-3719_164-3718i others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113020924 | |||||
| chr13:113020926
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-3718T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020926 | ||||||
| chr13:113020935
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-3709A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020935 | ||||||
| chr13:113020956
|
T | A | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.164-3688T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113020956 | ||||||
| chr13:113021011
|
CTGTA | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3630_164-3627d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113021011 | |||||
| chr13:113021044
|
GTGTGTA | G | 35 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(32): Show | 35 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.164-3598_164-3593d others(8): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113021044 | |||||
| chr13:113021066
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3578A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021066 | ||||||
| chr13:113021073
|
T | C | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.164-3571T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021073 | ||||||
| chr13:113021152
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3492G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021152 | ||||||
| chr13:113021178
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-3466G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021178 | ||||||
| chr13:113021282
|
C | CTGTGTGT others(9): Show |
59 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(56): Show | 59 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-3358_164-3343d others(18): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113021282 | |||||
| chr13:113021339
|
C | T | 3 | a0001c0003t0002g0019a0001c0003t0002g0064a0001c0003t0020g0089 | 3 | HG02074.hp2 HG02129.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.164-3305C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021339 | ||||||
| chr13:113021436
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3208G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021436 | ||||||
| chr13:113021446
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3198A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021446 | ||||||
| chr13:113021488
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-3156C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021488 | ||||||
| chr13:113021608
|
C | T | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.164-3036C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021608 | ||||||
| chr13:113021654
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.164-2990C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021654 | ||||||
| chr13:113021824
|
GAAGA | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-2814_164-2811d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113021824 | |||||
| chr13:113021861
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-2783T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021861 | ||||||
| chr13:113021934
|
G | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-2710G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021934 | ||||||
| chr13:113021944
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0086others(3): Show | 6 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-2700G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113021944 | ||||||
| chr13:113022092
|
G | A | 1 | a0001c0015t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164-2552G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022092 | ||||||
| chr13:113022112
|
G | A | 1 | a0001c0001t0008g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.164-2532G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022112 | ||||||
| chr13:113022318
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.164-2326C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022318 | ||||||
| chr13:113022382
|
C | T | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.164-2262C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022382 | ||||||
| chr13:113022481
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0086others(2): Show | 5 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-2163C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022481 | ||||||
| chr13:113022487
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0086others(3): Show | 6 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-2157C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022487 | ||||||
| chr13:113022546
|
C | A | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.164-2098C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022546 | ||||||
| chr13:113022566
|
G | A | 8 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0001t0006g0108others(5): Show | 8 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-2078G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022566 | ||||||
| chr13:113022587
|
G | T | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.164-2057G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022587 | ||||||
| chr13:113022648
|
C | T | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.164-1996C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022648 | ||||||
| chr13:113022656
|
C | G | 3 | a0001c0001t0008g0061a0001c0001t0008g0066a0001c0008t0003g0044 | 3 | HG02572.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.164-1988C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022656 | ||||||
| chr13:113022721
|
G | A | 2 | a0001c0002t0005g0060a0001c0015t0001g0013 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.164-1923G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022721 | ||||||
| chr13:113022856
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0086others(2): Show | 5 | HG01346.hp2 HG01358.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1788G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022856 | ||||||
| chr13:113022929
|
G | C | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.164-1715G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022929 | ||||||
| chr13:113022956
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.164-1688A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113022956 | ||||||
| chr13:113023022
|
A | G | 3 | a0001c0001t0008g0061a0001c0001t0008g0066a0001c0008t0003g0044 | 3 | HG02572.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.164-1622A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023022 | ||||||
| chr13:113023096
|
C | T | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.164-1548C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023096 | ||||||
| chr13:113023134
|
G | A | 9 | a0001c0004t0001g0102a0001c0004t0004g0084a0001c0004t0004g0097others(6): Show | 9 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-1510G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023134 | ||||||
| chr13:113023156
|
C | T | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.164-1488C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023156 | ||||||
| chr13:113023226
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.164-1418C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023226 | ||||||
| chr13:113023307
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.164-1337G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023307 | ||||||
| chr13:113023363
|
C | G | 10 | a0001c0002t0027g0065a0001c0004t0001g0102a0001c0004t0004g0084others(7): Show | 10 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-1281C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023363 | ||||||
| chr13:113023475
|
A | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(68): Show | 71 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.164-1169A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023475 | ||||||
| chr13:113023514
|
G | A | 2 | a0001c0006t0030g0096a0001c0008t0003g0039 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.164-1130G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023514 | ||||||
| chr13:113023581
|
G | A | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.164-1063G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113023581 | ||||||
| chr13:113024025
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-619T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113024025 | ||||||
| chr13:113024032
|
C | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.164-612C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113024032 | ||||||
| chr13:113024037
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0075others(13): Show | 16 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-607G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113024037 | ||||||
| chr13:113024049
|
G | A | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.164-595G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113024049 | ||||||
| chr13:113024203
|
G | T | 1 | a0001c0001t0018g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.164-441G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113024203 | ||||||
| chr13:113024352
|
T | TA | 47 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0051others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.164-286dupA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | 113024352 | |||||
| chr13:113024516
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-128T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 2/29 | chr13 | 113024516 | ||||||
| chr13:113024875
|
T | C | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+117T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024875 | ||||||
| chr13:113024876
|
G | A | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+118G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024876 | ||||||
| chr13:113024879
|
A | ATGCAGTC others(155): Show |
2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+123_278+124ins others(162): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024879 | |||||
| chr13:113024879
|
A | ATGCGGTC others(155): Show |
1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.278+123_278+124ins others(162): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024879 | |||||
| chr13:113024904
|
GGGCAGAG others(209): Show |
G | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.278+210_278+425del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024904 | |||||
| chr13:113024930
|
A | G | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+172A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024930 | ||||||
| chr13:113024936
|
C | G | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+178C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024936 | ||||||
| chr13:113024936
|
CGGTCCCC others(1181): Show |
C | 1 | a0001c0004t0004g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.278+199_278+1386de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024936 | |||||
| chr13:113024957
|
A | AGGGCAGA others(209): Show |
1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.278+222_278+223ins others(216): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024957 | |||||
| chr13:113024957
|
A | AGGGCAGA others(209): Show |
43 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(40): Show | 43 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.278+222_278+223ins others(216): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024957 | |||||
| chr13:113024957
|
A | G | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+199A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024957 | ||||||
| chr13:113024968
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+210T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024968 | ||||||
| chr13:113024970
|
T | C | 6 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+212T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024970 | ||||||
| chr13:113024981
|
A | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+223A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024981 | ||||||
| chr13:113024982
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+224T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024982 | ||||||
| chr13:113024986
|
G | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+228G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113024986 | ||||||
| chr13:113024986
|
GGTGGGGT others(209): Show |
G | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+252_278+467del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113024986 | |||||
| chr13:113025006
|
G | C | 1 | a0001c0003t0002g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.278+248G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025006 | ||||||
| chr13:113025010
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(56): Show | 59 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.278+252T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025010 | ||||||
| chr13:113025019
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(58): Show | 61 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.278+261A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025019 | ||||||
| chr13:113025022
|
T | C | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+264T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025022 | ||||||
| chr13:113025026
|
T | G | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+268T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025026 | ||||||
| chr13:113025035
|
A | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+277A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025035 | ||||||
| chr13:113025036
|
T | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+278T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025036 | ||||||
| chr13:113025038
|
A | G | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+280A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025038 | ||||||
| chr13:113025040
|
G | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+282G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025040 | ||||||
| chr13:113025041
|
G | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+283G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025041 | ||||||
| chr13:113025064
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.278+306C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025064 | ||||||
| chr13:113025073
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+315G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025073 | ||||||
| chr13:113025076
|
C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+318C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025076 | ||||||
| chr13:113025078
|
T | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+320T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025078 | ||||||
| chr13:113025084
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(58): Show | 61 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.278+326A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025084 | ||||||
| chr13:113025087
|
T | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+329T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025087 | ||||||
| chr13:113025089
|
A | C | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+331A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025089 | ||||||
| chr13:113025090
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+332C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025090 | ||||||
| chr13:113025093
|
G | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(58): Show | 61 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.278+335G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025093 | ||||||
| chr13:113025094
|
G | T | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+336G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025094 | ||||||
| chr13:113025098
|
GGGTCCCT others(47): Show |
G | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+347_278+400del others(54): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025098 | |||||
| chr13:113025105
|
T | C | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+347T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025105 | ||||||
| chr13:113025107
|
C | T | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+349C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025107 | ||||||
| chr13:113025108
|
A | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+350A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025108 | ||||||
| chr13:113025111
|
T | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+353T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025111 | ||||||
| chr13:113025112
|
A | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+354A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025112 | ||||||
| chr13:113025117
|
A | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+359A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025117 | ||||||
| chr13:113025118
|
T | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+360T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025118 | ||||||
| chr13:113025120
|
A | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+362A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025120 | ||||||
| chr13:113025120
|
AGGCAGAG others(101): Show |
A | 4 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0092others(1): Show | 4 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+388_278+495del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025120 | |||||
| chr13:113025130
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+372C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025130 | ||||||
| chr13:113025132
|
T | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+374T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025132 | ||||||
| chr13:113025138
|
A | G | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+380A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025138 | ||||||
| chr13:113025143
|
C | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+385C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025143 | ||||||
| chr13:113025144
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+386C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025144 | ||||||
| chr13:113025145
|
C | T | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+387C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025145 | ||||||
| chr13:113025146
|
A | G | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+388A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025146 | ||||||
| chr13:113025146
|
A | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+388A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025146 | ||||||
| chr13:113025148
|
C | G | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+390C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025148 | ||||||
| chr13:113025148
|
C | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+390C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025148 | ||||||
| chr13:113025149
|
A | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+391A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025149 | ||||||
| chr13:113025152
|
C | G | 51 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.278+394C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025152 | ||||||
| chr13:113025160
|
G | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+402G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025160 | ||||||
| chr13:113025164
|
C | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+406C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025164 | ||||||
| chr13:113025165
|
T | G | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+407T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025165 | ||||||
| chr13:113025171
|
T | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+413T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025171 | ||||||
| chr13:113025171
|
T | TTGGGGCA others(47): Show |
3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+413_278+414ins others(54): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025171 | ||||||
| chr13:113025173
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(58): Show | 61 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.278+415A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025173 | ||||||
| chr13:113025184
|
C | T | 5 | a0001c0001t0007g0017a0001c0004t0005g0011a0001c0004t0005g0012others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.278+426C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025184 | ||||||
| chr13:113025192
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+434G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025192 | ||||||
| chr13:113025197
|
C | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+439C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025197 | ||||||
| chr13:113025198
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+440C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025198 | ||||||
| chr13:113025201
|
T | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+443T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025201 | ||||||
| chr13:113025201
|
T | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+443T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025201 | ||||||
| chr13:113025202
|
T | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+444T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025202 | ||||||
| chr13:113025203
|
G | A | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+445G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025203 | ||||||
| chr13:113025213
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+455C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025213 | ||||||
| chr13:113025215
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+457T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025215 | ||||||
| chr13:113025216
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+458G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025216 | ||||||
| chr13:113025219
|
T | C | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+461T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025219 | ||||||
| chr13:113025220
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+462G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025220 | ||||||
| chr13:113025225
|
T | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.278+467T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025225 | ||||||
| chr13:113025226
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+468C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025226 | ||||||
| chr13:113025227
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+469G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025227 | ||||||
| chr13:113025228
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+470G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025228 | ||||||
| chr13:113025238
|
C | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+480C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025238 | ||||||
| chr13:113025246
|
A | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+488A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025246 | ||||||
| chr13:113025249
|
T | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+491T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025249 | ||||||
| chr13:113025251
|
C | A | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+493C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025251 | ||||||
| chr13:113025252
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+494C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025252 | ||||||
| chr13:113025253
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(56): Show | 59 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.278+495C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025253 | ||||||
| chr13:113025254
|
G | A | 7 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(4): Show | 7 | HG01109.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.278+496G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025254 | ||||||
| chr13:113025254
|
G | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+496G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025254 | ||||||
| chr13:113025256
|
C | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+498C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025256 | ||||||
| chr13:113025256
|
C | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+498C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025256 | ||||||
| chr13:113025257
|
A | G | 7 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0004t0005g0011others(4): Show | 7 | HG01515.hp1 HG01517.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+499A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025257 | ||||||
| chr13:113025260
|
G | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+502G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025260 | ||||||
| chr13:113025268
|
G | A | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+510G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025268 | ||||||
| chr13:113025273
|
T | G | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+515T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025273 | ||||||
| chr13:113025279
|
T | A | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+521T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025279 | ||||||
| chr13:113025280
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.278+522C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025280 | ||||||
| chr13:113025281
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.278+523A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025281 | ||||||
| chr13:113025288
|
AGTCTCCG others(20): Show |
A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+534_278+560del others(27): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025288 | |||||
| chr13:113025292
|
T | C | 49 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.278+534T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025292 | ||||||
| chr13:113025294
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.278+536C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025294 | ||||||
| chr13:113025296
|
T | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+538T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025296 | ||||||
| chr13:113025300
|
G | A | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+542G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025300 | ||||||
| chr13:113025305
|
A | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+547A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025305 | ||||||
| chr13:113025306
|
T | C | 49 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.278+548T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025306 | ||||||
| chr13:113025309
|
T | G | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+551T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025309 | ||||||
| chr13:113025310
|
G | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+552G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025310 | ||||||
| chr13:113025321
|
C | T | 48 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.278+563C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025321 | ||||||
| chr13:113025323
|
T | C | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+565T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025323 | ||||||
| chr13:113025324
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+566G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025324 | ||||||
| chr13:113025328
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+570G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025328 | ||||||
| chr13:113025331
|
G | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+573G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025331 | ||||||
| chr13:113025333
|
T | A | 48 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.278+575T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025333 | ||||||
| chr13:113025334
|
C | CGGGGCAG others(47): Show |
2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+587_278+588ins others(54): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025334 | |||||
| chr13:113025334
|
C | CGGGTCAG others(47): Show |
1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.278+579_278+580ins others(54): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025334 | |||||
| chr13:113025334
|
C | T | 50 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.278+576C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025334 | ||||||
| chr13:113025336
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+578G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025336 | ||||||
| chr13:113025343
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+585G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025343 | ||||||
| chr13:113025346
|
T | C | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+588T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025346 | ||||||
| chr13:113025354
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+596G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025354 | ||||||
| chr13:113025357
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+599T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025357 | ||||||
| chr13:113025358
|
C | CCCT | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+600_278+601ins others(3): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025358 | ||||||
| chr13:113025359
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(17): Show | 20 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.278+601G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025359 | ||||||
| chr13:113025359
|
G | C | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+601G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025359 | ||||||
| chr13:113025359
|
GTCATGGT others(47): Show |
G | 1 | a0001c0001t0001g0005 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.278+714_278+767del others(54): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025359 | |||||
| chr13:113025360
|
T | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(16): Show | 19 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.278+602T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025360 | ||||||
| chr13:113025362
|
ATGG | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+608_278+610del others(3): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025362 | |||||
| chr13:113025364
|
G | T | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+606G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025364 | ||||||
| chr13:113025375
|
C | T | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+617C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025375 | ||||||
| chr13:113025381
|
T | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+623T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025381 | ||||||
| chr13:113025382
|
G | T | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+624G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025382 | ||||||
| chr13:113025387
|
T | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(16): Show | 19 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.278+629T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025387 | ||||||
| chr13:113025388
|
C | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+630C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025388 | ||||||
| chr13:113025393
|
C | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+635C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025393 | ||||||
| chr13:113025397
|
G | A | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.278+639G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025397 | ||||||
| chr13:113025400
|
T | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(16): Show | 19 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.278+642T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025400 | ||||||
| chr13:113025404
|
T | G | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+646T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025404 | ||||||
| chr13:113025408
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+650G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025408 | ||||||
| chr13:113025411
|
T | C | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+653T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025411 | ||||||
| chr13:113025413
|
A | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(16): Show | 19 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.278+655A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025413 | ||||||
| chr13:113025413
|
A | G | 2 | a0001c0001t0023g0018a0001c0004t0001g0103 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.278+655A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025413 | ||||||
| chr13:113025414
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.278+656T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025414 | ||||||
| chr13:113025416
|
A | ACTG | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+658_278+659ins others(3): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025416 | ||||||
| chr13:113025416
|
A | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+658A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025416 | ||||||
| chr13:113025417
|
T | G | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+659T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025417 | ||||||
| chr13:113025418
|
G | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+660G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025418 | ||||||
| chr13:113025418
|
G | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.278+660G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025418 | ||||||
| chr13:113025419
|
G | C | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+661G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025419 | ||||||
| chr13:113025419
|
G | GGGTCCCT others(44): Show |
2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+661_278+662ins others(51): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025419 | ||||||
| chr13:113025426
|
C | A | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+668C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025426 | ||||||
| chr13:113025429
|
C | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+671C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025429 | ||||||
| chr13:113025430
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.278+672G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025430 | ||||||
| chr13:113025434
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0092 | 3 | HG01346.hp2 HG01358.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+676C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025434 | ||||||
| chr13:113025435
|
T | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+677T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025435 | ||||||
| chr13:113025441
|
T | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+683T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025441 | ||||||
| chr13:113025454
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+696T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025454 | ||||||
| chr13:113025462
|
G | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(2): Show | 5 | HG01109.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+704G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025462 | ||||||
| chr13:113025465
|
T | C | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+707T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025465 | ||||||
| chr13:113025467
|
A | C | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+709A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025467 | ||||||
| chr13:113025468
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(65): Show | 68 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.278+710T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025468 | ||||||
| chr13:113025471
|
T | G | 4 | a0001c0003t0001g0086a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01515.hp1 HG01517.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+713T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025471 | ||||||
| chr13:113025472
|
G | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+714G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025472 | ||||||
| chr13:113025472
|
G | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+714G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025472 | ||||||
| chr13:113025473
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+715G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025473 | ||||||
| chr13:113025473
|
G | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+715G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025473 | ||||||
| chr13:113025476
|
G | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+718G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025476 | ||||||
| chr13:113025482
|
C | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+724C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025482 | ||||||
| chr13:113025483
|
C | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+725C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025483 | ||||||
| chr13:113025485
|
T | C | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+727T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025485 | ||||||
| chr13:113025486
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+728G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025486 | ||||||
| chr13:113025490
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+732G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025490 | ||||||
| chr13:113025495
|
T | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+737T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025495 | ||||||
| chr13:113025495
|
T | TTGGGGCA others(20): Show |
3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+737_278+738ins others(27): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025495 | ||||||
| chr13:113025496
|
C | T | 49 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.278+738C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025496 | ||||||
| chr13:113025497
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+739G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025497 | ||||||
| chr13:113025498
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+740G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025498 | ||||||
| chr13:113025508
|
T | C | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+750T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025508 | ||||||
| chr13:113025516
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+758G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025516 | ||||||
| chr13:113025519
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+761T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025519 | ||||||
| chr13:113025521
|
A | C | 49 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.278+763A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025521 | ||||||
| chr13:113025522
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(62): Show | 65 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.278+764T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025522 | ||||||
| chr13:113025523
|
C | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+765C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025523 | ||||||
| chr13:113025524
|
A | G | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+766A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025524 | ||||||
| chr13:113025526
|
C | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(18): Show | 21 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.278+768C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025526 | ||||||
| chr13:113025526
|
C | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+768C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025526 | ||||||
| chr13:113025527
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+769G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025527 | ||||||
| chr13:113025537
|
C | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+779C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025537 | ||||||
| chr13:113025544
|
G | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+786G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025544 | ||||||
| chr13:113025549
|
T | A | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+791T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025549 | ||||||
| chr13:113025550
|
T | C | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.278+792T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025550 | ||||||
| chr13:113025558
|
AGTCTCTG others(20): Show |
A | 2 | a0001c0001t0001g0002a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.278+804_278+830del others(27): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025558 | |||||
| chr13:113025558
|
AGTCTCTG others(128): Show |
A | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+804_278+938del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025558 | |||||
| chr13:113025558
|
AGTCTCTG others(236): Show |
A | 2 | a0001c0001t0001g0024a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.278+804_278+1046de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025558 | |||||
| chr13:113025558
|
AGTCTCTG others(344): Show |
A | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.278+804_278+1154de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025558 | |||||
| chr13:113025566
|
G | T | 52 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(49): Show | 52 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.278+808G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025566 | ||||||
| chr13:113025573
|
T | C | 5 | a0001c0001t0007g0017a0001c0003t0001g0086a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+815T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025573 | ||||||
| chr13:113025576
|
T | C | 49 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.278+818T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025576 | ||||||
| chr13:113025579
|
T | G | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+821T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025579 | ||||||
| chr13:113025580
|
G | A | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+822G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025580 | ||||||
| chr13:113025581
|
G | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+823G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025581 | ||||||
| chr13:113025588
|
C | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+830C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025588 | ||||||
| chr13:113025590
|
C | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+832C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025590 | ||||||
| chr13:113025591
|
C | T | 2 | a0001c0001t0001g0002a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.278+833C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025591 | ||||||
| chr13:113025592
|
G | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+834G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025592 | ||||||
| chr13:113025597
|
T | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+839T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025597 | ||||||
| chr13:113025601
|
G | A | 2 | a0001c0001t0001g0002a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.278+843G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025601 | ||||||
| chr13:113025603
|
T | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0045others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+845T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025603 | ||||||
| chr13:113025604
|
C | T | 2 | a0001c0001t0001g0002a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.278+846C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025604 | ||||||
| chr13:113025616
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0045others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.278+858C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025616 | ||||||
| chr13:113025627
|
T | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+869T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025627 | ||||||
| chr13:113025629
|
C | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+871C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025629 | ||||||
| chr13:113025632
|
ATTGTGGG others(316): Show |
A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+875_278+1197de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025632 | ||||||
| chr13:113025633
|
T | C | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+875T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025633 | ||||||
| chr13:113025634
|
TGTGGGGT others(209): Show |
T | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+887_278+1102de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025634 | |||||
| chr13:113025635
|
G | A | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+877G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025635 | ||||||
| chr13:113025645
|
T | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+887T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025645 | ||||||
| chr13:113025645
|
TGCAACTA others(155): Show |
T | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.278+889_278+1050de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025645 | |||||
| chr13:113025647
|
C | T | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+889C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025647 | ||||||
| chr13:113025648
|
A | G | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+890A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025648 | ||||||
| chr13:113025651
|
T | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+893T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025651 | ||||||
| chr13:113025652
|
A | G | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+894A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025652 | ||||||
| chr13:113025652
|
A | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+894A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025652 | ||||||
| chr13:113025658
|
T | C | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+900T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025658 | ||||||
| chr13:113025660
|
A | G | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+902A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025660 | ||||||
| chr13:113025670
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+912C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025670 | ||||||
| chr13:113025678
|
A | G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+920A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025678 | ||||||
| chr13:113025681
|
T | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+923T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025681 | ||||||
| chr13:113025683
|
C | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+925C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025683 | ||||||
| chr13:113025685
|
T | C | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+927T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025685 | ||||||
| chr13:113025686
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+928G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025686 | ||||||
| chr13:113025686
|
G | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+928G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025686 | ||||||
| chr13:113025688
|
C | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+930C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025688 | ||||||
| chr13:113025688
|
C | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+930C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025688 | ||||||
| chr13:113025689
|
A | G | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+931A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025689 | ||||||
| chr13:113025699
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+941C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025699 | ||||||
| chr13:113025700
|
G | A | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+942G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025700 | ||||||
| chr13:113025705
|
T | G | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+947T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025705 | ||||||
| chr13:113025709
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+951G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025709 | ||||||
| chr13:113025711
|
T | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.278+953T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025711 | ||||||
| chr13:113025712
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+954C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025712 | ||||||
| chr13:113025724
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+966C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025724 | ||||||
| chr13:113025732
|
A | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.278+974A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025732 | ||||||
| chr13:113025735
|
T | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+977T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025735 | ||||||
| chr13:113025737
|
A | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+979A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025737 | ||||||
| chr13:113025741
|
G | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.278+983G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025741 | ||||||
| chr13:113025742
|
G | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+984G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025742 | ||||||
| chr13:113025743
|
G | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+985G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025743 | ||||||
| chr13:113025752
|
C | CCGTGACC others(49): Show |
2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+994_278+995ins others(56): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025752 | ||||||
| chr13:113025752
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+994C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025752 | ||||||
| chr13:113025753
|
T | C | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+995T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025753 | ||||||
| chr13:113025754
|
GCA | G | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+997_278+998del others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025754 | ||||||
| chr13:113025755
|
C | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+997C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025755 | ||||||
| chr13:113025756
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.278+998A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025756 | ||||||
| chr13:113025759
|
T | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1001T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025759 | ||||||
| chr13:113025760
|
A | G | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+1002A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025760 | ||||||
| chr13:113025760
|
A | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+1002A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025760 | ||||||
| chr13:113025765
|
A | T | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+1007A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025765 | ||||||
| chr13:113025766
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.278+1008T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025766 | ||||||
| chr13:113025768
|
A | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.278+1010A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025768 | ||||||
| chr13:113025778
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1020C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025778 | ||||||
| chr13:113025786
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1028A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025786 | ||||||
| chr13:113025789
|
T | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1031T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025789 | ||||||
| chr13:113025791
|
C | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1033C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025791 | ||||||
| chr13:113025791
|
C | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1033C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025791 | ||||||
| chr13:113025793
|
T | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(56): Show | 59 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.278+1035T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025793 | ||||||
| chr13:113025794
|
G | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.278+1036G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025794 | ||||||
| chr13:113025794
|
G | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1036G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025794 | ||||||
| chr13:113025796
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+1038C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025796 | ||||||
| chr13:113025796
|
C | G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+1038C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025796 | ||||||
| chr13:113025796
|
C | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1038C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025796 | ||||||
| chr13:113025797
|
A | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.278+1039A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025797 | ||||||
| chr13:113025807
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.278+1049C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025807 | ||||||
| chr13:113025808
|
G | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1050G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025808 | ||||||
| chr13:113025809
|
T | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1051T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025809 | ||||||
| chr13:113025813
|
T | G | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1055T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025813 | ||||||
| chr13:113025814
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.278+1056G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025814 | ||||||
| chr13:113025817
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.278+1059G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025817 | ||||||
| chr13:113025819
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0037others(2): Show | 5 | HG01346.hp2 HG01358.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1061T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025819 | ||||||
| chr13:113025820
|
C | T | 50 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.278+1062C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025820 | ||||||
| chr13:113025832
|
T | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1074T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025832 | ||||||
| chr13:113025836
|
T | G | 4 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1078T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025836 | ||||||
| chr13:113025843
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.278+1085T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025843 | ||||||
| chr13:113025845
|
A | C | 46 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1087A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025845 | ||||||
| chr13:113025846
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(56): Show | 59 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.278+1088T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025846 | ||||||
| chr13:113025849
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1091T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025849 | ||||||
| chr13:113025850
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.278+1092G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025850 | ||||||
| chr13:113025850
|
G | T | 46 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1092G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025850 | ||||||
| chr13:113025851
|
G | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1093G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025851 | ||||||
| chr13:113025858
|
C | A | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1100C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025858 | ||||||
| chr13:113025860
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1102C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025860 | ||||||
| chr13:113025861
|
C | T | 46 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1103C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025861 | ||||||
| chr13:113025862
|
G | A | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1104G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025862 | ||||||
| chr13:113025868
|
G | T | 46 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1110G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025868 | ||||||
| chr13:113025873
|
T | A | 46 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0038others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1115T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025873 | ||||||
| chr13:113025875
|
G | A | 1 | a0001c0003t0002g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.278+1117G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025875 | ||||||
| chr13:113025879
|
C | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1121C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025879 | ||||||
| chr13:113025886
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.278+1128C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025886 | ||||||
| chr13:113025890
|
T | G | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1132T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025890 | ||||||
| chr13:113025894
|
G | A | 5 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(2): Show | 5 | HG01109.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1136G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025894 | ||||||
| chr13:113025897
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.278+1139T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025897 | ||||||
| chr13:113025899
|
C | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.278+1141C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025899 | ||||||
| chr13:113025899
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1141C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025899 | ||||||
| chr13:113025900
|
C | T | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1142C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025900 | ||||||
| chr13:113025902
|
A | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+1144A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025902 | ||||||
| chr13:113025902
|
A | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1144A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025902 | ||||||
| chr13:113025903
|
T | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0045others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1145T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025903 | ||||||
| chr13:113025904
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.278+1146T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025904 | ||||||
| chr13:113025904
|
T | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+1146T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025904 | ||||||
| chr13:113025904
|
T | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.278+1146T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025904 | ||||||
| chr13:113025905
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+1147G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025905 | ||||||
| chr13:113025905
|
G | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0045others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1147G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025905 | ||||||
| chr13:113025905
|
G | GTGGGGTC others(101): Show |
3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1169_278+1170i others(110): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113025905 | |||||
| chr13:113025914
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.278+1156C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025914 | ||||||
| chr13:113025915
|
C | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1157C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025915 | ||||||
| chr13:113025917
|
T | C | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0002c0017t0001g0109 | 3 | HG01346.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1159T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025917 | ||||||
| chr13:113025918
|
G | A | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1160G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025918 | ||||||
| chr13:113025922
|
G | A | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1164G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025922 | ||||||
| chr13:113025925
|
G | A | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.278+1167G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025925 | ||||||
| chr13:113025927
|
T | A | 2 | a0001c0003t0001g0092a0002c0017t0001g0109 | 2 | HG01346.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+1169T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025927 | ||||||
| chr13:113025928
|
C | T | 4 | a0001c0003t0001g0092a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG01346.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1170C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025928 | ||||||
| chr13:113025930
|
G | A | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1172G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025930 | ||||||
| chr13:113025940
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+1182C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025940 | ||||||
| chr13:113025948
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+1190A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025948 | ||||||
| chr13:113025951
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(54): Show | 57 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.278+1193T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025951 | ||||||
| chr13:113025953
|
C | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.278+1195C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025953 | ||||||
| chr13:113025954
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+1196C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025954 | ||||||
| chr13:113025955
|
C | T | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1197C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025955 | ||||||
| chr13:113025956
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.278+1198G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025956 | ||||||
| chr13:113025957
|
T | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.278+1199T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025957 | ||||||
| chr13:113025958
|
C | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.278+1200C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025958 | ||||||
| chr13:113025958
|
C | T | 3 | a0001c0003t0001g0092a0001c0004t0005g0011a0001c0004t0005g0012 | 3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+1200C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025958 | ||||||
| chr13:113025958
|
CA | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+1201delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025958 | ||||||
| chr13:113025959
|
A | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+1201A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025959 | ||||||
| chr13:113025959
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0045others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.278+1201A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025959 | ||||||
| chr13:113025968
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0037 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.278+1210C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025968 | ||||||
| chr13:113025969
|
C | T | 3 | a0001c0003t0001g0092a0001c0004t0005g0011a0001c0004t0005g0012 | 3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+1211C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025969 | ||||||
| chr13:113025976
|
G | T | 3 | a0001c0003t0001g0092a0001c0004t0005g0011a0001c0004t0005g0012 | 3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+1218G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025976 | ||||||
| chr13:113025981
|
T | A | 3 | a0001c0003t0001g0092a0001c0004t0005g0011a0001c0004t0005g0012 | 3 | HG01515.hp1 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+1223T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025981 | ||||||
| chr13:113025982
|
C | T | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+1224C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025982 | ||||||
| chr13:113025987
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1229C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025987 | ||||||
| chr13:113025993
|
C | CCCTGTGA others(261): Show |
3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1235_278+1236i others(270): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025993 | ||||||
| chr13:113025996
|
C | CCT | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1238_278+1239i others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025996 | ||||||
| chr13:113025996
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.278+1238C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113025996 | ||||||
| chr13:113026005
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.278+1247T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026005 | ||||||
| chr13:113026007
|
A | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1249A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026007 | ||||||
| chr13:113026008
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.278+1250T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026008 | ||||||
| chr13:113026011
|
T | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.278+1253T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026011 | ||||||
| chr13:113026012
|
G | A | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.278+1254G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026012 | ||||||
| chr13:113026012
|
G | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1254G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026012 | ||||||
| chr13:113026013
|
G | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+1255G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026013 | ||||||
| chr13:113026022
|
C | T | 2 | a0001c0003t0001g0092a0003c0009t0011g0101 | 2 | HG01243.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.278+1264C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026022 | ||||||
| chr13:113026023
|
C | T | 46 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.278+1265C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026023 | ||||||
| chr13:113026024
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+1266G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026024 | ||||||
| chr13:113026029
|
T | C | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1271T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026029 | ||||||
| chr13:113026030
|
G | T | 44 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1272G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026030 | ||||||
| chr13:113026035
|
T | A | 45 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.278+1277T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026035 | ||||||
| chr13:113026048
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+1290C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026048 | ||||||
| chr13:113026056
|
A | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.278+1298A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026056 | ||||||
| chr13:113026059
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(59): Show | 62 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.278+1301T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026059 | ||||||
| chr13:113026061
|
C | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(59): Show | 62 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.278+1303C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026061 | ||||||
| chr13:113026061
|
C | CCCGTCGT others(101): Show |
3 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015 | 3 | HG02486.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1305_278+1306i others(110): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113026061 | |||||
| chr13:113026065
|
T | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+1307T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026065 | ||||||
| chr13:113026066
|
C | A | 47 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.278+1308C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026066 | ||||||
| chr13:113026066
|
C | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.278+1308C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026066 | ||||||
| chr13:113026066
|
C | T | 1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1308C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026066 | ||||||
| chr13:113026067
|
A | ATGGGGTC others(425): Show |
1 | a0002c0017t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278+1311_278+1312i others(434): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113026067 | |||||
| chr13:113026067
|
A | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+1309A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026067 | ||||||
| chr13:113026067
|
A | G | 49 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0049others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.278+1309A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026067 | ||||||
| chr13:113026070
|
C | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.278+1312C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026070 | ||||||
| chr13:113026070
|
CGGTCCCC others(47): Show |
C | 1 | a0001c0001t0004g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.278+1355_278+1408d others(56): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113026070 | |||||
| chr13:113026076
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0086others(1): Show | 4 | HG01346.hp2 HG01358.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1318C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026076 | ||||||
| chr13:113026078
|
G | A | 3 | a0001c0001t0001g0037a0001c0003t0001g0086a0004c0011t0002g0090 | 3 | HG01346.hp2 NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.278+1320G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026078 | ||||||
| chr13:113026090
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1332C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026090 | ||||||
| chr13:113026091
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0002g0008others(9): Show | 12 | HG00323.hp1 HG01069.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.278+1333G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026091 | ||||||
| chr13:113026110
|
G | A | 15 | a0001c0001t0001g0094a0001c0001t0003g0099a0001c0001t0006g0108others(12): Show | 15 | HG01175.hp2 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.278+1352G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026110 | ||||||
| chr13:113026113
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.278+1355T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026113 | ||||||
| chr13:113026115
|
A | C | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1357A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026115 | ||||||
| chr13:113026116
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(63): Show | 66 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.278+1358T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026116 | ||||||
| chr13:113026119
|
T | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.278+1361T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026119 | ||||||
| chr13:113026120
|
G | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1362G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026120 | ||||||
| chr13:113026121
|
G | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.278+1363G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026121 | ||||||
| chr13:113026130
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(57): Show | 60 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.278+1372C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026130 | ||||||
| chr13:113026131
|
C | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1373C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026131 | ||||||
| chr13:113026132
|
G | A | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.278+1374G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026132 | ||||||
| chr13:113026138
|
G | T | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1380G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026138 | ||||||
| chr13:113026143
|
T | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.278+1385T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026143 | ||||||
| chr13:113026253
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0003t0001g0086others(3): Show | 6 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.278+1495G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026253 | ||||||
| chr13:113026419
|
T | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+1661T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026419 | ||||||
| chr13:113026448
|
G | A | 2 | a0001c0001t0008g0061a0001c0008t0003g0044 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.278+1690G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026448 | ||||||
| chr13:113026491
|
C | T | 2 | a0001c0002t0001g0040a0001c0002t0002g0003 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.278+1733C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026491 | ||||||
| chr13:113026531
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.278+1773T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026531 | ||||||
| chr13:113026547
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0007g0017a0001c0005t0025g0016others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1789A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026547 | ||||||
| chr13:113026568
|
G | A | 2 | a0001c0001t0002g0048a0001c0002t0001g0071 | 2 | HG01361.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.278+1810G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026568 | ||||||
| chr13:113026604
|
G | C | 4 | a0001c0001t0007g0017a0001c0005t0025g0016a0001c0010t0021g0015others(1): Show | 4 | HG01243.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1846G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026604 | ||||||
| chr13:113026635
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+1877G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026635 | ||||||
| chr13:113026659
|
A | C | 3 | a0001c0001t0007g0017a0001c0005t0025g0016a0003c0009t0011g0101 | 3 | HG01243.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+1901A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026659 | ||||||
| chr13:113026663
|
C | T | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.278+1905C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026663 | ||||||
| chr13:113026668
|
A | G | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.278+1910A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026668 | ||||||
| chr13:113026685
|
C | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0037others(4): Show | 7 | HG01243.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.278+1927C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026685 | ||||||
| chr13:113026762
|
A | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(68): Show | 71 | HG00323.hp2 HG00544.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.278+2004A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026762 | ||||||
| chr13:113026929
|
C | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0033others(53): Show | 56 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.278+2171C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026929 | ||||||
| chr13:113026953
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.278+2195C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113026953 | ||||||
| chr13:113027081
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0023g0018a0001c0004t0001g0103 | 3 | HG01496.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+2323A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113027081 | ||||||
| chr13:113027086
|
G | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.278+2328G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113027086 | ||||||
| chr13:113027337
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278+2579G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113027337 | ||||||
| chr13:113027704
|
A | G | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278+2946A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113027704 | ||||||
| chr13:113027932
|
T | C | 20 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0063others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.278+3174T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113027932 | ||||||
| chr13:113028003
|
CT | C | 6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+3246delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028003 | ||||||
| chr13:113028008
|
G | A | 1 | a0001c0001t0026g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.278+3250G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028008 | ||||||
| chr13:113028474
|
C | G | 4 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(1): Show | 4 | HG01358.hp1 HG01517.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+3716C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028474 | ||||||
| chr13:113028541
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.278+3783C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028541 | ||||||
| chr13:113028602
|
A | G | 2 | a0001c0001t0007g0017a0001c0005t0025g0016 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+3844A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028602 | ||||||
| chr13:113028656
|
A | C | 6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+3898A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028656 | ||||||
| chr13:113028731
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+3973A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113028731 | ||||||
| chr13:113029151
|
A | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.278+4393A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113029151 | ||||||
| chr13:113029395
|
C | T | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+4637C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113029395 | ||||||
| chr13:113029547
|
G | A | 1 | a0001c0001t0006g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.278+4789G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113029547 | ||||||
| chr13:113029658
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.278+4900G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113029658 | ||||||
| chr13:113029703
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.278+4945G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113029703 | ||||||
| chr13:113030019
|
A | G | 2 | a0001c0005t0032g0106a0003c0009t0011g0101 | 2 | HG01243.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.278+5261A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030019 | ||||||
| chr13:113030021
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.278+5263G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030021 | ||||||
| chr13:113030153
|
A | C | 10 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(7): Show | 10 | HG01346.hp1 HG01358.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.278+5395A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030153 | ||||||
| chr13:113030279
|
A | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+5521A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030279 | ||||||
| chr13:113030306
|
C | T | 11 | a0001c0001t0001g0024a0001c0001t0007g0017a0001c0003t0001g0086others(8): Show | 11 | HG01346.hp1 HG01358.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.278+5548C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030306 | ||||||
| chr13:113030310
|
C | CGGTGTGA others(23): Show |
20 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.278+5558_278+5559i others(32): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113030310 | |||||
| chr13:113030310
|
C | CGGTGTGG others(23): Show |
5 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0005t0025g0016others(2): Show | 5 | HG01496.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.278+5561_278+5562i others(32): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113030310 | |||||
| chr13:113030310
|
C | CGGTGTGG others(23): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+5561_278+5562i others(32): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113030310 | |||||
| chr13:113030353
|
T | A | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+5595T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030353 | ||||||
| chr13:113030365
|
T | C | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.278+5607T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030365 | ||||||
| chr13:113030365
|
T | TGACGCAG others(23): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+5615_278+5644d others(32): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113030365 | |||||
| chr13:113030395
|
C | T | 4 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.278+5637C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030395 | ||||||
| chr13:113030459
|
C | T | 1 | a0001c0002t0027g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+5701C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030459 | ||||||
| chr13:113030547
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+5789C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030547 | ||||||
| chr13:113030605
|
G | A | 26 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.278+5847G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030605 | ||||||
| chr13:113030796
|
A | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+6038A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030796 | ||||||
| chr13:113030814
|
C | T | 19 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.278+6056C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030814 | ||||||
| chr13:113030954
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+6196G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030954 | ||||||
| chr13:113030983
|
G | A | 28 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.278+6225G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113030983 | ||||||
| chr13:113031028
|
GAGACAGA others(21): Show |
G | 26 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.278+6308_278+6335d others(30): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031028 | |||||
| chr13:113031038
|
G | C | 3 | a0001c0004t0004g0084a0001c0004t0004g0097a0001c0016t0004g0085 | 3 | HG01175.hp2 HG01257.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.278+6280G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031038 | ||||||
| chr13:113031148
|
GAGAGACA others(22): Show |
G | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+6394_278+6422d others(31): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031148 | |||||
| chr13:113031174
|
TGACA | T | 10 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(7): Show | 10 | HG01346.hp1 HG01358.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.278+6423_278+6426d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031174 | |||||
| chr13:113031189
|
G | GAC | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+6432_278+6433i others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031189 | |||||
| chr13:113031205
|
C | CAGAGACA others(9): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+6459_278+6474d others(18): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031205 | |||||
| chr13:113031205
|
C | G | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+6447C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031205 | ||||||
| chr13:113031236
|
GAGAC | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.278+6482_278+6485d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031236 | |||||
| chr13:113031258
|
GAGAC | G | 3 | a0001c0001t0006g0108a0001c0001t0019g0107a0003c0009t0011g0101 | 3 | HG01243.hp1 HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.278+6512_278+6515d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031258 | |||||
| chr13:113031304
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.278+6546G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031304 | ||||||
| chr13:113031340
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.278+6582A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031340 | ||||||
| chr13:113031374
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+6616G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031374 | ||||||
| chr13:113031394
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.278+6636G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031394 | ||||||
| chr13:113031418
|
G | A | 6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+6660G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031418 | ||||||
| chr13:113031456
|
C | T | 6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+6698C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031456 | ||||||
| chr13:113031518
|
C | G | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+6760C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031518 | ||||||
| chr13:113031569
|
A | AGGGTGGA others(11): Show |
1 | a0001c0002t0027g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278+6824_278+6841d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031569 | |||||
| chr13:113031627
|
G | A | 1 | a0001c0008t0004g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.278+6869G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031627 | ||||||
| chr13:113031644
|
C | T | 6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+6886C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031644 | ||||||
| chr13:113031711
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0063others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.278+6953G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031711 | ||||||
| chr13:113031800
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7042C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031800 | ||||||
| chr13:113031801
|
A | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7043A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031801 | ||||||
| chr13:113031802
|
T | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7044T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031802 | ||||||
| chr13:113031818
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7060C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031818 | ||||||
| chr13:113031844
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7086C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031844 | ||||||
| chr13:113031866
|
CCA | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.278+7131_278+7132d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031866 | |||||
| chr13:113031866
|
CCACA | C | 13 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0001t0007g0017others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.278+7129_278+7132d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031866 | |||||
| chr13:113031866
|
CCACACAC others(1): Show |
C | 10 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(7): Show | 10 | HG01346.hp1 HG01358.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.278+7125_278+7132d others(10): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113031866 | |||||
| chr13:113031895
|
C | T | 22 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.278+7137C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031895 | ||||||
| chr13:113031915
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7157C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031915 | ||||||
| chr13:113031917
|
T | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7159T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031917 | ||||||
| chr13:113031923
|
T | C | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7165T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031923 | ||||||
| chr13:113031925
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7167C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031925 | ||||||
| chr13:113031928
|
A | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7170A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031928 | ||||||
| chr13:113031939
|
C | G | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+7181C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031939 | ||||||
| chr13:113031942
|
G | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7184G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031942 | ||||||
| chr13:113031949
|
A | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7191A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031949 | ||||||
| chr13:113031950
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7192C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031950 | ||||||
| chr13:113031962
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(14): Show | 17 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.278+7204G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031962 | ||||||
| chr13:113031974
|
A | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7216A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031974 | ||||||
| chr13:113031991
|
C | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7233C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031991 | ||||||
| chr13:113031992
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7234C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031992 | ||||||
| chr13:113031994
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7236C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031994 | ||||||
| chr13:113031995
|
C | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7237C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031995 | ||||||
| chr13:113031996
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+7238C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113031996 | ||||||
| chr13:113032056
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+7298G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032056 | ||||||
| chr13:113032060
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(76): Show | 79 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.278+7302A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032060 | ||||||
| chr13:113032256
|
C | T | 1 | a0001c0005t0001g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.278+7498C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032256 | ||||||
| chr13:113032565
|
A | G | 6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+7807A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032565 | ||||||
| chr13:113032571
|
T | A | 3 | a0001c0001t0007g0017a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+7813T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032571 | ||||||
| chr13:113032731
|
G | A | 3 | a0001c0001t0007g0017a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+7973G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032731 | ||||||
| chr13:113032829
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.278+8071A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032829 | ||||||
| chr13:113032947
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.278+8189G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032947 | ||||||
| chr13:113032964
|
T | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8206T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032964 | ||||||
| chr13:113032978
|
G | GTGACGTG others(101): Show |
2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8223_278+8224i others(110): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113032978 | |||||
| chr13:113032982
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(76): Show | 79 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.278+8224T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032982 | ||||||
| chr13:113032987
|
G | T | 2 | a0001c0002t0001g0071a0001c0002t0016g0054 | 2 | HG01361.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.278+8229G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032987 | ||||||
| chr13:113032991
|
C | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8233C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032991 | ||||||
| chr13:113032995
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8237C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032995 | ||||||
| chr13:113032996
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+8238G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113032996 | ||||||
| chr13:113033000
|
T | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8242T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033000 | ||||||
| chr13:113033027
|
A | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8269A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033027 | ||||||
| chr13:113033031
|
C | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+8273C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033031 | ||||||
| chr13:113033035
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8277G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033035 | ||||||
| chr13:113033035
|
G | GCGTGAGT others(29): Show |
2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8291_278+8292i others(38): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033035 | |||||
| chr13:113033037
|
G | A | 2 | a0001c0003t0002g0047a0001c0004t0001g0102 | 2 | HG02074.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.278+8279G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033037 | ||||||
| chr13:113033050
|
A | G | 3 | a0001c0004t0001g0102a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.278+8292A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033050 | ||||||
| chr13:113033050
|
ATGACGTG others(137): Show |
A | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+8309_278+8452d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033050 | |||||
| chr13:113033054
|
C | CGTGAGTG others(281): Show |
1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8308_278+8309i others(290): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033054 | |||||
| chr13:113033072
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8314C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033072 | ||||||
| chr13:113033086
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8328G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033086 | ||||||
| chr13:113033091
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.278+8333A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033091 | ||||||
| chr13:113033100
|
T | C | 3 | a0001c0004t0001g0102a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.278+8342T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033100 | ||||||
| chr13:113033101
|
G | C | 3 | a0001c0004t0001g0102a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.278+8343G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033101 | ||||||
| chr13:113033126
|
T | C | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8368T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033126 | ||||||
| chr13:113033135
|
C | T | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8377C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033135 | ||||||
| chr13:113033139
|
C | CGTGACGT others(11): Show |
1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8386_278+8387i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033139 | |||||
| chr13:113033139
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8381C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033139 | ||||||
| chr13:113033140
|
G | A | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8382G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033140 | ||||||
| chr13:113033153
|
A | C | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8395A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033153 | ||||||
| chr13:113033158
|
G | A | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8400G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033158 | ||||||
| chr13:113033161
|
G | A | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8403G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033161 | ||||||
| chr13:113033176
|
A | G | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8418A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033176 | ||||||
| chr13:113033180
|
C | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8422C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033180 | ||||||
| chr13:113033189
|
A | C | 3 | a0001c0004t0001g0102a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.278+8431A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033189 | ||||||
| chr13:113033194
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8436G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033194 | ||||||
| chr13:113033198
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.278+8440C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033198 | ||||||
| chr13:113033216
|
C | T | 4 | a0001c0001t0023g0018a0001c0004t0001g0103a0001c0005t0025g0016others(1): Show | 4 | HG01496.hp1 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+8458C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033216 | ||||||
| chr13:113033217
|
A | G | 20 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.278+8459A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033217 | ||||||
| chr13:113033217
|
ATGAGTGG others(11): Show |
A | 1 | a0001c0004t0003g0009 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.278+8477_278+8494d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033217 | |||||
| chr13:113033219
|
G | GAGTGGCC others(227): Show |
10 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(7): Show | 10 | HG01346.hp1 HG01358.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.278+8488_278+8489i others(236): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033219 | |||||
| chr13:113033219
|
G | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8461G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033219 | ||||||
| chr13:113033226
|
C | T | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8468C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033226 | ||||||
| chr13:113033230
|
G | GTGACGTG others(531): Show |
1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+8488_278+8489i others(540): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033230 | |||||
| chr13:113033233
|
A | ACGTGAGT others(11): Show |
1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+8492_278+8493i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033233 | |||||
| chr13:113033235
|
G | A | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8477G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033235 | ||||||
| chr13:113033247
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0001t0007g0017others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.278+8489C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033247 | ||||||
| chr13:113033247
|
CGTGACAT others(29): Show |
C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+8529_278+8564d others(38): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033247 | |||||
| chr13:113033252
|
C | CGTGAGTG others(407): Show |
1 | a0001c0003t0001g0073 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.278+8494_278+8495i others(416): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033252 | ||||||
| chr13:113033252
|
C | CGTGAGTG others(533): Show |
1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.278+8494_278+8495i others(542): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033252 | ||||||
| chr13:113033252
|
C | CGTGAGTG others(533): Show |
50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(47): Show | 50 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.278+8494_278+8495i others(542): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033252 | ||||||
| chr13:113033252
|
C | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+8494C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033252 | ||||||
| chr13:113033253
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.278+8495A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033253 | ||||||
| chr13:113033255
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.278+8497T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033255 | ||||||
| chr13:113033261
|
A | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.278+8503A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033261 | ||||||
| chr13:113033269
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.278+8511G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033269 | ||||||
| chr13:113033269
|
G | GCGTGAGT others(47): Show |
1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278+8524_278+8525i others(56): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033269 | |||||
| chr13:113033269
|
G | GCGTGAGT others(11): Show |
1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+8524_278+8525i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033269 | |||||
| chr13:113033270
|
C | CATGAGTG others(137): Show |
6 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+8512_278+8513i others(146): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033270 | ||||||
| chr13:113033283
|
T | C | 20 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.278+8525T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033283 | ||||||
| chr13:113033284
|
G | A | 13 | a0001c0001t0001g0024a0001c0001t0007g0026a0001c0001t0007g0035others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.278+8526G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033284 | ||||||
| chr13:113033287
|
A | G | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+8529A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033287 | ||||||
| chr13:113033288
|
C | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+8530C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033288 | ||||||
| chr13:113033289
|
A | G | 15 | a0001c0001t0001g0024a0001c0001t0007g0026a0001c0001t0007g0035others(12): Show | 15 | HG01109.hp2 HG01346.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.278+8531A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033289 | ||||||
| chr13:113033291
|
T | G | 21 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.278+8533T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033291 | ||||||
| chr13:113033297
|
A | C | 21 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.278+8539A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033297 | ||||||
| chr13:113033305
|
G | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.278+8547G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033305 | ||||||
| chr13:113033306
|
C | CGTGAGTG others(29): Show |
2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8560_278+8561i others(38): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033306 | |||||
| chr13:113033306
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0007g0026a0001c0001t0007g0035others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.278+8548C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033306 | ||||||
| chr13:113033307
|
G | A | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+8549G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033307 | ||||||
| chr13:113033309
|
G | GAGTGGCC others(335): Show |
1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8560_278+8561i others(344): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033309 | |||||
| chr13:113033309
|
G | T | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+8551G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033309 | ||||||
| chr13:113033315
|
C | A | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+8557C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033315 | ||||||
| chr13:113033315
|
C | CCCCCGTG others(101): Show |
1 | a0001c0008t0004g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.278+8560_278+8561i others(110): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033315 | |||||
| chr13:113033319
|
T | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.278+8561T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033319 | ||||||
| chr13:113033323
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.278+8565G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033323 | ||||||
| chr13:113033323
|
G | C | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+8565G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033323 | ||||||
| chr13:113033324
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+8566C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033324 | ||||||
| chr13:113033337
|
C | T | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8579C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033337 | ||||||
| chr13:113033341
|
ACATTAGT others(11): Show |
A | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+8585_278+8602d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033341 | |||||
| chr13:113033345
|
TAGTGGAC others(47): Show |
T | 1 | a0002c0007t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.278+8616_278+8669d others(56): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033345 | |||||
| chr13:113033356
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.278+8598G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033356 | ||||||
| chr13:113033359
|
G | A | 2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8601G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033359 | ||||||
| chr13:113033359
|
G | GCGTGAGT others(11): Show |
16 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+8614_278+8615i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033359 | |||||
| chr13:113033361
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.278+8603G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033361 | ||||||
| chr13:113033374
|
G | A | 2 | a0001c0001t0007g0017a0001c0005t0032g0106 | 2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.278+8616G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033374 | ||||||
| chr13:113033378
|
C | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+8620C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033378 | ||||||
| chr13:113033381
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+8623G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033381 | ||||||
| chr13:113033391
|
C | CGTGACGT others(11): Show |
1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.278+8637_278+8638i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033391 | |||||
| chr13:113033396
|
T | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.278+8638T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033396 | ||||||
| chr13:113033399
|
G | GAGTGGCC others(767): Show |
1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8646_278+8647i others(776): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033399 | |||||
| chr13:113033399
|
G | GAGTGGCC others(191): Show |
1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+8646_278+8647i others(200): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033399 | |||||
| chr13:113033399
|
G | GAGTGGCC others(47): Show |
3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.278+8646_278+8647i others(56): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033399 | |||||
| chr13:113033399
|
G | GAGTGGCC others(47): Show |
53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.278+8646_278+8647i others(56): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033399 | |||||
| chr13:113033399
|
G | GAGTGGCC others(29): Show |
2 | a0001c0004t0001g0103a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.278+8646_278+8647i others(38): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033399 | |||||
| chr13:113033423
|
C | CCCCTGTG others(11): Show |
17 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.278+8668_278+8669i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033423 | |||||
| chr13:113033428
|
A | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.278+8670A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033428 | ||||||
| chr13:113033431
|
A | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.278+8673A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033431 | ||||||
| chr13:113033432
|
T | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.278+8674T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033432 | ||||||
| chr13:113033446
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.278+8688G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033446 | ||||||
| chr13:113033463
|
C | T | 3 | a0001c0001t0007g0017a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.278+8705C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033463 | ||||||
| chr13:113033467
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.278+8709G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033467 | ||||||
| chr13:113033468
|
C | T | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.278+8710C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033468 | ||||||
| chr13:113033503
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+8745G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033503 | ||||||
| chr13:113033615
|
T | C | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+8857T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033615 | ||||||
| chr13:113033630
|
AT | A | 2 | a0001c0001t0007g0017a0001c0005t0032g0106 | 2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.278+8875delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033630 | |||||
| chr13:113033636
|
C | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.278+8878C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033636 | ||||||
| chr13:113033788
|
A | G | 2 | a0001c0001t0023g0018a0001c0005t0025g0016 | 2 | HG01496.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278+9030A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033788 | ||||||
| chr13:113033802
|
G | A | 1 | a0001c0003t0001g0086 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.278+9044G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033802 | ||||||
| chr13:113033819
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.278+9061G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033819 | ||||||
| chr13:113033914
|
A | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(77): Show | 80 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.278+9156A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033914 | ||||||
| chr13:113033955
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+9197G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033955 | ||||||
| chr13:113033962
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.278+9204G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113033962 | ||||||
| chr13:113033972
|
TC | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.278+9220delC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113033972 | |||||
| chr13:113034002
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.278+9244C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034002 | ||||||
| chr13:113034135
|
C | CT | 34 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(31): Show | 34 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.278+9396dupT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034135 | |||||
| chr13:113034135
|
C | CTT | 30 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0033others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.278+9395_278+9396d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034135 | |||||
| chr13:113034135
|
CT | C | 5 | a0001c0001t0004g0070a0001c0003t0001g0073a0001c0004t0001g0103others(2): Show | 5 | HG01168.hp1 HG01243.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.278+9396delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034135 | |||||
| chr13:113034397
|
A | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0005g0062others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+9639A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034397 | ||||||
| chr13:113034432
|
C | G | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.278+9674C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034432 | ||||||
| chr13:113034495
|
TTATGCTG others(34): Show |
T | 1 | a0001c0001t0018g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.278+9738_278+9778d others(43): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034495 | ||||||
| chr13:113034548
|
C | T | 11 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(8): Show | 11 | HG01243.hp1 HG01346.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.278+9790C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034548 | ||||||
| chr13:113034575
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.278+9817T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034575 | ||||||
| chr13:113034601
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.278+9843G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034601 | ||||||
| chr13:113034609
|
C | G | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.278+9851C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034609 | ||||||
| chr13:113034622
|
T | TCGCCCTG others(10): Show |
1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278+9880_278+9881i others(19): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034622 | |||||
| chr13:113034639
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.278+9881A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034639 | ||||||
| chr13:113034653
|
GCCCTGGT others(10): Show |
G | 1 | a0001c0004t0003g0009 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.278+9927_278+9943d others(19): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034653 | |||||
| chr13:113034737
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278+9979G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034737 | ||||||
| chr13:113034830
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.278+10072G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034830 | ||||||
| chr13:113034863
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.278+10105C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034863 | ||||||
| chr13:113034864
|
G | GGAGGTGA others(13): Show |
1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278+10151_278+1017 others(24): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034864 | |||||
| chr13:113034864
|
GGAGGTGA others(13): Show |
G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+10151_278+1017 others(24): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113034864 | |||||
| chr13:113034878
|
T | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.278+10120T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034878 | ||||||
| chr13:113034900
|
T | G | 2 | a0001c0002t0001g0036a0001c0008t0004g0083 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.278+10142T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034900 | ||||||
| chr13:113034937
|
G | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.278+10179G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034937 | ||||||
| chr13:113034938
|
C | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278+10180C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113034938 | ||||||
| chr13:113035060
|
G | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-10211G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035060 | ||||||
| chr13:113035081
|
C | G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-10190C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035081 | ||||||
| chr13:113035105
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-10166C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035105 | ||||||
| chr13:113035215
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-10056G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035215 | ||||||
| chr13:113035592
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-9679G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035592 | ||||||
| chr13:113035597
|
C | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.279-9674C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035597 | ||||||
| chr13:113035642
|
G | C | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.279-9629G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035642 | ||||||
| chr13:113035645
|
T | G | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.279-9626T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035645 | ||||||
| chr13:113035646
|
G | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.279-9625G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035646 | ||||||
| chr13:113035721
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.279-9550G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035721 | ||||||
| chr13:113035740
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279-9531G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113035740 | ||||||
| chr13:113036234
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-9037C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113036234 | ||||||
| chr13:113036494
|
CAG | C | 2 | a0001c0001t0007g0017a0001c0001t0023g0018 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.279-8772_279-8771d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113036494 | |||||
| chr13:113036556
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279-8715G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113036556 | ||||||
| chr13:113036613
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-8658C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113036613 | ||||||
| chr13:113036699
|
T | TTTC | 7 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(4): Show | 7 | HG01109.hp2 HG01496.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.279-8568_279-8566d others(5): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113036699 | |||||
| chr13:113036769
|
G | A | 10 | a0001c0001t0001g0024a0001c0003t0001g0086a0001c0003t0001g0092others(7): Show | 10 | HG01346.hp1 HG01358.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-8502G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113036769 | ||||||
| chr13:113036805
|
G | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-8466G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113036805 | ||||||
| chr13:113036812
|
A | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(77): Show | 80 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.279-8459A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113036812 | ||||||
| chr13:113037102
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.279-8169G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037102 | ||||||
| chr13:113037104
|
C | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.279-8167C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037104 | ||||||
| chr13:113037232
|
A | G | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279-8039A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037232 | ||||||
| chr13:113037477
|
C | A | 2 | a0001c0012t0031g0021a0003c0009t0011g0101 | 2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.279-7794C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037477 | ||||||
| chr13:113037483
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(32): Show | 35 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.279-7788G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037483 | ||||||
| chr13:113037607
|
A | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(60): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.279-7664A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037607 | ||||||
| chr13:113037749
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.279-7522G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113037749 | ||||||
| chr13:113038019
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.279-7252A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038019 | ||||||
| chr13:113038242
|
G | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.279-7029G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038242 | ||||||
| chr13:113038262
|
G | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.279-7009G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038262 | ||||||
| chr13:113038422
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279-6849G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038422 | ||||||
| chr13:113038464
|
CA | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.279-6790delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113038464 | |||||
| chr13:113038771
|
A | T | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.279-6500A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038771 | ||||||
| chr13:113038914
|
A | G | 7 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.279-6357A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038914 | ||||||
| chr13:113038941
|
G | A | 3 | a0001c0001t0007g0017a0001c0001t0023g0018a0001c0012t0031g0021 | 3 | HG01496.hp1 HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.279-6330G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113038941 | ||||||
| chr13:113039014
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.279-6257C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039014 | ||||||
| chr13:113039060
|
C | T | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.279-6211C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039060 | ||||||
| chr13:113039061
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(15): Show | 18 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.279-6210G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039061 | ||||||
| chr13:113039061
|
G | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.279-6210G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039061 | ||||||
| chr13:113039079
|
T | C | 1 | a0001c0002t0002g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.279-6192T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039079 | ||||||
| chr13:113039205
|
G | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(17): Show | 20 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.279-6066G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039205 | ||||||
| chr13:113039329
|
G | A | 1 | a0001c0002t0002g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.279-5942G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039329 | ||||||
| chr13:113039347
|
T | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-5924T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039347 | ||||||
| chr13:113039450
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.279-5821A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039450 | ||||||
| chr13:113039501
|
T | G | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.279-5770T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039501 | ||||||
| chr13:113039577
|
A | G | 7 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.279-5694A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039577 | ||||||
| chr13:113039589
|
C | G | 4 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-5682C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039589 | ||||||
| chr13:113039636
|
G | GTAGAAAA others(9): Show |
1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279-5634_279-5619d others(18): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113039636 | |||||
| chr13:113039830
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(31): Show | 34 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.279-5441C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039830 | ||||||
| chr13:113039866
|
A | G | 1 | a0001c0001t0002g0008 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.279-5405A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113039866 | ||||||
| chr13:113040082
|
A | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279-5189A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040082 | ||||||
| chr13:113040086
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.279-5185C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040086 | ||||||
| chr13:113040167
|
C | T | 3 | a0001c0004t0004g0084a0001c0004t0004g0097a0001c0016t0004g0085 | 3 | HG01175.hp2 HG01257.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.279-5104C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040167 | ||||||
| chr13:113040185
|
T | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279-5086T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040185 | ||||||
| chr13:113040195
|
A | G | 9 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.279-5076A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040195 | ||||||
| chr13:113040201
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(32): Show | 35 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.279-5070G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040201 | ||||||
| chr13:113040219
|
C | T | 2 | a0001c0001t0007g0017a0001c0001t0023g0018 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.279-5052C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040219 | ||||||
| chr13:113040412
|
C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0022a0001c0001t0003g0099a0001c0005t0029g0091 | 3 | HG01069.hp1 HG02293.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279-4847_279-4834d others(16): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(9): Show |
44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(41): Show | 44 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.279-4849_279-4834d others(18): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(11): Show |
11 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0063others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.279-4851_279-4834d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(13): Show |
3 | a0001c0001t0028g0098a0001c0003t0001g0073a0005c0014t0024g0100 | 3 | HG01515.hp2 HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.279-4853_279-4834d others(22): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(15): Show |
15 | a0001c0001t0005g0062a0001c0001t0008g0066a0001c0001t0014g0001others(12): Show | 15 | HG00733.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.279-4855_279-4834d others(24): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(17): Show |
6 | a0001c0001t0022g0104a0001c0002t0002g0093a0001c0002t0015g0007others(3): Show | 6 | HG01891.hp1 HG01978.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.279-4857_279-4834d others(26): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(19): Show |
9 | a0001c0001t0001g0037a0001c0001t0002g0048a0001c0001t0004g0070others(6): Show | 9 | HG01109.hp1 HG01168.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.279-4834_279-4833i others(28): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(21): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0058others(1): Show | 4 | HG01496.hp2 HG02886.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-4834_279-4833i others(30): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040412
|
C | CTGTGTGT others(27): Show |
1 | a0001c0001t0001g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.279-4834_279-4833i others(36): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040412 | |||||
| chr13:113040436
|
G | GTGTGTGT others(17): Show |
1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.279-4834_279-4833i others(26): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040436 | |||||
| chr13:113040436
|
G | GTGTGTGT others(15): Show |
2 | a0001c0012t0031g0021a0003c0009t0011g0101 | 2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.279-4834_279-4833i others(24): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040436 | |||||
| chr13:113040436
|
G | GTGTGTGT others(11): Show |
1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-4834_279-4833i others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040436 | |||||
| chr13:113040436
|
G | GTGTGTGT others(7): Show |
3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279-4834_279-4833i others(16): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040436 | |||||
| chr13:113040436
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.279-4834_279-4833i others(12): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113040436 | |||||
| chr13:113040437
|
T | TGTGTGTG others(20): Show |
1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.279-4834_279-4833i others(29): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040437 | ||||||
| chr13:113040438
|
T | G | 1 | a0002c0007t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.279-4833T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040438 | ||||||
| chr13:113040479
|
C | T | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-4792C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040479 | ||||||
| chr13:113040499
|
T | C | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-4772T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040499 | ||||||
| chr13:113040526
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(32): Show | 35 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.279-4745G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040526 | ||||||
| chr13:113040582
|
G | C | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-4689G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040582 | ||||||
| chr13:113040648
|
T | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-4623T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040648 | ||||||
| chr13:113040762
|
C | T | 7 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0023g0018others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.279-4509C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040762 | ||||||
| chr13:113040904
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-4367C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040904 | ||||||
| chr13:113040915
|
T | C | 9 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.279-4356T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040915 | ||||||
| chr13:113040916
|
G | A | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-4355G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113040916 | ||||||
| chr13:113041201
|
T | C | 2 | a0001c0001t0007g0017a0001c0001t0023g0018 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.279-4070T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041201 | ||||||
| chr13:113041280
|
C | T | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-3991C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041280 | ||||||
| chr13:113041355
|
G | A | 1 | a0001c0015t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.279-3916G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041355 | ||||||
| chr13:113041392
|
G | T | 8 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.279-3879G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041392 | ||||||
| chr13:113041396
|
G | C | 4 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-3875G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041396 | ||||||
| chr13:113041465
|
C | CCATGACC others(34): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.279-3805_279-3804i others(43): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113041465 | |||||
| chr13:113041467
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-3804G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041467 | ||||||
| chr13:113041467
|
G | ATGACCAC others(34): Show |
6 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(3): Show | 6 | HG01109.hp2 HG01496.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.279-3805_279-3804i others(43): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041467 | ||||||
| chr13:113041534
|
CGTGGCCC others(34): Show |
C | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.279-3702_279-3662d others(43): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | 113041534 | |||||
| chr13:113041589
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(41): Show | 44 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.279-3682C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041589 | ||||||
| chr13:113041590
|
A | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(43): Show | 46 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.279-3681A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041590 | ||||||
| chr13:113041653
|
T | C | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.279-3618T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041653 | ||||||
| chr13:113041788
|
G | A | 4 | a0001c0001t0007g0017a0001c0001t0023g0018a0001c0004t0001g0103others(1): Show | 4 | HG01496.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-3483G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041788 | ||||||
| chr13:113041894
|
A | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(18): Show | 21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.279-3377A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113041894 | ||||||
| chr13:113042138
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.279-3133C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042138 | ||||||
| chr13:113042158
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.279-3113A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042158 | ||||||
| chr13:113042199
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(29): Show | 32 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.279-3072G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042199 | ||||||
| chr13:113042322
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-2949G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042322 | ||||||
| chr13:113042347
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(38): Show | 41 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.279-2924C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042347 | ||||||
| chr13:113042380
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.279-2891T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042380 | ||||||
| chr13:113042513
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279-2758C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042513 | ||||||
| chr13:113042517
|
G | A | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279-2754G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042517 | ||||||
| chr13:113042843
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.279-2428G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113042843 | ||||||
| chr13:113043048
|
C | T | 1 | a0001c0001t0006g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.279-2223C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043048 | ||||||
| chr13:113043150
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.279-2121G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043150 | ||||||
| chr13:113043232
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.279-2039G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043232 | ||||||
| chr13:113043452
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-1819G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043452 | ||||||
| chr13:113043540
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.279-1731T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043540 | ||||||
| chr13:113043650
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0002g0048others(1): Show | 4 | HG01346.hp2 HG02738.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-1621G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043650 | ||||||
| chr13:113043847
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-1424G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113043847 | ||||||
| chr13:113044349
|
G | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-922G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044349 | ||||||
| chr13:113044414
|
C | T | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.279-857C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044414 | ||||||
| chr13:113044471
|
G | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(34): Show | 37 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.279-800G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044471 | ||||||
| chr13:113044616
|
A | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-655A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044616 | ||||||
| chr13:113044684
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-587G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044684 | ||||||
| chr13:113044895
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.279-376G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044895 | ||||||
| chr13:113044975
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0049 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.279-296A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113044975 | ||||||
| chr13:113045007
|
C | T | 1 | a0001c0001t0026g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.279-264C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113045007 | ||||||
| chr13:113045020
|
G | A | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.279-251G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113045020 | ||||||
| chr13:113045166
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.279-105C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113045166 | ||||||
| chr13:113045174
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.279-97T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 3/29 | chr13 | 113045174 | ||||||
| chr13:113045368
|
G | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.369+7G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045368 | ||||||
| chr13:113045418
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.369+57G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045418 | ||||||
| chr13:113045564
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(31): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+203T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045564 | ||||||
| chr13:113045612
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369+251G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045612 | ||||||
| chr13:113045785
|
C | G | 7 | a0001c0004t0001g0102a0001c0004t0004g0084a0001c0004t0004g0097others(4): Show | 7 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+424C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045785 | ||||||
| chr13:113045891
|
T | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+530T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045891 | ||||||
| chr13:113045928
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369+567C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045928 | ||||||
| chr13:113045948
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+587C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113045948 | ||||||
| chr13:113046021
|
A | G | 3 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018 | 3 | HG01496.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.369+660A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046021 | ||||||
| chr13:113046044
|
C | T | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.369+683C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046044 | ||||||
| chr13:113046049
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+688C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046049 | ||||||
| chr13:113046228
|
C | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+867C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046228 | ||||||
| chr13:113046319
|
T | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+958T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046319 | ||||||
| chr13:113046409
|
A | G | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.369+1048A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046409 | ||||||
| chr13:113046432
|
C | T | 4 | a0001c0003t0001g0086a0001c0005t0001g0088a0001c0012t0031g0021others(1): Show | 4 | HG02135.hp1 HG02145.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1071C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046432 | ||||||
| chr13:113046480
|
C | T | 1 | a0001c0001t0004g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.369+1119C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046480 | ||||||
| chr13:113046483
|
C | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+1122C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046483 | ||||||
| chr13:113046493
|
C | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+1132C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046493 | ||||||
| chr13:113046542
|
C | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+1181C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046542 | ||||||
| chr13:113046599
|
A | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.369+1238A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046599 | ||||||
| chr13:113046717
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1356C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046717 | ||||||
| chr13:113046739
|
G | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+1378G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046739 | ||||||
| chr13:113046784
|
A | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+1423A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046784 | ||||||
| chr13:113046877
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.369+1516A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046877 | ||||||
| chr13:113046881
|
C | T | 3 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018 | 3 | HG01496.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.369+1520C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113046881 | ||||||
| chr13:113047215
|
A | G | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+1854A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047215 | ||||||
| chr13:113047218
|
A | G | 2 | a0001c0001t0008g0061a0001c0001t0008g0066 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.369+1857A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047218 | ||||||
| chr13:113047242
|
C | T | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.369+1881C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047242 | ||||||
| chr13:113047259
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.369+1898C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047259 | ||||||
| chr13:113047494
|
G | A | 5 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0002t0003g0014others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+2133G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047494 | ||||||
| chr13:113047527
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.369+2166G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047527 | ||||||
| chr13:113047580
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.369+2219C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047580 | ||||||
| chr13:113047625
|
G | A | 1 | a0001c0001t0026g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.369+2264G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047625 | ||||||
| chr13:113047706
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+2345C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047706 | ||||||
| chr13:113047744
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.369+2383C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047744 | ||||||
| chr13:113047745
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.369+2384G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047745 | ||||||
| chr13:113047824
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.369+2463C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047824 | ||||||
| chr13:113047838
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.369+2477T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047838 | ||||||
| chr13:113047863
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0001t0014g0001others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2502C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047863 | ||||||
| chr13:113047876
|
G | GCCTCCGC others(27): Show |
1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.369+2525_369+2526i others(36): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113047876 | |||||
| chr13:113047881
|
C | CGCTGACG others(27): Show |
59 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0032others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.369+2525_369+2526i others(36): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113047881 | |||||
| chr13:113047887
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.369+2526T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047887 | ||||||
| chr13:113047893
|
G | A | 6 | a0001c0001t0007g0017a0001c0005t0001g0079a0001c0005t0001g0080others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2532G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047893 | ||||||
| chr13:113047915
|
C | T | 2 | a0001c0001t0007g0017a0001c0012t0031g0021 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.369+2554C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113047915 | ||||||
| chr13:113048000
|
T | G | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+2639T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048000 | ||||||
| chr13:113048004
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.369+2643T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048004 | ||||||
| chr13:113048017
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369+2656C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048017 | ||||||
| chr13:113048089
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.369+2728C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048089 | ||||||
| chr13:113048101
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.369+2740C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048101 | ||||||
| chr13:113048260
|
T | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.369+2899T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048260 | ||||||
| chr13:113048304
|
T | G | 9 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0001t0014g0001others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2943T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048304 | ||||||
| chr13:113048410
|
T | C | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+3049T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048410 | ||||||
| chr13:113048433
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(52): Show | 55 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.369+3072C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048433 | ||||||
| chr13:113048437
|
C | CT | 48 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0032others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.369+3097dupT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113048437 | |||||
| chr13:113048437
|
C | CTT | 9 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0006g0056others(6): Show | 9 | HG01175.hp2 HG01243.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+3096_369+3097d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113048437 | |||||
| chr13:113048437
|
CT | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(28): Show | 31 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.369+3097delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113048437 | |||||
| chr13:113048530
|
TC | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.369+3173delC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113048530 | |||||
| chr13:113048535
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.369+3174G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048535 | ||||||
| chr13:113048721
|
T | C | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+3360T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048721 | ||||||
| chr13:113048903
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+3542C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113048903 | ||||||
| chr13:113049026
|
G | A | 4 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+3665G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049026 | ||||||
| chr13:113049037
|
C | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+3676C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049037 | ||||||
| chr13:113049047
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(31): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+3686C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049047 | ||||||
| chr13:113049048
|
G | A | 2 | a0001c0001t0003g0099a0001c0001t0026g0034 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.369+3687G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049048 | ||||||
| chr13:113049090
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.369+3729C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049090 | ||||||
| chr13:113049111
|
GA | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.369+3751delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049111 | ||||||
| chr13:113049128
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(13): Show | 16 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.369+3767G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049128 | ||||||
| chr13:113049330
|
T | C | 3 | a0001c0002t0003g0014a0001c0002t0003g0023a0001c0005t0025g0016 | 3 | HG01069.hp2 HG01071.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.369+3969T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049330 | ||||||
| chr13:113049352
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.369+3991T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049352 | ||||||
| chr13:113049458
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.369+4097A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049458 | ||||||
| chr13:113049504
|
C | T | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.369+4143C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049504 | ||||||
| chr13:113049868
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.369+4507C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113049868 | ||||||
| chr13:113050018
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(48): Show | 51 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.369+4657A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050018 | ||||||
| chr13:113050052
|
C | CAT | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.369+4691_369+4692i others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050052 | ||||||
| chr13:113050093
|
A | G | 4 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+4732A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050093 | ||||||
| chr13:113050125
|
A | C | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+4764A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050125 | ||||||
| chr13:113050157
|
TGTGA | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+4800_369+4803d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050157 | |||||
| chr13:113050189
|
C | T | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+4828C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050189 | ||||||
| chr13:113050191
|
A | T | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+4830A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050191 | ||||||
| chr13:113050216
|
GAGAC | G | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+4856_369+4859d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050216 | ||||||
| chr13:113050225
|
T | A | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+4864T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050225 | ||||||
| chr13:113050228
|
G | C | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+4867G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050228 | ||||||
| chr13:113050245
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(31): Show | 34 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+4884C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050245 | ||||||
| chr13:113050246
|
G | C | 3 | a0001c0001t0002g0008a0001c0001t0006g0010a0001c0001t0006g0056 | 3 | HG00323.hp1 HG01256.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.369+4885G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050246 | ||||||
| chr13:113050276
|
C | CTGTGAGT others(1): Show |
102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.369+4918_369+4925d others(10): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050276 | |||||
| chr13:113050287
|
A | T | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.369+4926A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050287 | ||||||
| chr13:113050289
|
A | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(34): Show | 37 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.369+4928A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050289 | ||||||
| chr13:113050666
|
G | GC | 35 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(32): Show | 35 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.369+5306dupC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050666 | |||||
| chr13:113050672
|
GA | G | 2 | a0001c0002t0003g0014a0001c0002t0003g0023 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.369+5312delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050672 | ||||||
| chr13:113050675
|
G | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.369+5314G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050675 | ||||||
| chr13:113050678
|
G | C | 5 | a0001c0001t0007g0017a0001c0005t0001g0079a0001c0005t0001g0080others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+5317G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050678 | ||||||
| chr13:113050682
|
TGGCTGGG others(10): Show |
T | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.369+5325_369+5341d others(19): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050682 | |||||
| chr13:113050686
|
T | G | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+5325T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050686 | ||||||
| chr13:113050689
|
G | A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+5328G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050689 | ||||||
| chr13:113050692
|
AGCGGGGA others(25): Show |
A | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+5338_369+5369d others(34): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050692 | |||||
| chr13:113050712
|
A | AG | 11 | a0001c0001t0007g0026a0001c0001t0008g0066a0001c0001t0026g0034others(8): Show | 11 | HG01257.hp1 HG01515.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.369+5358dupG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050712 | |||||
| chr13:113050712
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.369+5351A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050712 | ||||||
| chr13:113050714
|
G | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.369+5353G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050714 | ||||||
| chr13:113050720
|
C | G | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.369+5359C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050720 | ||||||
| chr13:113050720
|
C | T | 1 | a0001c0001t0006g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.369+5359C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050720 | ||||||
| chr13:113050724
|
GGCGGGGG others(11): Show |
G | 2 | a0001c0005t0025g0016a0001c0016t0004g0085 | 2 | HG01175.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.369+5373_369+5390d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050724 | |||||
| chr13:113050726
|
C | CG | 25 | a0001c0001t0001g0006a0001c0001t0001g0058a0001c0001t0002g0048others(22): Show | 25 | HG01069.hp2 HG01168.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.369+5373dupG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050726 | |||||
| chr13:113050726
|
C | G | 3 | a0001c0001t0001g0024a0001c0001t0007g0035a0001c0006t0009g0028 | 3 | HG01109.hp2 HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.369+5365C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050726 | ||||||
| chr13:113050726
|
CGGGGGGG others(12): Show |
C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.369+5372_369+5390d others(21): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050726 | |||||
| chr13:113050729
|
G | C | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+5368G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050729 | ||||||
| chr13:113050729
|
G | T | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+5368G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050729 | ||||||
| chr13:113050733
|
G | C | 1 | a0001c0001t0006g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.369+5372G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050733 | ||||||
| chr13:113050733
|
GGCGGGGG others(12): Show |
G | 3 | a0001c0001t0014g0001a0001c0001t0023g0018a0001c0001t0028g0098 | 3 | HG01496.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.369+5381_369+5399d others(21): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050733 | |||||
| chr13:113050734
|
GCGGGGGG others(11): Show |
G | 1 | a0001c0001t0022g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.369+5374_369+5391d others(20): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050734 | ||||||
| chr13:113050735
|
C | G | 1 | a0001c0004t0004g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.369+5374C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050735 | ||||||
| chr13:113050735
|
CGGGGGGA others(3): Show |
C | 1 | a0001c0001t0005g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.369+5381_369+5390d others(12): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050735 | |||||
| chr13:113050742
|
A | G | 2 | a0001c0002t0003g0014a0001c0002t0003g0023 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.369+5381A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050742 | ||||||
| chr13:113050742
|
AGCGGGGG others(3): Show |
A | 3 | a0001c0001t0018g0077a0001c0005t0032g0106a0001c0013t0001g0067 | 3 | HG00544.hp1 HG00544.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.369+5390_369+5399d others(12): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050742 | |||||
| chr13:113050744
|
C | G | 1 | a0001c0002t0003g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.369+5383C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050744 | ||||||
| chr13:113050745
|
G | C | 3 | a0001c0002t0003g0014a0001c0003t0001g0086a0004c0011t0002g0090 | 3 | HG01069.hp2 NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.369+5384G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050745 | ||||||
| chr13:113050752
|
T | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(48): Show | 51 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.369+5391T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050752 | ||||||
| chr13:113050752
|
T | C | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.369+5391T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050752 | ||||||
| chr13:113050752
|
T | G | 1 | a0001c0001t0005g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.369+5391T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050752 | ||||||
| chr13:113050754
|
C | CG | 6 | a0001c0001t0007g0035a0001c0002t0001g0040a0001c0003t0001g0092others(3): Show | 6 | HG01109.hp2 HG01175.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+5399dupG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050754 | |||||
| chr13:113050764
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.369+5403T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050764 | ||||||
| chr13:113050765
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.369+5404G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050765 | ||||||
| chr13:113050767
|
C | CG | 6 | a0001c0001t0001g0024a0001c0001t0018g0077a0001c0004t0005g0095others(3): Show | 6 | HG00544.hp1 HG00544.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+5412dupG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113050767 | |||||
| chr13:113050829
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.369+5468G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050829 | ||||||
| chr13:113050938
|
C | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.369+5577C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050938 | ||||||
| chr13:113050946
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.369+5585G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113050946 | ||||||
| chr13:113051029
|
T | G | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+5668T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051029 | ||||||
| chr13:113051068
|
A | G | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369+5707A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051068 | ||||||
| chr13:113051188
|
G | A | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.369+5827G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051188 | ||||||
| chr13:113051274
|
TGGGGCGG others(5): Show |
T | 18 | a0001c0001t0001g0024a0001c0002t0001g0040a0001c0003t0001g0053others(15): Show | 18 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.369+5922_369+5933d others(14): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113051274 | |||||
| chr13:113051309
|
C | G | 5 | a0001c0001t0005g0062a0001c0001t0028g0098a0001c0002t0003g0014others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+5948C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051309 | ||||||
| chr13:113051489
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369+6128G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051489 | ||||||
| chr13:113051499
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.369+6138G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051499 | ||||||
| chr13:113051608
|
C | CT | 14 | a0001c0001t0005g0062a0001c0001t0028g0098a0001c0002t0003g0014others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.369+6248dupT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113051608 | |||||
| chr13:113051625
|
G | C | 6 | a0001c0003t0001g0086a0001c0005t0001g0079a0001c0005t0001g0080others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+6264G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051625 | ||||||
| chr13:113051710
|
A | G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.369+6349A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051710 | ||||||
| chr13:113051899
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.369+6538G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113051899 | ||||||
| chr13:113052044
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(45): Show | 48 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.369+6683A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052044 | ||||||
| chr13:113052101
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.369+6740A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052101 | ||||||
| chr13:113052220
|
T | A | 2 | a0001c0001t0001g0113a0001c0002t0001g0069 | 2 | HG01168.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.369+6859T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052220 | ||||||
| chr13:113052573
|
G | A | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369+7212G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052573 | ||||||
| chr13:113052606
|
C | G | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.369+7245C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052606 | ||||||
| chr13:113052754
|
C | CGT | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(39): Show | 42 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.369+7407_369+7408d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113052754 | |||||
| chr13:113052805
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.369+7444A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052805 | ||||||
| chr13:113052815
|
ATC | A | 9 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+7455_369+7456d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113052815 | ||||||
| chr13:113053040
|
A | G | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(40): Show | 43 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.370-7553A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053040 | ||||||
| chr13:113053159
|
C | T | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-7434C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053159 | ||||||
| chr13:113053344
|
T | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(40): Show | 43 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.370-7249T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053344 | ||||||
| chr13:113053388
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(37): Show | 40 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-7205C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053388 | ||||||
| chr13:113053553
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.370-7040A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053553 | ||||||
| chr13:113053570
|
C | T | 1 | a0001c0004t0003g0009 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.370-7023C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053570 | ||||||
| chr13:113053777
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-6816G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053777 | ||||||
| chr13:113053971
|
G | A | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.370-6622G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113053971 | ||||||
| chr13:113054095
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-6498G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113054095 | ||||||
| chr13:113054164
|
G | A | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.370-6429G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113054164 | ||||||
| chr13:113054372
|
T | C | 3 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018 | 3 | HG01496.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.370-6221T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113054372 | ||||||
| chr13:113054383
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(40): Show | 43 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.370-6210C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113054383 | ||||||
| chr13:113054492
|
C | T | 5 | a0001c0001t0005g0062a0001c0001t0028g0098a0001c0002t0003g0014others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-6101C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113054492 | ||||||
| chr13:113054604
|
T | C | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-5989T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113054604 | ||||||
| chr13:113055122
|
C | T | 9 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(6): Show | 9 | HG01243.hp1 HG01496.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-5471C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055122 | ||||||
| chr13:113055218
|
A | C | 4 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-5375A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055218 | ||||||
| chr13:113055380
|
CG | C | 25 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(22): Show | 25 | HG00323.hp1 HG00544.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.370-5212delG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055380 | ||||||
| chr13:113055381
|
G | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.370-5212G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055381 | ||||||
| chr13:113055382
|
C | CCA | 3 | a0001c0001t0001g0004a0001c0003t0002g0078a0002c0017t0001g0109 | 3 | HG01346.hp1 HG01993.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.370-5149_370-5148d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055382
|
C | CCACA | 2 | a0001c0006t0002g0029a0001c0006t0009g0028 | 2 | HG01993.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.370-5151_370-5148d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055382
|
C | CGCCA | 3 | a0001c0001t0002g0008a0001c0001t0007g0017a0001c0005t0029g0091 | 3 | HG01256.hp2 HG02293.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.370-5211_370-5210i others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055382 | ||||||
| chr13:113055382
|
C | G | 15 | a0001c0001t0001g0063a0001c0001t0001g0094a0001c0001t0001g0113others(12): Show | 15 | HG01168.hp2 HG01257.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.370-5211C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055382 | ||||||
| chr13:113055382
|
CCACACAC others(1): Show |
C | 2 | a0001c0003t0002g0064a0003c0009t0011g0101 | 2 | HG01243.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.370-5155_370-5148d others(10): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055382
|
CCACACAC others(3): Show |
C | 1 | a0001c0003t0020g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.370-5157_370-5148d others(12): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055382
|
CCACACAC others(13): Show |
C | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.370-5167_370-5148d others(22): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055382
|
CCACACAC others(17): Show |
C | 1 | a0001c0005t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.370-5171_370-5148d others(26): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055382
|
CCACACAC others(21): Show |
C | 1 | a0001c0005t0001g0080 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.370-5175_370-5148d others(30): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113055382 | |||||
| chr13:113055383
|
C | CG | 2 | a0001c0004t0004g0097a0001c0013t0001g0067 | 2 | HG00544.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.370-5210_370-5209i others(3): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
C | G | 4 | a0001c0001t0001g0045a0001c0001t0006g0010a0001c0001t0006g0027others(1): Show | 4 | HG00323.hp1 HG01515.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-5210C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACA | C | 6 | a0001c0001t0001g0063a0001c0001t0001g0094a0001c0001t0001g0113others(3): Show | 6 | HG01168.hp2 HG01517.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-5209_370-5207d others(5): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACACA | C | 3 | a0001c0001t0003g0099a0001c0003t0001g0053a0001c0003t0002g0019 | 3 | HG02074.hp2 HG02602.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.370-5209_370-5205d others(7): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACACACA others(12): Show |
C | 1 | a0004c0011t0002g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.370-5209_370-5191d others(21): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACACACA others(14): Show |
C | 2 | a0001c0003t0001g0086a0001c0005t0032g0106 | 2 | HG02572.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.370-5209_370-5189d others(23): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACACACA others(18): Show |
C | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0087others(4): Show | 7 | HG00733.hp1 HG00733.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-5209_370-5185d others(27): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACACACA others(20): Show |
C | 3 | a0001c0005t0001g0079a0001c0005t0001g0081a0001c0008t0003g0039 | 3 | HG01257.hp1 HG01361.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.370-5209_370-5183d others(29): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055383
|
CACACACA others(22): Show |
C | 1 | a0002c0007t0001g0114 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.370-5209_370-5181d others(31): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055383 | ||||||
| chr13:113055384
|
A | C | 11 | a0001c0001t0001g0045a0001c0001t0006g0010a0001c0001t0006g0027others(8): Show | 11 | HG00323.hp1 HG00544.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.370-5209A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055384 | ||||||
| chr13:113055384
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 55 | HG00323.hp2 HG00544.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.370-5209A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055384 | ||||||
| chr13:113055385
|
C | G | 2 | a0001c0004t0005g0012a0001c0016t0004g0085 | 2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.370-5208C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CA | C | 4 | a0001c0001t0006g0056a0001c0001t0006g0108a0001c0002t0027g0065others(1): Show | 4 | HG01243.hp2 HG02129.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-5207delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACA | C | 5 | a0001c0001t0001g0052a0001c0001t0012g0055a0001c0001t0018g0077others(2): Show | 5 | HG00544.hp2 HG02145.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-5207_370-5205d others(5): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACA | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0075a0001c0001t0019g0107others(1): Show | 4 | HG01978.hp1 NA19005.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-5207_370-5203d others(7): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACACA others(2): Show |
C | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0003t0002g0111 | 3 | HG03490.hp1 HG03492.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.370-5207_370-5199d others(11): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACACA others(6): Show |
C | 2 | a0001c0001t0001g0002a0001c0001t0014g0001 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.370-5207_370-5195d others(15): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACACA others(8): Show |
C | 1 | a0001c0001t0022g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.370-5207_370-5193d others(17): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACACA others(16): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.370-5207_370-5185d others(25): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACACA others(18): Show |
C | 3 | a0001c0006t0030g0096a0001c0008t0004g0083a0002c0007t0001g0074 | 3 | HG01978.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.370-5207_370-5183d others(27): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055385
|
CACACACA others(20): Show |
C | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(29): Show | 32 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.370-5207_370-5181d others(29): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055385 | ||||||
| chr13:113055386
|
A | C | 2 | a0001c0004t0005g0012a0001c0016t0004g0085 | 2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.370-5207A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055386 | ||||||
| chr13:113055386
|
A | G | 2 | a0001c0004t0001g0103a0001c0004t0005g0011 | 2 | HG01517.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.370-5207A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055386 | ||||||
| chr13:113055387
|
CACACACA others(22): Show |
C | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-5205_370-5177d others(31): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055387 | ||||||
| chr13:113055388
|
A | G | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.370-5205A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055388 | ||||||
| chr13:113055410
|
A | G | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0087others(4): Show | 7 | HG00733.hp1 HG00733.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-5183A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055410 | ||||||
| chr13:113055411
|
CA | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0087others(4): Show | 7 | HG00733.hp1 HG00733.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-5181delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055411 | ||||||
| chr13:113055414
|
A | G | 1 | a0002c0007t0001g0114 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.370-5179A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055414 | ||||||
| chr13:113055459
|
T | C | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(51): Show | 54 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-5134T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055459 | ||||||
| chr13:113055517
|
C | T | 9 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(6): Show | 9 | HG01243.hp1 HG01496.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-5076C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055517 | ||||||
| chr13:113055988
|
A | C | 1 | a0001c0004t0004g0097 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.370-4605A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113055988 | ||||||
| chr13:113056116
|
C | T | 1 | a0001c0004t0003g0009 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.370-4477C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056116 | ||||||
| chr13:113056165
|
C | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.370-4428C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056165 | ||||||
| chr13:113056166
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(37): Show | 40 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-4427G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056166 | ||||||
| chr13:113056333
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-4260G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056333 | ||||||
| chr13:113056407
|
A | G | 9 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(6): Show | 9 | HG01243.hp1 HG01496.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-4186A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056407 | ||||||
| chr13:113056440
|
G | T | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.370-4153G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056440 | ||||||
| chr13:113056444
|
C | T | 1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-4149C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056444 | ||||||
| chr13:113056676
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(39): Show | 42 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.370-3917C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056676 | ||||||
| chr13:113056702
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-3891G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056702 | ||||||
| chr13:113056753
|
G | GGGTGCTG others(23): Show |
8 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-3815_370-3814i others(32): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113056753 | |||||
| chr13:113056769
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.370-3824G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056769 | ||||||
| chr13:113056779
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3814G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056779 | ||||||
| chr13:113056783
|
T | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3810T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056783 | ||||||
| chr13:113056786
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3807C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056786 | ||||||
| chr13:113056787
|
A | G | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3806A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056787 | ||||||
| chr13:113056791
|
A | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3802A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056791 | ||||||
| chr13:113056792
|
GTGTT | G | 8 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-3798_370-3795d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113056792 | |||||
| chr13:113056806
|
T | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3787T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056806 | ||||||
| chr13:113056813
|
G | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3780G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056813 | ||||||
| chr13:113056816
|
T | C | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3777T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056816 | ||||||
| chr13:113056817
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3776G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056817 | ||||||
| chr13:113056856
|
TTCGGCGC others(15): Show |
T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3735_370-3714d others(24): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113056856 | |||||
| chr13:113056880
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3713G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056880 | ||||||
| chr13:113056893
|
TTGGGTGC others(4): Show |
T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-3686_370-3676d others(13): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113056893 | |||||
| chr13:113056904
|
G | GTGTT | 8 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-3687_370-3686i others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113056904 | |||||
| chr13:113056948
|
CTG | C | 8 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-3639_370-3638d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113056948 | |||||
| chr13:113056989
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-3604G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113056989 | ||||||
| chr13:113057090
|
GTGTT | G | 2 | a0001c0003t0001g0086a0004c0011t0002g0090 | 2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.370-3500_370-3497d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113057090 | |||||
| chr13:113057126
|
G | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.370-3467G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113057126 | ||||||
| chr13:113057173
|
T | C | 2 | a0001c0001t0014g0001a0001c0001t0022g0104 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.370-3420T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113057173 | ||||||
| chr13:113057274
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-3319G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113057274 | ||||||
| chr13:113057318
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(37): Show | 40 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.370-3275G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113057318 | ||||||
| chr13:113057444
|
G | GTGTT | 6 | a0001c0003t0001g0086a0001c0005t0025g0016a0001c0005t0032g0106others(3): Show | 6 | HG01243.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-3147_370-3146i others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113057444 | |||||
| chr13:113057502
|
GTGTT | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(41): Show | 44 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.370-3088_370-3085d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113057502 | |||||
| chr13:113057547
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0002t0027g0065others(7): Show | 10 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.370-3046G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113057547 | ||||||
| chr13:113057603
|
GTGTT | G | 3 | a0001c0001t0014g0001a0001c0001t0022g0104a0001c0001t0023g0018 | 3 | HG01496.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.370-2987_370-2984d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113057603 | |||||
| chr13:113057633
|
GTGTT | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.370-2957_370-2954d others(6): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113057633 | |||||
| chr13:113057636
|
T | TTTGGGTG others(37): Show |
1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-2939_370-2896d others(46): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113057636 | |||||
| chr13:113057684
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.370-2909G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113057684 | ||||||
| chr13:113058042
|
AGGTGCTG others(8): Show |
A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-2536_370-2522d others(17): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113058042 | |||||
| chr13:113058073
|
G | A | 1 | a0001c0003t0002g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.370-2520G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058073 | ||||||
| chr13:113058143
|
G | A | 1 | a0001c0008t0003g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.370-2450G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058143 | ||||||
| chr13:113058224
|
C | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.370-2369C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058224 | ||||||
| chr13:113058392
|
T | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.370-2201T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058392 | ||||||
| chr13:113058420
|
G | T | 5 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-2173G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058420 | ||||||
| chr13:113058741
|
A | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-1852A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058741 | ||||||
| chr13:113058747
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-1846C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058747 | ||||||
| chr13:113058752
|
T | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-1841T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058752 | ||||||
| chr13:113058753
|
G | GTGGGCGC | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-1838_370-1837i others(9): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113058753 | |||||
| chr13:113058757
|
T | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.370-1836T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058757 | ||||||
| chr13:113058787
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.370-1806A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058787 | ||||||
| chr13:113058886
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.370-1707G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058886 | ||||||
| chr13:113058930
|
G | C | 1 | a0001c0003t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.370-1663G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058930 | ||||||
| chr13:113058938
|
C | T | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.370-1655C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058938 | ||||||
| chr13:113058943
|
C | CTGTTTGG others(8): Show |
2 | a0001c0001t0001g0082a0001c0001t0007g0017 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.370-1644_370-1630d others(17): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113058943 | |||||
| chr13:113058964
|
C | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.370-1629C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058964 | ||||||
| chr13:113058965
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.370-1628A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058965 | ||||||
| chr13:113058967
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.370-1626C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113058967 | ||||||
| chr13:113058969
|
C | CTGAGTGT others(23): Show |
52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(49): Show | 52 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.370-1622_370-1621i others(32): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113058969 | |||||
| chr13:113058969
|
C | CTGTTTGG others(8): Show |
46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(43): Show | 46 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.370-1618_370-1604d others(17): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | 113058969 | |||||
| chr13:113059160
|
C | T | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-1433C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113059160 | ||||||
| chr13:113059357
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.370-1236G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113059357 | ||||||
| chr13:113059591
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.370-1002A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113059591 | ||||||
| chr13:113059708
|
C | T | 4 | a0001c0001t0001g0024a0001c0003t0001g0053a0001c0003t0001g0073others(1): Show | 4 | HG01358.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-885C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113059708 | ||||||
| chr13:113059760
|
C | T | 1 | a0001c0004t0004g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.370-833C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113059760 | ||||||
| chr13:113060032
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.370-561G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113060032 | ||||||
| chr13:113060135
|
C | T | 2 | a0001c0001t0014g0001a0001c0001t0022g0104 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.370-458C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113060135 | ||||||
| chr13:113060505
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.370-88C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 4/29 | chr13 | 113060505 | ||||||
| chr13:113060846
|
G | A | 3 | a0001c0003t0002g0047a0001c0003t0002g0111a0001c0013t0001g0067 | 3 | HG00544.hp1 HG02074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.489+134G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113060846 | ||||||
| chr13:113060951
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.489+239A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113060951 | ||||||
| chr13:113061014
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.489+302G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061014 | ||||||
| chr13:113061061
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0026g0034 | 3 | HG01109.hp2 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.489+349C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061061 | ||||||
| chr13:113061081
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+369G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061081 | ||||||
| chr13:113061088
|
C | A | 4 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+376C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061088 | ||||||
| chr13:113061169
|
A | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(48): Show | 51 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.489+457A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061169 | ||||||
| chr13:113061180
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.489+468G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061180 | ||||||
| chr13:113061351
|
G | A | 1 | a0001c0015t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.489+639G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061351 | ||||||
| chr13:113061473
|
A | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.489+761A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061473 | ||||||
| chr13:113061634
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.489+922C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061634 | ||||||
| chr13:113061691
|
CCCCTCCC others(10): Show |
C | 40 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(37): Show | 40 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.489+1009_489+1025d others(19): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061691 | |||||
| chr13:113061696
|
CCCCTCCC others(9): Show |
C | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+988_489+1003de others(17): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061696 | |||||
| chr13:113061709
|
CCCTCCCC others(9): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.489+1000_489+1015d others(18): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061709 | |||||
| chr13:113061715
|
C | CCTCCCTC others(22): Show |
2 | a0001c0001t0001g0082a0001c0003t0002g0047 | 2 | HG02074.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.489+1008_489+1009i others(31): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061715 | |||||
| chr13:113061715
|
C | CCTCCCTC others(45): Show |
1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.489+1008_489+1009i others(54): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061715 | |||||
| chr13:113061716
|
CTCCCCCT others(33): Show |
C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+1009_489+1048d others(42): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061716 | |||||
| chr13:113061722
|
C | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489+1010C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061722 | ||||||
| chr13:113061725
|
G | C | 4 | a0001c0001t0001g0082a0001c0003t0002g0047a0001c0003t0002g0111others(1): Show | 4 | HG02074.hp1 HG03195.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1013G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061725 | ||||||
| chr13:113061733
|
C | T | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489+1021C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061733 | ||||||
| chr13:113061741
|
T | C | 4 | a0001c0001t0001g0082a0001c0003t0002g0047a0001c0003t0002g0111others(1): Show | 4 | HG02074.hp1 HG03195.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1029T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061741 | ||||||
| chr13:113061745
|
T | C | 3 | a0001c0001t0001g0082a0001c0003t0002g0047a0001c0006t0002g0110 | 3 | HG02074.hp1 HG03195.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.489+1033T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061745 | ||||||
| chr13:113061756
|
T | C | 4 | a0001c0001t0001g0082a0001c0003t0002g0047a0001c0003t0002g0111others(1): Show | 4 | HG02074.hp1 HG03195.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1044T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061756 | ||||||
| chr13:113061758
|
C | A | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.489+1046C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061758 | ||||||
| chr13:113061764
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+1052C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061764 | ||||||
| chr13:113061768
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+1056C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061768 | ||||||
| chr13:113061771
|
CCCCTCCC others(15): Show |
C | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.489+1063_489+1084d others(24): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061771 | |||||
| chr13:113061779
|
C | CCTCCCTC others(66): Show |
1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+1067_489+1068i others(75): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061779 | ||||||
| chr13:113061779
|
C | CTCCCTCT others(65): Show |
1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.489+1079_489+1080i others(74): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061779 | |||||
| chr13:113061779
|
C | CTCCCTCT others(63): Show |
39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(36): Show | 39 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.489+1089_489+1090i others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061779 | |||||
| chr13:113061779
|
C | CTCCCTCT others(63): Show |
3 | a0001c0002t0003g0014a0001c0002t0003g0023a0001c0005t0029g0091 | 3 | HG01069.hp2 HG01071.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.489+1089_489+1090i others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061779 | |||||
| chr13:113061779
|
C | CTCCCTCT others(63): Show |
1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.489+1084_489+1085i others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061779 | |||||
| chr13:113061779
|
C | T | 3 | a0001c0003t0002g0047a0001c0006t0002g0110a0003c0009t0011g0101 | 3 | HG01243.hp1 HG02074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.489+1067C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061779 | ||||||
| chr13:113061779
|
CTCCCTCT others(16): Show |
C | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(41): Show | 44 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.489+1088_489+1110d others(25): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061779 | |||||
| chr13:113061781
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.489+1069C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061781 | ||||||
| chr13:113061802
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0030others(47): Show | 50 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.489+1090T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061802 | ||||||
| chr13:113061802
|
T | TTCCCTCT others(16): Show |
1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.489+1110_489+1111i others(25): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061802 | |||||
| chr13:113061804
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489+1092C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061804 | ||||||
| chr13:113061809
|
T | TCCCCCTT others(41): Show |
1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489+1104_489+1105i others(50): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061809 | |||||
| chr13:113061844
|
C | CTCCTCCT others(14): Show |
1 | a0001c0005t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.489+1136_489+1156d others(23): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113061844 | |||||
| chr13:113061855
|
C | T | 1 | a0001c0004t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.489+1143C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061855 | ||||||
| chr13:113061872
|
T | C | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489+1160T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061872 | ||||||
| chr13:113061928
|
T | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+1216T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113061928 | ||||||
| chr13:113062195
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+1483G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062195 | ||||||
| chr13:113062212
|
G | A | 11 | a0001c0001t0001g0082a0001c0002t0027g0065a0001c0004t0001g0025others(8): Show | 11 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+1500G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062212 | ||||||
| chr13:113062261
|
C | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(48): Show | 51 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.489+1549C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062261 | ||||||
| chr13:113062261
|
C | T | 3 | a0001c0004t0001g0103a0001c0005t0025g0016a0003c0009t0011g0101 | 3 | HG01243.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489+1549C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062261 | ||||||
| chr13:113062311
|
A | C | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489+1599A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062311 | ||||||
| chr13:113062427
|
C | T | 2 | a0001c0001t0014g0001a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489+1715C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062427 | ||||||
| chr13:113062496
|
G | A | 3 | a0001c0002t0003g0014a0001c0002t0003g0023a0001c0005t0029g0091 | 3 | HG01069.hp2 HG01071.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.489+1784G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062496 | ||||||
| chr13:113062534
|
C | G | 2 | a0001c0001t0014g0001a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.490-1770C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062534 | ||||||
| chr13:113062699
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-1605C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062699 | ||||||
| chr13:113062708
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0037others(45): Show | 48 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-1596G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062708 | ||||||
| chr13:113062717
|
A | G | 2 | a0001c0005t0025g0016a0003c0009t0011g0101 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.490-1587A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062717 | ||||||
| chr13:113062784
|
C | T | 2 | a0001c0001t0014g0001a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.490-1520C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062784 | ||||||
| chr13:113062785
|
C | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0058 | 2 | HG01346.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.490-1519C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062785 | ||||||
| chr13:113062866
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-1438G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062866 | ||||||
| chr13:113062887
|
C | T | 3 | a0001c0003t0002g0019a0001c0003t0002g0064a0001c0003t0020g0089 | 3 | HG02074.hp2 HG02129.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.490-1417C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062887 | ||||||
| chr13:113062926
|
C | T | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.490-1378C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062926 | ||||||
| chr13:113062930
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(44): Show | 47 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.490-1374C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062930 | ||||||
| chr13:113062977
|
G | A | 3 | a0001c0001t0014g0001a0001c0004t0001g0103a0001c0012t0031g0021 | 3 | HG02145.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.490-1327G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113062977 | ||||||
| chr13:113063112
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.490-1192T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063112 | ||||||
| chr13:113063220
|
C | T | 1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.490-1084C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063220 | ||||||
| chr13:113063413
|
CCCCTGTC others(28): Show |
C | 19 | a0001c0001t0007g0026a0001c0001t0007g0035a0001c0001t0023g0018others(16): Show | 19 | HG01109.hp2 HG01346.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-840_490-806del others(35): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113063413 | |||||
| chr13:113063429
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-875C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063429 | ||||||
| chr13:113063436
|
A | G | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-868A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063436 | ||||||
| chr13:113063438
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-866C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063438 | ||||||
| chr13:113063441
|
T | C | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-863T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063441 | ||||||
| chr13:113063445
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-859G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063445 | ||||||
| chr13:113063447
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-857G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063447 | ||||||
| chr13:113063448
|
T | C | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-856T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063448 | ||||||
| chr13:113063464
|
C | CGCCCACA others(203): Show |
1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-787_490-786ins others(210): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113063464 | |||||
| chr13:113063483
|
T | TCCCTGTC others(28): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.490-805_490-771dup others(35): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | 113063483 | |||||
| chr13:113063494
|
A | G | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.490-810A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063494 | ||||||
| chr13:113063538
|
C | T | 2 | a0001c0003t0002g0078a0001c0005t0001g0068 | 2 | HG01993.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.490-766C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063538 | ||||||
| chr13:113063571
|
T | G | 1 | a0001c0003t0001g0073 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.490-733T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063571 | ||||||
| chr13:113063948
|
G | C | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-356G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113063948 | ||||||
| chr13:113064187
|
G | A | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-117G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113064187 | ||||||
| chr13:113064196
|
A | T | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-108A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113064196 | ||||||
| chr13:113064290
|
C | T | 4 | a0001c0004t0001g0103a0001c0005t0025g0016a0001c0012t0031g0021others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-14C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 5/29 | chr13 | 113064290 | ||||||
| chr13:113064638
|
C | CA | 51 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0031others(48): Show | 51 | HG00544.hp1 HG00544.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.606+234dupA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr13 | 113064638 | |||||
| chr13:113064801
|
G | A | 1 | a0001c0003t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.607-135G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 6/29 | chr13 | 113064801 | ||||||
| chr13:113065339
|
G | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0050others(9): Show | 12 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.756+254G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065339 | ||||||
| chr13:113065489
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.756+404G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065489 | ||||||
| chr13:113065502
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.756+417G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065502 | ||||||
| chr13:113065520
|
C | T | 14 | a0001c0001t0001g0006a0001c0003t0001g0053a0001c0003t0001g0073others(11): Show | 14 | HG01109.hp1 HG01346.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.756+435C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065520 | ||||||
| chr13:113065587
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.757-459G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065587 | ||||||
| chr13:113065602
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.757-444C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065602 | ||||||
| chr13:113065844
|
G | C | 1 | a0004c0011t0002g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.757-202G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065844 | ||||||
| chr13:113065845
|
C | G | 1 | a0004c0011t0002g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.757-201C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065845 | ||||||
| chr13:113065845
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.757-201C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 7/29 | chr13 | 113065845 | ||||||
| chr13:113066466
|
G | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.881+296G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066466 | ||||||
| chr13:113066697
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.881+527C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066697 | ||||||
| chr13:113066726
|
G | A | 6 | a0001c0003t0001g0086a0001c0003t0002g0019a0001c0003t0002g0042others(3): Show | 6 | HG02074.hp2 HG02129.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+556G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066726 | ||||||
| chr13:113066818
|
G | A | 3 | a0001c0002t0003g0014a0001c0002t0003g0023a0003c0009t0011g0101 | 3 | HG01069.hp2 HG01071.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.881+648G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066818 | ||||||
| chr13:113066832
|
C | A | 1 | a0001c0002t0015g0007 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.881+662C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066832 | ||||||
| chr13:113066833
|
G | A | 2 | a0001c0001t0001g0002a0001c0002t0001g0036 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.881+663G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066833 | ||||||
| chr13:113066924
|
G | A | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.881+754G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113066924 | ||||||
| chr13:113067007
|
G | A | 1 | a0001c0013t0001g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.881+837G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067007 | ||||||
| chr13:113067057
|
A | G | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.881+887A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067057 | ||||||
| chr13:113067094
|
T | A | 3 | a0001c0006t0030g0096a0001c0008t0003g0039a0001c0008t0004g0083 | 3 | HG02109.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.881+924T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067094 | ||||||
| chr13:113067176
|
ACTGGGTG others(59): Show |
A | 1 | a0001c0005t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.881+1095_881+1160d others(68): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067176 | |||||
| chr13:113067195
|
G | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.881+1025G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067195 | ||||||
| chr13:113067208
|
GCGGAGGC others(1841): Show |
G | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.881+1095_882-947de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067208 | |||||
| chr13:113067233
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0057 | 2 | HG00323.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.881+1063G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067233 | ||||||
| chr13:113067317
|
TGCACAGC others(59): Show |
T | 1 | a0001c0015t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.881+1227_881+1292d others(68): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067317 | |||||
| chr13:113067331
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(2): Show | 5 | HG01243.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1161G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067331 | ||||||
| chr13:113067340
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(2): Show | 5 | HG01243.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1170T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067340 | ||||||
| chr13:113067383
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0037others(63): Show | 66 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.881+1213C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067383 | ||||||
| chr13:113067406
|
TCGGAGGC others(59): Show |
T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.881+1279_881+1344d others(68): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067406 | |||||
| chr13:113067449
|
CGCACAGC others(1709): Show |
C | 2 | a0001c0005t0025g0016a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.881+1425_882-749de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067449 | |||||
| chr13:113067450
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.881+1280G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067450 | ||||||
| chr13:113067463
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+1293C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067463 | ||||||
| chr13:113067472
|
G | A | 17 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(14): Show | 17 | HG01109.hp2 HG01346.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+1302G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067472 | ||||||
| chr13:113067472
|
G | T | 4 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+1302G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067472 | ||||||
| chr13:113067515
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+1345T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067515 | ||||||
| chr13:113067529
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+1359G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067529 | ||||||
| chr13:113067538
|
T | G | 6 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0003t0002g0047others(3): Show | 6 | HG01515.hp1 HG01517.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+1368T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067538 | ||||||
| chr13:113067538
|
T | TCGGAGGC others(521): Show |
1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.881+1424_881+1425i others(530): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067538 | |||||
| chr13:113067538
|
TCGGAGGC others(125): Show |
T | 5 | a0001c0002t0002g0003a0001c0002t0002g0093a0001c0005t0001g0020others(2): Show | 5 | HG00733.hp1 HG02129.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1425_881+1556d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067538 | |||||
| chr13:113067581
|
T | C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.881+1411T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067581 | ||||||
| chr13:113067595
|
G | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.881+1425G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067595 | ||||||
| chr13:113067603
|
C | A | 2 | a0001c0001t0003g0099a0001c0001t0022g0104 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881+1433C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067603 | ||||||
| chr13:113067604
|
G | T | 4 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+1434G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067604 | ||||||
| chr13:113067661
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0002g0116a0001c0004t0005g0011others(2): Show | 5 | HG01243.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1491C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067661 | ||||||
| chr13:113067670
|
G | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.881+1500G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067670 | ||||||
| chr13:113067670
|
GCGGAGGC others(653): Show |
G | 1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.881+1557_882-1673d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067670 | |||||
| chr13:113067727
|
C | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.881+1557C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067727 | ||||||
| chr13:113067737
|
C | T | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.881+1567C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067737 | ||||||
| chr13:113067784
|
AGCTGGAG others(983): Show |
A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.881+1623_882-1277d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067784 | |||||
| chr13:113067793
|
C | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(31): Show | 34 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.881+1623C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067793 | ||||||
| chr13:113067802
|
G | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(31): Show | 34 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.881+1632G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067802 | ||||||
| chr13:113067802
|
GCGGAGGC others(521): Show |
G | 1 | a0001c0004t0005g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.881+1689_882-1673d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067802 | |||||
| chr13:113067803
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(2): Show | 5 | HG01109.hp2 HG01496.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1633C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067803 | ||||||
| chr13:113067804
|
GGAGGCAG others(1511): Show |
G | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.881+1689_882-683de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067804 | |||||
| chr13:113067859
|
C | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 40 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.881+1689C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067859 | ||||||
| chr13:113067868
|
G | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.881+1698G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067868 | ||||||
| chr13:113067868
|
GCGGAGGC others(455): Show |
G | 43 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0022others(40): Show | 43 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.882-1606_882-1145d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067868 | |||||
| chr13:113067911
|
T | C | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.881+1741T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067911 | ||||||
| chr13:113067916
|
AGCTGGAG others(389): Show |
A | 5 | a0001c0001t0001g0004a0001c0001t0002g0048a0001c0001t0023g0018others(2): Show | 5 | HG01496.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1887_882-1607d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113067916 | |||||
| chr13:113067925
|
G | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.881+1755G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067925 | ||||||
| chr13:113067934
|
T | A | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.881+1764T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067934 | ||||||
| chr13:113067934
|
T | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.881+1764T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067934 | ||||||
| chr13:113067991
|
G | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(30): Show | 33 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.881+1821G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113067991 | ||||||
| chr13:113068000
|
T | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.881+1830T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068000 | ||||||
| chr13:113068000
|
T | TCGGAGGC others(521): Show |
4 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+1886_881+1887i others(530): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068000 | |||||
| chr13:113068039
|
G | A | 2 | a0001c0002t0002g0003a0001c0002t0002g0093 | 2 | HG00733.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.881+1869G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068039 | ||||||
| chr13:113068057
|
C | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.881+1887C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068057 | ||||||
| chr13:113068066
|
T | G | 45 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.881+1896T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068066 | ||||||
| chr13:113068109
|
T | TGCACAGC others(455): Show |
1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.882-1871_882-1870i others(464): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068109 | |||||
| chr13:113068132
|
G | T | 11 | a0001c0001t0002g0116a0001c0003t0001g0053a0001c0003t0001g0073others(8): Show | 11 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-1927G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068132 | ||||||
| chr13:113068180
|
AGCTGGAG others(587): Show |
A | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.882-1860_882-1267d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068180 | |||||
| chr13:113068189
|
G | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(46): Show | 49 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.882-1870G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068189 | ||||||
| chr13:113068198
|
T | G | 53 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.882-1861T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068198 | ||||||
| chr13:113068199
|
T | C | 54 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 54 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.882-1860T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068199 | ||||||
| chr13:113068255
|
C | G | 10 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(7): Show | 10 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-1804C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068255 | ||||||
| chr13:113068264
|
G | T | 10 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(7): Show | 10 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-1795G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068264 | ||||||
| chr13:113068265
|
CGGAGGCA others(389): Show |
C | 2 | a0001c0002t0002g0003a0001c0002t0002g0093 | 2 | HG00733.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.882-1748_882-1353d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068265 | |||||
| chr13:113068310
|
AACGCTGG others(453): Show |
A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.882-1748_882-1289d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068310 | ||||||
| chr13:113068311
|
A | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.882-1748A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068311 | ||||||
| chr13:113068312
|
C | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.882-1747C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068312 | ||||||
| chr13:113068312
|
CGCTGGAG others(59): Show |
C | 2 | a0001c0003t0002g0047a0001c0003t0002g0111 | 2 | HG02074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.882-1606_882-1541d others(68): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068312 | |||||
| chr13:113068321
|
G | C | 51 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0037others(48): Show | 51 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.882-1738G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068321 | ||||||
| chr13:113068330
|
T | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0037others(48): Show | 51 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.882-1729T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068330 | ||||||
| chr13:113068377
|
C | A | 10 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(7): Show | 10 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-1682C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068377 | ||||||
| chr13:113068378
|
A | C | 10 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(7): Show | 10 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-1681A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068378 | ||||||
| chr13:113068387
|
G | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.882-1672G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068387 | ||||||
| chr13:113068396
|
T | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.882-1663T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068396 | ||||||
| chr13:113068408
|
G | C | 1 | a0001c0004t0001g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.882-1651G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068408 | ||||||
| chr13:113068453
|
G | C | 5 | a0001c0001t0001g0041a0001c0002t0001g0036a0001c0006t0002g0043others(2): Show | 5 | HG01243.hp1 HG02109.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.882-1606G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068453 | ||||||
| chr13:113068462
|
T | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.882-1597T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068462 | ||||||
| chr13:113068519
|
C | CCCAGCTA others(59): Show |
1 | a0001c0002t0001g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882-1532_882-1531i others(68): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068519 | |||||
| chr13:113068519
|
C | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(31): Show | 34 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.882-1540C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068519 | ||||||
| chr13:113068519
|
CCCAGCTA others(257): Show |
C | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.882-1474_882-1211d others(2): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113068519 | |||||
| chr13:113068528
|
T | G | 17 | a0001c0001t0001g0041a0001c0001t0023g0018a0001c0003t0001g0053others(14): Show | 17 | HG01346.hp1 HG01496.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.882-1531T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068528 | ||||||
| chr13:113068585
|
C | G | 2 | a0001c0006t0002g0043a0002c0007t0001g0076 | 2 | HG02738.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.882-1474C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068585 | ||||||
| chr13:113068601
|
C | A | 1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.882-1458C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068601 | ||||||
| chr13:113068651
|
G | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.882-1408G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068651 | ||||||
| chr13:113068660
|
T | G | 35 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0041others(32): Show | 35 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.882-1399T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068660 | ||||||
| chr13:113068661
|
T | C | 57 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.882-1398T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068661 | ||||||
| chr13:113068717
|
C | G | 1 | a0001c0002t0001g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882-1342C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068717 | ||||||
| chr13:113068773
|
A | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.882-1286A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068773 | ||||||
| chr13:113068774
|
C | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 53 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.882-1285C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068774 | ||||||
| chr13:113068783
|
G | C | 19 | a0001c0001t0002g0116a0001c0001t0023g0018a0001c0002t0002g0003others(16): Show | 19 | HG00733.hp1 HG01346.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.882-1276G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068783 | ||||||
| chr13:113068792
|
T | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(61): Show | 64 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.882-1267T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068792 | ||||||
| chr13:113068794
|
G | A | 8 | a0001c0004t0001g0102a0001c0004t0003g0009a0001c0004t0004g0084others(5): Show | 8 | HG01175.hp2 HG01257.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.882-1265G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068794 | ||||||
| chr13:113068849
|
G | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(35): Show | 38 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.882-1210G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068849 | ||||||
| chr13:113068858
|
T | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(35): Show | 38 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.882-1201T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068858 | ||||||
| chr13:113068859
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.882-1200C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068859 | ||||||
| chr13:113068915
|
C | G | 2 | a0001c0006t0002g0043a0002c0007t0001g0076 | 2 | HG02738.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.882-1144C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068915 | ||||||
| chr13:113068981
|
C | G | 17 | a0001c0001t0023g0018a0001c0002t0002g0003a0001c0002t0002g0093others(14): Show | 17 | HG00733.hp1 HG01243.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.882-1078C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113068981 | ||||||
| chr13:113069047
|
G | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(49): Show | 52 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.882-1012G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069047 | ||||||
| chr13:113069047
|
G | GCCAGCTA others(917): Show |
1 | a0001c0002t0001g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882-1004_882-1003i others(926): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069047 | |||||
| chr13:113069047
|
GCCAGCTA others(455): Show |
G | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.882-1003_882-542de others(1): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069047 | |||||
| chr13:113069056
|
T | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.882-1003T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069056 | ||||||
| chr13:113069056
|
TCGGAGGC others(59): Show |
T | 14 | a0001c0001t0023g0018a0001c0003t0001g0053a0001c0003t0001g0073others(11): Show | 14 | HG01346.hp1 HG01496.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.882-946_882-881del others(66): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069056 | |||||
| chr13:113069099
|
T | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-960T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069099 | ||||||
| chr13:113069113
|
G | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0050others(37): Show | 40 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.882-946G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069113 | ||||||
| chr13:113069122
|
G | T | 3 | a0001c0001t0014g0001a0001c0002t0005g0060a0002c0007t0001g0076 | 3 | HG03471.hp2 HG03492.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.882-937G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069122 | ||||||
| chr13:113069165
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.882-894T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069165 | ||||||
| chr13:113069165
|
T | TGCACAGC others(257): Show |
1 | a0001c0001t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.882-815_882-814ins others(264): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069165 | |||||
| chr13:113069179
|
C | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(35): Show | 38 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.882-880C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069179 | ||||||
| chr13:113069188
|
G | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(31): Show | 34 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.882-871G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069188 | ||||||
| chr13:113069190
|
G | A | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.882-869G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069190 | ||||||
| chr13:113069245
|
G | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(48): Show | 51 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.882-814G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069245 | ||||||
| chr13:113069245
|
GCCAGCTA others(191): Show |
G | 2 | a0001c0005t0025g0016a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.882-737_882-540del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069245 | |||||
| chr13:113069245
|
GCCAGCTA others(257): Show |
G | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.882-805_882-542del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069245 | |||||
| chr13:113069254
|
T | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.882-805T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069254 | ||||||
| chr13:113069276
|
G | C | 1 | a0001c0003t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.882-783G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069276 | ||||||
| chr13:113069311
|
C | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.882-748C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069311 | ||||||
| chr13:113069311
|
CCCAGCTA others(59): Show |
C | 2 | a0001c0002t0002g0093a0002c0007t0001g0076 | 2 | HG06807.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.882-737_882-672del others(66): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069311 | |||||
| chr13:113069320
|
G | T | 1 | a0001c0001t0014g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882-739G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069320 | ||||||
| chr13:113069320
|
GCAGAGGC others(125): Show |
G | 1 | a0001c0002t0002g0003 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.882-737_882-606del | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069320 | |||||
| chr13:113069321
|
C | T | 14 | a0001c0001t0023g0018a0001c0003t0001g0053a0001c0003t0001g0073others(11): Show | 14 | HG01346.hp1 HG01496.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.882-738C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069321 | ||||||
| chr13:113069322
|
A | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.882-737A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069322 | ||||||
| chr13:113069377
|
G | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(46): Show | 49 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.882-682G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069377 | ||||||
| chr13:113069386
|
G | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 37 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.882-673G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069386 | ||||||
| chr13:113069443
|
C | G | 1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.882-616C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069443 | ||||||
| chr13:113069452
|
T | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.882-607T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069452 | ||||||
| chr13:113069452
|
TCGGAGGC others(59): Show |
T | 14 | a0001c0001t0023g0018a0001c0003t0001g0053a0001c0003t0001g0073others(11): Show | 14 | HG01346.hp1 HG01496.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.882-540_882-475del others(66): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069452 | |||||
| chr13:113069509
|
C | G | 3 | a0001c0001t0014g0001a0001c0002t0002g0093a0005c0014t0024g0100 | 3 | HG01891.hp2 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882-550C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069509 | ||||||
| chr13:113069518
|
G | GCGGAGGC others(257): Show |
5 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-476_882-475ins others(264): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069518 | |||||
| chr13:113069519
|
CGGAGGCA others(59): Show |
C | 1 | a0001c0002t0002g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.882-474_882-409del others(66): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069519 | |||||
| chr13:113069529
|
G | A | 1 | a0001c0003t0002g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.882-530G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069529 | ||||||
| chr13:113069575
|
C | CCCAGCTA others(59): Show |
2 | a0001c0001t0001g0041a0001c0002t0001g0036 | 2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.882-475_882-474ins others(66): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr13 | 113069575 | |||||
| chr13:113069575
|
C | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.882-484C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069575 | ||||||
| chr13:113069585
|
T | C | 45 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0038others(42): Show | 45 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.882-474T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069585 | ||||||
| chr13:113069866
|
C | G | 2 | a0001c0005t0025g0016a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.882-193C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069866 | ||||||
| chr13:113069888
|
A | G | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882-171A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 8/29 | chr13 | 113069888 | ||||||
| chr13:113070229
|
G | C | 1 | a0001c0004t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.996+56G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113070229 | ||||||
| chr13:113070286
|
T | G | 1 | a0001c0002t0001g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.996+113T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113070286 | ||||||
| chr13:113070533
|
C | T | 1 | a0001c0008t0004g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.996+360C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113070533 | ||||||
| chr13:113070624
|
T | TCCCTCCC others(7): Show |
15 | a0001c0001t0014g0001a0001c0002t0003g0014a0001c0002t0003g0023others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.996+457_996+458ins others(14): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr13 | 113070624 | |||||
| chr13:113070639
|
C | T | 1 | a0001c0015t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.996+466C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113070639 | ||||||
| chr13:113070771
|
C | T | 2 | a0001c0001t0001g0045a0001c0004t0001g0103 | 2 | HG02300.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.996+598C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113070771 | ||||||
| chr13:113070794
|
C | T | 1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.996+621C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113070794 | ||||||
| chr13:113071053
|
G | A | 13 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(10): Show | 13 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.996+880G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113071053 | ||||||
| chr13:113071444
|
T | A | 26 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(23): Show | 26 | HG01109.hp2 HG01496.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.996+1271T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113071444 | ||||||
| chr13:113071880
|
T | C | 2 | a0001c0005t0025g0016a0001c0012t0031g0021 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.996+1707T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113071880 | ||||||
| chr13:113072300
|
C | G | 7 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.996+2127C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072300 | ||||||
| chr13:113072357
|
G | A | 1 | a0001c0003t0001g0073 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.997-2087G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072357 | ||||||
| chr13:113072572
|
G | A | 9 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.997-1872G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072572 | ||||||
| chr13:113072657
|
C | T | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-1787C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072657 | ||||||
| chr13:113072837
|
T | G | 2 | a0001c0001t0014g0001a0005c0014t0024g0100 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.997-1607T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072837 | ||||||
| chr13:113072838
|
C | A | 62 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(59): Show | 62 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.997-1606C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072838 | ||||||
| chr13:113072950
|
A | G | 3 | a0001c0003t0002g0047a0001c0003t0002g0111a0001c0006t0002g0110 | 3 | HG02074.hp1 NA18946.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.997-1494A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113072950 | ||||||
| chr13:113073023
|
C | G | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-1421C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073023 | ||||||
| chr13:113073029
|
CT | C | 24 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0007g0017others(21): Show | 24 | HG01109.hp2 HG01243.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.997-1398delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr13 | 113073029 | |||||
| chr13:113073029
|
CTT | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(32): Show | 35 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.997-1399_997-1398d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr13 | 113073029 | |||||
| chr13:113073227
|
G | A | 35 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(32): Show | 35 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.997-1217G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073227 | ||||||
| chr13:113073247
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0004g0070 | 2 | HG01168.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.997-1197T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073247 | ||||||
| chr13:113073300
|
T | C | 24 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(21): Show | 24 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.997-1144T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073300 | ||||||
| chr13:113073360
|
C | T | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.997-1084C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073360 | ||||||
| chr13:113073776
|
G | A | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-668G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073776 | ||||||
| chr13:113073845
|
G | A | 2 | a0001c0001t0023g0018a0001c0005t0032g0106 | 2 | HG01496.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.997-599G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073845 | ||||||
| chr13:113073895
|
A | G | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.997-549A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073895 | ||||||
| chr13:113073915
|
C | CA | 25 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(22): Show | 25 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.997-517dupA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr13 | 113073915 | |||||
| chr13:113073928
|
T | A | 1 | a0001c0001t0004g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.997-516T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113073928 | ||||||
| chr13:113074031
|
T | C | 17 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(14): Show | 17 | HG01515.hp2 HG01517.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.997-413T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074031 | ||||||
| chr13:113074081
|
T | C | 9 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.997-363T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074081 | ||||||
| chr13:113074104
|
G | A | 1 | a0001c0005t0001g0088 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.997-340G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074104 | ||||||
| chr13:113074134
|
T | G | 9 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.997-310T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074134 | ||||||
| chr13:113074167
|
GT | G | 2 | a0003c0009t0010g0115a0003c0009t0011g0101 | 2 | HG01243.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.997-275delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr13 | 113074167 | |||||
| chr13:113074184
|
C | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(11): Show | 14 | HG00544.hp2 HG01168.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.997-260C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074184 | ||||||
| chr13:113074252
|
C | T | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.997-192C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074252 | ||||||
| chr13:113074264
|
G | A | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-180G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 9/29 | chr13 | 113074264 | ||||||
| chr13:113074573
|
G | A | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1116+10G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074573 | ||||||
| chr13:113074588
|
G | A | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1116+25G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074588 | ||||||
| chr13:113074700
|
G | A | 2 | a0003c0009t0010g0115a0003c0009t0011g0101 | 2 | HG01243.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1116+137G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074700 | ||||||
| chr13:113074726
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1116+163T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074726 | ||||||
| chr13:113074777
|
G | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(9): Show | 12 | HG00544.hp2 HG01168.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116+214G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074777 | ||||||
| chr13:113074783
|
G | A | 2 | a0001c0001t0014g0001a0005c0014t0024g0100 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1117-215G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074783 | ||||||
| chr13:113074788
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1117-210C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074788 | ||||||
| chr13:113074914
|
C | T | 7 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117-84C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 10/29 | chr13 | 113074914 | ||||||
| chr13:113075197
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.1308+8G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | chr13 | 113075197 | ||||||
| chr13:113075221
|
C | T | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1308+32C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | chr13 | 113075221 | ||||||
| chr13:113075225
|
G | A | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1308+36G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | chr13 | 113075225 | ||||||
| chr13:113075372
|
A | G | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1308+183A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | chr13 | 113075372 | ||||||
| chr13:113075382
|
CT | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(49): Show | 52 | HG00544.hp2 HG00733.hp1 HG01168.hp2 others(49): Show |
intron_variant | MODIFIER | c.1308+208delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr13 | 113075382 | |||||
| chr13:113075596
|
G | A | 26 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1309-370G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | chr13 | 113075596 | ||||||
| chr13:113075711
|
C | T | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1309-255C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | chr13 | 113075711 | ||||||
| chr13:113075733
|
GTTGTCCA others(25): Show |
G | 27 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(24): Show | 27 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1309-175_1309-144d others(34): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr13 | 113075733 | |||||
| chr13:113076246
|
G | T | 5 | a0001c0001t0014g0001a0001c0001t0023g0018a0001c0005t0032g0106others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500+89G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076246 | ||||||
| chr13:113076271
|
AT | A | 17 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1500+124delT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr13 | 113076271 | |||||
| chr13:113076286
|
T | A | 48 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(45): Show | 48 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.1500+129T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076286 | ||||||
| chr13:113076404
|
A | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(34): Show | 37 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1500+247A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076404 | ||||||
| chr13:113076555
|
G | A | 8 | a0001c0001t0023g0018a0001c0005t0001g0020a0001c0005t0001g0068others(5): Show | 8 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1500+398G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076555 | ||||||
| chr13:113076661
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1501-391C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076661 | ||||||
| chr13:113076840
|
C | T | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1501-212C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076840 | ||||||
| chr13:113076854
|
C | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1501-198C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076854 | ||||||
| chr13:113076901
|
G | T | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1501-151G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076901 | ||||||
| chr13:113076965
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1501-87G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 12/29 | chr13 | 113076965 | ||||||
| chr13:113077330
|
C | T | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1660+119C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077330 | ||||||
| chr13:113077417
|
C | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 69 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1660+206C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077417 | ||||||
| chr13:113077418
|
C | T | 1 | a0001c0001t0006g0010 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1660+207C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077418 | ||||||
| chr13:113077588
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1660+377G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077588 | ||||||
| chr13:113077592
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1660+381T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077592 | ||||||
| chr13:113077666
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1660+455G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077666 | ||||||
| chr13:113077677
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 50 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1660+466G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077677 | ||||||
| chr13:113077716
|
G | A | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1660+505G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077716 | ||||||
| chr13:113077728
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1660+517G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077728 | ||||||
| chr13:113077772
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1660+561T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077772 | ||||||
| chr13:113077784
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1660+573C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077784 | ||||||
| chr13:113077885
|
G | T | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1661-478G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077885 | ||||||
| chr13:113077985
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1661-378G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113077985 | ||||||
| chr13:113078033
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(44): Show | 47 | HG00544.hp2 HG00733.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.1661-330C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113078033 | ||||||
| chr13:113078046
|
G | A | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1661-317G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113078046 | ||||||
| chr13:113078067
|
A | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1661-296A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113078067 | ||||||
| chr13:113078067
|
AAGGCCAA others(31): Show |
A | 8 | a0001c0001t0023g0018a0001c0005t0001g0020a0001c0005t0001g0068others(5): Show | 8 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661-223_1661-186d others(40): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr13 | 113078067 | |||||
| chr13:113078124
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1661-239G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 13/29 | chr13 | 113078124 | ||||||
| chr13:113078633
|
G | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1735-33G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 14/29 | chr13 | 113078633 | ||||||
| chr13:113078648
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1735-18C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 14/29 | chr13 | 113078648 | ||||||
| chr13:113078773
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1808+34C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113078773 | ||||||
| chr13:113078803
|
C | A | 2 | a0001c0001t0001g0052a0001c0004t0005g0095 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1808+64C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113078803 | ||||||
| chr13:113078815
|
G | A | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1808+76G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113078815 | ||||||
| chr13:113079021
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(29): Show | 32 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1808+282C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079021 | ||||||
| chr13:113079256
|
C | A | 2 | a0001c0003t0001g0073a0001c0003t0001g0092 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1808+517C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079256 | ||||||
| chr13:113079494
|
G | A | 1 | a0001c0002t0027g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1808+755G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079494 | ||||||
| chr13:113079494
|
G | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1808+755G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079494 | ||||||
| chr13:113079582
|
C | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1808+843C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079582 | ||||||
| chr13:113079778
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1808+1039C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079778 | ||||||
| chr13:113079786
|
C | T | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1808+1047C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079786 | ||||||
| chr13:113079794
|
G | GGTCCAGG others(169): Show |
1 | a0001c0001t0007g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(180): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(169): Show |
1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(180): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(169): Show |
82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 82 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1808+1070_1808+107 others(180): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(489): Show |
2 | a0001c0003t0002g0078a0001c0003t0020g0089 | 2 | HG01993.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1808+1070_1808+107 others(500): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(649): Show |
1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(660): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(489): Show |
1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(500): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(169): Show |
1 | a0001c0001t0026g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(180): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(169): Show |
1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(180): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(169): Show |
15 | a0001c0003t0001g0053a0001c0003t0001g0073a0001c0003t0001g0086others(12): Show | 15 | HG01515.hp2 HG01517.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1808+1070_1808+107 others(180): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(329): Show |
1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(340): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(489): Show |
7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1808+1070_1808+107 others(500): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079794
|
G | GGTCCAGG others(201): Show |
1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1808+1070_1808+107 others(212): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079794 | |||||
| chr13:113079810
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1808+1071T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079810 | ||||||
| chr13:113079869
|
A | G | 3 | a0001c0003t0002g0078a0001c0003t0020g0089a0001c0006t0030g0096 | 3 | HG01993.hp2 HG02129.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1808+1130A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079869 | ||||||
| chr13:113079879
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1808+1140G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079879 | ||||||
| chr13:113079901
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1808+1162G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079901 | ||||||
| chr13:113079902
|
G | A | 3 | a0001c0003t0002g0078a0001c0003t0020g0089a0001c0006t0030g0096 | 3 | HG01993.hp2 HG02129.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1808+1163G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079902 | ||||||
| chr13:113079902
|
G | GGAGTGTT others(153): Show |
11 | a0001c0003t0001g0053a0001c0003t0001g0086a0001c0003t0002g0019others(8): Show | 11 | HG01993.hp1 HG02074.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1809-1131_1809-972 others(163): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113079902 | |||||
| chr13:113079943
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1808+1204A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079943 | ||||||
| chr13:113079970
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 95 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1808+1231C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113079970 | ||||||
| chr13:113080029
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1809-1184G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113080029 | ||||||
| chr13:113080062
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1809-1151A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113080062 | ||||||
| chr13:113080378
|
C | T | 16 | a0001c0003t0001g0053a0001c0003t0001g0086a0001c0003t0002g0019others(13): Show | 16 | HG01243.hp1 HG01993.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.1809-835C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113080378 | ||||||
| chr13:113080453
|
C | T | 2 | a0001c0002t0001g0036a0001c0002t0001g0040 | 2 | HG01175.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1809-760C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113080453 | ||||||
| chr13:113080717
|
C | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0030others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1809-496C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113080717 | ||||||
| chr13:113080913
|
CA | C | 15 | a0001c0002t0001g0036a0001c0002t0001g0040a0001c0002t0001g0069others(12): Show | 15 | HG00733.hp1 HG01168.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1809-296delA | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr13 | 113080913 | |||||
| chr13:113080929
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1809-284G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113080929 | ||||||
| chr13:113081021
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1809-192G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113081021 | ||||||
| chr13:113081076
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 88 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1809-137T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 15/29 | chr13 | 113081076 | ||||||
| chr13:113081294
|
G | A | 8 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(5): Show | 8 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1875+15G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081294 | ||||||
| chr13:113081391
|
G | A | 1 | a0005c0014t0024g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1875+112G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081391 | ||||||
| chr13:113081419
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1875+140G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081419 | ||||||
| chr13:113081597
|
C | T | 3 | a0001c0001t0023g0018a0001c0005t0032g0106a0003c0009t0010g0115 | 3 | HG01496.hp1 HG02300.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1875+318C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081597 | ||||||
| chr13:113081768
|
C | T | 8 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(5): Show | 8 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1875+489C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081768 | ||||||
| chr13:113081812
|
G | A | 14 | a0001c0003t0001g0053a0001c0003t0001g0086a0001c0003t0002g0019others(11): Show | 14 | HG01993.hp1 HG01993.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1875+533G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081812 | ||||||
| chr13:113081854
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1876-573C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081854 | ||||||
| chr13:113081871
|
G | A | 2 | a0001c0005t0029g0091a0003c0009t0011g0101 | 2 | HG01243.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1876-556G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081871 | ||||||
| chr13:113081878
|
C | A | 1 | a0004c0011t0002g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1876-549C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081878 | ||||||
| chr13:113081919
|
A | G | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1876-508A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081919 | ||||||
| chr13:113081937
|
GTCACCTG others(28): Show |
G | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1876-459_1876-425d others(37): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr13 | 113081937 | |||||
| chr13:113081953
|
C | T | 17 | a0001c0003t0001g0053a0001c0003t0001g0086a0001c0003t0002g0019others(14): Show | 17 | HG01993.hp1 HG01993.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1876-474C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081953 | ||||||
| chr13:113081988
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1876-439C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113081988 | ||||||
| chr13:113082048
|
G | A | 7 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1876-379G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113082048 | ||||||
| chr13:113082229
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1876-198C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113082229 | ||||||
| chr13:113082243
|
C | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1876-184C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113082243 | ||||||
| chr13:113082336
|
T | G | 1 | a0001c0002t0001g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1876-91T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113082336 | ||||||
| chr13:113082378
|
C | A | 1 | a0001c0002t0027g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1876-49C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113082378 | ||||||
| chr13:113082420
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | splice_region_variant&intron_variant | LOW | c.1876-7C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 16/29 | chr13 | 113082420 | ||||||
| chr13:113082559
|
G | A | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1991+17G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082559 | ||||||
| chr13:113082668
|
T | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1991+126T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082668 | ||||||
| chr13:113082763
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1991+221A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082763 | ||||||
| chr13:113082778
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1991+236C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082778 | ||||||
| chr13:113082785
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1991+243C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082785 | ||||||
| chr13:113082808
|
G | C | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1991+266G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082808 | ||||||
| chr13:113082830
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1991+288C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082830 | ||||||
| chr13:113082914
|
C | A | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1991+372C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113082914 | ||||||
| chr13:113083042
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1991+500C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083042 | ||||||
| chr13:113083071
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1991+529C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083071 | ||||||
| chr13:113083137
|
G | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1991+595G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083137 | ||||||
| chr13:113083182
|
A | T | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1991+640A>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083182 | ||||||
| chr13:113083189
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1991+647A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083189 | ||||||
| chr13:113083398
|
C | T | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1992-600C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083398 | ||||||
| chr13:113083399
|
G | A | 15 | a0001c0001t0002g0116a0001c0003t0001g0053a0001c0003t0001g0086others(12): Show | 15 | HG01993.hp1 HG01993.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1992-599G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083399 | ||||||
| chr13:113083440
|
C | T | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1992-558C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083440 | ||||||
| chr13:113083590
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1992-408G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083590 | ||||||
| chr13:113083777
|
C | T | 1 | a0001c0003t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1992-221C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083777 | ||||||
| chr13:113083861
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1992-137G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083861 | ||||||
| chr13:113083863
|
C | T | 7 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1992-135C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 17/29 | chr13 | 113083863 | ||||||
| chr13:113084324
|
T | TACCCCAG others(10): Show |
70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 70 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2061+270_2061+286d others(19): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr13 | 113084324 | |||||
| chr13:113084489
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 70 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2062-403A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084489 | ||||||
| chr13:113084707
|
G | A | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2062-185G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084707 | ||||||
| chr13:113084762
|
C | A | 6 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0050others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-130C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084762 | ||||||
| chr13:113084799
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2062-93C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084799 | ||||||
| chr13:113084811
|
C | T | 16 | a0001c0001t0002g0116a0001c0003t0001g0053a0001c0003t0001g0086others(13): Show | 16 | HG01993.hp1 HG01993.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.2062-81C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084811 | ||||||
| chr13:113084812
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0063others(1): Show | 4 | HG01358.hp1 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2062-80G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084812 | ||||||
| chr13:113084816
|
T | G | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2062-76T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084816 | ||||||
| chr13:113084826
|
G | A | 1 | a0001c0003t0002g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2062-66G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 18/29 | chr13 | 113084826 | ||||||
| chr13:113085043
|
A | C | 11 | a0001c0005t0001g0020a0001c0005t0001g0068a0001c0005t0001g0079others(8): Show | 11 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2155-43A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 19/29 | chr13 | 113085043 | ||||||
| chr13:113085204
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2247+26G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085204 | ||||||
| chr13:113085354
|
G | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2247+176G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085354 | ||||||
| chr13:113085441
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2247+263G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085441 | ||||||
| chr13:113085688
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2248-436C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085688 | ||||||
| chr13:113085713
|
G | T | 26 | a0001c0001t0002g0116a0001c0003t0001g0053a0001c0003t0001g0086others(23): Show | 26 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.2248-411G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085713 | ||||||
| chr13:113085746
|
G | C | 16 | a0001c0002t0001g0036a0001c0002t0001g0040a0001c0002t0001g0069others(13): Show | 16 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2248-378G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085746 | ||||||
| chr13:113085767
|
AGGGTGGC others(50): Show |
A | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2248-264_2248-208d others(59): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr13 | 113085767 | |||||
| chr13:113085824
|
C | A | 16 | a0001c0002t0001g0036a0001c0002t0001g0040a0001c0002t0001g0069others(13): Show | 16 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2248-300C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085824 | ||||||
| chr13:113085904
|
G | A | 1 | a0003c0009t0010g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2248-220G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113085904 | ||||||
| chr13:113086099
|
G | A | 1 | a0001c0004t0004g0097 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2248-25G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 20/29 | chr13 | 113086099 | ||||||
| chr13:113086288
|
G | A | 16 | a0001c0002t0001g0036a0001c0002t0001g0040a0001c0002t0001g0069others(13): Show | 16 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2373+39G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113086288 | ||||||
| chr13:113086392
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2373+143A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113086392 | ||||||
| chr13:113086525
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2373+276C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113086525 | ||||||
| chr13:113086743
|
G | GT | 7 | a0001c0005t0001g0079a0001c0005t0001g0080a0001c0005t0001g0081others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.2374-482dupT | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr13 | 113086743 | |||||
| chr13:113086964
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.2374-271C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113086964 | ||||||
| chr13:113087027
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0028g0098 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2374-208C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113087027 | ||||||
| chr13:113087135
|
G | A | 1 | a0001c0013t0001g0067 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2374-100G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113087135 | ||||||
| chr13:113087150
|
A | C | 2 | a0001c0003t0002g0047a0001c0003t0002g0111 | 2 | HG02074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.2374-85A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113087150 | ||||||
| chr13:113087198
|
T | C | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2374-37T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 21/29 | chr13 | 113087198 | ||||||
| chr13:113087479
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2595+23C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 22/29 | chr13 | 113087479 | ||||||
| chr13:113087485
|
G | A | 5 | a0001c0003t0001g0086a0001c0003t0002g0047a0001c0003t0002g0111others(2): Show | 5 | HG02074.hp1 NA18946.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595+29G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 22/29 | chr13 | 113087485 | ||||||
| chr13:113087537
|
C | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.2595+81C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 22/29 | chr13 | 113087537 | ||||||
| chr13:113088079
|
C | T | 24 | a0001c0002t0001g0036a0001c0002t0001g0040a0001c0002t0001g0069others(21): Show | 24 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2689-248C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 23/29 | chr13 | 113088079 | ||||||
| chr13:113088084
|
C | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.2689-243C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 23/29 | chr13 | 113088084 | ||||||
| chr13:113088113
|
G | T | 1 | a0001c0010t0021g0015 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2689-214G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 23/29 | chr13 | 113088113 | ||||||
| chr13:113088141
|
C | T | 2 | a0001c0004t0004g0084a0005c0014t0024g0100 | 2 | HG01891.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2689-186C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 23/29 | chr13 | 113088141 | ||||||
| chr13:113088281
|
C | T | 18 | a0001c0001t0003g0099a0001c0001t0022g0104a0001c0002t0001g0036others(15): Show | 18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2689-46C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 23/29 | chr13 | 113088281 | ||||||
| chr13:113088463
|
C | T | 25 | a0001c0001t0002g0048a0001c0001t0002g0116a0001c0001t0003g0099others(22): Show | 25 | HG01109.hp2 HG01891.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.2767+58C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 24/29 | chr13 | 113088463 | ||||||
| chr13:113088491
|
C | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2768-71C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 24/29 | chr13 | 113088491 | ||||||
| chr13:113088496
|
C | T | 7 | a0001c0001t0003g0099a0001c0001t0007g0017a0001c0001t0007g0026others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2768-66C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 24/29 | chr13 | 113088496 | ||||||
| chr13:113088512
|
G | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2768-50G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 24/29 | chr13 | 113088512 | ||||||
| chr13:113088699
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2834+71G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113088699 | ||||||
| chr13:113088828
|
C | T | 16 | a0001c0001t0017g0059a0001c0002t0001g0036a0001c0002t0001g0040others(13): Show | 16 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2834+200C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113088828 | ||||||
| chr13:113088867
|
G | A | 1 | a0001c0006t0002g0110 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2834+239G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113088867 | ||||||
| chr13:113088872
|
T | C | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2834+244T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113088872 | ||||||
| chr13:113088880
|
T | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2834+252T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113088880 | ||||||
| chr13:113088990
|
C | T | 1 | a0001c0002t0015g0007 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2834+362C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113088990 | ||||||
| chr13:113089163
|
TCCCCCGC others(5): Show |
T | 7 | a0001c0001t0003g0099a0001c0001t0007g0017a0001c0001t0007g0026others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2835-434_2835-423d others(14): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089163 | |||||
| chr13:113089169
|
G | GC | 30 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0058others(27): Show | 30 | HG00544.hp2 HG01109.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.2835-430dupC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089169 | |||||
| chr13:113089169
|
G | GCC | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0008g0061others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2835-431_2835-430d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089169 | |||||
| chr13:113089169
|
GC | G | 18 | a0001c0001t0001g0022a0001c0001t0001g0050a0001c0001t0001g0051others(15): Show | 18 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.2835-430delC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089169 | |||||
| chr13:113089233
|
T | TTCTCATC others(133): Show |
1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2835-313_2835-312i others(142): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089233 | |||||
| chr13:113089233
|
T | TTCTCATC others(203): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0003t0001g0053 | 3 | HG02486.hp1 HG02602.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2835-313_2835-312i others(212): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089233 | |||||
| chr13:113089244
|
C | CCCGTCCG others(63): Show |
41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2835-313_2835-312i others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089244 | |||||
| chr13:113089244
|
C | CCCGTCCG others(133): Show |
1 | a0001c0001t0001g0002 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2835-313_2835-312i others(142): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089244 | |||||
| chr13:113089244
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2835-366C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089244 | ||||||
| chr13:113089250
|
C | CGGGTTTA others(133): Show |
1 | a0001c0001t0019g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2835-313_2835-312i others(142): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089250 | |||||
| chr13:113089250
|
C | CGGGTTTA others(273): Show |
1 | a0001c0001t0004g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2835-313_2835-312i others(282): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089250 | |||||
| chr13:113089250
|
CGGGTTTA others(63): Show |
C | 3 | a0001c0002t0002g0003a0001c0002t0002g0093a0001c0005t0029g0091 | 3 | HG00733.hp1 HG02293.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2835-312_2835-243d others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089250 | |||||
| chr13:113089298
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2835-312A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089298 | ||||||
| chr13:113089314
|
C | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0002g0048others(27): Show | 30 | HG01109.hp1 HG01175.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.2835-296C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089314 | ||||||
| chr13:113089320
|
T | C | 27 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0002g0048others(24): Show | 27 | HG01109.hp1 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.2835-290T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089320 | ||||||
| chr13:113089320
|
T | TGGGTTTA others(63): Show |
1 | a0001c0002t0001g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2835-226_2835-157d others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089320 | |||||
| chr13:113089320
|
T | TGGGTTTA others(133): Show |
1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2835-274_2835-135d others(142): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089320 | |||||
| chr13:113089384
|
C | T | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(36): Show | 39 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2835-226C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089384 | ||||||
| chr13:113089390
|
C | CGGGTTTA others(203): Show |
4 | a0001c0004t0004g0046a0001c0004t0004g0084a0001c0004t0004g0097others(1): Show | 4 | HG01109.hp1 HG01175.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2835-157_2835-156i others(212): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089390 | |||||
| chr13:113089390
|
C | CGGGTTTA others(133): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2835-157_2835-156i others(142): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089390 | |||||
| chr13:113089390
|
C | CGGGTTTA others(63): Show |
1 | a0001c0001t0006g0108 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2835-151_2835-150i others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089390 | |||||
| chr13:113089390
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(39): Show | 42 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.2835-220C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089390 | ||||||
| chr13:113089454
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(35): Show | 38 | HG00323.hp1 HG00544.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.2835-156T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089454 | ||||||
| chr13:113089454
|
T | TCCGTCCG others(133): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0049 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2835-135_2835-134i others(142): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089454 | |||||
| chr13:113089454
|
T | TCCGTCTG others(63): Show |
33 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0041others(30): Show | 33 | HG00323.hp2 HG00544.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.2835-151_2835-150i others(72): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | 113089454 | |||||
| chr13:113089544
|
C | A | 1 | a0001c0005t0025g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2835-66C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 25/29 | chr13 | 113089544 | ||||||
| chr13:113089825
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.2953+97G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113089825 | ||||||
| chr13:113090045
|
A | G | 2 | a0001c0002t0003g0014a0001c0002t0003g0023 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2953+317A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090045 | ||||||
| chr13:113090127
|
C | T | 11 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0002t0002g0003others(8): Show | 11 | HG00733.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2953+399C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090127 | ||||||
| chr13:113090145
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG03490.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2953+417C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090145 | ||||||
| chr13:113090253
|
C | T | 1 | a0002c0007t0001g0076 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2953+525C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090253 | ||||||
| chr13:113090341
|
C | T | 5 | a0001c0002t0003g0014a0001c0002t0003g0023a0001c0008t0003g0039others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2953+613C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090341 | ||||||
| chr13:113090355
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2953+627A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090355 | ||||||
| chr13:113090560
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2953+832A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090560 | ||||||
| chr13:113090621
|
G | A | 12 | a0001c0001t0017g0059a0001c0002t0001g0071a0001c0002t0003g0014others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2953+893G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090621 | ||||||
| chr13:113090689
|
G | A | 2 | a0001c0001t0012g0055a0003c0009t0010g0115 | 2 | HG02300.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2953+961G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090689 | ||||||
| chr13:113090920
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.2953+1192A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113090920 | ||||||
| chr13:113091063
|
C | T | 1 | a0001c0001t0028g0098 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2953+1335C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091063 | ||||||
| chr13:113091078
|
A | ACTCTCTC others(42): Show |
1 | a0001c0001t0008g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2953+1383_2953+138 others(53): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr13 | 113091078 | |||||
| chr13:113091088
|
C | T | 13 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0113others(10): Show | 13 | HG00544.hp1 HG00733.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2953+1360C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091088 | ||||||
| chr13:113091297
|
T | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2953+1569T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091297 | ||||||
| chr13:113091299
|
G | A | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2953+1571G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091299 | ||||||
| chr13:113091416
|
A | G | 4 | a0001c0001t0002g0116a0001c0003t0002g0047a0001c0003t0002g0111others(1): Show | 4 | HG02074.hp1 NA18946.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.2953+1688A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091416 | ||||||
| chr13:113091569
|
G | A | 2 | a0001c0001t0012g0055a0003c0009t0010g0115 | 2 | HG02300.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2953+1841G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091569 | ||||||
| chr13:113091577
|
C | T | 22 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0001t0007g0017others(19): Show | 22 | HG00544.hp1 HG01109.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2953+1849C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091577 | ||||||
| chr13:113091619
|
G | GCCGACCC others(41): Show |
2 | a0001c0001t0012g0055a0003c0009t0010g0115 | 2 | HG02300.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2953+1918_2953+191 others(52): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr13 | 113091619 | |||||
| chr13:113091627
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.2953+1899G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091627 | ||||||
| chr13:113091642
|
G | GGGGCTGA others(40): Show |
1 | a0001c0003t0002g0111 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2953+1918_2953+191 others(51): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr13 | 113091642 | |||||
| chr13:113091647
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.2953+1919C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091647 | ||||||
| chr13:113091648
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2953+1920A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091648 | ||||||
| chr13:113091650
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2953+1922T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091650 | ||||||
| chr13:113091675
|
G | A | 2 | a0001c0003t0001g0073a0001c0003t0001g0092 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2953+1947G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091675 | ||||||
| chr13:113091822
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2953+2094G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091822 | ||||||
| chr13:113091936
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.2953+2208A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113091936 | ||||||
| chr13:113092088
|
A | G | 2 | a0001c0001t0001g0063a0001c0004t0001g0025 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2953+2360A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092088 | ||||||
| chr13:113092222
|
C | T | 2 | a0001c0006t0002g0110a0005c0014t0024g0100 | 2 | HG01891.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2954-2292C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092222 | ||||||
| chr13:113092334
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2954-2180G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092334 | ||||||
| chr13:113092378
|
AGAGCCGG others(44): Show |
A | 3 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG03490.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2954-2135_2954-208 others(55): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092378 | ||||||
| chr13:113092379
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 110 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.2954-2135G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092379 | ||||||
| chr13:113092396
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(108): Show | 111 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2954-2118G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092396 | ||||||
| chr13:113092446
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG03490.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2954-2068T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092446 | ||||||
| chr13:113092447
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG03490.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2954-2067G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092447 | ||||||
| chr13:113092586
|
G | A | 1 | a0003c0009t0011g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2954-1928G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092586 | ||||||
| chr13:113092662
|
G | A | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2954-1852G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092662 | ||||||
| chr13:113092756
|
A | C | 13 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0002t0001g0040others(10): Show | 13 | HG00544.hp1 HG01175.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2954-1758A>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092756 | ||||||
| chr13:113092779
|
TG | T | 27 | a0001c0001t0001g0063a0001c0001t0005g0062a0001c0001t0007g0017others(24): Show | 27 | HG01109.hp1 HG01109.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.2954-1734delG | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092779 | ||||||
| chr13:113092788
|
C | G | 2 | a0001c0001t0001g0063a0001c0004t0001g0025 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2954-1726C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092788 | ||||||
| chr13:113092795
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2954-1719G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092795 | ||||||
| chr13:113092810
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.2954-1704A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092810 | ||||||
| chr13:113092821
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.2954-1693T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092821 | ||||||
| chr13:113092944
|
T | C | 18 | a0001c0001t0001g0063a0001c0001t0008g0066a0001c0001t0017g0059others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2954-1570T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092944 | ||||||
| chr13:113092957
|
G | C | 2 | a0001c0001t0012g0055a0003c0009t0010g0115 | 2 | HG02300.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2954-1557G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113092957 | ||||||
| chr13:113093103
|
G | A | 1 | a0001c0001t0012g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2954-1411G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093103 | ||||||
| chr13:113093197
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.2954-1317C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093197 | ||||||
| chr13:113093395
|
G | A | 1 | a0001c0005t0032g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2954-1119G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093395 | ||||||
| chr13:113093485
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2954-1029C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093485 | ||||||
| chr13:113093582
|
TC | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 70 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2954-928delC | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr13 | 113093582 | |||||
| chr13:113093723
|
C | G | 3 | a0001c0001t0005g0062a0001c0005t0025g0016a0005c0014t0024g0100 | 3 | HG01891.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2954-791C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093723 | ||||||
| chr13:113093769
|
G | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2954-745G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093769 | ||||||
| chr13:113093775
|
C | T | 18 | a0001c0001t0001g0063a0001c0001t0008g0066a0001c0001t0017g0059others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2954-739C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093775 | ||||||
| chr13:113093912
|
T | A | 1 | a0001c0005t0029g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2954-602T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093912 | ||||||
| chr13:113093984
|
C | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0002t0001g0040others(10): Show | 13 | HG00544.hp1 HG01175.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2954-530C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093984 | ||||||
| chr13:113093988
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2954-526C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113093988 | ||||||
| chr13:113094065
|
C | A | 17 | a0001c0001t0001g0063a0001c0001t0008g0066a0001c0001t0017g0059others(14): Show | 17 | HG01109.hp1 HG01175.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2954-449C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094065 | ||||||
| chr13:113094238
|
G | A | 17 | a0001c0001t0001g0063a0001c0001t0017g0059a0001c0002t0001g0071others(14): Show | 17 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2954-276G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094238 | ||||||
| chr13:113094241
|
G | A | 2 | a0001c0001t0001g0037a0001c0002t0001g0069 | 2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2954-273G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094241 | ||||||
| chr13:113094352
|
G | A | 2 | a0001c0001t0001g0058a0001c0003t0001g0053 | 2 | HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2954-162G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094352 | ||||||
| chr13:113094376
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2954-138C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094376 | ||||||
| chr13:113094469
|
C | T | 2 | a0001c0001t0006g0108a0001c0001t0019g0107 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2954-45C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094469 | ||||||
| chr13:113094495
|
G | A | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2954-19G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 26/29 | chr13 | 113094495 | ||||||
| chr13:113094783
|
C | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3075+148C>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113094783 | ||||||
| chr13:113094834
|
G | C | 6 | a0001c0001t0003g0099a0001c0002t0003g0014a0001c0002t0003g0023others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3075+199G>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113094834 | ||||||
| chr13:113094864
|
ACT | A | 6 | a0001c0001t0007g0017a0001c0001t0007g0026a0001c0001t0007g0035others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3075+236_3075+237d others(4): Show |
MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | 113094864 | |||||
| chr13:113095000
|
G | A | 6 | a0001c0001t0003g0099a0001c0002t0003g0014a0001c0002t0003g0023others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3075+365G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095000 | ||||||
| chr13:113095049
|
T | G | 3 | a0001c0001t0005g0062a0001c0005t0025g0016a0005c0014t0024g0100 | 3 | HG01891.hp2 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3075+414T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095049 | ||||||
| chr13:113095161
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 67 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3075+526G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095161 | ||||||
| chr13:113095181
|
G | T | 2 | a0001c0001t0022g0104a0001c0001t0023g0018 | 2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3075+546G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095181 | ||||||
| chr13:113095259
|
C | T | 1 | a0001c0006t0030g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3075+624C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095259 | ||||||
| chr13:113095323
|
G | A | 3 | a0001c0002t0005g0060a0001c0004t0005g0011a0001c0004t0005g0012 | 3 | HG01515.hp1 HG01517.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3075+688G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095323 | ||||||
| chr13:113095331
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.3075+696A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095331 | ||||||
| chr13:113095370
|
C | G | 18 | a0001c0001t0001g0063a0001c0001t0017g0059a0001c0002t0001g0071others(15): Show | 18 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3075+735C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095370 | ||||||
| chr13:113095397
|
A | G | 2 | a0001c0001t0012g0055a0003c0009t0010g0115 | 2 | HG02300.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.3075+762A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095397 | ||||||
| chr13:113095420
|
C | T | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3075+785C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095420 | ||||||
| chr13:113095628
|
T | A | 7 | a0001c0001t0005g0062a0001c0001t0007g0017a0001c0001t0007g0026others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3076-743T>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095628 | ||||||
| chr13:113095819
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.3076-552C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095819 | ||||||
| chr13:113095889
|
G | T | 3 | a0001c0001t0008g0061a0001c0001t0008g0066a0001c0001t0028g0098 | 3 | HG02559.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3076-482G>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113095889 | ||||||
| chr13:113096094
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.3076-277A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113096094 | ||||||
| chr13:113096128
|
A | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0094a0001c0002t0001g0040others(10): Show | 13 | HG00544.hp1 HG01175.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3076-243A>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113096128 | ||||||
| chr13:113096183
|
C | G | 12 | a0001c0001t0003g0099a0001c0001t0023g0018a0001c0002t0001g0036others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.3076-188C>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113096183 | ||||||
| chr13:113096210
|
C | T | 2 | a0001c0001t0023g0018a0001c0006t0030g0096 | 2 | HG01496.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3076-161C>T | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113096210 | ||||||
| chr13:113096272
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.3076-99G>A | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113096272 | ||||||
| chr13:113096318
|
T | G | 1 | a0001c0012t0031g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3076-53T>G | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 27/29 | chr13 | 113096318 | ||||||
| chr13:113096537
|
T | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0012g0055others(3): Show | 6 | HG01978.hp1 HG02300.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.3189-13T>C | MCF2L | ENSG00000126217.22 | transcript | ENST00000535094.7 | protein_coding | 28/29 | chr13 | 113096537 |