Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10150 |
|---|---|
| ensemblid | ENSG00000139793.21 |
| hgncid | 16746 |
| symbol | MBNL2 |
| name | muscleblind like splicing regulator 2 |
| refseq_nuc | NM_001382683.1 |
| refseq_prot | NP_001369612.1 |
| ensembl_nuc | ENST00000679496.1 |
| ensembl_prot | ENSP00000505596.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 97222333 |
| end | 97394120 |
| strand | + |
| ver | v1.2 |
| region | chr13:97222333-97394120 |
| region5000 | chr13:97217333-97399120 |
| regionname0 | MBNL2_chr13_97222333_97394120 |
| regionname5000 | MBNL2_chr13_97217333_97399120 |
| 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 | 391 | 252 | 87 | 54 | 69 | 12 | 28 | 43 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0002 | 0/0 | 391 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0003 | 0/0 | 391 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| 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 | 1176 | 241 | 81 | 53 | 66 | 11 | 28 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| c0002 | 0/0 | 1176 | 9 | 6 | 0 | 3 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| c0003 | 0/0 | 1176 | 2 | 0 | 1 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| c0004 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| c0005 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| 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 | 1/1 | 3475 | 181 | 53 | 41 | 52 | 12 | 21 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0002 | 0/0 | 3475 | 30 | 10 | 1 | 15 | 0 | 4 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0003 | 0/0 | 3475 | 11 | 0 | 5 | 3 | 0 | 3 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0004 | 0/0 | 3475 | 8 | 7 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0005 | 0/0 | 3475 | 6 | 4 | 2 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0006 | 0/0 | 3475 | 5 | 5 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0007 | 0/0 | 3475 | 2 | 2 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0008 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0009 | 0/0 | 3475 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0010 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0011 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0012 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0013 | 0/0 | 3475 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0014 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0015 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0016 | 0/0 | 3475 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0017 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| t0018 | 0/0 | 3475 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| 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 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| 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 | 1176 | 241 | 81 | 53 | 66 | 11 | 28 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0002 | 0/0 | 1176 | 9 | 6 | 0 | 3 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0003 | 0/0 | 1176 | 2 | 0 | 1 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0002c0004 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0003c0005 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4650 | 172 | 50 | 40 | 48 | 11 | 21 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0002 | 0/0 | 4650 | 30 | 10 | 1 | 15 | 0 | 4 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0003 | 0/0 | 4650 | 11 | 0 | 5 | 3 | 0 | 3 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0004 | 0/0 | 4650 | 8 | 7 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0005 | 0/0 | 4650 | 6 | 4 | 2 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0006 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0007 | 0/0 | 4650 | 2 | 2 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0008 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0009 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0010 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0011 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0012 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0013 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0014 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0015 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0016 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0017 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0001t0018 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0002t0001 | 0/0 | 4650 | 5 | 2 | 0 | 3 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0002t0006 | 0/0 | 4650 | 4 | 4 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0001c0003t0001 | 0/0 | 4650 | 2 | 0 | 1 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0002c0004t0001 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| a0003c0005t0001 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | copy fasta | chr13 | 97217333 | 97399120 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0012g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0013g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0016g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0001t0018g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0002t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| a0003c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0243 | EUR | FIN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00642 | hp1 | a0001 | c0001 | t0018 | g0012 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0250 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0244 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0221 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0197 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02717 | hp2 | a0001 | c0002 | t0006 | g0248 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02818 | hp1 | a0001 | c0002 | t0006 | g0212 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0253 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02970 | hp2 | a0001 | c0002 | t0006 | g0126 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0234 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03098 | hp2 | a0003 | c0005 | t0001 | g0171 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0216 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | YRI | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | YRI | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | LWK | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19056 | hp2 | a0002 | c0004 | t0001 | g0232 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0117 | AFR | ASW | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | GIH | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01123 | hp1 | a0001 | c0001 | t0016 | g0245 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0177 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0227 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0206 | AFR | USA | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | USA | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0230 | REF | REF | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | MBNL2_chr13_97217333_97399120 | MBNL2 | chr13 | 97217333 | 97399120 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97276368
|
G | A | 1 | a0002 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.133G>A | p.Val45Ile | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | 936/4650 | 133/1176 | 45/391 | chr13 | 97276368 | ||
| chr13:97391348
|
G | A | 1 | a0003 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1075G>A | p.Gly359Arg | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1878/4650 | 1075/1176 | 359/391 | chr13 | 97391348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97276361
|
T | C | 1 | a0001c0003 | 2 | HG00280.hp2 HG01361.hp2 |
synonymous_variant | LOW | c.126T>C | p.Ser42Ser | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | 929/4650 | 126/1176 | 42/391 | chr13 | 97276361 | ||
| chr13:97343132
|
G | A | 2 | a0001c0002a0002c0004 | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
synonymous_variant | LOW | c.456G>A | p.Thr152Thr | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/9 | 1259/4650 | 456/1176 | 152/391 | chr13 | 97343132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97275713
|
A | G | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(5): Show | 18 | HG00642.hp1 HG01123.hp1 HG01192.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-523A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | 523 | chr13 | 97275713 | |||||
| chr13:97275863
|
A | G | 1 | a0001c0001t0018 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-373A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | 373 | chr13 | 97275863 | |||||
| chr13:97275977
|
C | T | 1 | a0001c0001t0017 | 1 | HG02486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-259C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | chr13 | 97275977 | ||||||
| chr13:97276011
|
T | C | 6 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(3): Show | 9 | HG00642.hp1 HG01123.hp1 HG02572.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-225T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | 225 | chr13 | 97276011 | |||||
| chr13:97276209
|
A | G | 1 | a0001c0001t0013 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-27A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/9 | 27 | chr13 | 97276209 | |||||
| chr13:97391758
|
A | G | 1 | a0001c0001t0007 | 2 | HG03130.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*309A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 309 | chr13 | 97391758 | |||||
| chr13:97391783
|
G | A | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 334 | chr13 | 97391783 | |||||
| chr13:97392904
|
A | G | 3 | a0001c0001t0002a0001c0001t0012a0001c0001t0016 | 32 | HG00609.hp1 HG01123.hp1 HG01243.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1455A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1455 | chr13 | 97392904 | |||||
| chr13:97392909
|
A | T | 1 | a0001c0001t0011 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1460A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1460 | chr13 | 97392909 | |||||
| chr13:97393045
|
T | C | 1 | a0001c0001t0008 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1596T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1596 | chr13 | 97393045 | |||||
| chr13:97393115
|
C | T | 1 | a0001c0001t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1666 | chr13 | 97393115 | |||||
| chr13:97393231
|
C | T | 2 | a0001c0001t0005a0001c0001t0015 | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1782C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1782 | chr13 | 97393231 | |||||
| chr13:97393274
|
T | C | 2 | a0001c0001t0003a0001c0001t0009 | 12 | HG01943.hp2 HG01981.hp2 HG01993.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1825T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1825 | chr13 | 97393274 | |||||
| chr13:97393314
|
A | G | 1 | a0001c0001t0009 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 1865 | chr13 | 97393314 | |||||
| chr13:97393575
|
T | C | 1 | a0001c0001t0010 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2126T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 2126 | chr13 | 97393575 | |||||
| chr13:97394011
|
C | T | 2 | a0001c0001t0008a0001c0001t0017 | 2 | HG02258.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2562C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 9/9 | 2562 | chr13 | 97394011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97222766
|
A | G | 14 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0246others(11): Show | 14 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+235A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97222766 | ||||||
| chr13:97223109
|
A | G | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-605+578A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223109 | ||||||
| chr13:97223161
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-605+630G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223161 | ||||||
| chr13:97223777
|
C | T | 6 | a0001c0001t0004g0233a0001c0001t0014g0234a0001c0002t0001g0235others(3): Show | 6 | HG02976.hp1 HG03098.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-605+1246C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223777 | ||||||
| chr13:97223779
|
CATTT | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(41): Show | 44 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-605+1250_-605+125 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97223779 | |||||
| chr13:97223892
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-605+1361G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223892 | ||||||
| chr13:97223938
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18950.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-605+1407T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223938 | ||||||
| chr13:97223948
|
A | G | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-605+1417A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223948 | ||||||
| chr13:97223952
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-605+1421A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223952 | ||||||
| chr13:97223985
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0230 | 2 | HG04199.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-605+1454A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97223985 | ||||||
| chr13:97224016
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-605+1485A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224016 | ||||||
| chr13:97224021
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-605+1490A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224021 | ||||||
| chr13:97224158
|
A | G | 1 | a0001c0001t0012g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-605+1627A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224158 | ||||||
| chr13:97224169
|
G | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0035others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-605+1638G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224169 | ||||||
| chr13:97224174
|
G | A | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-605+1643G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224174 | ||||||
| chr13:97224283
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-605+1752G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224283 | ||||||
| chr13:97224435
|
C | T | 9 | a0001c0001t0001g0219a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01167.hp1 HG01257.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.-605+1904C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224435 | ||||||
| chr13:97224465
|
T | C | 6 | a0001c0001t0004g0233a0001c0001t0014g0234a0001c0002t0001g0235others(3): Show | 6 | HG02976.hp1 HG03098.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-605+1934T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224465 | ||||||
| chr13:97224474
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0003g0099 | 2 | HG00558.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-605+1943C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224474 | ||||||
| chr13:97224584
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-605+2053C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224584 | ||||||
| chr13:97224628
|
C | CA | 23 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 23 | HG01175.hp2 HG01496.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.-605+2121dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224628
|
C | CAA | 30 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.-605+2120_-605+212 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224628
|
CA | C | 51 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(48): Show | 51 | HG00609.hp2 HG01071.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.-605+2121delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224628
|
CAA | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0058others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.-605+2120_-605+212 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224628
|
CAAA | C | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG02572.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+2119_-605+212 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224628
|
CAAAAAAA | C | 5 | a0001c0001t0004g0233a0001c0001t0014g0234a0001c0002t0001g0235others(2): Show | 5 | HG02976.hp1 HG03098.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-605+2115_-605+212 others(11): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224628
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+2112_-605+212 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97224628 | |||||
| chr13:97224853
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-605+2322G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97224853 | ||||||
| chr13:97225170
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-605+2639A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225170 | ||||||
| chr13:97225181
|
T | A | 2 | a0001c0001t0001g0176a0001c0001t0017g0177 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-605+2650T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225181 | ||||||
| chr13:97225181
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-605+2650T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225181 | ||||||
| chr13:97225707
|
T | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0118a0001c0001t0001g0119others(11): Show | 14 | HG01192.hp1 HG02109.hp2 HG02965.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+3176T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225707 | ||||||
| chr13:97225712
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0005g0252a0001c0001t0005g0253 | 3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-605+3181G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225712 | ||||||
| chr13:97225768
|
C | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-605+3237C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225768 | ||||||
| chr13:97225963
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0002g0205a0001c0001t0007g0206 | 3 | HG02976.hp2 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-605+3432G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225963 | ||||||
| chr13:97225964
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-605+3433G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97225964 | ||||||
| chr13:97226021
|
G | GTT | 7 | a0001c0001t0001g0002a0001c0001t0001g0178a0001c0001t0004g0233others(4): Show | 7 | HG02965.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-605+3499_-605+350 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97226021 | |||||
| chr13:97226068
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-605+3537G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226068 | ||||||
| chr13:97226085
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-605+3554A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226085 | ||||||
| chr13:97226104
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-605+3573G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226104 | ||||||
| chr13:97226115
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-605+3584T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226115 | ||||||
| chr13:97226116
|
G | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-605+3585G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226116 | ||||||
| chr13:97226144
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+3613G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226144 | ||||||
| chr13:97226180
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-605+3649G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226180 | ||||||
| chr13:97226323
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+3792G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226323 | ||||||
| chr13:97226463
|
A | G | 1 | a0001c0001t0003g0019 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-605+3932A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226463 | ||||||
| chr13:97226555
|
T | A | 12 | a0001c0001t0001g0203a0001c0001t0001g0241a0001c0001t0001g0242others(9): Show | 12 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.-605+4024T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226555 | ||||||
| chr13:97226571
|
T | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-605+4040T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226571 | ||||||
| chr13:97226928
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+4397G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97226928 | ||||||
| chr13:97227012
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-605+4481T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227012 | ||||||
| chr13:97227040
|
CA | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-605+4521delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97227040 | |||||
| chr13:97227051
|
A | AC | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-605+4520_-605+452 others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227051 | ||||||
| chr13:97227052
|
A | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+4521A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227052 | ||||||
| chr13:97227053
|
C | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(14): Show | 17 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-605+4522C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227053 | ||||||
| chr13:97227054
|
A | C | 2 | a0001c0001t0002g0205a0001c0001t0007g0206 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-605+4523A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227054 | ||||||
| chr13:97227058
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-605+4527A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227058 | ||||||
| chr13:97227065
|
CA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(145): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-605+4546delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97227065 | |||||
| chr13:97227065
|
CAA | C | 13 | a0001c0001t0001g0026a0001c0001t0001g0094a0001c0001t0001g0095others(10): Show | 13 | HG00140.hp1 HG01109.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-605+4545_-605+454 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97227065 | |||||
| chr13:97227079
|
A | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+4548A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227079 | ||||||
| chr13:97227087
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-605+4556T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227087 | ||||||
| chr13:97227452
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-605+4921C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227452 | ||||||
| chr13:97227612
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG01981.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-605+5081C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227612 | ||||||
| chr13:97227656
|
A | G | 1 | a0001c0001t0002g0165 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-605+5125A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227656 | ||||||
| chr13:97227750
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-605+5219C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227750 | ||||||
| chr13:97227766
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-605+5235G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227766 | ||||||
| chr13:97227988
|
G | T | 1 | a0001c0001t0003g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-605+5457G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97227988 | ||||||
| chr13:97228297
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-605+5766G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228297 | ||||||
| chr13:97228344
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+5813G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228344 | ||||||
| chr13:97228505
|
A | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+5974A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228505 | ||||||
| chr13:97228529
|
C | CT | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-605+6015dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97228529 | |||||
| chr13:97228529
|
C | CTT | 13 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0087others(10): Show | 13 | HG00735.hp2 HG01261.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+6014_-605+601 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97228529 | |||||
| chr13:97228668
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+6137C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228668 | ||||||
| chr13:97228688
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-605+6157C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228688 | ||||||
| chr13:97228749
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01981.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-605+6218C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228749 | ||||||
| chr13:97228975
|
G | A | 1 | a0001c0001t0018g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-605+6444G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97228975 | ||||||
| chr13:97229337
|
C | T | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+6806C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97229337 | ||||||
| chr13:97229527
|
T | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18943.hp2 NA18946.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-605+6996T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97229527 | ||||||
| chr13:97229666
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-605+7135C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97229666 | ||||||
| chr13:97229843
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-605+7312G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97229843 | ||||||
| chr13:97229896
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-605+7365C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97229896 | ||||||
| chr13:97229992
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0002g0179 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-605+7461T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97229992 | ||||||
| chr13:97230114
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0209 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-605+7583A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97230114 | ||||||
| chr13:97230357
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0027others(6): Show | 9 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-605+7826G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97230357 | ||||||
| chr13:97230703
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-605+8172T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97230703 | ||||||
| chr13:97230887
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-605+8356T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97230887 | ||||||
| chr13:97231011
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-605+8480T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97231011 | ||||||
| chr13:97231048
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-605+8517G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97231048 | ||||||
| chr13:97231227
|
A | T | 1 | a0001c0001t0002g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-605+8696A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97231227 | ||||||
| chr13:97231801
|
G | GT | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0246others(4): Show | 7 | HG00642.hp1 HG01123.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+9281dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97231801 | |||||
| chr13:97231901
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG01256.hp1 HG01257.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-605+9370G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97231901 | ||||||
| chr13:97231913
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+9382A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97231913 | ||||||
| chr13:97232093
|
CGAA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0023others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-605+9565_-605+956 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232093 | |||||
| chr13:97232168
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-605+9637C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232168 | ||||||
| chr13:97232177
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-605+9646T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232177 | ||||||
| chr13:97232350
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-605+9819T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232350 | ||||||
| chr13:97232603
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-605+10072C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232603 | ||||||
| chr13:97232800
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-605+10269C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232800 | ||||||
| chr13:97232826
|
C | T | 6 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0004g0184others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+10295C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232826 | ||||||
| chr13:97232851
|
A | ATG | 30 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(27): Show | 30 | HG00609.hp1 HG01123.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-605+10359_-605+10 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
A | ATGTG | 21 | a0001c0001t0001g0036a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 21 | HG00280.hp2 HG00438.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.-605+10357_-605+10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
A | ATGTGTG | 12 | a0001c0001t0001g0053a0001c0001t0001g0187a0001c0001t0001g0188others(9): Show | 12 | HG01243.hp1 HG01928.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-605+10355_-605+10 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-605+10353_-605+10 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
A | ATGTGTGT others(3): Show |
1 | a0001c0002t0006g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-605+10351_-605+10 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-605+10349_-605+10 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-605+10320A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232851 | ||||||
| chr13:97232851
|
ATG | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0023others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-605+10359_-605+10 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
ATGTG | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0096others(6): Show | 9 | HG01192.hp1 HG01192.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-605+10357_-605+10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
ATGTGTG | A | 4 | a0001c0001t0001g0176a0001c0001t0011g0117a0001c0001t0013g0250others(1): Show | 4 | HG01109.hp1 HG01109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-605+10355_-605+10 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
ATGTGTGT others(3): Show |
A | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0104others(18): Show | 21 | HG00423.hp2 HG02027.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.-605+10351_-605+10 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232851
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-605+10345_-605+10 others(22): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232851 | |||||
| chr13:97232882
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-605+10351T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232882 | ||||||
| chr13:97232888
|
TGTGC | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0061 | 3 | HG01070.hp1 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-605+10359_-605+10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232888 | |||||
| chr13:97232890
|
T | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0180a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG02109.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+10359T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97232890 | ||||||
| chr13:97232890
|
T | TGTGC | 7 | a0001c0001t0001g0014a0001c0001t0001g0116a0001c0001t0001g0124others(4): Show | 7 | HG00642.hp1 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-605+10360_-605+10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232890 | |||||
| chr13:97232890
|
T | TGTGTGC | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0020others(6): Show | 9 | HG02027.hp1 HG02055.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-605+10360_-605+10 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232890 | |||||
| chr13:97232890
|
T | TGTGTGTG others(1): Show |
6 | a0001c0001t0001g0031a0001c0001t0001g0168a0001c0001t0002g0017others(3): Show | 6 | HG03669.hp2 HG04115.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+10360_-605+10 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232890 | |||||
| chr13:97232890
|
T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0186 | 2 | HG03540.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-605+10360_-605+10 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232890 | |||||
| chr13:97232890
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0170 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-605+10360_-605+10 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97232890 | |||||
| chr13:97233057
|
C | T | 1 | a0001c0002t0006g0197 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-605+10526C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233057 | ||||||
| chr13:97233126
|
C | CAT | 27 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0026others(24): Show | 27 | HG00735.hp1 HG01175.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.-605+10644_-605+10 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
C | CATAT | 6 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0175others(3): Show | 6 | HG00280.hp1 HG00280.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+10642_-605+10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
C | CATATAT | 5 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0060others(2): Show | 5 | HG01167.hp2 HG01884.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-605+10640_-605+10 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
C | CATATATA others(3): Show |
1 | a0001c0002t0001g0235 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-605+10636_-605+10 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CAT | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0039others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.-605+10644_-605+10 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATAT | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0050others(21): Show | 24 | HG00558.hp2 HG01243.hp1 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.-605+10642_-605+10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATAT | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG00609.hp2 HG02630.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.-605+10640_-605+10 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG01243.hp2 HG01261.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+10638_-605+10 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0003g0019 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-605+10636_-605+10 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(5): Show |
C | 4 | a0001c0001t0001g0091a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG02148.hp1 HG03239.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-605+10634_-605+10 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0082a0001c0001t0004g0210 | 2 | HG01192.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-605+10632_-605+10 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0001g0183a0001c0001t0004g0184 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-605+10630_-605+10 others(22): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0176a0001c0001t0004g0185a0001c0001t0017g0177 | 3 | HG01109.hp2 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-605+10628_-605+10 others(24): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(13): Show |
C | 2 | a0001c0001t0001g0033a0001c0001t0001g0164 | 2 | NA18944.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-605+10626_-605+10 others(26): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(15): Show |
C | 5 | a0001c0001t0001g0034a0001c0001t0001g0132a0001c0001t0002g0103others(2): Show | 5 | HG02486.hp2 HG02523.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-605+10624_-605+10 others(28): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(17): Show |
C | 17 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0133others(14): Show | 17 | HG00423.hp2 HG00609.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-605+10622_-605+10 others(30): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(19): Show |
C | 3 | a0001c0001t0002g0111a0001c0001t0002g0165a0001c0001t0003g0047 | 3 | NA18944.hp2 NA18967.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-605+10620_-605+10 others(32): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(21): Show |
C | 3 | a0001c0001t0001g0115a0001c0001t0007g0114a0001c0001t0015g0216 | 3 | HG03130.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-605+10618_-605+10 others(34): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(25): Show |
C | 4 | a0001c0001t0001g0228a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-605+10614_-605+10 others(38): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(27): Show |
C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-605+10612_-605+10 others(40): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(31): Show |
C | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+10608_-605+10 others(44): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233126
|
CATATATA others(33): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-605+10606_-605+10 others(46): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233126 | |||||
| chr13:97233143
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-605+10612A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233143 | ||||||
| chr13:97233343
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+10812C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233343 | ||||||
| chr13:97233406
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-605+10875G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233406 | ||||||
| chr13:97233417
|
C | T | 6 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0004g0184others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+10886C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233417 | ||||||
| chr13:97233674
|
G | GT | 13 | a0001c0001t0001g0081a0001c0001t0001g0176a0001c0001t0001g0183others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+11156dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97233674 | |||||
| chr13:97233749
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0023others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-605+11218C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233749 | ||||||
| chr13:97233914
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0027others(6): Show | 9 | HG02258.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-605+11383A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233914 | ||||||
| chr13:97233932
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0209 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-605+11401G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97233932 | ||||||
| chr13:97234157
|
G | C | 19 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0001g0208others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-605+11626G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234157 | ||||||
| chr13:97234398
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-605+11867C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234398 | ||||||
| chr13:97234474
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-605+11943T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234474 | ||||||
| chr13:97234482
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-605+11951G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234482 | ||||||
| chr13:97234501
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-605+11970G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234501 | ||||||
| chr13:97234644
|
C | G | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-605+12113C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234644 | ||||||
| chr13:97234761
|
G | T | 6 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0004g0184others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+12230G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234761 | ||||||
| chr13:97234808
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-605+12277C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234808 | ||||||
| chr13:97234986
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+12455C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97234986 | ||||||
| chr13:97234990
|
TAGA | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+12462_-605+12 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97234990 | |||||
| chr13:97235099
|
A | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0175others(4): Show | 7 | HG01975.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+12568A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235099 | ||||||
| chr13:97235104
|
G | T | 6 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0004g0184others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+12573G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235104 | ||||||
| chr13:97235129
|
G | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+12598G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235129 | ||||||
| chr13:97235205
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-605+12674A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235205 | ||||||
| chr13:97235223
|
T | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0002g0174others(3): Show | 6 | HG02572.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+12692T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235223 | ||||||
| chr13:97235358
|
C | CAG | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+12827_-605+12 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235358 | ||||||
| chr13:97235402
|
A | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+12871A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235402 | ||||||
| chr13:97235660
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-605+13129G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235660 | ||||||
| chr13:97235878
|
G | GA | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG01109.hp1 HG01261.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-605+13360dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97235878 | |||||
| chr13:97235878
|
GA | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(11): Show | 14 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-605+13360delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97235878 | |||||
| chr13:97235976
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+13445G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235976 | ||||||
| chr13:97235989
|
G | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-605+13458G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97235989 | ||||||
| chr13:97236131
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-605+13600A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97236131 | ||||||
| chr13:97236197
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+13666C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97236197 | ||||||
| chr13:97236366
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0209 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-605+13835T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97236366 | ||||||
| chr13:97236427
|
A | T | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+13896A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97236427 | ||||||
| chr13:97236477
|
G | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+13946G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97236477 | ||||||
| chr13:97236513
|
CT | C | 24 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(21): Show | 24 | HG00642.hp1 HG01109.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.-605+13996delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97236513 | |||||
| chr13:97236886
|
TTTTTA | T | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-605+14363_-605+14 others(11): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97236886 | |||||
| chr13:97237143
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0061 | 3 | HG01070.hp1 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-605+14612G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97237143 | ||||||
| chr13:97237839
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0002g0084 | 3 | HG02056.hp2 HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-605+15308G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97237839 | ||||||
| chr13:97238498
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-605+15967G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238498 | ||||||
| chr13:97238520
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18950.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-605+15989T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238520 | ||||||
| chr13:97238551
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-605+16020G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238551 | ||||||
| chr13:97238587
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-605+16056G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238587 | ||||||
| chr13:97238654
|
A | G | 9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(6): Show | 9 | HG01884.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-605+16123A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238654 | ||||||
| chr13:97238885
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-605+16354T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238885 | ||||||
| chr13:97238911
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-605+16380T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238911 | ||||||
| chr13:97238933
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-605+16402T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97238933 | ||||||
| chr13:97239040
|
T | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 15 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-605+16509T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97239040 | ||||||
| chr13:97239072
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-605+16541T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97239072 | ||||||
| chr13:97239722
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-605+17191G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97239722 | ||||||
| chr13:97239974
|
GAGA | G | 6 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0004g0184others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+17449_-605+17 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97239974 | |||||
| chr13:97240035
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-605+17504G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240035 | ||||||
| chr13:97240061
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-605+17530T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240061 | ||||||
| chr13:97240092
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+17561G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240092 | ||||||
| chr13:97240145
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0004g0173 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-605+17614G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240145 | ||||||
| chr13:97240156
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-605+17625G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240156 | ||||||
| chr13:97240306
|
C | G | 6 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0004g0184others(3): Show | 6 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-605+17775C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240306 | ||||||
| chr13:97240405
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0150a0001c0001t0001g0167 | 3 | HG02559.hp1 HG02622.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-605+17874C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240405 | ||||||
| chr13:97240471
|
A | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0059 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-605+17940A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240471 | ||||||
| chr13:97240564
|
T | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01981.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-605+18033T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240564 | ||||||
| chr13:97240604
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-605+18073C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240604 | ||||||
| chr13:97240969
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+18438G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97240969 | ||||||
| chr13:97241002
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-605+18471C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241002 | ||||||
| chr13:97241007
|
T | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-605+18476T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241007 | ||||||
| chr13:97241154
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+18623T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241154 | ||||||
| chr13:97241439
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0196 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-605+18908C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241439 | ||||||
| chr13:97241465
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.-605+18934T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241465 | ||||||
| chr13:97241517
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-605+18986C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241517 | ||||||
| chr13:97241692
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+19161G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241692 | ||||||
| chr13:97241695
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-605+19164C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97241695 | ||||||
| chr13:97242228
|
T | A | 1 | a0001c0001t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-605+19697T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242228 | ||||||
| chr13:97242312
|
G | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-605+19781G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242312 | ||||||
| chr13:97242489
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-605+19958A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242489 | ||||||
| chr13:97242694
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+20163C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242694 | ||||||
| chr13:97242743
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-605+20212G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242743 | ||||||
| chr13:97242779
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-605+20248T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242779 | ||||||
| chr13:97242780
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-605+20249C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242780 | ||||||
| chr13:97242813
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+20282G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242813 | ||||||
| chr13:97242927
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-605+20396C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242927 | ||||||
| chr13:97242953
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-605+20422C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97242953 | ||||||
| chr13:97243132
|
G | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0175others(4): Show | 7 | HG01975.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+20601G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243132 | ||||||
| chr13:97243315
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-605+20784T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243315 | ||||||
| chr13:97243328
|
T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(13): Show | 16 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-605+20797T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243328 | ||||||
| chr13:97243403
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0209 | 2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-605+20872C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243403 | ||||||
| chr13:97243443
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+20912G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243443 | ||||||
| chr13:97243742
|
A | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(13): Show | 16 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-605+21211A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243742 | ||||||
| chr13:97243743
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-605+21212A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243743 | ||||||
| chr13:97243861
|
G | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0175others(4): Show | 7 | HG01975.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-605+21330G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243861 | ||||||
| chr13:97243968
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-605+21437A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97243968 | ||||||
| chr13:97244240
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-605+21709C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97244240 | ||||||
| chr13:97244474
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-605+21943A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97244474 | ||||||
| chr13:97245004
|
TAA | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0030others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-605+22475_-605+22 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97245004 | |||||
| chr13:97245125
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0025others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-605+22594A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97245125 | ||||||
| chr13:97245287
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-605+22756T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97245287 | ||||||
| chr13:97245290
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-605+22759C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97245290 | ||||||
| chr13:97246092
|
T | C | 1 | a0001c0001t0003g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-605+23561T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246092 | ||||||
| chr13:97246275
|
T | TCA | 19 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0069others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-605+23778_-605+23 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246275
|
T | TCACA | 7 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0030others(4): Show | 7 | HG02523.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-605+23776_-605+23 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246275
|
TCA | T | 16 | a0001c0001t0001g0053a0001c0001t0001g0116a0001c0001t0001g0118others(13): Show | 16 | HG00423.hp2 HG01109.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.-605+23778_-605+23 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246275
|
TCACA | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00642.hp1 HG01071.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.-605+23776_-605+23 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246275
|
TCACACA | T | 8 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG02055.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-605+23774_-605+23 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246275
|
TCACACAC others(1): Show |
T | 3 | a0001c0001t0001g0031a0001c0001t0002g0205a0001c0001t0007g0206 | 3 | HG03139.hp1 HG06807.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-605+23772_-605+23 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246275
|
TCACACAC others(7): Show |
T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-605+23766_-605+23 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97246275 | |||||
| chr13:97246309
|
A | C | 4 | a0001c0001t0001g0183a0001c0001t0004g0184a0001c0001t0004g0185others(1): Show | 4 | HG01192.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-605+23778A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246309 | ||||||
| chr13:97246645
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-605+24114G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246645 | ||||||
| chr13:97246679
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-605+24148C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246679 | ||||||
| chr13:97246680
|
C | T | 4 | a0001c0002t0001g0235a0001c0002t0001g0236a0001c0002t0001g0237others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-605+24149C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246680 | ||||||
| chr13:97246757
|
G | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(13): Show | 16 | HG00642.hp1 HG02027.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-605+24226G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246757 | ||||||
| chr13:97246764
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-605+24233G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246764 | ||||||
| chr13:97246772
|
C | T | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-605+24241C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246772 | ||||||
| chr13:97246811
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+24280A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246811 | ||||||
| chr13:97246815
|
C | T | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0005g0238others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-605+24284C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246815 | ||||||
| chr13:97246944
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-605+24413T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97246944 | ||||||
| chr13:97247585
|
A | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0061 | 3 | HG01070.hp1 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-605+25054A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97247585 | ||||||
| chr13:97247672
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-605+25141G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97247672 | ||||||
| chr13:97247748
|
GTTCA | G | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0004g0233others(1): Show | 4 | HG02965.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-605+25223_-605+25 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97247748 | |||||
| chr13:97247838
|
C | G | 9 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0001g0191others(6): Show | 9 | HG01109.hp2 HG01192.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-605+25307C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97247838 | ||||||
| chr13:97248106
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-605+25575G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248106 | ||||||
| chr13:97248202
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0030others(3): Show | 6 | HG02056.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-605+25671G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248202 | ||||||
| chr13:97248267
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-605+25736G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248267 | ||||||
| chr13:97248356
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(10): Show | 13 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(10): Show |
intron_variant | MODIFIER | c.-605+25825T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248356 | ||||||
| chr13:97248357
|
G | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(9): Show | 12 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(9): Show |
intron_variant | MODIFIER | c.-605+25826G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248357 | ||||||
| chr13:97248731
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(8): Show | 11 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.-605+26200C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248731 | ||||||
| chr13:97248751
|
A | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0178others(22): Show | 25 | HG01192.hp2 HG02083.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.-605+26220A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97248751 | ||||||
| chr13:97249136
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.-604-26496G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97249136 | ||||||
| chr13:97250160
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0060 | 2 | NA18941.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-604-25472T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250160 | ||||||
| chr13:97250267
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-604-25365A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250267 | ||||||
| chr13:97250290
|
C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-604-25342C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250290 | ||||||
| chr13:97250390
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-604-25242C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250390 | ||||||
| chr13:97250481
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-604-25151A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250481 | ||||||
| chr13:97250538
|
AT | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-604-25084delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97250538 | |||||
| chr13:97250807
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-604-24825T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250807 | ||||||
| chr13:97250880
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0150a0001c0001t0001g0167 | 3 | HG02559.hp1 HG02622.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-604-24752T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97250880 | ||||||
| chr13:97251173
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-604-24459C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251173 | ||||||
| chr13:97251174
|
GTGAGATC others(5): Show |
G | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-604-24455_-604-24 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251174 | |||||
| chr13:97251385
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0191a0001c0001t0004g0173 | 3 | HG01109.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-604-24247C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251385 | ||||||
| chr13:97251424
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-604-24208A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251424 | ||||||
| chr13:97251485
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-604-24147T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251485 | ||||||
| chr13:97251529
|
AAGTC | A | 10 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0195others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-604-24100_-604-24 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251529 | |||||
| chr13:97251552
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0228a0001c0001t0001g0249others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-604-24080C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251552 | ||||||
| chr13:97251701
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-604-23931G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251701 | ||||||
| chr13:97251834
|
C | CT | 18 | a0001c0001t0001g0033a0001c0001t0001g0102a0001c0001t0001g0108others(15): Show | 18 | HG00642.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-604-23771dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251834 | |||||
| chr13:97251834
|
C | CTT | 8 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0168others(5): Show | 8 | HG00642.hp1 HG02735.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-604-23772_-604-23 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251834 | |||||
| chr13:97251834
|
C | CTTTT | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0004g0112others(2): Show | 5 | HG01975.hp1 HG02809.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-604-23774_-604-23 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251834 | |||||
| chr13:97251834
|
CT | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0025others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.-604-23771delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251834 | |||||
| chr13:97251834
|
CTT | C | 13 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0001t0001g0065others(10): Show | 13 | HG01192.hp1 HG01361.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.-604-23772_-604-23 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251834 | |||||
| chr13:97251834
|
CTTTTTT | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0178others(22): Show | 25 | HG01192.hp2 HG01981.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.-604-23776_-604-23 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97251834 | |||||
| chr13:97251874
|
C | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00642.hp1 HG01975.hp1 HG02735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-604-23758C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251874 | ||||||
| chr13:97251879
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0178others(24): Show | 27 | HG01192.hp2 HG01981.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.-604-23753C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251879 | ||||||
| chr13:97251990
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-604-23642A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97251990 | ||||||
| chr13:97252059
|
C | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0119others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-604-23573C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97252059 | ||||||
| chr13:97252106
|
T | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0031others(9): Show | 12 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(9): Show |
intron_variant | MODIFIER | c.-604-23526T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97252106 | ||||||
| chr13:97252400
|
T | TA | 47 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(44): Show | 47 | HG00642.hp1 HG01192.hp2 HG01975.hp1 others(44): Show |
intron_variant | MODIFIER | c.-604-23231dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97252400 | |||||
| chr13:97252448
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-604-23184G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97252448 | ||||||
| chr13:97252643
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-604-22989A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97252643 | ||||||
| chr13:97253132
|
A | G | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-604-22500A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97253132 | ||||||
| chr13:97253367
|
G | T | 1 | a0001c0001t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-604-22265G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97253367 | ||||||
| chr13:97253747
|
TATTTATT others(11): Show |
T | 28 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0178others(25): Show | 28 | HG01192.hp2 HG01981.hp1 HG02083.hp1 others(25): Show |
intron_variant | MODIFIER | c.-604-21864_-604-21 others(24): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97253747 | |||||
| chr13:97254488
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-604-21144G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97254488 | ||||||
| chr13:97254489
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0178others(6): Show | 9 | HG02083.hp1 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-604-21143T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97254489 | ||||||
| chr13:97254679
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-604-20953C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97254679 | ||||||
| chr13:97254989
|
C | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0007g0114others(1): Show | 4 | HG03130.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-604-20643C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97254989 | ||||||
| chr13:97255106
|
C | T | 4 | a0001c0002t0001g0235a0001c0002t0001g0236a0001c0002t0001g0237others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-604-20526C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255106 | ||||||
| chr13:97255107
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG00735.hp1 HG01175.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-604-20525G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255107 | ||||||
| chr13:97255331
|
A | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01981.hp1 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-604-20301A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255331 | ||||||
| chr13:97255629
|
G | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0116a0001c0001t0001g0186others(7): Show | 10 | HG00642.hp1 HG01975.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-604-20003G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255629 | ||||||
| chr13:97255740
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0054others(43): Show | 46 | HG01109.hp1 HG01123.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-604-19892T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255740 | ||||||
| chr13:97255767
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0007g0114a0001c0001t0015g0216 | 3 | HG03130.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-604-19865G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255767 | ||||||
| chr13:97255822
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00140.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-604-19810C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97255822 | ||||||
| chr13:97256168
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-604-19464A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256168 | ||||||
| chr13:97256192
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-604-19440C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256192 | ||||||
| chr13:97256352
|
A | AT | 18 | a0001c0001t0001g0004a0001c0001t0001g0176a0001c0001t0001g0187others(15): Show | 18 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-604-19269dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97256352 | |||||
| chr13:97256352
|
A | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-604-19280A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256352 | ||||||
| chr13:97256364
|
A | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0180a0001c0001t0002g0010others(2): Show | 5 | HG03195.hp1 NA18979.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.-604-19268A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256364 | ||||||
| chr13:97256420
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214 | 3 | HG02055.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-604-19212G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256420 | ||||||
| chr13:97256444
|
C | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0214 | 3 | HG02055.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-604-19188C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256444 | ||||||
| chr13:97256531
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-604-19101G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256531 | ||||||
| chr13:97256576
|
C | A | 1 | a0001c0001t0002g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-604-19056C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256576 | ||||||
| chr13:97256753
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02922.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-604-18879T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256753 | ||||||
| chr13:97256851
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-604-18781T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97256851 | ||||||
| chr13:97257071
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-604-18561T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97257071 | ||||||
| chr13:97257457
|
T | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-18175T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97257457 | ||||||
| chr13:97257608
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01123.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-604-18024G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97257608 | ||||||
| chr13:97257827
|
T | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0083others(8): Show | 11 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.-604-17805T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97257827 | ||||||
| chr13:97257867
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-604-17765G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97257867 | ||||||
| chr13:97258031
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0063 | 3 | HG01257.hp2 HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-604-17601C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258031 | ||||||
| chr13:97258189
|
A | T | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-604-17443A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258189 | ||||||
| chr13:97258193
|
T | C | 1 | a0001c0001t0002g0011 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-604-17439T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258193 | ||||||
| chr13:97258210
|
G | GT | 21 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0083others(18): Show | 21 | HG00642.hp1 HG01975.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.-604-17410dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97258210 | |||||
| chr13:97258481
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0002g0084 | 3 | HG02056.hp2 HG02074.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-604-17151C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258481 | ||||||
| chr13:97258666
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-604-16966G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258666 | ||||||
| chr13:97258796
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0199 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-604-16836G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258796 | ||||||
| chr13:97258804
|
A | T | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-604-16828A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97258804 | ||||||
| chr13:97259150
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-604-16482C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259150 | ||||||
| chr13:97259309
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-604-16323A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259309 | ||||||
| chr13:97259408
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-604-16224C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259408 | ||||||
| chr13:97259420
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-604-16212G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259420 | ||||||
| chr13:97259445
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-604-16187G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259445 | ||||||
| chr13:97259555
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0199 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-604-16077G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259555 | ||||||
| chr13:97259837
|
C | T | 1 | a0001c0001t0003g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-604-15795C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259837 | ||||||
| chr13:97259931
|
T | C | 2 | a0001c0001t0003g0224a0001c0001t0009g0221 | 2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-604-15701T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97259931 | ||||||
| chr13:97260041
|
A | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0199 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-604-15591A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97260041 | ||||||
| chr13:97260278
|
G | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0118others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-604-15354G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97260278 | ||||||
| chr13:97260449
|
A | C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-604-15183A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97260449 | ||||||
| chr13:97260465
|
C | T | 12 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0083others(9): Show | 12 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(9): Show |
intron_variant | MODIFIER | c.-604-15167C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97260465 | ||||||
| chr13:97260525
|
GAA | G | 9 | a0001c0001t0001g0130a0001c0001t0002g0131a0001c0001t0005g0238others(6): Show | 9 | HG01192.hp1 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-604-15106_-604-15 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97260525 | ||||||
| chr13:97260677
|
T | C | 12 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0083others(9): Show | 12 | HG00642.hp1 HG02735.hp1 HG03540.hp2 others(9): Show |
intron_variant | MODIFIER | c.-604-14955T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97260677 | ||||||
| chr13:97261051
|
T | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0054others(32): Show | 35 | HG01192.hp2 HG02027.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.-604-14581T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97261051 | ||||||
| chr13:97261084
|
TCTC | T | 9 | a0001c0001t0001g0180a0001c0001t0002g0174a0001c0001t0002g0199others(6): Show | 9 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-604-14545_-604-14 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97261084 | |||||
| chr13:97261177
|
A | T | 3 | a0001c0001t0001g0106a0001c0001t0002g0136a0001c0001t0002g0139 | 3 | HG02040.hp1 HG02056.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-604-14455A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97261177 | ||||||
| chr13:97261589
|
G | A | 3 | a0001c0001t0005g0113a0001c0001t0005g0252a0001c0001t0005g0253 | 3 | HG01975.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-604-14043G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97261589 | ||||||
| chr13:97261734
|
C | G | 1 | a0001c0001t0010g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-604-13898C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97261734 | ||||||
| chr13:97261737
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0251 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-604-13895A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97261737 | ||||||
| chr13:97262042
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-604-13590G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262042 | ||||||
| chr13:97262133
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.-604-13499G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262133 | ||||||
| chr13:97262138
|
C | A | 1 | a0001c0001t0004g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-604-13494C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262138 | ||||||
| chr13:97262376
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0004g0173 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-604-13256G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262376 | ||||||
| chr13:97262382
|
C | T | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-604-13250C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262382 | ||||||
| chr13:97262499
|
C | T | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-604-13133C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262499 | ||||||
| chr13:97262728
|
C | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0167a0001c0001t0002g0205others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-604-12904C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262728 | ||||||
| chr13:97262959
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-604-12673T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262959 | ||||||
| chr13:97262979
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-604-12653G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97262979 | ||||||
| chr13:97263104
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-604-12528C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263104 | ||||||
| chr13:97263150
|
T | G | 15 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0118others(12): Show | 15 | HG00140.hp2 HG00280.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-604-12482T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263150 | ||||||
| chr13:97263217
|
G | A | 16 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0118others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-604-12415G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263217 | ||||||
| chr13:97263291
|
A | G | 7 | a0001c0001t0001g0180a0001c0001t0002g0174a0001c0001t0002g0199others(4): Show | 7 | HG01192.hp2 HG02886.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-604-12341A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263291 | ||||||
| chr13:97263380
|
T | G | 22 | a0001c0001t0001g0027a0001c0001t0001g0116a0001c0001t0001g0124others(19): Show | 22 | HG01109.hp1 HG01123.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-604-12252T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263380 | ||||||
| chr13:97263505
|
A | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0004g0172 | 3 | HG02486.hp2 NA18962.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-604-12127A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263505 | ||||||
| chr13:97263573
|
T | G | 20 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0050others(17): Show | 20 | HG01109.hp1 HG01981.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.-604-12059T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263573 | ||||||
| chr13:97263673
|
G | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18950.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-604-11959G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263673 | ||||||
| chr13:97263698
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-604-11934A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263698 | ||||||
| chr13:97263806
|
C | T | 3 | a0001c0001t0010g0003a0001c0001t0013g0250a0001c0002t0001g0156 | 3 | HG01109.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-604-11826C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263806 | ||||||
| chr13:97263810
|
A | T | 7 | a0001c0001t0001g0115a0001c0001t0001g0176a0001c0001t0001g0180others(4): Show | 7 | HG01109.hp2 HG02976.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-604-11822A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263810 | ||||||
| chr13:97263877
|
G | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-604-11755G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263877 | ||||||
| chr13:97263944
|
C | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0077 | 3 | NA18941.hp1 NA18945.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-604-11688C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97263944 | ||||||
| chr13:97264013
|
CT | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0027others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.-604-11604delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97264013 | |||||
| chr13:97264119
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-604-11513G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97264119 | ||||||
| chr13:97264636
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-604-10996C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97264636 | ||||||
| chr13:97264682
|
T | G | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-10950T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97264682 | ||||||
| chr13:97264761
|
G | C | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-604-10871G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97264761 | ||||||
| chr13:97264935
|
C | G | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-10697C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97264935 | ||||||
| chr13:97265215
|
G | T | 2 | a0001c0001t0001g0115a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-604-10417G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265215 | ||||||
| chr13:97265332
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-604-10300C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265332 | ||||||
| chr13:97265411
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-604-10221A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265411 | ||||||
| chr13:97265443
|
C | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-604-10189C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265443 | ||||||
| chr13:97265529
|
G | A | 9 | a0001c0001t0004g0172a0001c0001t0006g0127a0001c0001t0014g0234others(6): Show | 9 | HG01123.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-604-10103G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265529 | ||||||
| chr13:97265532
|
A | G | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-10100A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265532 | ||||||
| chr13:97265560
|
G | A | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-604-10072G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265560 | ||||||
| chr13:97265669
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-604-9963G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265669 | ||||||
| chr13:97265892
|
A | G | 9 | a0001c0001t0004g0172a0001c0001t0006g0127a0001c0001t0014g0234others(6): Show | 9 | HG01123.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-604-9740A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265892 | ||||||
| chr13:97265963
|
C | T | 7 | a0001c0001t0006g0127a0001c0001t0014g0234a0001c0001t0015g0216others(4): Show | 7 | HG01123.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-604-9669C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97265963 | ||||||
| chr13:97266070
|
C | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-604-9562C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266070 | ||||||
| chr13:97266128
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-604-9504A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266128 | ||||||
| chr13:97266259
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0142 | 3 | HG00099.hp2 HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-604-9373A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266259 | ||||||
| chr13:97266263
|
T | A | 31 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0080others(28): Show | 31 | HG01071.hp1 HG01123.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.-604-9369T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266263 | ||||||
| chr13:97266516
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-604-9116A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266516 | ||||||
| chr13:97266534
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-604-9098T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266534 | ||||||
| chr13:97266831
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-604-8801A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97266831 | ||||||
| chr13:97267006
|
T | A | 2 | a0001c0001t0004g0184a0001c0001t0004g0210 | 2 | HG01192.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-604-8626T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267006 | ||||||
| chr13:97267079
|
T | C | 1 | a0001c0001t0003g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-604-8553T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267079 | ||||||
| chr13:97267125
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0167 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-604-8507C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267125 | ||||||
| chr13:97267230
|
T | C | 1 | a0001c0001t0018g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-604-8402T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267230 | ||||||
| chr13:97267268
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-604-8364G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267268 | ||||||
| chr13:97267396
|
C | G | 14 | a0001c0001t0001g0027a0001c0001t0001g0187a0001c0001t0001g0188others(11): Show | 14 | HG01123.hp1 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-604-8236C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267396 | ||||||
| chr13:97267648
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-604-7984G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267648 | ||||||
| chr13:97267869
|
T | C | 20 | a0001c0001t0001g0027a0001c0001t0001g0115a0001c0001t0001g0187others(17): Show | 20 | HG01123.hp1 HG01192.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-604-7763T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267869 | ||||||
| chr13:97267885
|
T | C | 2 | a0001c0001t0004g0184a0001c0001t0004g0210 | 2 | HG01192.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-604-7747T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267885 | ||||||
| chr13:97267927
|
A | T | 2 | a0001c0001t0001g0191a0001c0002t0001g0156 | 2 | HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-604-7705A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267927 | ||||||
| chr13:97267934
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0004g0185a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-604-7698C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267934 | ||||||
| chr13:97267935
|
G | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.-604-7697G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267935 | ||||||
| chr13:97267935
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-604-7697G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97267935 | ||||||
| chr13:97268062
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-604-7570T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268062 | ||||||
| chr13:97268073
|
T | TTTCC | 66 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-604-7532_-604-752 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97268073 | |||||
| chr13:97268073
|
T | TTTCCTTC others(1): Show |
7 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0071others(4): Show | 7 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(4): Show |
intron_variant | MODIFIER | c.-604-7536_-604-752 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97268073 | |||||
| chr13:97268073
|
TTTCC | T | 42 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0102others(39): Show | 42 | HG01109.hp1 HG01192.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-604-7532_-604-752 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97268073 | |||||
| chr13:97268089
|
C | CTTCCTTC others(5): Show |
1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-604-7532_-604-753 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97268089 | |||||
| chr13:97268089
|
C | CTTCCTTC others(1): Show |
8 | a0001c0001t0004g0172a0001c0001t0006g0127a0001c0001t0014g0234others(5): Show | 8 | HG01123.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-604-7536_-604-753 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97268089 | |||||
| chr13:97268104
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-604-7528T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268104 | ||||||
| chr13:97268122
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-604-7510G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268122 | ||||||
| chr13:97268125
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-604-7507G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268125 | ||||||
| chr13:97268157
|
C | T | 8 | a0001c0001t0001g0191a0001c0001t0006g0127a0001c0001t0014g0234others(5): Show | 8 | HG01123.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-604-7475C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268157 | ||||||
| chr13:97268400
|
C | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-7232C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268400 | ||||||
| chr13:97268424
|
T | A | 2 | a0001c0002t0001g0236a0002c0004t0001g0232 | 2 | NA18948.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-604-7208T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268424 | ||||||
| chr13:97268479
|
C | G | 73 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.-604-7153C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268479 | ||||||
| chr13:97268951
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-604-6681C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268951 | ||||||
| chr13:97268971
|
C | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0115a0001c0001t0001g0187others(15): Show | 18 | HG01123.hp1 HG02280.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-604-6661C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268971 | ||||||
| chr13:97268973
|
T | A | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-604-6659T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268973 | ||||||
| chr13:97268988
|
G | A | 6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-604-6644G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268988 | ||||||
| chr13:97268993
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-604-6639G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97268993 | ||||||
| chr13:97269012
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-604-6620C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269012 | ||||||
| chr13:97269276
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-604-6356T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269276 | ||||||
| chr13:97269297
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0249others(1): Show | 4 | HG02572.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-604-6335C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269297 | ||||||
| chr13:97269331
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-604-6301G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269331 | ||||||
| chr13:97269359
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-604-6273G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269359 | ||||||
| chr13:97269507
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-604-6125G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269507 | ||||||
| chr13:97269510
|
A | T | 1 | a0001c0001t0002g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-604-6122A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269510 | ||||||
| chr13:97269789
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0011g0117 | 3 | HG02965.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-604-5843T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269789 | ||||||
| chr13:97269856
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02055.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-604-5776T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269856 | ||||||
| chr13:97269877
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-604-5755G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97269877 | ||||||
| chr13:97270082
|
G | A | 26 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(23): Show | 26 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-604-5550G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270082 | ||||||
| chr13:97270195
|
G | T | 4 | a0001c0001t0004g0112a0001c0001t0004g0184a0001c0001t0004g0210others(1): Show | 4 | HG01192.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-604-5437G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270195 | ||||||
| chr13:97270610
|
C | A | 120 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.-604-5022C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270610 | ||||||
| chr13:97270733
|
T | G | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-4899T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270733 | ||||||
| chr13:97270789
|
T | C | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-604-4843T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270789 | ||||||
| chr13:97270839
|
G | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0249others(1): Show | 4 | HG02572.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-604-4793G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270839 | ||||||
| chr13:97270869
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-604-4763T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270869 | ||||||
| chr13:97270922
|
T | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-604-4710T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270922 | ||||||
| chr13:97270999
|
T | C | 4 | a0001c0001t0004g0112a0001c0001t0004g0184a0001c0001t0004g0210others(1): Show | 4 | HG01192.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-604-4633T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97270999 | ||||||
| chr13:97271112
|
G | GT | 12 | a0001c0001t0001g0175a0001c0001t0002g0006a0001c0001t0002g0009others(9): Show | 12 | HG00609.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-604-4507dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97271112 | |||||
| chr13:97271112
|
GT | G | 93 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0025others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-604-4507delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97271112 | |||||
| chr13:97271126
|
G | T | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-604-4506G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271126 | ||||||
| chr13:97271138
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-604-4494T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271138 | ||||||
| chr13:97271390
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-604-4242G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271390 | ||||||
| chr13:97271406
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-604-4226C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271406 | ||||||
| chr13:97271423
|
G | GATTT | 120 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.-604-4192_-604-418 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97271423 | |||||
| chr13:97271444
|
C | A | 17 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(14): Show | 17 | HG01109.hp1 HG01109.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-604-4188C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271444 | ||||||
| chr13:97271445
|
T | TTTCTA | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0249others(1): Show | 4 | HG02572.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-604-4187_-604-418 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271445 | ||||||
| chr13:97271446
|
A | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-604-4186A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271446 | ||||||
| chr13:97271447
|
A | T | 12 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(9): Show | 12 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-604-4185A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271447 | ||||||
| chr13:97271448
|
A | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(9): Show | 12 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-604-4184A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271448 | ||||||
| chr13:97271449
|
A | T | 12 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(9): Show | 12 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-604-4183A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271449 | ||||||
| chr13:97271451
|
A | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-604-4181A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271451 | ||||||
| chr13:97271455
|
C | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(9): Show | 12 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-604-4177C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271455 | ||||||
| chr13:97271460
|
AAAAAACA others(4): Show |
A | 4 | a0001c0001t0004g0112a0001c0001t0004g0184a0001c0001t0004g0210others(1): Show | 4 | HG01192.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-604-4166_-604-415 others(15): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97271460 | |||||
| chr13:97271586
|
G | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-604-4046G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271586 | ||||||
| chr13:97271644
|
A | T | 5 | a0001c0001t0004g0112a0001c0001t0004g0173a0001c0001t0004g0184others(2): Show | 5 | HG01192.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-604-3988A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271644 | ||||||
| chr13:97271673
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-604-3959C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271673 | ||||||
| chr13:97271678
|
C | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-604-3954C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271678 | ||||||
| chr13:97271922
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-604-3710C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97271922 | ||||||
| chr13:97272043
|
C | T | 5 | a0001c0001t0004g0112a0001c0001t0004g0173a0001c0001t0004g0184others(2): Show | 5 | HG01192.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-604-3589C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272043 | ||||||
| chr13:97272187
|
T | C | 133 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-604-3445T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272187 | ||||||
| chr13:97272426
|
C | A | 6 | a0001c0001t0003g0101a0001c0001t0003g0220a0001c0001t0003g0222others(3): Show | 6 | HG01943.hp2 HG01981.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-604-3206C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272426 | ||||||
| chr13:97272620
|
A | G | 10 | a0001c0001t0004g0172a0001c0001t0006g0127a0001c0001t0014g0234others(7): Show | 10 | HG01123.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-604-3012A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272620 | ||||||
| chr13:97272624
|
G | A | 10 | a0001c0001t0004g0172a0001c0001t0006g0127a0001c0001t0014g0234others(7): Show | 10 | HG01123.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-604-3008G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272624 | ||||||
| chr13:97272679
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-604-2953G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272679 | ||||||
| chr13:97272715
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-604-2917C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272715 | ||||||
| chr13:97272794
|
A | G | 10 | a0001c0001t0004g0172a0001c0001t0006g0127a0001c0001t0014g0234others(7): Show | 10 | HG01123.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-604-2838A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272794 | ||||||
| chr13:97272928
|
CA | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-604-2703delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97272928 | ||||||
| chr13:97273206
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-604-2426A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273206 | ||||||
| chr13:97273219
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-604-2413A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273219 | ||||||
| chr13:97273271
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-604-2361C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273271 | ||||||
| chr13:97273411
|
G | A | 2 | a0001c0001t0004g0184a0001c0001t0004g0210 | 2 | HG01192.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-604-2221G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273411 | ||||||
| chr13:97273477
|
C | T | 7 | a0001c0001t0001g0204a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-604-2155C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273477 | ||||||
| chr13:97273733
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-604-1899T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273733 | ||||||
| chr13:97273980
|
G | A | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-604-1652G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97273980 | ||||||
| chr13:97274164
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-604-1468A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274164 | ||||||
| chr13:97274213
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-604-1419G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274213 | ||||||
| chr13:97274217
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-604-1415G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274217 | ||||||
| chr13:97274244
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0096others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-604-1388T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274244 | ||||||
| chr13:97274353
|
C | G | 27 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(24): Show | 27 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-604-1279C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274353 | ||||||
| chr13:97274355
|
G | T | 1 | a0001c0001t0002g0010 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-604-1277G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274355 | ||||||
| chr13:97274357
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-604-1275C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274357 | ||||||
| chr13:97274364
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-604-1268T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274364 | ||||||
| chr13:97274515
|
C | CA | 6 | a0001c0001t0001g0146a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG01358.hp1 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-604-1104dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr13 | 97274515 | |||||
| chr13:97274683
|
T | C | 85 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.-604-949T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274683 | ||||||
| chr13:97274738
|
T | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0199 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-604-894T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274738 | ||||||
| chr13:97274855
|
C | T | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-604-777C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274855 | ||||||
| chr13:97274868
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-604-764G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274868 | ||||||
| chr13:97274964
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-604-668A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274964 | ||||||
| chr13:97274989
|
G | A | 3 | a0001c0001t0004g0172a0001c0001t0004g0173a0001c0001t0017g0177 | 3 | HG02486.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-604-643G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97274989 | ||||||
| chr13:97275017
|
T | C | 2 | a0001c0001t0016g0245a0001c0001t0018g0012 | 2 | HG00642.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-604-615T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275017 | ||||||
| chr13:97275152
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-604-480C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275152 | ||||||
| chr13:97275340
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-604-292T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275340 | ||||||
| chr13:97275350
|
A | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0087a0001c0001t0001g0231 | 3 | HG00735.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-604-282A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275350 | ||||||
| chr13:97275363
|
G | A | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-604-269G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275363 | ||||||
| chr13:97275466
|
G | A | 1 | a0001c0001t0003g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-604-166G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275466 | ||||||
| chr13:97275523
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-604-109A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 1/8 | chr13 | 97275523 | ||||||
| chr13:97276645
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.174+236A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97276645 | ||||||
| chr13:97276877
|
C | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+468C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97276877 | ||||||
| chr13:97276900
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0031others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.174+491G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97276900 | ||||||
| chr13:97276977
|
T | C | 84 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0031others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.174+568T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97276977 | ||||||
| chr13:97277225
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.174+816A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277225 | ||||||
| chr13:97277227
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+818G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277227 | ||||||
| chr13:97277294
|
T | G | 5 | a0001c0001t0004g0112a0001c0001t0004g0172a0001c0001t0004g0173others(2): Show | 5 | HG02486.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+885T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277294 | ||||||
| chr13:97277360
|
G | A | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+951G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277360 | ||||||
| chr13:97277381
|
T | G | 32 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(29): Show | 32 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.174+972T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277381 | ||||||
| chr13:97277393
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+984A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277393 | ||||||
| chr13:97277426
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.174+1017C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277426 | ||||||
| chr13:97277533
|
C | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+1124C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277533 | ||||||
| chr13:97277547
|
T | C | 1 | a0001c0001t0001g0002 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.174+1138T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277547 | ||||||
| chr13:97277651
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+1242G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277651 | ||||||
| chr13:97277860
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.174+1451C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277860 | ||||||
| chr13:97277966
|
G | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+1557G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277966 | ||||||
| chr13:97277977
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0004g0173 | 2 | HG03225.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.174+1568C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277977 | ||||||
| chr13:97277978
|
G | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0054others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+1569G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97277978 | ||||||
| chr13:97278071
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.174+1662T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278071 | ||||||
| chr13:97278144
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.174+1735C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278144 | ||||||
| chr13:97278251
|
C | CA | 11 | a0001c0001t0001g0007a0001c0001t0001g0108a0001c0001t0001g0150others(8): Show | 11 | HG01109.hp1 HG01175.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+1868dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278251
|
C | CAAAA | 18 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(15): Show | 18 | HG01192.hp2 HG02083.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+1865_174+1868d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278251
|
C | CAAAAA | 8 | a0001c0001t0002g0157a0001c0001t0002g0160a0001c0001t0002g0179others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1864_174+1868d others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278251
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.174+1859_174+1868d others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278251
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0004g0211 | 3 | HG02572.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.174+1858_174+1868d others(13): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278251
|
CA | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.174+1868delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278251
|
CAA | C | 6 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0002g0028others(3): Show | 6 | HG02486.hp1 HG02486.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+1867_174+1868d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97278251 | |||||
| chr13:97278567
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.174+2158C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278567 | ||||||
| chr13:97278569
|
C | G | 30 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(27): Show | 30 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.174+2160C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278569 | ||||||
| chr13:97278581
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18950.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.174+2172G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278581 | ||||||
| chr13:97278636
|
A | G | 119 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.174+2227A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278636 | ||||||
| chr13:97278986
|
A | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0125a0001c0001t0001g0176others(14): Show | 17 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.174+2577A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278986 | ||||||
| chr13:97278988
|
T | C | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+2579T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97278988 | ||||||
| chr13:97279014
|
C | G | 15 | a0001c0001t0001g0027a0001c0001t0001g0125a0001c0001t0001g0176others(12): Show | 15 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.174+2605C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279014 | ||||||
| chr13:97279037
|
A | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0066a0001c0001t0001g0092others(5): Show | 8 | HG00423.hp2 HG02040.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+2628A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279037 | ||||||
| chr13:97279038
|
C | T | 6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+2629C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279038 | ||||||
| chr13:97279115
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0187 | 3 | HG02895.hp2 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.174+2706A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279115 | ||||||
| chr13:97279271
|
T | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+2862T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279271 | ||||||
| chr13:97279310
|
G | A | 68 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.174+2901G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279310 | ||||||
| chr13:97279455
|
A | G | 135 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.174+3046A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279455 | ||||||
| chr13:97279554
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.174+3145C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279554 | ||||||
| chr13:97279654
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+3245C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279654 | ||||||
| chr13:97279724
|
C | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0228a0001c0002t0001g0008 | 3 | HG02559.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.174+3315C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279724 | ||||||
| chr13:97279805
|
T | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+3396T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97279805 | ||||||
| chr13:97280139
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.174+3730C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97280139 | ||||||
| chr13:97280662
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+4253G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97280662 | ||||||
| chr13:97280762
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174+4353C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97280762 | ||||||
| chr13:97280924
|
C | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+4515C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97280924 | ||||||
| chr13:97280962
|
C | T | 27 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(24): Show | 27 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.174+4553C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97280962 | ||||||
| chr13:97281018
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.174+4609C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281018 | ||||||
| chr13:97281163
|
T | C | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+4754T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281163 | ||||||
| chr13:97281264
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.174+4855G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281264 | ||||||
| chr13:97281271
|
C | G | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+4862C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281271 | ||||||
| chr13:97281385
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.174+4976T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281385 | ||||||
| chr13:97281762
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0228a0001c0002t0001g0008 | 3 | HG02559.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.174+5353A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281762 | ||||||
| chr13:97281773
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0180 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.174+5364G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281773 | ||||||
| chr13:97281817
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0130a0001c0001t0001g0167others(7): Show | 10 | HG01109.hp1 HG02717.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+5408G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281817 | ||||||
| chr13:97281965
|
C | T | 7 | a0001c0001t0006g0127a0001c0001t0014g0234a0001c0001t0016g0245others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+5556C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97281965 | ||||||
| chr13:97281970
|
T | TA | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.174+5564dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97281970 | |||||
| chr13:97282050
|
C | CA | 82 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.174+5653dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97282050 | |||||
| chr13:97282277
|
C | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+5868C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97282277 | ||||||
| chr13:97282332
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+5923G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97282332 | ||||||
| chr13:97282655
|
G | C | 13 | a0001c0001t0004g0112a0001c0001t0004g0184a0001c0001t0004g0210others(10): Show | 13 | HG00642.hp1 HG01123.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+6246G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97282655 | ||||||
| chr13:97282765
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.174+6356A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97282765 | ||||||
| chr13:97282982
|
A | C | 36 | a0001c0001t0001g0050a0001c0001t0001g0102a0001c0001t0001g0118others(33): Show | 36 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.174+6573A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97282982 | ||||||
| chr13:97283125
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.174+6716G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283125 | ||||||
| chr13:97283160
|
C | T | 8 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0100others(5): Show | 8 | HG00438.hp2 HG00558.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+6751C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283160 | ||||||
| chr13:97283179
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.174+6770C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283179 | ||||||
| chr13:97283245
|
G | GA | 120 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.174+6839dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97283245 | |||||
| chr13:97283277
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+6868C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283277 | ||||||
| chr13:97283286
|
G | A | 28 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(25): Show | 28 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.174+6877G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283286 | ||||||
| chr13:97283531
|
A | G | 162 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.174+7122A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283531 | ||||||
| chr13:97283544
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.174+7135C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283544 | ||||||
| chr13:97283599
|
A | G | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+7190A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283599 | ||||||
| chr13:97283620
|
G | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0200 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.174+7211G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283620 | ||||||
| chr13:97283648
|
T | A | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+7239T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283648 | ||||||
| chr13:97283653
|
A | G | 1 | a0001c0002t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.174+7244A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283653 | ||||||
| chr13:97283748
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.174+7339A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283748 | ||||||
| chr13:97283768
|
T | G | 32 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(29): Show | 32 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.174+7359T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283768 | ||||||
| chr13:97283842
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.174+7433G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283842 | ||||||
| chr13:97283914
|
T | C | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+7505T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283914 | ||||||
| chr13:97283926
|
G | T | 7 | a0001c0001t0001g0102a0001c0001t0001g0130a0001c0001t0001g0167others(4): Show | 7 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+7517G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97283926 | ||||||
| chr13:97284090
|
T | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+7681T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284090 | ||||||
| chr13:97284100
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174+7691C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284100 | ||||||
| chr13:97284291
|
G | A | 30 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(27): Show | 30 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.174+7882G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284291 | ||||||
| chr13:97284416
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.174+8007T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284416 | ||||||
| chr13:97284431
|
C | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.174+8022C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284431 | ||||||
| chr13:97284538
|
A | G | 1 | a0001c0001t0018g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.174+8129A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284538 | ||||||
| chr13:97284617
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.174+8208G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284617 | ||||||
| chr13:97284634
|
T | G | 7 | a0001c0001t0001g0102a0001c0001t0001g0130a0001c0001t0001g0167others(4): Show | 7 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+8225T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284634 | ||||||
| chr13:97284759
|
C | T | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+8350C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284759 | ||||||
| chr13:97284785
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.174+8376G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284785 | ||||||
| chr13:97284858
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.174+8449T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97284858 | ||||||
| chr13:97285014
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.174+8605G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285014 | ||||||
| chr13:97285144
|
A | T | 52 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0118others(49): Show | 52 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.174+8735A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285144 | ||||||
| chr13:97285290
|
T | C | 73 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.174+8881T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285290 | ||||||
| chr13:97285358
|
A | G | 12 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0070others(9): Show | 12 | HG00280.hp1 HG01123.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+8949A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285358 | ||||||
| chr13:97285390
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.174+8981C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285390 | ||||||
| chr13:97285478
|
G | T | 2 | a0001c0001t0004g0172a0001c0001t0017g0177 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.174+9069G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285478 | ||||||
| chr13:97285540
|
G | C | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+9131G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285540 | ||||||
| chr13:97285610
|
A | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+9201A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285610 | ||||||
| chr13:97285626
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.174+9217T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285626 | ||||||
| chr13:97285680
|
T | C | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.174+9271T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285680 | ||||||
| chr13:97285762
|
T | TTTATCAA others(314): Show |
1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+9368_174+9369i others(323): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97285762 | |||||
| chr13:97285762
|
T | TTTATCAA others(307): Show |
1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+9365_174+9366i others(316): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97285762 | |||||
| chr13:97285823
|
C | G | 1 | a0001c0001t0003g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.174+9414C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97285823 | ||||||
| chr13:97286108
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+9699A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286108 | ||||||
| chr13:97286117
|
C | T | 7 | a0001c0001t0006g0127a0001c0001t0014g0234a0001c0001t0016g0245others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+9708C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286117 | ||||||
| chr13:97286153
|
A | G | 2 | a0001c0001t0004g0185a0001c0001t0013g0250 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.174+9744A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286153 | ||||||
| chr13:97286183
|
T | G | 1 | a0001c0001t0002g0017 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.174+9774T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286183 | ||||||
| chr13:97286395
|
T | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.174+9986T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286395 | ||||||
| chr13:97286413
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+10004T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286413 | ||||||
| chr13:97286454
|
C | T | 72 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.174+10045C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286454 | ||||||
| chr13:97286455
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.174+10046G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286455 | ||||||
| chr13:97286463
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.174+10054C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286463 | ||||||
| chr13:97286612
|
A | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.174+10203A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286612 | ||||||
| chr13:97286612
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+10203A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286612 | ||||||
| chr13:97286715
|
C | T | 3 | a0001c0001t0004g0185a0001c0001t0004g0211a0001c0001t0013g0250 | 3 | HG01109.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.174+10306C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286715 | ||||||
| chr13:97286780
|
A | C | 3 | a0001c0001t0004g0185a0001c0001t0004g0211a0001c0001t0013g0250 | 3 | HG01109.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.174+10371A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286780 | ||||||
| chr13:97286784
|
C | T | 3 | a0001c0001t0004g0185a0001c0001t0004g0211a0001c0001t0013g0250 | 3 | HG01109.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.174+10375C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286784 | ||||||
| chr13:97286814
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG01256.hp1 HG01257.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+10405C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286814 | ||||||
| chr13:97286851
|
T | A | 2 | a0001c0001t0004g0185a0001c0001t0013g0250 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.174+10442T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286851 | ||||||
| chr13:97286927
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+10518C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97286927 | ||||||
| chr13:97287046
|
G | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0249 | 3 | HG03579.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.174+10637G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287046 | ||||||
| chr13:97287048
|
T | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.174+10639T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287048 | ||||||
| chr13:97287149
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.174+10740G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287149 | ||||||
| chr13:97287249
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.174+10840G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287249 | ||||||
| chr13:97287257
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.174+10848G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287257 | ||||||
| chr13:97287460
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.174+11051C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287460 | ||||||
| chr13:97287582
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.174+11173G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287582 | ||||||
| chr13:97287605
|
C | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+11196C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287605 | ||||||
| chr13:97287668
|
A | G | 7 | a0001c0001t0001g0251a0001c0001t0006g0127a0001c0001t0016g0245others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+11259A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287668 | ||||||
| chr13:97287691
|
TTC | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+11284_174+1128 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287691 | |||||
| chr13:97287716
|
CTTTTCTT others(2): Show |
C | 15 | a0001c0001t0001g0027a0001c0001t0001g0115a0001c0001t0001g0176others(12): Show | 15 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.174+11312_174+1132 others(13): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287716 | |||||
| chr13:97287716
|
CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+11312_174+1132 others(15): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287716 | |||||
| chr13:97287721
|
C | CT | 13 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0178others(10): Show | 13 | HG01981.hp1 HG02071.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+11333dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287721 | |||||
| chr13:97287721
|
CT | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0083others(11): Show | 14 | HG00438.hp2 HG00558.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+11333delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287721 | |||||
| chr13:97287721
|
CTT | C | 7 | a0001c0001t0001g0251a0001c0001t0006g0127a0001c0001t0016g0245others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+11332_174+1133 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287721 | |||||
| chr13:97287721
|
CTTTTT | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+11329_174+1133 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287721 | |||||
| chr13:97287727
|
T | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.174+11318T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287727 | ||||||
| chr13:97287829
|
G | GATTCTCC others(12): Show |
36 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+11438_174+1143 others(23): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287829 | |||||
| chr13:97287846
|
G | C | 1 | a0001c0001t0002g0010 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.174+11437G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287846 | ||||||
| chr13:97287895
|
C | G | 21 | a0001c0001t0001g0050a0001c0001t0001g0118a0001c0001t0001g0119others(18): Show | 21 | HG01192.hp2 HG01243.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.174+11486C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287895 | ||||||
| chr13:97287918
|
G | GT | 77 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.174+11519dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287918 | |||||
| chr13:97287918
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+11510_174+1151 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287918 | |||||
| chr13:97287918
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0176a0001c0001t0014g0234 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174+11519_174+1152 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287918 | |||||
| chr13:97287918
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174+11519_174+1152 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287918 | |||||
| chr13:97287918
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.174+11519_174+1152 others(21): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287918 | |||||
| chr13:97287925
|
TTTTGTTT others(7): Show |
T | 2 | a0001c0001t0004g0173a0001c0001t0015g0216 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+11520_174+1153 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287925 | |||||
| chr13:97287926
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.174+11517T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287926 | ||||||
| chr13:97287926
|
TTTGTTTT others(6): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.174+11520_174+1153 others(17): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287926 | |||||
| chr13:97287927
|
TTGTTTTG others(5): Show |
T | 33 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.174+11520_174+1153 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287927 | |||||
| chr13:97287928
|
TGTTTTGT others(4): Show |
T | 3 | a0001c0001t0001g0027a0001c0001t0001g0075a0001c0001t0013g0250 | 3 | HG01109.hp1 HG02896.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.174+11520_174+1153 others(15): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287928 | ||||||
| chr13:97287929
|
G | T | 15 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0176others(12): Show | 15 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.174+11520G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287929 | ||||||
| chr13:97287934
|
G | T | 15 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0176others(12): Show | 15 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.174+11525G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287934 | ||||||
| chr13:97287939
|
G | GT | 71 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.174+11544dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287939 | |||||
| chr13:97287939
|
G | GTTT | 6 | a0001c0001t0001g0251a0001c0001t0006g0127a0001c0002t0006g0126others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+11542_174+1154 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97287939 | |||||
| chr13:97287939
|
G | T | 21 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0125others(18): Show | 21 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.174+11530G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287939 | ||||||
| chr13:97287944
|
T | G | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0183others(3): Show | 6 | HG02717.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+11535T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287944 | ||||||
| chr13:97287966
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.174+11557G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97287966 | ||||||
| chr13:97288023
|
T | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0115a0001c0001t0001g0124others(22): Show | 25 | HG01109.hp2 HG01123.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+11614T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288023 | ||||||
| chr13:97288038
|
T | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+11629T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288038 | ||||||
| chr13:97288070
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+11661G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288070 | ||||||
| chr13:97288145
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.174+11736T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288145 | ||||||
| chr13:97288174
|
C | CTA | 37 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+11766_174+1176 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97288174 | |||||
| chr13:97288378
|
A | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.174+11969A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288378 | ||||||
| chr13:97288738
|
T | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+12329T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288738 | ||||||
| chr13:97288768
|
C | G | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+12359C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288768 | ||||||
| chr13:97288834
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+12425G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288834 | ||||||
| chr13:97288847
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.174+12438T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97288847 | ||||||
| chr13:97289010
|
A | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.174+12601A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289010 | ||||||
| chr13:97289059
|
T | C | 66 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.174+12650T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289059 | ||||||
| chr13:97289141
|
C | T | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.174+12732C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289141 | ||||||
| chr13:97289243
|
T | G | 137 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.174+12834T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289243 | ||||||
| chr13:97289254
|
A | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+12845A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289254 | ||||||
| chr13:97289400
|
TAAAATTA others(2505): Show |
T | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.174+12996_174+1550 others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97289400 | |||||
| chr13:97289477
|
T | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+13068T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289477 | ||||||
| chr13:97289498
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.174+13089C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289498 | ||||||
| chr13:97289528
|
A | C | 1 | a0001c0001t0003g0224 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.174+13119A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289528 | ||||||
| chr13:97289529
|
T | C | 66 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.174+13120T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289529 | ||||||
| chr13:97289845
|
A | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.174+13436A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97289845 | ||||||
| chr13:97290056
|
C | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+13647C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290056 | ||||||
| chr13:97290169
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.174+13760A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290169 | ||||||
| chr13:97290256
|
T | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+13847T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290256 | ||||||
| chr13:97290308
|
T | C | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+13899T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290308 | ||||||
| chr13:97290310
|
A | AT | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+13901_174+1390 others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290310 | ||||||
| chr13:97290311
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+13902G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290311 | ||||||
| chr13:97290316
|
G | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+13907G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290316 | ||||||
| chr13:97290381
|
A | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+13972A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290381 | ||||||
| chr13:97290398
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+13989C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290398 | ||||||
| chr13:97290399
|
G | A | 8 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0167others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+13990G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290399 | ||||||
| chr13:97290415
|
G | C | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+14006G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290415 | ||||||
| chr13:97290441
|
T | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+14032T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290441 | ||||||
| chr13:97290447
|
C | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+14038C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290447 | ||||||
| chr13:97290473
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.174+14064A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290473 | ||||||
| chr13:97290599
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+14190C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290599 | ||||||
| chr13:97290663
|
A | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+14254A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290663 | ||||||
| chr13:97290682
|
C | CA | 5 | a0001c0001t0001g0057a0001c0001t0001g0149a0001c0001t0002g0006others(2): Show | 5 | HG01261.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+14292dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97290682 | |||||
| chr13:97290682
|
CA | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0027others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.174+14292delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97290682 | |||||
| chr13:97290682
|
CAA | C | 84 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.174+14291_174+1429 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97290682 | |||||
| chr13:97290687
|
A | C | 1 | a0001c0001t0016g0245 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.174+14278A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290687 | ||||||
| chr13:97290698
|
A | G | 7 | a0001c0001t0001g0251a0001c0001t0006g0127a0001c0001t0016g0245others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+14289A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290698 | ||||||
| chr13:97290747
|
T | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+14338T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290747 | ||||||
| chr13:97290874
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0004g0172a0001c0001t0017g0177 | 3 | HG02486.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.174+14465G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290874 | ||||||
| chr13:97290927
|
CCTGG | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+14523_174+1452 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97290927 | |||||
| chr13:97290955
|
A | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+14546A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290955 | ||||||
| chr13:97290972
|
G | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+14563G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97290972 | ||||||
| chr13:97291175
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+14766G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291175 | ||||||
| chr13:97291198
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.174+14789T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291198 | ||||||
| chr13:97291282
|
C | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+14873C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291282 | ||||||
| chr13:97291404
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0014g0234 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174+14995G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291404 | ||||||
| chr13:97291433
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+15024G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291433 | ||||||
| chr13:97291449
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.174+15040G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291449 | ||||||
| chr13:97291450
|
C | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+15041C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291450 | ||||||
| chr13:97291477
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+15068G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291477 | ||||||
| chr13:97291525
|
T | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+15116T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291525 | ||||||
| chr13:97291620
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+15211C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291620 | ||||||
| chr13:97291649
|
A | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.174+15240A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291649 | ||||||
| chr13:97291724
|
T | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+15315T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291724 | ||||||
| chr13:97291846
|
G | A | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+15437G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291846 | ||||||
| chr13:97291882
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.174+15473G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291882 | ||||||
| chr13:97291900
|
C | CAAA | 7 | a0001c0001t0001g0023a0001c0001t0003g0101a0001c0001t0003g0220others(4): Show | 7 | HG01943.hp2 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+15506_174+1550 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAA | 33 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0118others(30): Show | 33 | HG00609.hp2 HG01123.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.174+15503_174+1550 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA | 60 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0029others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.174+15502_174+1550 others(11): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0044others(9): Show | 12 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+15501_174+1550 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01981.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+15499_174+1550 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(4): Show |
5 | a0001c0001t0001g0125a0001c0001t0001g0182a0001c0001t0001g0202others(2): Show | 5 | HG01109.hp1 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+15498_174+1550 others(15): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0122a0001c0001t0001g0135others(1): Show | 4 | HG00423.hp2 NA18946.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+15497_174+1550 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(6): Show |
15 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG01192.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.174+15496_174+1550 others(17): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(7): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0054others(8): Show | 11 | HG00280.hp2 HG00438.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+15495_174+1550 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0198a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG00140.hp2 HG01361.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+15494_174+1550 others(19): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(9): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0180a0001c0001t0001g0204others(3): Show | 6 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+15493_174+1550 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0176a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01109.hp2 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.174+15492_174+1550 others(21): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(11): Show |
6 | a0001c0001t0001g0027a0001c0001t0001g0143a0001c0001t0001g0191others(3): Show | 6 | HG02280.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(22): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0178a0001c0001t0007g0114others(1): Show | 4 | HG02071.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(23): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(13): Show |
5 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0002g0154others(2): Show | 5 | HG01175.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(24): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+15508_174+1550 others(25): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0004g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.174+15508_174+1550 others(26): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0150 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(28): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0229a0001c0001t0003g0163 | 2 | HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(29): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.174+15508_174+1550 others(30): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(22): Show |
7 | a0001c0001t0001g0132a0001c0001t0001g0207a0001c0001t0001g0209others(4): Show | 7 | HG02040.hp1 HG02523.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(33): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(23): Show |
7 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0096others(4): Show | 7 | HG02055.hp2 HG02165.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(34): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(24): Show |
6 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0001t0001g0162others(3): Show | 6 | HG00438.hp2 HG01255.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(35): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(25): Show |
4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0141others(1): Show | 4 | HG04199.hp1 NA18941.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(36): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(26): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0001g0217others(1): Show | 4 | HG02809.hp2 HG03239.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(37): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(27): Show |
4 | a0001c0001t0001g0164a0001c0001t0001g0183a0001c0001t0002g0161others(1): Show | 4 | HG00609.hp1 HG02717.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+15508_174+1550 others(38): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(28): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0226a0001c0001t0002g0111 | 3 | HG01167.hp1 HG01975.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(39): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0147 | 2 | HG00558.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(40): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(30): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0225a0001c0002t0001g0008 | 3 | HG01928.hp1 HG02630.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(41): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0167 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.174+15508_174+1550 others(42): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(32): Show |
2 | a0001c0001t0001g0106a0001c0001t0002g0010 | 2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(43): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(34): Show |
1 | a0001c0001t0002g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174+15508_174+1550 others(45): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291900
|
C | CAAAAAAA others(36): Show |
1 | a0001c0001t0001g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.174+15508_174+1550 others(47): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291900 | |||||
| chr13:97291917
|
A | AAAAAAAA others(26): Show |
1 | a0001c0002t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.174+15508_174+1550 others(37): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291917 | ||||||
| chr13:97291917
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0102a0001c0001t0002g0193 | 2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.174+15508_174+1550 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291917 | ||||||
| chr13:97291918
|
G | A | 91 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.174+15509G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291918 | ||||||
| chr13:97291931
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+15522G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97291931 | ||||||
| chr13:97291943
|
CTGTAATC others(8): Show |
C | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.174+15536_174+1555 others(19): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97291943 | |||||
| chr13:97292045
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+15636A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292045 | ||||||
| chr13:97292077
|
T | G | 70 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.174+15668T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292077 | ||||||
| chr13:97292132
|
C | T | 7 | a0001c0001t0001g0251a0001c0001t0006g0127a0001c0001t0016g0245others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+15723C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292132 | ||||||
| chr13:97292157
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+15748C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292157 | ||||||
| chr13:97292158
|
G | A | 78 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.174+15749G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292158 | ||||||
| chr13:97292167
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.174+15758C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292167 | ||||||
| chr13:97292200
|
C | CA | 31 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0079others(28): Show | 31 | HG00099.hp1 HG01123.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.174+15813dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97292200 | |||||
| chr13:97292200
|
C | CAAA | 5 | a0001c0001t0001g0124a0001c0001t0001g0178a0001c0001t0001g0191others(2): Show | 5 | HG01192.hp2 HG01884.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+15811_174+1581 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97292200 | |||||
| chr13:97292200
|
CAA | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0033others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.174+15812_174+1581 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97292200 | |||||
| chr13:97292200
|
CAAAA | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0176a0001c0001t0001g0180others(8): Show | 11 | HG01109.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+15810_174+1581 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97292200 | |||||
| chr13:97292248
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.174+15839C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292248 | ||||||
| chr13:97292350
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0014g0234 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174+15941G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292350 | ||||||
| chr13:97292424
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+16015A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292424 | ||||||
| chr13:97292450
|
T | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+16041T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292450 | ||||||
| chr13:97292503
|
A | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+16094A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292503 | ||||||
| chr13:97292612
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0004g0172a0001c0001t0017g0177 | 3 | HG02486.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.174+16203C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292612 | ||||||
| chr13:97292852
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+16443C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97292852 | ||||||
| chr13:97293039
|
CTCA | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+16638_174+1664 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97293039 | |||||
| chr13:97293047
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0183a0001c0001t0001g0228others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+16638C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97293047 | ||||||
| chr13:97293072
|
T | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+16663T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97293072 | ||||||
| chr13:97293228
|
T | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+16819T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97293228 | ||||||
| chr13:97293559
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0010g0003 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.174+17150T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97293559 | ||||||
| chr13:97293974
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+17565C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97293974 | ||||||
| chr13:97294081
|
A | C | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+17672A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294081 | ||||||
| chr13:97294377
|
A | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.174+17968A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294377 | ||||||
| chr13:97294497
|
A | C | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.174+18088A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294497 | ||||||
| chr13:97294558
|
T | G | 1 | a0001c0002t0001g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.174+18149T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294558 | ||||||
| chr13:97294579
|
T | G | 1 | a0001c0001t0001g0014 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.174+18170T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294579 | ||||||
| chr13:97294610
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.174+18201G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294610 | ||||||
| chr13:97294750
|
G | A | 7 | a0001c0001t0001g0204a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+18341G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294750 | ||||||
| chr13:97294966
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.174+18557C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97294966 | ||||||
| chr13:97295096
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0087a0001c0001t0001g0231 | 3 | HG00735.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.174+18687G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295096 | ||||||
| chr13:97295140
|
A | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.174+18731A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295140 | ||||||
| chr13:97295195
|
T | C | 1 | a0001c0001t0018g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.174+18786T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295195 | ||||||
| chr13:97295323
|
G | GT | 10 | a0001c0001t0001g0130a0001c0001t0002g0006a0001c0001t0002g0009others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.174+18925dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97295323 | |||||
| chr13:97295357
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.174+18948C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295357 | ||||||
| chr13:97295361
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+18952C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295361 | ||||||
| chr13:97295505
|
A | ATGT | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.174+19097_174+1909 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97295505 | |||||
| chr13:97295813
|
T | A | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+19404T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295813 | ||||||
| chr13:97295872
|
G | C | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+19463G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97295872 | ||||||
| chr13:97296121
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+19712C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296121 | ||||||
| chr13:97296176
|
A | C | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+19767A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296176 | ||||||
| chr13:97296208
|
C | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+19799C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296208 | ||||||
| chr13:97296435
|
A | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+20026A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296435 | ||||||
| chr13:97296444
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.174+20035C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296444 | ||||||
| chr13:97296480
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.174+20071C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296480 | ||||||
| chr13:97296523
|
T | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.174+20114T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296523 | ||||||
| chr13:97296608
|
C | T | 1 | a0001c0001t0016g0245 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.174+20199C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296608 | ||||||
| chr13:97296610
|
G | T | 4 | a0001c0001t0001g0130a0001c0001t0002g0157a0001c0001t0002g0160others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+20201G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296610 | ||||||
| chr13:97296663
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+20254G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296663 | ||||||
| chr13:97296742
|
A | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+20333A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296742 | ||||||
| chr13:97296778
|
T | C | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.174+20369T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296778 | ||||||
| chr13:97296930
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0180 | 2 | HG01109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.174+20521T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97296930 | ||||||
| chr13:97297031
|
C | A | 6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+20622C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297031 | ||||||
| chr13:97297097
|
C | G | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+20688C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297097 | ||||||
| chr13:97297135
|
A | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+20726A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297135 | ||||||
| chr13:97297170
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.174+20761T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297170 | ||||||
| chr13:97297226
|
A | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+20817A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297226 | ||||||
| chr13:97297258
|
C | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+20849C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297258 | ||||||
| chr13:97297432
|
T | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 18 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+21023T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297432 | ||||||
| chr13:97297495
|
A | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+21086A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297495 | ||||||
| chr13:97297568
|
A | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+21159A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297568 | ||||||
| chr13:97297599
|
T | G | 1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.174+21190T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297599 | ||||||
| chr13:97297632
|
C | A | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.174+21223C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297632 | ||||||
| chr13:97297687
|
A | T | 14 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0175others(11): Show | 14 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+21278A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297687 | ||||||
| chr13:97297696
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.174+21287C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297696 | ||||||
| chr13:97297718
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01175.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.174+21309G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297718 | ||||||
| chr13:97297765
|
T | A | 23 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0049others(20): Show | 23 | HG00423.hp2 HG00438.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.174+21356T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297765 | ||||||
| chr13:97297810
|
A | G | 1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.174+21401A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297810 | ||||||
| chr13:97297956
|
TAAAC | T | 66 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.174+21551_174+2155 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97297956 | |||||
| chr13:97297982
|
G | A | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.174+21573G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97297982 | ||||||
| chr13:97298152
|
A | G | 2 | a0001c0001t0004g0173a0001c0001t0015g0216 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+21743A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97298152 | ||||||
| chr13:97298158
|
C | A | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+21749C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97298158 | ||||||
| chr13:97298212
|
T | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.174+21803T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97298212 | ||||||
| chr13:97298503
|
C | G | 1 | a0001c0001t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.174+22094C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97298503 | ||||||
| chr13:97298729
|
A | G | 2 | a0001c0001t0004g0173a0001c0001t0015g0216 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+22320A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97298729 | ||||||
| chr13:97299010
|
A | G | 3 | a0001c0001t0004g0173a0001c0001t0013g0250a0001c0001t0015g0216 | 3 | HG01109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+22601A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299010 | ||||||
| chr13:97299065
|
A | G | 3 | a0001c0001t0004g0173a0001c0001t0013g0250a0001c0001t0015g0216 | 3 | HG01109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+22656A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299065 | ||||||
| chr13:97299181
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+22772C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299181 | ||||||
| chr13:97299266
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+22857C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299266 | ||||||
| chr13:97299419
|
G | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.174+23010G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299419 | ||||||
| chr13:97299462
|
G | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.174+23053G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299462 | ||||||
| chr13:97299648
|
A | ATATC | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0026others(36): Show | 39 | HG00099.hp2 HG00609.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.174+23276_174+2327 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97299648 | |||||
| chr13:97299648
|
A | ATATCTAT others(1): Show |
45 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0030others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.174+23272_174+2327 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97299648 | |||||
| chr13:97299648
|
A | ATATCTAT others(5): Show |
24 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0035others(21): Show | 24 | HG00423.hp1 HG00558.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.174+23268_174+2327 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97299648 | |||||
| chr13:97299648
|
A | ATATCTAT others(9): Show |
5 | a0001c0001t0001g0048a0001c0001t0001g0124a0001c0001t0001g0138others(2): Show | 5 | HG01257.hp1 HG01884.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+23264_174+2327 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97299648 | |||||
| chr13:97299648
|
ATATC | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0031others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.174+23276_174+2327 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97299648 | |||||
| chr13:97299666
|
A | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.174+23257A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299666 | ||||||
| chr13:97299737
|
G | T | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+23328G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299737 | ||||||
| chr13:97299829
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG01256.hp1 HG01257.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+23420G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299829 | ||||||
| chr13:97299940
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+23531C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97299940 | ||||||
| chr13:97300059
|
C | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+23650C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300059 | ||||||
| chr13:97300093
|
G | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+23684G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300093 | ||||||
| chr13:97300218
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+23809C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300218 | ||||||
| chr13:97300395
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.174+23986C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300395 | ||||||
| chr13:97300445
|
A | T | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.174+24036A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300445 | ||||||
| chr13:97300476
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.174+24067A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300476 | ||||||
| chr13:97300552
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0181 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.174+24143C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300552 | ||||||
| chr13:97300563
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+24154C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300563 | ||||||
| chr13:97300632
|
G | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+24223G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300632 | ||||||
| chr13:97300792
|
C | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.174+24383C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300792 | ||||||
| chr13:97300836
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+24427C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300836 | ||||||
| chr13:97300939
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0049others(19): Show | 22 | HG00423.hp2 HG00438.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.174+24530C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97300939 | ||||||
| chr13:97301136
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.174+24727C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301136 | ||||||
| chr13:97301185
|
C | T | 76 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.174+24776C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301185 | ||||||
| chr13:97301252
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.174+24843C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301252 | ||||||
| chr13:97301380
|
G | C | 2 | a0001c0001t0002g0174a0001c0001t0002g0199 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.174+24971G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301380 | ||||||
| chr13:97301444
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.174+25035G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301444 | ||||||
| chr13:97301504
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.174+25095G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301504 | ||||||
| chr13:97301676
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.174+25267G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301676 | ||||||
| chr13:97301711
|
C | G | 1 | a0001c0001t0006g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.174+25302C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301711 | ||||||
| chr13:97301750
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.174+25341C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301750 | ||||||
| chr13:97301814
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.174+25405A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301814 | ||||||
| chr13:97301959
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0191a0001c0001t0007g0114 | 3 | HG03130.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.174+25550T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301959 | ||||||
| chr13:97301969
|
G | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+25560G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97301969 | ||||||
| chr13:97302065
|
A | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.174+25656A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97302065 | ||||||
| chr13:97302171
|
G | T | 162 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.174+25762G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97302171 | ||||||
| chr13:97302433
|
G | A | 1 | a0002c0004t0001g0232 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.174+26024G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97302433 | ||||||
| chr13:97302866
|
C | T | 1 | a0001c0001t0003g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.174+26457C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97302866 | ||||||
| chr13:97302880
|
G | A | 15 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0167others(12): Show | 15 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.174+26471G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97302880 | ||||||
| chr13:97302897
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.174+26488G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97302897 | ||||||
| chr13:97303342
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+26933G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97303342 | ||||||
| chr13:97303568
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0014g0234 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174+27159G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97303568 | ||||||
| chr13:97303637
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.174+27228C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97303637 | ||||||
| chr13:97303672
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.174+27263C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97303672 | ||||||
| chr13:97303699
|
C | T | 2 | a0001c0001t0001g0116a0001c0002t0001g0008 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.174+27290C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97303699 | ||||||
| chr13:97303752
|
A | C | 3 | a0001c0001t0004g0173a0001c0001t0013g0250a0001c0001t0015g0216 | 3 | HG01109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+27343A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97303752 | ||||||
| chr13:97304007
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.174+27598T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304007 | ||||||
| chr13:97304011
|
C | T | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.174+27602C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304011 | ||||||
| chr13:97304075
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.174+27666T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304075 | ||||||
| chr13:97304087
|
A | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.174+27678A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304087 | ||||||
| chr13:97304272
|
G | T | 5 | a0001c0001t0001g0124a0001c0001t0004g0173a0001c0001t0013g0250others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+27863G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304272 | ||||||
| chr13:97304285
|
G | C | 5 | a0001c0001t0001g0124a0001c0001t0004g0173a0001c0001t0013g0250others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+27876G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304285 | ||||||
| chr13:97304357
|
A | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0147a0001c0001t0001g0225others(1): Show | 4 | HG01167.hp1 HG01928.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+27948A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304357 | ||||||
| chr13:97304379
|
A | G | 6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+27970A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304379 | ||||||
| chr13:97304500
|
A | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.174+28091A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304500 | ||||||
| chr13:97304541
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.174+28132A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304541 | ||||||
| chr13:97304576
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0013g0250a0001c0001t0014g0234 | 3 | HG01109.hp1 HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.174+28167A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304576 | ||||||
| chr13:97304584
|
G | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0111a0001c0001t0002g0165 | 3 | NA18948.hp1 NA18967.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.174+28175G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304584 | ||||||
| chr13:97304585
|
A | G | 173 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+28176A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304585 | ||||||
| chr13:97304650
|
A | G | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.174+28241A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304650 | ||||||
| chr13:97304718
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.174+28309A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304718 | ||||||
| chr13:97304765
|
T | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0164a0001c0001t0002g0010others(9): Show | 12 | HG02040.hp1 HG02056.hp1 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+28356T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304765 | ||||||
| chr13:97304876
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.174+28467G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304876 | ||||||
| chr13:97304894
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+28485T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304894 | ||||||
| chr13:97304906
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0004g0173a0001c0001t0013g0250others(1): Show | 4 | HG01109.hp1 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+28497C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97304906 | ||||||
| chr13:97305098
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0147a0001c0001t0001g0225others(1): Show | 4 | HG01167.hp1 HG01928.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+28689G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97305098 | ||||||
| chr13:97305542
|
T | C | 1 | a0001c0001t0004g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.175-28734T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97305542 | ||||||
| chr13:97305544
|
A | T | 1 | a0003c0005t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175-28732A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97305544 | ||||||
| chr13:97305609
|
C | CA | 78 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.175-28661dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97305609 | |||||
| chr13:97305612
|
A | G | 5 | a0001c0001t0001g0124a0001c0001t0002g0174a0001c0001t0002g0199others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-28664A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97305612 | ||||||
| chr13:97305764
|
G | A | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.175-28512G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97305764 | ||||||
| chr13:97305769
|
A | AAAAC | 81 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.175-28490_175-2848 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97305769 | |||||
| chr13:97305809
|
A | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0031others(23): Show | 26 | HG00423.hp2 HG01167.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.175-28467A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97305809 | ||||||
| chr13:97306043
|
T | C | 31 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0050others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.175-28233T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97306043 | ||||||
| chr13:97306150
|
C | A | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-28126C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97306150 | ||||||
| chr13:97306186
|
G | T | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-28090G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97306186 | ||||||
| chr13:97306387
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.175-27889G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97306387 | ||||||
| chr13:97306525
|
A | C | 3 | a0001c0001t0004g0112a0001c0001t0004g0233a0001c0001t0013g0250 | 3 | HG01109.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.175-27751A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97306525 | ||||||
| chr13:97307024
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.175-27252A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307024 | ||||||
| chr13:97307114
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175-27162C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307114 | ||||||
| chr13:97307115
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-27161G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307115 | ||||||
| chr13:97307140
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.175-27136C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307140 | ||||||
| chr13:97307180
|
T | G | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-27096T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307180 | ||||||
| chr13:97307386
|
A | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0199 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175-26890A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307386 | ||||||
| chr13:97307506
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-26770G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307506 | ||||||
| chr13:97307609
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.175-26667A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307609 | ||||||
| chr13:97307859
|
G | A | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-26417G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97307859 | ||||||
| chr13:97308052
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG02280.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.175-26224T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97308052 | ||||||
| chr13:97308090
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.175-26186T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97308090 | ||||||
| chr13:97308372
|
C | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.175-25904C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97308372 | ||||||
| chr13:97308750
|
C | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0147a0001c0001t0001g0225others(1): Show | 4 | HG01167.hp1 HG01928.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-25526C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97308750 | ||||||
| chr13:97308751
|
T | G | 139 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.175-25525T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97308751 | ||||||
| chr13:97309041
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-25235G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309041 | ||||||
| chr13:97309050
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-25226G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309050 | ||||||
| chr13:97309173
|
C | T | 61 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.175-25103C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309173 | ||||||
| chr13:97309242
|
A | C | 1 | a0001c0001t0002g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.175-25034A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309242 | ||||||
| chr13:97309324
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0002g0205others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-24952T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309324 | ||||||
| chr13:97309390
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG02280.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-24886A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309390 | ||||||
| chr13:97309393
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.175-24883G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309393 | ||||||
| chr13:97309525
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.175-24751C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309525 | ||||||
| chr13:97309539
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175-24737A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309539 | ||||||
| chr13:97309895
|
T | C | 12 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-24381T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309895 | ||||||
| chr13:97309925
|
G | C | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-24351G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309925 | ||||||
| chr13:97309951
|
G | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0082a0001c0001t0001g0088others(3): Show | 6 | HG01261.hp2 HG01943.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-24325G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309951 | ||||||
| chr13:97309999
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.175-24277G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97309999 | ||||||
| chr13:97310120
|
A | C | 1 | a0001c0001t0003g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.175-24156A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310120 | ||||||
| chr13:97310207
|
G | C | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-24069G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310207 | ||||||
| chr13:97310268
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175-24008G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310268 | ||||||
| chr13:97310418
|
C | CT | 7 | a0001c0001t0001g0020a0001c0001t0001g0064a0001c0001t0001g0128others(4): Show | 7 | HG00423.hp1 HG02027.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-23847dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310418 | |||||
| chr13:97310418
|
CT | C | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0167others(2): Show | 5 | HG02895.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-23847delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310418 | |||||
| chr13:97310439
|
C | CT | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0002g0205others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-23829dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310439 | |||||
| chr13:97310509
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.175-23767A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310509 | ||||||
| chr13:97310557
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0153others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-23719G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310557 | ||||||
| chr13:97310579
|
G | A | 19 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(16): Show | 19 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.175-23697G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310579 | ||||||
| chr13:97310611
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-23665A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97310611 | ||||||
| chr13:97310782
|
C | CT | 33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(30): Show | 33 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.175-23474dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310782 | |||||
| chr13:97310782
|
C | CTTT | 17 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(14): Show | 17 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-23476_175-2347 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310782 | |||||
| chr13:97310782
|
CT | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.175-23474delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310782 | |||||
| chr13:97310782
|
CTT | C | 12 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0055others(9): Show | 12 | HG01070.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-23475_175-2347 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97310782 | |||||
| chr13:97311052
|
A | C | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175-23224A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311052 | ||||||
| chr13:97311116
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175-23160G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311116 | ||||||
| chr13:97311122
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.175-23154G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311122 | ||||||
| chr13:97311188
|
C | A | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.175-23088C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311188 | ||||||
| chr13:97311502
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.175-22774A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311502 | ||||||
| chr13:97311523
|
T | C | 9 | a0001c0001t0004g0185a0001c0001t0006g0127a0001c0001t0016g0245others(6): Show | 9 | HG01123.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-22753T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311523 | ||||||
| chr13:97311649
|
AT | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.175-22619delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97311649 | |||||
| chr13:97311650
|
T | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-22626T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311650 | ||||||
| chr13:97311668
|
T | A | 12 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-22608T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311668 | ||||||
| chr13:97311668
|
T | TA | 9 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(6): Show | 9 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-22599dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97311668 | |||||
| chr13:97311669
|
A | T | 37 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.175-22607A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311669 | ||||||
| chr13:97311725
|
T | C | 76 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.175-22551T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97311725 | ||||||
| chr13:97312136
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0015g0216 | 3 | HG02895.hp2 HG02897.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-22140A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312136 | ||||||
| chr13:97312195
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175-22081C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312195 | ||||||
| chr13:97312498
|
G | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175-21778G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312498 | ||||||
| chr13:97312666
|
T | G | 11 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(8): Show | 11 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.175-21610T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312666 | ||||||
| chr13:97312840
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00140.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.175-21436C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312840 | ||||||
| chr13:97312871
|
A | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-21405A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312871 | ||||||
| chr13:97312876
|
C | A | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-21400C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312876 | ||||||
| chr13:97312987
|
A | G | 6 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-21289A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97312987 | ||||||
| chr13:97313011
|
T | A | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-21265T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313011 | ||||||
| chr13:97313242
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-21034G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313242 | ||||||
| chr13:97313309
|
T | C | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-20967T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313309 | ||||||
| chr13:97313326
|
C | A | 12 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-20950C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313326 | ||||||
| chr13:97313512
|
TA | T | 6 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-20761delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97313512 | |||||
| chr13:97313526
|
A | C | 66 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.175-20750A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313526 | ||||||
| chr13:97313819
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.175-20457C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313819 | ||||||
| chr13:97313925
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.175-20351T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97313925 | ||||||
| chr13:97314014
|
T | C | 81 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 81 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.175-20262T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314014 | ||||||
| chr13:97314048
|
T | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-20228T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314048 | ||||||
| chr13:97314302
|
A | T | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-19974A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314302 | ||||||
| chr13:97314310
|
T | C | 12 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-19966T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314310 | ||||||
| chr13:97314377
|
T | A | 7 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(4): Show | 7 | HG02559.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-19899T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314377 | ||||||
| chr13:97314494
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0014g0234 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-19782G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314494 | ||||||
| chr13:97314617
|
T | C | 6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-19659T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314617 | ||||||
| chr13:97314716
|
A | C | 12 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-19560A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97314716 | ||||||
| chr13:97315064
|
C | T | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.175-19212C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315064 | ||||||
| chr13:97315278
|
T | A | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0118others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.175-18998T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315278 | ||||||
| chr13:97315384
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.175-18892C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315384 | ||||||
| chr13:97315446
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0060 | 2 | HG02523.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.175-18830A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315446 | ||||||
| chr13:97315670
|
C | T | 15 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0130others(12): Show | 15 | HG01109.hp1 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-18606C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315670 | ||||||
| chr13:97315741
|
T | G | 2 | a0001c0001t0001g0191a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.175-18535T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315741 | ||||||
| chr13:97315747
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.175-18529T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97315747 | ||||||
| chr13:97315790
|
ATGGGTGA others(21): Show |
A | 1 | a0001c0001t0001g0031 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.175-18462_175-1843 others(32): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97315790 | |||||
| chr13:97315814
|
G | GCTCGTGG others(21): Show |
1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.175-18434_175-1840 others(32): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97315814 | |||||
| chr13:97315842
|
ACTCGTGG others(21): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-18420_175-1839 others(32): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97315842 | |||||
| chr13:97316140
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-18136C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316140 | ||||||
| chr13:97316149
|
A | C | 52 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.175-18127A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316149 | ||||||
| chr13:97316161
|
C | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0033others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.175-18115C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316161 | ||||||
| chr13:97316163
|
C | T | 11 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(8): Show | 11 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-18113C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316163 | ||||||
| chr13:97316356
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0194others(1): Show | 4 | HG03579.hp2 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-17920G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316356 | ||||||
| chr13:97316507
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.175-17769C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316507 | ||||||
| chr13:97316721
|
T | C | 25 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG01192.hp2 HG01981.hp1 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-17555T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316721 | ||||||
| chr13:97316745
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0033others(49): Show | 52 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.175-17531C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316745 | ||||||
| chr13:97316920
|
T | C | 11 | a0001c0001t0003g0099a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-17356T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316920 | ||||||
| chr13:97316947
|
G | A | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175-17329G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316947 | ||||||
| chr13:97316953
|
T | A | 1 | a0001c0001t0001g0002 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.175-17323T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316953 | ||||||
| chr13:97316973
|
G | A | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175-17303G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97316973 | ||||||
| chr13:97317113
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0033others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.175-17163G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317113 | ||||||
| chr13:97317208
|
A | G | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-17068A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317208 | ||||||
| chr13:97317250
|
C | T | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175-17026C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317250 | ||||||
| chr13:97317403
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0133 | 3 | NA18950.hp1 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.175-16873C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317403 | ||||||
| chr13:97317491
|
T | A | 9 | a0001c0001t0003g0099a0001c0002t0001g0235a0001c0002t0001g0236others(6): Show | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-16785T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317491 | ||||||
| chr13:97317509
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-16767G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317509 | ||||||
| chr13:97317511
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.175-16765A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317511 | ||||||
| chr13:97317578
|
T | C | 7 | a0001c0001t0001g0124a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-16698T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317578 | ||||||
| chr13:97317779
|
G | A | 20 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(17): Show | 20 | HG01981.hp1 HG02572.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.175-16497G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317779 | ||||||
| chr13:97317802
|
A | G | 6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-16474A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317802 | ||||||
| chr13:97317986
|
G | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.175-16290G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97317986 | ||||||
| chr13:97318241
|
G | T | 25 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG01981.hp1 HG02486.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-16035G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318241 | ||||||
| chr13:97318350
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-15926C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318350 | ||||||
| chr13:97318632
|
T | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.175-15644T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318632 | ||||||
| chr13:97318909
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0149 | 2 | NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.175-15367C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318909 | ||||||
| chr13:97318925
|
C | T | 1 | a0001c0001t0011g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175-15351C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318925 | ||||||
| chr13:97318926
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-15350G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318926 | ||||||
| chr13:97318976
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0020others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.175-15300T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97318976 | ||||||
| chr13:97319086
|
G | C | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-15190G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319086 | ||||||
| chr13:97319229
|
G | GT | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.175-15045dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97319229 | |||||
| chr13:97319273
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.175-15003A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319273 | ||||||
| chr13:97319287
|
G | A | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175-14989G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319287 | ||||||
| chr13:97319321
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-14955A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319321 | ||||||
| chr13:97319449
|
G | A | 7 | a0001c0001t0001g0124a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-14827G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319449 | ||||||
| chr13:97319487
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-14789C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319487 | ||||||
| chr13:97319541
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-14735G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319541 | ||||||
| chr13:97319593
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-14683C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319593 | ||||||
| chr13:97319743
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-14533A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319743 | ||||||
| chr13:97319818
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.175-14458A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319818 | ||||||
| chr13:97319819
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.175-14457T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97319819 | ||||||
| chr13:97320061
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175-14215A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320061 | ||||||
| chr13:97320143
|
T | C | 1 | a0001c0001t0002g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.175-14133T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320143 | ||||||
| chr13:97320202
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 39 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.175-14074A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320202 | ||||||
| chr13:97320258
|
G | T | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-14018G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320258 | ||||||
| chr13:97320261
|
C | CT | 45 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(42): Show | 45 | HG00140.hp1 HG00423.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.175-13999dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97320261 | |||||
| chr13:97320512
|
T | C | 1 | a0001c0001t0016g0245 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.175-13764T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320512 | ||||||
| chr13:97320572
|
A | C | 25 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG01981.hp1 HG02486.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-13704A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320572 | ||||||
| chr13:97320631
|
C | T | 12 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-13645C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320631 | ||||||
| chr13:97320632
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.175-13644G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320632 | ||||||
| chr13:97320638
|
G | T | 2 | a0001c0001t0001g0102a0001c0001t0007g0206 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175-13638G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320638 | ||||||
| chr13:97320711
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.175-13565C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320711 | ||||||
| chr13:97320864
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0012g0227 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.175-13412G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97320864 | ||||||
| chr13:97321246
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.175-13030C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321246 | ||||||
| chr13:97321363
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-12913G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321363 | ||||||
| chr13:97321398
|
T | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-12878T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321398 | ||||||
| chr13:97321467
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-12809A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321467 | ||||||
| chr13:97321468
|
G | T | 1 | a0001c0001t0002g0111 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.175-12808G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321468 | ||||||
| chr13:97321520
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-12756C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321520 | ||||||
| chr13:97321758
|
G | A | 12 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-12518G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321758 | ||||||
| chr13:97321874
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.175-12402T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321874 | ||||||
| chr13:97321898
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.175-12378T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321898 | ||||||
| chr13:97321902
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0033others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.175-12374A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97321902 | ||||||
| chr13:97322015
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.175-12261C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322015 | ||||||
| chr13:97322427
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-11849G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322427 | ||||||
| chr13:97322641
|
A | C | 1 | a0001c0002t0006g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175-11635A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322641 | ||||||
| chr13:97322666
|
T | C | 25 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG01981.hp1 HG02486.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-11610T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322666 | ||||||
| chr13:97322771
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.175-11505C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322771 | ||||||
| chr13:97322790
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.175-11486G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322790 | ||||||
| chr13:97322809
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175-11467C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97322809 | ||||||
| chr13:97323174
|
C | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-11102C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323174 | ||||||
| chr13:97323346
|
T | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(79): Show | 82 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.175-10930T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323346 | ||||||
| chr13:97323421
|
C | T | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175-10855C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323421 | ||||||
| chr13:97323473
|
T | C | 1 | a0001c0002t0001g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.175-10803T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323473 | ||||||
| chr13:97323528
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.175-10748A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323528 | ||||||
| chr13:97323788
|
A | T | 4 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0004g0211others(1): Show | 4 | HG02572.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-10488A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323788 | ||||||
| chr13:97323893
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.175-10383T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97323893 | ||||||
| chr13:97324130
|
A | T | 4 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0004g0211others(1): Show | 4 | HG02572.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-10146A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324130 | ||||||
| chr13:97324188
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.175-10088A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324188 | ||||||
| chr13:97324249
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.175-10027T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324249 | ||||||
| chr13:97324278
|
A | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0176others(11): Show | 14 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.175-9998A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324278 | ||||||
| chr13:97324379
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.175-9897G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324379 | ||||||
| chr13:97324444
|
A | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-9832A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324444 | ||||||
| chr13:97324451
|
T | C | 25 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(22): Show | 25 | HG01981.hp1 HG02486.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-9825T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324451 | ||||||
| chr13:97324833
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.175-9443A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324833 | ||||||
| chr13:97324881
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-9395G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324881 | ||||||
| chr13:97324951
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0007g0114 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.175-9325C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97324951 | ||||||
| chr13:97325287
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.175-8989T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97325287 | ||||||
| chr13:97325407
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-8869G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97325407 | ||||||
| chr13:97325818
|
C | T | 9 | a0001c0001t0003g0099a0001c0002t0001g0235a0001c0002t0001g0236others(6): Show | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-8458C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97325818 | ||||||
| chr13:97325921
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.175-8355A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97325921 | ||||||
| chr13:97325973
|
G | GT | 61 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(58): Show | 61 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.175-8298dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97325973 | |||||
| chr13:97326099
|
AGTCCAGG others(14): Show |
A | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.175-8175_175-8155d others(23): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97326099 | |||||
| chr13:97326186
|
T | G | 2 | a0001c0001t0003g0224a0001c0001t0009g0221 | 2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.175-8090T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97326186 | ||||||
| chr13:97326231
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0033others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.175-8045A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97326231 | ||||||
| chr13:97326450
|
G | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.175-7826G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97326450 | ||||||
| chr13:97326561
|
T | A | 1 | a0001c0001t0011g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175-7715T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97326561 | ||||||
| chr13:97326655
|
G | A | 4 | a0001c0001t0002g0174a0001c0001t0002g0199a0001c0001t0004g0211others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-7621G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97326655 | ||||||
| chr13:97326805
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.175-7471G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97326805 | ||||||
| chr13:97327037
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-7239C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327037 | ||||||
| chr13:97327189
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.175-7087T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327189 | ||||||
| chr13:97327353
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.175-6923G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327353 | ||||||
| chr13:97327499
|
TC | T | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175-6776delC | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327499 | ||||||
| chr13:97327560
|
T | TA | 18 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0123others(15): Show | 18 | HG00438.hp1 HG01261.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.175-6693dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97327560 | |||||
| chr13:97327560
|
T | TAAAA | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(61): Show | 64 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.175-6696_175-6693d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97327560 | |||||
| chr13:97327560
|
T | TAAAAA | 32 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0027others(29): Show | 32 | HG01192.hp1 HG01243.hp1 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.175-6697_175-6693d others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97327560 | |||||
| chr13:97327560
|
T | TAAAAAA | 41 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0043others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.175-6698_175-6693d others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97327560 | |||||
| chr13:97327560
|
T | TAAAAAAA | 27 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0057others(24): Show | 27 | HG00423.hp2 HG00609.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.175-6699_175-6693d others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97327560 | |||||
| chr13:97327584
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.175-6692G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327584 | ||||||
| chr13:97327645
|
A | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-6631A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327645 | ||||||
| chr13:97327757
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-6519G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327757 | ||||||
| chr13:97327773
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175-6503G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327773 | ||||||
| chr13:97327919
|
T | C | 1 | a0001c0001t0005g0239 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.175-6357T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97327919 | ||||||
| chr13:97328037
|
G | T | 2 | a0001c0001t0001g0102a0001c0001t0007g0206 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175-6239G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328037 | ||||||
| chr13:97328038
|
C | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-6238C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328038 | ||||||
| chr13:97328119
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.175-6157G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328119 | ||||||
| chr13:97328141
|
A | G | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-6135A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328141 | ||||||
| chr13:97328173
|
C | CT | 29 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0020others(26): Show | 29 | HG01123.hp1 HG01175.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.175-6081dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97328173 | |||||
| chr13:97328173
|
CTT | C | 15 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0130others(12): Show | 15 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-6082_175-6081d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97328173 | |||||
| chr13:97328173
|
CTTT | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-6083_175-6081d others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97328173 | |||||
| chr13:97328243
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175-6033T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328243 | ||||||
| chr13:97328243
|
TG | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.175-6032delG | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328243 | ||||||
| chr13:97328405
|
G | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175-5871G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328405 | ||||||
| chr13:97328426
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-5850C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328426 | ||||||
| chr13:97328482
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.175-5794A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328482 | ||||||
| chr13:97328573
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.175-5703G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328573 | ||||||
| chr13:97328641
|
A | ACACAGTT | 23 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG01981.hp1 HG02572.hp2 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.175-5632_175-5626d others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97328641 | |||||
| chr13:97328663
|
G | A | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-5613G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328663 | ||||||
| chr13:97328704
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-5572G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328704 | ||||||
| chr13:97328825
|
T | A | 11 | a0001c0001t0003g0099a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-5451T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328825 | ||||||
| chr13:97328881
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175-5395C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328881 | ||||||
| chr13:97328936
|
T | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-5340T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328936 | ||||||
| chr13:97328954
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-5322G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97328954 | ||||||
| chr13:97329274
|
A | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175-5002A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329274 | ||||||
| chr13:97329362
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.175-4914C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329362 | ||||||
| chr13:97329451
|
C | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.175-4825C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329451 | ||||||
| chr13:97329464
|
G | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.175-4812G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329464 | ||||||
| chr13:97329545
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.175-4731G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329545 | ||||||
| chr13:97329560
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0020others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.175-4716T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329560 | ||||||
| chr13:97329561
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-4715G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329561 | ||||||
| chr13:97329640
|
C | CACACACA others(281): Show |
1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-4628_175-4627i others(290): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329640 | |||||
| chr13:97329640
|
C | CACACACA others(280): Show |
12 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-4622_175-4621i others(289): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329640 | |||||
| chr13:97329640
|
C | CACACACA others(281): Show |
106 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.175-4622_175-4621i others(290): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329640 | |||||
| chr13:97329640
|
C | CACACACA others(279): Show |
1 | a0001c0001t0001g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.175-4622_175-4621i others(288): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329640 | |||||
| chr13:97329640
|
C | CACACACA others(281): Show |
131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(128): Show | 131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.175-4622_175-4621i others(290): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329640 | |||||
| chr13:97329640
|
C | CACACACA others(281): Show |
1 | a0001c0002t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.175-4622_175-4621i others(290): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329640 | |||||
| chr13:97329642
|
C | CACACAAT others(279): Show |
1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175-4622_175-4621i others(288): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329642 | |||||
| chr13:97329694
|
A | G | 9 | a0001c0001t0003g0099a0001c0002t0001g0235a0001c0002t0001g0236others(6): Show | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-4582A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329694 | ||||||
| chr13:97329726
|
A | AACACACA others(79): Show |
80 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.175-4547_175-4546i others(88): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329726 | |||||
| chr13:97329726
|
A | AACACACA others(77): Show |
53 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-4547_175-4546i others(86): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329726 | |||||
| chr13:97329726
|
A | AACACACA others(79): Show |
119 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.175-4547_175-4546i others(88): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329726 | |||||
| chr13:97329726
|
A | AACACACA others(79): Show |
1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-4547_175-4546i others(88): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329726 | |||||
| chr13:97329753
|
TAC | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.175-4515_175-4514d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329753 | |||||
| chr13:97329768
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.175-4508C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329768 | ||||||
| chr13:97329776
|
AG | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.175-4498delG | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329776 | |||||
| chr13:97329778
|
G | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0061others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-4498G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329778 | ||||||
| chr13:97329795
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0020others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.175-4481T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329795 | ||||||
| chr13:97329826
|
A | AAC | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0016others(57): Show | 60 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.175-4429_175-4428d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329826 | |||||
| chr13:97329826
|
A | AACAC | 6 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0093others(3): Show | 6 | HG00438.hp2 HG02056.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-4431_175-4428d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329826 | |||||
| chr13:97329826
|
A | AACACAC | 8 | a0001c0001t0003g0099a0001c0002t0001g0235a0001c0002t0001g0236others(5): Show | 8 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-4433_175-4428d others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329826 | |||||
| chr13:97329826
|
AACACACA others(5): Show |
A | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0020others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.175-4439_175-4428d others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97329826 | |||||
| chr13:97329861
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0020others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.175-4415A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329861 | ||||||
| chr13:97329899
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175-4377C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329899 | ||||||
| chr13:97329980
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.175-4296T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97329980 | ||||||
| chr13:97330016
|
A | C | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.175-4260A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330016 | ||||||
| chr13:97330031
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0085others(2): Show | 5 | HG02071.hp2 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-4245A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330031 | ||||||
| chr13:97330044
|
A | G | 1 | a0001c0001t0008g0005 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175-4232A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330044 | ||||||
| chr13:97330283
|
G | T | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-3993G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330283 | ||||||
| chr13:97330366
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175-3910G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330366 | ||||||
| chr13:97330545
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-3731T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330545 | ||||||
| chr13:97330642
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-3634C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330642 | ||||||
| chr13:97330760
|
A | T | 1 | a0001c0001t0001g0031 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.175-3516A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330760 | ||||||
| chr13:97330773
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.175-3503G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330773 | ||||||
| chr13:97330853
|
T | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0199a0001c0001t0017g0177 | 3 | HG02486.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175-3423T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330853 | ||||||
| chr13:97330857
|
G | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.175-3419G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330857 | ||||||
| chr13:97330861
|
A | T | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG01192.hp1 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.175-3415A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330861 | ||||||
| chr13:97330867
|
C | T | 11 | a0001c0001t0003g0099a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-3409C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330867 | ||||||
| chr13:97330927
|
A | C | 23 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG01981.hp1 HG02572.hp2 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.175-3349A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330927 | ||||||
| chr13:97330929
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.175-3347T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330929 | ||||||
| chr13:97330951
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.175-3325T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97330951 | ||||||
| chr13:97331162
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.175-3114C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331162 | ||||||
| chr13:97331253
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.175-3023A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331253 | ||||||
| chr13:97331405
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.175-2871C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331405 | ||||||
| chr13:97331492
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.175-2784C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331492 | ||||||
| chr13:97331514
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0020others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.175-2762A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331514 | ||||||
| chr13:97331535
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.175-2741A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331535 | ||||||
| chr13:97331835
|
T | C | 23 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG01981.hp1 HG02572.hp2 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.175-2441T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97331835 | ||||||
| chr13:97332098
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-2178C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97332098 | ||||||
| chr13:97332208
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.175-2068T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97332208 | ||||||
| chr13:97332466
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-1810C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97332466 | ||||||
| chr13:97332940
|
C | T | 12 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-1336C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97332940 | ||||||
| chr13:97332941
|
G | A | 9 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-1335G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97332941 | ||||||
| chr13:97333312
|
G | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.175-964G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333312 | ||||||
| chr13:97333491
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.175-785T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333491 | ||||||
| chr13:97333514
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.175-762T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333514 | ||||||
| chr13:97333515
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0061others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-761A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333515 | ||||||
| chr13:97333606
|
C | G | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-670C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333606 | ||||||
| chr13:97333795
|
CCTT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(73): Show | 76 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.175-478_175-476del others(3): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97333795 | |||||
| chr13:97333943
|
AAAAG | A | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-322_175-319del others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97333943 | |||||
| chr13:97333954
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-322A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333954 | ||||||
| chr13:97333968
|
A | G | 6 | a0001c0001t0001g0098a0001c0001t0001g0116a0001c0001t0001g0130others(3): Show | 6 | HG01255.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-308A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333968 | ||||||
| chr13:97333968
|
AAGGG | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(41): Show | 44 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.175-290_175-287del others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97333968 | |||||
| chr13:97333972
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175-304G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333972 | ||||||
| chr13:97333990
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.175-286A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333990 | ||||||
| chr13:97333991
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.175-285A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97333991 | ||||||
| chr13:97333996
|
GAGAA | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.175-276_175-273del others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97333996 | |||||
| chr13:97334002
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.175-274G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97334002 | ||||||
| chr13:97334008
|
AAGAGAGA others(1): Show |
A | 5 | a0001c0001t0001g0016a0001c0001t0001g0098a0001c0001t0002g0157others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-265_175-258del others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334008 | |||||
| chr13:97334016
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.175-260G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97334016 | ||||||
| chr13:97334148
|
C | A | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.175-128C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97334148 | ||||||
| chr13:97334148
|
C | CCACA | 17 | a0001c0001t0001g0027a0001c0001t0001g0066a0001c0001t0001g0090others(14): Show | 17 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-103_175-100dup others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334148
|
C | CCACACA | 35 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(32): Show | 35 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.175-105_175-100dup others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334148
|
C | CCACACAC others(1): Show |
31 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(28): Show | 31 | HG00438.hp2 HG00558.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.175-107_175-100dup others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334148
|
C | CCACACAC others(3): Show |
15 | a0001c0001t0001g0024a0001c0001t0001g0074a0001c0001t0001g0102others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-109_175-100dup others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334148
|
C | CCACACAC others(5): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0093 | 2 | HG00099.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.175-111_175-100dup others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334148
|
C | CCACACAC others(11): Show |
1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175-117_175-100dup others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334148
|
CCA | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(68): Show | 71 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.175-101_175-100del others(2): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr13 | 97334148 | |||||
| chr13:97334152
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.175-124A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97334152 | ||||||
| chr13:97334194
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.175-82C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97334194 | ||||||
| chr13:97334231
|
G | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0199a0001c0001t0017g0177 | 3 | HG02486.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175-45G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 2/8 | chr13 | 97334231 | ||||||
| chr13:97334532
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.339+92G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97334532 | ||||||
| chr13:97335048
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.339+608T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97335048 | ||||||
| chr13:97335285
|
CT | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(40): Show | 43 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.339+859delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97335285 | |||||
| chr13:97335286
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0014g0234 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.339+846T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97335286 | ||||||
| chr13:97335331
|
T | C | 1 | a0001c0001t0011g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.339+891T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97335331 | ||||||
| chr13:97335546
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(31): Show | 34 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+1106C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97335546 | ||||||
| chr13:97336085
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+1645G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336085 | ||||||
| chr13:97336093
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(80): Show | 83 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.339+1653G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336093 | ||||||
| chr13:97336241
|
T | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(102): Show | 105 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.339+1801T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336241 | ||||||
| chr13:97336292
|
A | C | 3 | a0001c0001t0001g0102a0001c0001t0004g0185a0001c0001t0007g0206 | 3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.339+1852A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336292 | ||||||
| chr13:97336414
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.339+1974G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336414 | ||||||
| chr13:97336435
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(41): Show | 44 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.339+1995A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336435 | ||||||
| chr13:97336802
|
A | G | 22 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(19): Show | 22 | HG01981.hp1 HG02572.hp2 HG02630.hp1 others(19): Show |
intron_variant | MODIFIER | c.339+2362A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97336802 | ||||||
| chr13:97337131
|
A | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0143a0001c0001t0001g0217 | 3 | HG01175.hp2 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.339+2691A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337131 | ||||||
| chr13:97337188
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.339+2748G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337188 | ||||||
| chr13:97337305
|
A | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.339+2865A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337305 | ||||||
| chr13:97337438
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0014g0234 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.339+2998G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337438 | ||||||
| chr13:97337467
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.339+3027A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337467 | ||||||
| chr13:97337475
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.339+3035A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337475 | ||||||
| chr13:97337489
|
G | C | 33 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0106others(30): Show | 33 | HG00609.hp1 HG01123.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.339+3049G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337489 | ||||||
| chr13:97337497
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.339+3057C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337497 | ||||||
| chr13:97337632
|
C | T | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.339+3192C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337632 | ||||||
| chr13:97337657
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(99): Show | 102 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.339+3217A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337657 | ||||||
| chr13:97337780
|
T | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.339+3340T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337780 | ||||||
| chr13:97337801
|
T | C | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.339+3361T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97337801 | ||||||
| chr13:97338365
|
C | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.339+3925C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338365 | ||||||
| chr13:97338488
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.339+4048T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338488 | ||||||
| chr13:97338528
|
C | A | 1 | a0001c0001t0002g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.339+4088C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338528 | ||||||
| chr13:97338656
|
C | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.339+4216C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338656 | ||||||
| chr13:97338857
|
C | T | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340-4159C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338857 | ||||||
| chr13:97338925
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.340-4091C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338925 | ||||||
| chr13:97338955
|
C | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-4061C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97338955 | ||||||
| chr13:97339040
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.340-3976T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339040 | ||||||
| chr13:97339052
|
T | C | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340-3964T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339052 | ||||||
| chr13:97339102
|
G | GTGTGCTA others(1856): Show |
1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1865): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
1 | a0001c0001t0002g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1868): Show |
1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1877): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
1 | a0001c0001t0002g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | NA18997.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1871): Show |
1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1880): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1859): Show |
1 | a0001c0001t0002g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1868): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
1 | a0001c0001t0002g0111 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1864): Show |
16 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0106others(13): Show | 16 | HG01123.hp1 HG01255.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1873): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1862): Show |
2 | a0001c0001t0002g0017a0001c0001t0002g0103 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1871): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1876): Show |
1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1885): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1867): Show |
1 | a0001c0001t0001g0082 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1876): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1868): Show |
1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1877): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1870): Show |
30 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 30 | HG00140.hp1 HG00423.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1879): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1868): Show |
1 | a0001c0001t0001g0043 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1877): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1867): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0075 | 2 | HG01516.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1876): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0003g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0001g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1861): Show |
1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1870): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1865): Show |
1 | a0001c0001t0001g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1874): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1864): Show |
1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1873): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1868): Show |
1 | a0001c0001t0001g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1877): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
1 | a0001c0001t0001g0070 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1868): Show |
47 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(44): Show | 47 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1877): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0001g0035 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1871): Show |
1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1880): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1867): Show |
1 | a0001c0001t0001g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1876): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1871): Show |
1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1880): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1869): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0001g0214 | 3 | HG02647.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1878): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1869): Show |
1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1878): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1873): Show |
4 | a0001c0001t0001g0130a0001c0001t0001g0183a0001c0001t0002g0193others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1882): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1862): Show |
6 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(3): Show | 6 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1871): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1864): Show |
1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1873): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1857): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00140.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1866): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1864): Show |
1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1873): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1863): Show |
1 | a0001c0001t0011g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1872): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1864): Show |
21 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0118others(18): Show | 21 | HG01109.hp2 HG02083.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1873): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1862): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0003t0001g0243others(1): Show | 4 | HG00280.hp2 HG01361.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1871): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1860): Show |
1 | a0001c0001t0001g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1869): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1971): Show |
8 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1980): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1973): Show |
1 | a0001c0001t0001g0229 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1982): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1971): Show |
1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1980): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1871): Show |
1 | a0001c0001t0018g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1880): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1968): Show |
2 | a0001c0001t0001g0116a0001c0001t0004g0185 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1977): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1970): Show |
1 | a0001c0001t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1979): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1973): Show |
2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1982): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1975): Show |
7 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1984): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1973): Show |
1 | a0001c0001t0002g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1982): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1966): Show |
1 | a0001c0001t0001g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1975): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1975): Show |
1 | a0001c0001t0002g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1984): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1968): Show |
1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1977): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1970): Show |
1 | a0001c0001t0001g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1979): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1979): Show |
5 | a0001c0001t0002g0131a0001c0001t0002g0157a0001c0001t0002g0160others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1988): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1976): Show |
1 | a0001c0001t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1985): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1977): Show |
1 | a0001c0001t0002g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1986): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1971): Show |
6 | a0001c0001t0003g0101a0001c0001t0003g0220a0001c0001t0003g0222others(3): Show | 6 | HG01943.hp2 HG01981.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1980): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1973): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0141 | 2 | HG00558.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1982): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1973): Show |
27 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0020others(24): Show | 27 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1982): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1975): Show |
1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1984): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1977): Show |
1 | a0001c0001t0012g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1986): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1971): Show |
1 | a0001c0001t0001g0014 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1980): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1973): Show |
1 | a0001c0001t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1982): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1966): Show |
1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1975): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1971): Show |
1 | a0001c0001t0001g0108 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1980): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1864): Show |
1 | a0001c0001t0001g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1873): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1866): Show |
1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.340-3910_340-3909i others(1875): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339102
|
G | GTGTGCTA others(1969): Show |
2 | a0001c0001t0001g0204a0001c0001t0014g0234 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.340-3910_340-3909i others(1978): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339102 | |||||
| chr13:97339108
|
A | C | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3908A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339108 | ||||||
| chr13:97339114
|
G | C | 2 | a0001c0001t0001g0204a0001c0001t0014g0234 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.340-3902G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339114 | ||||||
| chr13:97339122
|
T | TCTGTAGT others(20): Show |
2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3894_340-3893i others(29): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339122 | ||||||
| chr13:97339123
|
G | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3893G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339123 | ||||||
| chr13:97339143
|
A | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3873A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339143 | ||||||
| chr13:97339148
|
A | AGTGAATG others(1697): Show |
2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3868_340-3867i others(1706): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339148 | ||||||
| chr13:97339151
|
G | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3865G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339151 | ||||||
| chr13:97339153
|
A | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3863A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339153 | ||||||
| chr13:97339158
|
G | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3858G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339158 | ||||||
| chr13:97339159
|
C | G | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3857C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339159 | ||||||
| chr13:97339165
|
A | G | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3851A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339165 | ||||||
| chr13:97339171
|
A | G | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3845A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339171 | ||||||
| chr13:97339174
|
A | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3842A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339174 | ||||||
| chr13:97339181
|
A | G | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3835A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339181 | ||||||
| chr13:97339187
|
T | C | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3829T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339187 | ||||||
| chr13:97339199
|
TTG | T | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3808_340-3807d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339199 | |||||
| chr13:97339202
|
T | C | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3814T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339202 | ||||||
| chr13:97339220
|
AGT | A | 24 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0128others(21): Show | 24 | HG01981.hp1 HG02559.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-3791_340-3790d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339220 | |||||
| chr13:97339236
|
G | A | 2 | a0001c0002t0001g0235a0001c0002t0001g0237 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3780G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339236 | ||||||
| chr13:97339366
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.340-3650G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339366 | ||||||
| chr13:97339456
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.340-3560C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339456 | ||||||
| chr13:97339506
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.340-3510A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339506 | ||||||
| chr13:97339554
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.340-3462T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339554 | ||||||
| chr13:97339710
|
T | G | 24 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0128others(21): Show | 24 | HG01981.hp1 HG02559.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-3306T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339710 | ||||||
| chr13:97339745
|
G | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0084 | 2 | HG02074.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.340-3271G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339745 | ||||||
| chr13:97339806
|
T | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(48): Show | 51 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.340-3210T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339806 | ||||||
| chr13:97339863
|
T | TTG | 20 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0052others(17): Show | 20 | HG00280.hp2 HG00609.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.340-3146_340-3145d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339863 | |||||
| chr13:97339863
|
TTG | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(19): Show | 22 | HG00558.hp2 HG00642.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-3146_340-3145d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339863 | |||||
| chr13:97339863
|
TTGTG | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0182a0001c0001t0001g0204others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-3148_340-3145d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339863 | |||||
| chr13:97339866
|
T | TG | 9 | a0001c0001t0001g0108a0001c0001t0001g0178a0001c0001t0004g0233others(6): Show | 9 | HG01109.hp1 HG01175.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.340-3149dupG | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339866 | |||||
| chr13:97339866
|
T | TGG | 3 | a0001c0002t0001g0235a0001c0002t0001g0237a0001c0002t0006g0212 | 3 | HG02818.hp1 NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.340-3149_340-3148i others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339866 | |||||
| chr13:97339866
|
T | TGGG | 3 | a0001c0001t0004g0185a0001c0002t0001g0008a0001c0002t0001g0236 | 3 | HG02630.hp1 HG03209.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.340-3149_340-3148i others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339866 | |||||
| chr13:97339866
|
T | TGGGGGGG others(3): Show |
1 | a0001c0001t0001g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.340-3149_340-3148i others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339866 | |||||
| chr13:97339867
|
GT | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0143a0001c0001t0001g0217others(3): Show | 6 | HG01256.hp2 HG01943.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-3148delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339867 | ||||||
| chr13:97339867
|
GTGT | G | 16 | a0001c0001t0001g0032a0001c0001t0001g0079a0001c0001t0001g0083others(13): Show | 16 | HG00099.hp1 HG00438.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.340-3148_340-3146d others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339867 | ||||||
| chr13:97339868
|
T | G | 26 | a0001c0001t0001g0016a0001c0001t0001g0108a0001c0001t0001g0116others(23): Show | 26 | HG01109.hp1 HG01175.hp2 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-3148T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339868 | ||||||
| chr13:97339870
|
T | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(52): Show | 55 | HG00558.hp2 HG00642.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.340-3146T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339870 | ||||||
| chr13:97339870
|
T | TGTG | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG01261.hp2 HG01993.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-3145_340-3144i others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97339870 | |||||
| chr13:97339871
|
G | GT | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.340-3145_340-3144i others(3): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339871 | ||||||
| chr13:97339872
|
G | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0147a0001c0001t0002g0161others(4): Show | 7 | HG00280.hp2 HG00609.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-3144G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339872 | ||||||
| chr13:97339873
|
G | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0033others(63): Show | 66 | HG00140.hp2 HG01109.hp2 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.340-3143G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339873 | ||||||
| chr13:97339874
|
C | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.340-3142C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339874 | ||||||
| chr13:97339882
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.340-3134G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339882 | ||||||
| chr13:97339883
|
C | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.340-3133C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339883 | ||||||
| chr13:97339976
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.340-3040C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97339976 | ||||||
| chr13:97340070
|
A | C | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340-2946A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340070 | ||||||
| chr13:97340211
|
C | G | 2 | a0001c0001t0001g0204a0001c0001t0014g0234 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.340-2805C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340211 | ||||||
| chr13:97340274
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.340-2742A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340274 | ||||||
| chr13:97340349
|
TA | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.340-2666delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340349 | ||||||
| chr13:97340581
|
C | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.340-2435C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340581 | ||||||
| chr13:97340624
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.340-2392G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340624 | ||||||
| chr13:97340685
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.340-2331T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340685 | ||||||
| chr13:97340869
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.340-2147A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340869 | ||||||
| chr13:97340905
|
G | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(40): Show | 43 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-2111G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97340905 | ||||||
| chr13:97341076
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.340-1940C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341076 | ||||||
| chr13:97341082
|
GTTTACGT others(10): Show |
G | 1 | a0001c0001t0002g0011 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.340-1932_340-1916d others(19): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr13 | 97341082 | |||||
| chr13:97341158
|
G | A | 24 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0106others(21): Show | 24 | HG00609.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-1858G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341158 | ||||||
| chr13:97341162
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.340-1854A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341162 | ||||||
| chr13:97341336
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.340-1680C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341336 | ||||||
| chr13:97341501
|
T | G | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340-1515T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341501 | ||||||
| chr13:97341568
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18950.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.340-1448G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341568 | ||||||
| chr13:97341657
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340-1359C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341657 | ||||||
| chr13:97341765
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.340-1251A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341765 | ||||||
| chr13:97341911
|
T | G | 2 | a0001c0001t0001g0204a0001c0001t0014g0234 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.340-1105T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341911 | ||||||
| chr13:97341973
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.340-1043C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97341973 | ||||||
| chr13:97342043
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.340-973A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342043 | ||||||
| chr13:97342048
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.340-968T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342048 | ||||||
| chr13:97342054
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.340-962G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342054 | ||||||
| chr13:97342088
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.340-928T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342088 | ||||||
| chr13:97342146
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340-870C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342146 | ||||||
| chr13:97342154
|
A | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.340-862A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342154 | ||||||
| chr13:97342349
|
A | G | 1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.340-667A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342349 | ||||||
| chr13:97342386
|
C | G | 2 | a0001c0002t0001g0236a0002c0004t0001g0232 | 2 | NA18948.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.340-630C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342386 | ||||||
| chr13:97342440
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(81): Show | 84 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.340-576C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342440 | ||||||
| chr13:97342728
|
A | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0103others(1): Show | 4 | HG00609.hp1 HG02735.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-288A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 3/8 | chr13 | 97342728 | ||||||
| chr13:97343220
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.540+4C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343220 | ||||||
| chr13:97343450
|
A | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540+234A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343450 | ||||||
| chr13:97343456
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.540+240C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343456 | ||||||
| chr13:97343554
|
AG | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(62): Show | 65 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.540+340delG | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 97343554 | |||||
| chr13:97343716
|
T | C | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.540+500T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343716 | ||||||
| chr13:97343748
|
C | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.540+532C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343748 | ||||||
| chr13:97343813
|
G | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.540+597G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343813 | ||||||
| chr13:97343837
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 76 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.540+621G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343837 | ||||||
| chr13:97343870
|
A | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0147a0001c0001t0001g0225others(1): Show | 4 | HG01167.hp1 HG01928.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+654A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343870 | ||||||
| chr13:97343970
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.540+754C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343970 | ||||||
| chr13:97343986
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.540+770A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343986 | ||||||
| chr13:97343990
|
G | C | 1 | a0001c0001t0005g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540+774G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97343990 | ||||||
| chr13:97344330
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.540+1114T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97344330 | ||||||
| chr13:97344610
|
T | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.540+1394T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97344610 | ||||||
| chr13:97344629
|
G | T | 27 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0128others(24): Show | 27 | HG01981.hp1 HG02486.hp2 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.540+1413G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97344629 | ||||||
| chr13:97344874
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+1658G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97344874 | ||||||
| chr13:97344935
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.540+1719G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97344935 | ||||||
| chr13:97344955
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.540+1739C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97344955 | ||||||
| chr13:97345045
|
T | TTA | 54 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.541-1758_541-1757i others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 97345045 | |||||
| chr13:97345284
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.541-1520A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345284 | ||||||
| chr13:97345368
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.541-1436T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345368 | ||||||
| chr13:97345462
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0181 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.541-1342T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345462 | ||||||
| chr13:97345549
|
T | G | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.541-1255T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345549 | ||||||
| chr13:97345739
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-1065G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345739 | ||||||
| chr13:97345817
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01123.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.541-987C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345817 | ||||||
| chr13:97345851
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541-953A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345851 | ||||||
| chr13:97345876
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.541-928C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345876 | ||||||
| chr13:97345878
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0060 | 2 | HG02523.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.541-926A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345878 | ||||||
| chr13:97345887
|
C | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0105 | 3 | NA18979.hp1 NA18997.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.541-917C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345887 | ||||||
| chr13:97345898
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-906T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345898 | ||||||
| chr13:97345918
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.541-886G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345918 | ||||||
| chr13:97345956
|
G | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-848G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97345956 | ||||||
| chr13:97346137
|
G | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-667G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346137 | ||||||
| chr13:97346187
|
G | T | 1 | a0001c0001t0002g0165 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.541-617G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346187 | ||||||
| chr13:97346218
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-586A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346218 | ||||||
| chr13:97346225
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-579G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346225 | ||||||
| chr13:97346227
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-577T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346227 | ||||||
| chr13:97346229
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-575G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346229 | ||||||
| chr13:97346231
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-573T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346231 | ||||||
| chr13:97346235
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-569C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346235 | ||||||
| chr13:97346243
|
AGATG | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(130): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.541-533_541-530del others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 97346243 | |||||
| chr13:97346243
|
AGATGGAT others(1): Show |
A | 25 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0001t0001g0183others(22): Show | 25 | HG02055.hp2 HG02258.hp1 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.541-537_541-530del others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 97346243 | |||||
| chr13:97346254
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-550T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346254 | ||||||
| chr13:97346255
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-549G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346255 | ||||||
| chr13:97346269
|
ATGGATAG others(9): Show |
A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.541-529_541-514del others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr13 | 97346269 | |||||
| chr13:97346287
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.541-517G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346287 | ||||||
| chr13:97346293
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-511A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346293 | ||||||
| chr13:97346299
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-505A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346299 | ||||||
| chr13:97346307
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-497A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346307 | ||||||
| chr13:97346315
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-489A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346315 | ||||||
| chr13:97346316
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-488T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346316 | ||||||
| chr13:97346317
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-487A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346317 | ||||||
| chr13:97346326
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-478G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346326 | ||||||
| chr13:97346327
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-477A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346327 | ||||||
| chr13:97346328
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-476T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346328 | ||||||
| chr13:97346330
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-474G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346330 | ||||||
| chr13:97346337
|
G | T | 2 | a0001c0001t0001g0180a0001c0001t0004g0211 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.541-467G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346337 | ||||||
| chr13:97346360
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.541-444A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346360 | ||||||
| chr13:97346383
|
G | T | 2 | a0001c0001t0001g0180a0001c0001t0004g0211 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.541-421G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346383 | ||||||
| chr13:97346529
|
G | GCTTTTTT others(9): Show |
1 | a0001c0001t0002g0011 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.541-275_541-274ins others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346529 | ||||||
| chr13:97346532
|
G | T | 1 | a0001c0001t0002g0011 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.541-272G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346532 | ||||||
| chr13:97346533
|
C | T | 1 | a0001c0001t0002g0011 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.541-271C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346533 | ||||||
| chr13:97346608
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.541-196C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346608 | ||||||
| chr13:97346670
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0004g0211 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.541-134A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346670 | ||||||
| chr13:97346743
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.541-61G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346743 | ||||||
| chr13:97346754
|
G | A | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-50G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 4/8 | chr13 | 97346754 | ||||||
| chr13:97347097
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.804+30C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347097 | ||||||
| chr13:97347184
|
G | A | 5 | a0001c0001t0001g0086a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+117G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347184 | ||||||
| chr13:97347341
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+274G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347341 | ||||||
| chr13:97347413
|
G | A | 20 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0183others(17): Show | 20 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.804+346G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347413 | ||||||
| chr13:97347481
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.804+414A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347481 | ||||||
| chr13:97347516
|
A | T | 1 | a0001c0001t0002g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+449A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347516 | ||||||
| chr13:97347520
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.804+453A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347520 | ||||||
| chr13:97347750
|
C | A | 2 | a0001c0003t0001g0243a0001c0003t0001g0244 | 2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.804+683C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97347750 | ||||||
| chr13:97348074
|
A | ATT | 19 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0074others(16): Show | 19 | HG01070.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.804+1028_804+1029d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348074
|
A | ATTT | 55 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(52): Show | 55 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.804+1027_804+1029d others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348074
|
A | ATTTT | 6 | a0001c0001t0001g0132a0001c0001t0001g0149a0001c0001t0004g0172others(3): Show | 6 | HG02486.hp2 HG02523.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+1026_804+1029d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348074
|
AT | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0027others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.804+1029delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348074
|
ATT | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0106others(5): Show | 8 | HG01192.hp2 HG01975.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.804+1028_804+1029d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348074
|
ATTT | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0050others(61): Show | 64 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.804+1027_804+1029d others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348074
|
ATTTT | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0102a0001c0001t0001g0167others(3): Show | 6 | HG01255.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1026_804+1029d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97348074 | |||||
| chr13:97348124
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(58): Show | 61 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.804+1057G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348124 | ||||||
| chr13:97348257
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.804+1190A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348257 | ||||||
| chr13:97348322
|
A | T | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.804+1255A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348322 | ||||||
| chr13:97348387
|
G | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0183a0001c0001t0002g0193 | 3 | HG02717.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.804+1320G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348387 | ||||||
| chr13:97348591
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.804+1524C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348591 | ||||||
| chr13:97348634
|
C | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.804+1567C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348634 | ||||||
| chr13:97348724
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.804+1657A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348724 | ||||||
| chr13:97348757
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.804+1690C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348757 | ||||||
| chr13:97348993
|
T | C | 1 | a0001c0001t0007g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.804+1926T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348993 | ||||||
| chr13:97348999
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(58): Show | 61 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.804+1932C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97348999 | ||||||
| chr13:97349186
|
A | AT | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.804+2120dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97349186 | |||||
| chr13:97349208
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0007g0206 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.804+2141A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97349208 | ||||||
| chr13:97349227
|
CCTT | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0153others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+2161_804+2163d others(5): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97349227 | ||||||
| chr13:97349371
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+2304C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97349371 | ||||||
| chr13:97349574
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.804+2507T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97349574 | ||||||
| chr13:97349631
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0133 | 3 | NA18950.hp1 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.804+2564G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97349631 | ||||||
| chr13:97349684
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.804+2617T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97349684 | ||||||
| chr13:97350016
|
A | G | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+2949A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350016 | ||||||
| chr13:97350254
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.804+3187G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350254 | ||||||
| chr13:97350303
|
C | G | 7 | a0001c0001t0001g0124a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+3236C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350303 | ||||||
| chr13:97350369
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(79): Show | 82 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+3302G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350369 | ||||||
| chr13:97350469
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+3402C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350469 | ||||||
| chr13:97350608
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804+3541C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350608 | ||||||
| chr13:97350614
|
T | G | 1 | a0001c0001t0004g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+3547T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350614 | ||||||
| chr13:97350626
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(4): Show | 7 | HG02055.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+3559A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350626 | ||||||
| chr13:97350680
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(57): Show | 60 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.804+3613G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350680 | ||||||
| chr13:97350777
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.804+3710C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350777 | ||||||
| chr13:97350971
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.804+3904A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97350971 | ||||||
| chr13:97351022
|
C | T | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.804+3955C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97351022 | ||||||
| chr13:97351493
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0228 | 3 | HG02559.hp1 HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.804+4426G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97351493 | ||||||
| chr13:97351670
|
T | C | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.804+4603T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97351670 | ||||||
| chr13:97351682
|
G | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.804+4615G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97351682 | ||||||
| chr13:97351719
|
G | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.804+4652G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97351719 | ||||||
| chr13:97351815
|
G | C | 1 | a0001c0001t0003g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.804+4748G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97351815 | ||||||
| chr13:97352014
|
A | ACT | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.805-4781_805-4780d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352014 | |||||
| chr13:97352035
|
T | TATAA | 12 | a0001c0001t0001g0014a0001c0001t0001g0132a0001c0001t0001g0162others(9): Show | 12 | HG00438.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.805-4736_805-4733d others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352035 | |||||
| chr13:97352035
|
T | TATAAATA others(1): Show |
41 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(38): Show | 41 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.805-4740_805-4733d others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352035 | |||||
| chr13:97352035
|
T | TATAAATA others(5): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0125others(1): Show | 4 | HG00099.hp1 HG01256.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-4744_805-4733d others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352035 | |||||
| chr13:97352035
|
T | TATAAATA others(9): Show |
4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | HG01109.hp1 HG01981.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-4748_805-4733d others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352035 | |||||
| chr13:97352035
|
TATAAATA others(1): Show |
T | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.805-4740_805-4733d others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352035 | |||||
| chr13:97352131
|
A | G | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.805-4665A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97352131 | ||||||
| chr13:97352142
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.805-4654C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97352142 | ||||||
| chr13:97352200
|
C | CA | 134 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.805-4595dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97352200 | |||||
| chr13:97352314
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.805-4482T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97352314 | ||||||
| chr13:97352355
|
C | T | 4 | a0001c0002t0001g0235a0001c0002t0001g0236a0001c0002t0001g0237others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-4441C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97352355 | ||||||
| chr13:97352898
|
T | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.805-3898T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97352898 | ||||||
| chr13:97353054
|
C | T | 3 | a0001c0001t0004g0210a0001c0001t0004g0211a0001c0001t0017g0177 | 3 | HG01192.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.805-3742C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353054 | ||||||
| chr13:97353265
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.805-3531A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353265 | ||||||
| chr13:97353380
|
C | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(51): Show | 54 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.805-3416C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353380 | ||||||
| chr13:97353493
|
C | T | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.805-3303C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353493 | ||||||
| chr13:97353611
|
T | G | 1 | a0001c0001t0016g0245 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.805-3185T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353611 | ||||||
| chr13:97353626
|
T | G | 1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.805-3170T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353626 | ||||||
| chr13:97353762
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0149 | 2 | NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.805-3034A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353762 | ||||||
| chr13:97353863
|
TG | T | 21 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0002g0010others(18): Show | 21 | HG00609.hp1 HG02027.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-2932delG | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97353863 | ||||||
| chr13:97354039
|
C | CA | 124 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.805-2740dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97354039 | |||||
| chr13:97354039
|
C | CAA | 8 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0180others(5): Show | 8 | HG02027.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.805-2741_805-2740d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97354039 | |||||
| chr13:97354049
|
A | AG | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.805-2747_805-2746i others(3): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354049 | ||||||
| chr13:97354134
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.805-2662C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354134 | ||||||
| chr13:97354162
|
AT | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.805-2631delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97354162 | |||||
| chr13:97354247
|
C | T | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805-2549C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354247 | ||||||
| chr13:97354412
|
A | G | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.805-2384A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354412 | ||||||
| chr13:97354450
|
C | G | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.805-2346C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354450 | ||||||
| chr13:97354537
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0228a0001c0001t0004g0185 | 3 | HG02559.hp2 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.805-2259G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354537 | ||||||
| chr13:97354761
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.805-2035A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97354761 | ||||||
| chr13:97355070
|
G | A | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.805-1726G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97355070 | ||||||
| chr13:97355456
|
G | A | 1 | a0001c0001t0004g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.805-1340G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97355456 | ||||||
| chr13:97355853
|
G | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(37): Show | 40 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.805-943G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97355853 | ||||||
| chr13:97356130
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.805-666C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97356130 | ||||||
| chr13:97356213
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.805-583G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | chr13 | 97356213 | ||||||
| chr13:97356237
|
AT | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(36): Show | 39 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.805-552delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97356237 | |||||
| chr13:97356422
|
AT | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.805-365delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr13 | 97356422 | |||||
| chr13:97357059
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.858+210G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 6/8 | chr13 | 97357059 | ||||||
| chr13:97357067
|
A | G | 21 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0002g0010others(18): Show | 21 | HG00609.hp1 HG02027.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.858+218A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 6/8 | chr13 | 97357067 | ||||||
| chr13:97358152
|
C | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(68): Show | 71 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1012+517C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97358152 | ||||||
| chr13:97358434
|
T | TAC | 9 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+803_1012+804d others(4): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97358434 | |||||
| chr13:97358505
|
A | C | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1012+870A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97358505 | ||||||
| chr13:97358559
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1012+924C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97358559 | ||||||
| chr13:97358575
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(4): Show | 7 | HG02055.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012+940T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97358575 | ||||||
| chr13:97358576
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1012+941C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97358576 | ||||||
| chr13:97358653
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1012+1018A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97358653 | ||||||
| chr13:97359033
|
TCA | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1012+1401_1012+140 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97359033 | |||||
| chr13:97359239
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1012+1604T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359239 | ||||||
| chr13:97359272
|
T | TA | 13 | a0001c0001t0001g0056a0001c0001t0001g0125a0001c0001t0001g0155others(10): Show | 13 | HG01123.hp2 HG01361.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1012+1650dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97359272 | |||||
| chr13:97359285
|
AT | A | 4 | a0001c0002t0001g0235a0001c0002t0001g0236a0001c0002t0001g0237others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+1652delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97359285 | |||||
| chr13:97359286
|
T | A | 6 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0006g0126others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1012+1651T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359286 | ||||||
| chr13:97359381
|
T | A | 1 | a0001c0001t0003g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1012+1746T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359381 | ||||||
| chr13:97359425
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1012+1790A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359425 | ||||||
| chr13:97359586
|
GATGAAAT others(7): Show |
G | 3 | a0001c0001t0001g0116a0001c0001t0001g0228a0001c0001t0004g0185 | 3 | HG02559.hp2 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1012+1957_1012+197 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97359586 | |||||
| chr13:97359612
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1012+1977A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359612 | ||||||
| chr13:97359647
|
C | T | 6 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 6 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1012+2012C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359647 | ||||||
| chr13:97359704
|
G | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1012+2069G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359704 | ||||||
| chr13:97359739
|
A | C | 9 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0131others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+2104A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359739 | ||||||
| chr13:97359826
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1012+2191G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97359826 | ||||||
| chr13:97360076
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+2441T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97360076 | ||||||
| chr13:97360103
|
A | C | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1012+2468A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97360103 | ||||||
| chr13:97360188
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1012+2553A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97360188 | ||||||
| chr13:97360354
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1012+2719T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97360354 | ||||||
| chr13:97360645
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1012+3010T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97360645 | ||||||
| chr13:97360839
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1012+3204T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97360839 | ||||||
| chr13:97361028
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1012+3393A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361028 | ||||||
| chr13:97361209
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1012+3574C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361209 | ||||||
| chr13:97361374
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0007g0206 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1012+3739T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361374 | ||||||
| chr13:97361410
|
G | A | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1013-3726G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361410 | ||||||
| chr13:97361498
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1013-3638A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361498 | ||||||
| chr13:97361503
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0109a0001c0001t0001g0115others(1): Show | 4 | HG02559.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-3633A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361503 | ||||||
| chr13:97361591
|
G | C | 2 | a0001c0001t0001g0191a0001c0001t0007g0206 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1013-3545G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361591 | ||||||
| chr13:97361608
|
C | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1013-3528C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361608 | ||||||
| chr13:97361635
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1013-3501A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361635 | ||||||
| chr13:97361758
|
A | AT | 10 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0196others(7): Show | 10 | HG01884.hp1 HG02027.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-3349dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361758
|
AT | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0020others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1013-3349delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361758
|
ATT | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1013-3350_1013-334 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361758
|
ATTT | A | 13 | a0001c0001t0001g0074a0001c0001t0001g0151a0001c0001t0001g0213others(10): Show | 13 | HG01070.hp2 HG01109.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-3351_1013-334 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361758
|
ATTTT | A | 14 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0064others(11): Show | 14 | HG00423.hp1 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1013-3352_1013-334 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361758
|
ATTTTT | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(32): Show | 35 | HG00140.hp1 HG00423.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.1013-3353_1013-334 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361758
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0002t0006g0197 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1013-3360_1013-334 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97361758 | |||||
| chr13:97361898
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1013-3238T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361898 | ||||||
| chr13:97361924
|
C | T | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-3212C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361924 | ||||||
| chr13:97361925
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1013-3211A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361925 | ||||||
| chr13:97361945
|
G | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1013-3191G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361945 | ||||||
| chr13:97361954
|
G | T | 3 | a0001c0001t0005g0113a0001c0001t0005g0252a0001c0001t0005g0253 | 3 | HG01975.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1013-3182G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361954 | ||||||
| chr13:97361987
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1013-3149G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97361987 | ||||||
| chr13:97362144
|
AT | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(39): Show | 42 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1013-2983delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97362144 | |||||
| chr13:97362433
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(37): Show | 40 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1013-2703A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97362433 | ||||||
| chr13:97362487
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0083others(2): Show | 5 | HG02027.hp1 HG02056.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-2649G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97362487 | ||||||
| chr13:97362627
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1013-2509C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97362627 | ||||||
| chr13:97362691
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1013-2445C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97362691 | ||||||
| chr13:97362973
|
G | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-2163G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97362973 | ||||||
| chr13:97362985
|
C | A | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1013-2151C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97362985 | ||||||
| chr13:97363055
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1013-2081C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97363055 | ||||||
| chr13:97363418
|
C | CTG | 30 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0036others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1013-1673_1013-167 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
C | CTGTG | 44 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(41): Show | 44 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1013-1675_1013-167 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
C | CTGTGTG | 22 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0066others(19): Show | 22 | HG00423.hp2 HG00609.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1013-1677_1013-167 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
C | CTGTGTGT others(1): Show |
18 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0050others(15): Show | 18 | HG01167.hp1 HG01261.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1013-1679_1013-167 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0001g0081a0001c0001t0001g0176a0001c0001t0003g0163others(1): Show | 4 | HG01109.hp2 HG03486.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1681_1013-167 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0225 | 2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1013-1683_1013-167 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTG | C | 9 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0059others(6): Show | 9 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1013-1673_1013-167 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTGTG | C | 5 | a0001c0001t0002g0193a0001c0001t0003g0019a0001c0001t0004g0184others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1675_1013-167 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTGTGTG | C | 4 | a0001c0001t0001g0195a0001c0001t0004g0210a0001c0001t0004g0211others(1): Show | 4 | HG01192.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1677_1013-167 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTGTGTGT others(1): Show |
C | 4 | a0001c0001t0002g0062a0001c0001t0002g0157a0001c0001t0004g0112others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1679_1013-167 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTGTGTGT others(5): Show |
C | 12 | a0001c0001t0001g0069a0001c0001t0001g0087a0001c0001t0002g0006others(9): Show | 12 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1013-1683_1013-167 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTGTGTGT others(7): Show |
C | 64 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1013-1685_1013-167 others(18): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363418
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0011g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1013-1693_1013-167 others(26): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr13 | 97363418 | |||||
| chr13:97363536
|
A | C | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1013-1600A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97363536 | ||||||
| chr13:97363842
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1013-1294C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97363842 | ||||||
| chr13:97364069
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1013-1067G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364069 | ||||||
| chr13:97364129
|
T | C | 6 | a0001c0001t0003g0101a0001c0001t0003g0220a0001c0001t0003g0222others(3): Show | 6 | HG01943.hp2 HG01981.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-1007T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364129 | ||||||
| chr13:97364162
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1013-974G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364162 | ||||||
| chr13:97364180
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1013-956A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364180 | ||||||
| chr13:97364447
|
G | A | 1 | a0001c0001t0008g0005 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1013-689G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364447 | ||||||
| chr13:97364656
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1013-480G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364656 | ||||||
| chr13:97364957
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1013-179A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 7/8 | chr13 | 97364957 | ||||||
| chr13:97365197
|
C | A | 11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+26C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365197 | ||||||
| chr13:97365211
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1048+40A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365211 | ||||||
| chr13:97365386
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1048+215A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365386 | ||||||
| chr13:97365464
|
C | T | 11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+293C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365464 | ||||||
| chr13:97365492
|
G | A | 11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+321G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365492 | ||||||
| chr13:97365630
|
G | A | 1 | a0001c0002t0006g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1048+459G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365630 | ||||||
| chr13:97365778
|
C | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+607C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365778 | ||||||
| chr13:97365898
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1048+727G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365898 | ||||||
| chr13:97365967
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1048+796T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97365967 | ||||||
| chr13:97365969
|
G | GA | 7 | a0001c0001t0004g0112a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048+808dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97365969 | |||||
| chr13:97365969
|
GA | G | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+808delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97365969 | |||||
| chr13:97366079
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048+908A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97366079 | ||||||
| chr13:97366089
|
T | C | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+918T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97366089 | ||||||
| chr13:97366614
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1048+1443A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97366614 | ||||||
| chr13:97366782
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(50): Show | 53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1048+1611C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97366782 | ||||||
| chr13:97367317
|
C | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0249 | 3 | HG03579.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1048+2146C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97367317 | ||||||
| chr13:97367444
|
T | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048+2273T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97367444 | ||||||
| chr13:97367538
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1048+2367C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97367538 | ||||||
| chr13:97367828
|
G | A | 8 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+2657G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97367828 | ||||||
| chr13:97367918
|
G | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1048+2747G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97367918 | ||||||
| chr13:97367921
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1048+2750T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97367921 | ||||||
| chr13:97368175
|
C | T | 1 | a0001c0002t0006g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1048+3004C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368175 | ||||||
| chr13:97368333
|
A | G | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048+3162A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368333 | ||||||
| chr13:97368412
|
T | TTAAAA | 12 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0001t0001g0119others(9): Show | 12 | HG01192.hp2 HG01496.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048+3264_1048+326 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368412
|
T | TTAAAATA others(3): Show |
36 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(33): Show | 36 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1048+3259_1048+326 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368412
|
T | TTAAAATA others(8): Show |
17 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0130others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1048+3254_1048+326 others(19): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368412
|
T | TTAAAATA others(13): Show |
11 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(8): Show | 11 | HG01109.hp1 HG01981.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1048+3249_1048+326 others(24): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368412
|
T | TTAAAATA others(18): Show |
39 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(36): Show | 39 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1048+3244_1048+326 others(29): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368412
|
T | TTAAAATA others(23): Show |
8 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0217others(5): Show | 8 | HG00423.hp1 HG01952.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048+3268_1048+326 others(34): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368412
|
T | TTAAAATA others(28): Show |
5 | a0001c0001t0001g0007a0001c0002t0006g0126a0001c0002t0006g0197others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+3268_1048+326 others(39): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368412 | |||||
| chr13:97368475
|
G | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG00423.hp2 HG01943.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+3304G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368475 | ||||||
| chr13:97368483
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048+3312C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368483 | ||||||
| chr13:97368578
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0147 | 3 | HG01943.hp1 HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1048+3407A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368578 | ||||||
| chr13:97368591
|
AATAAATA others(14): Show |
A | 38 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1048+3424_1048+344 others(25): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368591 | |||||
| chr13:97368593
|
TAAATATT others(10): Show |
T | 3 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0181 | 3 | HG02055.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1048+3423_1048+343 others(21): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368593 | ||||||
| chr13:97368612
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0181 | 3 | HG02055.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1048+3441C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368612 | ||||||
| chr13:97368658
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01981.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1048+3487A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368658 | ||||||
| chr13:97368700
|
T | TTG | 17 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG01192.hp1 HG01192.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1048+3555_1048+355 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
T | TTGTG | 6 | a0001c0001t0001g0030a0001c0001t0001g0100a0001c0001t0001g0116others(3): Show | 6 | HG00423.hp2 HG00558.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+3553_1048+355 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
T | TTGTGTG | 31 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1048+3551_1048+355 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
T | TTGTGTGT others(1): Show |
61 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0020others(58): Show | 61 | HG00438.hp2 HG00642.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.1048+3549_1048+355 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
T | TTGTGTGT others(3): Show |
7 | a0001c0001t0002g0157a0001c0001t0002g0193a0001c0001t0014g0234others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048+3547_1048+355 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+3545_1048+355 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
TTG | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(4): Show | 7 | HG02055.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048+3555_1048+355 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
TTGTG | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0191a0001c0001t0007g0206 | 3 | HG02071.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1048+3553_1048+355 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368700
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1048+3545_1048+355 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368700 | |||||
| chr13:97368824
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0183a0001c0001t0002g0193 | 3 | HG02717.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1048+3653A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368824 | ||||||
| chr13:97368855
|
T | G | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048+3684T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97368855 | ||||||
| chr13:97368997
|
AATG | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(34): Show | 37 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1048+3831_1048+383 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97368997 | |||||
| chr13:97369052
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1048+3881A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369052 | ||||||
| chr13:97369099
|
G | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+3928G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369099 | ||||||
| chr13:97369180
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1048+4009A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369180 | ||||||
| chr13:97369595
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1048+4424C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369595 | ||||||
| chr13:97369645
|
G | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1048+4474G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369645 | ||||||
| chr13:97369753
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1048+4582A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369753 | ||||||
| chr13:97369770
|
A | G | 1 | a0001c0001t0003g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1048+4599A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369770 | ||||||
| chr13:97369947
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1048+4776T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97369947 | ||||||
| chr13:97370090
|
A | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1048+4919A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97370090 | ||||||
| chr13:97370223
|
TG | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048+5054delG | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97370223 | |||||
| chr13:97370395
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+5224C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97370395 | ||||||
| chr13:97370467
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1048+5296C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97370467 | ||||||
| chr13:97370645
|
G | A | 11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+5474G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97370645 | ||||||
| chr13:97370667
|
C | CA | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1048+5508dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97370667 | |||||
| chr13:97370676
|
A | G | 13 | a0001c0001t0001g0130a0001c0001t0001g0183a0001c0001t0017g0177others(10): Show | 13 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1048+5505A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97370676 | ||||||
| chr13:97370686
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1048+5515A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97370686 | ||||||
| chr13:97371395
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1048+6224C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97371395 | ||||||
| chr13:97371797
|
A | T | 8 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+6626A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97371797 | ||||||
| chr13:97372026
|
G | A | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+6855G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97372026 | ||||||
| chr13:97372099
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1048+6928C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97372099 | ||||||
| chr13:97372340
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1048+7169T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97372340 | ||||||
| chr13:97372428
|
G | A | 1 | a0001c0002t0006g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1048+7257G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97372428 | ||||||
| chr13:97372665
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1048+7494G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97372665 | ||||||
| chr13:97372679
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1048+7508A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97372679 | ||||||
| chr13:97373099
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0007g0206 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1048+7928C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97373099 | ||||||
| chr13:97373192
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0002g0145 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1048+8021G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97373192 | ||||||
| chr13:97373319
|
G | A | 1 | a0001c0001t0003g0099 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1048+8148G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97373319 | ||||||
| chr13:97373351
|
T | C | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048+8180T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97373351 | ||||||
| chr13:97373465
|
T | TA | 5 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0049others(2): Show | 5 | HG02071.hp1 NA18946.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+8307dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373465 | |||||
| chr13:97373465
|
T | TAA | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+8306_1048+830 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373465 | |||||
| chr13:97373465
|
TA | T | 6 | a0001c0001t0003g0101a0001c0001t0003g0220a0001c0001t0003g0222others(3): Show | 6 | HG01943.hp2 HG01981.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+8307delA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373465 | |||||
| chr13:97373471
|
A | T | 21 | a0001c0001t0001g0104a0001c0001t0002g0010a0001c0001t0002g0011others(18): Show | 21 | HG00609.hp1 HG01123.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.1048+8300A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97373471 | ||||||
| chr13:97373605
|
A | AAT | 21 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0053others(18): Show | 21 | HG01192.hp1 HG01496.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1048+8453_1048+845 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373605 | |||||
| chr13:97373605
|
A | AATAT | 37 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1048+8451_1048+845 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373605 | |||||
| chr13:97373605
|
A | AATATAT | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0020others(38): Show | 41 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1048+8449_1048+845 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373605 | |||||
| chr13:97373605
|
A | AATATATA others(1): Show |
18 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0032others(15): Show | 18 | HG01257.hp1 HG01261.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1048+8447_1048+845 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373605 | |||||
| chr13:97373605
|
A | AATATATA others(3): Show |
6 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0115others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+8445_1048+845 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373605 | |||||
| chr13:97373652
|
CTCTG | C | 11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+8485_1048+848 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97373652 | |||||
| chr13:97373658
|
C | T | 8 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+8487C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97373658 | ||||||
| chr13:97374063
|
A | AT | 16 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0077others(13): Show | 16 | HG00438.hp1 HG00735.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1048+8921dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT | 5 | a0001c0001t0001g0204a0001c0001t0002g0006a0001c0001t0002g0160others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+8915_1048+892 others(11): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(1): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0115others(8): Show | 11 | HG01261.hp1 HG01884.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+8914_1048+892 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(2): Show |
15 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0079others(12): Show | 15 | HG00099.hp1 HG01243.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1048+8913_1048+892 others(13): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(3): Show |
12 | a0001c0001t0001g0016a0001c0001t0001g0098a0001c0001t0001g0108others(9): Show | 12 | HG00438.hp2 HG01175.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048+8912_1048+892 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(4): Show |
11 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0032others(8): Show | 11 | HG00423.hp1 HG01496.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+8911_1048+892 others(15): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(5): Show |
5 | a0001c0001t0001g0024a0001c0001t0001g0067a0001c0001t0001g0093others(2): Show | 5 | HG01070.hp2 HG01358.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+8910_1048+892 others(16): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0148 | 2 | HG00642.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1048+8909_1048+892 others(17): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1048+8906_1048+892 others(20): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+8898_1048+892 others(28): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
AT | A | 25 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(22): Show | 25 | HG00280.hp1 HG01167.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1048+8921delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
ATT | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0119a0001c0001t0001g0124others(11): Show | 14 | HG00140.hp2 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1048+8920_1048+892 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
ATTT | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0128a0001c0001t0001g0129others(8): Show | 11 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+8919_1048+892 others(7): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
ATTTTT | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0030others(28): Show | 31 | HG00280.hp2 HG00423.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1048+8917_1048+892 others(9): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
ATTTTTT | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0095others(2): Show | 5 | HG00140.hp1 HG01975.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+8916_1048+892 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
ATTTTTTT others(1): Show |
A | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG02055.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+8914_1048+892 others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374063
|
ATTTTTTT others(3): Show |
A | 8 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(5): Show | 8 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+8912_1048+892 others(14): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97374063 | |||||
| chr13:97374170
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1048+8999C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97374170 | ||||||
| chr13:97374227
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0085others(2): Show | 5 | HG02071.hp2 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+9056C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97374227 | ||||||
| chr13:97374366
|
C | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(59): Show | 62 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1048+9195C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97374366 | ||||||
| chr13:97374686
|
C | G | 1 | a0001c0001t0003g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1048+9515C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97374686 | ||||||
| chr13:97374811
|
T | G | 11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+9640T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97374811 | ||||||
| chr13:97374975
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048+9804G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97374975 | ||||||
| chr13:97375045
|
G | A | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+9874G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97375045 | ||||||
| chr13:97375075
|
CT | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048+9908delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97375075 | |||||
| chr13:97375386
|
C | T | 1 | a0001c0001t0015g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048+10215C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97375386 | ||||||
| chr13:97375620
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1048+10449C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97375620 | ||||||
| chr13:97375764
|
T | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 37 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1048+10593T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97375764 | ||||||
| chr13:97375821
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(78): Show | 81 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1048+10650A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97375821 | ||||||
| chr13:97375918
|
G | A | 1 | a0001c0001t0017g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048+10747G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97375918 | ||||||
| chr13:97376010
|
A | AACAGG | 2 | a0001c0001t0001g0191a0001c0001t0007g0206 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1048+10850_1048+10 others(11): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97376010 | |||||
| chr13:97376325
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1048+11154T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376325 | ||||||
| chr13:97376514
|
C | A | 1 | a0001c0002t0001g0235 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1048+11343C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376514 | ||||||
| chr13:97376530
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(39): Show | 42 | HG00140.hp1 HG00423.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1048+11359C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376530 | ||||||
| chr13:97376531
|
G | A | 1 | a0001c0002t0001g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1048+11360G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376531 | ||||||
| chr13:97376651
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1048+11480A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376651 | ||||||
| chr13:97376882
|
A | G | 2 | a0001c0002t0001g0008a0001c0002t0001g0156 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1048+11711A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376882 | ||||||
| chr13:97376997
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+11826T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97376997 | ||||||
| chr13:97377150
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00140.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1048+11979G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97377150 | ||||||
| chr13:97377298
|
G | A | 7 | a0001c0001t0001g0124a0001c0001t0005g0113a0001c0001t0005g0238others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+12127G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97377298 | ||||||
| chr13:97377328
|
C | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0156a0001c0002t0001g0235others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+12157C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97377328 | ||||||
| chr13:97377456
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0203 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1048+12285A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97377456 | ||||||
| chr13:97377688
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1048+12517T>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97377688 | ||||||
| chr13:97377944
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1048+12773G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97377944 | ||||||
| chr13:97378122
|
A | ATGAAAAT others(44): Show |
11 | a0001c0001t0017g0177a0001c0002t0001g0008a0001c0002t0001g0156others(8): Show | 11 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+12968_1048+13 others(57): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97378122 | |||||
| chr13:97378194
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1048+13023T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97378194 | ||||||
| chr13:97378198
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1048+13027G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97378198 | ||||||
| chr13:97378704
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1049-12618C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97378704 | ||||||
| chr13:97378726
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1049-12596T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97378726 | ||||||
| chr13:97378769
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1049-12553T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97378769 | ||||||
| chr13:97379072
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1049-12250G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379072 | ||||||
| chr13:97379172
|
G | A | 1 | a0001c0001t0013g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1049-12150G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379172 | ||||||
| chr13:97379223
|
T | A | 1 | a0001c0001t0004g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1049-12099T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379223 | ||||||
| chr13:97379423
|
A | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(15): Show | 18 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1049-11899A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379423 | ||||||
| chr13:97379675
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(9): Show | 12 | HG02055.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1049-11647G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379675 | ||||||
| chr13:97379699
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1049-11623G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379699 | ||||||
| chr13:97379746
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1049-11576G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97379746 | ||||||
| chr13:97380211
|
G | A | 1 | a0001c0001t0004g0210 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1049-11111G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380211 | ||||||
| chr13:97380226
|
GCTCATGC others(9): Show |
G | 3 | a0001c0001t0004g0112a0001c0001t0004g0210a0001c0001t0004g0233 | 3 | HG01192.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1049-11094_1049-11 others(22): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97380226 | |||||
| chr13:97380269
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1049-11053G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380269 | ||||||
| chr13:97380393
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0142 | 2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1049-10929C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380393 | ||||||
| chr13:97380409
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1049-10913G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380409 | ||||||
| chr13:97380493
|
AAACC | A | 52 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(49): Show | 52 | HG00438.hp1 HG00558.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1049-10826_1049-10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97380493 | |||||
| chr13:97380496
|
C | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1049-10826C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380496 | ||||||
| chr13:97380509
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1049-10813C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380509 | ||||||
| chr13:97380543
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1049-10779A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380543 | ||||||
| chr13:97380556
|
G | C | 3 | a0001c0001t0005g0113a0001c0001t0005g0252a0001c0001t0005g0253 | 3 | HG01975.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1049-10766G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97380556 | ||||||
| chr13:97381062
|
CCTCT | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0181 | 3 | HG02055.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1049-10253_1049-10 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97381062 | |||||
| chr13:97381073
|
ATCTCTCC others(19): Show |
A | 2 | a0001c0001t0004g0112a0001c0001t0004g0233 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1049-10235_1049-10 others(32): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97381073 | |||||
| chr13:97381115
|
G | GAC | 48 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0020others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1049-10186_1049-10 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97381115 | |||||
| chr13:97381438
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1049-9884A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97381438 | ||||||
| chr13:97382238
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1049-9084C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382238 | ||||||
| chr13:97382446
|
C | T | 2 | a0001c0003t0001g0243a0001c0003t0001g0244 | 2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1049-8876C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382446 | ||||||
| chr13:97382508
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1049-8814G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382508 | ||||||
| chr13:97382510
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1049-8812G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382510 | ||||||
| chr13:97382598
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00140.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1049-8724C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382598 | ||||||
| chr13:97382602
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1049-8720G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382602 | ||||||
| chr13:97382657
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0142a0001c0002t0006g0126others(3): Show | 6 | HG00099.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-8665T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382657 | ||||||
| chr13:97382669
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1049-8653A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382669 | ||||||
| chr13:97382672
|
A | AT | 8 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0094others(5): Show | 8 | HG00140.hp1 HG00423.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1049-8631dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97382672 | |||||
| chr13:97382672
|
AT | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0044others(38): Show | 41 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1049-8631delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97382672 | |||||
| chr13:97382707
|
C | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0111a0001c0001t0002g0165 | 3 | NA18948.hp1 NA18967.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1049-8615C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97382707 | ||||||
| chr13:97383012
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(84): Show | 87 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1049-8310G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383012 | ||||||
| chr13:97383049
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1049-8273C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383049 | ||||||
| chr13:97383084
|
T | C | 1 | a0001c0002t0006g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1049-8238T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383084 | ||||||
| chr13:97383108
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1049-8214T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383108 | ||||||
| chr13:97383129
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1049-8193G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383129 | ||||||
| chr13:97383318
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0001g0207others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1049-8004A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383318 | ||||||
| chr13:97383438
|
G | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1049-7884G>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383438 | ||||||
| chr13:97383807
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1049-7515A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97383807 | ||||||
| chr13:97383903
|
A | AT | 32 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1049-7405dupT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97383903 | |||||
| chr13:97383903
|
AT | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0153a0001c0001t0001g0200others(4): Show | 7 | HG01981.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-7405delT | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97383903 | |||||
| chr13:97384045
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0254 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1049-7277G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97384045 | ||||||
| chr13:97384126
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1049-7196C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97384126 | ||||||
| chr13:97384657
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0041others(1): Show | 4 | HG01167.hp2 HG01256.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-6665G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97384657 | ||||||
| chr13:97384667
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1049-6655C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97384667 | ||||||
| chr13:97384706
|
A | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0015others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1049-6616A>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97384706 | ||||||
| chr13:97384818
|
G | T | 1 | a0001c0001t0003g0099 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1049-6504G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97384818 | ||||||
| chr13:97385007
|
C | G | 8 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0001g0142others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-6315C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97385007 | ||||||
| chr13:97385016
|
C | A | 107 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0021others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1049-6306C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97385016 | ||||||
| chr13:97385637
|
C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0021others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1049-5685C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97385637 | ||||||
| chr13:97385812
|
G | A | 6 | a0001c0001t0001g0104a0001c0001t0001g0142a0001c0002t0006g0126others(3): Show | 6 | HG00099.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-5510G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97385812 | ||||||
| chr13:97386101
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1049-5221C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97386101 | ||||||
| chr13:97386173
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0132 | 2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1049-5149C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97386173 | ||||||
| chr13:97386323
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0021others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1049-4999G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97386323 | ||||||
| chr13:97386516
|
G | T | 2 | a0001c0001t0001g0191a0001c0001t0007g0206 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1049-4806G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97386516 | ||||||
| chr13:97386592
|
G | A | 19 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0013others(16): Show | 19 | HG00609.hp1 HG02027.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1049-4730G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97386592 | ||||||
| chr13:97386763
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01981.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1049-4559G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97386763 | ||||||
| chr13:97387204
|
T | C | 7 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0001g0142others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-4118T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97387204 | ||||||
| chr13:97387322
|
G | A | 7 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-4000G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97387322 | ||||||
| chr13:97387720
|
T | A | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1049-3602T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97387720 | ||||||
| chr13:97387905
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0180 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1049-3417A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97387905 | ||||||
| chr13:97388023
|
C | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1049-3299C>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97388023 | ||||||
| chr13:97388314
|
C | CAT | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(140): Show | 143 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1049-2987_1049-298 others(6): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATAT | 30 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0061others(27): Show | 30 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1049-2989_1049-298 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATATAT | 3 | a0001c0001t0001g0007a0001c0001t0001g0150a0001c0001t0018g0012 | 3 | HG00642.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-2991_1049-298 others(10): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATATATA others(11): Show |
2 | a0001c0002t0006g0126a0001c0002t0006g0248 | 2 | HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1049-3003_1049-298 others(22): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATATATA others(13): Show |
1 | a0001c0002t0006g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1049-3005_1049-298 others(24): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATATATA others(15): Show |
1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1049-3007_1049-298 others(26): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATATATA others(19): Show |
3 | a0001c0001t0001g0142a0001c0001t0001g0191a0001c0002t0006g0197 | 3 | HG00099.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1049-2986_1049-298 others(30): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
C | CATATATA others(29): Show |
1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1049-2986_1049-298 others(40): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388314
|
CATAT | C | 7 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-2989_1049-298 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97388314 | |||||
| chr13:97388337
|
C | A | 1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1049-2985C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97388337 | ||||||
| chr13:97388483
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0230 | 2 | HG02735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1049-2839G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97388483 | ||||||
| chr13:97388586
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0059 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1049-2736C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97388586 | ||||||
| chr13:97388733
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1049-2589A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97388733 | ||||||
| chr13:97388955
|
G | A | 7 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-2367G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97388955 | ||||||
| chr13:97389026
|
G | GCAGCAGT others(14): Show |
1 | a0001c0001t0014g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1049-2293_1049-227 others(25): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97389026 | |||||
| chr13:97389298
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0121a0001c0001t0001g0146others(3): Show | 6 | HG00642.hp2 HG01070.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1049-2024C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97389298 | ||||||
| chr13:97389712
|
AAAAG | A | 40 | a0001c0001t0001g0087a0001c0001t0001g0125a0001c0001t0001g0175others(37): Show | 40 | HG00609.hp1 HG00735.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1049-1586_1049-158 others(8): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97389712 | |||||
| chr13:97389831
|
C | T | 3 | a0001c0001t0008g0005a0001c0001t0014g0234a0001c0001t0017g0177 | 3 | HG02258.hp1 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1049-1491C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97389831 | ||||||
| chr13:97390313
|
T | TA | 17 | a0001c0001t0001g0104a0001c0001t0001g0142a0001c0001t0001g0191others(14): Show | 17 | HG00099.hp2 HG01192.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1049-1008dupA | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr13 | 97390313 | |||||
| chr13:97390574
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049-748G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390574 | ||||||
| chr13:97390613
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1049-709A>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390613 | ||||||
| chr13:97390869
|
T | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0084 | 2 | HG02074.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1049-453T>C | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390869 | ||||||
| chr13:97390882
|
T | A | 7 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-440T>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390882 | ||||||
| chr13:97390898
|
TATATTTA others(3): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1049-423_1049-414d others(12): Show |
MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390898 | ||||||
| chr13:97390918
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1049-404G>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390918 | ||||||
| chr13:97390958
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1049-364A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97390958 | ||||||
| chr13:97391015
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1049-307A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97391015 | ||||||
| chr13:97391105
|
C | A | 7 | a0001c0001t0005g0113a0001c0001t0005g0238a0001c0001t0005g0239others(4): Show | 7 | HG01192.hp1 HG01975.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-217C>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97391105 | ||||||
| chr13:97391169
|
C | T | 1 | a0001c0001t0007g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1049-153C>T | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97391169 | ||||||
| chr13:97391177
|
G | A | 3 | a0001c0001t0005g0113a0001c0001t0005g0252a0001c0001t0005g0253 | 3 | HG01975.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1049-145G>A | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97391177 | ||||||
| chr13:97391241
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1049-81A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97391241 | ||||||
| chr13:97391288
|
A | G | 3 | a0001c0001t0004g0112a0001c0001t0004g0210a0001c0001t0004g0233 | 3 | HG01192.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1049-34A>G | MBNL2 | ENSG00000139793.21 | transcript | ENST00000679496.1 | protein_coding | 8/8 | chr13 | 97391288 |