Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 153769 |
|---|---|
| ensemblid | ENSG00000156463.18 |
| hgncid | 26299 |
| symbol | SH3RF2 |
| name | SH3 domain containing ring finger 2 |
| refseq_nuc | NM_152550.4 |
| refseq_prot | NP_689763.4 |
| ensembl_nuc | ENST00000359120.9 |
| ensembl_prot | ENSP00000352028.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 145936578 |
| end | 146063292 |
| strand | + |
| ver | v1.2 |
| region | chr5:145936578-146063292 |
| region5000 | chr5:145931578-146068292 |
| regionname0 | SH3RF2_chr5_145936578_146063292 |
| regionname5000 | SH3RF2_chr5_145931578_146068292 |
| 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 | 0/1 | 729 | 103 | 33 | 20 | 37 | 4 | 8 | 23 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002 | 0/0 | 729 | 79 | 14 | 18 | 31 | 5 | 11 | 20 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0003 | 0/0 | 729 | 49 | 1 | 12 | 26 | 3 | 7 | 14 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0004 | 0/0 | 729 | 10 | 8 | 0 | 1 | 0 | 1 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0005 | 0/0 | 729 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0006 | 1/0 | 729 | 6 | 5 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0007 | 0/0 | 729 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0008 | 0/0 | 729 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0009 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0010 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0011 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0012 | 0/0 | 729 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0013 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0014 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0015 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0016 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0017 | 0/0 | 491 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0018 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0019 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0020 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0021 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0022 | 0/0 | 729 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| 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 | 0/1 | 2190 | 90 | 22 | 19 | 36 | 4 | 8 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0002 | 0/0 | 2190 | 77 | 14 | 18 | 31 | 5 | 9 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0003 | 0/0 | 2190 | 49 | 1 | 12 | 26 | 3 | 7 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0004 | 0/0 | 2190 | 7 | 7 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0005 | 0/0 | 2190 | 6 | 6 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0006 | 0/0 | 2190 | 5 | 3 | 0 | 1 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0007 | 1/0 | 2190 | 5 | 4 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0008 | 0/0 | 2190 | 5 | 5 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0009 | 0/0 | 2190 | 3 | 1 | 2 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0010 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0011 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0012 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0013 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0014 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0015 | 0/0 | 2180 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0016 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0017 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0018 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0019 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0020 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0021 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0022 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0023 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0024 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0025 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0026 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0027 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0028 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0029 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0030 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| c0031 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| 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 | 1/0 | 815 | 187 | 64 | 32 | 64 | 8 | 18 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| t0002 | 0/1 | 815 | 80 | 8 | 19 | 40 | 4 | 8 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| t0003 | 0/0 | 815 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| t0004 | 0/0 | 815 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| t0005 | 0/0 | 815 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| t0006 | 0/0 | 815 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| t0007 | 0/0 | 815 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| 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 | 0/1 | 2190 | 90 | 22 | 19 | 36 | 4 | 8 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0005 | 0/0 | 2190 | 6 | 6 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0010 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0011 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0014 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0016 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0002 | 0/0 | 2190 | 77 | 14 | 18 | 31 | 5 | 9 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0022 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0023 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0003c0003 | 0/0 | 2190 | 49 | 1 | 12 | 26 | 3 | 7 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0004c0006 | 0/0 | 2190 | 5 | 3 | 0 | 1 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0004c0008 | 0/0 | 2190 | 5 | 5 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0005c0004 | 0/0 | 2190 | 7 | 7 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0006c0007 | 1/0 | 2190 | 5 | 4 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0006c0025 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0007c0009 | 0/0 | 2190 | 3 | 1 | 2 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0008c0028 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0009c0027 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0010c0021 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0011c0024 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0012c0020 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0013c0019 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0014c0017 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0015c0012 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0016c0013 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0017c0015 | 0/0 | 2180 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0018c0018 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0019c0026 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0020c0030 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0021c0029 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0022c0031 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3004 | 18 | 17 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0001t0002 | 0/1 | 3004 | 72 | 5 | 18 | 36 | 4 | 8 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0005t0001 | 0/0 | 3004 | 6 | 6 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0010t0001 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0010t0002 | 0/0 | 3004 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0011t0001 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0014t0002 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0001c0016t0002 | 0/0 | 3004 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0002t0001 | 0/0 | 3004 | 76 | 14 | 18 | 31 | 5 | 8 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0002t0007 | 0/0 | 3004 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0022t0005 | 0/0 | 3004 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0002c0023t0001 | 0/0 | 3004 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0003c0003t0001 | 0/0 | 3004 | 47 | 1 | 10 | 26 | 3 | 7 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0003c0003t0004 | 0/0 | 3004 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0003c0003t0006 | 0/0 | 3004 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0004c0006t0001 | 0/0 | 3004 | 5 | 3 | 0 | 1 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0004c0008t0001 | 0/0 | 3004 | 5 | 5 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0005c0004t0001 | 0/0 | 3004 | 5 | 5 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0005c0004t0002 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0006c0007t0001 | 1/0 | 3004 | 5 | 4 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0006c0025t0001 | 0/0 | 3004 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0007c0009t0001 | 0/0 | 3004 | 3 | 1 | 2 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0008c0028t0001 | 0/0 | 3004 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0009c0027t0001 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0010c0021t0001 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0011c0024t0001 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0012c0020t0001 | 0/0 | 3004 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0013c0019t0001 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0014c0017t0001 | 0/0 | 3004 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0015c0012t0001 | 0/0 | 3004 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0016c0013t0002 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0017c0015t0002 | 0/0 | 2994 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0018c0018t0001 | 0/0 | 3004 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0019c0026t0001 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0020c0030t0001 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0021c0029t0002 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| a0022c0031t0003 | 0/0 | 3004 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | copy fasta | chr5 | 145931578 | 146068292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0010t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0010t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0011t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0011t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0014t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0001c0016t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0022t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0002c0023t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0003c0003t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0006t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0006t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0008t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0008t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0008t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0004c0008t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0005c0004t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0006c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0006c0007t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0006c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0006c0007t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0006c0007t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0006c0025t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0007c0009t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0007c0009t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0007c0009t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0008c0028t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0009c0027t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0010c0021t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0011c0024t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0012c0020t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0013c0019t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0014c0017t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0015c0012t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0016c0013t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0017c0015t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0018c0018t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0019c0026t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0020c0030t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0021c0029t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| a0022c0031t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0043 | EUR | GBR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0064 | EUR | GBR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0246 | EUR | GBR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | GBR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | FIN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0237 | EUR | FIN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0214 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0021 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0266 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0218 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00673 | hp1 | a0019 | c0026 | t0001 | g0228 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0232 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01069 | hp2 | a0007 | c0009 | t0001 | g0251 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0242 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01071 | hp2 | a0007 | c0009 | t0001 | g0250 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0035 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01099 | hp2 | a0022 | c0031 | t0003 | g0007 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0107 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0034 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0029 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01257 | hp1 | a0008 | c0028 | t0001 | g0221 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01257 | hp2 | a0001 | c0016 | t0002 | g0122 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | IBS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0044 | EUR | IBS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0070 | EUR | IBS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0038 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01952 | hp2 | a0003 | c0003 | t0004 | g0220 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02004 | hp1 | a0003 | c0003 | t0006 | g0241 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0223 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0219 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02055 | hp2 | a0005 | c0004 | t0001 | g0103 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0231 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02132 | hp1 | a0021 | c0029 | t0002 | g0126 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0109 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02135 | hp2 | a0020 | c0030 | t0001 | g0123 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0260 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CDX | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | CDX | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0217 | EAS | CDX | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CDX | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02258 | hp1 | a0005 | c0004 | t0001 | g0150 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0222 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02451 | hp1 | a0004 | c0008 | t0001 | g0262 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | KHV | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0211 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02615 | hp2 | a0005 | c0004 | t0001 | g0151 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02630 | hp1 | a0005 | c0004 | t0002 | g0204 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0210 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02647 | hp2 | a0004 | c0008 | t0001 | g0159 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0067 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0227 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02809 | hp2 | a0001 | c0011 | t0001 | g0071 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02886 | hp2 | a0018 | c0018 | t0001 | g0095 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02895 | hp1 | a0001 | c0010 | t0002 | g0270 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0212 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02896 | hp1 | a0014 | c0017 | t0001 | g0249 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02896 | hp2 | a0006 | c0007 | t0001 | g0094 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0213 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02897 | hp2 | a0006 | c0007 | t0001 | g0093 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02970 | hp2 | a0004 | c0006 | t0001 | g0081 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02976 | hp2 | a0006 | c0007 | t0001 | g0097 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03098 | hp2 | a0006 | c0025 | t0001 | g0259 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03130 | hp2 | a0001 | c0010 | t0001 | g0257 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03139 | hp1 | a0004 | c0008 | t0001 | g0267 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03195 | hp2 | a0004 | c0006 | t0001 | g0085 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03225 | hp1 | a0006 | c0007 | t0001 | g0096 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0020 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03453 | hp1 | a0015 | c0012 | t0001 | g0202 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0042 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03540 | hp1 | a0004 | c0006 | t0001 | g0139 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03579 | hp1 | a0001 | c0011 | t0001 | g0160 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03579 | hp2 | a0005 | c0004 | t0001 | g0079 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0196 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03710 | hp1 | a0002 | c0023 | t0001 | g0048 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0235 | SAS | BEB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0226 | SAS | BEB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0229 | SAS | BEB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0008 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04199 | hp1 | a0002 | c0022 | t0005 | g0075 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04199 | hp2 | a0004 | c0006 | t0001 | g0124 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04204 | hp1 | a0002 | c0002 | t0007 | g0106 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0243 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG04228 | hp2 | a0012 | c0020 | t0001 | g0261 | SAS | STU | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18522 | hp1 | a0001 | c0010 | t0001 | g0041 | AFR | YRI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | CHB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | YRI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18906 | hp2 | a0007 | c0009 | t0001 | g0248 | AFR | YRI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18957 | hp1 | a0004 | c0006 | t0001 | g0152 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0234 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18962 | hp1 | a0016 | c0013 | t0002 | g0161 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18965 | hp2 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18978 | hp1 | a0003 | c0003 | t0001 | g0225 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18985 | hp1 | a0017 | c0015 | t0002 | g0184 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0065 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18989 | hp1 | a0009 | c0027 | t0001 | g0010 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18992 | hp1 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18992 | hp2 | a0010 | c0021 | t0001 | g0240 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19002 | hp1 | a0013 | c0019 | t0001 | g0033 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0244 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0224 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | LWK | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19043 | hp2 | a0004 | c0008 | t0001 | g0077 | AFR | LWK | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0216 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19063 | hp1 | a0001 | c0014 | t0002 | g0153 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19074 | hp1 | a0011 | c0024 | t0001 | g0238 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0230 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | ASW | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | TSI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | TSI | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02109 | hp2 | a0005 | c0004 | t0002 | g0205 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02486 | hp2 | a0004 | c0008 | t0001 | g0078 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0209 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| HG03471 | hp2 | a0005 | c0004 | t0001 | g0145 | AFR | MSL | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | USA | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0146 | AFR | USA | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0142 | REF | REF | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| homoSapiens_grch38 | hp1 | a0006 | c0007 | t0001 | g0131 | REF | REF | SH3RF2_chr5_145931578_146068292 | SH3RF2 | chr5 | 145931578 | 146068292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:145936694
|
G | C | 1 | a0022 | 1 | HG01099.hp2 | splice_region_variant | LOW | c.-107G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/10 | chr5 | 145936694 | ||||||
| chr5:145938070
|
C | T | 1 | a0022 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.142C>T | p.Arg48Trp | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/10 | 365/3004 | 142/2190 | 48/729 | chr5 | 145938070 | ||
| chr5:145938122
|
C | T | 2 | a0020a0021 | 2 | HG02132.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.194C>T | p.Ala65Val | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/10 | 417/3004 | 194/2190 | 65/729 | chr5 | 145938122 | ||
| chr5:145938193
|
C | T | 1 | a0008 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.265C>T | p.Arg89Cys | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/10 | 488/3004 | 265/2190 | 89/729 | chr5 | 145938193 | ||
| chr5:146000199
|
T | G | 1 | a0007 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.520T>G | p.Phe174Val | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/10 | 743/3004 | 520/2190 | 174/729 | chr5 | 146000199 | ||
| chr5:146000286
|
A | G | 1 | a0009 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.607A>G | p.Lys203Glu | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/10 | 830/3004 | 607/2190 | 203/729 | chr5 | 146000286 | ||
| chr5:146004064
|
A | G | 1 | a0019 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.655A>G | p.Ile219Val | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/10 | 878/3004 | 655/2190 | 219/729 | chr5 | 146004064 | ||
| chr5:146013801
|
C | T | 12 | a0002a0003a0005others(9): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
missense_variant | MODERATE | c.799C>T | p.Arg267Cys | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/10 | 1022/3004 | 799/2190 | 267/729 | chr5 | 146013801 | ||
| chr5:146013856
|
T | G | 1 | a0013 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.854T>G | p.Leu285Arg | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/10 | 1077/3004 | 854/2190 | 285/729 | chr5 | 146013856 | ||
| chr5:146013925
|
T | C | 1 | a0012 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.923T>C | p.Leu308Pro | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/10 | 1146/3004 | 923/2190 | 308/729 | chr5 | 146013925 | ||
| chr5:146013930
|
C | T | 1 | a0018 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.928C>T | p.Arg310Trp | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/10 | 1151/3004 | 928/2190 | 310/729 | chr5 | 146013930 | ||
| chr5:146047818
|
C | T | 1 | a0011 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.1106C>T | p.Ala369Val | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/10 | 1329/3004 | 1106/2190 | 369/729 | chr5 | 146047818 | ||
| chr5:146049184
|
G | A | 1 | a0014 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.1261G>A | p.Val421Ile | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/10 | 1484/3004 | 1261/2190 | 421/729 | chr5 | 146049184 | ||
| chr5:146056007
|
G | A | 1 | a0010 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.1349G>A | p.Arg450Gln | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/10 | 1572/3004 | 1349/2190 | 450/729 | chr5 | 146056007 | ||
| chr5:146056088
|
G | A | 1 | a0015 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1430G>A | p.Arg477Gln | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/10 | 1653/3004 | 1430/2190 | 477/729 | chr5 | 146056088 | ||
| chr5:146056130
|
TAGTCAAC others(3): Show |
T | 1 | a0017 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.1473_1482delAGTCAA others(4): Show |
p.Ile491fs | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/10 | 1696/3004 | 1473/2190 | 491/729 | chr5 | 146056130 | ||
| chr5:146060084
|
T | C | 20 | a0001a0002a0003others(17): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
missense_variant | MODERATE | c.1774T>C | p.Trp592Arg | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/10 | 1997/3004 | 1774/2190 | 592/729 | chr5 | 146060084 | ||
| chr5:146060165
|
G | A | 1 | a0016 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.1855G>A | p.Ala619Thr | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/10 | 2078/3004 | 1855/2190 | 619/729 | chr5 | 146060165 | ||
| chr5:146062570
|
G | A | 5 | a0003a0008a0011others(2): Show | 53 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(50): Show |
missense_variant | MODERATE | c.2059G>A | p.Val687Ile | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 2282/3004 | 2059/2190 | 687/729 | chr5 | 146062570 | ||
| chr5:146062640
|
G | C | 12 | a0002a0003a0004others(9): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
missense_variant | MODERATE | c.2129G>C | p.Gly710Ala | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 2352/3004 | 2129/2190 | 710/729 | chr5 | 146062640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146013752
|
C | T | 4 | a0001c0005a0001c0010a0004c0008others(1): Show | 15 | HG02451.hp1 HG02486.hp2 HG02615.hp1 others(12): Show |
synonymous_variant | LOW | c.750C>T | p.Asn250Asn | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/10 | 973/3004 | 750/2190 | 250/729 | chr5 | 146013752 | ||
| chr5:146014037
|
C | T | 2 | a0001c0011a0014c0017 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.1035C>T | p.Asp345Asp | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/10 | 1258/3004 | 1035/2190 | 345/729 | chr5 | 146014037 | ||
| chr5:146049102
|
C | A | 1 | a0001c0010 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1179C>A | p.Ala393Ala | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/10 | 1402/3004 | 1179/2190 | 393/729 | chr5 | 146049102 | ||
| chr5:146049183
|
C | T | 1 | a0001c0010 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1260C>T | p.Gly420Gly | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/10 | 1483/3004 | 1260/2190 | 420/729 | chr5 | 146049183 | ||
| chr5:146049195
|
C | T | 1 | a0001c0016 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.1272C>T | p.Val424Val | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/10 | 1495/3004 | 1272/2190 | 424/729 | chr5 | 146049195 | ||
| chr5:146056167
|
T | A | 1 | a0002c0022 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1509T>A | p.Thr503Thr | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/10 | 1732/3004 | 1509/2190 | 503/729 | chr5 | 146056167 | ||
| chr5:146060005
|
C | T | 1 | a0001c0014 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.1695C>T | p.Ala565Ala | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/10 | 1918/3004 | 1695/2190 | 565/729 | chr5 | 146060005 | ||
| chr5:146060185
|
C | A | 1 | a0002c0023 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.1875C>A | p.Ile625Ile | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/10 | 2098/3004 | 1875/2190 | 625/729 | chr5 | 146060185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:145937844
|
A | G | 1 | a0002c0002t0007 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-85A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/10 | 85 | chr5 | 145937844 | |||||
| chr5:146062710
|
G | C | 1 | a0003c0003t0004 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 9 | chr5 | 146062710 | |||||
| chr5:146062804
|
G | A | 1 | a0002c0022t0005 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 103 | chr5 | 146062804 | |||||
| chr5:146062928
|
G | T | 1 | a0003c0003t0006 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 227 | chr5 | 146062928 | |||||
| chr5:146062932
|
G | A | 8 | a0001c0001t0002a0001c0010t0002a0001c0014t0002others(5): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 231 | chr5 | 146062932 | |||||
| chr5:146063009
|
C | T | 8 | a0001c0001t0002a0001c0010t0002a0001c0014t0002others(5): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*308C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 10/10 | 308 | chr5 | 146063009 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:145936743
|
T | C | 40 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(37): Show | 41 | HG00544.hp2 HG00639.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-107+49T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145936743 | ||||||
| chr5:145936921
|
G | C | 1 | a0001c0005t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-107+227G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145936921 | ||||||
| chr5:145937169
|
GA | G | 5 | a0001c0010t0002g0270a0002c0002t0001g0002a0002c0002t0001g0268others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-107+488delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 145937169 | |||||
| chr5:145937375
|
C | T | 1 | a0003c0003t0001g0266 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-106-448C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937375 | ||||||
| chr5:145937395
|
T | C | 32 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0050others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.-106-428T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937395 | ||||||
| chr5:145937504
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-106-319G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937504 | ||||||
| chr5:145937533
|
G | A | 1 | a0001c0011t0001g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-106-290G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937533 | ||||||
| chr5:145937536
|
A | G | 1 | a0002c0002t0001g0264 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-106-287A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937536 | ||||||
| chr5:145937581
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-106-242G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937581 | ||||||
| chr5:145937608
|
A | G | 2 | a0001c0001t0001g0263a0004c0008t0001g0262 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-106-215A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937608 | ||||||
| chr5:145937781
|
G | T | 1 | a0012c0020t0001g0261 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-106-42G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937781 | ||||||
| chr5:145937810
|
C | G | 1 | a0002c0002t0001g0260 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-106-13C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 1/9 | chr5 | 145937810 | ||||||
| chr5:145938383
|
T | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.378+77T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938383 | ||||||
| chr5:145938456
|
C | G | 15 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.378+150C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938456 | ||||||
| chr5:145938529
|
G | A | 1 | a0002c0022t0005g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+223G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938529 | ||||||
| chr5:145938642
|
G | A | 7 | a0001c0001t0001g0076a0002c0002t0001g0072a0002c0002t0001g0260others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+336G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938642 | ||||||
| chr5:145938658
|
CAAAAG | C | 3 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0247 | 3 | HG01175.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.378+354_378+358del others(5): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145938658 | |||||
| chr5:145938676
|
T | C | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.378+370T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938676 | ||||||
| chr5:145938720
|
G | A | 2 | a0002c0002t0001g0080a0022c0031t0003g0007 | 2 | HG01099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.378+414G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938720 | ||||||
| chr5:145938785
|
G | A | 2 | a0001c0001t0001g0263a0004c0006t0001g0081 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.378+479G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938785 | ||||||
| chr5:145938818
|
A | C | 1 | a0003c0003t0001g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378+512A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938818 | ||||||
| chr5:145938924
|
T | G | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+618T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938924 | ||||||
| chr5:145938935
|
C | A | 5 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0002g0084others(2): Show | 5 | HG01934.hp1 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+629C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145938935 | ||||||
| chr5:145939050
|
A | G | 5 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0002g0084others(2): Show | 5 | HG01934.hp1 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+744A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939050 | ||||||
| chr5:145939059
|
G | A | 2 | a0002c0002t0001g0043a0003c0003t0001g0044 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.378+753G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939059 | ||||||
| chr5:145939083
|
C | A | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.378+777C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939083 | ||||||
| chr5:145939091
|
A | T | 50 | a0001c0001t0002g0040a0002c0002t0001g0226a0002c0002t0001g0229others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+785A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939091 | ||||||
| chr5:145939283
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.378+977G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939283 | ||||||
| chr5:145939430
|
G | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+1124G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939430 | ||||||
| chr5:145939498
|
C | T | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.378+1192C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939498 | ||||||
| chr5:145939503
|
C | G | 94 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(91): Show | 94 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.378+1197C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939503 | ||||||
| chr5:145939564
|
C | T | 110 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(107): Show | 110 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.378+1258C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939564 | ||||||
| chr5:145939818
|
C | G | 1 | a0002c0002t0001g0070 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.378+1512C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939818 | ||||||
| chr5:145939858
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.378+1552G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939858 | ||||||
| chr5:145939890
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.378+1584C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145939890 | ||||||
| chr5:145940187
|
G | C | 94 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(91): Show | 94 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.378+1881G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145940187 | ||||||
| chr5:145940516
|
A | T | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+2210A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145940516 | ||||||
| chr5:145940791
|
A | C | 95 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(92): Show | 95 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.378+2485A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145940791 | ||||||
| chr5:145940860
|
GA | G | 50 | a0001c0001t0002g0040a0002c0002t0001g0226a0002c0002t0001g0229others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+2555delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145940860 | ||||||
| chr5:145941059
|
G | C | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+2753G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941059 | ||||||
| chr5:145941063
|
G | T | 26 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(23): Show | 26 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.378+2757G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941063 | ||||||
| chr5:145941124
|
C | T | 4 | a0002c0002t0001g0258a0007c0009t0001g0250a0007c0009t0001g0251others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+2818C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941124 | ||||||
| chr5:145941151
|
G | A | 6 | a0001c0001t0001g0098a0006c0007t0001g0093a0006c0007t0001g0094others(3): Show | 6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+2845G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941151 | ||||||
| chr5:145941295
|
C | A | 2 | a0005c0004t0002g0204a0005c0004t0002g0205 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.378+2989C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941295 | ||||||
| chr5:145941351
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0265 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.378+3045C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941351 | ||||||
| chr5:145941370
|
C | G | 1 | a0001c0001t0002g0201 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.378+3064C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941370 | ||||||
| chr5:145941396
|
C | T | 8 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+3090C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941396 | ||||||
| chr5:145941425
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+3119G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941425 | ||||||
| chr5:145941538
|
G | A | 1 | a0002c0002t0007g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.378+3232G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941538 | ||||||
| chr5:145941659
|
T | C | 50 | a0001c0001t0002g0040a0002c0002t0001g0226a0002c0002t0001g0229others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+3353T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941659 | ||||||
| chr5:145941711
|
C | A | 2 | a0003c0003t0001g0008a0003c0003t0001g0107 | 2 | HG01109.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.378+3405C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941711 | ||||||
| chr5:145941932
|
C | T | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.378+3626C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941932 | ||||||
| chr5:145941933
|
T | C | 50 | a0001c0001t0002g0040a0002c0002t0001g0226a0002c0002t0001g0229others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+3627T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145941933 | ||||||
| chr5:145942053
|
A | T | 1 | a0002c0002t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.378+3747A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942053 | ||||||
| chr5:145942129
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+3823G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942129 | ||||||
| chr5:145942336
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+4030G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942336 | ||||||
| chr5:145942356
|
G | A | 51 | a0001c0001t0002g0040a0002c0002t0001g0226a0002c0002t0001g0229others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+4050G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942356 | ||||||
| chr5:145942508
|
C | T | 146 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(143): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.378+4202C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942508 | ||||||
| chr5:145942583
|
C | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+4277C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942583 | ||||||
| chr5:145942669
|
G | T | 6 | a0001c0001t0001g0098a0006c0007t0001g0093a0006c0007t0001g0094others(3): Show | 6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+4363G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942669 | ||||||
| chr5:145942759
|
A | T | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+4453A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942759 | ||||||
| chr5:145942789
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.378+4483T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942789 | ||||||
| chr5:145942814
|
A | G | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.378+4508A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145942814 | ||||||
| chr5:145943062
|
G | T | 110 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(107): Show | 110 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.378+4756G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145943062 | ||||||
| chr5:145943230
|
T | TA | 89 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(86): Show | 89 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.378+4936dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145943230 | |||||
| chr5:145943490
|
T | C | 1 | a0004c0006t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.378+5184T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145943490 | ||||||
| chr5:145943654
|
C | T | 11 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(8): Show | 12 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.378+5348C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145943654 | ||||||
| chr5:145943692
|
T | TTTTTTG | 59 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0186others(56): Show | 61 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.378+5415_378+5420d others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145943692 | |||||
| chr5:145943737
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+5431G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145943737 | ||||||
| chr5:145943949
|
C | T | 3 | a0002c0002t0001g0189a0002c0002t0001g0197a0002c0002t0001g0198 | 3 | HG01256.hp2 HG01934.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.378+5643C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145943949 | ||||||
| chr5:145943967
|
T | A | 111 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(108): Show | 111 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.378+5661T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145943967 | ||||||
| chr5:145944056
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+5750G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944056 | ||||||
| chr5:145944120
|
A | G | 1 | a0002c0002t0001g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.378+5814A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944120 | ||||||
| chr5:145944138
|
C | T | 19 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(16): Show | 19 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.378+5832C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944138 | ||||||
| chr5:145944337
|
C | CT | 14 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.378+6049dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145944337 | |||||
| chr5:145944337
|
CTT | C | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+6048_378+6049d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145944337 | |||||
| chr5:145944337
|
CTTT | C | 14 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(11): Show | 14 | HG02258.hp2 HG02451.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.378+6047_378+6049d others(5): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145944337 | |||||
| chr5:145944355
|
T | A | 49 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(46): Show | 49 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.378+6049T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944355 | ||||||
| chr5:145944479
|
G | A | 8 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0087others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+6173G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944479 | ||||||
| chr5:145944518
|
C | T | 90 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(87): Show | 90 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.378+6212C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944518 | ||||||
| chr5:145944669
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.378+6363C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944669 | ||||||
| chr5:145944670
|
G | A | 2 | a0005c0004t0001g0079a0007c0009t0001g0248 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.378+6364G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944670 | ||||||
| chr5:145944778
|
G | A | 3 | a0003c0003t0001g0030a0003c0003t0001g0214a0003c0003t0001g0215 | 3 | HG00408.hp2 HG00423.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.378+6472G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145944778 | ||||||
| chr5:145945005
|
A | C | 26 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0104others(23): Show | 26 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.378+6699A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145945005 | ||||||
| chr5:145945048
|
G | C | 71 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.378+6742G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145945048 | ||||||
| chr5:145945168
|
C | G | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+6862C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145945168 | ||||||
| chr5:145945230
|
AGT | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+6927_378+6928d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145945230 | |||||
| chr5:145945355
|
C | T | 21 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(18): Show | 21 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.378+7049C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145945355 | ||||||
| chr5:145945372
|
A | T | 20 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(17): Show | 20 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.378+7066A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145945372 | ||||||
| chr5:145946127
|
C | T | 49 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(46): Show | 49 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.378+7821C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946127 | ||||||
| chr5:145946364
|
C | G | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.378+8058C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946364 | ||||||
| chr5:145946666
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.378+8360G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946666 | ||||||
| chr5:145946826
|
G | C | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+8520G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946826 | ||||||
| chr5:145946832
|
G | T | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+8526G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946832 | ||||||
| chr5:145946833
|
C | A | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+8527C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946833 | ||||||
| chr5:145946917
|
G | A | 7 | a0003c0003t0001g0030a0003c0003t0001g0214a0003c0003t0001g0215others(4): Show | 7 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+8611G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145946917 | ||||||
| chr5:145947136
|
T | C | 51 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+8830T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947136 | ||||||
| chr5:145947153
|
C | CAT | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(7): Show | 10 | HG01255.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+8864_378+8865d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145947153 | |||||
| chr5:145947153
|
CAT | C | 6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0185others(3): Show | 6 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+8864_378+8865d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145947153 | |||||
| chr5:145947361
|
G | A | 3 | a0002c0002t0001g0009a0002c0002t0001g0264a0009c0027t0001g0010 | 3 | NA18975.hp2 NA18989.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.378+9055G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947361 | ||||||
| chr5:145947457
|
A | G | 2 | a0003c0003t0001g0008a0003c0003t0001g0107 | 2 | HG01109.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.378+9151A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947457 | ||||||
| chr5:145947817
|
G | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+9511G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947817 | ||||||
| chr5:145947823
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.378+9517G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947823 | ||||||
| chr5:145947833
|
A | G | 1 | a0003c0003t0001g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378+9527A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947833 | ||||||
| chr5:145947860
|
T | C | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+9554T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947860 | ||||||
| chr5:145947957
|
T | G | 1 | a0003c0003t0001g0006 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.378+9651T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947957 | ||||||
| chr5:145947991
|
A | C | 8 | a0001c0001t0001g0076a0002c0002t0001g0072a0002c0002t0001g0260others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+9685A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145947991 | ||||||
| chr5:145948028
|
T | C | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+9722T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948028 | ||||||
| chr5:145948058
|
C | G | 2 | a0001c0001t0001g0076a0002c0002t0001g0260 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.378+9752C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948058 | ||||||
| chr5:145948422
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+10116G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948422 | ||||||
| chr5:145948566
|
A | C | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+10260A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948566 | ||||||
| chr5:145948581
|
C | T | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+10275C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948581 | ||||||
| chr5:145948789
|
C | A | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+10483C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948789 | ||||||
| chr5:145948855
|
T | C | 32 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(29): Show | 32 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.378+10549T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948855 | ||||||
| chr5:145948882
|
CCATGGGT others(31): Show |
C | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.378+10579_378+1061 others(42): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145948882 | |||||
| chr5:145948896
|
G | T | 1 | a0001c0001t0002g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.378+10590G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948896 | ||||||
| chr5:145948965
|
T | C | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+10659T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145948965 | ||||||
| chr5:145949006
|
A | G | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+10700A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949006 | ||||||
| chr5:145949161
|
C | T | 2 | a0001c0001t0002g0162a0016c0013t0002g0161 | 2 | HG03710.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.378+10855C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949161 | ||||||
| chr5:145949353
|
G | A | 29 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(26): Show | 29 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.378+11047G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949353 | ||||||
| chr5:145949417
|
T | C | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+11111T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949417 | ||||||
| chr5:145949421
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.378+11115C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949421 | ||||||
| chr5:145949438
|
A | C | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+11132A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949438 | ||||||
| chr5:145949539
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.378+11233C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949539 | ||||||
| chr5:145949554
|
C | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+11248C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145949554 | ||||||
| chr5:145949820
|
G | GA | 63 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.378+11519dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145949820 | |||||
| chr5:145950065
|
A | AG | 94 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(91): Show | 94 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.378+11759_378+1176 others(5): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145950065 | ||||||
| chr5:145950103
|
C | T | 12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+11797C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145950103 | ||||||
| chr5:145950109
|
TCATGTAG others(4): Show |
T | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+11806_378+1181 others(15): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145950109 | |||||
| chr5:145950254
|
G | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+11948G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145950254 | ||||||
| chr5:145950781
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+12475G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145950781 | ||||||
| chr5:145950847
|
G | A | 9 | a0001c0001t0001g0206a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 9 | HG01934.hp1 HG02559.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+12541G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145950847 | ||||||
| chr5:145951228
|
C | T | 4 | a0001c0005t0001g0210a0001c0005t0001g0211a0001c0005t0001g0212others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+12922C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951228 | ||||||
| chr5:145951294
|
T | A | 1 | a0003c0003t0001g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.378+12988T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951294 | ||||||
| chr5:145951420
|
C | T | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+13114C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951420 | ||||||
| chr5:145951440
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378+13134T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951440 | ||||||
| chr5:145951494
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.378+13188T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951494 | ||||||
| chr5:145951501
|
T | C | 1 | a0002c0002t0001g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.378+13195T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951501 | ||||||
| chr5:145951528
|
C | G | 8 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(5): Show | 8 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+13222C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951528 | ||||||
| chr5:145951535
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+13229C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951535 | ||||||
| chr5:145951543
|
C | A | 5 | a0003c0003t0001g0065a0003c0003t0001g0216a0003c0003t0001g0222others(2): Show | 5 | HG01257.hp1 HG01952.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+13237C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951543 | ||||||
| chr5:145951758
|
G | A | 1 | a0002c0002t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378+13452G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951758 | ||||||
| chr5:145951893
|
C | G | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.378+13587C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145951893 | ||||||
| chr5:145952013
|
T | G | 12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+13707T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952013 | ||||||
| chr5:145952020
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.378+13714C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952020 | ||||||
| chr5:145952088
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.378+13782A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952088 | ||||||
| chr5:145952133
|
C | G | 4 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(1): Show | 4 | HG01934.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+13827C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952133 | ||||||
| chr5:145952487
|
C | T | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+14181C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952487 | ||||||
| chr5:145952541
|
T | G | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+14235T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952541 | ||||||
| chr5:145952639
|
T | C | 12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+14333T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952639 | ||||||
| chr5:145952641
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+14335C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952641 | ||||||
| chr5:145952749
|
C | T | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+14443C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952749 | ||||||
| chr5:145952881
|
T | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+14575T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145952881 | ||||||
| chr5:145953103
|
GTCTC | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(27): Show | 30 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+14813_378+1481 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145953103 | |||||
| chr5:145953119
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.378+14813C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953119 | ||||||
| chr5:145953124
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.378+14818T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953124 | ||||||
| chr5:145953124
|
T | TCA | 9 | a0001c0001t0001g0076a0001c0001t0002g0019a0001c0001t0002g0056others(6): Show | 9 | HG00673.hp2 HG02896.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+14841_378+1484 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145953124 | |||||
| chr5:145953124
|
T | TCACA | 18 | a0001c0001t0002g0058a0001c0001t0002g0158a0002c0002t0001g0003others(15): Show | 18 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.378+14839_378+1484 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145953124 | |||||
| chr5:145953124
|
TCA | T | 18 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.378+14841_378+1484 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145953124 | |||||
| chr5:145953124
|
TCACA | T | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+14839_378+1484 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145953124 | |||||
| chr5:145953203
|
A | G | 1 | a0001c0001t0002g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.378+14897A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953203 | ||||||
| chr5:145953413
|
C | T | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+15107C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953413 | ||||||
| chr5:145953671
|
T | C | 2 | a0003c0003t0001g0066a0003c0003t0001g0223 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.378+15365T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953671 | ||||||
| chr5:145953818
|
A | T | 94 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(91): Show | 94 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.378+15512A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953818 | ||||||
| chr5:145953880
|
G | T | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+15574G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145953880 | ||||||
| chr5:145954065
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.378+15759A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145954065 | ||||||
| chr5:145954090
|
G | A | 1 | a0002c0002t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.378+15784G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145954090 | ||||||
| chr5:145954208
|
C | T | 51 | a0001c0001t0002g0110a0002c0002t0001g0226a0002c0002t0001g0229others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+15902C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145954208 | ||||||
| chr5:145954223
|
T | C | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.378+15917T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145954223 | ||||||
| chr5:145954326
|
T | C | 102 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.378+16020T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145954326 | ||||||
| chr5:145954647
|
C | G | 94 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(91): Show | 94 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.378+16341C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145954647 | ||||||
| chr5:145954868
|
C | CGA | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+16578_378+1657 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145954868 | |||||
| chr5:145955026
|
T | C | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | NA18981.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.378+16720T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955026 | ||||||
| chr5:145955143
|
T | C | 2 | a0003c0003t0001g0224a0003c0003t0001g0225 | 2 | NA18978.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.378+16837T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955143 | ||||||
| chr5:145955215
|
C | G | 2 | a0003c0003t0001g0039a0003c0003t0001g0068 | 2 | NA18965.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.378+16909C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955215 | ||||||
| chr5:145955227
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+16921T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955227 | ||||||
| chr5:145955305
|
C | T | 17 | a0001c0001t0002g0058a0001c0001t0002g0158a0002c0002t0001g0043others(14): Show | 17 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.378+16999C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955305 | ||||||
| chr5:145955464
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.378+17158T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955464 | ||||||
| chr5:145955840
|
G | T | 1 | a0001c0005t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.378+17534G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145955840 | ||||||
| chr5:145956159
|
A | G | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+17853A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956159 | ||||||
| chr5:145956207
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.378+17901G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956207 | ||||||
| chr5:145956305
|
T | C | 12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+17999T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956305 | ||||||
| chr5:145956388
|
G | A | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+18082G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956388 | ||||||
| chr5:145956424
|
C | T | 1 | a0005c0004t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.378+18118C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956424 | ||||||
| chr5:145956692
|
A | T | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.378+18386A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956692 | ||||||
| chr5:145956858
|
G | A | 5 | a0006c0007t0001g0093a0006c0007t0001g0094a0006c0007t0001g0096others(2): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+18552G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145956858 | ||||||
| chr5:145957086
|
A | G | 1 | a0001c0001t0002g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.378+18780A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145957086 | ||||||
| chr5:145957211
|
A | T | 1 | a0002c0002t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.378+18905A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145957211 | ||||||
| chr5:145957279
|
A | G | 5 | a0006c0007t0001g0093a0006c0007t0001g0094a0006c0007t0001g0096others(2): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+18973A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145957279 | ||||||
| chr5:145957483
|
T | C | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+19177T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145957483 | ||||||
| chr5:145957803
|
A | T | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+19497A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145957803 | ||||||
| chr5:145957876
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+19570G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145957876 | ||||||
| chr5:145958076
|
A | G | 44 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(41): Show | 44 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.378+19770A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145958076 | ||||||
| chr5:145958128
|
AAAAAC | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(1): Show | 4 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+19837_378+1984 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145958128 | |||||
| chr5:145958276
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.378+19970G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145958276 | ||||||
| chr5:145958511
|
T | G | 1 | a0003c0003t0001g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378+20205T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145958511 | ||||||
| chr5:145958614
|
G | A | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+20308G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145958614 | ||||||
| chr5:145958896
|
C | T | 18 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.378+20590C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145958896 | ||||||
| chr5:145958923
|
T | C | 50 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(47): Show | 50 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+20617T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145958923 | ||||||
| chr5:145959097
|
G | T | 32 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(29): Show | 32 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.378+20791G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959097 | ||||||
| chr5:145959605
|
C | CTA | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+21309_378+2131 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959605 | |||||
| chr5:145959615
|
A | ATG | 15 | a0001c0001t0002g0110a0001c0001t0002g0149a0001c0001t0002g0181others(12): Show | 15 | HG01256.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.378+21341_378+2134 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959615 | |||||
| chr5:145959615
|
A | ATGTG | 3 | a0002c0002t0001g0200a0003c0003t0001g0246a0005c0004t0002g0205 | 3 | HG00140.hp1 HG01361.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.378+21339_378+2134 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959615 | |||||
| chr5:145959615
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.378+21309A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959615 | ||||||
| chr5:145959615
|
ATG | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0207a0001c0001t0001g0208others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.378+21341_378+2134 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959615 | |||||
| chr5:145959615
|
ATGTG | A | 51 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0191others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+21339_378+2134 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959615 | |||||
| chr5:145959615
|
ATGTGTG | A | 8 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(5): Show | 8 | HG00673.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+21337_378+2134 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959615 | |||||
| chr5:145959617
|
G | A | 23 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(20): Show | 23 | HG01934.hp1 HG02145.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.378+21311G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959617 | ||||||
| chr5:145959619
|
G | A | 1 | a0005c0004t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.378+21313G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959619 | ||||||
| chr5:145959645
|
G | A | 9 | a0001c0001t0001g0206a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 9 | HG01934.hp1 HG02559.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+21339G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959645 | ||||||
| chr5:145959649
|
A | G | 2 | a0004c0006t0001g0081a0006c0025t0001g0259 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.378+21343A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959649 | ||||||
| chr5:145959655
|
G | A | 1 | a0004c0008t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.378+21349G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959655 | ||||||
| chr5:145959666
|
C | CAT | 4 | a0001c0001t0001g0090a0001c0001t0002g0110a0002c0002t0001g0047others(1): Show | 4 | HG02155.hp2 HG03579.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+21375_378+2137 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959666 | |||||
| chr5:145959666
|
C | CATAT | 26 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(23): Show | 26 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.378+21373_378+2137 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959666 | |||||
| chr5:145959666
|
C | CATATAT | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(1): Show | 4 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+21371_378+2137 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145959666 | |||||
| chr5:145959732
|
T | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+21426T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959732 | ||||||
| chr5:145959887
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.378+21581G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959887 | ||||||
| chr5:145959948
|
A | T | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.378+21642A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959948 | ||||||
| chr5:145959986
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+21680C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959986 | ||||||
| chr5:145959998
|
C | T | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+21692C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145959998 | ||||||
| chr5:145960052
|
T | C | 1 | a0003c0003t0001g0031 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.378+21746T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145960052 | ||||||
| chr5:145960281
|
C | G | 1 | a0002c0002t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.378+21975C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145960281 | ||||||
| chr5:145960471
|
A | G | 4 | a0001c0001t0002g0104a0001c0001t0002g0179a0001c0001t0002g0180others(1): Show | 4 | NA18948.hp2 NA18978.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+22165A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145960471 | ||||||
| chr5:145960523
|
C | G | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+22217C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145960523 | ||||||
| chr5:145960652
|
C | T | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+22346C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145960652 | ||||||
| chr5:145960919
|
A | T | 2 | a0002c0002t0001g0059a0003c0003t0001g0021 | 2 | HG00544.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.378+22613A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145960919 | ||||||
| chr5:145961043
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.378+22737C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961043 | ||||||
| chr5:145961053
|
G | A | 8 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(5): Show | 9 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+22747G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961053 | ||||||
| chr5:145961107
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.378+22801G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961107 | ||||||
| chr5:145961136
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378+22830T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961136 | ||||||
| chr5:145961174
|
C | CT | 33 | a0001c0001t0001g0076a0001c0001t0002g0046a0001c0001t0002g0053others(30): Show | 33 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.378+22892dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961174
|
C | CTT | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0252others(7): Show | 10 | HG01934.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.378+22891_378+2289 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961174
|
C | CTTT | 10 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0090others(7): Show | 10 | HG02145.hp1 HG02976.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+22890_378+2289 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961174
|
C | CTTTT | 6 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG02055.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+22889_378+2289 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961174
|
C | CTTTTT | 6 | a0002c0002t0001g0102a0006c0007t0001g0093a0006c0007t0001g0094others(3): Show | 6 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+22888_378+2289 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961174
|
CT | C | 19 | a0001c0001t0002g0110a0001c0001t0002g0113a0001c0001t0002g0162others(16): Show | 20 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.378+22892delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961174
|
CTTTTTTT others(1): Show |
C | 12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+22885_378+2289 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145961174 | |||||
| chr5:145961354
|
C | G | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+23048C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961354 | ||||||
| chr5:145961509
|
G | A | 1 | a0002c0002t0001g0156 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.378+23203G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961509 | ||||||
| chr5:145961545
|
C | T | 102 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.378+23239C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961545 | ||||||
| chr5:145961790
|
T | C | 27 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0022others(24): Show | 28 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.378+23484T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961790 | ||||||
| chr5:145961809
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+23503G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145961809 | ||||||
| chr5:145962030
|
C | T | 16 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(13): Show | 16 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.378+23724C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962030 | ||||||
| chr5:145962308
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.378+24002C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962308 | ||||||
| chr5:145962385
|
A | G | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+24079A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962385 | ||||||
| chr5:145962416
|
T | G | 1 | a0003c0003t0001g0230 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.378+24110T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962416 | ||||||
| chr5:145962477
|
G | A | 1 | a0004c0006t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.378+24171G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962477 | ||||||
| chr5:145962529
|
T | C | 102 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.378+24223T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962529 | ||||||
| chr5:145962656
|
C | T | 1 | a0001c0010t0001g0257 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.378+24350C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962656 | ||||||
| chr5:145962712
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.378+24406A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962712 | ||||||
| chr5:145962768
|
A | C | 102 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.378+24462A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962768 | ||||||
| chr5:145962770
|
C | T | 1 | a0003c0003t0001g0068 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.378+24464C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962770 | ||||||
| chr5:145962862
|
T | C | 2 | a0001c0001t0002g0201a0003c0003t0001g0146 | 2 | HG01978.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.378+24556T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962862 | ||||||
| chr5:145962888
|
C | CT | 25 | a0001c0001t0001g0076a0001c0001t0002g0052a0001c0001t0002g0110others(22): Show | 25 | HG00741.hp1 HG01106.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.378+24608dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145962888 | |||||
| chr5:145962888
|
C | CTT | 25 | a0001c0001t0001g0074a0001c0001t0001g0082a0001c0001t0001g0088others(22): Show | 25 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.378+24607_378+2460 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145962888 | |||||
| chr5:145962888
|
CT | C | 69 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0053others(66): Show | 69 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.378+24608delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145962888 | |||||
| chr5:145962888
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.378+24594_378+2460 others(19): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145962888 | |||||
| chr5:145962940
|
C | G | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+24634C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145962940 | ||||||
| chr5:145963236
|
CTGGATGA others(9): Show |
C | 1 | a0002c0002t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.378+24937_378+2495 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963236 | |||||
| chr5:145963243
|
A | AATGG | 17 | a0001c0001t0002g0056a0001c0001t0002g0117a0001c0001t0002g0118others(14): Show | 17 | HG00735.hp2 HG01069.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.378+24980_378+2498 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963243 | |||||
| chr5:145963243
|
A | AATGGATG others(1): Show |
2 | a0001c0010t0002g0270a0004c0008t0001g0267 | 2 | HG02895.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.378+24976_378+2498 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963243 | |||||
| chr5:145963243
|
AATGG | A | 52 | a0001c0001t0001g0076a0001c0001t0002g0058a0001c0001t0002g0149others(49): Show | 52 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.378+24980_378+2498 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963243 | |||||
| chr5:145963243
|
AATGGATG others(1): Show |
A | 3 | a0002c0002t0001g0195a0005c0004t0001g0079a0007c0009t0001g0248 | 3 | HG02055.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.378+24976_378+2498 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963243 | |||||
| chr5:145963243
|
AATGGATG others(5): Show |
A | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+24972_378+2498 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963243 | |||||
| chr5:145963282
|
GGATGGAT others(1): Show |
G | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(1): Show | 4 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+24977_378+2498 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963282 | ||||||
| chr5:145963286
|
GGATT | G | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(7): Show | 10 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+24981_378+2498 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963286 | ||||||
| chr5:145963290
|
T | G | 17 | a0001c0001t0001g0082a0001c0001t0001g0098a0001c0001t0001g0100others(14): Show | 17 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.378+24984T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963290 | ||||||
| chr5:145963362
|
G | C | 1 | a0002c0002t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.378+25056G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963362 | ||||||
| chr5:145963565
|
T | C | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.378+25259T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963565 | ||||||
| chr5:145963575
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.378+25269A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963575 | ||||||
| chr5:145963632
|
A | C | 1 | a0001c0001t0002g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.378+25326A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963632 | ||||||
| chr5:145963658
|
C | T | 25 | a0002c0002t0001g0001a0002c0002t0001g0022a0002c0002t0001g0023others(22): Show | 26 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.378+25352C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963658 | ||||||
| chr5:145963688
|
C | G | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+25382C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963688 | ||||||
| chr5:145963829
|
G | GT | 13 | a0001c0001t0002g0017a0001c0001t0002g0132a0001c0001t0002g0133others(10): Show | 13 | HG00639.hp2 HG02451.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.378+25537dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963829 | |||||
| chr5:145963829
|
GT | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0206others(12): Show | 15 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+25537delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145963829 | |||||
| chr5:145963892
|
C | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+25586C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963892 | ||||||
| chr5:145963918
|
C | T | 8 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(5): Show | 8 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+25612C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963918 | ||||||
| chr5:145963958
|
C | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+25652C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963958 | ||||||
| chr5:145963977
|
C | G | 3 | a0002c0002t0001g0200a0003c0003t0001g0029a0003c0003t0001g0246 | 3 | HG00140.hp1 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.378+25671C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963977 | ||||||
| chr5:145963977
|
C | T | 9 | a0003c0003t0001g0006a0003c0003t0001g0034a0003c0003t0001g0035others(6): Show | 9 | HG01070.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+25671C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145963977 | ||||||
| chr5:145964128
|
G | A | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+25822G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964128 | ||||||
| chr5:145964136
|
C | T | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+25830C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964136 | ||||||
| chr5:145964145
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.378+25839C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964145 | ||||||
| chr5:145964188
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.378+25882C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964188 | ||||||
| chr5:145964191
|
C | A | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+25885C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964191 | ||||||
| chr5:145964221
|
CTTCT | C | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+25922_378+2592 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964221 | |||||
| chr5:145964233
|
C | G | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+25927C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964233 | ||||||
| chr5:145964266
|
C | G | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+25960C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964266 | ||||||
| chr5:145964272
|
T | TTTCC | 83 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0017others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.378+25997_378+2600 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964272 | |||||
| chr5:145964272
|
TTTCC | T | 5 | a0001c0001t0001g0208a0001c0001t0002g0058a0001c0001t0002g0158others(2): Show | 5 | HG00408.hp1 HG01167.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+25997_378+2600 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964272 | |||||
| chr5:145964299
|
C | T | 6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+25993C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964299 | ||||||
| chr5:145964303
|
C | CCTTCCTT others(1): Show |
3 | a0001c0001t0002g0110a0002c0002t0001g0233a0003c0003t0001g0217 | 3 | HG02165.hp1 HG02523.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.378+26000_378+2600 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964303 | |||||
| chr5:145964303
|
C | CCTTT | 43 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(40): Show | 43 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.378+26006_378+2600 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964303 | |||||
| chr5:145964303
|
C | T | 35 | a0001c0001t0001g0073a0001c0001t0001g0100a0001c0001t0001g0101others(32): Show | 35 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.378+25997C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964303 | ||||||
| chr5:145964307
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0265a0001c0001t0002g0054others(6): Show | 9 | HG02056.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+26001T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964307 | ||||||
| chr5:145964308
|
CTTTCT | C | 6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+26006_378+2601 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964308 | |||||
| chr5:145964312
|
C | CTTTCTT | 9 | a0003c0003t0001g0006a0003c0003t0001g0034a0003c0003t0001g0035others(6): Show | 9 | HG01070.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+26009_378+2601 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964312 | |||||
| chr5:145964312
|
C | CTTTCTTT others(3): Show |
1 | a0003c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.378+26009_378+2601 others(14): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964312 | |||||
| chr5:145964312
|
CT | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+26020delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964312 | |||||
| chr5:145964313
|
T | TTTC | 12 | a0001c0001t0001g0074a0001c0001t0001g0082a0001c0001t0001g0088others(9): Show | 12 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.378+26009_378+2601 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145964313 | |||||
| chr5:145964336
|
T | C | 1 | a0002c0002t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.378+26030T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964336 | ||||||
| chr5:145964340
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.378+26034T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964340 | ||||||
| chr5:145964463
|
C | A | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+26157C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964463 | ||||||
| chr5:145964464
|
G | A | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.378+26158G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145964464 | ||||||
| chr5:145965161
|
C | T | 1 | a0002c0022t0005g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+26855C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965161 | ||||||
| chr5:145965173
|
A | G | 2 | a0001c0005t0001g0210a0001c0005t0001g0211 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.378+26867A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965173 | ||||||
| chr5:145965212
|
G | A | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+26906G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965212 | ||||||
| chr5:145965282
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.378+26976C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965282 | ||||||
| chr5:145965297
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+26991A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965297 | ||||||
| chr5:145965357
|
G | T | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+27051G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965357 | ||||||
| chr5:145965458
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.378+27152C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965458 | ||||||
| chr5:145965621
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+27315G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965621 | ||||||
| chr5:145965629
|
T | C | 1 | a0001c0005t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.378+27323T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965629 | ||||||
| chr5:145965710
|
G | C | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.378+27404G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965710 | ||||||
| chr5:145965767
|
T | C | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.378+27461T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965767 | ||||||
| chr5:145965783
|
A | T | 1 | a0004c0006t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.378+27477A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145965783 | ||||||
| chr5:145966288
|
A | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+27982A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966288 | ||||||
| chr5:145966411
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.378+28105A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966411 | ||||||
| chr5:145966476
|
A | ATTG | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+28176_378+2817 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145966476 | |||||
| chr5:145966668
|
A | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+28362A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966668 | ||||||
| chr5:145966685
|
G | T | 1 | a0003c0003t0006g0241 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.378+28379G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966685 | ||||||
| chr5:145966748
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+28442G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966748 | ||||||
| chr5:145966754
|
A | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+28448A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966754 | ||||||
| chr5:145966776
|
T | C | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+28470T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966776 | ||||||
| chr5:145966790
|
A | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+28484A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966790 | ||||||
| chr5:145966978
|
A | G | 50 | a0002c0002t0001g0226a0002c0002t0001g0229a0002c0002t0001g0233others(47): Show | 50 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.378+28672A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145966978 | ||||||
| chr5:145967188
|
C | T | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+28882C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967188 | ||||||
| chr5:145967395
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.378+29089G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967395 | ||||||
| chr5:145967623
|
C | T | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.378+29317C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967623 | ||||||
| chr5:145967654
|
T | C | 2 | a0005c0004t0001g0079a0005c0004t0001g0103 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.378+29348T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967654 | ||||||
| chr5:145967762
|
T | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+29456T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967762 | ||||||
| chr5:145967820
|
C | T | 3 | a0002c0002t0001g0200a0003c0003t0001g0029a0003c0003t0001g0246 | 3 | HG00140.hp1 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.378+29514C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967820 | ||||||
| chr5:145967880
|
A | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29574A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967880 | ||||||
| chr5:145967903
|
A | T | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(1): Show | 4 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+29597A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967903 | ||||||
| chr5:145967952
|
G | T | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.378+29646G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967952 | ||||||
| chr5:145967963
|
C | T | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29657C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967963 | ||||||
| chr5:145967986
|
G | GTTAT | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29680_378+2968 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967986 | ||||||
| chr5:145967987
|
A | T | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29681A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145967987 | ||||||
| chr5:145968046
|
GATATTTG others(7): Show |
G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29758_378+2977 others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145968046 | |||||
| chr5:145968120
|
G | A | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29814G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145968120 | ||||||
| chr5:145968183
|
T | C | 1 | a0002c0022t0005g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+29877T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145968183 | ||||||
| chr5:145968295
|
C | T | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+29989C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145968295 | ||||||
| chr5:145968331
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.378+30025T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145968331 | ||||||
| chr5:145968345
|
G | A | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+30039G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145968345 | ||||||
| chr5:145968402
|
A | G | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+30096A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145968402 | ||||||
| chr5:145969139
|
A | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+30833A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969139 | ||||||
| chr5:145969296
|
T | C | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.379-30762T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969296 | ||||||
| chr5:145969317
|
C | G | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.379-30741C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969317 | ||||||
| chr5:145969365
|
G | A | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-30693G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969365 | ||||||
| chr5:145969460
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.379-30598C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969460 | ||||||
| chr5:145969463
|
T | C | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(27): Show | 30 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.379-30595T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969463 | ||||||
| chr5:145969606
|
G | A | 100 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(97): Show | 100 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.379-30452G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969606 | ||||||
| chr5:145969705
|
A | G | 1 | a0002c0002t0001g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.379-30353A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969705 | ||||||
| chr5:145969787
|
G | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-30271G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969787 | ||||||
| chr5:145969817
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.379-30241C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969817 | ||||||
| chr5:145969896
|
T | C | 32 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(29): Show | 32 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.379-30162T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145969896 | ||||||
| chr5:145970002
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.379-30056G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970002 | ||||||
| chr5:145970008
|
A | G | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-30050A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970008 | ||||||
| chr5:145970126
|
A | AT | 11 | a0001c0001t0002g0104a0001c0001t0002g0164a0001c0001t0002g0165others(8): Show | 11 | HG00438.hp1 HG00438.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-29922dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145970126 | |||||
| chr5:145970160
|
A | G | 4 | a0001c0001t0002g0104a0001c0001t0002g0179a0001c0001t0002g0180others(1): Show | 4 | NA18948.hp2 NA18978.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-29898A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970160 | ||||||
| chr5:145970170
|
A | C | 103 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.379-29888A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970170 | ||||||
| chr5:145970177
|
A | G | 18 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.379-29881A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970177 | ||||||
| chr5:145970272
|
C | T | 14 | a0001c0001t0002g0015a0001c0001t0002g0050a0001c0001t0002g0051others(11): Show | 14 | HG00280.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-29786C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970272 | ||||||
| chr5:145970280
|
C | A | 5 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-29778C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970280 | ||||||
| chr5:145970345
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0098 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.379-29713T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970345 | ||||||
| chr5:145970346
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0098 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.379-29712C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970346 | ||||||
| chr5:145970611
|
G | A | 1 | a0004c0006t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.379-29447G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970611 | ||||||
| chr5:145970799
|
CT | C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-29251delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145970799 | |||||
| chr5:145970839
|
A | G | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-29219A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145970839 | ||||||
| chr5:145971071
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-28987G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145971071 | ||||||
| chr5:145971188
|
G | T | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.379-28870G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145971188 | ||||||
| chr5:145971196
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258 | 3 | HG01167.hp2 HG01496.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.379-28862T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145971196 | ||||||
| chr5:145971558
|
T | C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-28500T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145971558 | ||||||
| chr5:145971618
|
A | T | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-28440A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145971618 | ||||||
| chr5:145971738
|
G | A | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-28320G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145971738 | ||||||
| chr5:145971871
|
A | AATG | 4 | a0002c0002t0001g0189a0002c0002t0001g0200a0005c0004t0001g0150others(1): Show | 4 | HG01361.hp1 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-28150_379-2814 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145971871 | |||||
| chr5:145971871
|
A | AATGATG | 3 | a0001c0001t0002g0016a0001c0001t0002g0119a0002c0002t0001g0012 | 3 | HG02056.hp2 NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.379-28153_379-2814 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145971871 | |||||
| chr5:145971871
|
AATG | A | 58 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0177others(55): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.379-28150_379-2814 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145971871 | |||||
| chr5:145971871
|
AATGATG | A | 18 | a0001c0001t0002g0110a0001c0005t0001g0042a0001c0005t0001g0209others(15): Show | 18 | HG01255.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.379-28153_379-2814 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145971871 | |||||
| chr5:145971871
|
AATGATGA others(2): Show |
A | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-28156_379-2814 others(13): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145971871 | |||||
| chr5:145971871
|
AATGATGA others(5): Show |
A | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.379-28159_379-2814 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145971871 | |||||
| chr5:145972140
|
G | T | 102 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(99): Show | 102 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.379-27918G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972140 | ||||||
| chr5:145972168
|
T | A | 26 | a0002c0002t0001g0001a0002c0002t0001g0022a0002c0002t0001g0023others(23): Show | 27 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.379-27890T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972168 | ||||||
| chr5:145972268
|
C | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0002t0001g0258others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-27790C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972268 | ||||||
| chr5:145972274
|
C | A | 1 | a0004c0006t0001g0152 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.379-27784C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972274 | ||||||
| chr5:145972317
|
C | T | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-27741C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972317 | ||||||
| chr5:145972445
|
G | A | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-27613G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972445 | ||||||
| chr5:145972482
|
A | C | 5 | a0006c0007t0001g0093a0006c0007t0001g0094a0006c0007t0001g0096others(2): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-27576A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972482 | ||||||
| chr5:145972544
|
C | T | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-27514C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972544 | ||||||
| chr5:145972560
|
C | T | 1 | a0002c0002t0007g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.379-27498C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972560 | ||||||
| chr5:145972737
|
A | G | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379-27321A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972737 | ||||||
| chr5:145972836
|
C | T | 34 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(31): Show | 34 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.379-27222C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972836 | ||||||
| chr5:145972840
|
C | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-27218C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972840 | ||||||
| chr5:145972873
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.379-27185G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972873 | ||||||
| chr5:145972927
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.379-27131T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145972927 | ||||||
| chr5:145973086
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.379-26972G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973086 | ||||||
| chr5:145973286
|
C | T | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379-26772C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973286 | ||||||
| chr5:145973309
|
A | G | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-26749A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973309 | ||||||
| chr5:145973458
|
T | C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-26600T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973458 | ||||||
| chr5:145973788
|
A | G | 34 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(31): Show | 34 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.379-26270A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973788 | ||||||
| chr5:145973882
|
A | G | 1 | a0002c0002t0001g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379-26176A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973882 | ||||||
| chr5:145973903
|
T | C | 2 | a0006c0007t0001g0093a0006c0007t0001g0094 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.379-26155T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145973903 | ||||||
| chr5:145974017
|
A | G | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-26041A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974017 | ||||||
| chr5:145974021
|
G | A | 10 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(7): Show | 10 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.379-26037G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974021 | ||||||
| chr5:145974159
|
A | C | 1 | a0003c0003t0001g0006 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379-25899A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974159 | ||||||
| chr5:145974328
|
G | T | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-25730G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974328 | ||||||
| chr5:145974393
|
C | T | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-25665C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974393 | ||||||
| chr5:145974457
|
A | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-25601A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974457 | ||||||
| chr5:145974458
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.379-25600G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974458 | ||||||
| chr5:145974507
|
G | A | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379-25551G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974507 | ||||||
| chr5:145974635
|
G | C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-25423G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974635 | ||||||
| chr5:145974855
|
C | T | 1 | a0002c0002t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.379-25203C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974855 | ||||||
| chr5:145974910
|
G | T | 1 | a0003c0003t0001g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.379-25148G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974910 | ||||||
| chr5:145974986
|
T | C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-25072T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145974986 | ||||||
| chr5:145975050
|
A | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-25008A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145975050 | ||||||
| chr5:145975122
|
G | A | 46 | a0002c0002t0001g0229a0002c0002t0001g0233a0002c0002t0001g0236others(43): Show | 46 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.379-24936G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145975122 | ||||||
| chr5:145975262
|
A | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-24796A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145975262 | ||||||
| chr5:145975724
|
C | T | 1 | a0002c0002t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379-24334C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145975724 | ||||||
| chr5:145975726
|
C | G | 7 | a0002c0002t0001g0009a0002c0002t0001g0140a0002c0002t0001g0141others(4): Show | 7 | HG00609.hp2 HG02027.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-24332C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145975726 | ||||||
| chr5:145975792
|
T | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-24266T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145975792 | ||||||
| chr5:145976023
|
G | A | 1 | a0002c0002t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.379-24035G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976023 | ||||||
| chr5:145976121
|
C | A | 1 | a0004c0006t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.379-23937C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976121 | ||||||
| chr5:145976146
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-23912G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976146 | ||||||
| chr5:145976151
|
A | T | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-23907A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976151 | ||||||
| chr5:145976304
|
A | G | 2 | a0002c0002t0001g0004a0002c0002t0001g0005 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.379-23754A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976304 | ||||||
| chr5:145976443
|
G | GA | 29 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(26): Show | 29 | HG00280.hp1 HG01934.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.379-23602dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145976443 | |||||
| chr5:145976443
|
GA | G | 9 | a0001c0001t0002g0060a0001c0001t0002g0144a0001c0001t0002g0179others(6): Show | 9 | HG01255.hp2 HG02738.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-23602delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145976443 | |||||
| chr5:145976448
|
A | T | 1 | a0009c0027t0001g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.379-23610A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976448 | ||||||
| chr5:145976479
|
C | T | 137 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(134): Show | 138 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.379-23579C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976479 | ||||||
| chr5:145976524
|
C | T | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-23534C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976524 | ||||||
| chr5:145976611
|
G | A | 2 | a0007c0009t0001g0250a0007c0009t0001g0251 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.379-23447G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976611 | ||||||
| chr5:145976622
|
C | T | 1 | a0003c0003t0001g0243 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.379-23436C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976622 | ||||||
| chr5:145976627
|
G | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(1): Show | 4 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-23431G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976627 | ||||||
| chr5:145976640
|
G | T | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-23418G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976640 | ||||||
| chr5:145976714
|
T | C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-23344T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976714 | ||||||
| chr5:145976720
|
C | T | 2 | a0005c0004t0002g0204a0005c0004t0002g0205 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.379-23338C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976720 | ||||||
| chr5:145976784
|
A | G | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-23274A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976784 | ||||||
| chr5:145976884
|
T | C | 1 | a0002c0002t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.379-23174T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976884 | ||||||
| chr5:145976963
|
C | A | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-23095C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145976963 | ||||||
| chr5:145977091
|
G | A | 11 | a0001c0001t0002g0040a0001c0001t0002g0117a0001c0001t0002g0118others(8): Show | 11 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-22967G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977091 | ||||||
| chr5:145977111
|
G | A | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.379-22947G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977111 | ||||||
| chr5:145977179
|
T | A | 31 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(28): Show | 31 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.379-22879T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977179 | ||||||
| chr5:145977188
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.379-22870C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977188 | ||||||
| chr5:145977219
|
G | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0007c0009t0001g0248others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-22839G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977219 | ||||||
| chr5:145977242
|
C | T | 2 | a0001c0011t0001g0160a0014c0017t0001g0249 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-22816C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977242 | ||||||
| chr5:145977246
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-22812T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977246 | ||||||
| chr5:145977422
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.379-22636C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977422 | ||||||
| chr5:145977660
|
A | G | 1 | a0002c0002t0001g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.379-22398A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977660 | ||||||
| chr5:145977872
|
A | G | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.379-22186A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145977872 | ||||||
| chr5:145978339
|
C | T | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-21719C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145978339 | ||||||
| chr5:145978685
|
G | GA | 80 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.379-21360dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145978685 | |||||
| chr5:145978747
|
G | A | 2 | a0005c0004t0001g0150a0005c0004t0001g0151 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.379-21311G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145978747 | ||||||
| chr5:145978872
|
G | T | 2 | a0007c0009t0001g0250a0007c0009t0001g0251 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.379-21186G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145978872 | ||||||
| chr5:145979152
|
A | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-20906A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145979152 | ||||||
| chr5:145979263
|
G | T | 1 | a0002c0002t0001g0057 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.379-20795G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145979263 | ||||||
| chr5:145979687
|
C | T | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379-20371C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145979687 | ||||||
| chr5:145979694
|
T | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-20364T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145979694 | ||||||
| chr5:145979934
|
T | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-20124T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145979934 | ||||||
| chr5:145979974
|
C | G | 1 | a0001c0001t0002g0017 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379-20084C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145979974 | ||||||
| chr5:145980010
|
C | T | 64 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.379-20048C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980010 | ||||||
| chr5:145980142
|
T | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-19916T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980142 | ||||||
| chr5:145980167
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.379-19891C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980167 | ||||||
| chr5:145980226
|
T | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-19832T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980226 | ||||||
| chr5:145980239
|
G | C | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-19819G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980239 | ||||||
| chr5:145980243
|
C | A | 7 | a0002c0002t0001g0236a0003c0003t0001g0062a0003c0003t0001g0109others(4): Show | 7 | HG00280.hp2 HG02135.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-19815C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980243 | ||||||
| chr5:145980356
|
A | AT | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-19695dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145980356 | |||||
| chr5:145980450
|
C | G | 1 | a0004c0006t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.379-19608C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980450 | ||||||
| chr5:145980463
|
CACAGTAG others(5): Show |
C | 1 | a0001c0001t0002g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.379-19594_379-1958 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980463 | ||||||
| chr5:145980713
|
G | A | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379-19345G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145980713 | ||||||
| chr5:145981194
|
A | G | 1 | a0002c0002t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.379-18864A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981194 | ||||||
| chr5:145981350
|
G | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-18708G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981350 | ||||||
| chr5:145981400
|
G | A | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.379-18658G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981400 | ||||||
| chr5:145981519
|
C | G | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.379-18539C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981519 | ||||||
| chr5:145981809
|
T | C | 64 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.379-18249T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981809 | ||||||
| chr5:145981830
|
T | C | 1 | a0002c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.379-18228T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981830 | ||||||
| chr5:145981924
|
T | G | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254others(1): Show | 4 | HG03098.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-18134T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981924 | ||||||
| chr5:145981936
|
A | G | 108 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(105): Show | 108 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.379-18122A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145981936 | ||||||
| chr5:145982054
|
C | T | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-18004C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145982054 | ||||||
| chr5:145982301
|
C | T | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-17757C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145982301 | ||||||
| chr5:145982315
|
C | T | 2 | a0002c0002t0001g0043a0003c0003t0001g0044 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.379-17743C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145982315 | ||||||
| chr5:145982556
|
G | A | 1 | a0006c0007t0001g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.379-17502G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145982556 | ||||||
| chr5:145983092
|
G | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379-16966G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145983092 | ||||||
| chr5:145983207
|
A | C | 64 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.379-16851A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145983207 | ||||||
| chr5:145983247
|
C | CT | 11 | a0001c0001t0002g0127a0001c0001t0002g0133a0001c0001t0002g0134others(8): Show | 11 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-16794dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145983247 | |||||
| chr5:145983247
|
CT | C | 93 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(90): Show | 93 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.379-16794delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145983247 | |||||
| chr5:145983247
|
CTT | C | 5 | a0001c0005t0001g0213a0004c0006t0001g0139a0007c0009t0001g0250others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-16795_379-1679 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145983247 | |||||
| chr5:145983299
|
C | T | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-16759C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145983299 | ||||||
| chr5:145983300
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.379-16758G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145983300 | ||||||
| chr5:145983982
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.379-16076G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145983982 | ||||||
| chr5:145984068
|
T | A | 107 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.379-15990T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984068 | ||||||
| chr5:145984082
|
T | C | 1 | a0001c0014t0002g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.379-15976T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984082 | ||||||
| chr5:145984121
|
A | G | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-15937A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984121 | ||||||
| chr5:145984174
|
G | A | 1 | a0003c0003t0001g0230 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.379-15884G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984174 | ||||||
| chr5:145984296
|
A | G | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-15762A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984296 | ||||||
| chr5:145984300
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.379-15758G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984300 | ||||||
| chr5:145984420
|
T | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-15638T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984420 | ||||||
| chr5:145984441
|
A | G | 64 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.379-15617A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984441 | ||||||
| chr5:145984675
|
G | A | 1 | a0004c0008t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.379-15383G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984675 | ||||||
| chr5:145984738
|
T | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-15320T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984738 | ||||||
| chr5:145984766
|
G | A | 49 | a0002c0002t0001g0059a0002c0002t0001g0229a0002c0002t0001g0233others(46): Show | 49 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.379-15292G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145984766 | ||||||
| chr5:145985013
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.379-15045G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985013 | ||||||
| chr5:145985028
|
T | C | 1 | a0002c0002t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.379-15030T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985028 | ||||||
| chr5:145985162
|
GA | G | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-14890delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145985162 | |||||
| chr5:145985236
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.379-14822A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985236 | ||||||
| chr5:145985273
|
A | G | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-14785A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985273 | ||||||
| chr5:145985497
|
C | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0265 | 3 | HG02976.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.379-14561C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985497 | ||||||
| chr5:145985499
|
T | G | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-14559T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985499 | ||||||
| chr5:145985560
|
T | C | 64 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.379-14498T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985560 | ||||||
| chr5:145985673
|
T | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-14385T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985673 | ||||||
| chr5:145985709
|
T | A | 106 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.379-14349T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985709 | ||||||
| chr5:145985872
|
A | C | 65 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0110others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.379-14186A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145985872 | ||||||
| chr5:145986002
|
C | CAAAT | 53 | a0001c0001t0002g0046a0001c0001t0002g0117a0001c0001t0002g0118others(50): Show | 54 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.379-14015_379-1401 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986002
|
C | CAAATAAA others(1): Show |
47 | a0001c0001t0002g0040a0001c0001t0002g0058a0001c0001t0002g0104others(44): Show | 47 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.379-14019_379-1401 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986002
|
C | CAAATAAA others(5): Show |
7 | a0003c0003t0001g0034a0003c0003t0001g0035a0003c0003t0001g0036others(4): Show | 7 | HG01070.hp1 HG01099.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-14023_379-1401 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986002
|
CAAAT | C | 72 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.379-14015_379-1401 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986002
|
CAAATAAA others(5): Show |
C | 1 | a0001c0001t0002g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.379-14023_379-1401 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986002
|
CAAATAAA others(13): Show |
C | 33 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(30): Show | 33 | HG01934.hp1 HG02109.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-14031_379-1401 others(24): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986002
|
CAAATAAA others(21): Show |
C | 2 | a0002c0002t0001g0072a0002c0002t0001g0256 | 2 | HG01255.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.379-14039_379-1401 others(32): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145986002 | |||||
| chr5:145986045
|
A | G | 32 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(29): Show | 32 | HG01255.hp2 HG01934.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.379-14013A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986045 | ||||||
| chr5:145986056
|
C | T | 1 | a0003c0003t0001g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.379-14002C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986056 | ||||||
| chr5:145986057
|
G | T | 35 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(32): Show | 35 | HG01255.hp2 HG01934.hp1 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.379-14001G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986057 | ||||||
| chr5:145986266
|
G | A | 1 | a0002c0023t0001g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.379-13792G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986266 | ||||||
| chr5:145986370
|
T | C | 96 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(93): Show | 96 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.379-13688T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986370 | ||||||
| chr5:145986389
|
T | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-13669T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986389 | ||||||
| chr5:145986481
|
T | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379-13577T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986481 | ||||||
| chr5:145986686
|
T | G | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.379-13372T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986686 | ||||||
| chr5:145986723
|
G | C | 1 | a0002c0002t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.379-13335G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986723 | ||||||
| chr5:145986832
|
C | T | 3 | a0002c0002t0001g0245a0003c0003t0001g0227a0003c0003t0001g0232 | 3 | HG01069.hp1 HG01515.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.379-13226C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986832 | ||||||
| chr5:145986844
|
T | C | 2 | a0002c0002t0001g0166a0020c0030t0001g0123 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.379-13214T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986844 | ||||||
| chr5:145986926
|
A | G | 2 | a0002c0002t0001g0080a0022c0031t0003g0007 | 2 | HG01099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.379-13132A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145986926 | ||||||
| chr5:145987222
|
G | A | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0004c0006t0001g0081others(8): Show | 11 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-12836G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987222 | ||||||
| chr5:145987280
|
G | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0007c0009t0001g0248others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-12778G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987280 | ||||||
| chr5:145987302
|
A | G | 80 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.379-12756A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987302 | ||||||
| chr5:145987309
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.379-12749C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987309 | ||||||
| chr5:145987310
|
T | C | 2 | a0005c0004t0001g0079a0005c0004t0001g0103 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.379-12748T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987310 | ||||||
| chr5:145987417
|
T | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254 | 3 | HG03098.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.379-12641T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987417 | ||||||
| chr5:145987442
|
A | G | 1 | a0019c0026t0001g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379-12616A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987442 | ||||||
| chr5:145987610
|
C | A | 48 | a0002c0002t0001g0059a0002c0002t0001g0233a0002c0002t0001g0236others(45): Show | 48 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.379-12448C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987610 | ||||||
| chr5:145987698
|
G | C | 2 | a0003c0003t0001g0029a0003c0003t0001g0246 | 2 | HG00140.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.379-12360G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987698 | ||||||
| chr5:145987729
|
CA | C | 48 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(45): Show | 48 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.379-12322delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145987729 | |||||
| chr5:145987751
|
A | C | 32 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(29): Show | 32 | HG01934.hp1 HG02145.hp1 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.379-12307A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987751 | ||||||
| chr5:145987772
|
T | C | 2 | a0002c0002t0001g0072a0002c0002t0001g0256 | 2 | HG01255.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.379-12286T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987772 | ||||||
| chr5:145987853
|
T | A | 9 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-12205T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987853 | ||||||
| chr5:145987903
|
A | G | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379-12155A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145987903 | ||||||
| chr5:145988037
|
A | T | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(16): Show | 19 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-12021A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988037 | ||||||
| chr5:145988266
|
C | A | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-11792C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988266 | ||||||
| chr5:145988266
|
C | T | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-11792C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988266 | ||||||
| chr5:145988318
|
G | A | 1 | a0018c0018t0001g0095 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.379-11740G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988318 | ||||||
| chr5:145988357
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.379-11701T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988357 | ||||||
| chr5:145988534
|
G | A | 5 | a0001c0001t0001g0206a0001c0001t0002g0083a0001c0001t0002g0084others(2): Show | 5 | HG01934.hp1 HG02559.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-11524G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988534 | ||||||
| chr5:145988955
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.379-11103G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988955 | ||||||
| chr5:145988958
|
G | A | 2 | a0003c0003t0001g0065a0003c0003t0001g0216 | 2 | NA18986.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.379-11100G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145988958 | ||||||
| chr5:145989044
|
G | A | 9 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-11014G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989044 | ||||||
| chr5:145989070
|
C | G | 8 | a0001c0001t0001g0206a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG01934.hp1 HG02559.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-10988C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989070 | ||||||
| chr5:145989092
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.379-10966C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989092 | ||||||
| chr5:145989129
|
T | C | 2 | a0002c0002t0001g0011a0002c0002t0001g0047 | 2 | HG02155.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.379-10929T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989129 | ||||||
| chr5:145989138
|
T | C | 105 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(102): Show | 105 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.379-10920T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989138 | ||||||
| chr5:145989242
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.379-10816T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989242 | ||||||
| chr5:145989462
|
T | C | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.379-10596T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989462 | ||||||
| chr5:145989466
|
G | A | 1 | a0002c0002t0001g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.379-10592G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989466 | ||||||
| chr5:145989511
|
T | A | 1 | a0019c0026t0001g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379-10547T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989511 | ||||||
| chr5:145989597
|
G | A | 9 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-10461G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989597 | ||||||
| chr5:145989734
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | NA18949.hp1 NA19063.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.379-10324G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989734 | ||||||
| chr5:145989791
|
A | AT | 46 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(43): Show | 46 | HG00280.hp2 HG00544.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.379-10266dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145989791 | |||||
| chr5:145989916
|
G | A | 11 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(8): Show | 12 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.379-10142G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989916 | ||||||
| chr5:145989955
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-10103T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989955 | ||||||
| chr5:145989960
|
A | G | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.379-10098A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145989960 | ||||||
| chr5:145990005
|
A | G | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.379-10053A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145990005 | ||||||
| chr5:145990259
|
T | C | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-9799T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145990259 | ||||||
| chr5:145990378
|
A | G | 2 | a0002c0002t0001g0043a0003c0003t0001g0044 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.379-9680A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145990378 | ||||||
| chr5:145990516
|
T | G | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-9542T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145990516 | ||||||
| chr5:145990627
|
T | G | 1 | a0002c0002t0001g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.379-9431T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145990627 | ||||||
| chr5:145991118
|
A | C | 145 | a0001c0011t0001g0071a0001c0011t0001g0160a0002c0002t0001g0001others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.379-8940A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991118 | ||||||
| chr5:145991255
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0265 | 3 | HG02976.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.379-8803C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991255 | ||||||
| chr5:145991569
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0265 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.379-8489C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991569 | ||||||
| chr5:145991629
|
G | C | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-8429G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991629 | ||||||
| chr5:145991757
|
A | G | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.379-8301A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991757 | ||||||
| chr5:145991780
|
A | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0265 | 3 | HG02976.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.379-8278A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991780 | ||||||
| chr5:145991827
|
G | T | 1 | a0002c0002t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.379-8231G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145991827 | ||||||
| chr5:145992200
|
C | T | 1 | a0005c0004t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.379-7858C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992200 | ||||||
| chr5:145992217
|
C | A | 145 | a0001c0011t0001g0071a0001c0011t0001g0160a0002c0002t0001g0001others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.379-7841C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992217 | ||||||
| chr5:145992230
|
C | G | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(8): Show | 11 | HG01167.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-7828C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992230 | ||||||
| chr5:145992340
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.379-7718T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992340 | ||||||
| chr5:145992476
|
T | G | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-7582T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992476 | ||||||
| chr5:145992644
|
G | C | 195 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.379-7414G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992644 | ||||||
| chr5:145992682
|
C | T | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-7376C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992682 | ||||||
| chr5:145992708
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.379-7350C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992708 | ||||||
| chr5:145992742
|
T | C | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-7316T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992742 | ||||||
| chr5:145992807
|
C | T | 1 | a0003c0003t0001g0232 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.379-7251C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992807 | ||||||
| chr5:145992986
|
C | T | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-7072C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145992986 | ||||||
| chr5:145993039
|
C | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-7019C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993039 | ||||||
| chr5:145993059
|
C | T | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-6999C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993059 | ||||||
| chr5:145993129
|
G | A | 1 | a0002c0002t0001g0247 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.379-6929G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993129 | ||||||
| chr5:145993144
|
A | C | 1 | a0002c0002t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.379-6914A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993144 | ||||||
| chr5:145993173
|
A | G | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.379-6885A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993173 | ||||||
| chr5:145993209
|
G | T | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379-6849G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993209 | ||||||
| chr5:145993352
|
G | A | 2 | a0005c0004t0002g0204a0005c0004t0002g0205 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.379-6706G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993352 | ||||||
| chr5:145993364
|
C | T | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-6694C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993364 | ||||||
| chr5:145993462
|
G | T | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.379-6596G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993462 | ||||||
| chr5:145993640
|
G | A | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-6418G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993640 | ||||||
| chr5:145993708
|
G | A | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-6350G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993708 | ||||||
| chr5:145993807
|
A | T | 145 | a0001c0011t0001g0071a0001c0011t0001g0160a0002c0002t0001g0001others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.379-6251A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993807 | ||||||
| chr5:145993926
|
A | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-6132A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145993926 | ||||||
| chr5:145994012
|
C | A | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-6046C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994012 | ||||||
| chr5:145994151
|
T | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.379-5907T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994151 | ||||||
| chr5:145994157
|
C | T | 1 | a0002c0023t0001g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.379-5901C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994157 | ||||||
| chr5:145994342
|
C | T | 6 | a0002c0002t0001g0195a0002c0002t0001g0255a0002c0002t0001g0256others(3): Show | 6 | HG01255.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-5716C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994342 | ||||||
| chr5:145994602
|
C | T | 8 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(5): Show | 9 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-5456C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994602 | ||||||
| chr5:145994608
|
T | G | 1 | a0002c0002t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.379-5450T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994608 | ||||||
| chr5:145994812
|
G | A | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.379-5246G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994812 | ||||||
| chr5:145994913
|
T | C | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-5145T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145994913 | ||||||
| chr5:145995007
|
T | TA | 5 | a0001c0001t0001g0206a0001c0011t0001g0071a0001c0011t0001g0160others(2): Show | 5 | HG00099.hp2 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-5042dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145995007 | |||||
| chr5:145995007
|
T | TAA | 140 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(137): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.379-5043_379-5042d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145995007 | |||||
| chr5:145995051
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.379-5007T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995051 | ||||||
| chr5:145995231
|
C | T | 1 | a0001c0005t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.379-4827C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995231 | ||||||
| chr5:145995232
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0158 | 2 | HG00408.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.379-4826G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995232 | ||||||
| chr5:145995250
|
G | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-4808G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995250 | ||||||
| chr5:145995272
|
C | T | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.379-4786C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995272 | ||||||
| chr5:145995300
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.379-4758A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995300 | ||||||
| chr5:145995320
|
A | G | 2 | a0003c0003t0001g0029a0003c0003t0001g0246 | 2 | HG00140.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.379-4738A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995320 | ||||||
| chr5:145995359
|
T | G | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-4699T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995359 | ||||||
| chr5:145995385
|
A | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-4673A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995385 | ||||||
| chr5:145995515
|
G | A | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-4543G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995515 | ||||||
| chr5:145995519
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.379-4539A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995519 | ||||||
| chr5:145995686
|
G | A | 1 | a0003c0003t0001g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.379-4372G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995686 | ||||||
| chr5:145995874
|
A | T | 1 | a0001c0001t0002g0180 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.379-4184A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995874 | ||||||
| chr5:145995897
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.379-4161T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995897 | ||||||
| chr5:145995991
|
C | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-4067C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145995991 | ||||||
| chr5:145996018
|
G | T | 1 | a0001c0011t0001g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.379-4040G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996018 | ||||||
| chr5:145996072
|
G | T | 1 | a0002c0002t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.379-3986G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996072 | ||||||
| chr5:145996411
|
G | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-3647G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996411 | ||||||
| chr5:145996518
|
AT | A | 147 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.379-3532delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145996518 | |||||
| chr5:145996546
|
TCTGA | T | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-3509_379-3506d others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145996546 | |||||
| chr5:145996705
|
G | A | 160 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.379-3353G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996705 | ||||||
| chr5:145996747
|
A | G | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-3311A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996747 | ||||||
| chr5:145996763
|
TA | T | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-3294delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996763 | ||||||
| chr5:145996899
|
G | A | 195 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.379-3159G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145996899 | ||||||
| chr5:145997043
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.379-3015C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997043 | ||||||
| chr5:145997194
|
C | T | 195 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.379-2864C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997194 | ||||||
| chr5:145997230
|
A | G | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379-2828A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997230 | ||||||
| chr5:145997327
|
C | G | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379-2731C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997327 | ||||||
| chr5:145997328
|
C | T | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(27): Show | 30 | HG01934.hp1 HG02145.hp1 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.379-2730C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997328 | ||||||
| chr5:145997346
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-2712G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997346 | ||||||
| chr5:145997498
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.379-2560A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997498 | ||||||
| chr5:145997573
|
T | C | 161 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-2485T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997573 | ||||||
| chr5:145997727
|
T | A | 1 | a0003c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.379-2331T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997727 | ||||||
| chr5:145997772
|
AG | A | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(16): Show | 19 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-2285delG | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997772 | ||||||
| chr5:145997821
|
G | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-2237G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997821 | ||||||
| chr5:145997860
|
T | C | 195 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.379-2198T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997860 | ||||||
| chr5:145997879
|
C | A | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(16): Show | 19 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-2179C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997879 | ||||||
| chr5:145997888
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.379-2170G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997888 | ||||||
| chr5:145997916
|
C | T | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.379-2142C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997916 | ||||||
| chr5:145997984
|
A | G | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(16): Show | 19 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-2074A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145997984 | ||||||
| chr5:145998015
|
C | T | 145 | a0001c0011t0001g0071a0001c0011t0001g0160a0002c0002t0001g0001others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.379-2043C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998015 | ||||||
| chr5:145998053
|
G | A | 1 | a0002c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.379-2005G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998053 | ||||||
| chr5:145998064
|
C | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-1994C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998064 | ||||||
| chr5:145998134
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.379-1924C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998134 | ||||||
| chr5:145998147
|
A | T | 1 | a0002c0002t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.379-1911A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998147 | ||||||
| chr5:145998281
|
T | TAA | 6 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(3): Show | 6 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1761_379-1760d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145998281 | |||||
| chr5:145998281
|
TA | T | 6 | a0001c0001t0001g0090a0001c0001t0002g0053a0001c0001t0002g0105others(3): Show | 6 | HG00733.hp1 HG01169.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1760delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145998281 | |||||
| chr5:145998281
|
TAA | T | 140 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.379-1761_379-1760d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145998281 | |||||
| chr5:145998402
|
A | G | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.379-1656A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998402 | ||||||
| chr5:145998499
|
GA | G | 162 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.379-1551delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145998499 | |||||
| chr5:145998631
|
A | G | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-1427A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998631 | ||||||
| chr5:145998731
|
T | C | 5 | a0001c0001t0002g0019a0001c0001t0002g0056a0001c0001t0002g0154others(2): Show | 5 | HG00673.hp2 NA18945.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-1327T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998731 | ||||||
| chr5:145998782
|
G | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.379-1276G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998782 | ||||||
| chr5:145998840
|
G | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379-1218G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998840 | ||||||
| chr5:145998961
|
A | G | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-1097A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145998961 | ||||||
| chr5:145999014
|
T | C | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(16): Show | 19 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-1044T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145999014 | ||||||
| chr5:145999023
|
A | AC | 141 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.379-1034dupC | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 145999023 | |||||
| chr5:145999025
|
T | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.379-1033T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145999025 | ||||||
| chr5:145999142
|
G | A | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-916G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145999142 | ||||||
| chr5:145999363
|
T | C | 1 | a0002c0002t0001g0003 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.379-695T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145999363 | ||||||
| chr5:145999696
|
C | T | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-362C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 2/9 | chr5 | 145999696 | ||||||
| chr5:146000448
|
G | A | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.648+121G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000448 | ||||||
| chr5:146000449
|
T | A | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.648+122T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000449 | ||||||
| chr5:146000451
|
A | AT | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.648+124_648+125ins others(1): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000451 | ||||||
| chr5:146000452
|
A | T | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.648+125A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000452 | ||||||
| chr5:146000490
|
C | T | 3 | a0002c0002t0001g0189a0002c0002t0001g0197a0002c0002t0001g0198 | 3 | HG01256.hp2 HG01934.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.648+163C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000490 | ||||||
| chr5:146000534
|
A | G | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.648+207A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000534 | ||||||
| chr5:146000707
|
C | T | 165 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.648+380C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000707 | ||||||
| chr5:146000898
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.648+571A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000898 | ||||||
| chr5:146000969
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.648+642G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146000969 | ||||||
| chr5:146001052
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.648+725G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001052 | ||||||
| chr5:146001055
|
C | T | 145 | a0001c0011t0001g0071a0001c0011t0001g0160a0002c0002t0001g0001others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.648+728C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001055 | ||||||
| chr5:146001075
|
C | A | 3 | a0002c0002t0001g0116a0002c0002t0001g0137a0002c0002t0001g0138 | 3 | HG02486.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.648+748C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001075 | ||||||
| chr5:146001183
|
C | G | 9 | a0001c0001t0002g0104a0001c0001t0002g0164a0001c0001t0002g0165others(6): Show | 9 | HG00438.hp1 HG02132.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+856C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001183 | ||||||
| chr5:146001485
|
C | T | 1 | a0001c0005t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.648+1158C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001485 | ||||||
| chr5:146001645
|
C | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+1318C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001645 | ||||||
| chr5:146001743
|
A | G | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.648+1416A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001743 | ||||||
| chr5:146001773
|
G | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.648+1446G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001773 | ||||||
| chr5:146001893
|
A | G | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.648+1566A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001893 | ||||||
| chr5:146001996
|
C | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.648+1669C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146001996 | ||||||
| chr5:146002047
|
T | G | 26 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(23): Show | 26 | HG01167.hp2 HG01934.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.648+1720T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002047 | ||||||
| chr5:146002048
|
A | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254 | 3 | HG03098.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.648+1721A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002048 | ||||||
| chr5:146002106
|
T | C | 195 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.648+1779T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002106 | ||||||
| chr5:146002118
|
A | T | 26 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(23): Show | 26 | HG01167.hp2 HG01934.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.648+1791A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002118 | ||||||
| chr5:146002174
|
G | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.648+1847G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002174 | ||||||
| chr5:146002271
|
C | A | 1 | a0003c0003t0001g0227 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.649-1787C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002271 | ||||||
| chr5:146002303
|
T | C | 1 | a0003c0003t0001g0227 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.649-1755T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002303 | ||||||
| chr5:146002320
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.649-1738G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002320 | ||||||
| chr5:146002322
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.649-1736G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002322 | ||||||
| chr5:146002380
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.649-1678G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002380 | ||||||
| chr5:146002406
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.649-1652G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002406 | ||||||
| chr5:146002415
|
C | T | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-1643C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002415 | ||||||
| chr5:146002460
|
AAAGAAAG others(26): Show |
A | 1 | a0002c0002t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.649-1594_649-1562d others(35): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002460 | |||||
| chr5:146002469
|
A | AAAGG | 36 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0100others(33): Show | 37 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.649-1523_649-1520d others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
A | AAAGGAAG others(1): Show |
24 | a0001c0001t0001g0098a0001c0001t0001g0253a0001c0001t0001g0265others(21): Show | 25 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-1527_649-1520d others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
A | AAAGGAAG others(5): Show |
7 | a0002c0002t0001g0027a0002c0002t0001g0059a0002c0002t0001g0191others(4): Show | 7 | HG02071.hp1 HG02970.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-1531_649-1520d others(14): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
A | AAAGGAAG others(13): Show |
1 | a0013c0019t0001g0033 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.649-1539_649-1520d others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
AAAGG | A | 90 | a0001c0001t0001g0090a0001c0001t0001g0207a0001c0001t0001g0208others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.649-1523_649-1520d others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
AAAGGAAG others(1): Show |
A | 40 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0263others(37): Show | 40 | HG00609.hp2 HG00735.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.649-1527_649-1520d others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
AAAGGAAG others(5): Show |
A | 9 | a0002c0002t0001g0013a0002c0002t0001g0141a0002c0002t0001g0155others(6): Show | 9 | HG00438.hp2 HG00673.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.649-1531_649-1520d others(14): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
AAAGGAAG others(9): Show |
A | 7 | a0001c0001t0002g0015a0001c0005t0001g0212a0001c0005t0001g0213others(4): Show | 7 | HG00621.hp1 HG01346.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-1535_649-1520d others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
AAAGGAAG others(13): Show |
A | 5 | a0001c0001t0002g0136a0001c0011t0001g0071a0002c0002t0001g0003others(2): Show | 5 | HG00140.hp2 HG02809.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-1539_649-1520d others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002469
|
AAAGGAAG others(21): Show |
A | 1 | a0001c0001t0002g0086 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.649-1547_649-1520d others(30): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 146002469 | |||||
| chr5:146002529
|
G | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.649-1529G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002529 | ||||||
| chr5:146002535
|
A | G | 3 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0267 | 3 | HG02486.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.649-1523A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002535 | ||||||
| chr5:146002586
|
A | G | 4 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-1472A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146002586 | ||||||
| chr5:146003178
|
T | A | 1 | a0001c0001t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.649-880T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146003178 | ||||||
| chr5:146003721
|
T | G | 1 | a0001c0001t0002g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.649-337T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 3/9 | chr5 | 146003721 | ||||||
| chr5:146004158
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.744+5G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004158 | ||||||
| chr5:146004291
|
G | T | 1 | a0005c0004t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.744+138G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004291 | ||||||
| chr5:146004504
|
A | G | 2 | a0002c0002t0001g0177a0003c0003t0001g0055 | 2 | NA18991.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.744+351A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004504 | ||||||
| chr5:146004562
|
A | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0254 | 3 | HG03098.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.744+409A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004562 | ||||||
| chr5:146004572
|
A | G | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.744+419A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004572 | ||||||
| chr5:146004632
|
A | G | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+479A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004632 | ||||||
| chr5:146004654
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.744+501T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004654 | ||||||
| chr5:146004655
|
ATATGGAG others(9): Show |
A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744+518_744+533del others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 146004655 | |||||
| chr5:146004671
|
TTATGGAG others(5): Show |
T | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.744+534_744+545del others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 146004671 | |||||
| chr5:146004738
|
A | C | 1 | a0002c0002t0001g0156 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.744+585A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004738 | ||||||
| chr5:146004779
|
T | G | 1 | a0003c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+626T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004779 | ||||||
| chr5:146004782
|
G | C | 1 | a0003c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+629G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004782 | ||||||
| chr5:146004790
|
A | C | 1 | a0003c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+637A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004790 | ||||||
| chr5:146004793
|
G | T | 1 | a0003c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+640G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004793 | ||||||
| chr5:146004794
|
T | A | 1 | a0003c0003t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+641T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004794 | ||||||
| chr5:146004961
|
G | A | 195 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.744+808G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146004961 | ||||||
| chr5:146005155
|
A | G | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1002A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005155 | ||||||
| chr5:146005174
|
A | G | 1 | a0003c0003t0001g0038 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.744+1021A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005174 | ||||||
| chr5:146005333
|
T | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744+1180T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005333 | ||||||
| chr5:146005393
|
C | T | 2 | a0002c0002t0001g0087a0002c0002t0001g0258 | 2 | HG01496.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.744+1240C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005393 | ||||||
| chr5:146005854
|
T | A | 1 | a0003c0003t0001g0216 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.744+1701T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005854 | ||||||
| chr5:146005854
|
T | TA | 152 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0252others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.744+1718dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 146005854 | |||||
| chr5:146005854
|
T | TAA | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.744+1717_744+1718d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 146005854 | |||||
| chr5:146005855
|
A | T | 1 | a0001c0001t0002g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.744+1702A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005855 | ||||||
| chr5:146005871
|
A | AG | 4 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+1719dupG | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 146005871 | |||||
| chr5:146005875
|
T | C | 1 | a0005c0004t0002g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.744+1722T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005875 | ||||||
| chr5:146005892
|
G | A | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.744+1739G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005892 | ||||||
| chr5:146005937
|
T | A | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.744+1784T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005937 | ||||||
| chr5:146005942
|
A | G | 143 | a0001c0001t0002g0133a0002c0002t0001g0001a0002c0002t0001g0002others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.744+1789A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146005942 | ||||||
| chr5:146006095
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.744+1942A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006095 | ||||||
| chr5:146006118
|
G | A | 1 | a0002c0002t0001g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.744+1965G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006118 | ||||||
| chr5:146006321
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.744+2168T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006321 | ||||||
| chr5:146006335
|
G | C | 165 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0133others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.744+2182G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006335 | ||||||
| chr5:146006351
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.744+2198G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006351 | ||||||
| chr5:146006366
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.744+2213A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006366 | ||||||
| chr5:146006387
|
C | A | 2 | a0005c0004t0001g0079a0005c0004t0001g0103 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.744+2234C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006387 | ||||||
| chr5:146006492
|
G | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.744+2339G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006492 | ||||||
| chr5:146006575
|
T | G | 165 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0133others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.744+2422T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146006575 | ||||||
| chr5:146007002
|
C | T | 1 | a0002c0002t0001g0191 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.744+2849C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007002 | ||||||
| chr5:146007034
|
C | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744+2881C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007034 | ||||||
| chr5:146007082
|
A | G | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.744+2929A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007082 | ||||||
| chr5:146007182
|
C | G | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0004c0008t0001g0077others(4): Show | 7 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+3029C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007182 | ||||||
| chr5:146007273
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.744+3120C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007273 | ||||||
| chr5:146007361
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.744+3208G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007361 | ||||||
| chr5:146007445
|
T | C | 196 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.744+3292T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007445 | ||||||
| chr5:146007691
|
G | C | 196 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.744+3538G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007691 | ||||||
| chr5:146007756
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.744+3603C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007756 | ||||||
| chr5:146007937
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.744+3784T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146007937 | ||||||
| chr5:146008281
|
G | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744+4128G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008281 | ||||||
| chr5:146008283
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0098 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.744+4130C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008283 | ||||||
| chr5:146008388
|
A | T | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(27): Show | 30 | HG01934.hp1 HG02145.hp1 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.744+4235A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008388 | ||||||
| chr5:146008446
|
C | T | 1 | a0004c0006t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.744+4293C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008446 | ||||||
| chr5:146008601
|
G | T | 141 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.744+4448G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008601 | ||||||
| chr5:146008617
|
C | T | 15 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(12): Show | 15 | HG02451.hp1 HG02486.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+4464C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008617 | ||||||
| chr5:146008720
|
C | A | 6 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(3): Show | 6 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.744+4567C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008720 | ||||||
| chr5:146008932
|
G | A | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+4779G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146008932 | ||||||
| chr5:146009134
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-4613A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009134 | ||||||
| chr5:146009330
|
C | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.745-4417C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009330 | ||||||
| chr5:146009437
|
C | A | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-4310C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009437 | ||||||
| chr5:146009500
|
C | G | 9 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.745-4247C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009500 | ||||||
| chr5:146009563
|
T | C | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.745-4184T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009563 | ||||||
| chr5:146009568
|
C | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.745-4179C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009568 | ||||||
| chr5:146009863
|
T | C | 1 | a0002c0002t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.745-3884T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009863 | ||||||
| chr5:146009923
|
C | A | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(27): Show | 30 | HG01934.hp1 HG02145.hp1 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.745-3824C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146009923 | ||||||
| chr5:146010013
|
T | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.745-3734T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010013 | ||||||
| chr5:146010124
|
C | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0056a0001c0001t0002g0154others(2): Show | 5 | HG00673.hp2 NA18945.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-3623C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010124 | ||||||
| chr5:146010148
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.745-3599G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010148 | ||||||
| chr5:146010283
|
G | A | 4 | a0003c0003t0001g0146a0003c0003t0001g0222a0003c0003t0004g0220others(1): Show | 4 | HG01257.hp1 HG01952.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3464G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010283 | ||||||
| chr5:146010292
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0265 | 3 | HG02976.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.745-3455G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010292 | ||||||
| chr5:146010384
|
T | G | 1 | a0002c0002t0001g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.745-3363T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010384 | ||||||
| chr5:146010405
|
G | T | 1 | a0002c0002t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.745-3342G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010405 | ||||||
| chr5:146010422
|
T | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.745-3325T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010422 | ||||||
| chr5:146010429
|
T | A | 8 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(5): Show | 9 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.745-3318T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010429 | ||||||
| chr5:146010486
|
G | C | 30 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(27): Show | 30 | HG01934.hp1 HG02145.hp1 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.745-3261G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010486 | ||||||
| chr5:146010577
|
G | T | 1 | a0001c0001t0002g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.745-3170G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010577 | ||||||
| chr5:146010626
|
C | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0154 | 2 | NA18945.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.745-3121C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010626 | ||||||
| chr5:146010692
|
C | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.745-3055C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010692 | ||||||
| chr5:146010707
|
C | A | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.745-3040C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010707 | ||||||
| chr5:146010712
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-3035T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010712 | ||||||
| chr5:146010833
|
T | G | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.745-2914T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010833 | ||||||
| chr5:146010843
|
G | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.745-2904G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010843 | ||||||
| chr5:146010906
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.745-2841G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010906 | ||||||
| chr5:146010934
|
A | T | 196 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.745-2813A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010934 | ||||||
| chr5:146010948
|
C | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.745-2799C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010948 | ||||||
| chr5:146010960
|
G | T | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.745-2787G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010960 | ||||||
| chr5:146010962
|
T | C | 1 | a0001c0001t0002g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.745-2785T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146010962 | ||||||
| chr5:146011122
|
T | A | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.745-2625T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011122 | ||||||
| chr5:146011140
|
G | C | 5 | a0003c0003t0001g0008a0003c0003t0001g0107a0007c0009t0001g0248others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-2607G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011140 | ||||||
| chr5:146011205
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-2542C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011205 | ||||||
| chr5:146011219
|
G | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.745-2528G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011219 | ||||||
| chr5:146011237
|
A | G | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.745-2510A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011237 | ||||||
| chr5:146011297
|
T | A | 1 | a0003c0003t0001g0222 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.745-2450T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011297 | ||||||
| chr5:146011312
|
G | T | 1 | a0001c0010t0002g0270 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.745-2435G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011312 | ||||||
| chr5:146011399
|
T | A | 1 | a0002c0002t0001g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.745-2348T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011399 | ||||||
| chr5:146011480
|
G | A | 11 | a0002c0002t0001g0001a0002c0002t0001g0023a0002c0002t0001g0024others(8): Show | 12 | HG00609.hp1 HG00621.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.745-2267G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011480 | ||||||
| chr5:146011564
|
G | A | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-2183G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011564 | ||||||
| chr5:146011608
|
T | C | 1 | a0003c0003t0001g0020 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.745-2139T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011608 | ||||||
| chr5:146011659
|
G | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.745-2088G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011659 | ||||||
| chr5:146011841
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.745-1906C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011841 | ||||||
| chr5:146011884
|
C | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.745-1863C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011884 | ||||||
| chr5:146011889
|
T | C | 1 | a0002c0002t0001g0003 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.745-1858T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146011889 | ||||||
| chr5:146012050
|
G | A | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.745-1697G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012050 | ||||||
| chr5:146012090
|
AG | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.745-1654delG | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 146012090 | |||||
| chr5:146012383
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.745-1364G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012383 | ||||||
| chr5:146012384
|
A | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.745-1363A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012384 | ||||||
| chr5:146012420
|
A | G | 1 | a0003c0003t0001g0243 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.745-1327A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012420 | ||||||
| chr5:146012752
|
T | C | 165 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.745-995T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012752 | ||||||
| chr5:146012784
|
C | T | 196 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.745-963C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012784 | ||||||
| chr5:146012884
|
T | C | 165 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0005t0001g0042others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.745-863T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146012884 | ||||||
| chr5:146013039
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-708T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146013039 | ||||||
| chr5:146013049
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.745-698A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146013049 | ||||||
| chr5:146013172
|
C | T | 196 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.745-575C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146013172 | ||||||
| chr5:146013519
|
G | C | 1 | a0001c0001t0002g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.745-228G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 4/9 | chr5 | 146013519 | ||||||
| chr5:146014111
|
T | C | 6 | a0001c0005t0001g0042a0001c0005t0001g0209a0001c0005t0001g0210others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+50T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146014111 | ||||||
| chr5:146014118
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1059+57C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146014118 | ||||||
| chr5:146014356
|
T | C | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1059+295T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146014356 | ||||||
| chr5:146014394
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1059+333C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146014394 | ||||||
| chr5:146014708
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0265 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1059+647C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146014708 | ||||||
| chr5:146014837
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+776A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146014837 | ||||||
| chr5:146015313
|
C | T | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1059+1252C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146015313 | ||||||
| chr5:146015696
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0265 | 3 | HG02976.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1059+1635G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146015696 | ||||||
| chr5:146015749
|
A | C | 8 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1059+1688A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146015749 | ||||||
| chr5:146015792
|
C | T | 8 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1059+1731C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146015792 | ||||||
| chr5:146015805
|
T | A | 73 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059+1744T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146015805 | ||||||
| chr5:146015861
|
A | G | 2 | a0006c0025t0001g0259a0015c0012t0001g0202 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+1800A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146015861 | ||||||
| chr5:146016041
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1059+1980C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016041 | ||||||
| chr5:146016120
|
G | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1059+2059G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016120 | ||||||
| chr5:146016249
|
T | C | 1 | a0002c0002t0001g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1059+2188T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016249 | ||||||
| chr5:146016326
|
G | A | 3 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0247 | 3 | HG01175.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1059+2265G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016326 | ||||||
| chr5:146016354
|
A | AGATG | 62 | a0001c0001t0002g0015a0001c0001t0002g0054a0001c0001t0002g0056others(59): Show | 63 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+2341_1059+234 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146016354 | |||||
| chr5:146016354
|
A | AGATGGAT others(1): Show |
14 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0046others(11): Show | 14 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+2337_1059+234 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146016354 | |||||
| chr5:146016354
|
A | AGATGGAT others(5): Show |
2 | a0001c0001t0002g0014a0001c0001t0002g0040 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1059+2333_1059+234 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146016354 | |||||
| chr5:146016354
|
AGATG | A | 63 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(60): Show | 63 | HG00280.hp2 HG00621.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+2341_1059+234 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146016354 | |||||
| chr5:146016354
|
AGATGGAT others(1): Show |
A | 13 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0252others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+2337_1059+234 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146016354 | |||||
| chr5:146016354
|
AGATGGAT others(5): Show |
A | 2 | a0002c0002t0001g0070a0004c0006t0001g0139 | 2 | HG01516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1059+2333_1059+234 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146016354 | |||||
| chr5:146016370
|
G | T | 10 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(7): Show | 10 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1059+2309G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016370 | ||||||
| chr5:146016398
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1059+2337G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016398 | ||||||
| chr5:146016402
|
G | A | 10 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(7): Show | 10 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1059+2341G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016402 | ||||||
| chr5:146016541
|
G | A | 10 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(7): Show | 10 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1059+2480G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016541 | ||||||
| chr5:146016609
|
G | A | 152 | a0001c0011t0001g0071a0001c0011t0001g0160a0002c0002t0001g0001others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1059+2548G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016609 | ||||||
| chr5:146016704
|
C | T | 157 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1059+2643C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016704 | ||||||
| chr5:146016769
|
T | C | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+2708T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016769 | ||||||
| chr5:146016784
|
T | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+2723T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016784 | ||||||
| chr5:146016989
|
T | C | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+2928T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146016989 | ||||||
| chr5:146017022
|
G | A | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+2961G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017022 | ||||||
| chr5:146017045
|
T | C | 1 | a0005c0004t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1059+2984T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017045 | ||||||
| chr5:146017139
|
G | A | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1059+3078G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017139 | ||||||
| chr5:146017373
|
G | GAA | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+3313_1059+331 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146017373 | |||||
| chr5:146017433
|
T | G | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+3372T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017433 | ||||||
| chr5:146017495
|
T | G | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+3434T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017495 | ||||||
| chr5:146017609
|
C | T | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+3548C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017609 | ||||||
| chr5:146017624
|
T | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1059+3563T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017624 | ||||||
| chr5:146017697
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1059+3636A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017697 | ||||||
| chr5:146017811
|
C | T | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+3750C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017811 | ||||||
| chr5:146017812
|
T | C | 2 | a0007c0009t0001g0250a0007c0009t0001g0251 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1059+3751T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017812 | ||||||
| chr5:146017815
|
G | T | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+3754G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017815 | ||||||
| chr5:146017816
|
C | T | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1059+3755C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017816 | ||||||
| chr5:146017896
|
T | C | 253 | a0001c0001t0001g0076a0001c0001t0001g0100a0001c0001t0001g0101others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1059+3835T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017896 | ||||||
| chr5:146017965
|
T | G | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+3904T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146017965 | ||||||
| chr5:146018125
|
G | A | 1 | a0009c0027t0001g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1059+4064G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018125 | ||||||
| chr5:146018147
|
T | C | 4 | a0001c0005t0001g0210a0001c0005t0001g0211a0001c0005t0001g0212others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+4086T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018147 | ||||||
| chr5:146018196
|
C | T | 1 | a0003c0003t0004g0220 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1059+4135C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018196 | ||||||
| chr5:146018197
|
G | A | 73 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059+4136G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018197 | ||||||
| chr5:146018223
|
A | T | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+4162A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018223 | ||||||
| chr5:146018233
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1059+4172T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018233 | ||||||
| chr5:146018342
|
T | C | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+4281T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018342 | ||||||
| chr5:146018473
|
T | G | 1 | a0001c0001t0002g0125 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1059+4412T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018473 | ||||||
| chr5:146018512
|
AC | A | 3 | a0003c0003t0001g0032a0003c0003t0001g0109a0020c0030t0001g0123 | 3 | HG02135.hp1 HG02135.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1059+4454delC | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146018512 | |||||
| chr5:146018526
|
ACAC | A | 47 | a0002c0002t0001g0200a0002c0002t0001g0239a0003c0003t0001g0006others(44): Show | 47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.1059+4469_1059+447 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146018526 | |||||
| chr5:146018528
|
AC | A | 4 | a0002c0002t0001g0236a0003c0003t0001g0032a0003c0003t0001g0109others(1): Show | 4 | HG02135.hp1 HG02135.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+4469delC | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146018528 | |||||
| chr5:146018685
|
C | T | 233 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1059+4624C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018685 | ||||||
| chr5:146018760
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1059+4699C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018760 | ||||||
| chr5:146018786
|
C | A | 233 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1059+4725C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146018786 | ||||||
| chr5:146018836
|
AG | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+4778delG | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146018836 | |||||
| chr5:146018895
|
A | AT | 233 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1059+4839dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146018895 | |||||
| chr5:146019010
|
T | C | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+4949T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019010 | ||||||
| chr5:146019095
|
G | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+5034G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019095 | ||||||
| chr5:146019128
|
A | G | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1059+5067A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019128 | ||||||
| chr5:146019170
|
C | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+5109C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019170 | ||||||
| chr5:146019241
|
C | G | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+5180C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019241 | ||||||
| chr5:146019370
|
C | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1059+5309C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019370 | ||||||
| chr5:146019374
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+5313C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019374 | ||||||
| chr5:146019517
|
G | A | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+5456G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019517 | ||||||
| chr5:146019622
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1059+5561G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019622 | ||||||
| chr5:146019655
|
C | G | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+5594C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019655 | ||||||
| chr5:146019691
|
C | T | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1059+5630C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019691 | ||||||
| chr5:146019708
|
G | A | 15 | a0002c0002t0001g0200a0003c0003t0001g0006a0003c0003t0001g0008others(12): Show | 15 | HG00140.hp1 HG01070.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+5647G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019708 | ||||||
| chr5:146019838
|
G | T | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+5777G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019838 | ||||||
| chr5:146019887
|
GTTCT | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+5829_1059+583 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146019887 | |||||
| chr5:146019930
|
G | A | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+5869G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146019930 | ||||||
| chr5:146020054
|
G | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+5993G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020054 | ||||||
| chr5:146020154
|
T | C | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+6093T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020154 | ||||||
| chr5:146020160
|
A | T | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+6099A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020160 | ||||||
| chr5:146020318
|
G | A | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+6257G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020318 | ||||||
| chr5:146020474
|
T | A | 5 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+6413T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020474 | ||||||
| chr5:146020508
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1059+6447C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020508 | ||||||
| chr5:146020522
|
A | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+6461A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020522 | ||||||
| chr5:146020555
|
G | A | 82 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1059+6494G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020555 | ||||||
| chr5:146020574
|
A | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+6513A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020574 | ||||||
| chr5:146020898
|
A | G | 250 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0206others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1059+6837A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020898 | ||||||
| chr5:146020937
|
C | A | 1 | a0002c0002t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1059+6876C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146020937 | ||||||
| chr5:146021079
|
T | C | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+7018T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146021079 | ||||||
| chr5:146021153
|
AT | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+7093delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146021153 | ||||||
| chr5:146021313
|
T | C | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+7252T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146021313 | ||||||
| chr5:146021595
|
A | T | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+7534A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146021595 | ||||||
| chr5:146021797
|
T | C | 91 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1059+7736T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146021797 | ||||||
| chr5:146021848
|
C | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+7787C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146021848 | ||||||
| chr5:146022053
|
C | A | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+7992C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022053 | ||||||
| chr5:146022078
|
G | A | 3 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0267 | 3 | HG02486.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+8017G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022078 | ||||||
| chr5:146022252
|
G | A | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+8191G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022252 | ||||||
| chr5:146022365
|
G | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+8304G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022365 | ||||||
| chr5:146022407
|
C | A | 142 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1059+8346C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022407 | ||||||
| chr5:146022603
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1059+8542G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022603 | ||||||
| chr5:146022818
|
G | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+8757G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022818 | ||||||
| chr5:146022832
|
G | A | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+8771G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022832 | ||||||
| chr5:146022835
|
G | T | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1059+8774G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022835 | ||||||
| chr5:146022869
|
A | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+8808A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022869 | ||||||
| chr5:146022873
|
AAACACAC others(6): Show |
A | 1 | a0002c0023t0001g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1059+8814_1059+882 others(17): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022873 | |||||
| chr5:146022873
|
AAACACAC others(8): Show |
A | 1 | a0003c0003t0001g0223 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1059+8814_1059+882 others(19): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022873 | |||||
| chr5:146022874
|
A | AAC | 4 | a0001c0001t0001g0101a0006c0007t0001g0093a0006c0007t0001g0094others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+8861_1059+886 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
A | AACACAC | 3 | a0001c0001t0001g0207a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+8857_1059+886 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AAC | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+8861_1059+886 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACAC | A | 13 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0208others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+8859_1059+886 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACAC | A | 10 | a0001c0001t0001g0082a0001c0001t0002g0040a0001c0001t0002g0060others(7): Show | 10 | HG00438.hp1 HG00735.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059+8857_1059+886 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACACA others(1): Show |
A | 68 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0014others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1059+8855_1059+886 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACACA others(3): Show |
A | 5 | a0001c0011t0001g0160a0004c0008t0001g0077a0004c0008t0001g0078others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+8853_1059+886 others(14): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACACA others(5): Show |
A | 17 | a0001c0005t0001g0042a0001c0011t0001g0071a0002c0002t0001g0001others(14): Show | 18 | HG01099.hp1 HG01109.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1059+8851_1059+886 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACACA others(7): Show |
A | 111 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1059+8849_1059+886 others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACACA others(9): Show |
A | 14 | a0002c0002t0001g0239a0003c0003t0001g0030a0003c0003t0001g0031others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.1059+8847_1059+886 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022874
|
AACACACA others(11): Show |
A | 1 | a0019c0026t0001g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1059+8845_1059+886 others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146022874 | |||||
| chr5:146022884
|
C | A | 1 | a0004c0008t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1059+8823C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022884 | ||||||
| chr5:146022886
|
C | A | 5 | a0001c0011t0001g0160a0004c0008t0001g0077a0004c0008t0001g0078others(2): Show | 5 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+8825C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022886 | ||||||
| chr5:146022888
|
C | A | 2 | a0001c0011t0001g0071a0014c0017t0001g0249 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+8827C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022888 | ||||||
| chr5:146022957
|
A | G | 9 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0077others(6): Show | 9 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+8896A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146022957 | ||||||
| chr5:146023066
|
T | C | 81 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1059+9005T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146023066 | ||||||
| chr5:146023229
|
G | A | 81 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1059+9168G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146023229 | ||||||
| chr5:146023270
|
A | G | 174 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1059+9209A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146023270 | ||||||
| chr5:146023424
|
G | T | 90 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1059+9363G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146023424 | ||||||
| chr5:146023456
|
G | A | 4 | a0003c0003t0001g0034a0003c0003t0001g0035a0003c0003t0001g0036others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+9395G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146023456 | ||||||
| chr5:146023663
|
T | C | 252 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0206others(249): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1059+9602T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146023663 | ||||||
| chr5:146024018
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+9957G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024018 | ||||||
| chr5:146024138
|
G | A | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+10077G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024138 | ||||||
| chr5:146024213
|
G | C | 85 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1059+10152G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024213 | ||||||
| chr5:146024367
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1059+10306G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024367 | ||||||
| chr5:146024420
|
C | T | 221 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(218): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1059+10359C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024420 | ||||||
| chr5:146024568
|
C | A | 2 | a0002c0002t0001g0193a0002c0002t0001g0264 | 2 | NA18942.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1059+10507C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024568 | ||||||
| chr5:146024753
|
G | T | 16 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1059+10692G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024753 | ||||||
| chr5:146024799
|
G | A | 5 | a0001c0001t0002g0061a0001c0001t0002g0171a0001c0001t0002g0172others(2): Show | 5 | HG00544.hp1 HG02027.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+10738G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024799 | ||||||
| chr5:146024956
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1059+10895A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024956 | ||||||
| chr5:146024980
|
G | A | 1 | a0005c0004t0002g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1059+10919G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146024980 | ||||||
| chr5:146025006
|
G | A | 8 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(5): Show | 9 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+10945G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025006 | ||||||
| chr5:146025043
|
T | C | 1 | a0004c0006t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1059+10982T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025043 | ||||||
| chr5:146025101
|
T | C | 6 | a0004c0008t0001g0077a0004c0008t0001g0078a0004c0008t0001g0159others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+11040T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025101 | ||||||
| chr5:146025383
|
A | G | 1 | a0002c0022t0005g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1059+11322A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025383 | ||||||
| chr5:146025419
|
G | C | 6 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(3): Show | 6 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+11358G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025419 | ||||||
| chr5:146025450
|
C | T | 81 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1059+11389C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025450 | ||||||
| chr5:146025518
|
G | A | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+11457G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025518 | ||||||
| chr5:146025717
|
GTTT | G | 84 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1059+11659_1059+11 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146025717 | |||||
| chr5:146025813
|
T | G | 1 | a0002c0002t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1059+11752T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025813 | ||||||
| chr5:146025867
|
A | G | 81 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1059+11806A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025867 | ||||||
| chr5:146025962
|
C | T | 81 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1059+11901C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025962 | ||||||
| chr5:146025965
|
T | A | 3 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | HG01167.hp1 HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1059+11904T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146025965 | ||||||
| chr5:146026164
|
T | A | 1 | a0001c0001t0002g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1059+12103T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026164 | ||||||
| chr5:146026213
|
T | G | 1 | a0001c0001t0002g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1059+12152T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026213 | ||||||
| chr5:146026307
|
T | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+12246T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026307 | ||||||
| chr5:146026308
|
T | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+12247T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026308 | ||||||
| chr5:146026474
|
G | C | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+12413G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026474 | ||||||
| chr5:146026490
|
C | A | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+12429C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026490 | ||||||
| chr5:146026599
|
C | G | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1059+12538C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026599 | ||||||
| chr5:146026618
|
T | G | 251 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0206others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1059+12557T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026618 | ||||||
| chr5:146026644
|
G | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1059+12583G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026644 | ||||||
| chr5:146026672
|
G | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1059+12611G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026672 | ||||||
| chr5:146026735
|
C | T | 1 | a0002c0002t0001g0059 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1059+12674C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026735 | ||||||
| chr5:146026737
|
A | G | 1 | a0002c0002t0001g0059 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1059+12676A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146026737 | ||||||
| chr5:146027218
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1059+13157G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027218 | ||||||
| chr5:146027228
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+13167A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027228 | ||||||
| chr5:146027332
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1059+13271A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027332 | ||||||
| chr5:146027354
|
G | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+13293G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027354 | ||||||
| chr5:146027522
|
A | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+13461A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027522 | ||||||
| chr5:146027554
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1059+13493A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027554 | ||||||
| chr5:146027595
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1059+13534C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027595 | ||||||
| chr5:146027598
|
G | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+13537G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027598 | ||||||
| chr5:146027646
|
T | C | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+13585T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027646 | ||||||
| chr5:146027708
|
A | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+13647A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027708 | ||||||
| chr5:146027752
|
C | T | 1 | a0004c0006t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1059+13691C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027752 | ||||||
| chr5:146027760
|
G | A | 8 | a0001c0001t0001g0206a0001c0001t0002g0083a0001c0001t0002g0084others(5): Show | 8 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+13699G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027760 | ||||||
| chr5:146027828
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1059+13767G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027828 | ||||||
| chr5:146027870
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1059+13809C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146027870 | ||||||
| chr5:146028067
|
G | A | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+14006G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028067 | ||||||
| chr5:146028073
|
T | C | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14012T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028073 | ||||||
| chr5:146028097
|
T | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1059+14036T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028097 | ||||||
| chr5:146028122
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+14061G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028122 | ||||||
| chr5:146028155
|
A | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14094A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028155 | ||||||
| chr5:146028163
|
A | AAC | 11 | a0001c0001t0001g0076a0002c0002t0001g0236a0002c0002t0007g0106others(8): Show | 11 | HG01169.hp2 HG02055.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+14148_1059+14 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
A | AACAC | 11 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(8): Show | 11 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+14146_1059+14 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
A | AACACAC | 3 | a0001c0001t0001g0089a0001c0001t0001g0263a0003c0003t0001g0021 | 3 | HG00544.hp2 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1059+14144_1059+14 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AAC | A | 34 | a0001c0001t0002g0086a0001c0001t0002g0099a0001c0005t0001g0042others(31): Show | 34 | HG00099.hp1 HG00438.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1059+14148_1059+14 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AACAC | A | 35 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(32): Show | 36 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1059+14146_1059+14 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AACACAC | A | 4 | a0002c0002t0001g0072a0005c0004t0001g0150a0005c0004t0001g0151others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+14144_1059+14 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AACACACA others(3): Show |
A | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+14140_1059+14 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AACACACA others(5): Show |
A | 4 | a0006c0025t0001g0259a0007c0009t0001g0248a0007c0009t0001g0250others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+14138_1059+14 others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1059+14136_1059+14 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028163
|
AACACACA others(23): Show |
A | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14120_1059+14 others(36): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028163 | |||||
| chr5:146028207
|
C | G | 77 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0014others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1059+14146C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028207 | ||||||
| chr5:146028207
|
CACAG | C | 20 | a0002c0002t0001g0022a0002c0002t0001g0024a0002c0002t0001g0025others(17): Show | 20 | HG00741.hp1 HG01256.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1059+14148_1059+14 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028207 | |||||
| chr5:146028209
|
C | G | 84 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0002g0014others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1059+14148C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028209 | ||||||
| chr5:146028209
|
CAG | C | 5 | a0002c0002t0001g0003a0002c0002t0001g0140a0002c0002t0001g0188others(2): Show | 5 | HG00609.hp2 HG00621.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14152_1059+14 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028209 | |||||
| chr5:146028211
|
G | C | 4 | a0002c0002t0001g0001a0002c0002t0001g0023a0002c0002t0001g0028others(1): Show | 5 | HG00609.hp1 HG01361.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14150G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028211 | ||||||
| chr5:146028263
|
CAAA | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+14204_1059+14 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028263 | |||||
| chr5:146028267
|
A | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+14206A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028267 | ||||||
| chr5:146028294
|
A | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14233A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028294 | ||||||
| chr5:146028525
|
C | T | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14464C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028525 | ||||||
| chr5:146028545
|
G | T | 1 | a0002c0002t0001g0012 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1059+14484G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028545 | ||||||
| chr5:146028558
|
C | T | 4 | a0002c0002t0001g0087a0007c0009t0001g0248a0007c0009t0001g0250others(1): Show | 4 | HG01069.hp2 HG01071.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+14497C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028558 | ||||||
| chr5:146028588
|
T | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1059+14527T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028588 | ||||||
| chr5:146028589
|
G | A | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14528G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028589 | ||||||
| chr5:146028595
|
CCCACCA | C | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+14543_1059+14 others(12): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146028595 | |||||
| chr5:146028611
|
A | C | 1 | a0002c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1059+14550A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028611 | ||||||
| chr5:146028670
|
G | A | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1059+14609G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028670 | ||||||
| chr5:146028776
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1059+14715A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028776 | ||||||
| chr5:146028792
|
C | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+14731C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028792 | ||||||
| chr5:146028894
|
C | T | 1 | a0006c0025t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1059+14833C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028894 | ||||||
| chr5:146028966
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1059+14905C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146028966 | ||||||
| chr5:146029036
|
A | G | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1059+14975A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029036 | ||||||
| chr5:146029076
|
A | G | 1 | a0002c0002t0001g0063 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1059+15015A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029076 | ||||||
| chr5:146029130
|
C | A | 1 | a0004c0008t0001g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1059+15069C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029130 | ||||||
| chr5:146029247
|
A | T | 1 | a0001c0001t0002g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1059+15186A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029247 | ||||||
| chr5:146029302
|
T | C | 1 | a0003c0003t0001g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059+15241T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029302 | ||||||
| chr5:146029473
|
G | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1059+15412G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029473 | ||||||
| chr5:146029499
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1059+15438C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029499 | ||||||
| chr5:146029507
|
G | A | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1059+15446G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029507 | ||||||
| chr5:146029538
|
G | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+15477G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029538 | ||||||
| chr5:146029784
|
G | C | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+15723G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029784 | ||||||
| chr5:146029852
|
A | G | 75 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1059+15791A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029852 | ||||||
| chr5:146029866
|
T | C | 1 | a0002c0002t0001g0064 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1059+15805T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029866 | ||||||
| chr5:146029904
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+15843A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029904 | ||||||
| chr5:146029974
|
G | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1059+15913G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029974 | ||||||
| chr5:146029992
|
G | A | 1 | a0005c0004t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1059+15931G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146029992 | ||||||
| chr5:146030203
|
C | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0233 | 2 | HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1059+16142C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030203 | ||||||
| chr5:146030287
|
G | C | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1059+16226G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030287 | ||||||
| chr5:146030517
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+16456C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030517 | ||||||
| chr5:146030714
|
A | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+16653A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030714 | ||||||
| chr5:146030728
|
C | T | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1059+16667C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030728 | ||||||
| chr5:146030884
|
A | C | 79 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1059+16823A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030884 | ||||||
| chr5:146030884
|
A | T | 9 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+16823A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146030884 | ||||||
| chr5:146031177
|
A | G | 1 | a0002c0002t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1060-16595A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031177 | ||||||
| chr5:146031234
|
C | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1060-16538C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031234 | ||||||
| chr5:146031250
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1060-16522C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031250 | ||||||
| chr5:146031283
|
C | T | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-16489C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031283 | ||||||
| chr5:146031356
|
A | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-16416A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031356 | ||||||
| chr5:146031367
|
G | A | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-16405G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031367 | ||||||
| chr5:146031430
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1060-16342C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031430 | ||||||
| chr5:146031452
|
A | G | 1 | a0002c0002t0001g0009 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1060-16320A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031452 | ||||||
| chr5:146031513
|
T | C | 1 | a0002c0002t0001g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1060-16259T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031513 | ||||||
| chr5:146031664
|
C | T | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-16108C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031664 | ||||||
| chr5:146031705
|
T | C | 6 | a0001c0011t0001g0071a0001c0011t0001g0160a0004c0008t0001g0159others(3): Show | 6 | HG02451.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-16067T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031705 | ||||||
| chr5:146031772
|
A | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-16000A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031772 | ||||||
| chr5:146031819
|
A | G | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-15953A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031819 | ||||||
| chr5:146031865
|
G | A | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-15907G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031865 | ||||||
| chr5:146031879
|
A | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-15893A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031879 | ||||||
| chr5:146031879
|
A | G | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-15893A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031879 | ||||||
| chr5:146031915
|
A | T | 1 | a0004c0006t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1060-15857A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146031915 | ||||||
| chr5:146032008
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-15764C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032008 | ||||||
| chr5:146032090
|
G | A | 1 | a0003c0003t0001g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1060-15682G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032090 | ||||||
| chr5:146032103
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1060-15669G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032103 | ||||||
| chr5:146032195
|
C | T | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(4): Show | 7 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-15577C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032195 | ||||||
| chr5:146032277
|
A | G | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-15495A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032277 | ||||||
| chr5:146032366
|
C | G | 1 | a0009c0027t0001g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1060-15406C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032366 | ||||||
| chr5:146032443
|
C | A | 1 | a0001c0001t0002g0178 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1060-15329C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032443 | ||||||
| chr5:146032666
|
A | G | 5 | a0001c0001t0002g0014a0001c0001t0002g0105a0001c0001t0002g0127others(2): Show | 5 | HG00639.hp2 HG00733.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-15106A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032666 | ||||||
| chr5:146032922
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1060-14850G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032922 | ||||||
| chr5:146032924
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1060-14848G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146032924 | ||||||
| chr5:146033019
|
A | G | 78 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-14753A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033019 | ||||||
| chr5:146033163
|
GATT | G | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-14606_1060-14 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033163 | |||||
| chr5:146033303
|
G | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-14469G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033303 | ||||||
| chr5:146033451
|
C | CT | 68 | a0001c0001t0001g0082a0001c0001t0001g0089a0001c0001t0001g0206others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1060-14285dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
C | CTT | 31 | a0001c0001t0001g0263a0001c0001t0002g0135a0002c0002t0001g0005others(28): Show | 31 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.1060-14286_1060-14 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
C | CTTT | 6 | a0002c0002t0001g0001a0002c0002t0001g0023a0002c0023t0001g0048others(3): Show | 7 | HG03710.hp1 HG03831.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-14287_1060-14 others(9): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
C | CTTTT | 5 | a0002c0002t0001g0027a0002c0002t0001g0043a0002c0002t0001g0197others(2): Show | 5 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-14288_1060-14 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CT | C | 16 | a0001c0001t0001g0090a0002c0002t0001g0012a0002c0002t0001g0013others(13): Show | 16 | HG00733.hp2 HG02132.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1060-14285delT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT | C | 9 | a0001c0001t0001g0207a0001c0010t0001g0041a0001c0010t0001g0257others(6): Show | 9 | HG01069.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-14291_1060-14 others(13): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0080 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1060-14294_1060-14 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT others(5): Show |
C | 1 | a0022c0031t0003g0007 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1060-14296_1060-14 others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1060-14297_1060-14 others(19): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0002g0110a0001c0001t0002g0180 | 2 | HG03834.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1060-14302_1060-14 others(24): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT others(12): Show |
C | 70 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-14303_1060-14 others(25): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033451
|
CTTTTTTT others(28): Show |
C | 1 | a0007c0009t0001g0250 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1060-14319_1060-14 others(41): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146033451 | |||||
| chr5:146033459
|
T | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-14313T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033459 | ||||||
| chr5:146033470
|
T | C | 2 | a0001c0001t0002g0110a0001c0001t0002g0180 | 2 | HG03834.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1060-14302T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033470 | ||||||
| chr5:146033471
|
T | C | 70 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-14301T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033471 | ||||||
| chr5:146033488
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1060-14284G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033488 | ||||||
| chr5:146033596
|
A | G | 251 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0206others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1060-14176A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033596 | ||||||
| chr5:146033849
|
G | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-13923G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033849 | ||||||
| chr5:146033900
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-13872G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146033900 | ||||||
| chr5:146034254
|
C | G | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(4): Show | 7 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-13518C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034254 | ||||||
| chr5:146034289
|
T | C | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-13483T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034289 | ||||||
| chr5:146034290
|
G | A | 5 | a0001c0001t0002g0019a0001c0001t0002g0056a0001c0001t0002g0154others(2): Show | 5 | HG00673.hp2 NA18945.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-13482G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034290 | ||||||
| chr5:146034334
|
T | C | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-13438T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034334 | ||||||
| chr5:146034549
|
G | A | 1 | a0005c0004t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-13223G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034549 | ||||||
| chr5:146034569
|
G | C | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-13203G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034569 | ||||||
| chr5:146034669
|
T | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-13103T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034669 | ||||||
| chr5:146034681
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1060-13091A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034681 | ||||||
| chr5:146034758
|
G | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-13014G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034758 | ||||||
| chr5:146034793
|
C | T | 147 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1060-12979C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034793 | ||||||
| chr5:146034835
|
A | G | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-12937A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034835 | ||||||
| chr5:146034908
|
C | T | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-12864C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034908 | ||||||
| chr5:146034970
|
G | T | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1060-12802G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034970 | ||||||
| chr5:146034979
|
C | A | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-12793C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146034979 | ||||||
| chr5:146035105
|
CA | C | 86 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1060-12654delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146035105 | |||||
| chr5:146035125
|
A | G | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-12647A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035125 | ||||||
| chr5:146035262
|
G | C | 4 | a0006c0025t0001g0259a0007c0009t0001g0248a0007c0009t0001g0250others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-12510G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035262 | ||||||
| chr5:146035351
|
A | C | 1 | a0003c0003t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1060-12421A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035351 | ||||||
| chr5:146035353
|
C | CT | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-12410dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146035353 | |||||
| chr5:146035455
|
A | AAAAGCTA others(2): Show |
87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-12312_1060-12 others(15): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146035455 | |||||
| chr5:146035528
|
G | A | 1 | a0003c0003t0001g0006 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1060-12244G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035528 | ||||||
| chr5:146035555
|
A | G | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-12217A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035555 | ||||||
| chr5:146035584
|
A | T | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-12188A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035584 | ||||||
| chr5:146035906
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060-11866C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146035906 | ||||||
| chr5:146036049
|
G | T | 147 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1060-11723G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036049 | ||||||
| chr5:146036113
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0197 | 2 | HG01934.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1060-11659G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036113 | ||||||
| chr5:146036270
|
G | A | 3 | a0001c0001t0002g0046a0001c0001t0002g0058a0001c0001t0002g0158 | 3 | HG00408.hp1 HG00597.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1060-11502G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036270 | ||||||
| chr5:146036280
|
C | T | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-11492C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036280 | ||||||
| chr5:146036296
|
C | T | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0025t0001g0259others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-11476C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036296 | ||||||
| chr5:146036332
|
G | A | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-11440G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036332 | ||||||
| chr5:146036438
|
T | C | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-11334T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036438 | ||||||
| chr5:146036516
|
A | C | 1 | a0002c0002t0001g0264 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1060-11256A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036516 | ||||||
| chr5:146036602
|
C | T | 1 | a0002c0002t0001g0268 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1060-11170C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036602 | ||||||
| chr5:146036652
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1060-11120G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036652 | ||||||
| chr5:146036693
|
T | G | 1 | a0003c0003t0001g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1060-11079T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036693 | ||||||
| chr5:146036968
|
C | T | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-10804C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036968 | ||||||
| chr5:146036969
|
A | C | 1 | a0003c0003t0001g0055 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1060-10803A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146036969 | ||||||
| chr5:146037151
|
G | A | 1 | a0003c0003t0001g0237 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1060-10621G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037151 | ||||||
| chr5:146037238
|
G | A | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-10534G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037238 | ||||||
| chr5:146037278
|
C | A | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-10494C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037278 | ||||||
| chr5:146037385
|
G | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1060-10387G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037385 | ||||||
| chr5:146037410
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1060-10362T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037410 | ||||||
| chr5:146037484
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1060-10288C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037484 | ||||||
| chr5:146037563
|
C | A | 1 | a0001c0001t0002g0147 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1060-10209C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037563 | ||||||
| chr5:146037596
|
CAG | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-10175_1060-10 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037596 | ||||||
| chr5:146037671
|
A | C | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1060-10101A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037671 | ||||||
| chr5:146037773
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1060-9999A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037773 | ||||||
| chr5:146037829
|
T | G | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-9943T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146037829 | ||||||
| chr5:146038046
|
T | C | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-9726T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038046 | ||||||
| chr5:146038091
|
C | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-9681C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038091 | ||||||
| chr5:146038094
|
T | C | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-9678T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038094 | ||||||
| chr5:146038225
|
T | C | 2 | a0001c0001t0001g0263a0001c0005t0001g0209 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1060-9547T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038225 | ||||||
| chr5:146038623
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1060-9149T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038623 | ||||||
| chr5:146038711
|
A | G | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-9061A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038711 | ||||||
| chr5:146038875
|
G | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-8897G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146038875 | ||||||
| chr5:146039201
|
A | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-8571A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146039201 | ||||||
| chr5:146039281
|
A | T | 1 | a0003c0003t0001g0109 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1060-8491A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146039281 | ||||||
| chr5:146039430
|
G | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-8342G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146039430 | ||||||
| chr5:146039891
|
A | T | 87 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0014others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-7881A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146039891 | ||||||
| chr5:146039898
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1060-7874A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146039898 | ||||||
| chr5:146040127
|
G | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-7645G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040127 | ||||||
| chr5:146040137
|
G | A | 2 | a0003c0003t0001g0008a0003c0003t0001g0107 | 2 | HG01109.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1060-7635G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040137 | ||||||
| chr5:146040263
|
G | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-7509G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040263 | ||||||
| chr5:146040268
|
T | C | 2 | a0002c0002t0001g0177a0002c0002t0001g0236 | 2 | NA18991.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1060-7504T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040268 | ||||||
| chr5:146040416
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1060-7356G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040416 | ||||||
| chr5:146040487
|
G | A | 1 | a0003c0003t0001g0232 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1060-7285G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040487 | ||||||
| chr5:146040631
|
G | A | 89 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1060-7141G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040631 | ||||||
| chr5:146040813
|
G | A | 1 | a0008c0028t0001g0221 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1060-6959G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040813 | ||||||
| chr5:146040848
|
G | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-6924G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040848 | ||||||
| chr5:146040893
|
A | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-6879A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040893 | ||||||
| chr5:146040959
|
G | A | 2 | a0002c0002t0001g0255a0002c0002t0001g0260 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1060-6813G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040959 | ||||||
| chr5:146040982
|
G | A | 170 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1060-6790G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146040982 | ||||||
| chr5:146041013
|
G | A | 88 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1060-6759G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041013 | ||||||
| chr5:146041047
|
T | C | 96 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(93): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1060-6725T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041047 | ||||||
| chr5:146041289
|
G | A | 2 | a0002c0002t0001g0193a0002c0002t0001g0264 | 2 | NA18942.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1060-6483G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041289 | ||||||
| chr5:146041336
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1060-6436T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041336 | ||||||
| chr5:146041404
|
G | A | 6 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-6368G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041404 | ||||||
| chr5:146041515
|
T | G | 1 | a0002c0002t0001g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1060-6257T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041515 | ||||||
| chr5:146041658
|
C | G | 1 | a0002c0023t0001g0048 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1060-6114C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041658 | ||||||
| chr5:146041670
|
T | C | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-6102T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041670 | ||||||
| chr5:146041749
|
G | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-6023G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041749 | ||||||
| chr5:146041837
|
G | A | 2 | a0003c0003t0001g0224a0003c0003t0001g0225 | 2 | NA18978.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1060-5935G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041837 | ||||||
| chr5:146041849
|
T | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-5923T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041849 | ||||||
| chr5:146041855
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1060-5917C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041855 | ||||||
| chr5:146041892
|
T | C | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-5880T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041892 | ||||||
| chr5:146041932
|
A | T | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-5840A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041932 | ||||||
| chr5:146041938
|
T | A | 1 | a0002c0022t0005g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1060-5834T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041938 | ||||||
| chr5:146041958
|
A | G | 9 | a0003c0003t0001g0006a0003c0003t0001g0034a0003c0003t0001g0035others(6): Show | 9 | HG01070.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-5814A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041958 | ||||||
| chr5:146041971
|
C | T | 3 | a0002c0002t0001g0072a0002c0002t0001g0102a0002c0002t0001g0112 | 3 | HG02109.hp1 HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1060-5801C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146041971 | ||||||
| chr5:146042168
|
T | TA | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-5603dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146042168 | |||||
| chr5:146042411
|
T | C | 12 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1060-5361T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146042411 | ||||||
| chr5:146042480
|
C | A | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-5292C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146042480 | ||||||
| chr5:146042585
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1060-5187C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146042585 | ||||||
| chr5:146042770
|
T | C | 1 | a0002c0002t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1060-5002T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146042770 | ||||||
| chr5:146042775
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1060-4997G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146042775 | ||||||
| chr5:146043009
|
G | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-4763G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043009 | ||||||
| chr5:146043034
|
A | G | 9 | a0001c0001t0001g0206a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 9 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1060-4738A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043034 | ||||||
| chr5:146043089
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1060-4683A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043089 | ||||||
| chr5:146043352
|
A | G | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-4420A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043352 | ||||||
| chr5:146043401
|
G | GGAATTCC | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-4371_1060-437 others(11): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043401 | ||||||
| chr5:146043404
|
T | A | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-4368T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043404 | ||||||
| chr5:146043405
|
C | CCAA | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-4367_1060-436 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043405 | ||||||
| chr5:146043406
|
A | G | 3 | a0007c0009t0001g0248a0007c0009t0001g0250a0007c0009t0001g0251 | 3 | HG01069.hp2 HG01071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-4366A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043406 | ||||||
| chr5:146043584
|
T | C | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-4188T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043584 | ||||||
| chr5:146043657
|
A | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0005c0004t0002g0204others(1): Show | 4 | HG01167.hp2 HG02109.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-4115A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043657 | ||||||
| chr5:146043718
|
T | A | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-4054T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043718 | ||||||
| chr5:146043734
|
A | T | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-4038A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043734 | ||||||
| chr5:146043747
|
T | C | 1 | a0002c0002t0001g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1060-4025T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043747 | ||||||
| chr5:146043769
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1060-4003G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043769 | ||||||
| chr5:146043817
|
G | A | 4 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0001t0002g0181others(1): Show | 4 | HG02074.hp1 NA18949.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-3955G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043817 | ||||||
| chr5:146043898
|
A | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-3874A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146043898 | ||||||
| chr5:146044128
|
G | A | 3 | a0002c0002t0001g0255a0002c0002t0001g0260a0004c0006t0001g0085 | 3 | HG02145.hp2 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1060-3644G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044128 | ||||||
| chr5:146044133
|
G | A | 3 | a0002c0002t0001g0116a0002c0002t0001g0137a0002c0002t0001g0138 | 3 | HG02486.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1060-3639G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044133 | ||||||
| chr5:146044139
|
GTTTTTTT others(6): Show |
G | 3 | a0001c0014t0002g0153a0005c0004t0002g0204a0005c0004t0002g0205 | 3 | HG02109.hp2 HG02630.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1060-3623_1060-361 others(17): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146044139 | |||||
| chr5:146044139
|
GTTTTTTT others(7): Show |
G | 87 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1060-3617_1060-360 others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146044139 | |||||
| chr5:146044149
|
G | GT | 10 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(7): Show | 10 | HG01168.hp1 HG02155.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-3610dupT | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146044149 | |||||
| chr5:146044182
|
G | C | 1 | a0002c0002t0001g0191 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-3590G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044182 | ||||||
| chr5:146044210
|
G | T | 1 | a0001c0001t0002g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1060-3562G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044210 | ||||||
| chr5:146044292
|
A | G | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0007c0009t0001g0248others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-3480A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044292 | ||||||
| chr5:146044343
|
G | T | 1 | a0002c0002t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1060-3429G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044343 | ||||||
| chr5:146044456
|
T | C | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1060-3316T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044456 | ||||||
| chr5:146044579
|
T | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-3193T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044579 | ||||||
| chr5:146044912
|
G | A | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-2860G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044912 | ||||||
| chr5:146044964
|
C | T | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-2808C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146044964 | ||||||
| chr5:146045099
|
A | G | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-2673A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146045099 | ||||||
| chr5:146045286
|
G | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-2486G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146045286 | ||||||
| chr5:146045465
|
G | A | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-2307G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146045465 | ||||||
| chr5:146045754
|
G | A | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-2018G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146045754 | ||||||
| chr5:146045854
|
T | G | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-1918T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146045854 | ||||||
| chr5:146045890
|
T | A | 2 | a0005c0004t0001g0079a0005c0004t0001g0103 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1060-1882T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146045890 | ||||||
| chr5:146046013
|
G | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1060-1759G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046013 | ||||||
| chr5:146046020
|
C | T | 146 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1060-1752C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046020 | ||||||
| chr5:146046049
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1060-1723A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046049 | ||||||
| chr5:146046085
|
G | A | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-1687G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046085 | ||||||
| chr5:146046321
|
C | A | 2 | a0005c0004t0002g0204a0005c0004t0002g0205 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1060-1451C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046321 | ||||||
| chr5:146046364
|
C | T | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-1408C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046364 | ||||||
| chr5:146046365
|
A | G | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-1407A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046365 | ||||||
| chr5:146046372
|
T | C | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-1400T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046372 | ||||||
| chr5:146046424
|
T | TC | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-1346dupC | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146046424 | |||||
| chr5:146046594
|
G | A | 8 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(5): Show | 9 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1060-1178G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046594 | ||||||
| chr5:146046597
|
C | T | 1 | a0002c0002t0001g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1060-1175C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046597 | ||||||
| chr5:146046685
|
T | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1060-1087T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046685 | ||||||
| chr5:146046963
|
T | C | 1 | a0016c0013t0002g0161 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1060-809T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046963 | ||||||
| chr5:146046995
|
G | A | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-777G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146046995 | ||||||
| chr5:146047154
|
C | CGT | 6 | a0001c0001t0001g0206a0002c0002t0001g0028a0002c0002t0001g0111others(3): Show | 6 | HG00597.hp1 HG00741.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-595_1060-594d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146047154 | |||||
| chr5:146047154
|
C | CGTGTGTG others(7): Show |
5 | a0001c0001t0002g0017a0001c0001t0002g0185a0001c0010t0002g0270others(2): Show | 5 | HG02895.hp1 NA18957.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-607_1060-594d others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146047154 | |||||
| chr5:146047154
|
C | CGTGTGTG others(9): Show |
66 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1060-609_1060-594d others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146047154 | |||||
| chr5:146047154
|
C | CGTGTGTG others(11): Show |
7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0127others(4): Show | 7 | HG01106.hp2 HG01167.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-611_1060-594d others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146047154 | |||||
| chr5:146047154
|
C | CGTGTGTG others(13): Show |
6 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0011t0001g0160others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-613_1060-594d others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146047154 | |||||
| chr5:146047154
|
C | CGTGTGTG others(15): Show |
5 | a0001c0011t0001g0071a0004c0008t0001g0159a0005c0004t0002g0204others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-615_1060-594d others(24): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 146047154 | |||||
| chr5:146047178
|
T | TGTGTGTG others(10): Show |
1 | a0001c0001t0002g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1060-594_1060-593i others(19): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146047178 | ||||||
| chr5:146047448
|
G | A | 2 | a0005c0004t0001g0150a0005c0004t0001g0151 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1060-324G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146047448 | ||||||
| chr5:146047542
|
G | T | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1060-230G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146047542 | ||||||
| chr5:146047696
|
G | A | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-76G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146047696 | ||||||
| chr5:146047737
|
T | C | 8 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060-35T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 5/9 | chr5 | 146047737 | ||||||
| chr5:146047964
|
T | A | 90 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1151+101T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146047964 | ||||||
| chr5:146048199
|
T | C | 2 | a0003c0003t0001g0029a0003c0003t0001g0246 | 2 | HG00140.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1151+336T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146048199 | ||||||
| chr5:146048314
|
C | CA | 49 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(46): Show | 49 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.1151+464dupA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 146048314 | |||||
| chr5:146048314
|
C | CAA | 30 | a0001c0001t0002g0054a0001c0001t0002g0060a0001c0001t0002g0061others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1151+463_1151+464d others(4): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 146048314 | |||||
| chr5:146048464
|
A | G | 92 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0207others(89): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1151+601A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146048464 | ||||||
| chr5:146048540
|
A | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1152-535A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146048540 | ||||||
| chr5:146048541
|
C | T | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1152-534C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146048541 | ||||||
| chr5:146048567
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1152-508C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146048567 | ||||||
| chr5:146048654
|
T | A | 1 | a0002c0002t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1152-421T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 6/9 | chr5 | 146048654 | ||||||
| chr5:146049380
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | NA18949.hp1 NA19063.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1322+135G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146049380 | ||||||
| chr5:146049456
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1322+211A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146049456 | ||||||
| chr5:146049694
|
A | C | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1322+449A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146049694 | ||||||
| chr5:146049778
|
G | C | 72 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1322+533G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146049778 | ||||||
| chr5:146050091
|
G | T | 2 | a0002c0002t0001g0001a0002c0002t0001g0023 | 3 | NA18981.hp2 NA18983.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1322+846G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050091 | ||||||
| chr5:146050096
|
G | A | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1322+851G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050096 | ||||||
| chr5:146050356
|
C | G | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1322+1111C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050356 | ||||||
| chr5:146050400
|
C | T | 54 | a0002c0002t0001g0239a0003c0003t0001g0006a0003c0003t0001g0008others(51): Show | 54 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1322+1155C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050400 | ||||||
| chr5:146050439
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1322+1194C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050439 | ||||||
| chr5:146050609
|
T | C | 1 | a0002c0002t0001g0013 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1322+1364T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050609 | ||||||
| chr5:146050747
|
A | T | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1322+1502A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146050747 | ||||||
| chr5:146051053
|
G | A | 144 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1322+1808G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051053 | ||||||
| chr5:146051056
|
G | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01167.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1322+1811G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051056 | ||||||
| chr5:146051072
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1322+1827T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051072 | ||||||
| chr5:146051286
|
T | C | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1322+2041T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051286 | ||||||
| chr5:146051366
|
G | T | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1322+2121G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051366 | ||||||
| chr5:146051420
|
A | G | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(4): Show | 7 | HG01167.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1322+2175A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051420 | ||||||
| chr5:146051520
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1322+2275C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051520 | ||||||
| chr5:146051620
|
C | T | 9 | a0003c0003t0001g0006a0003c0003t0001g0034a0003c0003t0001g0035others(6): Show | 9 | HG01070.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1322+2375C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051620 | ||||||
| chr5:146051923
|
G | A | 2 | a0003c0003t0001g0224a0003c0003t0001g0225 | 2 | NA18978.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1322+2678G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146051923 | ||||||
| chr5:146052056
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1322+2811C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052056 | ||||||
| chr5:146052057
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1322+2812G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052057 | ||||||
| chr5:146052105
|
A | G | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1322+2860A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052105 | ||||||
| chr5:146052346
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0002c0002t0001g0157 | 3 | HG02809.hp1 HG03139.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1322+3101G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052346 | ||||||
| chr5:146052477
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1322+3232G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052477 | ||||||
| chr5:146052628
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0010t0001g0041others(3): Show | 6 | HG01167.hp2 HG02895.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323-3353G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052628 | ||||||
| chr5:146052651
|
C | A | 1 | a0002c0002t0001g0013 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1323-3330C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052651 | ||||||
| chr5:146052831
|
T | TATG | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0005c0004t0001g0145 | 3 | HG01167.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1323-3148_1323-314 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 146052831 | |||||
| chr5:146052955
|
A | G | 97 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1323-3026A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146052955 | ||||||
| chr5:146053050
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1323-2931C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053050 | ||||||
| chr5:146053380
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1323-2601C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053380 | ||||||
| chr5:146053422
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1323-2559G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053422 | ||||||
| chr5:146053571
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1323-2410G>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053571 | ||||||
| chr5:146053654
|
T | C | 100 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1323-2327T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053654 | ||||||
| chr5:146053736
|
T | TCCTCTTT others(56): Show |
1 | a0001c0001t0002g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1323-2205_1323-220 others(67): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 146053736 | |||||
| chr5:146053756
|
G | A | 3 | a0001c0001t0002g0105a0001c0001t0002g0133a0001c0001t0002g0134 | 3 | HG00639.hp2 HG00733.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1323-2225G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053756 | ||||||
| chr5:146053777
|
G | A | 91 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1323-2204G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053777 | ||||||
| chr5:146053901
|
A | G | 1 | a0007c0009t0001g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1323-2080A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146053901 | ||||||
| chr5:146054000
|
G | A | 1 | a0004c0008t0001g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1323-1981G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054000 | ||||||
| chr5:146054200
|
C | T | 71 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1323-1781C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054200 | ||||||
| chr5:146054204
|
G | A | 2 | a0005c0004t0001g0150a0005c0004t0001g0151 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1323-1777G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054204 | ||||||
| chr5:146054247
|
GC | G | 3 | a0003c0003t0001g0055a0003c0003t0001g0109a0003c0003t0001g0230 | 3 | HG02135.hp1 NA19077.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1323-1733delC | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054247 | ||||||
| chr5:146054335
|
G | T | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323-1646G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054335 | ||||||
| chr5:146054359
|
T | TTGC | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323-1611_1323-160 others(7): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 146054359 | |||||
| chr5:146054743
|
T | A | 3 | a0004c0008t0001g0159a0004c0008t0001g0262a0015c0012t0001g0202 | 3 | HG02451.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1323-1238T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054743 | ||||||
| chr5:146054869
|
T | C | 71 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1323-1112T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146054869 | ||||||
| chr5:146055048
|
T | C | 2 | a0002c0002t0001g0193a0002c0002t0001g0264 | 2 | NA18942.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1323-933T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146055048 | ||||||
| chr5:146055152
|
T | G | 101 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1323-829T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146055152 | ||||||
| chr5:146055238
|
T | A | 3 | a0003c0003t0001g0217a0003c0003t0001g0218a0003c0003t0001g0266 | 3 | HG00597.hp1 HG00621.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1323-743T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 7/9 | chr5 | 146055238 | ||||||
| chr5:146056251
|
TG | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0265 | 3 | HG02976.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1555+39delG | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146056251 | ||||||
| chr5:146056569
|
G | A | 2 | a0001c0005t0001g0210a0001c0005t0001g0211 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1555+356G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146056569 | ||||||
| chr5:146056901
|
C | G | 1 | a0002c0002t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1555+688C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146056901 | ||||||
| chr5:146056934
|
G | A | 1 | a0003c0003t0001g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1555+721G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146056934 | ||||||
| chr5:146057136
|
T | C | 3 | a0001c0011t0001g0071a0001c0011t0001g0160a0014c0017t0001g0249 | 3 | HG02809.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1555+923T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057136 | ||||||
| chr5:146057246
|
T | A | 2 | a0005c0004t0002g0204a0005c0004t0002g0205 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1555+1033T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057246 | ||||||
| chr5:146057273
|
T | A | 1 | a0001c0001t0002g0125 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1555+1060T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057273 | ||||||
| chr5:146057277
|
T | C | 97 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1555+1064T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057277 | ||||||
| chr5:146057288
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1555+1075T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057288 | ||||||
| chr5:146057311
|
C | T | 97 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1555+1098C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057311 | ||||||
| chr5:146057389
|
C | T | 12 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0005t0001g0042others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1555+1176C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057389 | ||||||
| chr5:146057424
|
C | T | 4 | a0004c0006t0001g0081a0004c0008t0001g0077a0004c0008t0001g0078others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1555+1211C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057424 | ||||||
| chr5:146057740
|
G | T | 2 | a0005c0004t0002g0204a0005c0004t0002g0205 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1555+1527G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057740 | ||||||
| chr5:146057780
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1555+1567A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057780 | ||||||
| chr5:146057785
|
T | A | 1 | a0002c0002t0001g0003 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1555+1572T>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057785 | ||||||
| chr5:146057928
|
G | GTC | 13 | a0001c0001t0001g0088a0002c0002t0001g0004a0002c0002t0001g0005others(10): Show | 13 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1555+1755_1555+175 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
G | GTCTC | 10 | a0002c0002t0001g0013a0002c0002t0001g0022a0002c0002t0001g0111others(7): Show | 10 | HG02004.hp1 HG02486.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1555+1753_1555+175 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
G | GTCTCTC | 3 | a0002c0002t0001g0236a0004c0006t0001g0139a0012c0020t0001g0261 | 3 | HG03540.hp1 HG04228.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1555+1751_1555+175 others(10): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
GTC | G | 3 | a0002c0002t0001g0059a0002c0002t0001g0233a0002c0002t0001g0255 | 3 | HG02523.hp1 NA18994.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1555+1755_1555+175 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
GTCTC | G | 26 | a0001c0001t0001g0082a0001c0010t0001g0041a0001c0010t0001g0257others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1555+1753_1555+175 others(8): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
GTCTCTCT others(3): Show |
G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0005c0004t0001g0145 | 3 | HG01167.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1555+1747_1555+175 others(14): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
GTCTCTCT others(5): Show |
G | 6 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(3): Show | 6 | HG01934.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1555+1745_1555+175 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057928
|
GTCTCTCT others(9): Show |
G | 3 | a0001c0001t0001g0206a0005c0004t0001g0079a0005c0004t0001g0103 | 3 | HG02055.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1555+1741_1555+175 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057928 | |||||
| chr5:146057950
|
CTCTCTCT others(13): Show |
C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1555+1741_1555+176 others(24): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057950 | |||||
| chr5:146057954
|
CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0002g0125 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1555+1745_1555+176 others(24): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057954 | |||||
| chr5:146057958
|
CTCTCTCT others(9): Show |
C | 65 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1555+1749_1555+176 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057958 | |||||
| chr5:146057960
|
CTCTCTCT others(7): Show |
C | 5 | a0001c0001t0002g0058a0001c0001t0002g0104a0001c0001t0002g0136others(2): Show | 5 | HG00140.hp2 HG02155.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1555+1751_1555+176 others(18): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057960 | |||||
| chr5:146057962
|
C | A | 7 | a0001c0005t0001g0210a0003c0003t0001g0018a0003c0003t0001g0055others(4): Show | 7 | HG00280.hp2 HG02135.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1555+1749C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057962 | ||||||
| chr5:146057966
|
C | A | 13 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(10): Show | 13 | HG00280.hp2 HG02055.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1555+1753C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057966 | ||||||
| chr5:146057966
|
C | CTA | 6 | a0001c0005t0001g0212a0001c0005t0001g0213a0002c0002t0001g0009others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1555+1754_1555+175 others(6): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057966 | |||||
| chr5:146057966
|
C | CTCTCTCT others(11): Show |
2 | a0001c0011t0001g0071a0001c0011t0001g0160 | 2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1555+1756_1555+175 others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057966 | |||||
| chr5:146057966
|
C | CTCTCTCT others(9): Show |
2 | a0005c0004t0001g0150a0014c0017t0001g0249 | 2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1555+1756_1555+175 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057966 | |||||
| chr5:146057966
|
C | CTCTCTCT others(11): Show |
1 | a0005c0004t0001g0151 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1555+1756_1555+175 others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057966 | |||||
| chr5:146057970
|
A | C | 4 | a0001c0001t0001g0092a0007c0009t0001g0248a0007c0009t0001g0250others(1): Show | 4 | HG01069.hp2 HG01071.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1555+1757A>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057970 | ||||||
| chr5:146057972
|
C | A | 1 | a0005c0004t0002g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1555+1759C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057972 | ||||||
| chr5:146057976
|
C | A | 1 | a0005c0004t0002g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1555+1763C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057976 | ||||||
| chr5:146057980
|
C | A | 3 | a0005c0004t0001g0150a0005c0004t0001g0151a0005c0004t0002g0205 | 3 | HG02109.hp2 HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1555+1767C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057980 | ||||||
| chr5:146057980
|
C | CTATATAT others(11): Show |
1 | a0001c0005t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1555+1770_1555+177 others(22): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057980 | |||||
| chr5:146057980
|
C | CTATATAT others(13): Show |
2 | a0001c0005t0001g0212a0001c0005t0001g0213 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1555+1770_1555+177 others(24): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057980 | |||||
| chr5:146057984
|
C | A | 95 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1555+1771C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146057984 | ||||||
| chr5:146057984
|
C | CTATATAT others(9): Show |
1 | a0001c0005t0001g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1555+1784_1555+178 others(20): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057984 | |||||
| chr5:146057984
|
C | CTATCTAT others(5): Show |
2 | a0007c0009t0001g0250a0007c0009t0001g0251 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1555+1774_1555+177 others(16): Show |
SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146057984 | |||||
| chr5:146058005
|
A | T | 1 | a0002c0002t0001g0013 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1555+1792A>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146058005 | ||||||
| chr5:146058011
|
C | G | 254 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0100others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1555+1798C>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146058011 | ||||||
| chr5:146058642
|
C | T | 1 | a0005c0004t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1556-1224C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146058642 | ||||||
| chr5:146058658
|
A | G | 5 | a0002c0002t0001g0009a0002c0002t0001g0140a0002c0002t0001g0169others(2): Show | 5 | HG00609.hp2 NA18747.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1556-1208A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146058658 | ||||||
| chr5:146058685
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1556-1181G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146058685 | ||||||
| chr5:146058686
|
C | T | 3 | a0001c0010t0001g0041a0001c0010t0001g0257a0001c0010t0002g0270 | 3 | HG02895.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1556-1180C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146058686 | ||||||
| chr5:146058871
|
TA | T | 75 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1556-979delA | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 146058871 | |||||
| chr5:146059178
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1556-688C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146059178 | ||||||
| chr5:146059306
|
CG | C | 5 | a0005c0004t0001g0150a0005c0004t0001g0151a0007c0009t0001g0248others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1556-559delG | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146059306 | ||||||
| chr5:146059534
|
G | A | 1 | a0003c0003t0001g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1556-332G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146059534 | ||||||
| chr5:146059535
|
C | T | 106 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1556-331C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146059535 | ||||||
| chr5:146059559
|
T | C | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0098others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1556-307T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146059559 | ||||||
| chr5:146059561
|
C | T | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0098others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1556-305C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 8/9 | chr5 | 146059561 | ||||||
| chr5:146060459
|
T | G | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0098others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1914+235T>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146060459 | ||||||
| chr5:146060519
|
T | C | 5 | a0001c0005t0001g0042a0001c0005t0001g0210a0001c0005t0001g0211others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1914+295T>C | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146060519 | ||||||
| chr5:146061081
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0168 | 2 | HG02040.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1914+857C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061081 | ||||||
| chr5:146061100
|
C | T | 88 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0088others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1914+876C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061100 | ||||||
| chr5:146061279
|
C | T | 1 | a0003c0003t0001g0244 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1914+1055C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061279 | ||||||
| chr5:146061317
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1914+1093C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061317 | ||||||
| chr5:146061501
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0011t0001g0071others(3): Show | 6 | HG01167.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1915-925G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061501 | ||||||
| chr5:146061508
|
G | T | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0011t0001g0071others(3): Show | 6 | HG01167.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1915-918G>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061508 | ||||||
| chr5:146061666
|
A | G | 263 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1915-760A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061666 | ||||||
| chr5:146061728
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1915-698C>T | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061728 | ||||||
| chr5:146061754
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0011t0001g0071others(3): Show | 6 | HG01167.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1915-672G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146061754 | ||||||
| chr5:146062277
|
A | G | 24 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1915-149A>G | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146062277 | ||||||
| chr5:146062324
|
G | A | 1 | a0015c0012t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1915-102G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146062324 | ||||||
| chr5:146062358
|
G | A | 1 | a0001c0011t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1915-68G>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146062358 | ||||||
| chr5:146062383
|
C | A | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0082others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1915-43C>A | SH3RF2 | ENSG00000156463.18 | transcript | ENST00000359120.9 | protein_coding | 9/9 | chr5 | 146062383 |