| geneid | 25759 |
|---|---|
| ensemblid | ENSG00000129946.11 |
| hgncid | 29869 |
| symbol | SHC2 |
| name | SHC adaptor protein 2 |
| refseq_nuc | NM_012435.3 |
| refseq_prot | NP_036567.2 |
| ensembl_nuc | ENST00000264554.11 |
| ensembl_prot | ENSP00000264554.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 416589 |
| end | 461033 |
| strand | - |
| ver | v1.2 |
| region | chr19:416589-461033 |
| region5000 | chr19:411589-466033 |
| regionname0 | SHC2_chr19_416589_461033 |
| regionname5000 | SHC2_chr19_411589_466033 |
| 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 | 0/0 | 582 | 179 | 46 | 35 | 75 | 5 | 18 | 45 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002 | 1/1 | 582 | 19 | 1 | 6 | 1 | 1 | 8 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0003 | 0/0 | 582 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0004 | 0/0 | 582 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0005 | 0/0 | 582 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0006 | 0/0 | 582 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0007 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0008 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0009 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0010 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0011 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| 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 | 0/0 | 1749 | 88 | 27 | 18 | 35 | 2 | 6 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0002 | 0/0 | 1749 | 38 | 2 | 7 | 23 | 0 | 6 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0003 | 0/0 | 1749 | 23 | 0 | 2 | 17 | 0 | 4 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0004 | 1/1 | 1749 | 16 | 0 | 6 | 0 | 1 | 7 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0005 | 0/0 | 1749 | 12 | 4 | 4 | 0 | 2 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0006 | 0/0 | 1749 | 6 | 4 | 1 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0007 | 0/0 | 1749 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0008 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0009 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0010 | 0/0 | 1749 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0011 | 0/0 | 1749 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0012 | 0/0 | 1749 | 2 | 0 | 0 | 1 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0013 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0014 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0015 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0016 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0017 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0018 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0019 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0020 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0021 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0022 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0023 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0024 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| c0025 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 777 | 104 | 5 | 28 | 51 | 4 | 15 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0002 | 0/0 | 777 | 28 | 9 | 1 | 14 | 1 | 3 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0003 | 0/0 | 777 | 20 | 9 | 3 | 6 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0004 | 0/0 | 777 | 19 | 2 | 7 | 6 | 0 | 4 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0005 | 1/0 | 777 | 17 | 11 | 2 | 0 | 1 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0006 | 0/0 | 777 | 13 | 13 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0007 | 0/0 | 777 | 2 | 2 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0008 | 0/0 | 777 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0009 | 0/0 | 777 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0010 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0011 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0012 | 0/0 | 777 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0013 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0014 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0015 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| t0016 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| 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 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| 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 | 0/0 | 1749 | 88 | 27 | 18 | 35 | 2 | 6 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0002 | 0/0 | 1749 | 38 | 2 | 7 | 23 | 0 | 6 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0003 | 0/0 | 1749 | 23 | 0 | 2 | 17 | 0 | 4 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0005 | 0/0 | 1749 | 12 | 4 | 4 | 0 | 2 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0006 | 0/0 | 1749 | 6 | 4 | 1 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0007 | 0/0 | 1749 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0013 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0014 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0016 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0017 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0018 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0020 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0023 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0004 | 1/1 | 1749 | 16 | 0 | 6 | 0 | 1 | 7 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0012 | 0/0 | 1749 | 2 | 0 | 0 | 1 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0024 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0003c0008 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0004c0010 | 0/0 | 1749 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0005c0009 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0006c0011 | 0/0 | 1749 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0007c0019 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0008c0021 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0009c0015 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0010c0022 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0011c0025 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2525 | 52 | 0 | 12 | 35 | 2 | 3 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0002 | 0/0 | 2525 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0003 | 0/0 | 2525 | 7 | 6 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0004 | 0/0 | 2525 | 7 | 2 | 3 | 0 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0005 | 0/0 | 2525 | 6 | 5 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0006 | 0/0 | 2525 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0007 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0008 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0009 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0011 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0013 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0001t0016 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0002t0001 | 0/0 | 2525 | 21 | 1 | 2 | 14 | 0 | 4 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0002t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0002t0003 | 0/0 | 2525 | 10 | 0 | 2 | 6 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0002t0004 | 0/0 | 2525 | 6 | 0 | 3 | 3 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0003t0001 | 0/0 | 2525 | 5 | 0 | 2 | 2 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0003t0002 | 0/0 | 2525 | 14 | 0 | 0 | 11 | 0 | 3 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0003t0004 | 0/0 | 2525 | 3 | 0 | 0 | 3 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0003t0010 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0005t0001 | 0/0 | 2525 | 8 | 0 | 4 | 0 | 2 | 2 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0005t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0005t0006 | 0/0 | 2525 | 2 | 2 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0005t0015 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0006t0001 | 0/0 | 2525 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0006t0002 | 0/0 | 2525 | 2 | 0 | 1 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0006t0006 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0007t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0007t0003 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0007t0006 | 0/0 | 2525 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0013t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0014t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0016t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0017t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0018t0006 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0020t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0001c0023t0007 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0004t0001 | 0/1 | 2525 | 10 | 0 | 4 | 0 | 0 | 5 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0004t0004 | 0/0 | 2525 | 2 | 0 | 1 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0004t0005 | 1/0 | 2525 | 4 | 0 | 1 | 0 | 1 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0012t0002 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0012t0004 | 0/0 | 2525 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0002c0024t0003 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0003c0008t0003 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0003c0008t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0003c0008t0006 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0004c0010t0002 | 0/0 | 2525 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0005c0009t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0005c0009t0014 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0006c0011t0005 | 0/0 | 2525 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0007c0019t0001 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0008c0021t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0009c0015t0012 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0010c0022t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| a0011c0025t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | copy fasta | chr19 | 411589 | 466033 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0016g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0013t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0014t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0016t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0017t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0018t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0020t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0023t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0012t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0012t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0024t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0003c0008t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0003c0008t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0003c0008t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0004c0010t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0004c0010t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0005c0009t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0005c0009t0014g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0006c0011t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0006c0011t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0007c0019t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0008c0021t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0009c0015t0012g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0010c0022t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0011c0025t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0001 | g0022 | EUR | GBR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0016 | EUR | GBR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00323 | hp2 | a0002 | c0004 | t0005 | g0201 | EUR | FIN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0111 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00621 | hp1 | a0001 | c0003 | t0010 | g0077 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00639 | hp1 | a0002 | c0004 | t0001 | g0187 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0025 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00733 | hp2 | a0002 | c0004 | t0001 | g0197 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00735 | hp1 | a0001 | c0014 | t0001 | g0021 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00735 | hp2 | a0001 | c0005 | t0001 | g0017 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0147 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01099 | hp1 | a0011 | c0025 | t0001 | g0206 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01099 | hp2 | a0001 | c0005 | t0001 | g0015 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01109 | hp1 | a0001 | c0005 | t0001 | g0012 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01109 | hp2 | a0006 | c0011 | t0005 | g0059 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0196 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01258 | hp1 | a0002 | c0004 | t0005 | g0190 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01358 | hp1 | a0001 | c0016 | t0001 | g0144 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01358 | hp2 | a0002 | c0004 | t0001 | g0192 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01361 | hp1 | a0001 | c0020 | t0001 | g0104 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01884 | hp2 | a0001 | c0023 | t0007 | g0186 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01943 | hp2 | a0001 | c0006 | t0002 | g0019 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01952 | hp1 | a0009 | c0015 | t0012 | g0027 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0148 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01981 | hp1 | a0002 | c0004 | t0004 | g0191 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0088 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0072 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02145 | hp1 | a0003 | c0008 | t0003 | g0183 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02148 | hp1 | a0001 | c0001 | t0008 | g0119 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | CDX | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0073 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0106 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0156 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0113 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02451 | hp2 | a0001 | c0007 | t0006 | g0037 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02622 | hp1 | a0001 | c0017 | t0005 | g0056 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02622 | hp2 | a0001 | c0013 | t0005 | g0007 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0149 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02735 | hp1 | a0001 | c0005 | t0001 | g0013 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02818 | hp1 | a0003 | c0008 | t0006 | g0185 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02922 | hp1 | a0008 | c0021 | t0002 | g0032 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02976 | hp1 | a0001 | c0007 | t0006 | g0042 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02976 | hp2 | a0001 | c0005 | t0015 | g0008 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03017 | hp1 | a0002 | c0012 | t0004 | g0193 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03098 | hp2 | a0001 | c0006 | t0006 | g0014 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03195 | hp1 | a0001 | c0007 | t0003 | g0030 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03209 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03225 | hp1 | a0001 | c0005 | t0006 | g0010 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03225 | hp2 | a0006 | c0011 | t0005 | g0063 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0194 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0065 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03540 | hp2 | a0001 | c0005 | t0006 | g0009 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03579 | hp1 | a0001 | c0007 | t0006 | g0055 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03579 | hp2 | a0001 | c0018 | t0006 | g0179 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0060 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03831 | hp1 | a0002 | c0004 | t0001 | g0204 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03927 | hp2 | a0001 | c0005 | t0001 | g0011 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0199 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04199 | hp2 | a0002 | c0004 | t0004 | g0200 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0181 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04204 | hp2 | a0002 | c0004 | t0001 | g0205 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0078 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0173 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18522 | hp2 | a0005 | c0009 | t0005 | g0048 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18612 | hp2 | a0001 | c0003 | t0004 | g0110 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0024 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0175 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0150 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0075 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18960 | hp1 | a0002 | c0012 | t0002 | g0203 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0178 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0174 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18985 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0096 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18989 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0076 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19009 | hp2 | a0004 | c0010 | t0002 | g0068 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19030 | hp1 | a0001 | c0007 | t0002 | g0080 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19043 | hp2 | a0002 | c0024 | t0003 | g0188 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0074 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19066 | hp2 | a0001 | c0003 | t0004 | g0109 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19080 | hp1 | a0004 | c0010 | t0002 | g0067 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19091 | hp2 | a0001 | c0003 | t0004 | g0108 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19240 | hp1 | a0005 | c0009 | t0014 | g0040 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19240 | hp2 | a0010 | c0022 | t0002 | g0184 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20752 | hp2 | a0001 | c0006 | t0002 | g0018 | EUR | TSI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0195 | SAS | GIH | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20905 | hp2 | a0002 | c0004 | t0005 | g0189 | SAS | GIH | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0163 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02559 | hp2 | a0003 | c0008 | t0005 | g0182 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0023 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG06807 | hp2 | a0007 | c0019 | t0001 | g0127 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0070 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA21309 | hp2 | a0001 | c0005 | t0005 | g0026 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0001 | g0198 | REF | REF | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| homoSapiens_grch38 | hp1 | a0002 | c0004 | t0005 | g0202 | REF | REF | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:418948
|
C | T | 1 | a0007 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1729G>A | p.Val577Met | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/13 | 1766/2525 | 1729/1749 | 577/582 | chr19 | 418948 | ||
| chr19:422229
|
C | T | 2 | a0005a0010 | 3 | NA18522.hp2 NA19240.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1537G>A | p.Val513Ile | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/13 | 1574/2525 | 1537/1749 | 513/582 | chr19 | 422229 | ||
| chr19:430696
|
A | G | 1 | a0004 | 2 | NA19009.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.1162T>C | p.Ser388Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/13 | 1199/2525 | 1162/1749 | 388/582 | chr19 | 430696 | ||
| chr19:434848
|
T | C | 1 | a0010 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.971A>G | p.Glu324Gly | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/13 | 1008/2525 | 971/1749 | 324/582 | chr19 | 434848 | ||
| chr19:436181
|
C | A | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.937G>T | p.Ala313Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/13 | 974/2525 | 937/1749 | 313/582 | chr19 | 436181 | ||
| chr19:438830
|
T | C | 1 | a0006 | 2 | HG01109.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.608A>G | p.Asn203Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/13 | 645/2525 | 608/1749 | 203/582 | chr19 | 438830 | ||
| chr19:460636
|
C | T | 1 | a0009 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.361G>A | p.Ala121Thr | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 398/2525 | 361/1749 | 121/582 | chr19 | 460636 | ||
| chr19:460642
|
C | A | 2 | a0003a0010 | 4 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.355G>T | p.Ala119Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 392/2525 | 355/1749 | 119/582 | chr19 | 460642 | ||
| chr19:460668
|
C | G | 10 | a0001a0003a0004others(7): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
missense_variant | MODERATE | c.329G>C | p.Gly110Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 366/2525 | 329/1749 | 110/582 | chr19 | 460668 | ||
| chr19:460729
|
G | A | 1 | a0011 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.268C>T | p.Pro90Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 305/2525 | 268/1749 | 90/582 | chr19 | 460729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:418973
|
G | A | 1 | a0001c0018 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1704C>T | p.Ala568Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/13 | 1741/2525 | 1704/1749 | 568/582 | chr19 | 418973 | ||
| chr19:422238
|
G | T | 1 | a0001c0002 | 38 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(35): Show |
synonymous_variant | LOW | c.1528C>A | p.Arg510Arg | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/13 | 1565/2525 | 1528/1749 | 510/582 | chr19 | 422238 | ||
| chr19:422452
|
G | C | 4 | a0001c0007a0001c0023a0002c0024others(1): Show | 9 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
synonymous_variant | LOW | c.1314C>G | p.Pro438Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/13 | 1351/2525 | 1314/1749 | 438/582 | chr19 | 422452 | ||
| chr19:425131
|
C | T | 3 | a0001c0013a0001c0017a0001c0018 | 3 | HG02622.hp1 HG02622.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1275G>A | p.Pro425Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/13 | 1312/2525 | 1275/1749 | 425/582 | chr19 | 425131 | ||
| chr19:425182
|
G | A | 3 | a0001c0014a0001c0020a0011c0025 | 3 | HG00735.hp1 HG01099.hp1 HG01361.hp1 |
synonymous_variant | LOW | c.1224C>T | p.Asp408Asp | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/13 | 1261/2525 | 1224/1749 | 408/582 | chr19 | 425182 | ||
| chr19:425224
|
C | T | 1 | a0001c0016 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1182G>A | p.Pro394Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/13 | 1219/2525 | 1182/1749 | 394/582 | chr19 | 425224 | ||
| chr19:434718
|
G | A | 5 | a0001c0003a0001c0006a0002c0012others(2): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
synonymous_variant | LOW | c.1101C>T | p.Ala367Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/13 | 1138/2525 | 1101/1749 | 367/582 | chr19 | 434718 | ||
| chr19:460658
|
C | A | 1 | a0001c0023 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.339G>T | p.Ala113Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 376/2525 | 339/1749 | 113/582 | chr19 | 460658 | ||
| chr19:460883
|
C | T | 4 | a0001c0005a0001c0006a0001c0013others(1): Show | 20 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(17): Show |
synonymous_variant | LOW | c.114G>A | p.Ala38Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 151/2525 | 114/1749 | 38/582 | chr19 | 460883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:416616
|
C | T | 1 | a0001c0003t0010 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2312 | chr19 | 416616 | |||||
| chr19:416664
|
C | T | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*664G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2264 | chr19 | 416664 | |||||
| chr19:416666
|
G | C | 7 | a0001c0001t0006a0001c0001t0013a0001c0005t0006others(4): Show | 14 | HG02258.hp1 HG02451.hp2 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*662C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2262 | chr19 | 416666 | |||||
| chr19:416694
|
C | T | 1 | a0001c0005t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2234 | chr19 | 416694 | |||||
| chr19:416834
|
A | G | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(17): Show | 54 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*494T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2094 | chr19 | 416834 | |||||
| chr19:416950
|
G | A | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1978 | chr19 | 416950 | |||||
| chr19:416963
|
C | T | 14 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(11): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*365G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1965 | chr19 | 416963 | |||||
| chr19:417014
|
A | C | 46 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(43): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*314T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1914 | chr19 | 417014 | |||||
| chr19:417157
|
C | T | 10 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(7): Show | 29 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1771 | chr19 | 417157 | |||||
| chr19:417196
|
C | T | 1 | a0001c0001t0009 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*132G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1732 | chr19 | 417196 | |||||
| chr19:417214
|
C | T | 1 | a0001c0001t0008 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1714 | chr19 | 417214 | |||||
| chr19:417256
|
C | T | 1 | a0009c0015t0012 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1672 | chr19 | 417256 | |||||
| chr19:417262
|
G | A | 6 | a0001c0001t0003a0001c0001t0016a0001c0002t0003others(3): Show | 21 | HG01071.hp2 HG01952.hp2 HG01978.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*66C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1666 | chr19 | 417262 | |||||
| chr19:417281
|
C | T | 15 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(12): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*47G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1647 | chr19 | 417281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:417396
|
T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.*6-74A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417396 | ||||||
| chr19:417556
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(142): Show | 151 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.*6-234T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417556 | ||||||
| chr19:417588
|
C | T | 19 | a0001c0001t0004g0035a0001c0001t0004g0064a0001c0001t0004g0065others(16): Show | 19 | HG01074.hp1 HG01981.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.*6-266G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417588 | ||||||
| chr19:417621
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*6-299G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417621 | ||||||
| chr19:417633
|
C | G | 1 | a0001c0001t0004g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*6-311G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417633 | ||||||
| chr19:417705
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*6-383G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417705 | ||||||
| chr19:417706
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*6-384C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417706 | ||||||
| chr19:417714
|
C | T | 4 | a0001c0001t0003g0036a0001c0001t0003g0050a0001c0001t0003g0071others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6-392G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417714 | ||||||
| chr19:417729
|
C | T | 1 | a0001c0005t0001g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*6-407G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417729 | ||||||
| chr19:417737
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.*6-415T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417737 | ||||||
| chr19:417826
|
TGGGTGGA others(15): Show |
T | 1 | a0001c0001t0001g0002 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*6-526_*6-505delTA others(20): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417826 | ||||||
| chr19:417870
|
G | C | 21 | a0001c0001t0001g0162a0001c0001t0002g0052a0001c0003t0002g0001others(18): Show | 22 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.*6-548C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417870 | ||||||
| chr19:417989
|
G | A | 1 | a0001c0003t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.*6-667C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417989 | ||||||
| chr19:418056
|
A | G | 33 | a0001c0001t0001g0170a0001c0001t0003g0004a0001c0001t0003g0171others(30): Show | 35 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.*6-734T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418056 | ||||||
| chr19:418065
|
A | G | 13 | a0001c0001t0001g0134a0001c0001t0007g0041a0001c0002t0001g0006others(10): Show | 14 | HG00558.hp2 HG01993.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.*6-743T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418065 | ||||||
| chr19:418126
|
C | G | 1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*5+797G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418126 | ||||||
| chr19:418131
|
C | T | 55 | a0001c0001t0001g0170a0001c0001t0003g0004a0001c0001t0003g0171others(52): Show | 57 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.*5+792G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418131 | ||||||
| chr19:418133
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.*5+790G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418133 | ||||||
| chr19:418178
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(191): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.*5+745T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418178 | ||||||
| chr19:418232
|
C | T | 3 | a0002c0004t0001g0187a0002c0004t0001g0199a0002c0004t0001g0205 | 3 | HG00639.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.*5+691G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418232 | ||||||
| chr19:418250
|
C | T | 1 | a0001c0002t0001g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*5+673G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418250 | ||||||
| chr19:418323
|
C | T | 13 | a0001c0001t0002g0057a0001c0001t0004g0064a0001c0001t0004g0065others(10): Show | 13 | HG01074.hp1 HG01358.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.*5+600G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418323 | ||||||
| chr19:418433
|
C | T | 1 | a0001c0003t0002g0117 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.*5+490G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418433 | ||||||
| chr19:418436
|
C | T | 21 | a0001c0001t0004g0035a0001c0001t0004g0064a0001c0001t0004g0065others(18): Show | 22 | HG01074.hp1 HG01109.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.*5+487G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418436 | ||||||
| chr19:418507
|
C | T | 16 | a0001c0001t0002g0101a0001c0001t0004g0159a0001c0001t0004g0161others(13): Show | 17 | HG00544.hp2 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.*5+416G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418507 | ||||||
| chr19:418549
|
G | A | 2 | a0001c0003t0002g0076a0002c0012t0002g0203 | 2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.*5+374C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418549 | ||||||
| chr19:418556
|
G | A | 19 | a0001c0001t0002g0101a0001c0001t0003g0050a0001c0001t0004g0064others(16): Show | 19 | HG00544.hp2 HG01074.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.*5+367C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418556 | ||||||
| chr19:418624
|
A | G | 7 | a0001c0001t0004g0035a0001c0001t0005g0028a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.*5+299T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418624 | ||||||
| chr19:418701
|
AGGGGACA others(16): Show |
A | 14 | a0001c0001t0002g0052a0001c0001t0003g0050a0001c0001t0011g0038others(11): Show | 14 | HG01109.hp2 HG02258.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.*5+199_*5+221delAC others(21): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418701 | ||||||
| chr19:418769
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0061others(65): Show | 69 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.*5+154C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418769 | ||||||
| chr19:418786
|
G | A | 51 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0002g0052others(48): Show | 52 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.*5+137C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418786 | ||||||
| chr19:418790
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0003g0050a0005c0009t0014g0040 | 3 | HG02559.hp1 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.*5+133G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418790 | ||||||
| chr19:418791
|
G | A | 4 | a0001c0001t0002g0101a0001c0001t0007g0041a0001c0005t0006g0009others(1): Show | 4 | HG02572.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5+132C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418791 | ||||||
| chr19:418805
|
CCT | C | 6 | a0001c0001t0002g0079a0001c0001t0004g0035a0001c0001t0005g0028others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.*5+116_*5+117delAG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418805 | ||||||
| chr19:418835
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.*5+88G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418835 | ||||||
| chr19:418892
|
A | G | 1 | a0002c0004t0004g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.*5+31T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418892 | ||||||
| chr19:418914
|
G | C | 1 | a0002c0012t0004g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*5+9C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418914 | ||||||
| chr19:418915
|
C | G | 4 | a0001c0003t0001g0058a0001c0006t0001g0020a0001c0006t0001g0023others(1): Show | 4 | HG01074.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.*5+8G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418915 | ||||||
| chr19:419075
|
G | A | 22 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0002g0001others(19): Show | 23 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1621-19C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419075 | ||||||
| chr19:419167
|
C | T | 1 | a0001c0018t0006g0179 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1621-111G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419167 | ||||||
| chr19:419204
|
A | C | 8 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0035others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621-148T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419204 | ||||||
| chr19:419232
|
C | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1621-176G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419232 | ||||||
| chr19:419246
|
C | T | 3 | a0001c0001t0003g0071a0001c0001t0011g0038a0001c0007t0003g0030 | 3 | HG02486.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1621-190G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419246 | ||||||
| chr19:419407
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(186): Show | 195 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1621-351T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419407 | ||||||
| chr19:419471
|
T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(186): Show | 195 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1621-415A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419471 | ||||||
| chr19:419498
|
T | C | 56 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0035others(53): Show | 57 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1621-442A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419498 | ||||||
| chr19:419531
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0005g0053 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1621-475C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419531 | ||||||
| chr19:419561
|
G | A | 1 | a0001c0007t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1621-505C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419561 | ||||||
| chr19:419593
|
G | A | 5 | a0001c0002t0001g0003a0001c0002t0004g0088a0001c0002t0004g0096others(2): Show | 6 | HG02004.hp2 HG02273.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1621-537C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419593 | ||||||
| chr19:419788
|
C | T | 24 | a0001c0002t0001g0006a0001c0002t0001g0083a0001c0002t0001g0087others(21): Show | 25 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1621-732G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419788 | ||||||
| chr19:419799
|
T | TA | 9 | a0001c0001t0002g0079a0001c0001t0004g0035a0001c0001t0005g0028others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1621-744dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419799 | ||||||
| chr19:419874
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1621-818A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419874 | ||||||
| chr19:420118
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1621-1062G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420118 | ||||||
| chr19:420349
|
C | A | 5 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621-1293G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420349 | ||||||
| chr19:420393
|
C | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1621-1337G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420393 | ||||||
| chr19:420436
|
C | T | 4 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(1): Show | 4 | HG02451.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621-1380G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420436 | ||||||
| chr19:420619
|
T | C | 3 | a0001c0003t0002g0001a0001c0003t0002g0111a0001c0003t0002g0150 | 4 | HG00544.hp2 NA18954.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1620+1527A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420619 | ||||||
| chr19:420636
|
G | C | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1620+1510C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420636 | ||||||
| chr19:420751
|
C | T | 2 | a0001c0002t0003g0085a0001c0002t0003g0157 | 2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1620+1395G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420751 | ||||||
| chr19:420755
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(142): Show | 150 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1620+1391C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420755 | ||||||
| chr19:420780
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1620+1366C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420780 | ||||||
| chr19:420834
|
A | G | 2 | a0001c0002t0004g0174a0001c0002t0004g0175 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1620+1312T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420834 | ||||||
| chr19:420918
|
T | C | 22 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(19): Show | 23 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1620+1228A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420918 | ||||||
| chr19:420922
|
C | T | 22 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(19): Show | 23 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1620+1224G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420922 | ||||||
| chr19:420941
|
T | G | 5 | a0001c0003t0001g0113a0001c0003t0004g0108a0001c0003t0004g0109others(2): Show | 5 | HG01952.hp1 HG02293.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1620+1205A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420941 | ||||||
| chr19:420975
|
G | A | 14 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0159others(11): Show | 15 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1620+1171C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420975 | ||||||
| chr19:421297
|
A | G | 2 | a0001c0002t0004g0174a0001c0002t0004g0175 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1620+849T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421297 | ||||||
| chr19:421305
|
C | T | 30 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0113others(27): Show | 31 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1620+841G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421305 | ||||||
| chr19:421397
|
CA | C | 31 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(28): Show | 33 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1620+748delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421397 | ||||||
| chr19:421397
|
CAA | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(124): Show | 131 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1620+747_1620+748d others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421397 | ||||||
| chr19:421408
|
A | AAAAG | 7 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(4): Show | 7 | HG01109.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1620+737_1620+738i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421408 | ||||||
| chr19:421412
|
A | G | 7 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(4): Show | 7 | HG01109.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1620+734T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421412 | ||||||
| chr19:421413
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(158): Show | 167 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1620+733T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421413 | ||||||
| chr19:421430
|
A | G | 5 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1620+716T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421430 | ||||||
| chr19:421433
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(159): Show | 168 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1620+713C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421433 | ||||||
| chr19:421454
|
G | T | 2 | a0006c0011t0005g0059a0006c0011t0005g0063 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1620+692C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421454 | ||||||
| chr19:421459
|
G | A | 1 | a0001c0002t0003g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1620+687C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421459 | ||||||
| chr19:421467
|
G | GAGGA | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(167): Show | 176 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1620+675_1620+678d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421467 | ||||||
| chr19:421499
|
T | G | 1 | a0003c0008t0003g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1620+647A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421499 | ||||||
| chr19:421567
|
A | G | 4 | a0001c0001t0011g0038a0005c0009t0005g0048a0005c0009t0014g0040others(1): Show | 4 | HG02486.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1620+579T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421567 | ||||||
| chr19:421571
|
T | C | 1 | a0002c0012t0002g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1620+575A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421571 | ||||||
| chr19:421597
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1620+549A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421597 | ||||||
| chr19:421661
|
G | A | 1 | a0001c0003t0001g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1620+485C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421661 | ||||||
| chr19:421825
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(134): Show | 141 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1620+321T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421825 | ||||||
| chr19:421842
|
C | T | 35 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(32): Show | 36 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1620+304G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421842 | ||||||
| chr19:421976
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1620+170A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421976 | ||||||
| chr19:422023
|
TCGAGACC others(44): Show |
T | 34 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(31): Show | 36 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1620+72_1620+122de others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 422023 | ||||||
| chr19:422033
|
TGAGACCC others(35): Show |
T | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(124): Show | 131 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1620+71_1620+112de others(43): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 422033 | ||||||
| chr19:422118
|
G | A | 2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1620+28C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 422118 | ||||||
| chr19:422481
|
G | A | 30 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0113others(27): Show | 31 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1310-25C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422481 | ||||||
| chr19:422512
|
C | T | 2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1310-56G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422512 | ||||||
| chr19:422534
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(96): Show | 102 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1310-78C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422534 | ||||||
| chr19:422537
|
T | A | 1 | a0001c0001t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1310-81A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422537 | ||||||
| chr19:422543
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(131): Show | 138 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1310-87C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422543 | ||||||
| chr19:422555
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(131): Show | 138 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1310-99C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422555 | ||||||
| chr19:422579
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(94): Show | 100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1310-123G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422579 | ||||||
| chr19:422584
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(131): Show | 138 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1310-128C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422584 | ||||||
| chr19:422592
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(94): Show | 100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1310-136G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422592 | ||||||
| chr19:422625
|
G | A | 2 | a0001c0002t0004g0174a0001c0002t0004g0175 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1310-169C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422625 | ||||||
| chr19:422625
|
G | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(65): Show | 70 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1310-169C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422625 | ||||||
| chr19:422665
|
G | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(30): Show | 35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1310-209C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422665 | ||||||
| chr19:422730
|
T | G | 1 | a0002c0004t0004g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1310-274A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422730 | ||||||
| chr19:422738
|
A | G | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1310-282T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422738 | ||||||
| chr19:422755
|
T | C | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1310-299A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422755 | ||||||
| chr19:422770
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1310-314G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422770 | ||||||
| chr19:422904
|
G | C | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1310-448C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422904 | ||||||
| chr19:422938
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(85): Show | 91 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1310-482G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422938 | ||||||
| chr19:423099
|
T | TCCTCCAG others(298): Show |
1 | a0001c0001t0008g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1310-948_1310-644d others(307): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | ||||||
| chr19:423099
|
TCCTCCAG others(237): Show |
T | 1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1310-887_1310-644d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | ||||||
| chr19:423099
|
TCCTCCAG others(298): Show |
T | 32 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(29): Show | 34 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1310-948_1310-644d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | ||||||
| chr19:423099
|
TCCTCCAG others(481): Show |
T | 5 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1310-1131_1310-644 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | ||||||
| chr19:423131
|
G | GCCCTGAC others(54): Show |
20 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(17): Show | 21 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1310-676_1310-675i others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423131 | ||||||
| chr19:423131
|
GCCCTGAC others(420): Show |
G | 36 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0002g0101others(33): Show | 36 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1310-1102_1310-676 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423131 | ||||||
| chr19:423142
|
C | T | 31 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(28): Show | 32 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1310-686G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423142 | ||||||
| chr19:423143
|
ACTCCCTG others(359): Show |
A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1310-1053_1310-688 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423143 | ||||||
| chr19:423157
|
C | A | 31 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(28): Show | 32 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1310-701G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423157 | ||||||
| chr19:423192
|
G | C | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1310-736C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423192 | ||||||
| chr19:423192
|
GCCCTGAC others(359): Show |
G | 42 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(39): Show | 43 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1310-1102_1310-737 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423192 | ||||||
| chr19:423204
|
ACTCCCTG others(420): Show |
A | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1310-1175_1310-749 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423204 | ||||||
| chr19:423241
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0166 | 3 | HG00609.hp1 NA18985.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1310-785C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423241 | ||||||
| chr19:423279
|
G | GGCCCCTC others(115): Show |
1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1310-945_1310-824d others(124): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423279 | ||||||
| chr19:423279
|
GGCCCCTC others(54): Show |
G | 1 | a0001c0001t0001g0142 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1310-884_1310-824d others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423279 | ||||||
| chr19:423279
|
GGCCCCTC others(115): Show |
G | 1 | a0001c0001t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1310-945_1310-824d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423279 | ||||||
| chr19:423340
|
C | CGCCCCTC others(54): Show |
4 | a0001c0005t0001g0022a0001c0014t0001g0021a0001c0020t0001g0104others(1): Show | 4 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1310-885_1310-884i others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423340 | ||||||
| chr19:423401
|
C | G | 20 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(17): Show | 21 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1310-945G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423401 | ||||||
| chr19:423436
|
G | GCCCTGAC others(115): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0124a0001c0001t0001g0128others(1): Show | 4 | HG00639.hp2 HG01071.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1310-1102_1310-981 others(125): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423436 | ||||||
| chr19:423436
|
GCCCTGAC others(115): Show |
G | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1310-1102_1310-981 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423436 | ||||||
| chr19:423462
|
C | A | 1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1310-1006G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423462 | ||||||
| chr19:423462
|
C | G | 32 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(29): Show | 34 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1310-1006G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423462 | ||||||
| chr19:423509
|
G | A | 20 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(17): Show | 21 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1310-1053C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423509 | ||||||
| chr19:423509
|
GCTCCCTG others(54): Show |
G | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1310-1114_1310-105 others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423509 | ||||||
| chr19:423558
|
C | G | 54 | a0001c0001t0001g0112a0001c0001t0002g0039a0001c0001t0002g0057others(51): Show | 57 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.1310-1102G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423558 | ||||||
| chr19:423569
|
C | T | 2 | a0001c0002t0001g0006a0009c0015t0012g0027 | 3 | HG00558.hp2 HG01952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1310-1113G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423569 | ||||||
| chr19:423570
|
A | G | 32 | a0001c0002t0001g0094a0001c0003t0001g0058a0001c0003t0001g0062others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1310-1114T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423570 | ||||||
| chr19:423570
|
ACTCCCTG others(54): Show |
A | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1310-1175_1310-111 others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423570 | ||||||
| chr19:423618
|
C | A | 32 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1310-1162G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423618 | ||||||
| chr19:423619
|
G | C | 34 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(31): Show | 36 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1310-1163C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423619 | ||||||
| chr19:423622
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1310-1166G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423622 | ||||||
| chr19:423631
|
G | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(30): Show | 35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1310-1175C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423631 | ||||||
| chr19:423734
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1310-1278C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423734 | ||||||
| chr19:423933
|
G | A | 32 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1309+1164C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423933 | ||||||
| chr19:424074
|
T | A | 2 | a0001c0002t0003g0085a0001c0002t0003g0157 | 2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1309+1023A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424074 | ||||||
| chr19:424142
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1309+955A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424142 | ||||||
| chr19:424168
|
G | A | 1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1309+929C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424168 | ||||||
| chr19:424216
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1309+881C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424216 | ||||||
| chr19:424267
|
G | A | 1 | a0001c0006t0006g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1309+830C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424267 | ||||||
| chr19:424326
|
C | T | 1 | a0001c0003t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1309+771G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424326 | ||||||
| chr19:424416
|
G | A | 4 | a0001c0001t0011g0038a0005c0009t0005g0048a0005c0009t0014g0040others(1): Show | 4 | HG02486.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309+681C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424416 | ||||||
| chr19:424505
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1309+592C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424505 | ||||||
| chr19:424531
|
C | T | 26 | a0001c0003t0001g0058a0001c0003t0001g0113a0001c0003t0002g0060others(23): Show | 26 | HG00558.hp1 HG00621.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1309+566G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424531 | ||||||
| chr19:424559
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1309+538C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424559 | ||||||
| chr19:424806
|
G | A | 35 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(32): Show | 37 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1309+291C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424806 | ||||||
| chr19:425020
|
T | G | 1 | a0001c0002t0001g0003 | 2 | NA18939.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1309+77A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 425020 | ||||||
| chr19:425250
|
G | C | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-19C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425250 | ||||||
| chr19:425290
|
G | A | 3 | a0001c0001t0003g0036a0001c0001t0003g0071a0001c0005t0006g0010 | 3 | HG02055.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1175-59C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425290 | ||||||
| chr19:425305
|
C | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0005t0001g0011others(7): Show | 10 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175-74G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425305 | ||||||
| chr19:425343
|
C | A | 2 | a0001c0002t0004g0174a0001c0002t0004g0175 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-112G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425343 | ||||||
| chr19:425370
|
C | A | 32 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1175-139G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425370 | ||||||
| chr19:425383
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1175-152C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425383 | ||||||
| chr19:425413
|
T | C | 2 | a0001c0001t0006g0054a0003c0008t0006g0185 | 2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1175-182A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425413 | ||||||
| chr19:425460
|
G | A | 1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1175-229C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425460 | ||||||
| chr19:425469
|
G | A | 31 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(28): Show | 32 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1175-238C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425469 | ||||||
| chr19:425530
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1175-299T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425530 | ||||||
| chr19:425559
|
T | C | 36 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(33): Show | 38 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1175-328A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425559 | ||||||
| chr19:425581
|
A | G | 2 | a0001c0002t0004g0174a0001c0002t0004g0175 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-350T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425581 | ||||||
| chr19:425755
|
G | A | 32 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1175-524C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425755 | ||||||
| chr19:425895
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1175-664C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425895 | ||||||
| chr19:426029
|
C | CA | 19 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0002g0057others(16): Show | 19 | HG00621.hp2 HG01071.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1175-799dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426029 | ||||||
| chr19:426029
|
CA | C | 5 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-799delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426029 | ||||||
| chr19:426043
|
A | C | 1 | a0001c0013t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1175-812T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426043 | ||||||
| chr19:426219
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1175-988C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426219 | ||||||
| chr19:426331
|
AAGAGTCC others(98): Show |
A | 1 | a0011c0025t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1175-1205_1175-110 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426331 | ||||||
| chr19:426359
|
CGAGAGGC others(168): Show |
C | 2 | a0001c0001t0001g0133a0001c0001t0002g0052 | 2 | HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1175-1303_1175-112 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426359 | ||||||
| chr19:426363
|
A | AGGCAGAG others(28): Show |
1 | a0002c0004t0001g0196 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1175-1167_1175-113 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426363 | ||||||
| chr19:426363
|
AGGCAGAG others(203): Show |
A | 5 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1342_1175-113 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426363 | ||||||
| chr19:426363
|
AGGCAGAG others(378): Show |
A | 1 | a0001c0001t0001g0002 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1175-1517_1175-113 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426363 | ||||||
| chr19:426428
|
G | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-1197C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426428 | ||||||
| chr19:426433
|
GGGCAGAG others(63): Show |
G | 2 | a0001c0002t0004g0174a0001c0002t0004g0175 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-1272_1175-120 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426433 | ||||||
| chr19:426440
|
G | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(30): Show | 35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1175-1209C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426440 | ||||||
| chr19:426463
|
G | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-1232C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426463 | ||||||
| chr19:426464
|
AGAGAGGC others(28): Show |
A | 33 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1268_1175-123 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426464 | ||||||
| chr19:426468
|
A | G | 2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1175-1237T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426468 | ||||||
| chr19:426503
|
A | G | 33 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1272T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426503 | ||||||
| chr19:426503
|
AGGCAGAG others(98): Show |
A | 33 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(30): Show | 35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1175-1377_1175-127 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426503 | ||||||
| chr19:426538
|
A | AGGCAGAG others(28): Show |
1 | a0001c0001t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1175-1342_1175-130 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | ||||||
| chr19:426538
|
A | AGGCAGAG others(63): Show |
1 | a0001c0001t0001g0132 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1175-1377_1175-130 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | ||||||
| chr19:426538
|
A | G | 4 | a0001c0002t0004g0174a0001c0002t0004g0175a0001c0003t0004g0109others(1): Show | 4 | NA18612.hp2 NA18947.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1307T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | ||||||
| chr19:426538
|
AGGCAGAG others(28): Show |
A | 7 | a0001c0001t0001g0141a0001c0001t0001g0176a0001c0001t0004g0035others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-1342_1175-130 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | ||||||
| chr19:426538
|
AGGCAGAG others(63): Show |
A | 24 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0002g0101others(21): Show | 25 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1175-1377_1175-130 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | ||||||
| chr19:426538
|
AGGCAGAG others(133): Show |
A | 8 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-1447_1175-130 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | ||||||
| chr19:426566
|
C | G | 33 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1335G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426566 | ||||||
| chr19:426568
|
G | A | 33 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1337C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426568 | ||||||
| chr19:426569
|
A | C | 33 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1338T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426569 | ||||||
| chr19:426573
|
G | A | 33 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1342C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426573 | ||||||
| chr19:426585
|
G | A | 1 | a0001c0003t0002g0111 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1175-1354C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426585 | ||||||
| chr19:426608
|
G | A | 27 | a0001c0002t0002g0046a0001c0003t0001g0058a0001c0003t0001g0062others(24): Show | 28 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1175-1377C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426608 | ||||||
| chr19:426670
|
ACCGAGAG others(134): Show |
A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1175-1580_1175-144 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426670 | ||||||
| chr19:426671
|
C | G | 1 | a0001c0005t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1440G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426671 | ||||||
| chr19:426672
|
C | T | 1 | a0001c0005t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1441G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426672 | ||||||
| chr19:426674
|
A | C | 1 | a0001c0005t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1443T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426674 | ||||||
| chr19:426800
|
G | GGAGGACG others(63): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0102 | 2 | NA18999.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1175-1570_1175-156 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426800 | ||||||
| chr19:426810
|
AC | A | 69 | a0001c0001t0002g0052a0001c0002t0001g0003a0001c0002t0001g0006others(66): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1175-1580delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426810 | ||||||
| chr19:426811
|
C | G | 4 | a0001c0001t0004g0159a0001c0001t0004g0161a0002c0004t0001g0192others(1): Show | 4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1580G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426811 | ||||||
| chr19:426812
|
C | T | 4 | a0001c0001t0004g0159a0001c0001t0004g0161a0002c0004t0001g0192others(1): Show | 4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1581G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426812 | ||||||
| chr19:426814
|
A | C | 4 | a0001c0001t0004g0159a0001c0001t0004g0161a0002c0004t0001g0192others(1): Show | 4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1583T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426814 | ||||||
| chr19:426814
|
AGAGGGGC others(28): Show |
A | 2 | a0001c0007t0003g0030a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1175-1618_1175-158 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426814 | ||||||
| chr19:426853
|
G | T | 67 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(64): Show | 70 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1175-1622C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426853 | ||||||
| chr19:426974
|
C | T | 75 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0003g0036others(72): Show | 78 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1175-1743G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426974 | ||||||
| chr19:427009
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1175-1778G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427009 | ||||||
| chr19:427455
|
GGGGGAAT others(18): Show |
G | 1 | a0002c0004t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1175-2249_1175-222 others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427455 | ||||||
| chr19:427466
|
ACACGGCA others(43): Show |
A | 1 | a0001c0001t0004g0065 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1175-2285_1175-223 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427466 | ||||||
| chr19:427476
|
G | A | 7 | a0001c0001t0002g0101a0001c0001t0007g0041a0001c0001t0011g0038others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-2245C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427476 | ||||||
| chr19:427491
|
A | ACACGGCA others(18): Show |
8 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-2285_1175-226 others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427491 | ||||||
| chr19:427491
|
A | G | 1 | a0002c0004t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1175-2260T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427491 | ||||||
| chr19:427491
|
ACACGGCA others(18): Show |
A | 1 | a0002c0004t0001g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1175-2285_1175-226 others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427491 | ||||||
| chr19:427516
|
G | A | 1 | a0001c0003t0002g0150 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1175-2285C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427516 | ||||||
| chr19:427548
|
ACAGGGAA others(143): Show |
A | 35 | a0001c0001t0002g0052a0001c0001t0005g0047a0001c0002t0002g0046others(32): Show | 36 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1175-2467_1175-231 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427548 | ||||||
| chr19:427573
|
ACAGGGAA others(19): Show |
A | 1 | a0001c0001t0004g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1175-2368_1175-234 others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427573 | ||||||
| chr19:427573
|
ACAGGGAA others(118): Show |
A | 39 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(36): Show | 41 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1175-2467_1175-234 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427573 | ||||||
| chr19:427580
|
AGGGGGAA others(93): Show |
A | 2 | a0001c0002t0001g0140a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2449_1175-235 others(104): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427580 | ||||||
| chr19:427645
|
GGCGCACA others(61): Show |
G | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1175-2482_1175-241 others(72): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427645 | ||||||
| chr19:427687
|
C | T | 2 | a0001c0002t0001g0140a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2456G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427687 | ||||||
| chr19:427691
|
A | G | 2 | a0001c0002t0001g0140a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2460T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427691 | ||||||
| chr19:427698
|
G | A | 2 | a0001c0002t0001g0140a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2467C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427698 | ||||||
| chr19:427727
|
GGAAGGGG others(144): Show |
G | 1 | a0001c0001t0001g0162 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1175-2647_1175-249 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427727 | ||||||
| chr19:427852
|
GGAAGGGG others(19): Show |
G | 4 | a0001c0001t0016g0070a0001c0013t0005g0007a0001c0017t0005g0056others(1): Show | 4 | HG02622.hp1 HG02622.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-2647_1175-262 others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427852 | ||||||
| chr19:427989
|
C | G | 1 | a0001c0002t0003g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1174+2695G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427989 | ||||||
| chr19:428066
|
A | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+2618T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428066 | ||||||
| chr19:428077
|
G | T | 70 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0003g0036others(67): Show | 73 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1174+2607C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428077 | ||||||
| chr19:428463
|
C | T | 1 | a0001c0005t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1174+2221G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428463 | ||||||
| chr19:428527
|
G | A | 1 | a0001c0001t0005g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1174+2157C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428527 | ||||||
| chr19:428530
|
T | G | 6 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0002g0001others(3): Show | 7 | HG00544.hp2 HG00621.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+2154A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428530 | ||||||
| chr19:428605
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1174+2079T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428605 | ||||||
| chr19:428608
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1174+2076T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428608 | ||||||
| chr19:428792
|
GAC | G | 73 | a0001c0001t0002g0101a0001c0001t0003g0071a0001c0001t0007g0041others(70): Show | 76 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1174+1890_1174+189 others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428792 | ||||||
| chr19:428832
|
T | C | 1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1174+1852A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428832 | ||||||
| chr19:428907
|
C | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+1777G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428907 | ||||||
| chr19:428955
|
C | G | 21 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(18): Show | 22 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1174+1729G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428955 | ||||||
| chr19:429109
|
GTGCACGG others(581): Show |
G | 2 | a0001c0001t0001g0160a0001c0016t0001g0144 | 2 | HG00733.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1174+987_1174+1574 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429109 | ||||||
| chr19:429128
|
TGTGTGGA others(42): Show |
T | 3 | a0001c0006t0001g0020a0001c0006t0001g0023a0001c0006t0001g0024 | 3 | HG03209.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1174+1507_1174+155 others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429128 | ||||||
| chr19:429139
|
T | C | 79 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0002g0101others(76): Show | 82 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1174+1545A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429139 | ||||||
| chr19:429227
|
G | A | 4 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0013g0073others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1457C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429227 | ||||||
| chr19:429304
|
C | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+1380G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429304 | ||||||
| chr19:429306
|
T | C | 1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1174+1378A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429306 | ||||||
| chr19:429404
|
T | G | 27 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174+1280A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429404 | ||||||
| chr19:429410
|
G | T | 1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1174+1274C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429410 | ||||||
| chr19:429533
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1174+1151G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429533 | ||||||
| chr19:429553
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174+1131G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429553 | ||||||
| chr19:429560
|
A | T | 33 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1174+1124T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429560 | ||||||
| chr19:429575
|
G | A | 1 | a0002c0004t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+1109C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429575 | ||||||
| chr19:429581
|
GCAGTACC others(42): Show |
G | 4 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0013g0073others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1054_1174+110 others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429581 | ||||||
| chr19:429599
|
A | G | 4 | a0001c0001t0011g0038a0005c0009t0005g0048a0005c0009t0014g0040others(1): Show | 4 | HG02486.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1085T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429599 | ||||||
| chr19:429604
|
G | C | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1080C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429604 | ||||||
| chr19:429613
|
AATACCGT others(42): Show |
A | 4 | a0001c0001t0003g0071a0005c0009t0005g0048a0005c0009t0014g0040others(1): Show | 4 | NA18522.hp2 NA19240.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+1022_1174+107 others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429613 | ||||||
| chr19:429615
|
T | C | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1069A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429615 | ||||||
| chr19:429630
|
A | G | 2 | a0001c0001t0011g0038a0001c0006t0002g0019 | 2 | HG01943.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1174+1054T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429630 | ||||||
| chr19:429653
|
C | G | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1031G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429653 | ||||||
| chr19:429654
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1030C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429654 | ||||||
| chr19:429659
|
T | C | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1025A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429659 | ||||||
| chr19:429662
|
C | A | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1022G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429662 | ||||||
| chr19:429664
|
TACCGTGT others(42): Show |
T | 1 | a0002c0004t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+971_1174+1019 others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429664 | ||||||
| chr19:429679
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1005C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429679 | ||||||
| chr19:429721
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+963C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429721 | ||||||
| chr19:429725
|
G | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0151a0001c0002t0001g0152 | 3 | HG02015.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1174+959C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429725 | ||||||
| chr19:429746
|
A | G | 33 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1174+938T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429746 | ||||||
| chr19:429751
|
C | T | 2 | a0001c0003t0004g0109a0001c0003t0004g0110 | 2 | NA18612.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1174+933G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429751 | ||||||
| chr19:429776
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174+908G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429776 | ||||||
| chr19:429815
|
G | A | 3 | a0001c0003t0002g0001a0001c0003t0002g0111a0001c0003t0002g0150 | 4 | HG00544.hp2 NA18954.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+869C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429815 | ||||||
| chr19:429850
|
A | G | 2 | a0001c0001t0004g0159a0001c0005t0006g0009 | 2 | HG02148.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174+834T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429850 | ||||||
| chr19:429891
|
A | G | 1 | a0002c0004t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1174+793T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429891 | ||||||
| chr19:429930
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1174+754A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429930 | ||||||
| chr19:429962
|
A | G | 94 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0002g0101others(91): Show | 97 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1174+722T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429962 | ||||||
| chr19:429976
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+708C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429976 | ||||||
| chr19:429991
|
A | G | 3 | a0001c0001t0002g0101a0001c0001t0007g0041a0008c0021t0002g0032 | 3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1174+693T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429991 | ||||||
| chr19:430029
|
C | T | 2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1174+655G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430029 | ||||||
| chr19:430034
|
CCCCAACG others(43): Show |
C | 1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1174+600_1174+649d others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430034 | ||||||
| chr19:430097
|
G | A | 1 | a0001c0018t0006g0179 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174+587C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430097 | ||||||
| chr19:430105
|
A | G | 1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1174+579T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430105 | ||||||
| chr19:430141
|
A | G | 36 | a0001c0001t0003g0004a0001c0001t0003g0180a0001c0002t0002g0046others(33): Show | 38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1174+543T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430141 | ||||||
| chr19:430148
|
GA | G | 33 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1174+535delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430148 | ||||||
| chr19:430178
|
C | T | 3 | a0001c0003t0002g0001a0001c0003t0002g0111a0001c0003t0002g0150 | 4 | HG00544.hp2 NA18954.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+506G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430178 | ||||||
| chr19:430184
|
C | A | 2 | a0001c0014t0001g0021a0001c0020t0001g0104 | 2 | HG00735.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1174+500G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430184 | ||||||
| chr19:430205
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1174+479T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430205 | ||||||
| chr19:430211
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1174+473C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430211 | ||||||
| chr19:430246
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1174+438C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430246 | ||||||
| chr19:430271
|
G | A | 19 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0004others(16): Show | 20 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1174+413C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430271 | ||||||
| chr19:430301
|
C | G | 5 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0003g0036others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+383G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430301 | ||||||
| chr19:430310
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1174+374C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430310 | ||||||
| chr19:430323
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1174+361C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430323 | ||||||
| chr19:430370
|
C | T | 38 | a0001c0001t0002g0101a0001c0001t0007g0041a0001c0002t0001g0003others(35): Show | 40 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1174+314G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430370 | ||||||
| chr19:430380
|
A | G | 12 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0159others(9): Show | 12 | HG00323.hp2 HG01258.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174+304T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430380 | ||||||
| chr19:430450
|
C | G | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1174+234G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430450 | ||||||
| chr19:430458
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1174+226C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430458 | ||||||
| chr19:430559
|
G | A | 5 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0005t0001g0025others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+125C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430559 | ||||||
| chr19:430613
|
G | A | 4 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0013g0073others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+71C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430613 | ||||||
| chr19:430807
|
ACCCCCAG others(3): Show |
A | 1 | a0001c0001t0001g0121 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1111-70_1111-61del others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430807 | ||||||
| chr19:430822
|
G | A | 1 | a0001c0001t0006g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1111-75C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430822 | ||||||
| chr19:430847
|
A | C | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-100T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430847 | ||||||
| chr19:430934
|
G | A | 5 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0003g0036others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-187C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430934 | ||||||
| chr19:431029
|
T | A | 141 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0143others(138): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1111-282A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431029 | ||||||
| chr19:431033
|
C | T | 2 | a0001c0007t0003g0030a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1111-286G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431033 | ||||||
| chr19:431097
|
C | T | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-350G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431097 | ||||||
| chr19:431104
|
AC | A | 38 | a0001c0001t0001g0143a0001c0001t0003g0071a0001c0003t0001g0058others(35): Show | 39 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1111-358delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431104 | ||||||
| chr19:431123
|
G | A | 1 | a0002c0004t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1111-376C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431123 | ||||||
| chr19:431187
|
G | A | 37 | a0001c0001t0003g0071a0001c0003t0001g0058a0001c0003t0001g0062others(34): Show | 38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1111-440C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431187 | ||||||
| chr19:431239
|
T | G | 4 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0013g0073others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-492A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431239 | ||||||
| chr19:431248
|
C | CAGAGGAG others(51): Show |
68 | a0001c0001t0001g0130a0001c0002t0001g0003a0001c0002t0001g0006others(65): Show | 71 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1111-559_1111-502d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | ||||||
| chr19:431248
|
C | CAGAGGAG others(167): Show |
2 | a0005c0009t0005g0048a0005c0009t0014g0040 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111-502_1111-501i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | ||||||
| chr19:431248
|
C | CAGAGGAG others(279): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-502_1111-501i others(288): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | ||||||
| chr19:431248
|
C | CAGAGGAG others(283): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-502_1111-501i others(292): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | ||||||
| chr19:431266
|
T | TAGATGGC others(395): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-520_1111-519i others(404): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431266 | ||||||
| chr19:431281
|
CGTGA | C | 4 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(1): Show | 4 | HG02486.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-538_1111-535d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431281 | ||||||
| chr19:431305
|
T | A | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-558A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431305 | ||||||
| chr19:431316
|
C | CGGGCAGA others(391): Show |
1 | a0001c0006t0006g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1111-570_1111-569i others(400): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431316 | ||||||
| chr19:431316
|
CGGGCAGA others(329): Show |
C | 1 | a0002c0004t0005g0190 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1111-905_1111-570d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431316 | ||||||
| chr19:431332
|
G | GCTTCATC others(167): Show |
6 | a0001c0007t0006g0037a0001c0007t0006g0055a0001c0023t0007g0186others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-586_1111-585i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431332 | ||||||
| chr19:431363
|
A | T | 15 | a0001c0001t0002g0052a0001c0001t0002g0101a0001c0001t0003g0036others(12): Show | 15 | HG00639.hp1 HG01943.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1111-616T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431363 | ||||||
| chr19:431375
|
A | G | 26 | a0001c0001t0001g0130a0001c0001t0002g0039a0001c0001t0002g0052others(23): Show | 26 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1111-628T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431375 | ||||||
| chr19:431390
|
A | G | 24 | a0001c0001t0001g0130a0001c0001t0002g0039a0001c0001t0002g0052others(21): Show | 24 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1111-643T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431390 | ||||||
| chr19:431421
|
T | A | 6 | a0001c0001t0002g0039a0001c0001t0003g0071a0001c0006t0002g0019others(3): Show | 6 | HG00639.hp1 HG01943.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-674A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431421 | ||||||
| chr19:431421
|
TTAGAGGA others(47): Show |
T | 2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1111-728_1111-675d others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431421 | ||||||
| chr19:431421
|
TTAGAGGA others(155): Show |
T | 1 | a0001c0001t0006g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111-836_1111-675d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431421 | ||||||
| chr19:431432
|
CGGGCAGA others(557): Show |
C | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-1249_1111-686 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431432 | ||||||
| chr19:431433
|
G | A | 1 | a0001c0006t0002g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-686C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431433 | ||||||
| chr19:431436
|
C | CAGAT | 15 | a0001c0001t0001g0130a0001c0001t0003g0071a0001c0006t0002g0019others(12): Show | 15 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1111-693_1111-690d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431436 | ||||||
| chr19:431436
|
C | CAGATAGA others(453): Show |
2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-690_1111-689i others(462): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431436 | ||||||
| chr19:431436
|
C | CAGATAGA others(55): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1111-690_1111-689i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431436 | ||||||
| chr19:431440
|
TGGCGCTT others(43): Show |
T | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-743_1111-694d others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431440 | ||||||
| chr19:431444
|
G | A | 1 | a0001c0006t0002g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-697C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431444 | ||||||
| chr19:431452
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-705C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431452 | ||||||
| chr19:431474
|
G | A | 1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-727C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431474 | ||||||
| chr19:431475
|
A | T | 6 | a0001c0001t0003g0071a0001c0006t0002g0019a0002c0004t0001g0187others(3): Show | 6 | HG00639.hp1 HG01943.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-728T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431475 | ||||||
| chr19:431486
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1111-739G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431486 | ||||||
| chr19:431487
|
G | A | 2 | a0001c0001t0001g0130a0001c0002t0004g0096 | 2 | HG01123.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1111-740C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431487 | ||||||
| chr19:431490
|
C | CAGAT | 20 | a0001c0001t0001g0130a0001c0001t0002g0039a0001c0001t0002g0101others(17): Show | 20 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-747_1111-744d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | ||||||
| chr19:431490
|
C | CAGATAGA others(55): Show |
1 | a0001c0002t0004g0096 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1111-744_1111-743i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | ||||||
| chr19:431490
|
C | CAGATGGC others(167): Show |
1 | a0002c0012t0004g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1111-744_1111-743i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | ||||||
| chr19:431490
|
CAGATGGC others(163): Show |
C | 12 | a0001c0001t0003g0171a0001c0001t0005g0168a0001c0001t0006g0043others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111-913_1111-744d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | ||||||
| chr19:431498
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0003g0036a0001c0005t0006g0010others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-751C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431498 | ||||||
| chr19:431529
|
A | ATAGAGGA others(109): Show |
1 | a0001c0003t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1111-783_1111-782i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | ||||||
| chr19:431529
|
A | ATAGAGGA others(167): Show |
4 | a0001c0003t0002g0072a0001c0003t0002g0181a0001c0003t0004g0108others(1): Show | 4 | HG01952.hp1 HG02132.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-783_1111-782i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | ||||||
| chr19:431529
|
A | T | 8 | a0001c0001t0001g0130a0001c0001t0002g0052a0001c0001t0003g0071others(5): Show | 8 | HG01123.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-782T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | ||||||
| chr19:431529
|
ATAGAGGA others(221): Show |
A | 1 | a0001c0005t0006g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1111-1010_1111-783 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | ||||||
| chr19:431540
|
C | G | 3 | a0001c0001t0002g0101a0001c0001t0007g0041a0008c0021t0002g0032 | 3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1111-793G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431540 | ||||||
| chr19:431540
|
CGGGCAGA others(105): Show |
C | 21 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111-905_1111-794d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431540 | ||||||
| chr19:431541
|
G | A | 6 | a0001c0001t0002g0039a0001c0001t0003g0071a0001c0002t0002g0046others(3): Show | 6 | HG00639.hp1 HG03942.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-794C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431541 | ||||||
| chr19:431544
|
C | CAGAT | 32 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0002g0079others(29): Show | 32 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1111-801_1111-798d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(229): Show |
1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-798_1111-797i others(238): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(573): Show |
1 | a0001c0017t0005g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1111-798_1111-797i others(582): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(399): Show |
1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-798_1111-797i others(408): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(457): Show |
1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-798_1111-797i others(466): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(225): Show |
7 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(4): Show | 8 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-798_1111-797i others(234): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(283): Show |
2 | a0001c0003t0002g0076a0002c0012t0002g0203 | 2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1111-798_1111-797i others(292): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(341): Show |
11 | a0001c0003t0001g0113a0001c0003t0002g0060a0001c0003t0002g0069others(8): Show | 11 | HG00558.hp1 HG00621.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-798_1111-797i others(350): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(689): Show |
1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-798_1111-797i others(698): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(55): Show |
2 | a0001c0002t0001g0140a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1111-798_1111-797i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431544
|
C | CAGATAGA others(113): Show |
30 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(27): Show | 32 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1111-798_1111-797i others(122): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | ||||||
| chr19:431549
|
G | A | 5 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(2): Show | 5 | HG00099.hp1 HG02486.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-802C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431549 | ||||||
| chr19:431551
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1111-804G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431551 | ||||||
| chr19:431552
|
G | A | 6 | a0001c0001t0002g0039a0001c0001t0003g0071a0001c0002t0002g0046others(3): Show | 6 | HG00639.hp1 HG03942.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-805C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431552 | ||||||
| chr19:431583
|
A | T | 50 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0002g0079others(47): Show | 52 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1111-836T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431583 | ||||||
| chr19:431583
|
ATAGAGGA others(283): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1111-1126_1111-837 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431583 | ||||||
| chr19:431594
|
C | G | 25 | a0001c0001t0002g0101a0001c0001t0003g0071a0001c0001t0004g0033others(22): Show | 26 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1111-847G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431594 | ||||||
| chr19:431595
|
G | A | 8 | a0001c0001t0002g0052a0001c0003t0002g0072a0001c0003t0002g0078others(5): Show | 8 | HG01952.hp1 HG02132.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-848C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431595 | ||||||
| chr19:431598
|
CAGAT | C | 7 | a0001c0001t0001g0130a0001c0001t0002g0039a0002c0004t0001g0187others(4): Show | 7 | HG00639.hp1 HG01123.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-855_1111-852d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431598 | ||||||
| chr19:431602
|
T | TAGATGGC others(47): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-856_1111-855i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431602 | ||||||
| chr19:431604
|
G | C | 1 | a0001c0017t0005g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1111-857C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431604 | ||||||
| chr19:431607
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1111-860C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431607 | ||||||
| chr19:431607
|
GGCGCTTC others(109): Show |
G | 1 | a0001c0005t0001g0022 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1111-976_1111-861d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431607 | ||||||
| chr19:431610
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-863C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431610 | ||||||
| chr19:431629
|
C | T | 1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-882G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431629 | ||||||
| chr19:431641
|
A | T | 56 | a0001c0001t0001g0126a0001c0001t0002g0057a0001c0001t0003g0004others(53): Show | 59 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1111-894T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431641 | ||||||
| chr19:431652
|
G | C | 88 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0002g0039others(85): Show | 92 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1111-905C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431652 | ||||||
| chr19:431653
|
G | A | 6 | a0001c0002t0002g0046a0001c0007t0006g0037a0001c0023t0007g0186others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-906C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431653 | ||||||
| chr19:431656
|
CAGAT | C | 7 | a0001c0001t0001g0130a0001c0001t0002g0039a0001c0001t0006g0054others(4): Show | 7 | HG00639.hp1 HG01123.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-913_1111-910d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431656 | ||||||
| chr19:431660
|
T | TAGATGGC others(47): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-914_1111-913i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | ||||||
| chr19:431660
|
T | TAGATGGC others(47): Show |
1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1111-914_1111-913i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | ||||||
| chr19:431660
|
T | TAGATGGC others(101): Show |
1 | a0008c0021t0002g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1111-914_1111-913i others(110): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | ||||||
| chr19:431660
|
T | TAGATGGC others(101): Show |
1 | a0001c0001t0002g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1111-914_1111-913i others(110): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | ||||||
| chr19:431660
|
T | TAGATGGC others(47): Show |
2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-914_1111-913i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | ||||||
| chr19:431660
|
T | TAGATGGC others(441): Show |
1 | a0001c0006t0002g0018 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1111-914_1111-913i others(450): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | ||||||
| chr19:431665
|
G | A | 21 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(18): Show | 21 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111-918C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431665 | ||||||
| chr19:431668
|
G | A | 36 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(33): Show | 38 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1111-921C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431668 | ||||||
| chr19:431699
|
A | ATAGAGGA others(51): Show |
2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1111-953_1111-952i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431699 | ||||||
| chr19:431699
|
A | T | 76 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0126others(73): Show | 80 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1111-952T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431699 | ||||||
| chr19:431708
|
G | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-961C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431708 | ||||||
| chr19:431710
|
C | G | 19 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(16): Show | 20 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-963G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431710 | ||||||
| chr19:431711
|
G | A | 5 | a0001c0002t0002g0046a0001c0006t0001g0020a0001c0006t0001g0023others(2): Show | 5 | HG03098.hp2 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-964C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431711 | ||||||
| chr19:431714
|
CAGAT | C | 9 | a0001c0001t0001g0126a0001c0001t0002g0057a0001c0001t0003g0050others(6): Show | 9 | HG00639.hp1 HG02015.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111-971_1111-968d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431714 | ||||||
| chr19:431720
|
G | C | 4 | a0001c0001t0004g0159a0001c0001t0004g0161a0002c0004t0001g0192others(1): Show | 4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-973C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431720 | ||||||
| chr19:431723
|
A | G | 130 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0097others(127): Show | 134 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1111-976T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431723 | ||||||
| chr19:431725
|
C | CGCTTCAT others(109): Show |
1 | a0001c0002t0003g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1111-979_1111-978i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431725 | ||||||
| chr19:431725
|
C | CGCTTCAT others(109): Show |
1 | a0001c0002t0001g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1111-979_1111-978i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431725 | ||||||
| chr19:431725
|
C | T | 31 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(28): Show | 33 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1111-978G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431725 | ||||||
| chr19:431726
|
G | A | 3 | a0001c0001t0001g0138a0006c0011t0005g0059a0006c0011t0005g0063 | 3 | HG01109.hp2 HG02040.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1111-979C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431726 | ||||||
| chr19:431726
|
G | ACTTCATC others(51): Show |
1 | a0001c0002t0003g0178 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1111-979_1111-978i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431726 | ||||||
| chr19:431726
|
G | ACTTCATC others(51): Show |
1 | a0001c0002t0001g0140 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1111-979_1111-978i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431726 | ||||||
| chr19:431745
|
C | A | 6 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0002g0001others(3): Show | 7 | HG00544.hp2 HG00621.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-998G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431745 | ||||||
| chr19:431757
|
T | A | 45 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0002g0052others(42): Show | 46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1111-1010A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431757 | ||||||
| chr19:431757
|
T | TTAGAGGA others(51): Show |
2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-1011_1111-101 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431757 | ||||||
| chr19:431768
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-1021G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431768 | ||||||
| chr19:431768
|
C | G | 11 | a0001c0003t0001g0139a0001c0003t0002g0072a0001c0003t0002g0076others(8): Show | 11 | HG01952.hp1 HG02132.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-1021G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431768 | ||||||
| chr19:431769
|
G | A | 6 | a0001c0001t0001g0126a0001c0001t0002g0057a0001c0001t0003g0050others(3): Show | 6 | HG02015.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1022C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431769 | ||||||
| chr19:431772
|
CAGAT | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0071a0001c0001t0003g0180 | 4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1029_1111-102 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431772 | ||||||
| chr19:431772
|
CAGATAGA others(341): Show |
C | 4 | a0001c0001t0004g0159a0001c0001t0004g0161a0002c0004t0001g0192others(1): Show | 4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1373_1111-102 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431772 | ||||||
| chr19:431781
|
G | A | 1 | a0001c0005t0006g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1111-1034C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431781 | ||||||
| chr19:431804
|
G | A | 2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-1057C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431804 | ||||||
| chr19:431804
|
G | GTGAGTGA others(561): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1058_1111-105 others(572): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431804 | ||||||
| chr19:431815
|
T | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0002g0057others(23): Show | 28 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1111-1068A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431815 | ||||||
| chr19:431815
|
T | TTAGAGGA others(449): Show |
3 | a0001c0007t0006g0037a0001c0007t0006g0055a0002c0024t0003g0188 | 3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1069_1111-106 others(460): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431815 | ||||||
| chr19:431826
|
C | CGGGCAGA others(109): Show |
1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1080_1111-107 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431826 | ||||||
| chr19:431826
|
C | G | 14 | a0001c0001t0001g0126a0001c0003t0001g0113a0001c0003t0002g0060others(11): Show | 14 | HG00558.hp1 HG00621.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-1079G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431826 | ||||||
| chr19:431827
|
G | A | 9 | a0001c0001t0001g0130a0001c0001t0003g0071a0001c0006t0001g0020others(6): Show | 9 | HG00639.hp1 HG01123.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111-1080C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431827 | ||||||
| chr19:431827
|
GGGCAGAT others(105): Show |
G | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-1192_1111-108 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431827 | ||||||
| chr19:431830
|
CAGAT | C | 3 | a0001c0001t0001g0130a0002c0004t0001g0187a0010c0022t0002g0184 | 3 | HG00639.hp1 HG01123.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-1087_1111-108 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431830 | ||||||
| chr19:431834
|
T | TGGCGCTT others(719): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1088_1111-108 others(730): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431834 | ||||||
| chr19:431861
|
C | A | 11 | a0001c0003t0001g0113a0001c0003t0002g0060a0001c0003t0002g0069others(8): Show | 11 | HG00558.hp1 HG00621.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-1114G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431861 | ||||||
| chr19:431873
|
T | A | 34 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0003g0071others(31): Show | 35 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1111-1126A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431873 | ||||||
| chr19:431874
|
T | C | 1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1127A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431874 | ||||||
| chr19:431884
|
C | G | 20 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0003g0071others(17): Show | 21 | HG00544.hp2 HG00621.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1111-1137G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431884 | ||||||
| chr19:431885
|
G | A | 6 | a0001c0001t0007g0041a0001c0007t0006g0037a0001c0007t0006g0055others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1138C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431885 | ||||||
| chr19:431888
|
C | CAGAT | 39 | a0001c0001t0001g0126a0001c0001t0002g0057a0001c0001t0003g0004others(36): Show | 41 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1111-1145_1111-114 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431888
|
C | CAGATAGA others(217): Show |
1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431888
|
C | CAGATAGA others(171): Show |
1 | a0001c0003t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(182): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431888
|
C | CAGATAGA others(171): Show |
1 | a0001c0003t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(182): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431888
|
C | CAGATAGA others(275): Show |
1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431888
|
C | CAGATGGC others(225): Show |
1 | a0001c0001t0001g0081 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(236): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431888
|
CAGATGGC others(457): Show |
C | 2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1111-1605_1111-114 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | ||||||
| chr19:431895
|
C | T | 2 | a0006c0011t0005g0059a0006c0011t0005g0063 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1111-1148G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431895 | ||||||
| chr19:431915
|
C | A | 2 | a0001c0003t0002g0076a0002c0012t0002g0203 | 2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1111-1168G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431915 | ||||||
| chr19:431927
|
A | T | 14 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0002g0001others(11): Show | 15 | HG00544.hp2 HG00621.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1111-1180T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431927 | ||||||
| chr19:431938
|
C | G | 6 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1191G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431938 | ||||||
| chr19:431938
|
C | T | 2 | a0005c0009t0005g0048a0005c0009t0014g0040 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111-1191G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431938 | ||||||
| chr19:431939
|
A | G | 51 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0130others(48): Show | 52 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1111-1192T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431939 | ||||||
| chr19:431939
|
A | GGGCAGAT others(109): Show |
1 | a0001c0001t0001g0142 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1111-1192_1111-119 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431939 | ||||||
| chr19:431942
|
CAGAT | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0004t0001g0199others(1): Show | 4 | HG01123.hp1 HG03239.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1199_1111-119 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431942 | ||||||
| chr19:431942
|
CAGATAGA others(55): Show |
C | 1 | a0002c0004t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1111-1257_1111-119 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431942 | ||||||
| chr19:431948
|
G | C | 1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1111-1201C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431948 | ||||||
| chr19:431954
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1111-1207C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431954 | ||||||
| chr19:431985
|
A | T | 15 | a0001c0001t0001g0142a0001c0001t0002g0079a0001c0001t0003g0004others(12): Show | 16 | HG01074.hp2 HG01109.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-1238T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431985 | ||||||
| chr19:431996
|
G | C | 19 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0142others(16): Show | 20 | HG01884.hp1 HG01884.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-1249C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | ||||||
| chr19:431996
|
G | GGGGCAGA others(51): Show |
2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-1250_1111-124 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | ||||||
| chr19:431996
|
G | GGGGCAGA others(51): Show |
1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-1250_1111-124 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | ||||||
| chr19:431996
|
GGGGCAGA others(109): Show |
G | 1 | a0001c0001t0006g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111-1365_1111-125 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | ||||||
| chr19:431997
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-1250C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431997 | ||||||
| chr19:432000
|
CAGAT | C | 4 | a0001c0001t0003g0004a0001c0001t0003g0180a0002c0004t0001g0199others(1): Show | 5 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1257_1111-125 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432000 | ||||||
| chr19:432006
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1111-1259C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432006 | ||||||
| chr19:432012
|
G | ACTTCATC others(109): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1265_1111-126 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432012 | ||||||
| chr19:432020
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1111-1273C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432020 | ||||||
| chr19:432031
|
C | A | 5 | a0001c0003t0001g0058a0001c0003t0002g0072a0001c0003t0004g0108others(2): Show | 5 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1284G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432031 | ||||||
| chr19:432031
|
C | CGTGAGTG others(167): Show |
1 | a0001c0006t0002g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-1285_1111-128 others(178): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432031 | ||||||
| chr19:432043
|
A | ATAGAGGA others(105): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1297_1111-129 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432043 | ||||||
| chr19:432043
|
A | T | 29 | a0001c0001t0001g0126a0001c0001t0002g0052a0001c0001t0003g0071others(26): Show | 30 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1111-1296T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432043 | ||||||
| chr19:432054
|
C | CGGGCAGA others(151): Show |
1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1308_1111-130 others(162): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432054 | ||||||
| chr19:432054
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1111-1307G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432054 | ||||||
| chr19:432055
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1111-1308C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432055 | ||||||
| chr19:432058
|
CAGAT | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0180a0001c0001t0011g0038 | 4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1315_1111-131 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432058 | ||||||
| chr19:432062
|
T | TAGATGGC others(47): Show |
3 | a0001c0003t0002g0001a0001c0003t0010g0077a0001c0017t0005g0056 | 4 | HG00621.hp1 HG02622.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1316_1111-131 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432062 | ||||||
| chr19:432067
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1111-1320C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432067 | ||||||
| chr19:432089
|
C | CGTGAGTG others(333): Show |
1 | a0001c0003t0004g0109 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1111-1343_1111-134 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | ||||||
| chr19:432089
|
C | CGTGAGTG others(333): Show |
9 | a0001c0003t0002g0060a0001c0003t0002g0074a0001c0003t0002g0078others(6): Show | 9 | HG00558.hp1 HG00621.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111-1343_1111-134 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | ||||||
| chr19:432089
|
C | CGTGAGTG others(109): Show |
1 | a0001c0006t0002g0018 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1111-1343_1111-134 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | ||||||
| chr19:432089
|
C | T | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-1342G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | ||||||
| chr19:432101
|
A | ATAGAGGA others(109): Show |
2 | a0001c0003t0001g0058a0002c0012t0004g0193 | 2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1111-1355_1111-135 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432101 | ||||||
| chr19:432101
|
A | ATAGAGGA others(51): Show |
1 | a0001c0002t0001g0006 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1111-1355_1111-135 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432101 | ||||||
| chr19:432101
|
A | T | 14 | a0001c0001t0001g0130a0001c0001t0002g0101a0001c0001t0004g0033others(11): Show | 14 | HG00544.hp2 HG01109.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1111-1354T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432101 | ||||||
| chr19:432112
|
C | G | 55 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0001g0143others(52): Show | 56 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1111-1365G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432112 | ||||||
| chr19:432113
|
G | A | 15 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0005g0168others(12): Show | 15 | HG01891.hp2 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1111-1366C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432113 | ||||||
| chr19:432120
|
T | TAGATGGC others(619): Show |
1 | a0001c0001t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-1374_1111-137 others(630): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | ||||||
| chr19:432120
|
T | TAGATGGC others(279): Show |
1 | a0001c0006t0006g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1111-1374_1111-137 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | ||||||
| chr19:432120
|
T | TAGATGGC others(275): Show |
2 | a0006c0011t0005g0059a0006c0011t0005g0063 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1111-1374_1111-137 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | ||||||
| chr19:432120
|
T | TGGCGCTT others(159): Show |
4 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0002g0111others(1): Show | 4 | HG00544.hp2 NA18940.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1374_1111-137 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | ||||||
| chr19:432125
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0003g0004a0001c0001t0003g0180 | 4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1378C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432125 | ||||||
| chr19:432128
|
G | A | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1381C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432128 | ||||||
| chr19:432144
|
G | C | 3 | a0001c0007t0006g0037a0001c0007t0006g0055a0002c0024t0003g0188 | 3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1397C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432144 | ||||||
| chr19:432147
|
C | A | 4 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0002g0111others(1): Show | 4 | HG00544.hp2 NA18940.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1400G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432147 | ||||||
| chr19:432147
|
C | CGTGAGTG others(275): Show |
4 | a0001c0003t0002g0069a0001c0003t0002g0075a0001c0003t0002g0076others(1): Show | 4 | NA18954.hp2 NA18960.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1401_1111-140 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432147 | ||||||
| chr19:432147
|
C | CGTGAGTG others(271): Show |
1 | a0001c0002t0001g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1111-1401_1111-140 others(282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432147 | ||||||
| chr19:432148
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-1401C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432148 | ||||||
| chr19:432150
|
G | GAGTGAGA others(101): Show |
1 | a0001c0003t0010g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1111-1404_1111-140 others(112): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432150 | ||||||
| chr19:432159
|
A | ATAGAGGA others(329): Show |
1 | a0001c0002t0003g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1413_1111-141 others(340): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432159 | ||||||
| chr19:432159
|
A | T | 70 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0052others(67): Show | 73 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1111-1412T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432159 | ||||||
| chr19:432170
|
C | CGGGCAGA others(109): Show |
1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1424_1111-142 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432170 | ||||||
| chr19:432170
|
C | G | 8 | a0001c0001t0001g0097a0001c0001t0002g0101a0001c0003t0001g0058others(5): Show | 8 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-1423G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432170 | ||||||
| chr19:432171
|
G | A | 5 | a0001c0001t0002g0039a0001c0007t0006g0037a0001c0007t0006g0055others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1424C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432171 | ||||||
| chr19:432171
|
G | GGGCAGAT others(109): Show |
1 | a0001c0001t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-1425_1111-142 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432171 | ||||||
| chr19:432176
|
GATAC | G | 3 | a0001c0007t0006g0037a0001c0007t0006g0055a0002c0024t0003g0188 | 3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1433_1111-143 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432176 | ||||||
| chr19:432178
|
T | TAGATGGC others(47): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1432_1111-143 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432178 | ||||||
| chr19:432180
|
C | G | 106 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0001g0126others(103): Show | 110 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1111-1433G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432180 | ||||||
| chr19:432183
|
G | A | 5 | a0001c0001t0001g0126a0001c0001t0011g0038a0002c0004t0001g0187others(2): Show | 5 | HG00639.hp1 HG02015.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1436C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432183 | ||||||
| chr19:432186
|
G | A | 2 | a0005c0009t0005g0048a0005c0009t0014g0040 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111-1439C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432186 | ||||||
| chr19:432194
|
G | A | 1 | a0001c0001t0016g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111-1447C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432194 | ||||||
| chr19:432205
|
C | CGTGAGTG others(387): Show |
1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1111-1459_1111-145 others(398): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432205 | ||||||
| chr19:432205
|
C | CGTGAGTG others(167): Show |
2 | a0001c0006t0001g0020a0001c0006t0001g0024 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1111-1459_1111-145 others(178): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432205 | ||||||
| chr19:432205
|
C | CGTGAGTG others(225): Show |
1 | a0001c0006t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1111-1459_1111-145 others(236): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432205 | ||||||
| chr19:432211
|
T | G | 1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1464A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432211 | ||||||
| chr19:432217
|
T | A | 62 | a0001c0001t0001g0142a0001c0001t0002g0039a0001c0001t0002g0101others(59): Show | 65 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1111-1470A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432217 | ||||||
| chr19:432218
|
T | C | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1471A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432218 | ||||||
| chr19:432228
|
C | CGGGCAGA others(449): Show |
1 | a0001c0003t0001g0113 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1111-1482_1111-148 others(460): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432228 | ||||||
| chr19:432228
|
C | G | 4 | a0001c0002t0001g0006a0001c0006t0006g0014a0001c0017t0005g0056others(1): Show | 5 | HG00558.hp2 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1481G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432228 | ||||||
| chr19:432232
|
CAGAT | C | 3 | a0001c0001t0001g0130a0001c0001t0003g0071a0003c0008t0005g0182 | 3 | HG01123.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1111-1489_1111-148 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432232 | ||||||
| chr19:432232
|
CAGATAGA others(287): Show |
C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-1779_1111-148 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432232 | ||||||
| chr19:432244
|
G | A | 1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-1497C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432244 | ||||||
| chr19:432263
|
C | CGTGAGTG others(329): Show |
3 | a0001c0002t0001g0092a0001c0002t0004g0174a0001c0002t0004g0175 | 3 | HG01993.hp2 NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1111-1517_1111-151 others(340): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432263 | ||||||
| chr19:432275
|
T | A | 70 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0143others(67): Show | 72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1111-1528A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432275 | ||||||
| chr19:432276
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1529A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432276 | ||||||
| chr19:432286
|
C | CGGGCAGA others(51): Show |
5 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0002g0111others(2): Show | 5 | HG00544.hp2 HG00621.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1597_1111-154 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432286 | ||||||
| chr19:432286
|
C | CGGGCAGA others(221): Show |
1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-1540_1111-153 others(232): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432286 | ||||||
| chr19:432286
|
C | G | 49 | a0001c0001t0003g0036a0001c0002t0001g0003a0001c0002t0001g0006others(46): Show | 52 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1111-1539G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432286 | ||||||
| chr19:432287
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0143 | 2 | HG00609.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1111-1540C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432287 | ||||||
| chr19:432287
|
G | GGGCAGAT others(47): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1541_1111-154 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432287 | ||||||
| chr19:432290
|
CAGAT | C | 6 | a0001c0001t0002g0079a0001c0001t0007g0041a0001c0001t0013g0073others(3): Show | 6 | HG01074.hp2 HG01361.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1547_1111-154 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | ||||||
| chr19:432290
|
CAGATAGA others(55): Show |
C | 3 | a0001c0001t0001g0129a0001c0001t0003g0004a0001c0001t0003g0180 | 4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1605_1111-154 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | ||||||
| chr19:432290
|
CAGATAGA others(403): Show |
C | 1 | a0011c0025t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1111-1953_1111-154 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | ||||||
| chr19:432290
|
CAGATAGA others(689): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1110+1723_1111-154 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | ||||||
| chr19:432296
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1111-1549C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432296 | ||||||
| chr19:432302
|
G | A | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1555C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432302 | ||||||
| chr19:432318
|
G | GATCGTGA others(383): Show |
1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1572_1111-157 others(394): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432318 | ||||||
| chr19:432321
|
C | A | 2 | a0001c0001t0011g0038a0001c0006t0002g0019 | 2 | HG01943.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1111-1574G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432321 | ||||||
| chr19:432321
|
C | CGTGAGTG others(275): Show |
1 | a0009c0015t0012g0027 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1111-1575_1111-157 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432321 | ||||||
| chr19:432333
|
A | T | 54 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0004g0159others(51): Show | 56 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1111-1586T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432333 | ||||||
| chr19:432344
|
G | C | 34 | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0002g0039others(31): Show | 34 | HG00639.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1111-1597C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | ||||||
| chr19:432344
|
G | GGGGCAGA others(93): Show |
1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1598_1111-159 others(104): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | ||||||
| chr19:432344
|
GGGGCAGA others(51): Show |
G | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-1655_1111-159 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | ||||||
| chr19:432344
|
GGGGCAGA others(457): Show |
G | 29 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0084others(26): Show | 30 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1110+1901_1111-159 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | ||||||
| chr19:432345
|
G | A | 6 | a0001c0001t0002g0039a0001c0001t0003g0071a0001c0001t0007g0041others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1598C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432345 | ||||||
| chr19:432348
|
CAGAT | C | 8 | a0001c0001t0001g0126a0001c0001t0004g0159a0001c0001t0004g0161others(5): Show | 8 | HG00639.hp1 HG01358.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-1605_1111-160 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432348 | ||||||
| chr19:432352
|
T | TAGATGGC others(47): Show |
1 | a0006c0011t0005g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111-1606_1111-160 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432352 | ||||||
| chr19:432352
|
T | TAGATGGC others(47): Show |
1 | a0006c0011t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1111-1606_1111-160 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432352 | ||||||
| chr19:432352
|
T | TGGCGCTT others(214): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1606_1111-160 others(225): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432352 | ||||||
| chr19:432376
|
G | GATCGTGA others(39): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0172 | 3 | HG00558.hp2 HG03942.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1111-1630_1111-162 others(50): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432376 | ||||||
| chr19:432379
|
C | A | 1 | a0001c0006t0002g0018 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1111-1632G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | ||||||
| chr19:432379
|
C | CGTGAGTG others(101): Show |
1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1111-1633_1111-163 others(112): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | ||||||
| chr19:432379
|
C | CGTGAGTG others(271): Show |
1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111-1633_1111-163 others(282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | ||||||
| chr19:432379
|
C | CGTGAGTG others(213): Show |
1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1111-1633_1111-163 others(224): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | ||||||
| chr19:432391
|
T | A | 28 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0130others(25): Show | 30 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1111-1644A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | ||||||
| chr19:432391
|
T | TTAGAGGA others(275): Show |
1 | a0001c0006t0006g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1111-1645_1111-164 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | ||||||
| chr19:432391
|
T | TTAGAGGA others(43): Show |
1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1111-1645_1111-164 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | ||||||
| chr19:432391
|
T | TTAGAGGA others(491): Show |
22 | a0001c0002t0001g0003a0001c0002t0001g0083a0001c0002t0001g0093others(19): Show | 23 | HG00423.hp2 HG01952.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1111-1645_1111-164 others(502): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | ||||||
| chr19:432391
|
T | TTAGAGGA others(565): Show |
2 | a0001c0003t0002g0072a0001c0003t0004g0108 | 2 | HG02132.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1111-1645_1111-164 others(576): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | ||||||
| chr19:432391
|
T | TTAGAGGA others(105): Show |
2 | a0001c0007t0006g0055a0002c0024t0003g0188 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1645_1111-164 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | ||||||
| chr19:432402
|
C | CGGGCAGA others(773): Show |
2 | a0001c0002t0003g0091a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1111-1656_1111-165 others(784): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432402 | ||||||
| chr19:432402
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0007g0041a0001c0002t0001g0089others(3): Show | 6 | HG01361.hp1 HG02293.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-1655G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432402 | ||||||
| chr19:432403
|
G | A | 15 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0002g0079others(12): Show | 16 | HG00639.hp1 HG01358.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-1656C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432403 | ||||||
| chr19:432403
|
G | GGGCAGAT others(213): Show |
1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-1657_1111-165 others(224): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432403 | ||||||
| chr19:432403
|
G | GGGCAGAT others(163): Show |
1 | a0001c0014t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1111-1657_1111-165 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432403 | ||||||
| chr19:432410
|
T | TAGATGGC others(47): Show |
19 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(16): Show | 19 | HG00423.hp1 HG00544.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1111-1664_1111-166 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432410 | ||||||
| chr19:432412
|
G | C | 1 | a0001c0001t0002g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1111-1665C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432412 | ||||||
| chr19:432418
|
G | A | 3 | a0001c0003t0001g0058a0001c0007t0002g0080a0002c0012t0004g0193 | 3 | HG01074.hp2 HG03017.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1111-1671C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432418 | ||||||
| chr19:432422
|
CATCGTGA others(5): Show |
C | 1 | a0001c0002t0003g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1687_1111-167 others(16): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432422 | ||||||
| chr19:432425
|
C | T | 1 | a0001c0013t0005g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1111-1678G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432425 | ||||||
| chr19:432437
|
C | A | 1 | a0001c0003t0001g0113 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1111-1690G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | ||||||
| chr19:432437
|
C | CGTGAGTG others(971): Show |
1 | a0001c0006t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1111-1691_1111-169 others(982): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | ||||||
| chr19:432437
|
C | CGTGAGTG others(47): Show |
2 | a0001c0003t0001g0058a0002c0012t0004g0193 | 2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1111-1691_1111-169 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | ||||||
| chr19:432437
|
C | T | 1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1111-1690G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | ||||||
| chr19:432449
|
A | ATAGAGGA others(391): Show |
2 | a0001c0006t0001g0020a0001c0006t0001g0024 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1111-1703_1111-170 others(402): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432449 | ||||||
| chr19:432449
|
A | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0099others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1111-1702T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432449 | ||||||
| chr19:432460
|
C | G | 21 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0142others(18): Show | 22 | HG00639.hp1 HG00735.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1111-1713G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432460 | ||||||
| chr19:432460
|
C | T | 3 | a0001c0001t0003g0036a0001c0005t0006g0010a0010c0022t0002g0184 | 3 | HG02055.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-1713G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432460 | ||||||
| chr19:432461
|
G | A | 5 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1714C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432461 | ||||||
| chr19:432464
|
CAGAT | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0102others(21): Show | 24 | HG00323.hp1 HG01071.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-1721_1111-171 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | ||||||
| chr19:432464
|
CAGATAGA others(55): Show |
C | 1 | a0001c0001t0016g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111-1779_1111-171 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | ||||||
| chr19:432464
|
CAGATAGA others(113): Show |
C | 1 | a0001c0005t0015g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1111-1837_1111-171 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | ||||||
| chr19:432464
|
CAGATAGA others(515): Show |
C | 21 | a0001c0001t0001g0098a0001c0001t0004g0035a0001c0001t0004g0064others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+1723_1111-171 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | ||||||
| chr19:432468
|
T | TAGATGGC others(205): Show |
1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1111-1722_1111-172 others(216): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432468 | ||||||
| chr19:432468
|
T | TAGATGGC others(163): Show |
1 | a0006c0011t0005g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111-1722_1111-172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432468 | ||||||
| chr19:432468
|
T | TAGATGGC others(105): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1722_1111-172 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432468 | ||||||
| chr19:432484
|
G | A | 26 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(23): Show | 28 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.1111-1737C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432484 | ||||||
| chr19:432495
|
C | A | 1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1111-1748G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432495 | ||||||
| chr19:432507
|
A | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1111-1760T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432507 | ||||||
| chr19:432516
|
G | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-1769C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432516 | ||||||
| chr19:432518
|
C | A | 1 | a0001c0006t0002g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-1771G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432518 | ||||||
| chr19:432518
|
C | G | 30 | a0001c0001t0002g0057a0001c0001t0002g0101a0001c0001t0003g0050others(27): Show | 31 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1111-1771G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432518 | ||||||
| chr19:432519
|
G | A | 16 | a0001c0001t0005g0168a0001c0001t0006g0043a0001c0001t0006g0049others(13): Show | 16 | HG01109.hp2 HG01358.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1111-1772C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432519 | ||||||
| chr19:432522
|
CAGAT | C | 3 | a0001c0001t0003g0071a0001c0002t0003g0147a0001c0020t0001g0104 | 3 | HG01071.hp2 HG01361.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1111-1779_1111-177 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432522 | ||||||
| chr19:432526
|
T | TAGATGGC others(259): Show |
3 | a0001c0002t0001g0092a0001c0002t0004g0174a0001c0002t0004g0175 | 3 | HG01993.hp2 NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1111-1780_1111-177 others(270): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432526 | ||||||
| chr19:432526
|
T | TAGATGGC others(43): Show |
22 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(19): Show | 24 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-1780_1111-177 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432526 | ||||||
| chr19:432526
|
T | TAGATGGC others(47): Show |
4 | a0001c0001t0001g0132a0001c0001t0001g0142a0001c0006t0002g0018others(1): Show | 4 | HG00544.hp1 HG01943.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1780_1111-177 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432526 | ||||||
| chr19:432528
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1111-1781C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432528 | ||||||
| chr19:432528
|
G | CATGGCGC others(279): Show |
1 | a0001c0001t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-1781_1111-178 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432528 | ||||||
| chr19:432542
|
G | A | 1 | a0001c0002t0003g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1795C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432542 | ||||||
| chr19:432553
|
C | A | 1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1111-1806G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432553 | ||||||
| chr19:432553
|
C | CGTGAGTG others(105): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1111-1807_1111-180 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432553 | ||||||
| chr19:432558
|
G | GTGAGAGA others(43): Show |
2 | a0001c0002t0001g0140a0001c0002t0003g0173 | 2 | HG04228.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1111-1812_1111-181 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432558 | ||||||
| chr19:432565
|
A | AGGAGGCC others(43): Show |
2 | a0001c0002t0003g0091a0001c0002t0003g0178 | 2 | NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1111-1819_1111-181 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432565 | ||||||
| chr19:432565
|
A | ATAGAGGA others(51): Show |
1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1819_1111-181 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432565 | ||||||
| chr19:432565
|
A | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0102others(21): Show | 24 | HG01071.hp1 HG01071.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-1818T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432565 | ||||||
| chr19:432566
|
T | C | 1 | a0001c0007t0006g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1111-1819A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432566 | ||||||
| chr19:432576
|
C | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(37): Show | 40 | HG00423.hp1 HG01358.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1111-1829G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432576 | ||||||
| chr19:432577
|
G | A | 31 | a0001c0001t0001g0103a0001c0001t0001g0131a0001c0001t0016g0070others(28): Show | 33 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1111-1830C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432577 | ||||||
| chr19:432584
|
T | TAGATGGC others(43): Show |
1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-1838_1111-183 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | ||||||
| chr19:432584
|
T | TAGATGGC others(333): Show |
1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1838_1111-183 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | ||||||
| chr19:432584
|
T | TAGATGGC others(1122): Show |
2 | a0001c0007t0006g0055a0002c0024t0003g0188 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1838_1111-183 others(1133): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | ||||||
| chr19:432584
|
T | TGGCGCTT others(275): Show |
1 | a0006c0011t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1111-1838_1111-183 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | ||||||
| chr19:432584
|
TAGATGGC others(337): Show |
T | 1 | a0001c0001t0001g0124 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1110+1781_1111-183 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | ||||||
| chr19:432586
|
G | C | 2 | a0001c0001t0011g0038a0003c0008t0005g0182 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1111-1839C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432586 | ||||||
| chr19:432591
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0004g0174a0001c0002t0004g0175 | 3 | HG01993.hp2 NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1111-1844G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432591 | ||||||
| chr19:432623
|
A | AGGAGGCC others(101): Show |
1 | a0001c0002t0003g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1877_1111-187 others(112): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432623 | ||||||
| chr19:432623
|
A | T | 68 | a0001c0001t0001g0132a0001c0001t0001g0142a0001c0001t0001g0143others(65): Show | 71 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1111-1876T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432623 | ||||||
| chr19:432631
|
G | A | 1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1884C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432631 | ||||||
| chr19:432634
|
C | CGGGCAGA others(321): Show |
1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1111-1888_1111-188 others(332): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432634 | ||||||
| chr19:432634
|
C | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0102others(52): Show | 57 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1111-1887G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432634 | ||||||
| chr19:432635
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(15): Show | 19 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1111-1888C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432635 | ||||||
| chr19:432642
|
T | TAGATGGC others(329): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1896_1111-189 others(340): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432642 | ||||||
| chr19:432644
|
G | C | 13 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0003g0171others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1111-1897C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432644 | ||||||
| chr19:432649
|
C | CGCTTCAT others(379): Show |
1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111-1903_1111-190 others(390): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432649 | ||||||
| chr19:432649
|
C | T | 3 | a0001c0002t0001g0089a0001c0002t0003g0091a0001c0002t0003g0178 | 3 | NA18960.hp2 NA19009.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1111-1902G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432649 | ||||||
| chr19:432650
|
G | A | 2 | a0001c0001t0002g0052a0003c0008t0005g0182 | 2 | HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1111-1903C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432650 | ||||||
| chr19:432669
|
C | A | 2 | a0001c0003t0002g0072a0001c0003t0004g0108 | 2 | HG02132.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1111-1922G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432669 | ||||||
| chr19:432669
|
C | CGTGAGTG others(51): Show |
21 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0001g0113others(18): Show | 22 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1111-1923_1111-192 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432669 | ||||||
| chr19:432681
|
A | ATAGAGGA others(51): Show |
2 | a0001c0003t0001g0058a0002c0012t0004g0193 | 2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1111-1935_1111-193 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432681 | ||||||
| chr19:432681
|
A | T | 35 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0130others(32): Show | 35 | HG00639.hp1 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1111-1934T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432681 | ||||||
| chr19:432682
|
T | C | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-1935A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432682 | ||||||
| chr19:432692
|
C | A | 1 | a0001c0016t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1111-1945G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | ||||||
| chr19:432692
|
C | CGGGCAGA others(51): Show |
1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1946_1111-194 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | ||||||
| chr19:432692
|
C | CGGGCAGA others(47): Show |
2 | a0001c0006t0002g0018a0001c0006t0002g0019 | 2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1111-1946_1111-194 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | ||||||
| chr19:432692
|
C | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(36): Show | 40 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1111-1945G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | ||||||
| chr19:432693
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0102others(5): Show | 8 | HG02040.hp2 HG02132.hp1 NA18999.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-1946C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432693 | ||||||
| chr19:432696
|
CAGAT | C | 5 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0013t0005g0007others(2): Show | 5 | HG02559.hp1 HG02622.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1953_1111-195 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432696 | ||||||
| chr19:432700
|
T | TAGATGGC others(155): Show |
1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1954_1111-195 others(166): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432700 | ||||||
| chr19:432700
|
T | TAGATGGC others(47): Show |
1 | a0001c0014t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1111-1954_1111-195 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432700 | ||||||
| chr19:432702
|
G | C | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1955C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432702 | ||||||
| chr19:432707
|
C | T | 29 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.1111-1960G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432707 | ||||||
| chr19:432724
|
G | GATCGTGA others(151): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-1978_1111-197 others(162): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432724 | ||||||
| chr19:432727
|
C | A | 1 | a0001c0006t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1111-1980G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432727 | ||||||
| chr19:432727
|
C | CGTGAGTG others(51): Show |
2 | a0001c0003t0002g0100a0009c0015t0012g0027 | 2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1110+1981_1111-198 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432727 | ||||||
| chr19:432739
|
A | T | 53 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(50): Show | 53 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1110+1970T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432739 | ||||||
| chr19:432750
|
C | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0131a0002c0004t0001g0204 | 3 | HG00323.hp1 HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1110+1959G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | ||||||
| chr19:432750
|
C | CGGGCAGA others(321): Show |
1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1958_1110+195 others(332): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | ||||||
| chr19:432750
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0102others(11): Show | 14 | HG01071.hp2 HG02040.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110+1959G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | ||||||
| chr19:432750
|
C | T | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1959G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | ||||||
| chr19:432751
|
G | A | 6 | a0001c0001t0001g0132a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG00544.hp1 HG00609.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+1958C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432751 | ||||||
| chr19:432758
|
T | TAGATGGC others(47): Show |
2 | a0001c0007t0006g0037a0006c0011t0005g0063 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1110+1950_1110+195 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432758 | ||||||
| chr19:432758
|
T | TAGATGGC others(105): Show |
4 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(1): Show | 4 | HG02486.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1950_1110+195 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432758 | ||||||
| chr19:432758
|
TAGATGGC others(163): Show |
T | 1 | a0001c0001t0002g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1110+1781_1110+195 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432758 | ||||||
| chr19:432785
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1924G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432785 | ||||||
| chr19:432797
|
A | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(56): Show | 62 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1110+1912T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432797 | ||||||
| chr19:432808
|
C | A | 1 | a0001c0020t0001g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1110+1901G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432808 | ||||||
| chr19:432808
|
C | G | 46 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0130others(43): Show | 47 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1110+1901G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432808 | ||||||
| chr19:432809
|
G | A | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1900C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432809 | ||||||
| chr19:432812
|
CAGAT | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(10): Show | 13 | HG00423.hp1 HG02027.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110+1893_1110+189 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432812 | ||||||
| chr19:432818
|
G | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1891C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432818 | ||||||
| chr19:432823
|
C | A | 1 | a0001c0005t0015g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1110+1886G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432823 | ||||||
| chr19:432823
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1886G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432823 | ||||||
| chr19:432824
|
G | A | 5 | a0001c0001t0004g0033a0001c0002t0001g0089a0001c0002t0001g0155others(2): Show | 5 | HG02698.hp2 HG03098.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+1885C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432824 | ||||||
| chr19:432824
|
G | GCTTCATC others(51): Show |
29 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.1110+1884_1110+188 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432824 | ||||||
| chr19:432828
|
CATCGTGA others(5): Show |
C | 1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1869_1110+188 others(16): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432828 | ||||||
| chr19:432840
|
G | C | 2 | a0001c0007t0006g0055a0002c0024t0003g0188 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1869C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432840 | ||||||
| chr19:432855
|
T | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(31): Show | 34 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1110+1854A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432855 | ||||||
| chr19:432855
|
T | TTAGAGGA others(47): Show |
8 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0102others(5): Show | 8 | HG02040.hp2 HG02132.hp1 NA18999.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+1853_1110+185 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432855 | ||||||
| chr19:432866
|
C | CGGGCAGA others(105): Show |
1 | a0001c0003t0001g0113 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1110+1842_1110+184 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | ||||||
| chr19:432866
|
C | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0131a0001c0001t0002g0101others(4): Show | 7 | HG00323.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+1843G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | ||||||
| chr19:432866
|
CGGGCAGA others(221): Show |
C | 2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1110+1615_1110+184 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | ||||||
| chr19:432866
|
CGGGCAGA others(337): Show |
C | 1 | a0001c0020t0001g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1110+1499_1110+184 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | ||||||
| chr19:432867
|
G | A | 2 | a0001c0007t0006g0055a0002c0024t0003g0188 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1842C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432867 | ||||||
| chr19:432870
|
CAGAT | C | 2 | a0001c0007t0006g0055a0002c0024t0003g0188 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1835_1110+183 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432870 | ||||||
| chr19:432874
|
TAGATGGC others(47): Show |
T | 1 | a0001c0001t0016g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1110+1781_1110+183 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432874 | ||||||
| chr19:432882
|
G | A | 8 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+1827C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432882 | ||||||
| chr19:432882
|
G | GCTTCATC others(333): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1826_1110+182 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432882 | ||||||
| chr19:432889
|
CGTGA | C | 2 | a0001c0006t0002g0018a0001c0006t0002g0019 | 2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1110+1816_1110+181 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432889 | ||||||
| chr19:432898
|
G | C | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1811C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432898 | ||||||
| chr19:432913
|
T | A | 6 | a0001c0002t0002g0046a0001c0002t0003g0147a0001c0003t0001g0113others(3): Show | 6 | HG01071.hp2 HG01884.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+1796A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432913 | ||||||
| chr19:432913
|
T | TTAGAGGA others(743): Show |
3 | a0001c0006t0001g0020a0001c0006t0001g0024a0001c0006t0006g0014 | 3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1795_1110+179 others(754): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432913 | ||||||
| chr19:432924
|
C | G | 24 | a0001c0001t0007g0041a0001c0003t0001g0062a0001c0003t0001g0066others(21): Show | 25 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1110+1785G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432924 | ||||||
| chr19:432924
|
CGGGCAGA others(163): Show |
C | 2 | a0001c0013t0005g0007a0001c0018t0006g0179 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1110+1615_1110+178 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432924 | ||||||
| chr19:432924
|
CGGGCAGA others(395): Show |
C | 2 | a0001c0001t0001g0103a0001c0001t0001g0131 | 2 | HG00323.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1110+1383_1110+178 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432924 | ||||||
| chr19:432925
|
G | A | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1784C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432925 | ||||||
| chr19:432928
|
C | CAGAT | 62 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(59): Show | 64 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1110+1777_1110+178 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | ||||||
| chr19:432928
|
C | CAGATAGA others(163): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+1780_1110+178 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | ||||||
| chr19:432928
|
C | CAGATGGC others(51): Show |
1 | a0001c0001t0006g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+1780_1110+178 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | ||||||
| chr19:432928
|
CAGATGGC others(51): Show |
C | 5 | a0001c0001t0004g0159a0001c0001t0004g0161a0001c0001t0011g0038others(2): Show | 5 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+1723_1110+178 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | ||||||
| chr19:432936
|
G | A | 2 | a0005c0009t0005g0048a0005c0009t0014g0040 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+1773C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432936 | ||||||
| chr19:432944
|
G | A | 1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1765C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432944 | ||||||
| chr19:432955
|
C | A | 28 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(25): Show | 29 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1110+1754G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432955 | ||||||
| chr19:432955
|
C | T | 2 | a0001c0006t0002g0018a0001c0006t0002g0019 | 2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1110+1754G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432955 | ||||||
| chr19:432956
|
G | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1110+1753C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432956 | ||||||
| chr19:432967
|
A | T | 11 | a0001c0001t0002g0052a0001c0001t0005g0053a0001c0003t0001g0058others(8): Show | 11 | HG00621.hp2 HG01074.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+1742T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432967 | ||||||
| chr19:432978
|
C | CGGGCAGA others(109): Show |
1 | a0001c0001t0001g0132 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1110+1730_1110+173 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432978 | ||||||
| chr19:432978
|
C | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(28): Show | 32 | HG00423.hp1 HG00621.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1110+1731G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432978 | ||||||
| chr19:432978
|
CGGGCAGA others(341): Show |
C | 1 | a0001c0001t0005g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1110+1383_1110+173 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432978 | ||||||
| chr19:432979
|
G | A | 9 | a0001c0001t0001g0165a0001c0003t0001g0062a0001c0003t0001g0066others(6): Show | 10 | HG00544.hp2 HG00621.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+1730C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432979 | ||||||
| chr19:432979
|
GGGCAGAT others(51): Show |
G | 1 | a0001c0005t0015g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1110+1672_1110+172 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432979 | ||||||
| chr19:432982
|
CAGAT | C | 2 | a0001c0001t0004g0033a0002c0004t0001g0204 | 2 | HG03098.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1110+1723_1110+172 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432982 | ||||||
| chr19:432986
|
T | TAGATGGC others(105): Show |
1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(221): Show |
1 | a0009c0015t0012g0027 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(232): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(163): Show |
1 | a0001c0003t0001g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(43): Show |
1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(163): Show |
10 | a0001c0003t0002g0001a0001c0003t0002g0060a0001c0003t0002g0069others(7): Show | 11 | HG02132.hp2 HG03688.hp1 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+1722_1110+172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(453): Show |
1 | a0002c0012t0004g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(464): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(221): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(232): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(723): Show |
1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(734): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(163): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1722_1110+172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:432986
|
T | TAGATGGC others(782): Show |
1 | a0001c0007t0006g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(793): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | ||||||
| chr19:433002
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1110+1707C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433002 | ||||||
| chr19:433002
|
G | GTGAGTGA others(109): Show |
2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1110+1706_1110+170 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433002 | ||||||
| chr19:433013
|
C | A | 4 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0051others(1): Show | 4 | HG00621.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1696G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433013 | ||||||
| chr19:433025
|
A | T | 29 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0003g0071others(26): Show | 29 | HG01109.hp2 HG01358.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1110+1684T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433025 | ||||||
| chr19:433034
|
G | A | 2 | a0005c0009t0005g0048a0005c0009t0014g0040 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+1675C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433034 | ||||||
| chr19:433036
|
C | G | 36 | a0001c0001t0002g0101a0001c0002t0001g0003a0001c0002t0001g0006others(33): Show | 38 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.1110+1673G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433036 | ||||||
| chr19:433037
|
A | G | 89 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(86): Show | 91 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1110+1672T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433037 | ||||||
| chr19:433040
|
CAGAT | C | 5 | a0001c0001t0003g0171a0001c0006t0002g0018a0001c0006t0002g0019others(2): Show | 5 | HG01358.hp1 HG01943.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+1665_1110+166 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433040 | ||||||
| chr19:433044
|
T | TAGATGGC others(47): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(217): Show |
1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(217): Show |
2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+1664_1110+166 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(727): Show |
1 | a0001c0003t0002g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(738): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(105): Show |
4 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0051others(1): Show | 4 | HG02622.hp1 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1664_1110+166 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(669): Show |
12 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0001g0139others(9): Show | 12 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+1664_1110+166 others(680): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(271): Show |
1 | a0001c0003t0001g0113 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433044
|
T | TAGATGGC others(47): Show |
1 | a0001c0001t0006g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | ||||||
| chr19:433052
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(5): Show | 8 | HG01109.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+1657C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433052 | ||||||
| chr19:433057
|
A | G | 1 | a0001c0002t0001g0006 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1110+1652T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433057 | ||||||
| chr19:433071
|
C | A | 3 | a0001c0001t0003g0071a0001c0016t0001g0144a0010c0022t0002g0184 | 3 | HG01358.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+1638G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433071 | ||||||
| chr19:433083
|
A | T | 18 | a0001c0001t0002g0101a0001c0001t0004g0033a0001c0001t0006g0043others(15): Show | 18 | HG01071.hp2 HG02015.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1110+1626T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433083 | ||||||
| chr19:433094
|
G | C | 57 | a0001c0001t0002g0052a0001c0001t0003g0036a0001c0001t0003g0071others(54): Show | 59 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1110+1615C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433094 | ||||||
| chr19:433095
|
G | A | 1 | a0006c0011t0005g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+1614C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433095 | ||||||
| chr19:433098
|
CAGAT | C | 10 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(7): Show | 10 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1110+1607_1110+161 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433098 | ||||||
| chr19:433102
|
T | TAGATGGC others(47): Show |
2 | a0001c0007t0006g0055a0002c0024t0003g0188 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1606_1110+160 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433102 | ||||||
| chr19:433102
|
T | TGGCGCTT others(214): Show |
1 | a0006c0011t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1110+1606_1110+160 others(225): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433102 | ||||||
| chr19:433102
|
T | TGGCGCTT others(97): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+1606_1110+160 others(108): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433102 | ||||||
| chr19:433110
|
G | GCTTCATC others(105): Show |
1 | a0006c0011t0005g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+1598_1110+159 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433110 | ||||||
| chr19:433121
|
A | AGTGAGAT others(43): Show |
2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+1587_1110+158 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433121 | ||||||
| chr19:433129
|
C | A | 11 | a0001c0001t0002g0052a0001c0001t0003g0071a0001c0001t0006g0043others(8): Show | 11 | HG01358.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1580G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433129 | ||||||
| chr19:433141
|
A | ATAGAGGA others(51): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1567_1110+156 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433141 | ||||||
| chr19:433141
|
A | ATAGAGGA others(47): Show |
31 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(28): Show | 32 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.1110+1567_1110+156 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433141 | ||||||
| chr19:433141
|
A | T | 11 | a0001c0001t0002g0039a0001c0001t0003g0171a0001c0001t0016g0070others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1568T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433141 | ||||||
| chr19:433152
|
C | G | 11 | a0001c0001t0002g0057a0001c0001t0003g0004a0001c0001t0003g0050others(8): Show | 12 | HG01978.hp1 HG02015.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+1557G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433152 | ||||||
| chr19:433152
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1110+1557G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433152 | ||||||
| chr19:433153
|
G | A | 4 | a0001c0001t0003g0171a0001c0007t0006g0055a0002c0024t0003g0188others(1): Show | 4 | HG02145.hp1 HG03195.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1556C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433153 | ||||||
| chr19:433153
|
G | GGGCAGAT others(449): Show |
1 | a0001c0007t0006g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+1555_1110+155 others(460): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433153 | ||||||
| chr19:433156
|
CAGAT | C | 13 | a0001c0003t0001g0058a0001c0003t0002g0001a0001c0003t0002g0060others(10): Show | 14 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+1549_1110+155 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433156 | ||||||
| chr19:433160
|
T | TGGCGCTT others(43): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1548_1110+154 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433160 | ||||||
| chr19:433160
|
T | TGGCGCTT others(159): Show |
1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1110+1548_1110+154 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433160 | ||||||
| chr19:433162
|
G | C | 3 | a0001c0001t0002g0052a0001c0002t0001g0006a0001c0002t0001g0151 | 3 | HG02015.hp1 HG02559.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1110+1547C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433162 | ||||||
| chr19:433167
|
C | T | 2 | a0001c0002t0001g0089a0001c0002t0003g0147 | 2 | HG01071.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1110+1542G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433167 | ||||||
| chr19:433168
|
G | A | 1 | a0006c0011t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1110+1541C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433168 | ||||||
| chr19:433187
|
C | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(5): Show | 8 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+1522G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433187 | ||||||
| chr19:433187
|
C | T | 2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+1522G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433187 | ||||||
| chr19:433188
|
G | GTGAGAGT others(217): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0151 | 2 | HG02015.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1110+1520_1110+152 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433188 | ||||||
| chr19:433199
|
A | ATAGAGGA others(109): Show |
1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+1509_1110+151 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433199 | ||||||
| chr19:433199
|
A | T | 32 | a0001c0001t0002g0052a0001c0001t0002g0101a0001c0001t0003g0004others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1110+1510T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433199 | ||||||
| chr19:433210
|
A | C | 39 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(36): Show | 40 | HG01071.hp2 HG01109.hp2 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1110+1499T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433210 | ||||||
| chr19:433210
|
A | G | 104 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0002g0079others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1110+1499T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433210 | ||||||
| chr19:433211
|
G | A | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1498C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433211 | ||||||
| chr19:433214
|
CAGAT | C | 4 | a0001c0001t0002g0039a0001c0001t0016g0070a0002c0004t0001g0204others(1): Show | 4 | HG03831.hp1 HG04204.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1491_1110+149 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433214 | ||||||
| chr19:433220
|
G | C | 1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1489C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433220 | ||||||
| chr19:433226
|
G | A | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1483C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433226 | ||||||
| chr19:433229
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1480A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433229 | ||||||
| chr19:433234
|
G | A | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+1475C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433234 | ||||||
| chr19:433245
|
C | A | 2 | a0001c0001t0002g0039a0002c0004t0001g0205 | 2 | HG04204.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1110+1464G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433245 | ||||||
| chr19:433245
|
CGTGAGTG others(391): Show |
C | 2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+1066_1110+146 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433245 | ||||||
| chr19:433246
|
G | A | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1463C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433246 | ||||||
| chr19:433257
|
T | A | 19 | a0001c0001t0002g0039a0001c0001t0004g0033a0001c0001t0006g0043others(16): Show | 19 | HG01358.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+1452A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433257 | ||||||
| chr19:433268
|
C | G | 6 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0003g0071others(3): Show | 6 | HG02486.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+1441G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433268 | ||||||
| chr19:433269
|
G | A | 1 | a0002c0004t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+1440C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433269 | ||||||
| chr19:433272
|
CAGAT | C | 11 | a0001c0001t0002g0052a0001c0001t0002g0101a0001c0001t0003g0004others(8): Show | 12 | HG01978.hp1 HG02015.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+1433_1110+143 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433272 | ||||||
| chr19:433276
|
T | TAGATGGC others(159): Show |
28 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0092others(25): Show | 29 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+1432_1110+143 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433276 | ||||||
| chr19:433276
|
T | TAGATGGC others(159): Show |
1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1110+1432_1110+143 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433276 | ||||||
| chr19:433276
|
T | TGGCGCTT others(43): Show |
1 | a0001c0016t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1110+1432_1110+143 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433276 | ||||||
| chr19:433278
|
G | GATGGCAC others(840): Show |
1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1430_1110+143 others(851): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433278 | ||||||
| chr19:433278
|
G | GATGGCGC others(159): Show |
1 | a0006c0011t0005g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+1430_1110+143 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433278 | ||||||
| chr19:433278
|
G | GATGGCGC others(217): Show |
1 | a0006c0011t0005g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1110+1430_1110+143 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433278 | ||||||
| chr19:433284
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1110+1425C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433284 | ||||||
| chr19:433295
|
A | AGTGAGAT others(3909): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1413_1110+141 others(3920): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433295 | ||||||
| chr19:433303
|
C | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0101a0002c0004t0001g0205others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1406G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433303 | ||||||
| chr19:433303
|
CGTGAGTG others(333): Show |
C | 2 | a0001c0007t0003g0030a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1110+1066_1110+140 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433303 | ||||||
| chr19:433315
|
A | T | 13 | a0001c0001t0003g0036a0001c0001t0006g0043a0001c0001t0006g0049others(10): Show | 13 | HG01978.hp2 HG02055.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+1394T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433315 | ||||||
| chr19:433326
|
G | C | 64 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(61): Show | 67 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.1110+1383C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433326 | ||||||
| chr19:433336
|
G | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1373C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433336 | ||||||
| chr19:433342
|
G | A | 5 | a0001c0001t0003g0036a0001c0001t0016g0070a0001c0002t0001g0089others(2): Show | 5 | HG01071.hp2 HG02055.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+1367C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433342 | ||||||
| chr19:433372
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1337C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433372 | ||||||
| chr19:433373
|
T | A | 39 | a0001c0001t0001g0103a0001c0001t0001g0131a0001c0001t0002g0079others(36): Show | 41 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1110+1336A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433373 | ||||||
| chr19:433373
|
T | TTAGAGGA others(51): Show |
3 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0051 | 3 | HG02970.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1110+1335_1110+133 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433373 | ||||||
| chr19:433373
|
TTAGAGGA others(217): Show |
T | 1 | a0002c0004t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+1112_1110+133 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433373 | ||||||
| chr19:433374
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1335A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433374 | ||||||
| chr19:433375
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1334T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433375 | ||||||
| chr19:433378
|
G | GTCTGTGA others(499): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1330_1110+133 others(510): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433378 | ||||||
| chr19:433382
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1327C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433382 | ||||||
| chr19:433383
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1326G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433383 | ||||||
| chr19:433384
|
C | G | 9 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(6): Show | 9 | HG01978.hp2 HG02083.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110+1325G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433384 | ||||||
| chr19:433386
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1323C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433386 | ||||||
| chr19:433388
|
CAGAT | C | 3 | a0001c0001t0004g0033a0001c0001t0016g0070a0001c0016t0001g0144 | 3 | HG01358.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+1317_1110+132 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433388 | ||||||
| chr19:433391
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1318T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433391 | ||||||
| chr19:433392
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1317A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433392 | ||||||
| chr19:433397
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1312C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433397 | ||||||
| chr19:433398
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1311C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433398 | ||||||
| chr19:433399
|
C | A | 27 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1110+1310G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433399 | ||||||
| chr19:433400
|
G | A | 10 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0003g0004others(7): Show | 11 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1309C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433400 | ||||||
| chr19:433401
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1308G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433401 | ||||||
| chr19:433402
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1307A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433402 | ||||||
| chr19:433404
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1305G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433404 | ||||||
| chr19:433407
|
CGTGA | C | 13 | a0001c0003t0001g0058a0001c0003t0002g0001a0001c0003t0002g0060others(10): Show | 14 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+1298_1110+130 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433407 | ||||||
| chr19:433419
|
C | A | 1 | a0001c0001t0016g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1110+1290G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433419 | ||||||
| chr19:433427
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1282T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433427 | ||||||
| chr19:433431
|
T | A | 12 | a0001c0001t0002g0052a0001c0001t0006g0034a0001c0001t0006g0043others(9): Show | 12 | HG01358.hp1 HG01978.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+1278A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433431 | ||||||
| chr19:433432
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1277A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433432 | ||||||
| chr19:433436
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1273C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433436 | ||||||
| chr19:433440
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1269C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433440 | ||||||
| chr19:433442
|
C | G | 6 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+1267G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433442 | ||||||
| chr19:433442
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1267G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433442 | ||||||
| chr19:433444
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1265C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433444 | ||||||
| chr19:433446
|
C | CAGAT | 11 | a0001c0001t0002g0101a0001c0001t0004g0033a0001c0001t0006g0043others(8): Show | 11 | HG02572.hp1 HG02572.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1259_1110+126 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATAGA others(557): Show |
1 | a0001c0002t0001g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(568): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATAGA others(1693): Show |
1 | a0001c0002t0003g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(1704): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATAGA others(677): Show |
2 | a0001c0001t0003g0036a0001c0005t0006g0010 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+1262_1110+126 others(688): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATAGA others(113): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(124): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATAGA others(55): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1262_1110+126 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATAGA others(109): Show |
1 | a0001c0001t0006g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATGGC others(561): Show |
1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(572): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433446
|
C | CAGATGGC others(47): Show |
1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | ||||||
| chr19:433448
|
G | GATAGATG others(3271): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1260_1110+126 others(3282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433448 | ||||||
| chr19:433450
|
TGGCGCTT others(101): Show |
T | 2 | a0001c0001t0002g0052a0001c0001t0016g0070 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+1151_1110+125 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433450 | ||||||
| chr19:433451
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1258C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433451 | ||||||
| chr19:433453
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1256G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433453 | ||||||
| chr19:433454
|
G | A | 5 | a0001c0001t0003g0036a0001c0001t0004g0033a0001c0002t0001g0083others(2): Show | 5 | HG01978.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+1255C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433454 | ||||||
| chr19:433455
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1254G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433455 | ||||||
| chr19:433456
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1253A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433456 | ||||||
| chr19:433458
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1251G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433458 | ||||||
| chr19:433462
|
G | A | 1 | a0002c0004t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+1247C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433462 | ||||||
| chr19:433473
|
C | A | 8 | a0001c0001t0001g0103a0001c0001t0001g0131a0001c0001t0002g0039others(5): Show | 9 | HG00323.hp1 HG01891.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110+1236G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433473 | ||||||
| chr19:433473
|
C | T | 14 | a0001c0001t0007g0041a0001c0003t0001g0058a0001c0003t0002g0001others(11): Show | 15 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1110+1236G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433473 | ||||||
| chr19:433473
|
CGTGAGTG others(163): Show |
C | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+1066_1110+123 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433473 | ||||||
| chr19:433474
|
G | A | 4 | a0001c0001t0003g0071a0005c0009t0005g0048a0005c0009t0014g0040others(1): Show | 4 | NA18522.hp2 NA19240.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+1235C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433474 | ||||||
| chr19:433483
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1226T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433483 | ||||||
| chr19:433485
|
A | T | 11 | a0001c0001t0002g0101a0001c0001t0006g0034a0001c0001t0007g0041others(8): Show | 11 | HG01978.hp2 HG02083.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+1224T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433485 | ||||||
| chr19:433485
|
ATAGAGGA others(221): Show |
A | 27 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1110+996_1110+1223 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433485 | ||||||
| chr19:433486
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1223A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433486 | ||||||
| chr19:433488
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1221C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433488 | ||||||
| chr19:433489
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1220T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433489 | ||||||
| chr19:433494
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1215C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433494 | ||||||
| chr19:433496
|
C | G | 3 | a0001c0001t0002g0101a0001c0006t0001g0023a0008c0021t0002g0032 | 3 | HG02572.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1110+1213G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433496 | ||||||
| chr19:433496
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1213G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433496 | ||||||
| chr19:433498
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1211C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433498 | ||||||
| chr19:433503
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1206T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433503 | ||||||
| chr19:433504
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1205A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433504 | ||||||
| chr19:433504
|
TAGATGGC others(47): Show |
T | 6 | a0001c0001t0002g0039a0001c0001t0003g0004a0001c0001t0003g0180others(3): Show | 7 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+1151_1110+120 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433504 | ||||||
| chr19:433512
|
G | A | 3 | a0001c0001t0006g0034a0001c0002t0001g0087a0001c0002t0003g0085 | 3 | HG02083.hp2 HG02135.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1110+1197C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | ||||||
| chr19:433512
|
G | GCTTCATC others(1017): Show |
1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1110+1196_1110+119 others(1028): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | ||||||
| chr19:433512
|
G | GCTTCATC others(51): Show |
22 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0051others(19): Show | 22 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1110+1196_1110+119 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | ||||||
| chr19:433512
|
G | GCTTCATC others(279): Show |
1 | a0001c0002t0003g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1110+1196_1110+119 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | ||||||
| chr19:433512
|
G | GCTTCATC others(7223): Show |
1 | a0001c0002t0003g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1110+1196_1110+119 others(7234): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | ||||||
| chr19:433519
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1190G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433519 | ||||||
| chr19:433531
|
C | A | 1 | a0001c0005t0015g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1110+1178G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433531 | ||||||
| chr19:433542
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1167C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433542 | ||||||
| chr19:433543
|
T | A | 11 | a0001c0001t0002g0101a0001c0001t0006g0043a0001c0001t0006g0049others(8): Show | 11 | HG01071.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1166A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433543 | ||||||
| chr19:433543
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1166A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433543 | ||||||
| chr19:433544
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1165A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433544 | ||||||
| chr19:433545
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1164T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433545 | ||||||
| chr19:433549
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1160C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433549 | ||||||
| chr19:433550
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1159T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433550 | ||||||
| chr19:433551
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1158C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433551 | ||||||
| chr19:433553
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1156G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433553 | ||||||
| chr19:433554
|
C | G | 4 | a0001c0001t0003g0071a0001c0002t0003g0147a0001c0016t0001g0144others(1): Show | 4 | HG01071.hp2 HG01358.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1155G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433554 | ||||||
| chr19:433555
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1154C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433555 | ||||||
| chr19:433557
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1152C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433557 | ||||||
| chr19:433558
|
C | CAGAT | 18 | a0001c0001t0002g0101a0001c0001t0003g0036a0001c0001t0004g0033others(15): Show | 18 | HG01071.hp2 HG01358.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1110+1147_1110+115 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | ||||||
| chr19:433558
|
C | CAGATAGA others(337): Show |
1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+1150_1110+115 others(348): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | ||||||
| chr19:433558
|
C | CAGATAGA others(1419): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1150_1110+115 others(1430): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | ||||||
| chr19:433558
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1151G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | ||||||
| chr19:433560
|
G | GATAGATG others(1014): Show |
3 | a0001c0007t0006g0037a0001c0007t0006g0055a0002c0024t0003g0188 | 3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1148_1110+114 others(1025): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433560 | ||||||
| chr19:433560
|
G | GATAGATG others(279): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1148_1110+114 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433560 | ||||||
| chr19:433563
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1146C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433563 | ||||||
| chr19:433565
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1144G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433565 | ||||||
| chr19:433566
|
G | A | 3 | a0001c0006t0001g0020a0001c0006t0001g0024a0001c0006t0006g0014 | 3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1143C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433566 | ||||||
| chr19:433567
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1142G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433567 | ||||||
| chr19:433568
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1141A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433568 | ||||||
| chr19:433573
|
C | T | 2 | a0001c0001t0003g0071a0001c0002t0001g0093 | 2 | NA18940.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+1136G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433573 | ||||||
| chr19:433574
|
G | A | 3 | a0001c0006t0001g0020a0001c0006t0001g0024a0001c0006t0006g0014 | 3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1135C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433574 | ||||||
| chr19:433585
|
A | C | 69 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0002g0101others(66): Show | 72 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.1110+1124T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433585 | ||||||
| chr19:433586
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1123C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433586 | ||||||
| chr19:433595
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1114T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433595 | ||||||
| chr19:433597
|
A | ATAGAGGA others(51): Show |
3 | a0001c0007t0002g0080a0006c0011t0005g0059a0006c0011t0005g0063 | 3 | HG01109.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1110+1111_1110+111 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433597 | ||||||
| chr19:433597
|
A | T | 38 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0092others(35): Show | 40 | HG00423.hp2 HG00558.hp2 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1110+1112T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433597 | ||||||
| chr19:433598
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1111A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433598 | ||||||
| chr19:433600
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1109C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433600 | ||||||
| chr19:433601
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1108T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433601 | ||||||
| chr19:433606
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1103C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433606 | ||||||
| chr19:433607
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1102G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433607 | ||||||
| chr19:433608
|
C | G | 14 | a0001c0003t0001g0058a0001c0003t0002g0001a0001c0003t0002g0060others(11): Show | 15 | HG01074.hp2 HG01358.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+1101G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433608 | ||||||
| chr19:433608
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1101G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433608 | ||||||
| chr19:433610
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1099C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433610 | ||||||
| chr19:433612
|
CAGAT | C | 3 | a0001c0006t0001g0020a0001c0006t0001g0024a0001c0006t0006g0014 | 3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1093_1110+109 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433612 | ||||||
| chr19:433615
|
A | T | 2 | a0001c0001t0003g0071a0001c0003t0004g0109 | 2 | NA19066.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+1094T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433615 | ||||||
| chr19:433616
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1093A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433616 | ||||||
| chr19:433616
|
T | TGGCGCTT others(159): Show |
1 | a0001c0006t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+1092_1110+109 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433616 | ||||||
| chr19:433618
|
G | C | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1091C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433618 | ||||||
| chr19:433623
|
C | A | 1 | a0002c0004t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+1086G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433623 | ||||||
| chr19:433624
|
G | A | 3 | a0001c0001t0003g0036a0001c0001t0004g0033a0001c0005t0006g0010 | 3 | HG02055.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+1085C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433624 | ||||||
| chr19:433625
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1084G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433625 | ||||||
| chr19:433626
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1083A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433626 | ||||||
| chr19:433627
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1082A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433627 | ||||||
| chr19:433628
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1081G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433628 | ||||||
| chr19:433631
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1078G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433631 | ||||||
| chr19:433632
|
G | A | 1 | a0001c0007t0006g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+1077C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433632 | ||||||
| chr19:433643
|
A | C | 110 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0081others(107): Show | 115 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1110+1066T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433643 | ||||||
| chr19:433643
|
A | T | 1 | a0002c0004t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+1066T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433643 | ||||||
| chr19:433651
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1058T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433651 | ||||||
| chr19:433655
|
A | ATAGAGGA others(47): Show |
1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1053_1110+105 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433655 | ||||||
| chr19:433655
|
A | T | 37 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0003g0036others(34): Show | 37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110+1054T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433655 | ||||||
| chr19:433660
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1049C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433660 | ||||||
| chr19:433664
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1045C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433664 | ||||||
| chr19:433666
|
C | G | 2 | a0001c0001t0002g0039a0001c0002t0001g0083 | 2 | HG01978.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1110+1043G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433666 | ||||||
| chr19:433668
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1041C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433668 | ||||||
| chr19:433676
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1033C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433676 | ||||||
| chr19:433680
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1029C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433680 | ||||||
| chr19:433681
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1028G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433681 | ||||||
| chr19:433682
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1027C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433682 | ||||||
| chr19:433684
|
T | TGTGAGTG others(3): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1024_1110+102 others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433684 | ||||||
| chr19:433689
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1020G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433689 | ||||||
| chr19:433701
|
C | T | 1 | a0002c0004t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+1008G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433701 | ||||||
| chr19:433702
|
G | A | 2 | a0001c0003t0004g0109a0001c0003t0004g0110 | 2 | NA18612.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1110+1007C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433702 | ||||||
| chr19:433713
|
T | A | 42 | a0001c0001t0002g0057a0001c0001t0002g0101a0001c0001t0003g0050others(39): Show | 44 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1110+996A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433713 | ||||||
| chr19:433714
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+995A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433714 | ||||||
| chr19:433718
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+991C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433718 | ||||||
| chr19:433719
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+990C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433719 | ||||||
| chr19:433721
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+988C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433721 | ||||||
| chr19:433724
|
C | CGGGCAGA others(47): Show |
1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1110+984_1110+985i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433724 | ||||||
| chr19:433724
|
C | G | 14 | a0001c0002t0003g0147a0001c0003t0001g0058a0001c0003t0002g0001others(11): Show | 15 | HG01071.hp2 HG01074.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+985G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433724 | ||||||
| chr19:433728
|
CAGAT | C | 6 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+977_1110+980d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433728 | ||||||
| chr19:433731
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+978T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433731 | ||||||
| chr19:433732
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+977A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433732 | ||||||
| chr19:433732
|
T | TAGATGGC others(43): Show |
2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+976_1110+977i others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433732 | ||||||
| chr19:433734
|
G | GATGGCGC others(1187): Show |
1 | a0001c0002t0001g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1110+974_1110+975i others(1196): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433734 | ||||||
| chr19:433737
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+972C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433737 | ||||||
| chr19:433739
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+970G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433739 | ||||||
| chr19:433740
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+969C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433740 | ||||||
| chr19:433741
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+968G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433741 | ||||||
| chr19:433742
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+967A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433742 | ||||||
| chr19:433744
|
C | CTGTGAGA others(47): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+964_1110+965i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433744 | ||||||
| chr19:433759
|
C | A | 6 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+950G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433759 | ||||||
| chr19:433759
|
C | CGTGAGTG others(221): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+949_1110+950i others(230): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433759 | ||||||
| chr19:433771
|
T | A | 11 | a0001c0001t0002g0101a0001c0001t0006g0043a0001c0001t0006g0049others(8): Show | 11 | HG01978.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+938A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | ||||||
| chr19:433771
|
T | TTAGAGGA others(337): Show |
26 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0092others(23): Show | 28 | HG00558.hp2 HG01952.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+937_1110+938i others(346): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | ||||||
| chr19:433771
|
T | TTAGAGGA others(2841): Show |
1 | a0001c0002t0001g0154 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1110+937_1110+938i others(2850): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | ||||||
| chr19:433771
|
T | TTAGAGGA others(337): Show |
1 | a0001c0002t0003g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1110+937_1110+938i others(346): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | ||||||
| chr19:433771
|
T | TTAGAGGA others(333): Show |
1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+937_1110+938i others(342): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | ||||||
| chr19:433772
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+937A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433772 | ||||||
| chr19:433773
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+936T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433773 | ||||||
| chr19:433775
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+934T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433775 | ||||||
| chr19:433777
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+932C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433777 | ||||||
| chr19:433779
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+930C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433779 | ||||||
| chr19:433782
|
C | G | 34 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0003g0004others(31): Show | 35 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1110+927G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433782 | ||||||
| chr19:433783
|
G | A | 1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+926C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433783 | ||||||
| chr19:433792
|
G | A | 3 | a0001c0002t0003g0085a0001c0002t0003g0157a0001c0002t0003g0173 | 3 | HG02083.hp2 HG04228.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1110+917C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433792 | ||||||
| chr19:433792
|
G | AATGGCGC others(51): Show |
2 | a0001c0002t0001g0087a0001c0002t0001g0089 | 2 | HG02135.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1110+917_1110+918i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433792 | ||||||
| chr19:433792
|
G | C | 7 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+917C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433792 | ||||||
| chr19:433794
|
T | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+915A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433794 | ||||||
| chr19:433798
|
G | A | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+911C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433798 | ||||||
| chr19:433800
|
T | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+909A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433800 | ||||||
| chr19:433801
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+908A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433801 | ||||||
| chr19:433801
|
T | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+908A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433801 | ||||||
| chr19:433802
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+907G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433802 | ||||||
| chr19:433802
|
C | CATTGTGA others(541): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+906_1110+907i others(550): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433802 | ||||||
| chr19:433806
|
G | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+903C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433806 | ||||||
| chr19:433810
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1110+899C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433810 | ||||||
| chr19:433817
|
C | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+892G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433817 | ||||||
| chr19:433825
|
A | AGTCTGT | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+883_1110+884i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433825 | ||||||
| chr19:433828
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+881C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433828 | ||||||
| chr19:433829
|
T | A | 68 | a0001c0001t0001g0112a0001c0001t0002g0039a0001c0001t0002g0052others(65): Show | 72 | HG00423.hp2 HG00558.hp2 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.1110+880A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433829 | ||||||
| chr19:433829
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+880A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433829 | ||||||
| chr19:433829
|
T | TTAGAGGA others(387): Show |
1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+879_1110+880i others(396): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433829 | ||||||
| chr19:433830
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+879A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433830 | ||||||
| chr19:433831
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+878T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433831 | ||||||
| chr19:433833
|
A | ATC | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+875_1110+876i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433833 | ||||||
| chr19:433835
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+874C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433835 | ||||||
| chr19:433837
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+872C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433837 | ||||||
| chr19:433838
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+871C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433838 | ||||||
| chr19:433839
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+870G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433839 | ||||||
| chr19:433840
|
G | C | 73 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0002g0052others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1110+869C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433840 | ||||||
| chr19:433840
|
G | GGGGCAGA others(51): Show |
2 | a0001c0002t0002g0046a0005c0009t0014g0040 | 2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+868_1110+869i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433840 | ||||||
| chr19:433841
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+868C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433841 | ||||||
| chr19:433842
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+867C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433842 | ||||||
| chr19:433843
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+866C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433843 | ||||||
| chr19:433843
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+866C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433843 | ||||||
| chr19:433844
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+865G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433844 | ||||||
| chr19:433844
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+865G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433844 | ||||||
| chr19:433844
|
CAGAT | C | 29 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+861_1110+864d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433844 | ||||||
| chr19:433847
|
A | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+862T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433847 | ||||||
| chr19:433848
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+861A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | ||||||
| chr19:433848
|
T | TAGATGGC others(2559): Show |
1 | a0001c0003t0002g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1110+860_1110+861i others(2568): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | ||||||
| chr19:433848
|
T | TAGATGGC others(163): Show |
17 | a0001c0003t0001g0062a0001c0003t0001g0066a0001c0003t0001g0113others(14): Show | 17 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1110+860_1110+861i others(172): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | ||||||
| chr19:433848
|
T | TAGATGGC others(735): Show |
1 | a0001c0003t0002g0072 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1110+860_1110+861i others(744): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | ||||||
| chr19:433848
|
T | TAGATGGC others(735): Show |
11 | a0001c0003t0001g0058a0001c0003t0002g0001a0001c0003t0002g0069others(8): Show | 12 | HG01074.hp2 HG01952.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+860_1110+861i others(744): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | ||||||
| chr19:433848
|
T | TAGATGGC others(221): Show |
3 | a0001c0006t0001g0020a0001c0006t0001g0023a0001c0006t0001g0024 | 3 | HG03209.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+860_1110+861i others(230): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | ||||||
| chr19:433853
|
G | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+856C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433853 | ||||||
| chr19:433855
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+854G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433855 | ||||||
| chr19:433856
|
G | A | 2 | a0001c0001t0003g0071a0001c0002t0003g0147 | 2 | HG01071.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+853C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433856 | ||||||
| chr19:433857
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+852G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433857 | ||||||
| chr19:433857
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+852G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433857 | ||||||
| chr19:433858
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+851A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433858 | ||||||
| chr19:433859
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+850A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433859 | ||||||
| chr19:433860
|
C | CTGTGAG | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+848_1110+849i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433860 | ||||||
| chr19:433860
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+849G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433860 | ||||||
| chr19:433864
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+845C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433864 | ||||||
| chr19:433872
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+837C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433872 | ||||||
| chr19:433875
|
C | A | 29 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+834G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433875 | ||||||
| chr19:433876
|
G | A | 1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+833C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433876 | ||||||
| chr19:433881
|
T | TTATATC | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+827_1110+828i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433881 | ||||||
| chr19:433883
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+826T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433883 | ||||||
| chr19:433885
|
A | AGATAGAG others(51): Show |
1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+823_1110+824i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433885 | ||||||
| chr19:433886
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+823C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433886 | ||||||
| chr19:433887
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+822T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433887 | ||||||
| chr19:433887
|
A | T | 6 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+822T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433887 | ||||||
| chr19:433888
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+821A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433888 | ||||||
| chr19:433889
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+820T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433889 | ||||||
| chr19:433891
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+818T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433891 | ||||||
| chr19:433893
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+816C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433893 | ||||||
| chr19:433893
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+816C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433893 | ||||||
| chr19:433894
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+815T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433894 | ||||||
| chr19:433895
|
G | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+814C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433895 | ||||||
| chr19:433896
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+813C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433896 | ||||||
| chr19:433897
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+812G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433897 | ||||||
| chr19:433898
|
G | C | 128 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0112others(125): Show | 132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1110+811C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433898 | ||||||
| chr19:433898
|
G | GGGGCAGA others(51): Show |
5 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0034others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+753_1110+810d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433898 | ||||||
| chr19:433898
|
G | GGGGCAGA others(109): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+695_1110+810d others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433898 | ||||||
| chr19:433899
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+810C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433899 | ||||||
| chr19:433899
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+810C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433899 | ||||||
| chr19:433901
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+808C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433901 | ||||||
| chr19:433901
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+808C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433901 | ||||||
| chr19:433902
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+807G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433902 | ||||||
| chr19:433903
|
A | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+806T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433903 | ||||||
| chr19:433905
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+804T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433905 | ||||||
| chr19:433906
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+803A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433906 | ||||||
| chr19:433908
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+801C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433908 | ||||||
| chr19:433909
|
A | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+800T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433909 | ||||||
| chr19:433909
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+800T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433909 | ||||||
| chr19:433910
|
T | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+799A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433910 | ||||||
| chr19:433910
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+799A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433910 | ||||||
| chr19:433911
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+798C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433911 | ||||||
| chr19:433911
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+798C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433911 | ||||||
| chr19:433913
|
C | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+796G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433913 | ||||||
| chr19:433913
|
C | T | 1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1110+796G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433913 | ||||||
| chr19:433914
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+795C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433914 | ||||||
| chr19:433915
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+794G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433915 | ||||||
| chr19:433916
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+793A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433916 | ||||||
| chr19:433916
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+793A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433916 | ||||||
| chr19:433917
|
T | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+792A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433917 | ||||||
| chr19:433918
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+791G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433918 | ||||||
| chr19:433922
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+787C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433922 | ||||||
| chr19:433924
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+785C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433924 | ||||||
| chr19:433926
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+783C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433926 | ||||||
| chr19:433933
|
C | A | 31 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1110+776G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433933 | ||||||
| chr19:433933
|
C | CGTGAGTG others(51): Show |
1 | a0001c0002t0003g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1110+775_1110+776i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433933 | ||||||
| chr19:433934
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+775C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433934 | ||||||
| chr19:433940
|
G | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+769C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433940 | ||||||
| chr19:433943
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+766T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433943 | ||||||
| chr19:433944
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+765C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433944 | ||||||
| chr19:433945
|
A | AGATCATG others(417): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+763_1110+764i others(426): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | ||||||
| chr19:433945
|
A | ATAGAGGA others(51): Show |
2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+763_1110+764i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | ||||||
| chr19:433945
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+764T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | ||||||
| chr19:433945
|
A | T | 1 | a0001c0002t0003g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+764T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | ||||||
| chr19:433946
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+763A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433946 | ||||||
| chr19:433947
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+762T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433947 | ||||||
| chr19:433948
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+761C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433948 | ||||||
| chr19:433950
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+759C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433950 | ||||||
| chr19:433954
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+755C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433954 | ||||||
| chr19:433954
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+755C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433954 | ||||||
| chr19:433955
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+754G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433955 | ||||||
| chr19:433956
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+753G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433956 | ||||||
| chr19:433958
|
G | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+751C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433958 | ||||||
| chr19:433959
|
GC | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+749delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433959 | ||||||
| chr19:433963
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+746T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433963 | ||||||
| chr19:433964
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+745A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433964 | ||||||
| chr19:433965
|
A | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+744T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433965 | ||||||
| chr19:433967
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+742T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433967 | ||||||
| chr19:433968
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+741A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433968 | ||||||
| chr19:433969
|
G | A | 6 | a0001c0001t0005g0053a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+740C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433969 | ||||||
| chr19:433970
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+739C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433970 | ||||||
| chr19:433971
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+738G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433971 | ||||||
| chr19:433972
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+737C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433972 | ||||||
| chr19:433973
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+736G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433973 | ||||||
| chr19:433973
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+736G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433973 | ||||||
| chr19:433974
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+735A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433974 | ||||||
| chr19:433975
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+734A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433975 | ||||||
| chr19:433976
|
C | CT | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+732_1110+733i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433976 | ||||||
| chr19:433976
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+733G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433976 | ||||||
| chr19:433978
|
T | TG | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+730_1110+731i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433978 | ||||||
| chr19:433979
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+730G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433979 | ||||||
| chr19:433980
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+729C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433980 | ||||||
| chr19:433982
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+727C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433982 | ||||||
| chr19:433984
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+725C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433984 | ||||||
| chr19:433991
|
C | CGTGAGTG others(445): Show |
1 | a0005c0009t0005g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1110+717_1110+718i others(454): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433991 | ||||||
| chr19:433992
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+717C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433992 | ||||||
| chr19:433997
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+712A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433997 | ||||||
| chr19:434001
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+708T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434001 | ||||||
| chr19:434003
|
A | T | 1 | a0001c0001t0007g0041 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+706T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434003 | ||||||
| chr19:434004
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+705A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434004 | ||||||
| chr19:434005
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+704T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434005 | ||||||
| chr19:434006
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+703C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434006 | ||||||
| chr19:434007
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+702T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434007 | ||||||
| chr19:434010
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+699T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434010 | ||||||
| chr19:434011
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+698C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434011 | ||||||
| chr19:434012
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+697C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434012 | ||||||
| chr19:434013
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+696G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434013 | ||||||
| chr19:434013
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+696G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434013 | ||||||
| chr19:434014
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+695G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434014 | ||||||
| chr19:434014
|
C | CGGGCAGA others(51): Show |
5 | a0001c0007t0002g0080a0001c0007t0006g0055a0002c0024t0003g0188others(2): Show | 5 | HG01109.hp2 HG03225.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+694_1110+695i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434014 | ||||||
| chr19:434014
|
C | G | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+695G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434014 | ||||||
| chr19:434015
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+694C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434015 | ||||||
| chr19:434016
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+693C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434016 | ||||||
| chr19:434017
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+692C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434017 | ||||||
| chr19:434018
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+691G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434018 | ||||||
| chr19:434020
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+689C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434020 | ||||||
| chr19:434020
|
G | GATAGATG others(51): Show |
1 | a0001c0002t0003g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1110+688_1110+689i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434020 | ||||||
| chr19:434023
|
A | C | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+686T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434023 | ||||||
| chr19:434024
|
GA | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+684delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434024 | ||||||
| chr19:434027
|
G | GAGTCTGT others(48): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+681_1110+682i others(57): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434027 | ||||||
| chr19:434027
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+682C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434027 | ||||||
| chr19:434029
|
C | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+680G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434029 | ||||||
| chr19:434031
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+678G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434031 | ||||||
| chr19:434031
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+678G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434031 | ||||||
| chr19:434032
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+677A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434032 | ||||||
| chr19:434033
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+676A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434033 | ||||||
| chr19:434033
|
T | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+676A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434033 | ||||||
| chr19:434034
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+675G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434034 | ||||||
| chr19:434037
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+672G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434037 | ||||||
| chr19:434038
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+671C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434038 | ||||||
| chr19:434053
|
A | AGTCT | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+655_1110+656i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434053 | ||||||
| chr19:434060
|
G | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+649C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434060 | ||||||
| chr19:434061
|
T | A | 3 | a0001c0001t0003g0071a0001c0002t0003g0147a0001c0007t0006g0037 | 3 | HG01071.hp2 HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+648A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434061 | ||||||
| chr19:434062
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+647A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434062 | ||||||
| chr19:434063
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+646T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434063 | ||||||
| chr19:434063
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+646T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434063 | ||||||
| chr19:434066
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+643C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434066 | ||||||
| chr19:434067
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+642C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434067 | ||||||
| chr19:434068
|
A | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+641T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434068 | ||||||
| chr19:434069
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+640C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434069 | ||||||
| chr19:434070
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+639C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434070 | ||||||
| chr19:434071
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+638G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434071 | ||||||
| chr19:434072
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+637G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434072 | ||||||
| chr19:434072
|
C | GGGGCAGA others(51): Show |
1 | a0001c0007t0006g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+637_1110+638i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434072 | ||||||
| chr19:434072
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+637G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434072 | ||||||
| chr19:434073
|
G | A | 6 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+636C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434073 | ||||||
| chr19:434074
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+635C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434074 | ||||||
| chr19:434075
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+634C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434075 | ||||||
| chr19:434076
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+633G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434076 | ||||||
| chr19:434079
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+630T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434079 | ||||||
| chr19:434080
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+629A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434080 | ||||||
| chr19:434080
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+629A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434080 | ||||||
| chr19:434082
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+627C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434082 | ||||||
| chr19:434082
|
GATGGCGC others(3): Show |
G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+617_1110+626d others(12): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434082 | ||||||
| chr19:434084
|
T | TCG | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+624_1110+625i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434084 | ||||||
| chr19:434085
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+624C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434085 | ||||||
| chr19:434087
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+622G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434087 | ||||||
| chr19:434089
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+620G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434089 | ||||||
| chr19:434091
|
T | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+618A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434091 | ||||||
| chr19:434092
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+617G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434092 | ||||||
| chr19:434101
|
T | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+608A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434101 | ||||||
| chr19:434108
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+601C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434108 | ||||||
| chr19:434112
|
G | GTC | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+596_1110+597i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434112 | ||||||
| chr19:434115
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+594T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434115 | ||||||
| chr19:434119
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+590A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434119 | ||||||
| chr19:434120
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+589A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434120 | ||||||
| chr19:434121
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+588T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434121 | ||||||
| chr19:434123
|
A | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+586T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434123 | ||||||
| chr19:434125
|
G | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+584C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434125 | ||||||
| chr19:434126
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+583T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434126 | ||||||
| chr19:434127
|
G | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+582C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434127 | ||||||
| chr19:434128
|
G | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+581C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434128 | ||||||
| chr19:434130
|
C | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+579G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434130 | ||||||
| chr19:434130
|
C | T | 2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+579G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434130 | ||||||
| chr19:434131
|
G | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+578C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434131 | ||||||
| chr19:434132
|
GGC | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+575_1110+576d others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434132 | ||||||
| chr19:434133
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+576C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434133 | ||||||
| chr19:434134
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+575G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434134 | ||||||
| chr19:434135
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+574T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434135 | ||||||
| chr19:434138
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+571A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434138 | ||||||
| chr19:434139
|
G | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+570C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434139 | ||||||
| chr19:434139
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+570C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434139 | ||||||
| chr19:434141
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+568G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434141 | ||||||
| chr19:434141
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+568G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434141 | ||||||
| chr19:434143
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+566G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434143 | ||||||
| chr19:434144
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+565A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434144 | ||||||
| chr19:434146
|
CA | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+562delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434146 | ||||||
| chr19:434149
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+560G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434149 | ||||||
| chr19:434159
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+550T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434159 | ||||||
| chr19:434161
|
A | C | 43 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(40): Show | 44 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1110+548T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434161 | ||||||
| chr19:434162
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+547C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434162 | ||||||
| chr19:434168
|
G | C | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+541C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434168 | ||||||
| chr19:434169
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+540T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434169 | ||||||
| chr19:434171
|
A | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+538T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434171 | ||||||
| chr19:434174
|
T | G | 7 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(4): Show | 7 | HG01361.hp1 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+535A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434174 | ||||||
| chr19:434175
|
A | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+534T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434175 | ||||||
| chr19:434178
|
G | GT | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+530_1110+531i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434178 | ||||||
| chr19:434181
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+528C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434181 | ||||||
| chr19:434182
|
G | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+527C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434182 | ||||||
| chr19:434183
|
C | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+526G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434183 | ||||||
| chr19:434185
|
G | GTGA | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+523_1110+524i others(5): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434185 | ||||||
| chr19:434187
|
G | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+522C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434187 | ||||||
| chr19:434188
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+521G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434188 | ||||||
| chr19:434192
|
TA | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+516delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434192 | ||||||
| chr19:434195
|
AC | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+513delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434195 | ||||||
| chr19:434197
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+512C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434197 | ||||||
| chr19:434199
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+510G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434199 | ||||||
| chr19:434201
|
C | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+508G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434201 | ||||||
| chr19:434202
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+507G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434202 | ||||||
| chr19:434203
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+506G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434203 | ||||||
| chr19:434203
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+506G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434203 | ||||||
| chr19:434204
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+505G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434204 | ||||||
| chr19:434207
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+502A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434207 | ||||||
| chr19:434207
|
T | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+502A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434207 | ||||||
| chr19:434208
|
G | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+501C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434208 | ||||||
| chr19:434213
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+496G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434213 | ||||||
| chr19:434213
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+496G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434213 | ||||||
| chr19:434214
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+495G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434214 | ||||||
| chr19:434215
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+494A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434215 | ||||||
| chr19:434220
|
T | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+489A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434220 | ||||||
| chr19:434222
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+487C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434222 | ||||||
| chr19:434227
|
A | AAATCGTG others(421): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+481_1110+482i others(430): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434227 | ||||||
| chr19:434239
|
C | CATAAGTG others(96): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+469_1110+470i others(105): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434239 | ||||||
| chr19:434240
|
C | CTGAGTGA others(85): Show |
5 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0004g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+377_1110+468d others(94): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434240 | ||||||
| chr19:434240
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+469G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434240 | ||||||
| chr19:434243
|
A | AATGAGAC others(1): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+465_1110+466i others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434243 | ||||||
| chr19:434256
|
GTGAGTGA others(5): Show |
G | 6 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0050others(3): Show | 6 | HG02486.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+441_1110+452d others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434256 | ||||||
| chr19:434259
|
A | AGTCAGTG others(337): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+449_1110+450i others(346): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434259 | ||||||
| chr19:434267
|
C | CGTGAGTC others(1): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+441_1110+442i others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434267 | ||||||
| chr19:434268
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+441T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434268 | ||||||
| chr19:434277
|
A | C | 35 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0083others(32): Show | 37 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1110+432T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434277 | ||||||
| chr19:434280
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+429T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434280 | ||||||
| chr19:434296
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+413T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434296 | ||||||
| chr19:434303
|
A | AGATC | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+405_1110+406i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434303 | ||||||
| chr19:434311
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+398G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434311 | ||||||
| chr19:434316
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+393G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434316 | ||||||
| chr19:434324
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+385T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434324 | ||||||
| chr19:434343
|
C | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+366G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434343 | ||||||
| chr19:434344
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+365T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434344 | ||||||
| chr19:434354
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+355C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434354 | ||||||
| chr19:434355
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+354T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434355 | ||||||
| chr19:434357
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+352T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434357 | ||||||
| chr19:434358
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+351A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434358 | ||||||
| chr19:434359
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+350G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434359 | ||||||
| chr19:434359
|
CATGAGAT others(13): Show |
C | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+330_1110+349d others(22): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434359 | ||||||
| chr19:434360
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+349T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434360 | ||||||
| chr19:434367
|
C | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+342G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434367 | ||||||
| chr19:434379
|
G | C | 94 | a0001c0001t0002g0052a0001c0001t0002g0079a0001c0001t0002g0101others(91): Show | 97 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1110+330C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434379 | ||||||
| chr19:434380
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+329T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434380 | ||||||
| chr19:434384
|
G | GAT | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+324_1110+325i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434384 | ||||||
| chr19:434386
|
C | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+323G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434386 | ||||||
| chr19:434389
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+320T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434389 | ||||||
| chr19:434390
|
G | GAGTGTGA others(3): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+318_1110+319i others(12): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434390 | ||||||
| chr19:434405
|
T | TGTGAGAT others(615): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+303_1110+304i others(624): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434405 | ||||||
| chr19:434416
|
T | TCATA | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+292_1110+293i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434416 | ||||||
| chr19:434417
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+292T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434417 | ||||||
| chr19:434425
|
A | AGGT | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+283_1110+284i others(5): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434425 | ||||||
| chr19:434428
|
C | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+281G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434428 | ||||||
| chr19:434436
|
G | A | 1 | a0001c0005t0001g0022 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1110+273C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434436 | ||||||
| chr19:434440
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+269T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434440 | ||||||
| chr19:434446
|
C | G | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+263G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434446 | ||||||
| chr19:434447
|
T | A | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+262A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434447 | ||||||
| chr19:434452
|
G | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+257C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434452 | ||||||
| chr19:434454
|
T | TCGTGAGT others(88): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+254_1110+255i others(97): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434454 | ||||||
| chr19:434455
|
A | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+254T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434455 | ||||||
| chr19:434461
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+248G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434461 | ||||||
| chr19:434461
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+248G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434461 | ||||||
| chr19:434462
|
A | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+247T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434462 | ||||||
| chr19:434462
|
A | T | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+247T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434462 | ||||||
| chr19:434463
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+246T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434463 | ||||||
| chr19:434463
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+246T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434463 | ||||||
| chr19:434476
|
G | A | 1 | a0001c0001t0005g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1110+233C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434476 | ||||||
| chr19:434483
|
TGTGA | T | 3 | a0001c0001t0002g0101a0001c0001t0007g0041a0008c0021t0002g0032 | 3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+222_1110+225d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434483 | ||||||
| chr19:434485
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+224A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434485 | ||||||
| chr19:434487
|
A | AGATG | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+221_1110+222i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434487 | ||||||
| chr19:434488
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+221C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434488 | ||||||
| chr19:434488
|
GTGAGTGA others(5): Show |
G | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+209_1110+220d others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434488 | ||||||
| chr19:434496
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+213T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434496 | ||||||
| chr19:434499
|
C | CGTGAGTC others(319): Show |
1 | a0001c0001t0006g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1110+209_1110+210i others(328): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434499 | ||||||
| chr19:434499
|
C | CGTGAGTC others(319): Show |
4 | a0001c0001t0006g0043a0001c0001t0006g0054a0001c0005t0006g0009others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+209_1110+210i others(328): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434499 | ||||||
| chr19:434500
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+209T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434500 | ||||||
| chr19:434501
|
T | C | 36 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(33): Show | 37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110+208A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434501 | ||||||
| chr19:434511
|
C | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+198G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434511 | ||||||
| chr19:434511
|
C | CGTGATTG others(371): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+197_1110+198i others(380): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434511 | ||||||
| chr19:434517
|
C | T | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+192G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434517 | ||||||
| chr19:434519
|
T | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+190A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434519 | ||||||
| chr19:434527
|
T | C | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+182A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434527 | ||||||
| chr19:434539
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+170A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434539 | ||||||
| chr19:434547
|
TGTGA | T | 7 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(4): Show | 7 | HG01109.hp2 HG02451.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+158_1110+161d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434547 | ||||||
| chr19:434552
|
G | GATCA | 5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+156_1110+157i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434552 | ||||||
| chr19:434554
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+155T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434554 | ||||||
| chr19:434556
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+153C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434556 | ||||||
| chr19:434560
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+149T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434560 | ||||||
| chr19:434564
|
A | G | 6 | a0001c0001t0003g0071a0001c0001t0006g0043a0001c0001t0006g0049others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+145T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434564 | ||||||
| chr19:434567
|
A | AGTGAGAT others(832): Show |
5 | a0001c0001t0006g0043a0001c0001t0006g0049a0001c0001t0006g0054others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(841): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTC others(39): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(48): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
1 | a0001c0001t0001g0105 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3693): Show |
1 | a0002c0012t0002g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3702): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
6 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0003g0050others(3): Show | 6 | HG02486.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
2 | a0001c0001t0003g0004a0001c0001t0003g0180 | 3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
4 | a0001c0001t0016g0070a0001c0013t0005g0007a0001c0017t0005g0056others(1): Show | 4 | HG02622.hp1 HG02622.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3681): Show |
1 | a0001c0002t0003g0045 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3690): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3669): Show |
3 | a0001c0001t0002g0101a0001c0001t0007g0041a0008c0021t0002g0032 | 3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3678): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3685): Show |
28 | a0001c0002t0001g0003a0001c0002t0001g0083a0001c0002t0001g0087others(25): Show | 29 | HG00423.hp2 HG01978.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3694): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3685): Show |
3 | a0001c0002t0001g0006a0001c0002t0001g0093a0001c0002t0001g0167 | 4 | HG00558.hp2 HG02027.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3694): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3673): Show |
2 | a0001c0002t0003g0147a0001c0002t0003g0148 | 2 | HG01071.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3682): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3685): Show |
1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3694): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3691): Show |
5 | a0001c0003t0002g0069a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | NA18954.hp2 NA18999.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3700): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3693): Show |
23 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(20): Show | 24 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3702): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
2 | a0001c0007t0003g0030a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3711): Show |
1 | a0001c0001t0005g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3720): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3712): Show |
1 | a0001c0001t0001g0123 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3721): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3711): Show |
2 | a0001c0001t0003g0171a0003c0008t0003g0183 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3720): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3709): Show |
1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3718): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3710): Show |
1 | a0001c0014t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3719): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
60 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(57): Show | 61 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3713): Show |
2 | a0005c0009t0005g0048a0010c0022t0002g0184 | 2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3729): Show |
1 | a0001c0001t0001g0002 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3738): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3707): Show |
1 | a0001c0005t0001g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3707): Show |
15 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0035others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3707): Show |
10 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0159others(7): Show | 10 | HG01258.hp1 HG01358.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3707): Show |
1 | a0002c0004t0005g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3755): Show |
1 | a0001c0001t0004g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3764): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3657): Show |
2 | a0006c0011t0005g0059a0006c0011t0005g0063 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3666): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3657): Show |
5 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3666): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3643): Show |
3 | a0001c0001t0003g0036a0001c0001t0004g0033a0001c0005t0006g0010 | 3 | HG02055.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3652): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3601): Show |
1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3610): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3643): Show |
2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3652): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3671): Show |
1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3680): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434567
|
A | AGTGAGTG others(3693): Show |
4 | a0001c0006t0001g0020a0001c0006t0001g0023a0001c0006t0001g0024others(1): Show | 4 | HG03098.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3702): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | ||||||
| chr19:434576
|
G | GATCATGA others(3639): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+132_1110+133i others(3648): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434576 | ||||||
| chr19:434970
|
CA | C | 33 | a0001c0003t0001g0058a0001c0003t0001g0062a0001c0003t0001g0066others(30): Show | 34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.954-106delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 434970 | ||||||
| chr19:434986
|
A | C | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.954-121T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 434986 | ||||||
| chr19:435076
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.954-211C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435076 | ||||||
| chr19:435080
|
T | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0093a0001c0002t0001g0167others(1): Show | 5 | HG00558.hp2 HG02027.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-215A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435080 | ||||||
| chr19:435138
|
C | T | 2 | a0001c0001t0002g0052a0001c0001t0011g0038 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.954-273G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435138 | ||||||
| chr19:435141
|
C | G | 39 | a0001c0001t0002g0052a0001c0001t0002g0101a0001c0001t0007g0041others(36): Show | 41 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.954-276G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435141 | ||||||
| chr19:435178
|
C | A | 5 | a0001c0003t0002g0069a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | NA18954.hp2 NA18999.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-313G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435178 | ||||||
| chr19:435307
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0003g0036a0001c0001t0004g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-442G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435307 | ||||||
| chr19:435337
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.954-472G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435337 | ||||||
| chr19:435386
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.954-521A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435386 | ||||||
| chr19:435493
|
C | T | 33 | a0001c0001t0007g0041a0001c0002t0001g0003a0001c0002t0001g0006others(30): Show | 35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.954-628G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435493 | ||||||
| chr19:435495
|
C | T | 1 | a0002c0004t0001g0196 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.954-630G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435495 | ||||||
| chr19:435551
|
T | C | 7 | a0001c0007t0002g0080a0001c0007t0006g0037a0001c0007t0006g0055others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.953+614A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435551 | ||||||
| chr19:435691
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.953+474T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435691 | ||||||
| chr19:435753
|
G | A | 2 | a0006c0011t0005g0059a0006c0011t0005g0063 | 2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.953+412C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435753 | ||||||
| chr19:435875
|
G | A | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.953+290C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435875 | ||||||
| chr19:436004
|
C | T | 1 | a0001c0003t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.953+161G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 436004 | ||||||
| chr19:436015
|
G | C | 1 | a0003c0008t0003g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.953+150C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 436015 | ||||||
| chr19:436053
|
G | A | 1 | a0003c0008t0003g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.953+112C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 436053 | ||||||
| chr19:436369
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.826+11C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 6/12 | chr19 | 436369 | ||||||
| chr19:436541
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.774+89G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 5/12 | chr19 | 436541 | ||||||
| chr19:436690
|
C | T | 36 | a0001c0001t0003g0036a0001c0003t0001g0058a0001c0003t0001g0062others(33): Show | 37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
splice_region_variant&intron_variant | LOW | c.721-7G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436690 | ||||||
| chr19:436727
|
G | A | 1 | a0003c0008t0003g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.721-44C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436727 | ||||||
| chr19:436741
|
C | T | 3 | a0001c0001t0003g0171a0005c0009t0005g0048a0005c0009t0014g0040 | 3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.721-58G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436741 | ||||||
| chr19:436770
|
G | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.721-87C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436770 | ||||||
| chr19:436975
|
T | C | 4 | a0001c0001t0002g0079a0001c0001t0004g0033a0001c0001t0013g0073others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-292A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436975 | ||||||
| chr19:437100
|
G | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.721-417C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437100 | ||||||
| chr19:437165
|
T | C | 3 | a0001c0001t0004g0033a0001c0005t0006g0010a0003c0008t0006g0185 | 3 | HG02818.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.721-482A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437165 | ||||||
| chr19:437206
|
G | A | 1 | a0003c0008t0003g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.721-523C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437206 | ||||||
| chr19:437217
|
C | CATCTGCG others(17): Show |
1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.721-535_721-534ins others(24): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437217 | ||||||
| chr19:437242
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.721-559T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437242 | ||||||
| chr19:437253
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.721-570G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437253 | ||||||
| chr19:437256
|
T | C | 91 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0002g0039others(88): Show | 95 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.721-573A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437256 | ||||||
| chr19:437266
|
G | A | 1 | a0008c0021t0002g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.721-583C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437266 | ||||||
| chr19:437266
|
GTCTGCGT others(17): Show |
G | 4 | a0001c0007t0002g0080a0001c0007t0006g0037a0002c0024t0003g0188others(1): Show | 4 | HG02451.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-607_721-584del others(24): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437266 | ||||||
| chr19:437320
|
ATGCTCAT others(5): Show |
A | 1 | a0001c0003t0002g0076 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.721-649_721-638del others(12): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437320 | ||||||
| chr19:437368
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.721-685C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437368 | ||||||
| chr19:437607
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.721-924C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437607 | ||||||
| chr19:437784
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.720+934C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437784 | ||||||
| chr19:437846
|
CCCT | C | 3 | a0001c0001t0003g0171a0005c0009t0005g0048a0005c0009t0014g0040 | 3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720+869_720+871del others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437846 | ||||||
| chr19:437958
|
T | C | 3 | a0001c0001t0003g0171a0005c0009t0005g0048a0005c0009t0014g0040 | 3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720+760A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437958 | ||||||
| chr19:438248
|
G | C | 1 | a0001c0001t0011g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.720+470C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438248 | ||||||
| chr19:438357
|
T | C | 71 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0002g0079others(68): Show | 73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.720+361A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438357 | ||||||
| chr19:438358
|
T | C | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.720+360A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438358 | ||||||
| chr19:438417
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0087a0001c0002t0001g0089others(1): Show | 4 | HG01978.hp2 HG02083.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+301C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438417 | ||||||
| chr19:438421
|
C | T | 44 | a0001c0001t0002g0079a0001c0001t0002g0101a0001c0001t0003g0171others(41): Show | 45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.720+297G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438421 | ||||||
| chr19:438430
|
G | C | 3 | a0001c0001t0003g0171a0005c0009t0005g0048a0005c0009t0014g0040 | 3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720+288C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438430 | ||||||
| chr19:438436
|
GGCGTCCT others(22): Show |
G | 2 | a0001c0001t0003g0171a0005c0009t0005g0048 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.720+253_720+281del others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438436 | ||||||
| chr19:438438
|
C | T | 1 | a0001c0005t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.720+280G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438438 | ||||||
| chr19:438468
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.720+250C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438468 | ||||||
| chr19:438475
|
C | G | 1 | a0001c0003t0001g0139 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.720+243G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438475 | ||||||
| chr19:438584
|
C | G | 5 | a0001c0001t0004g0035a0001c0001t0005g0028a0001c0001t0005g0029others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+134G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438584 | ||||||
| chr19:438868
|
G | A | 19 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0004g0064others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.601-31C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438868 | ||||||
| chr19:438911
|
C | T | 20 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0005g0168others(17): Show | 20 | HG00733.hp1 HG01358.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.600+59G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438911 | ||||||
| chr19:438915
|
C | T | 20 | a0001c0001t0001g0160a0001c0001t0002g0079a0001c0001t0004g0159others(17): Show | 20 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.600+55G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438915 | ||||||
| chr19:438916
|
C | T | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.600+54G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438916 | ||||||
| chr19:439055
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0112others(11): Show | 15 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.540-25C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439055 | ||||||
| chr19:439112
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.540-82C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439112 | ||||||
| chr19:439193
|
A | G | 79 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0086others(76): Show | 81 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.540-163T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439193 | ||||||
| chr19:439214
|
A | G | 11 | a0001c0001t0002g0052a0001c0001t0003g0004a0001c0001t0003g0171others(8): Show | 12 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.540-184T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439214 | ||||||
| chr19:439393
|
C | T | 11 | a0001c0001t0003g0004a0001c0001t0003g0171a0001c0001t0003g0180others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.540-363G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439393 | ||||||
| chr19:439431
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.540-401G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439431 | ||||||
| chr19:439457
|
C | A | 2 | a0001c0001t0003g0050a0001c0001t0006g0051 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.540-427G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439457 | ||||||
| chr19:439463
|
C | CCTGTCTG others(21): Show |
5 | a0001c0001t0011g0038a0001c0005t0006g0010a0001c0007t0002g0080others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-461_540-434dup others(28): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439463 | ||||||
| chr19:439510
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0004g0096 | 3 | NA18939.hp1 NA18988.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.540-480C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439510 | ||||||
| chr19:439547
|
T | C | 2 | a0001c0003t0002g0069a0001c0003t0002g0075 | 2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.540-517A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439547 | ||||||
| chr19:439566
|
C | T | 4 | a0001c0001t0005g0168a0001c0001t0006g0034a0003c0008t0003g0183others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-536G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439566 | ||||||
| chr19:439580
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.540-550G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439580 | ||||||
| chr19:439601
|
C | T | 3 | a0001c0003t0001g0113a0001c0003t0002g0001a0009c0015t0012g0027 | 4 | HG01952.hp1 HG02293.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-571G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439601 | ||||||
| chr19:439727
|
C | G | 1 | a0001c0005t0001g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.540-697G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439727 | ||||||
| chr19:439752
|
G | A | 1 | a0001c0005t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.540-722C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439752 | ||||||
| chr19:439801
|
G | A | 1 | a0001c0001t0016g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.540-771C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439801 | ||||||
| chr19:439841
|
C | T | 3 | a0001c0001t0003g0171a0001c0017t0005g0056a0005c0009t0005g0048 | 3 | HG02622.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.540-811G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439841 | ||||||
| chr19:439855
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.540-825C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439855 | ||||||
| chr19:439868
|
A | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.540-838T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439868 | ||||||
| chr19:440005
|
A | G | 90 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0177others(87): Show | 93 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.539+857T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440005 | ||||||
| chr19:440025
|
C | CA | 11 | a0001c0001t0001g0122a0001c0001t0001g0170a0001c0001t0003g0171others(8): Show | 11 | HG00544.hp2 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.539+836dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440025 | ||||||
| chr19:440025
|
C | CAA | 42 | a0001c0001t0001g0061a0001c0001t0002g0039a0001c0001t0002g0052others(39): Show | 43 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.539+835_539+836dup others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440025 | ||||||
| chr19:440088
|
A | AACGCCAT others(12): Show |
77 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0177others(74): Show | 80 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.539+755_539+773dup others(19): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440088 | ||||||
| chr19:440114
|
G | C | 1 | a0001c0016t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.539+748C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440114 | ||||||
| chr19:440128
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+734G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440128 | ||||||
| chr19:440282
|
A | G | 4 | a0001c0001t0003g0171a0001c0001t0007g0041a0001c0017t0005g0056others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+580T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440282 | ||||||
| chr19:440314
|
C | T | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.539+548G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440314 | ||||||
| chr19:440316
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.539+546A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440316 | ||||||
| chr19:440478
|
G | C | 87 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0176others(84): Show | 90 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.539+384C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440478 | ||||||
| chr19:440598
|
C | T | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0004g0174others(1): Show | 4 | HG00423.hp1 NA18947.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+264G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440598 | ||||||
| chr19:440655
|
C | T | 6 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0004g0174others(3): Show | 6 | HG00423.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+207G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440655 | ||||||
| chr19:440701
|
C | T | 2 | a0001c0003t0002g0076a0002c0012t0002g0203 | 2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.539+161G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440701 | ||||||
| chr19:440785
|
CGCTGCCG others(9): Show |
C | 4 | a0001c0001t0011g0038a0001c0007t0002g0080a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+61_539+76delAC others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440785 | ||||||
| chr19:440817
|
T | C | 50 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(47): Show | 52 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.539+45A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440817 | ||||||
| chr19:440846
|
A | G | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.539+16T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440846 | ||||||
| chr19:441027
|
T | A | 16 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(13): Show | 16 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.469-95A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441027 | ||||||
| chr19:441069
|
G | T | 35 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-137C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441069 | ||||||
| chr19:441100
|
T | C | 35 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-168A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441100 | ||||||
| chr19:441111
|
T | C | 51 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(48): Show | 53 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.469-179A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441111 | ||||||
| chr19:441114
|
G | A | 4 | a0001c0001t0009g0163a0001c0014t0001g0021a0001c0020t0001g0104others(1): Show | 4 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-182C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441114 | ||||||
| chr19:441130
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.469-198G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441130 | ||||||
| chr19:441148
|
G | C | 35 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-216C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441148 | ||||||
| chr19:441163
|
A | G | 35 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-231T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441163 | ||||||
| chr19:441186
|
C | A | 1 | a0001c0002t0001g0140 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.469-254G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441186 | ||||||
| chr19:441195
|
C | G | 35 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-263G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441195 | ||||||
| chr19:441226
|
C | T | 7 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0004g0174others(4): Show | 7 | HG00423.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-294G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441226 | ||||||
| chr19:441243
|
A | G | 35 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-311T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441243 | ||||||
| chr19:441252
|
G | A | 1 | a0001c0002t0003g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.469-320C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441252 | ||||||
| chr19:441257
|
C | T | 15 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(12): Show | 15 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-325G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441257 | ||||||
| chr19:441354
|
C | T | 1 | a0001c0005t0001g0016 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.469-422G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441354 | ||||||
| chr19:441373
|
C | G | 6 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0004g0174others(3): Show | 6 | HG00423.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-441G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441373 | ||||||
| chr19:441376
|
C | T | 5 | a0001c0003t0002g0069a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | NA18954.hp2 NA18999.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-444G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441376 | ||||||
| chr19:441448
|
A | G | 8 | a0001c0001t0001g0061a0001c0003t0001g0062a0001c0003t0001g0066others(5): Show | 9 | HG00544.hp2 HG00621.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-516T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441448 | ||||||
| chr19:441456
|
T | A | 8 | a0001c0001t0004g0035a0001c0001t0005g0028a0001c0001t0005g0029others(5): Show | 8 | HG00733.hp2 HG01256.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-524A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441456 | ||||||
| chr19:441457
|
A | G | 93 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0176others(90): Show | 96 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.469-525T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441457 | ||||||
| chr19:441686
|
C | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-754G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441686 | ||||||
| chr19:441718
|
T | C | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0004g0174others(1): Show | 4 | HG00423.hp1 NA18947.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-786A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441718 | ||||||
| chr19:441730
|
C | T | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-798G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441730 | ||||||
| chr19:441764
|
G | A | 33 | a0001c0001t0001g0061a0001c0001t0003g0036a0001c0003t0001g0058others(30): Show | 34 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.469-832C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441764 | ||||||
| chr19:441813
|
G | A | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-881C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441813 | ||||||
| chr19:442378
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-1446C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442378 | ||||||
| chr19:442437
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-1505C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442437 | ||||||
| chr19:442475
|
GTGGGTGG others(1): Show |
G | 28 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(25): Show | 30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-1551_469-1544d others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442475 | ||||||
| chr19:442511
|
ATGGATGG others(9): Show |
A | 4 | a0001c0001t0011g0038a0001c0007t0002g0080a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1595_469-1580d others(18): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442511 | ||||||
| chr19:442531
|
ATGGATGG others(9): Show |
A | 32 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(29): Show | 34 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.469-1615_469-1600d others(18): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442531 | ||||||
| chr19:442535
|
A | ATGGGTGG others(13): Show |
3 | a0001c0003t0001g0113a0001c0003t0002g0001a0009c0015t0012g0027 | 4 | HG01952.hp1 HG02293.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1604_469-1603i others(22): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442535 | ||||||
| chr19:442547
|
G | A | 56 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0001g0177others(53): Show | 57 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.469-1615C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442547 | ||||||
| chr19:442557
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.469-1625C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442557 | ||||||
| chr19:442568
|
C | T | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-1636G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442568 | ||||||
| chr19:442569
|
G | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0105others(2): Show | 5 | HG00544.hp1 HG02559.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1637C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442569 | ||||||
| chr19:442623
|
GTGAATGG others(9): Show |
G | 4 | a0001c0001t0011g0038a0001c0007t0002g0080a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1707_469-1692d others(18): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442623 | ||||||
| chr19:442626
|
A | G | 111 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(108): Show | 115 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-1694T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442626 | ||||||
| chr19:442631
|
G | GTGGA | 88 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0176others(85): Show | 91 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.469-1703_469-1700d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442631 | ||||||
| chr19:442662
|
G | GGTGGATG others(1): Show |
6 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0004g0174others(3): Show | 6 | HG00423.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-1738_469-1731d others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442662 | ||||||
| chr19:442696
|
C | T | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1764G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442696 | ||||||
| chr19:442704
|
C | T | 4 | a0001c0001t0003g0171a0001c0001t0004g0033a0001c0017t0005g0056others(1): Show | 4 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1772G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442704 | ||||||
| chr19:442707
|
A | G | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1775T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442707 | ||||||
| chr19:442711
|
C | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1779G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442711 | ||||||
| chr19:442712
|
T | C | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1780A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442712 | ||||||
| chr19:442731
|
A | G | 16 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(13): Show | 16 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.469-1799T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442731 | ||||||
| chr19:442733
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1801C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442733 | ||||||
| chr19:442736
|
C | T | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1804G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442736 | ||||||
| chr19:442738
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1806C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442738 | ||||||
| chr19:442743
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1811C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442743 | ||||||
| chr19:442750
|
G | T | 2 | a0001c0007t0003g0030a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.469-1818C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442750 | ||||||
| chr19:442759
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1827C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442759 | ||||||
| chr19:442767
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1835C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442767 | ||||||
| chr19:442772
|
T | C | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1840A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442772 | ||||||
| chr19:442775
|
A | G | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1843T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442775 | ||||||
| chr19:442779
|
A | G | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1847T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442779 | ||||||
| chr19:442808
|
TGAGTGGA others(97): Show |
T | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1980_469-1877d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442808 | ||||||
| chr19:442895
|
A | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0121others(9): Show | 12 | HG00558.hp1 HG01074.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.469-1963T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442895 | ||||||
| chr19:442898
|
A | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0121others(9): Show | 12 | HG00558.hp1 HG01074.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.469-1966T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442898 | ||||||
| chr19:442910
|
G | C | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-1978C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442910 | ||||||
| chr19:442913
|
G | A | 27 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(24): Show | 27 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(24): Show |
intron_variant | MODIFIER | c.469-1981C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442913 | ||||||
| chr19:442915
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1983C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442915 | ||||||
| chr19:442918
|
G | A | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1986C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442918 | ||||||
| chr19:442932
|
T | C | 26 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(23): Show | 26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-2000A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442932 | ||||||
| chr19:442932
|
T | TGGATGGG others(29): Show |
154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(151): Show | 160 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.469-2001_469-2000i others(38): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442932 | ||||||
| chr19:442932
|
T | TGGATGGG others(32): Show |
1 | a0001c0001t0001g0166 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.469-2001_469-2000i others(41): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442932 | ||||||
| chr19:443029
|
G | A | 2 | a0001c0001t0003g0071a0001c0001t0016g0070 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.469-2097C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443029 | ||||||
| chr19:443162
|
ATGGATGG others(21): Show |
A | 1 | a0001c0003t0002g0150 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.469-2258_469-2231d others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443162 | ||||||
| chr19:443309
|
A | G | 28 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(25): Show | 30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-2377T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443309 | ||||||
| chr19:443318
|
G | A | 28 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(25): Show | 30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-2386C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443318 | ||||||
| chr19:443320
|
G | GGACA | 28 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(25): Show | 30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-2389_469-2388i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443320 | ||||||
| chr19:443320
|
G | GGATGGAT others(5): Show |
27 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(24): Show | 27 | HG00423.hp1 HG02559.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.469-2389_469-2388i others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443320 | ||||||
| chr19:443379
|
TGGGTGGG others(189): Show |
T | 2 | a0001c0001t0001g0160a0001c0001t0004g0159 | 2 | HG00733.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.469-2643_469-2448d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443379 | ||||||
| chr19:443388
|
G | A | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-2456C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443388 | ||||||
| chr19:443527
|
CAGAT | C | 5 | a0001c0001t0006g0049a0001c0001t0006g0054a0001c0005t0015g0008others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2599_469-2596d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443527 | ||||||
| chr19:443575
|
CGGGTGGG others(105): Show |
C | 1 | a0001c0017t0005g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469-2755_469-2644d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443575 | ||||||
| chr19:443636
|
AGATGGAT others(105): Show |
A | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.469-2816_469-2705d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443636 | ||||||
| chr19:443782
|
ATGGATGG others(21): Show |
A | 4 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0105others(1): Show | 4 | HG00544.hp1 NA18999.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-2878_469-2851d others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443782 | ||||||
| chr19:443843
|
T | C | 1 | a0001c0003t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.469-2911A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443843 | ||||||
| chr19:443859
|
T | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0151a0001c0002t0001g0152 | 3 | HG02015.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.469-2927A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443859 | ||||||
| chr19:443879
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.469-2947A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443879 | ||||||
| chr19:443882
|
GTGGATGG others(13): Show |
G | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-2970_469-2951d others(22): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443882 | ||||||
| chr19:443906
|
A | ATGGG | 11 | a0001c0001t0001g0061a0001c0001t0003g0036a0001c0003t0001g0062others(8): Show | 12 | HG00544.hp2 HG00621.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-2978_469-2975d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443906 | ||||||
| chr19:443918
|
A | G | 22 | a0001c0003t0001g0058a0001c0003t0001g0139a0001c0003t0002g0060others(19): Show | 22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-2986T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443918 | ||||||
| chr19:443930
|
ATGGACGG others(100): Show |
A | 22 | a0001c0003t0001g0058a0001c0003t0001g0139a0001c0003t0002g0060others(19): Show | 22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3105_469-2999d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443930 | ||||||
| chr19:443936
|
G | A | 28 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(25): Show | 30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-3004C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443936 | ||||||
| chr19:443951
|
T | TGGGTGGA others(4): Show |
1 | a0001c0002t0001g0107 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.469-3030_469-3020d others(13): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443951 | ||||||
| chr19:444049
|
A | G | 22 | a0001c0003t0001g0058a0001c0003t0001g0139a0001c0003t0002g0060others(19): Show | 22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3117T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444049 | ||||||
| chr19:444052
|
G | A | 22 | a0001c0003t0001g0058a0001c0003t0001g0139a0001c0003t0002g0060others(19): Show | 22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3120C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444052 | ||||||
| chr19:444054
|
T | G | 4 | a0001c0001t0011g0038a0001c0007t0002g0080a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-3122A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444054 | ||||||
| chr19:444373
|
G | A | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-3441C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444373 | ||||||
| chr19:444386
|
G | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-3454C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444386 | ||||||
| chr19:444417
|
T | C | 33 | a0001c0001t0001g0061a0001c0001t0003g0036a0001c0003t0001g0058others(30): Show | 34 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.469-3485A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444417 | ||||||
| chr19:444489
|
A | G | 1 | a0001c0003t0002g0072 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.469-3557T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444489 | ||||||
| chr19:444567
|
C | T | 1 | a0001c0002t0003g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.469-3635G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444567 | ||||||
| chr19:444737
|
C | A | 28 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(25): Show | 30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-3805G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444737 | ||||||
| chr19:444797
|
G | A | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.469-3865C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444797 | ||||||
| chr19:444866
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.469-3934T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444866 | ||||||
| chr19:444872
|
C | T | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-3940G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444872 | ||||||
| chr19:444918
|
C | A | 32 | a0001c0001t0001g0061a0001c0001t0003g0036a0001c0003t0001g0058others(29): Show | 33 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.469-3986G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444918 | ||||||
| chr19:445070
|
C | T | 1 | a0001c0002t0003g0091 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.469-4138G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445070 | ||||||
| chr19:445406
|
G | C | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-4474C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445406 | ||||||
| chr19:445425
|
T | A | 1 | a0002c0004t0004g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.469-4493A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445425 | ||||||
| chr19:445434
|
G | A | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-4502C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445434 | ||||||
| chr19:445699
|
C | T | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-4767G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445699 | ||||||
| chr19:445746
|
C | A | 1 | a0001c0018t0006g0179 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469-4814G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445746 | ||||||
| chr19:446131
|
C | T | 3 | a0001c0006t0001g0020a0001c0006t0001g0023a0001c0006t0001g0024 | 3 | HG03209.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.469-5199G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446131 | ||||||
| chr19:446243
|
G | A | 32 | a0001c0001t0001g0061a0001c0001t0003g0036a0001c0003t0001g0058others(29): Show | 33 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.469-5311C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446243 | ||||||
| chr19:446378
|
A | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0145a0001c0001t0002g0079others(28): Show | 33 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.469-5446T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446378 | ||||||
| chr19:446380
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469-5448C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446380 | ||||||
| chr19:446405
|
G | T | 1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-5473C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446405 | ||||||
| chr19:446450
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18747.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.469-5518T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446450 | ||||||
| chr19:446455
|
C | T | 14 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0002g0101others(11): Show | 14 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.469-5523G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446455 | ||||||
| chr19:446460
|
A | G | 1 | a0001c0002t0003g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.469-5528T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446460 | ||||||
| chr19:446462
|
T | C | 1 | a0001c0002t0003g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.469-5530A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446462 | ||||||
| chr19:446472
|
G | A | 1 | a0001c0016t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.469-5540C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446472 | ||||||
| chr19:446552
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.469-5620C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446552 | ||||||
| chr19:446601
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.469-5669C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446601 | ||||||
| chr19:446821
|
G | A | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.469-5889C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446821 | ||||||
| chr19:446827
|
A | T | 82 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0176others(79): Show | 85 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.469-5895T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446827 | ||||||
| chr19:446840
|
G | A | 1 | a0001c0005t0005g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469-5908C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446840 | ||||||
| chr19:446887
|
A | G | 86 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0001g0176others(83): Show | 89 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.469-5955T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446887 | ||||||
| chr19:447078
|
A | G | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-6146T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447078 | ||||||
| chr19:447089
|
C | T | 1 | a0001c0017t0005g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469-6157G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447089 | ||||||
| chr19:447105
|
T | C | 1 | a0001c0001t0016g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.469-6173A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447105 | ||||||
| chr19:447262
|
T | C | 3 | a0001c0001t0006g0043a0001c0007t0003g0030a0001c0007t0006g0042 | 3 | HG02976.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.469-6330A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447262 | ||||||
| chr19:447286
|
G | A | 4 | a0001c0001t0011g0038a0001c0007t0002g0080a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-6354C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447286 | ||||||
| chr19:447307
|
G | C | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-6375C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447307 | ||||||
| chr19:447314
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.469-6382T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447314 | ||||||
| chr19:447320
|
G | C | 30 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(27): Show | 32 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.469-6388C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447320 | ||||||
| chr19:447402
|
C | A | 2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.469-6470G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447402 | ||||||
| chr19:447550
|
G | A | 15 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(12): Show | 15 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-6618C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447550 | ||||||
| chr19:447570
|
G | A | 1 | a0002c0004t0005g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.469-6638C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447570 | ||||||
| chr19:447641
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.469-6709C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447641 | ||||||
| chr19:447710
|
G | A | 1 | a0010c0022t0002g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-6778C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447710 | ||||||
| chr19:447727
|
G | A | 2 | a0001c0001t0002g0079a0001c0001t0013g0073 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.469-6795C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447727 | ||||||
| chr19:447777
|
T | TA | 40 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(37): Show | 42 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.469-6846dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447777 | ||||||
| chr19:447785
|
A | T | 2 | a0001c0005t0006g0009a0001c0007t0006g0055 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.469-6853T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447785 | ||||||
| chr19:447848
|
C | A | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.469-6916G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447848 | ||||||
| chr19:447964
|
C | G | 5 | a0001c0001t0003g0171a0001c0001t0006g0034a0001c0017t0005g0056others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-7032G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447964 | ||||||
| chr19:448041
|
C | T | 61 | a0001c0001t0001g0061a0001c0001t0001g0145a0001c0001t0002g0079others(58): Show | 64 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.469-7109G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448041 | ||||||
| chr19:448064
|
G | A | 26 | a0001c0001t0001g0145a0001c0001t0002g0079a0001c0001t0003g0004others(23): Show | 28 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.469-7132C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448064 | ||||||
| chr19:448093
|
G | A | 1 | a0001c0002t0001g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.469-7161C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448093 | ||||||
| chr19:448106
|
C | T | 1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.469-7174G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448106 | ||||||
| chr19:448109
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.469-7177G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448109 | ||||||
| chr19:448123
|
C | T | 7 | a0001c0001t0003g0171a0001c0001t0004g0033a0001c0001t0006g0034others(4): Show | 7 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-7191G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448123 | ||||||
| chr19:448173
|
T | C | 91 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(88): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.469-7241A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448173 | ||||||
| chr19:448177
|
C | A | 91 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(88): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.469-7245G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448177 | ||||||
| chr19:448253
|
C | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0166 | 3 | HG00609.hp1 NA18985.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.469-7321G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448253 | ||||||
| chr19:448271
|
G | A | 2 | a0001c0001t0001g0099a0001c0002t0001g0167 | 2 | HG02027.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.469-7339C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448271 | ||||||
| chr19:448289
|
A | G | 139 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(136): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-7357T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448289 | ||||||
| chr19:448292
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0007g0041 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.469-7360C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448292 | ||||||
| chr19:448342
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.469-7410G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448342 | ||||||
| chr19:448395
|
C | T | 60 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0084others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.469-7463G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448395 | ||||||
| chr19:448408
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469-7476C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448408 | ||||||
| chr19:448463
|
CTCT | C | 15 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(12): Show | 15 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-7534_469-7532d others(5): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448463 | ||||||
| chr19:448598
|
C | T | 4 | a0001c0001t0003g0171a0001c0001t0006g0034a0001c0017t0005g0056others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-7666G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448598 | ||||||
| chr19:448696
|
C | T | 23 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(20): Show | 23 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.469-7764G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448696 | ||||||
| chr19:448700
|
T | A | 23 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(20): Show | 23 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.469-7768A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448700 | ||||||
| chr19:448773
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.469-7841C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448773 | ||||||
| chr19:448874
|
C | T | 2 | a0001c0001t0003g0171a0002c0004t0001g0187 | 2 | HG00639.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-7942G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448874 | ||||||
| chr19:448932
|
G | A | 1 | a0005c0009t0014g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.469-8000C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448932 | ||||||
| chr19:448940
|
T | C | 143 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.469-8008A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448940 | ||||||
| chr19:448970
|
T | C | 1 | a0001c0006t0006g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-8038A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448970 | ||||||
| chr19:448997
|
AAAAAATA others(1): Show |
A | 12 | a0001c0001t0002g0039a0001c0001t0002g0052a0001c0001t0002g0057others(9): Show | 12 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-8073_469-8066d others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448997 | ||||||
| chr19:449146
|
C | T | 2 | a0001c0001t0001g0061a0001c0003t0001g0066 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.469-8214G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449146 | ||||||
| chr19:449175
|
T | A | 139 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(136): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-8243A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449175 | ||||||
| chr19:449252
|
A | G | 147 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.469-8320T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449252 | ||||||
| chr19:449289
|
C | T | 1 | a0001c0005t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.469-8357G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449289 | ||||||
| chr19:449357
|
C | A | 1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.469-8425G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449357 | ||||||
| chr19:449367
|
G | C | 1 | a0001c0002t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.469-8435C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449367 | ||||||
| chr19:449459
|
G | A | 10 | a0001c0001t0002g0039a0001c0001t0002g0057a0001c0001t0002g0101others(7): Show | 10 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-8527C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449459 | ||||||
| chr19:449483
|
T | C | 2 | a0001c0002t0001g0151a0001c0002t0001g0152 | 2 | HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.469-8551A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449483 | ||||||
| chr19:449591
|
G | A | 1 | a0001c0017t0005g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469-8659C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449591 | ||||||
| chr19:449627
|
G | A | 2 | a0001c0002t0001g0107a0001c0003t0002g0111 | 2 | HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.469-8695C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449627 | ||||||
| chr19:449659
|
C | G | 150 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(147): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.469-8727G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449659 | ||||||
| chr19:449822
|
G | A | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.469-8890C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449822 | ||||||
| chr19:449920
|
G | A | 1 | a0001c0005t0006g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-8988C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449920 | ||||||
| chr19:449982
|
C | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9050G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449982 | ||||||
| chr19:450013
|
A | G | 26 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0033others(23): Show | 26 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-9081T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450013 | ||||||
| chr19:450051
|
C | T | 3 | a0001c0001t0001g0082a0001c0002t0001g0083a0001c0002t0001g0089 | 3 | HG01978.hp2 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.469-9119G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450051 | ||||||
| chr19:450055
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.469-9123G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450055 | ||||||
| chr19:450056
|
G | A | 5 | a0001c0002t0001g0153a0001c0002t0001g0154a0003c0008t0003g0183others(2): Show | 5 | HG00423.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-9124C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450056 | ||||||
| chr19:450067
|
T | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9135A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450067 | ||||||
| chr19:450068
|
G | A | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.469-9136C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450068 | ||||||
| chr19:450117
|
C | T | 2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.469-9185G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450117 | ||||||
| chr19:450120
|
G | A | 20 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(17): Show | 20 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.469-9188C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450120 | ||||||
| chr19:450149
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469-9217C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450149 | ||||||
| chr19:450165
|
G | A | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.469-9233C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450165 | ||||||
| chr19:450168
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.469-9236C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450168 | ||||||
| chr19:450180
|
G | A | 20 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(17): Show | 20 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.469-9248C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450180 | ||||||
| chr19:450219
|
G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469-9287C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450219 | ||||||
| chr19:450231
|
A | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9299T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450231 | ||||||
| chr19:450238
|
T | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9306A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450238 | ||||||
| chr19:450282
|
C | T | 19 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(16): Show | 19 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.469-9350G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450282 | ||||||
| chr19:450294
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.469-9362G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450294 | ||||||
| chr19:450302
|
A | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9370T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450302 | ||||||
| chr19:450393
|
C | T | 1 | a0002c0012t0002g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.469-9461G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450393 | ||||||
| chr19:450489
|
A | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9557T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450489 | ||||||
| chr19:450493
|
CACTT | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9565_469-9562d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450493 | ||||||
| chr19:450507
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9575G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450507 | ||||||
| chr19:450515
|
C | T | 19 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(16): Show | 19 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.469-9583G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450515 | ||||||
| chr19:450626
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9694G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450626 | ||||||
| chr19:450627
|
A | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9695T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450627 | ||||||
| chr19:450643
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.469-9711G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450643 | ||||||
| chr19:450644
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9712C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450644 | ||||||
| chr19:450715
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9783G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450715 | ||||||
| chr19:450813
|
C | T | 7 | a0001c0001t0003g0180a0001c0001t0004g0035a0001c0001t0005g0028others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+9716G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450813 | ||||||
| chr19:450814
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9715C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450814 | ||||||
| chr19:450817
|
ATATTTCA others(31): Show |
A | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.468+9674_468+9711d others(40): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450817 | ||||||
| chr19:450882
|
G | A | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+9647C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450882 | ||||||
| chr19:450916
|
T | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9613A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450916 | ||||||
| chr19:450927
|
T | C | 25 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0003g0171others(22): Show | 25 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.468+9602A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450927 | ||||||
| chr19:450931
|
A | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9598T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450931 | ||||||
| chr19:450941
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.468+9588C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450941 | ||||||
| chr19:451005
|
C | A | 1 | a0001c0002t0004g0156 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.468+9524G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451005 | ||||||
| chr19:451007
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9522C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451007 | ||||||
| chr19:451033
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.468+9496G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451033 | ||||||
| chr19:451055
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+9474C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451055 | ||||||
| chr19:451069
|
G | A | 2 | a0001c0001t0005g0047a0002c0004t0005g0189 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+9460C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451069 | ||||||
| chr19:451072
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0003g0180a0001c0001t0004g0035others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+9457C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451072 | ||||||
| chr19:451079
|
C | T | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+9450G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451079 | ||||||
| chr19:451083
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.468+9446C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451083 | ||||||
| chr19:451089
|
T | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9440A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451089 | ||||||
| chr19:451093
|
G | GTGTGGAT others(69): Show |
6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9435_468+9436i others(78): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451093 | ||||||
| chr19:451158
|
T | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9371A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451158 | ||||||
| chr19:451206
|
CGTGTGGA others(31): Show |
C | 18 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(15): Show | 18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+9285_468+9322d others(40): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451206 | ||||||
| chr19:451259
|
G | A | 18 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(15): Show | 18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+9270C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451259 | ||||||
| chr19:451261
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9268G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451261 | ||||||
| chr19:451264
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+9265C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451264 | ||||||
| chr19:451320
|
C | G | 42 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(39): Show | 43 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.468+9209G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451320 | ||||||
| chr19:451335
|
G | A | 7 | a0001c0001t0004g0033a0001c0003t0010g0077a0001c0005t0015g0008others(4): Show | 7 | HG00621.hp1 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+9194C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451335 | ||||||
| chr19:451339
|
TGGCTGTG others(32): Show |
T | 1 | a0001c0002t0001g0003 | 2 | NA18939.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.468+9151_468+9189d others(41): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451339 | ||||||
| chr19:451377
|
TG | T | 147 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.468+9151delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451377 | ||||||
| chr19:451388
|
G | A | 6 | a0001c0003t0002g0069a0001c0003t0002g0074a0001c0003t0002g0075others(3): Show | 6 | HG03225.hp1 NA18954.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9141C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451388 | ||||||
| chr19:451465
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9064C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451465 | ||||||
| chr19:451583
|
C | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8946G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451583 | ||||||
| chr19:451666
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8863G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451666 | ||||||
| chr19:451746
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8783G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451746 | ||||||
| chr19:451814
|
G | C | 9 | a0001c0001t0004g0033a0001c0002t0002g0046a0001c0005t0015g0008others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+8715C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451814 | ||||||
| chr19:451849
|
T | A | 147 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+8680A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451849 | ||||||
| chr19:451876
|
A | C | 147 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0082others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+8653T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451876 | ||||||
| chr19:451908
|
A | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8621T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451908 | ||||||
| chr19:451959
|
G | A | 3 | a0001c0002t0002g0046a0001c0007t0002g0080a0002c0024t0003g0188 | 3 | NA18906.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.468+8570C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451959 | ||||||
| chr19:451981
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8548C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451981 | ||||||
| chr19:452062
|
C | T | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8467G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452062 | ||||||
| chr19:452105
|
T | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8424A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452105 | ||||||
| chr19:452197
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8332C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452197 | ||||||
| chr19:452226
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.468+8303G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452226 | ||||||
| chr19:452244
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8285C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452244 | ||||||
| chr19:452252
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8277C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452252 | ||||||
| chr19:452270
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8259C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452270 | ||||||
| chr19:452270
|
GTTTCATT others(188): Show |
G | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+8064_468+8258d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452270 | ||||||
| chr19:452296
|
T | C | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8233A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452296 | ||||||
| chr19:452309
|
G | GTTCCTGC others(58): Show |
1 | a0001c0001t0001g0098 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.468+8155_468+8219d others(67): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452309 | ||||||
| chr19:452309
|
GTTCCTGC others(58): Show |
G | 19 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(16): Show | 19 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.468+8155_468+8219d others(67): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452309 | ||||||
| chr19:452320
|
G | A | 16 | a0001c0001t0001g0145a0001c0001t0003g0004a0001c0001t0005g0168others(13): Show | 17 | HG00423.hp2 HG01071.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+8209C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452320 | ||||||
| chr19:452335
|
GTTTCATT others(123): Show |
G | 5 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+8064_468+8193d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452335 | ||||||
| chr19:452374
|
A | G | 5 | a0001c0001t0005g0053a0001c0007t0002g0080a0002c0024t0003g0188others(2): Show | 5 | HG02559.hp2 NA18522.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+8155T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452374 | ||||||
| chr19:452381
|
C | T | 40 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(37): Show | 42 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.468+8148G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452381 | ||||||
| chr19:452382
|
G | A | 1 | a0003c0008t0005g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+8147C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452382 | ||||||
| chr19:452385
|
G | A | 1 | a0001c0002t0003g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.468+8144C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452385 | ||||||
| chr19:452422
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.468+8107C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452422 | ||||||
| chr19:452447
|
A | G | 2 | a0001c0001t0001g0002a0001c0003t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.468+8082T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452447 | ||||||
| chr19:452449
|
A | G | 18 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(15): Show | 18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+8080T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452449 | ||||||
| chr19:452478
|
T | C | 2 | a0001c0001t0001g0061a0001c0003t0001g0066 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.468+8051A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452478 | ||||||
| chr19:452486
|
C | T | 17 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(14): Show | 17 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.468+8043G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452486 | ||||||
| chr19:452512
|
G | A | 5 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+8017C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452512 | ||||||
| chr19:452595
|
G | A | 18 | a0001c0001t0001g0099a0001c0001t0003g0171a0001c0001t0004g0161others(15): Show | 18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+7934C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452595 | ||||||
| chr19:452745
|
G | T | 7 | a0001c0001t0001g0044a0001c0001t0004g0033a0001c0005t0015g0008others(4): Show | 7 | HG02145.hp1 HG02165.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+7784C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452745 | ||||||
| chr19:452803
|
C | T | 2 | a0001c0001t0002g0101a0008c0021t0002g0032 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.468+7726G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452803 | ||||||
| chr19:452975
|
C | T | 1 | a0002c0012t0004g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.468+7554G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452975 | ||||||
| chr19:452976
|
G | A | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+7553C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452976 | ||||||
| chr19:453105
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(179): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.468+7424T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453105 | ||||||
| chr19:453127
|
T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.468+7402A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453127 | ||||||
| chr19:453160
|
A | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(184): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.468+7369T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453160 | ||||||
| chr19:453389
|
T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.468+7140A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453389 | ||||||
| chr19:453397
|
A | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(184): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.468+7132T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453397 | ||||||
| chr19:453439
|
T | G | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+7090A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453439 | ||||||
| chr19:453478
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.468+7051G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453478 | ||||||
| chr19:453687
|
G | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.468+6842C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453687 | ||||||
| chr19:453731
|
C | T | 1 | a0002c0004t0005g0190 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.468+6798G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453731 | ||||||
| chr19:453750
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(187): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.468+6779A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453750 | ||||||
| chr19:453782
|
C | A | 25 | a0001c0001t0001g0061a0001c0001t0004g0064a0001c0001t0004g0065others(22): Show | 26 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+6747G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453782 | ||||||
| chr19:453794
|
G | A | 7 | a0001c0001t0003g0180a0001c0001t0004g0035a0001c0001t0005g0028others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+6735C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453794 | ||||||
| chr19:453826
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(187): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.468+6703T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453826 | ||||||
| chr19:453898
|
G | A | 6 | a0001c0001t0004g0033a0001c0005t0015g0008a0003c0008t0003g0183others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+6631C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453898 | ||||||
| chr19:454015
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.468+6514T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454015 | ||||||
| chr19:454351
|
C | A | 3 | a0003c0008t0003g0183a0003c0008t0005g0182a0003c0008t0006g0185 | 3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+6178G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454351 | ||||||
| chr19:454430
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0081others(53): Show | 58 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.468+6099C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454430 | ||||||
| chr19:454524
|
C | T | 8 | a0001c0001t0003g0180a0001c0001t0004g0035a0001c0001t0005g0028others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+6005G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454524 | ||||||
| chr19:454605
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.468+5924C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454605 | ||||||
| chr19:454658
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+5871G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454658 | ||||||
| chr19:454668
|
T | C | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+5861A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454668 | ||||||
| chr19:454738
|
C | T | 3 | a0001c0001t0002g0057a0001c0001t0003g0050a0001c0001t0006g0051 | 3 | HG02970.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.468+5791G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454738 | ||||||
| chr19:454751
|
C | T | 1 | a0011c0025t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.468+5778G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454751 | ||||||
| chr19:454790
|
CA | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0081others(83): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.468+5738delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454790 | ||||||
| chr19:454821
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0102a0001c0001t0001g0103others(43): Show | 47 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.468+5708G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454821 | ||||||
| chr19:454849
|
G | A | 1 | a0001c0001t0004g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.468+5680C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454849 | ||||||
| chr19:454943
|
C | T | 9 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0001g0172others(6): Show | 9 | HG00423.hp1 HG00544.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+5586G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454943 | ||||||
| chr19:454955
|
C | G | 25 | a0001c0001t0001g0061a0001c0001t0004g0064a0001c0001t0004g0065others(22): Show | 26 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+5574G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454955 | ||||||
| chr19:455148
|
G | A | 1 | a0001c0001t0006g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.468+5381C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455148 | ||||||
| chr19:455200
|
G | A | 3 | a0001c0001t0003g0050a0001c0001t0006g0051a0001c0005t0015g0008 | 3 | HG02970.hp1 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.468+5329C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455200 | ||||||
| chr19:455256
|
C | T | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+5273G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455256 | ||||||
| chr19:455285
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0004g0159a0001c0001t0004g0161 | 3 | HG00733.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.468+5244C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455285 | ||||||
| chr19:455488
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.468+5041G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455488 | ||||||
| chr19:455661
|
A | G | 40 | a0001c0001t0001g0061a0001c0001t0002g0052a0001c0001t0003g0071others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.468+4868T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455661 | ||||||
| chr19:455663
|
G | A | 2 | a0001c0005t0005g0026a0001c0005t0006g0010 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.468+4866C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455663 | ||||||
| chr19:455664
|
C | T | 1 | a0001c0023t0007g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+4865G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455664 | ||||||
| chr19:455757
|
G | C | 21 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(18): Show | 23 | HG00558.hp2 HG00621.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+4772C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455757 | ||||||
| chr19:455878
|
C | A | 19 | a0001c0001t0003g0171a0001c0005t0001g0011a0001c0005t0001g0012others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+4651G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455878 | ||||||
| chr19:455957
|
G | C | 1 | a0008c0021t0002g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+4572C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455957 | ||||||
| chr19:455957
|
G | GC | 78 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0001g0177others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.468+4571_468+4572i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455957 | ||||||
| chr19:455993
|
C | A | 2 | a0001c0001t0001g0044a0001c0002t0003g0045 | 2 | HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+4536G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455993 | ||||||
| chr19:456054
|
A | G | 10 | a0001c0001t0002g0039a0001c0001t0005g0028a0001c0001t0005g0029others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+4475T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456054 | ||||||
| chr19:456118
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.468+4411A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456118 | ||||||
| chr19:456165
|
C | T | 3 | a0001c0003t0010g0077a0001c0020t0001g0104a0011c0025t0001g0206 | 3 | HG00621.hp1 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.468+4364G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456165 | ||||||
| chr19:456177
|
G | A | 7 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+4352C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456177 | ||||||
| chr19:456180
|
G | A | 18 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.468+4349C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456180 | ||||||
| chr19:456286
|
T | C | 57 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(54): Show | 58 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.468+4243A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456286 | ||||||
| chr19:456302
|
T | C | 81 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.468+4227A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456302 | ||||||
| chr19:456341
|
TG | T | 205 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(202): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.468+4187delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456341 | ||||||
| chr19:456358
|
G | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+4171C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456358 | ||||||
| chr19:456440
|
C | T | 49 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(46): Show | 50 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.468+4089G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456440 | ||||||
| chr19:456441
|
G | A | 1 | a0001c0001t0009g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.468+4088C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456441 | ||||||
| chr19:456516
|
C | T | 8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0001g0172others(5): Show | 8 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+4013G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456516 | ||||||
| chr19:456655
|
C | T | 2 | a0001c0001t0006g0043a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+3874G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456655 | ||||||
| chr19:456682
|
G | A | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+3847C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456682 | ||||||
| chr19:456736
|
C | T | 21 | a0001c0001t0001g0061a0001c0001t0003g0071a0001c0001t0004g0064others(18): Show | 22 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.468+3793G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456736 | ||||||
| chr19:456738
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.468+3791G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456738 | ||||||
| chr19:456739
|
G | A | 16 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+3790C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456739 | ||||||
| chr19:456768
|
C | A | 4 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3761G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456768 | ||||||
| chr19:456776
|
A | AGAACTCT others(51): Show |
4 | a0002c0004t0001g0187a0002c0004t0001g0192a0002c0004t0001g0205others(1): Show | 4 | HG00639.hp1 HG01358.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3695_468+3752d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456776 | ||||||
| chr19:456776
|
AGAACTCT others(51): Show |
A | 16 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0003g0036others(13): Show | 16 | HG00423.hp1 HG01258.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+3695_468+3752d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456776 | ||||||
| chr19:456828
|
CTGCCTGG others(52): Show |
C | 4 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3642_468+3700d others(61): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456828 | ||||||
| chr19:456834
|
G | A | 27 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(24): Show | 28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3695C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456834 | ||||||
| chr19:456834
|
G | GGAACTCT others(482): Show |
16 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+3694_468+3695i others(491): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456834 | ||||||
| chr19:456834
|
G | GGAACTCT others(482): Show |
1 | a0001c0005t0006g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+3694_468+3695i others(491): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456834 | ||||||
| chr19:456847
|
C | T | 34 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(31): Show | 35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3682G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456847 | ||||||
| chr19:456849
|
AT | A | 34 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(31): Show | 35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3679delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456849 | ||||||
| chr19:456850
|
T | A | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3679A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456850 | ||||||
| chr19:456851
|
C | A | 34 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(31): Show | 35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3678G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456851 | ||||||
| chr19:456858
|
A | G | 34 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(31): Show | 35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3671T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456858 | ||||||
| chr19:456860
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3669C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456860 | ||||||
| chr19:456862
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3667C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456862 | ||||||
| chr19:456863
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3666C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456863 | ||||||
| chr19:456875
|
CTGCTGTG others(44): Show |
C | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3603_468+3653d others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456875 | ||||||
| chr19:456883
|
C | CCCCGCCC others(55): Show |
26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3645_468+3646i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456883 | ||||||
| chr19:456886
|
CT | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3642delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456886 | ||||||
| chr19:456887
|
T | C | 26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3642A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456887 | ||||||
| chr19:456905
|
T | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3624A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456905 | ||||||
| chr19:456911
|
CACTGCGT others(48): Show |
C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3563_468+3617d others(57): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456911 | ||||||
| chr19:456914
|
T | C | 46 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(43): Show | 47 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.468+3615A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456914 | ||||||
| chr19:456917
|
G | A | 4 | a0001c0001t0005g0053a0001c0001t0006g0054a0001c0007t0006g0055others(1): Show | 4 | HG02622.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3612C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456917 | ||||||
| chr19:456944
|
GCC | G | 26 | a0001c0001t0001g0061a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3583_468+3584d others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456944 | ||||||
| chr19:456946
|
C | CTAGAACT others(83): Show |
1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+3582_468+3583i others(92): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456946 | ||||||
| chr19:456947
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0002g0079 | 2 | HG01884.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.468+3582G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456947 | ||||||
| chr19:456963
|
T | C | 27 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(24): Show | 28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3566A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456963 | ||||||
| chr19:456968
|
T | A | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3561A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456968 | ||||||
| chr19:456968
|
T | C | 27 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(24): Show | 28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3561A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456968 | ||||||
| chr19:456972
|
C | CCA | 27 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(24): Show | 28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3556_468+3557i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456972 | ||||||
| chr19:456973
|
A | C | 26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3556T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456973 | ||||||
| chr19:456973
|
A | T | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3556T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456973 | ||||||
| chr19:456973
|
AG | A | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3555delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456973 | ||||||
| chr19:456974
|
G | A | 27 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(24): Show | 28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3555C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456974 | ||||||
| chr19:456994
|
G | C | 35 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(32): Show | 36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3535C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456994 | ||||||
| chr19:457002
|
G | A | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3527C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457002 | ||||||
| chr19:457007
|
G | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3522C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457007 | ||||||
| chr19:457008
|
C | A | 26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3521G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457008 | ||||||
| chr19:457014
|
A | T | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3515T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457014 | ||||||
| chr19:457024
|
T | C | 35 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(32): Show | 36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3505A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457024 | ||||||
| chr19:457027
|
A | AC | 26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3501dupG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457027 | ||||||
| chr19:457034
|
G | A | 35 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(32): Show | 36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3495C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457034 | ||||||
| chr19:457035
|
C | T | 12 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0005g0028others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.468+3494G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457035 | ||||||
| chr19:457036
|
G | A | 27 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(24): Show | 28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3493C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457036 | ||||||
| chr19:457038
|
G | C | 35 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(32): Show | 36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3491C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457038 | ||||||
| chr19:457039
|
G | A | 35 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(32): Show | 36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3490C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457039 | ||||||
| chr19:457045
|
T | TTGCACC | 13 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0005g0028others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+3478_468+3483d others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457045 | ||||||
| chr19:457046
|
T | TGCACCA | 22 | a0001c0001t0003g0071a0001c0001t0004g0064a0001c0001t0004g0065others(19): Show | 23 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+3482_468+3483i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457046 | ||||||
| chr19:457058
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0005g0047a0002c0004t0005g0189 | 3 | HG01884.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3471C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457058 | ||||||
| chr19:457063
|
G | C | 2 | a0001c0001t0005g0047a0002c0004t0005g0189 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3466C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457063 | ||||||
| chr19:457064
|
C | A | 23 | a0001c0001t0003g0071a0001c0001t0004g0064a0001c0001t0004g0065others(20): Show | 24 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+3465G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457064 | ||||||
| chr19:457064
|
C | T | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3465G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457064 | ||||||
| chr19:457064
|
CCTAGAAC others(119): Show |
C | 6 | a0001c0001t0002g0057a0001c0023t0007g0186a0003c0008t0003g0183others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+3339_468+3464d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457064 | ||||||
| chr19:457070
|
A | T | 3 | a0001c0001t0002g0079a0001c0001t0005g0047a0002c0004t0005g0189 | 3 | HG01884.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3459T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457070 | ||||||
| chr19:457073
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3456G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457073 | ||||||
| chr19:457083
|
AC | A | 3 | a0001c0001t0002g0079a0001c0001t0005g0047a0002c0004t0005g0189 | 3 | HG01884.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3445delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457083 | ||||||
| chr19:457084
|
C | CCCCACCA others(55): Show |
1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+3444_468+3445i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457084 | ||||||
| chr19:457085
|
C | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3444G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457085 | ||||||
| chr19:457091
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3438T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457091 | ||||||
| chr19:457092
|
C | CATCAGGC others(54): Show |
1 | a0001c0003t0002g0075 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.468+3436_468+3437i others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457092 | ||||||
| chr19:457092
|
C | T | 4 | a0001c0001t0002g0079a0001c0001t0005g0047a0001c0002t0002g0046others(1): Show | 4 | HG01884.hp1 HG03017.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+3437G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457092 | ||||||
| chr19:457093
|
A | ATCAGGCC others(55): Show |
17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3435_468+3436i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457093 | ||||||
| chr19:457096
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3433T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457096 | ||||||
| chr19:457127
|
A | T | 23 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0005g0047others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+3402T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457127 | ||||||
| chr19:457136
|
C | A | 5 | a0001c0001t0002g0079a0001c0001t0005g0047a0001c0002t0002g0046others(2): Show | 5 | HG01884.hp1 HG03017.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3393G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457136 | ||||||
| chr19:457148
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3381G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457148 | ||||||
| chr19:457154
|
A | ATATCAGG others(117): Show |
21 | a0001c0001t0003g0071a0001c0001t0004g0064a0001c0001t0004g0065others(18): Show | 22 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.468+3374_468+3375i others(126): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457154 | ||||||
| chr19:457154
|
A | G | 5 | a0001c0001t0002g0079a0001c0001t0005g0047a0001c0002t0002g0046others(2): Show | 5 | HG01884.hp1 HG03017.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3375T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457154 | ||||||
| chr19:457159
|
A | G | 26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3370T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457159 | ||||||
| chr19:457172
|
A | T | 52 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(49): Show | 53 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.468+3357T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457172 | ||||||
| chr19:457189
|
G | A | 1 | a0001c0007t0002g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+3340C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457189 | ||||||
| chr19:457190
|
A | T | 26 | a0001c0001t0002g0079a0001c0001t0003g0071a0001c0001t0004g0064others(23): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3339T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457190 | ||||||
| chr19:457196
|
A | T | 1 | a0001c0001t0006g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3333T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457196 | ||||||
| chr19:457218
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0006g0043 | 2 | HG03540.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.468+3311G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457218 | ||||||
| chr19:457247
|
G | A | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3282C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457247 | ||||||
| chr19:457252
|
G | C | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3277C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457252 | ||||||
| chr19:457253
|
A | C | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3276T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457253 | ||||||
| chr19:457253
|
A | T | 1 | a0001c0001t0006g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3276T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457253 | ||||||
| chr19:457259
|
A | ACTCTGTC others(56): Show |
1 | a0001c0002t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.468+3207_468+3269d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457259 | ||||||
| chr19:457259
|
A | T | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3270T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457259 | ||||||
| chr19:457262
|
C | A | 1 | a0001c0001t0006g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3267G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457262 | ||||||
| chr19:457262
|
CTGTCTGC others(118): Show |
C | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.468+3142_468+3266d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457262 | ||||||
| chr19:457272
|
AC | A | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3256delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457272 | ||||||
| chr19:457280
|
A | G | 1 | a0001c0001t0006g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3249T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457280 | ||||||
| chr19:457281
|
C | T | 54 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0001g0177others(51): Show | 55 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.468+3248G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457281 | ||||||
| chr19:457281
|
CATCAGGC others(55): Show |
C | 1 | a0001c0001t0006g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3186_468+3247d others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457281 | ||||||
| chr19:457282
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3247T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457282 | ||||||
| chr19:457310
|
A | G | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3219T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457310 | ||||||
| chr19:457315
|
C | A | 3 | a0001c0001t0005g0053a0001c0001t0006g0054a0001c0007t0006g0055 | 3 | HG02922.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.468+3214G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457315 | ||||||
| chr19:457315
|
C | G | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3214G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457315 | ||||||
| chr19:457316
|
C | T | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3213G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457316 | ||||||
| chr19:457317
|
CT | C | 4 | a0001c0001t0003g0050a0001c0001t0006g0049a0001c0001t0006g0051others(1): Show | 4 | HG02572.hp1 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3211delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457317 | ||||||
| chr19:457322
|
T | A | 26 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+3207A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457322 | ||||||
| chr19:457325
|
C | A | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3204G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457325 | ||||||
| chr19:457335
|
A | AC | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3193dupG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457335 | ||||||
| chr19:457342
|
A | G | 9 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(6): Show | 9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3187T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457342 | ||||||
| chr19:457343
|
T | C | 26 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+3186A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457343 | ||||||
| chr19:457344
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3185T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457344 | ||||||
| chr19:457347
|
A | AGGCCTTT others(56): Show |
31 | a0001c0001t0002g0039a0001c0001t0002g0079a0001c0001t0003g0071others(28): Show | 32 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.468+3181_468+3182i others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | ||||||
| chr19:457347
|
A | AGGCCTTT others(307): Show |
13 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0171others(10): Show | 13 | HG01258.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+3181_468+3182i others(316): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | ||||||
| chr19:457347
|
A | AGGCCTTT others(306): Show |
1 | a0001c0001t0001g0177 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.468+3181_468+3182i others(315): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | ||||||
| chr19:457347
|
A | G | 10 | a0001c0001t0001g0061a0001c0001t0005g0028a0001c0001t0005g0029others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+3182T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | ||||||
| chr19:457363
|
A | ACCTGCTG others(56): Show |
17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3165_468+3166i others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457363 | ||||||
| chr19:457407
|
C | T | 3 | a0001c0001t0002g0101a0001c0001t0003g0004a0001c0001t0005g0168 | 4 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3122G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457407 | ||||||
| chr19:457423
|
C | T | 45 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0001g0177others(42): Show | 46 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.468+3106G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457423 | ||||||
| chr19:457720
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.468+2809A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457720 | ||||||
| chr19:457732
|
A | G | 21 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0005t0001g0011others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.468+2797T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457732 | ||||||
| chr19:457742
|
C | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2787G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457742 | ||||||
| chr19:457789
|
G | T | 2 | a0001c0001t0001g0044a0001c0002t0003g0045 | 2 | HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+2740C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457789 | ||||||
| chr19:457801
|
C | A | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2728G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457801 | ||||||
| chr19:457805
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2724G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457805 | ||||||
| chr19:457844
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2685A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457844 | ||||||
| chr19:457881
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2648G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457881 | ||||||
| chr19:457954
|
CGGGGAGG others(14): Show |
C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2554_468+2574d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457954 | ||||||
| chr19:458010
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2519T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458010 | ||||||
| chr19:458032
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2497T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458032 | ||||||
| chr19:458038
|
CGGGGAGG others(14): Show |
C | 1 | a0001c0003t0002g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.468+2470_468+2490d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458038 | ||||||
| chr19:458045
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2484C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458045 | ||||||
| chr19:458047
|
G | A | 1 | a0001c0003t0002g0074 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.468+2482C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458047 | ||||||
| chr19:458047
|
GGAAGCGG others(56): Show |
G | 1 | a0001c0001t0003g0171 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+2419_468+2481d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458047 | ||||||
| chr19:458052
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2477G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458052 | ||||||
| chr19:458057
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2472G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458057 | ||||||
| chr19:458058
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2471A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458058 | ||||||
| chr19:458059
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2470A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458059 | ||||||
| chr19:458067
|
C | G | 3 | a0001c0001t0001g0044a0001c0002t0003g0045a0002c0004t0001g0204 | 3 | HG02165.hp1 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+2462G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458067 | ||||||
| chr19:458068
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2461C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458068 | ||||||
| chr19:458071
|
A | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2458T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458071 | ||||||
| chr19:458073
|
CGGGTCTT others(14): Show |
C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2435_468+2455d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458073 | ||||||
| chr19:458099
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2430G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458099 | ||||||
| chr19:458100
|
C | T | 1 | a0001c0001t0006g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+2429G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458100 | ||||||
| chr19:458101
|
CGGGGAGG others(14): Show |
C | 1 | a0001c0001t0005g0047 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.468+2407_468+2427d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458101 | ||||||
| chr19:458110
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2419T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458110 | ||||||
| chr19:458116
|
G | T | 11 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0003g0036others(8): Show | 11 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+2413C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458116 | ||||||
| chr19:458121
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2408A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458121 | ||||||
| chr19:458122
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2407A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458122 | ||||||
| chr19:458144
|
G | A | 18 | a0001c0001t0001g0165a0001c0005t0001g0011a0001c0005t0001g0012others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.468+2385C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458144 | ||||||
| chr19:458150
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2379T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458150 | ||||||
| chr19:458162
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2367A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458162 | ||||||
| chr19:458173
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2356T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458173 | ||||||
| chr19:458176
|
C | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2353G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458176 | ||||||
| chr19:458179
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2350T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458179 | ||||||
| chr19:458180
|
T | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2349A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458180 | ||||||
| chr19:458181
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0081others(72): Show | 78 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+2348C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458181 | ||||||
| chr19:458186
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2343C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458186 | ||||||
| chr19:458188
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2341C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458188 | ||||||
| chr19:458192
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2337G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458192 | ||||||
| chr19:458192
|
CGGGGAAG others(36): Show |
C | 2 | a0001c0001t0006g0043a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+2294_468+2336d others(45): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458192 | ||||||
| chr19:458231
|
C | G | 77 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+2298G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458231 | ||||||
| chr19:458235
|
G | C | 11 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0022others(8): Show | 11 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.468+2294C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458235 | ||||||
| chr19:458235
|
G | T | 6 | a0001c0005t0001g0011a0001c0005t0001g0015a0001c0005t0001g0016others(3): Show | 6 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+2294C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458235 | ||||||
| chr19:458250
|
C | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2279G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458250 | ||||||
| chr19:458270
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2259A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458270 | ||||||
| chr19:458278
|
GCGGAAGT others(56): Show |
G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2188_468+2250d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458278 | ||||||
| chr19:458285
|
TGGGTCCC others(56): Show |
T | 1 | a0001c0003t0002g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.468+2181_468+2243d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458285 | ||||||
| chr19:458287
|
G | A | 38 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0001g0177others(35): Show | 39 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.468+2242C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458287 | ||||||
| chr19:458322
|
GGAAGCGG others(14): Show |
G | 23 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(20): Show | 24 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+2186_468+2206d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458322 | ||||||
| chr19:458327
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0044others(143): Show | 151 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+2202G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458327 | ||||||
| chr19:458341
|
A | G | 19 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(16): Show | 19 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+2188T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458341 | ||||||
| chr19:458343
|
A | G | 19 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0039others(16): Show | 19 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+2186T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458343 | ||||||
| chr19:458348
|
C | T | 23 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(20): Show | 24 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+2181G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458348 | ||||||
| chr19:458355
|
C | CG | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2173dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458355 | ||||||
| chr19:458363
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2166G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458363 | ||||||
| chr19:458376
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2153G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458376 | ||||||
| chr19:458385
|
G | A | 12 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0003g0036others(9): Show | 12 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.468+2144C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458385 | ||||||
| chr19:458389
|
T | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2140A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458389 | ||||||
| chr19:458397
|
C | CG | 16 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+2131dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458397 | ||||||
| chr19:458402
|
A | G | 1 | a0001c0006t0006g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.468+2127T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458402 | ||||||
| chr19:458405
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2124G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458405 | ||||||
| chr19:458412
|
G | A | 1 | a0008c0021t0002g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+2117C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458412 | ||||||
| chr19:458414
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.468+2115C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458414 | ||||||
| chr19:458416
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2113G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458416 | ||||||
| chr19:458427
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2102T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458427 | ||||||
| chr19:458458
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2071A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458458 | ||||||
| chr19:458469
|
AGACGCAT others(78): Show |
A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1975_468+2059d others(87): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458469 | ||||||
| chr19:458497
|
A | G | 53 | a0001c0001t0001g0061a0001c0001t0001g0176a0001c0001t0001g0177others(50): Show | 54 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.468+2032T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458497 | ||||||
| chr19:458498
|
G | T | 4 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+2031C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458498 | ||||||
| chr19:458524
|
T | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2005A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458524 | ||||||
| chr19:458545
|
CGGGGAGG others(14): Show |
C | 1 | a0008c0021t0002g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+1963_468+1983d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458545 | ||||||
| chr19:458553
|
TGGAAGCG others(121): Show |
T | 1 | a0002c0024t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.468+1848_468+1975d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458553 | ||||||
| chr19:458565
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1964G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458565 | ||||||
| chr19:458570
|
G | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1959C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458570 | ||||||
| chr19:458574
|
C | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1955G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458574 | ||||||
| chr19:458575
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1954C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458575 | ||||||
| chr19:458580
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1949G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458580 | ||||||
| chr19:458587
|
C | T | 3 | a0001c0001t0001g0044a0001c0002t0003g0045a0002c0004t0001g0204 | 3 | HG02165.hp1 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+1942G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458587 | ||||||
| chr19:458594
|
C | A | 3 | a0001c0001t0001g0044a0001c0002t0003g0045a0002c0004t0001g0204 | 3 | HG02165.hp1 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+1935G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458594 | ||||||
| chr19:458594
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1935G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458594 | ||||||
| chr19:458609
|
C | CGGGGAGG others(98): Show |
6 | a0001c0001t0005g0028a0001c0001t0005g0031a0001c0001t0007g0041others(3): Show | 6 | HG01891.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+1919_468+1920i others(107): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458609 | ||||||
| chr19:458609
|
C | CGGGGAGG others(99): Show |
1 | a0001c0001t0005g0029 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.468+1919_468+1920i others(108): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458609 | ||||||
| chr19:458610
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1919T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458610 | ||||||
| chr19:458613
|
G | GAGGCGGA others(98): Show |
1 | a0001c0005t0006g0009 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468+1915_468+1916i others(107): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458613 | ||||||
| chr19:458621
|
C | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1908G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458621 | ||||||
| chr19:458628
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1901A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458628 | ||||||
| chr19:458630
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1899G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458630 | ||||||
| chr19:458631
|
G | A | 8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0001g0172others(5): Show | 8 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+1898C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458631 | ||||||
| chr19:458642
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1887T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458642 | ||||||
| chr19:458645
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1884G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458645 | ||||||
| chr19:458646
|
G | A | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1883C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458646 | ||||||
| chr19:458649
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1880G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458649 | ||||||
| chr19:458650
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1879A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458650 | ||||||
| chr19:458651
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1878A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458651 | ||||||
| chr19:458665
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1864A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458665 | ||||||
| chr19:458668
|
GT | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1860delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458668 | ||||||
| chr19:458673
|
G | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1856C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458673 | ||||||
| chr19:458678
|
A | AG | 6 | a0001c0001t0002g0057a0001c0001t0005g0029a0001c0002t0001g0089others(3): Show | 6 | HG01099.hp1 HG01109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+1850dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458678 | ||||||
| chr19:458681
|
G | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1848C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458681 | ||||||
| chr19:458729
|
T | C | 1 | a0008c0021t0002g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+1800A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458729 | ||||||
| chr19:458736
|
C | CG | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1792dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458736 | ||||||
| chr19:458742
|
G | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1787C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458742 | ||||||
| chr19:458744
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1785G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458744 | ||||||
| chr19:458748
|
A | G | 7 | a0001c0001t0002g0057a0001c0017t0005g0056a0001c0023t0007g0186others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1781T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458748 | ||||||
| chr19:458750
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1779G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458750 | ||||||
| chr19:458755
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1774G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458755 | ||||||
| chr19:458755
|
CCCGGGGA others(14): Show |
C | 3 | a0001c0001t0005g0053a0001c0001t0006g0054a0001c0007t0006g0055 | 3 | HG02922.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.468+1753_468+1773d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458755 | ||||||
| chr19:458757
|
CGGGGAGG others(35): Show |
C | 1 | a0001c0002t0001g0169 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.468+1730_468+1771d others(44): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458757 | ||||||
| chr19:458765
|
C | T | 1 | a0002c0004t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.468+1764G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458765 | ||||||
| chr19:458769
|
G | A | 7 | a0001c0001t0002g0057a0001c0017t0005g0056a0001c0023t0007g0186others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1760C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458769 | ||||||
| chr19:458769
|
G | GGCGGGTT others(14): Show |
1 | a0001c0001t0005g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.468+1739_468+1759d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458769 | ||||||
| chr19:458771
|
C | CGGGTTCC others(56): Show |
1 | a0001c0003t0002g0075 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.468+1695_468+1757d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458771 | ||||||
| chr19:458778
|
C | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1751G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458778 | ||||||
| chr19:458778
|
CGGGGAGG others(14): Show |
C | 2 | a0001c0001t0006g0043a0001c0002t0003g0178 | 2 | HG03540.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.468+1730_468+1750d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458778 | ||||||
| chr19:458798
|
CTGGGGAG others(14): Show |
C | 1 | a0001c0003t0002g0076 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.468+1710_468+1730d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458798 | ||||||
| chr19:458829
|
G | A | 19 | a0001c0001t0006g0043a0001c0005t0001g0011a0001c0005t0001g0012others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+1700C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458829 | ||||||
| chr19:458832
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1697T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458832 | ||||||
| chr19:458841
|
C | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(4): Show | 7 | HG01978.hp2 HG02004.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1688G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458841 | ||||||
| chr19:458846
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1683T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458846 | ||||||
| chr19:458849
|
C | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1680G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458849 | ||||||
| chr19:458852
|
A | AGGGGCGG others(28): Show |
1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1676_468+1677i others(37): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458852 | ||||||
| chr19:458853
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1676T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458853 | ||||||
| chr19:458855
|
C | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1674G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458855 | ||||||
| chr19:458856
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.468+1673C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458856 | ||||||
| chr19:458859
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1670A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458859 | ||||||
| chr19:458860
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1669G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458860 | ||||||
| chr19:458861
|
C | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1668G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458861 | ||||||
| chr19:458862
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1667A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458862 | ||||||
| chr19:458867
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1662T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458867 | ||||||
| chr19:458882
|
G | A | 7 | a0001c0001t0003g0050a0001c0001t0005g0053a0001c0001t0006g0049others(4): Show | 7 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1647C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458882 | ||||||
| chr19:458919
|
G | A | 1 | a0002c0012t0002g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.468+1610C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458919 | ||||||
| chr19:458935
|
A | G | 88 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.468+1594T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458935 | ||||||
| chr19:458993
|
C | T | 4 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+1536G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458993 | ||||||
| chr19:459074
|
T | C | 88 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.468+1455A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459074 | ||||||
| chr19:459087
|
G | A | 88 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0176others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.468+1442C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459087 | ||||||
| chr19:459093
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1436C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459093 | ||||||
| chr19:459110
|
C | T | 8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0002t0001g0172others(5): Show | 8 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+1419G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459110 | ||||||
| chr19:459112
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1417A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459112 | ||||||
| chr19:459119
|
AATATAAG others(2): Show |
A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1401_468+1409d others(11): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459119 | ||||||
| chr19:459184
|
TGTAGGGG others(22): Show |
T | 8 | a0001c0001t0002g0052a0001c0001t0003g0050a0001c0001t0005g0053others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1316_468+1344d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459184 | ||||||
| chr19:459208
|
C | G | 2 | a0001c0005t0001g0012a0001c0005t0001g0013 | 2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.468+1321G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459208 | ||||||
| chr19:459237
|
CCCAGCGT others(51): Show |
C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1234_468+1291d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459237 | ||||||
| chr19:459260
|
T | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1269A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459260 | ||||||
| chr19:459263
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1266G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459263 | ||||||
| chr19:459267
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1262A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459267 | ||||||
| chr19:459269
|
G | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1260C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459269 | ||||||
| chr19:459270
|
G | A | 2 | a0001c0001t0002g0057a0001c0023t0007g0186 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.468+1259C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459270 | ||||||
| chr19:459271
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1258A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459271 | ||||||
| chr19:459275
|
G | GGGGGAAG others(109): Show |
1 | a0001c0005t0001g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.468+1253_468+1254i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459275 | ||||||
| chr19:459295
|
G | C | 1 | a0001c0005t0001g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.468+1234C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459295 | ||||||
| chr19:459295
|
G | GCCAGCGT others(109): Show |
1 | a0001c0005t0001g0012 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.468+1233_468+1234i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459295 | ||||||
| chr19:459324
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+1205G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459324 | ||||||
| chr19:459324
|
CCCAGCGT others(22): Show |
C | 5 | a0001c0001t0001g0081a0001c0001t0002g0039a0001c0001t0011g0038others(2): Show | 5 | HG02451.hp2 HG02486.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+1176_468+1204d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459324 | ||||||
| chr19:459325
|
C | CCAGCGTA others(167): Show |
14 | a0001c0005t0001g0015a0001c0005t0001g0016a0001c0005t0001g0017others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.468+1203_468+1204i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459325 | ||||||
| chr19:459325
|
C | CCAGCGTA others(167): Show |
1 | a0001c0005t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.468+1203_468+1204i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459325 | ||||||
| chr19:459347
|
A | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1182T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459347 | ||||||
| chr19:459350
|
G | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1179C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459350 | ||||||
| chr19:459353
|
G | C | 27 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.468+1176C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459353 | ||||||
| chr19:459353
|
G | GCCAGCGT others(22): Show |
1 | a0001c0002t0001g0006 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.468+1175_468+1176i others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459353 | ||||||
| chr19:459354
|
C | T | 23 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+1175G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459354 | ||||||
| chr19:459356
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1173T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459356 | ||||||
| chr19:459358
|
C | A | 2 | a0001c0005t0001g0012a0001c0005t0001g0013 | 2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.468+1171G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459358 | ||||||
| chr19:459358
|
C | T | 23 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+1171G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459358 | ||||||
| chr19:459362
|
G | A | 15 | a0001c0005t0001g0011a0001c0005t0001g0015a0001c0005t0001g0016others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.468+1167C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459362 | ||||||
| chr19:459362
|
G | GGGGGAAG others(51): Show |
2 | a0001c0005t0001g0012a0001c0005t0001g0013 | 2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.468+1166_468+1167i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459362 | ||||||
| chr19:459382
|
G | C | 158 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0061others(155): Show | 162 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.468+1147C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459382 | ||||||
| chr19:459382
|
G | GCCAGCGT others(22): Show |
1 | a0001c0002t0001g0006 | 2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.468+1118_468+1146d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459382 | ||||||
| chr19:459410
|
A | ACCCAGCG others(51): Show |
10 | a0001c0005t0001g0011a0001c0005t0001g0015a0001c0005t0001g0022others(7): Show | 10 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1118_468+1119i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459410 | ||||||
| chr19:459411
|
C | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1118G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459411 | ||||||
| chr19:459431
|
C | A | 2 | a0001c0001t0006g0043a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+1098G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459431 | ||||||
| chr19:459441
|
CCAGCGTA others(22): Show |
C | 4 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0007t0006g0037others(1): Show | 4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+1059_468+1087d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459441 | ||||||
| chr19:459463
|
T | A | 25 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1066A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459463 | ||||||
| chr19:459466
|
C | G | 25 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1063G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459466 | ||||||
| chr19:459468
|
A | G | 7 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0016others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1061T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459468 | ||||||
| chr19:459469
|
C | CCCAGCGT others(51): Show |
7 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0016others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1059_468+1060i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459469 | ||||||
| chr19:459469
|
C | G | 11 | a0001c0003t0001g0058a0001c0005t0001g0011a0001c0005t0001g0015others(8): Show | 11 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.468+1060G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459469 | ||||||
| chr19:459470
|
T | C | 25 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1059A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459470 | ||||||
| chr19:459472
|
A | C | 1 | a0001c0007t0006g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.468+1057T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459472 | ||||||
| chr19:459515
|
G | A | 2 | a0001c0001t0002g0079a0001c0007t0002g0080 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.468+1014C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459515 | ||||||
| chr19:459520
|
T | C | 25 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1009A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459520 | ||||||
| chr19:459521
|
T | A | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1008A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459521 | ||||||
| chr19:459524
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1005G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459524 | ||||||
| chr19:459524
|
CAACTCAG others(22): Show |
C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+976_468+1004de others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459524 | ||||||
| chr19:459527
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1002G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459527 | ||||||
| chr19:459528
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1001A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459528 | ||||||
| chr19:459532
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+997A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459532 | ||||||
| chr19:459537
|
A | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+992T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459537 | ||||||
| chr19:459549
|
T | C | 21 | a0001c0001t0002g0039a0001c0001t0011g0038a0001c0005t0001g0011others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.468+980A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459549 | ||||||
| chr19:459557
|
T | C | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+972A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459557 | ||||||
| chr19:459579
|
A | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+950T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459579 | ||||||
| chr19:459582
|
G | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+947C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459582 | ||||||
| chr19:459615
|
T | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+914A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459615 | ||||||
| chr19:459619
|
T | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+910A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459619 | ||||||
| chr19:459623
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+906T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459623 | ||||||
| chr19:459707
|
T | C | 8 | a0001c0001t0005g0028a0001c0001t0005g0029a0001c0001t0005g0031others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+822A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459707 | ||||||
| chr19:459740
|
C | T | 4 | a0001c0001t0003g0050a0001c0001t0006g0049a0001c0001t0006g0051others(1): Show | 4 | HG02572.hp1 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+789G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459740 | ||||||
| chr19:459922
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+607G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459922 | ||||||
| chr19:459949
|
C | A | 2 | a0001c0001t0006g0043a0001c0007t0006g0042 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+580G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459949 | ||||||
| chr19:459976
|
C | T | 2 | a0001c0001t0001g0044a0001c0002t0003g0045 | 2 | HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+553G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459976 | ||||||
| chr19:460025
|
A | G | 45 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0002g0079others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+504T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460025 | ||||||
| chr19:460027
|
G | A | 45 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0002g0079others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+502C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460027 | ||||||
| chr19:460049
|
C | T | 45 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0002g0079others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+480G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460049 | ||||||
| chr19:460073
|
T | A | 45 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0002g0079others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+456A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460073 | ||||||
| chr19:460190
|
G | C | 1 | a0001c0003t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.468+339C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460190 | ||||||
| chr19:460222
|
G | A | 2 | a0001c0001t0002g0057a0001c0023t0007g0186 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.468+307C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460222 | ||||||
| chr19:460260
|
T | TG | 9 | a0001c0001t0002g0052a0001c0001t0003g0050a0001c0001t0005g0053others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+268dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460260 | ||||||
| chr19:460274
|
C | A | 1 | a0001c0001t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.468+255G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460274 | ||||||
| chr19:460274
|
C | G | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+255G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460274 | ||||||
| chr19:460292
|
TC | T | 17 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+236delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460292 | ||||||
| chr19:460343
|
G | A | 24 | a0001c0001t0001g0061a0001c0001t0002g0079a0001c0001t0003g0071others(21): Show | 25 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+186C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460343 | ||||||
| chr19:460382
|
G | A | 16 | a0001c0005t0001g0011a0001c0005t0001g0012a0001c0005t0001g0013others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+147C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460382 | ||||||
| chr19:460403
|
G | A | 2 | a0003c0008t0006g0185a0010c0022t0002g0184 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.468+126C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460403 | ||||||
| chr19:460475
|
G | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0081others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.468+54C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460475 | ||||||
| chr19:460507
|
G | A | 11 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0003g0171others(8): Show | 11 | HG00423.hp1 HG02258.hp2 HG03195.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+22C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460507 | ||||||
| chr19:460515
|
T | G | 1 | a0002c0004t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.468+14A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460515 | ||||||
| chr19:460515
|
TG | T | 6 | a0001c0001t0005g0029a0001c0001t0005g0031a0001c0005t0006g0009others(3): Show | 6 | HG02145.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+13delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460515 | ||||||
| chr19:460516
|
G | T | 1 | a0001c0001t0005g0028 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.468+13C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460516 |