Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 53358 |
|---|---|
| ensemblid | ENSG00000148082.10 |
| hgncid | 18181 |
| symbol | SHC3 |
| name | SHC adaptor protein 3 |
| refseq_nuc | NM_016848.6 |
| refseq_prot | NP_058544.3 |
| ensembl_nuc | ENST00000375835.9 |
| ensembl_prot | ENSP00000364995.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 89005771 |
| end | 89178818 |
| strand | - |
| ver | v1.2 |
| region | chr9:89005771-89178818 |
| region5000 | chr9:89000771-89183818 |
| regionname0 | SHC3_chr9_89005771_89178818 |
| regionname5000 | SHC3_chr9_89000771_89183818 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 594 | 185 | 77 | 58 | 8 | 14 | 26 | 6 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0002 | 0/0 | 594 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| 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 | 1785 | 108 | 52 | 26 | 7 | 6 | 17 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0002 | 1/1 | 1785 | 49 | 12 | 21 | 1 | 6 | 7 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0003 | 0/0 | 1785 | 17 | 6 | 9 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0004 | 0/0 | 1785 | 5 | 3 | 0 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0005 | 0/0 | 1785 | 3 | 3 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0006 | 0/0 | 1785 | 2 | 1 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0007 | 0/0 | 1785 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0008 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| c0009 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8036 | 41 | 7 | 17 | 5 | 2 | 10 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0002 | 0/0 | 8034 | 36 | 9 | 18 | 0 | 6 | 3 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0003 | 0/0 | 8035 | 18 | 14 | 3 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0004 | 0/0 | 8035 | 11 | 3 | 5 | 0 | 1 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0005 | 0/0 | 8035 | 10 | 7 | 0 | 0 | 3 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0006 | 0/0 | 8035 | 6 | 0 | 2 | 0 | 1 | 3 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0007 | 0/0 | 8035 | 5 | 3 | 2 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0008 | 0/0 | 8035 | 4 | 2 | 0 | 1 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0009 | 0/1 | 8035 | 4 | 2 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0010 | 0/0 | 8034 | 4 | 2 | 0 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0011 | 0/0 | 8035 | 3 | 3 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0012 | 0/0 | 8035 | 3 | 3 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0013 | 0/0 | 8035 | 3 | 3 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0014 | 0/0 | 8035 | 3 | 2 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0015 | 0/0 | 8035 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0016 | 0/0 | 8035 | 2 | 0 | 1 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0017 | 0/0 | 8035 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0018 | 0/0 | 8035 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0019 | 0/0 | 8036 | 2 | 0 | 1 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0020 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0021 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0022 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0023 | 0/0 | 8035 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0024 | 0/0 | 8035 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0025 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0026 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0027 | 0/0 | 8034 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0028 | 0/0 | 8034 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0029 | 0/0 | 8034 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0030 | 0/0 | 8034 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0031 | 0/0 | 8034 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0032 | 0/0 | 8034 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0033 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0034 | 1/0 | 8035 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0035 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0036 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0037 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0038 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0039 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0040 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0041 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0042 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0043 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0044 | 0/0 | 8035 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0045 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| t0046 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| 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 | 2 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| 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 | 1785 | 108 | 52 | 26 | 7 | 6 | 17 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002 | 1/1 | 1785 | 49 | 12 | 21 | 1 | 6 | 7 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003 | 0/0 | 1785 | 17 | 6 | 9 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0004 | 0/0 | 1785 | 5 | 3 | 0 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0006 | 0/0 | 1785 | 2 | 1 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0007 | 0/0 | 1785 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0008 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0009 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0002c0005 | 0/0 | 1785 | 3 | 3 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9820 | 29 | 5 | 8 | 5 | 1 | 10 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0002 | 0/0 | 9818 | 18 | 6 | 7 | 0 | 4 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0003 | 0/0 | 9819 | 11 | 8 | 2 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0004 | 0/0 | 9819 | 5 | 2 | 3 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0005 | 0/0 | 9819 | 6 | 5 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0006 | 0/0 | 9819 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0007 | 0/0 | 9819 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0008 | 0/0 | 9819 | 3 | 2 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0009 | 0/0 | 9819 | 3 | 2 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0012 | 0/0 | 9819 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0013 | 0/0 | 9819 | 3 | 3 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0014 | 0/0 | 9819 | 3 | 2 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0016 | 0/0 | 9819 | 2 | 0 | 1 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0017 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0018 | 0/0 | 9819 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0019 | 0/0 | 9820 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0020 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0022 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0023 | 0/0 | 9819 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0025 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0026 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0028 | 0/0 | 9818 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0029 | 0/0 | 9818 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0030 | 0/0 | 9818 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0033 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0035 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0036 | 0/0 | 9820 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0037 | 0/0 | 9820 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0041 | 0/0 | 9820 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0042 | 0/0 | 9820 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0043 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0001t0044 | 0/0 | 9819 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0001 | 0/0 | 9820 | 5 | 0 | 4 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0002 | 0/0 | 9818 | 15 | 3 | 8 | 0 | 2 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0003 | 0/0 | 9819 | 4 | 3 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0004 | 0/0 | 9819 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0005 | 0/0 | 9819 | 4 | 2 | 0 | 0 | 2 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0006 | 0/0 | 9819 | 5 | 0 | 2 | 0 | 1 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0007 | 0/0 | 9819 | 2 | 0 | 2 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0008 | 0/0 | 9819 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0009 | 0/1 | 9819 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0012 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0015 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0017 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0019 | 0/0 | 9820 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0021 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0031 | 0/0 | 9818 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0032 | 0/0 | 9818 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0034 | 1/0 | 9819 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0038 | 0/0 | 9820 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0039 | 0/0 | 9820 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0002t0040 | 0/0 | 9820 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0001 | 0/0 | 9820 | 5 | 1 | 4 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0002 | 0/0 | 9818 | 3 | 0 | 3 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0003 | 0/0 | 9819 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0004 | 0/0 | 9819 | 4 | 0 | 2 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0011 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0045 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0003t0046 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0004t0001 | 0/0 | 9820 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0004t0010 | 0/0 | 9818 | 4 | 2 | 0 | 0 | 1 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0006t0004 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0006t0024 | 0/0 | 9819 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0007t0003 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0007t0015 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0008t0001 | 0/0 | 9820 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0001c0009t0027 | 0/0 | 9818 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0002c0005t0007 | 0/0 | 9819 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| a0002c0005t0011 | 0/0 | 9819 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | copy fasta | chr9 | 89000771 | 89183818 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0014g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0014g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0016g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0016g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0017g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0018g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0019g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0020g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0022g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0023g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0025g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0026g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0028g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0029g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0030g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0035g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0036g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0037g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0041g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0042g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0043g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0001t0044g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0006g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0007g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0009g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0017g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0019g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0021g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0031g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0032g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0034g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0038g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0039g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0002t0040g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0045g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0003t0046g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0004t0010g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0004t0010g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0004t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0004t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0006t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0006t0024g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0007t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0007t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0008t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0001c0009t0027g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0002c0005t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0002c0005t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| a0002c0005t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | GBR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0124 | EUR | GBR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0088 | EUR | GBR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00280 | hp1 | a0001 | c0002 | t0006 | g0173 | EUR | FIN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | FIN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | FIN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0128 | EUR | FIN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00408 | hp2 | a0001 | c0002 | t0032 | g0083 | EAS | CHS | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00642 | hp2 | a0001 | c0002 | t0007 | g0058 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00735 | hp1 | a0001 | c0001 | t0042 | g0079 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00735 | hp2 | a0001 | c0002 | t0006 | g0127 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00738 | hp2 | a0001 | c0001 | t0016 | g0160 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01070 | hp1 | a0001 | c0001 | t0014 | g0138 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0143 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01074 | hp1 | a0001 | c0001 | t0041 | g0174 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01074 | hp2 | a0001 | c0002 | t0039 | g0078 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01106 | hp1 | a0001 | c0008 | t0001 | g0015 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01167 | hp1 | a0001 | c0002 | t0038 | g0095 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0118 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0056 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0140 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01255 | hp2 | a0001 | c0001 | t0023 | g0023 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01257 | hp2 | a0001 | c0002 | t0007 | g0081 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01258 | hp1 | a0001 | c0003 | t0004 | g0021 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01261 | hp2 | a0001 | c0002 | t0006 | g0059 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01433 | hp1 | a0001 | c0006 | t0024 | g0168 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0117 | EUR | IBS | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01515 | hp2 | a0001 | c0003 | t0004 | g0011 | EUR | IBS | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01517 | hp1 | a0001 | c0002 | t0005 | g0147 | EUR | IBS | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0116 | EUR | IBS | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0050 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0106 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01891 | hp1 | a0001 | c0001 | t0033 | g0037 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0052 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0097 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0123 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01952 | hp2 | a0001 | c0002 | t0031 | g0064 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0066 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG01993 | hp2 | a0001 | c0002 | t0019 | g0126 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02055 | hp1 | a0001 | c0003 | t0045 | g0008 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02148 | hp2 | a0001 | c0003 | t0004 | g0014 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0042 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02258 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0105 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0112 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02572 | hp2 | a0002 | c0005 | t0011 | g0033 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0093 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02647 | hp1 | a0001 | c0002 | t0015 | g0043 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0166 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0135 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0053 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0109 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02818 | hp2 | a0002 | c0005 | t0007 | g0032 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0054 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02886 | hp2 | a0001 | c0001 | t0029 | g0024 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02896 | hp2 | a0001 | c0004 | t0010 | g0181 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02897 | hp1 | a0001 | c0004 | t0010 | g0182 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0022 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02970 | hp1 | a0001 | c0001 | t0043 | g0077 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0025 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0060 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03041 | hp2 | a0001 | c0002 | t0017 | g0031 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0028 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0034 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03130 | hp1 | a0002 | c0005 | t0011 | g0048 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0091 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03225 | hp2 | a0001 | c0003 | t0046 | g0007 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03239 | hp2 | a0001 | c0002 | t0006 | g0002 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03453 | hp1 | a0001 | c0001 | t0026 | g0172 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0040 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03486 | hp2 | a0001 | c0007 | t0015 | g0176 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03492 | hp1 | a0001 | c0001 | t0016 | g0098 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0152 | AFR | GWD | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03579 | hp1 | a0001 | c0007 | t0003 | g0177 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03654 | hp1 | a0001 | c0001 | t0044 | g0134 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03654 | hp2 | a0001 | c0004 | t0010 | g0180 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03669 | hp1 | a0001 | c0002 | t0040 | g0142 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03704 | hp1 | a0001 | c0002 | t0006 | g0002 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03704 | hp2 | a0001 | c0003 | t0004 | g0013 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0159 | SAS | BEB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03834 | hp1 | a0001 | c0002 | t0008 | g0148 | SAS | BEB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03834 | hp2 | a0001 | c0001 | t0036 | g0133 | SAS | BEB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG04115 | hp1 | a0001 | c0001 | t0019 | g0057 | SAS | STU | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | STU | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18522 | hp1 | a0001 | c0001 | t0017 | g0076 | AFR | YRI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | YRI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18906 | hp1 | a0001 | c0001 | t0035 | g0092 | AFR | YRI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | YRI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18961 | hp1 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18974 | hp2 | a0001 | c0001 | t0037 | g0113 | EAS | JPT | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0144 | AFR | LWK | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA19030 | hp2 | a0001 | c0003 | t0011 | g0010 | AFR | LWK | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0102 | AFR | LWK | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA19043 | hp2 | a0001 | c0009 | t0027 | g0178 | AFR | LWK | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0096 | AFR | YRI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | YRI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA20805 | hp1 | a0001 | c0004 | t0010 | g0179 | EUR | TSI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02486 | hp1 | a0001 | c0001 | t0028 | g0139 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0087 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG02559 | hp2 | a0001 | c0001 | t0030 | g0122 | AFR | ACB | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0161 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| HG03471 | hp2 | a0001 | c0002 | t0021 | g0051 | AFR | MSL | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | USA | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | USA | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA21309 | hp1 | a0001 | c0006 | t0004 | g0169 | AFR | LWK | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | LWK | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0009 | g0082 | REF | REF | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0034 | g0080 | REF | REF | SHC3_chr9_89000771_89183818 | SHC3 | chr9 | 89000771 | 89183818 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:89042094
|
G | A | 1 | a0002 | 3 | HG02572.hp2 HG02818.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1292C>T | p.Pro431Leu | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/12 | 1650/9819 | 1292/1785 | 431/594 | chr9 | 89042094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:89042048
|
T | C | 6 | a0001c0001a0001c0003a0001c0004others(3): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
synonymous_variant | LOW | c.1338A>G | p.Pro446Pro | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/12 | 1696/9819 | 1338/1785 | 446/594 | chr9 | 89042048 | ||
| chr9:89052051
|
G | A | 1 | a0001c0004 | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.948C>T | p.Pro316Pro | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/12 | 1306/9819 | 948/1785 | 316/594 | chr9 | 89052051 | ||
| chr9:89075121
|
C | T | 1 | a0001c0006 | 2 | HG01433.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.717G>A | p.Pro239Pro | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/12 | 1075/9819 | 717/1785 | 239/594 | chr9 | 89075121 | ||
| chr9:89178170
|
C | G | 2 | a0001c0003a0001c0008 | 18 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
synonymous_variant | LOW | c.291G>C | p.Ser97Ser | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/12 | 649/9819 | 291/1785 | 97/594 | chr9 | 89178170 | ||
| chr9:89178200
|
G | A | 1 | a0001c0007 | 2 | HG03486.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.261C>T | p.Ala87Ala | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/12 | 619/9819 | 261/1785 | 87/594 | chr9 | 89178200 | ||
| chr9:89178395
|
G | A | 1 | a0001c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.66C>T | p.Leu22Leu | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/12 | 424/9819 | 66/1785 | 22/594 | chr9 | 89178395 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:89005977
|
G | A | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7470C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 7470 | chr9 | 89005977 | |||||
| chr9:89006015
|
G | A | 3 | a0001c0001t0019a0001c0002t0019a0001c0002t0040 | 3 | HG01993.hp2 HG03669.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7432C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 7432 | chr9 | 89006015 | |||||
| chr9:89006177
|
C | T | 1 | a0001c0003t0046 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7270G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 7270 | chr9 | 89006177 | |||||
| chr9:89006282
|
A | G | 22 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(19): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*7165T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 7165 | chr9 | 89006282 | |||||
| chr9:89006346
|
C | G | 1 | a0001c0001t0016 | 2 | HG00738.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7101G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 7101 | chr9 | 89006346 | |||||
| chr9:89006490
|
G | A | 2 | a0001c0001t0005a0001c0002t0005 | 10 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6957C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 6957 | chr9 | 89006490 | |||||
| chr9:89006502
|
C | T | 1 | a0001c0003t0045 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6945G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 6945 | chr9 | 89006502 | |||||
| chr9:89007049
|
C | G | 1 | a0001c0001t0029 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6398G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 6398 | chr9 | 89007049 | |||||
| chr9:89007262
|
G | A | 52 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(49): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*6185C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 6185 | chr9 | 89007262 | |||||
| chr9:89007315
|
C | A | 1 | a0001c0002t0031 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6132G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 6132 | chr9 | 89007315 | |||||
| chr9:89007364
|
C | T | 1 | a0001c0001t0023 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6083G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 6083 | chr9 | 89007364 | |||||
| chr9:89007531
|
A | G | 5 | a0001c0001t0016a0001c0001t0018a0001c0001t0026others(2): Show | 7 | HG00738.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5916T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 5916 | chr9 | 89007531 | |||||
| chr9:89007776
|
A | G | 22 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(19): Show | 38 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*5671T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 5671 | chr9 | 89007776 | |||||
| chr9:89007955
|
T | C | 1 | a0001c0001t0018 | 2 | HG02258.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5492A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 5492 | chr9 | 89007955 | |||||
| chr9:89008349
|
G | C | 1 | a0001c0001t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5098C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 5098 | chr9 | 89008349 | |||||
| chr9:89008395
|
C | T | 1 | a0001c0002t0039 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5052G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 5052 | chr9 | 89008395 | |||||
| chr9:89008426
|
G | C | 1 | a0001c0004t0010 | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5021C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 5021 | chr9 | 89008426 | |||||
| chr9:89008521
|
G | C | 1 | a0001c0006t0024 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4926C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4926 | chr9 | 89008521 | |||||
| chr9:89008581
|
C | T | 1 | a0001c0002t0038 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4866G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4866 | chr9 | 89008581 | |||||
| chr9:89008590
|
G | C | 23 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(20): Show | 39 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4857C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4857 | chr9 | 89008590 | |||||
| chr9:89008696
|
C | T | 1 | a0001c0003t0046 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4751G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4751 | chr9 | 89008696 | |||||
| chr9:89008794
|
G | A | 52 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(49): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*4653C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4653 | chr9 | 89008794 | |||||
| chr9:89008896
|
A | G | 22 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(19): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*4551T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4551 | chr9 | 89008896 | |||||
| chr9:89009139
|
G | C | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*4308C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4308 | chr9 | 89009139 | |||||
| chr9:89009223
|
G | A | 7 | a0001c0001t0008a0001c0001t0009a0001c0001t0020others(4): Show | 11 | HG01943.hp2 HG02486.hp1 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4224C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4224 | chr9 | 89009223 | |||||
| chr9:89009309
|
C | T | 3 | a0001c0001t0008a0001c0002t0008a0001c0009t0027 | 5 | HG02809.hp2 HG03834.hp1 NA18906.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4138G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 4138 | chr9 | 89009309 | |||||
| chr9:89009482
|
A | G | 16 | a0001c0001t0001a0001c0001t0014a0001c0001t0019others(13): Show | 54 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3965T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3965 | chr9 | 89009482 | |||||
| chr9:89009522
|
G | A | 1 | a0001c0001t0018 | 2 | HG02258.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3925C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3925 | chr9 | 89009522 | |||||
| chr9:89009555
|
C | G | 1 | a0001c0001t0037 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3892G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3892 | chr9 | 89009555 | |||||
| chr9:89009600
|
C | T | 3 | a0001c0001t0012a0001c0001t0023a0001c0002t0012 | 4 | HG01255.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3847G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3847 | chr9 | 89009600 | |||||
| chr9:89009628
|
C | T | 1 | a0001c0001t0020 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3819G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3819 | chr9 | 89009628 | |||||
| chr9:89009816
|
G | A | 1 | a0001c0001t0025 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3631C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3631 | chr9 | 89009816 | |||||
| chr9:89009864
|
C | T | 1 | a0001c0001t0026 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3583G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3583 | chr9 | 89009864 | |||||
| chr9:89009927
|
A | G | 1 | a0001c0001t0018 | 2 | HG02258.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3520T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3520 | chr9 | 89009927 | |||||
| chr9:89010027
|
A | C | 1 | a0001c0001t0022 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3420T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3420 | chr9 | 89010027 | |||||
| chr9:89010043
|
C | T | 1 | a0001c0003t0045 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3404G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3404 | chr9 | 89010043 | |||||
| chr9:89010090
|
C | T | 1 | a0001c0004t0010 | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3357G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3357 | chr9 | 89010090 | |||||
| chr9:89010158
|
A | G | 2 | a0001c0001t0005a0001c0002t0005 | 10 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3289T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3289 | chr9 | 89010158 | |||||
| chr9:89010312
|
G | A | 1 | a0001c0004t0010 | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3135C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3135 | chr9 | 89010312 | |||||
| chr9:89010320
|
G | A | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*3127C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 3127 | chr9 | 89010320 | |||||
| chr9:89010475
|
G | C | 15 | a0001c0001t0001a0001c0001t0014a0001c0001t0019others(12): Show | 53 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2972C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2972 | chr9 | 89010475 | |||||
| chr9:89010637
|
C | T | 1 | a0001c0001t0036 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2810G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2810 | chr9 | 89010637 | |||||
| chr9:89010926
|
A | G | 15 | a0001c0001t0001a0001c0001t0014a0001c0001t0019others(12): Show | 53 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2521T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2521 | chr9 | 89010926 | |||||
| chr9:89011014
|
T | C | 3 | a0001c0001t0017a0001c0001t0033a0001c0002t0017 | 3 | HG01891.hp1 HG03041.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2433A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2433 | chr9 | 89011014 | |||||
| chr9:89011021
|
T | C | 7 | a0001c0001t0008a0001c0001t0009a0001c0001t0020others(4): Show | 11 | HG01943.hp2 HG02486.hp1 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2426A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2426 | chr9 | 89011021 | |||||
| chr9:89011064
|
C | T | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2383G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2383 | chr9 | 89011064 | |||||
| chr9:89011116
|
T | A | 8 | a0001c0001t0004a0001c0001t0006a0001c0002t0004others(5): Show | 20 | HG00280.hp1 HG00735.hp2 HG01106.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2331A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2331 | chr9 | 89011116 | |||||
| chr9:89011182
|
G | A | 1 | a0001c0001t0042 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2265C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2265 | chr9 | 89011182 | |||||
| chr9:89011198
|
A | G | 1 | a0001c0002t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2249T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2249 | chr9 | 89011198 | |||||
| chr9:89011345
|
C | G | 1 | a0001c0001t0043 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2102 | chr9 | 89011345 | |||||
| chr9:89011410
|
G | T | 1 | a0001c0001t0043 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2037C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 2037 | chr9 | 89011410 | |||||
| chr9:89011783
|
C | T | 3 | a0001c0001t0017a0001c0001t0033a0001c0002t0017 | 3 | HG01891.hp1 HG03041.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 1664 | chr9 | 89011783 | |||||
| chr9:89011855
|
C | T | 1 | a0001c0001t0016 | 2 | HG00738.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1592G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 1592 | chr9 | 89011855 | |||||
| chr9:89012185
|
C | T | 2 | a0001c0001t0006a0001c0002t0006 | 6 | HG00280.hp1 HG00735.hp2 HG01261.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1262G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 1262 | chr9 | 89012185 | |||||
| chr9:89012444
|
T | C | 1 | a0001c0003t0046 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1003A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 1003 | chr9 | 89012444 | |||||
| chr9:89012527
|
C | G | 7 | a0001c0001t0008a0001c0001t0009a0001c0001t0020others(4): Show | 11 | HG01943.hp2 HG02486.hp1 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*920G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 920 | chr9 | 89012527 | |||||
| chr9:89013141
|
C | CT | 14 | a0001c0001t0001a0001c0001t0019a0001c0001t0036others(11): Show | 50 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*305dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 305 | chr9 | 89013141 | |||||
| chr9:89013143
|
TA | T | 10 | a0001c0001t0002a0001c0001t0028a0001c0001t0029others(7): Show | 46 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*303delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 303 | chr9 | 89013143 | |||||
| chr9:89013144
|
A | T | 48 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(45): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*303T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 303 | chr9 | 89013144 | |||||
| chr9:89013167
|
T | C | 19 | a0001c0001t0001a0001c0001t0014a0001c0001t0019others(16): Show | 57 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*280A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 280 | chr9 | 89013167 | |||||
| chr9:89013269
|
C | T | 2 | a0001c0003t0011a0002c0005t0011 | 3 | HG02572.hp2 HG03130.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*178G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 12/12 | 178 | chr9 | 89013269 | |||||
| chr9:89178746
|
G | A | 1 | a0001c0004t0010 | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-286C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/12 | 286 | chr9 | 89178746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:89013631
|
A | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1657-56T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89013631 | ||||||
| chr9:89013669
|
C | T | 2 | a0001c0001t0016g0098a0001c0001t0016g0160 | 2 | HG00738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1657-94G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89013669 | ||||||
| chr9:89013685
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1657-110C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89013685 | ||||||
| chr9:89013935
|
G | T | 1 | a0001c0001t0029g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1657-360C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89013935 | ||||||
| chr9:89014024
|
G | T | 1 | a0001c0002t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1657-449C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014024 | ||||||
| chr9:89014125
|
C | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1657-550G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014125 | ||||||
| chr9:89014358
|
A | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1657-783T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014358 | ||||||
| chr9:89014459
|
C | T | 1 | a0001c0001t0007g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1657-884G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014459 | ||||||
| chr9:89014512
|
C | T | 5 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-937G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014512 | ||||||
| chr9:89014581
|
C | A | 5 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-1006G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014581 | ||||||
| chr9:89014728
|
T | C | 70 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0065others(67): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1657-1153A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014728 | ||||||
| chr9:89014968
|
C | G | 3 | a0001c0001t0017g0076a0001c0001t0033g0037a0001c0002t0017g0031 | 3 | HG01891.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1657-1393G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89014968 | ||||||
| chr9:89015028
|
G | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1657-1453C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89015028 | ||||||
| chr9:89015182
|
C | T | 1 | a0001c0001t0035g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1657-1607G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89015182 | ||||||
| chr9:89015633
|
G | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(30): Show | 36 | HG00099.hp1 HG00408.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1657-2058C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89015633 | ||||||
| chr9:89015653
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1657-2078C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89015653 | ||||||
| chr9:89015738
|
G | A | 10 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(7): Show | 10 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1657-2163C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89015738 | ||||||
| chr9:89015911
|
A | G | 42 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0065others(39): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.1657-2336T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89015911 | ||||||
| chr9:89016162
|
G | C | 3 | a0001c0001t0029g0024a0001c0002t0002g0094a0001c0002t0002g0118 | 3 | HG01167.hp2 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1657-2587C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016162 | ||||||
| chr9:89016298
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1657-2723T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016298 | ||||||
| chr9:89016364
|
C | G | 5 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-2789G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016364 | ||||||
| chr9:89016432
|
A | T | 2 | a0001c0001t0017g0076a0001c0002t0017g0031 | 2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1657-2857T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016432 | ||||||
| chr9:89016447
|
A | T | 1 | a0001c0002t0039g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1657-2872T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016447 | ||||||
| chr9:89016590
|
A | C | 5 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-3015T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016590 | ||||||
| chr9:89016653
|
C | T | 3 | a0001c0001t0017g0076a0001c0001t0033g0037a0001c0002t0017g0031 | 3 | HG01891.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1657-3078G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016653 | ||||||
| chr9:89016708
|
A | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1657-3133T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016708 | ||||||
| chr9:89016889
|
T | C | 2 | a0001c0001t0016g0098a0001c0001t0016g0160 | 2 | HG00738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1657-3314A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016889 | ||||||
| chr9:89016981
|
T | A | 141 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0071others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1657-3406A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89016981 | ||||||
| chr9:89017033
|
G | A | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1657-3458C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89017033 | ||||||
| chr9:89017046
|
C | T | 1 | a0001c0003t0001g0016 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1657-3471G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89017046 | ||||||
| chr9:89017085
|
T | C | 2 | a0001c0002t0002g0140a0001c0006t0024g0168 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1657-3510A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89017085 | ||||||
| chr9:89017216
|
C | G | 1 | a0001c0002t0032g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1657-3641G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89017216 | ||||||
| chr9:89017278
|
C | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1657-3703G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89017278 | ||||||
| chr9:89017396
|
G | A | 5 | a0001c0001t0008g0108a0001c0001t0008g0109a0001c0001t0008g0132others(2): Show | 5 | HG02809.hp2 HG03834.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1657-3821C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89017396 | ||||||
| chr9:89018191
|
C | T | 5 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-4616G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018191 | ||||||
| chr9:89018310
|
TA | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1657-4736delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018310 | ||||||
| chr9:89018400
|
C | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1657-4825G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018400 | ||||||
| chr9:89018432
|
A | C | 1 | a0001c0001t0013g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1657-4857T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018432 | ||||||
| chr9:89018622
|
A | G | 7 | a0001c0001t0006g0060a0001c0002t0004g0135a0001c0002t0006g0002others(4): Show | 8 | HG00280.hp1 HG00735.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657-5047T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018622 | ||||||
| chr9:89018698
|
TC | T | 21 | a0001c0001t0001g0099a0001c0001t0002g0065a0001c0001t0002g0121others(18): Show | 21 | HG00280.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1657-5124delG | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018698 | ||||||
| chr9:89018699
|
C | CTT | 12 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(9): Show | 12 | HG00099.hp2 HG00738.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1657-5126_1657-512 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018699 | ||||||
| chr9:89018699
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1657-5124G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018699 | ||||||
| chr9:89018811
|
T | C | 3 | a0001c0001t0026g0172a0001c0002t0015g0043a0001c0007t0015g0176 | 3 | HG02647.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1657-5236A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018811 | ||||||
| chr9:89018896
|
C | T | 6 | a0001c0001t0002g0103a0001c0001t0002g0116a0001c0002t0002g0119others(3): Show | 6 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1657-5321G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018896 | ||||||
| chr9:89018928
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1657-5353C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018928 | ||||||
| chr9:89018973
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 53 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1657-5398G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89018973 | ||||||
| chr9:89019062
|
G | GA | 5 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-5488dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89019062 | ||||||
| chr9:89019064
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1657-5489T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89019064 | ||||||
| chr9:89019239
|
C | T | 4 | a0001c0001t0003g0115a0001c0002t0003g0052a0001c0002t0003g0056others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1657-5664G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89019239 | ||||||
| chr9:89019868
|
A | G | 2 | a0001c0002t0015g0043a0001c0007t0015g0176 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1657-6293T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89019868 | ||||||
| chr9:89020189
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1657-6614C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020189 | ||||||
| chr9:89020294
|
G | T | 3 | a0001c0001t0013g0093a0001c0001t0013g0105a0001c0001t0013g0112 | 3 | HG02280.hp2 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1657-6719C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020294 | ||||||
| chr9:89020427
|
T | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 56 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1657-6852A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020427 | ||||||
| chr9:89020430
|
T | C | 2 | a0001c0001t0013g0093a0001c0001t0013g0112 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1657-6855A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020430 | ||||||
| chr9:89020501
|
G | A | 1 | a0001c0002t0039g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1657-6926C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020501 | ||||||
| chr9:89020619
|
G | A | 1 | a0001c0001t0025g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1657-7044C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020619 | ||||||
| chr9:89020870
|
C | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0071others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1657-7295G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020870 | ||||||
| chr9:89020905
|
G | T | 3 | a0001c0001t0026g0172a0001c0002t0015g0043a0001c0007t0015g0176 | 3 | HG02647.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1657-7330C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89020905 | ||||||
| chr9:89021165
|
C | T | 14 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(11): Show | 14 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1657-7590G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021165 | ||||||
| chr9:89021345
|
C | T | 2 | a0001c0001t0014g0025a0001c0001t0014g0106 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1657-7770G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021345 | ||||||
| chr9:89021375
|
G | A | 3 | a0001c0001t0017g0076a0001c0001t0033g0037a0001c0002t0017g0031 | 3 | HG01891.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1657-7800C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021375 | ||||||
| chr9:89021394
|
C | A | 2 | a0001c0002t0015g0043a0001c0007t0015g0176 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1657-7819G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021394 | ||||||
| chr9:89021629
|
C | T | 2 | a0001c0001t0018g0046a0001c0001t0018g0144 | 2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1657-8054G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021629 | ||||||
| chr9:89021815
|
T | G | 6 | a0001c0001t0003g0049a0001c0001t0003g0104a0001c0001t0003g0120others(3): Show | 6 | HG02258.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1657-8240A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021815 | ||||||
| chr9:89021910
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 51 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1657-8335G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89021910 | ||||||
| chr9:89022073
|
C | T | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1657-8498G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022073 | ||||||
| chr9:89022139
|
C | A | 4 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0023g0023others(1): Show | 4 | HG01255.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-8564G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022139 | ||||||
| chr9:89022227
|
G | C | 108 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0065others(105): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1657-8652C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022227 | ||||||
| chr9:89022389
|
G | A | 108 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0065others(105): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1657-8814C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022389 | ||||||
| chr9:89022550
|
G | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1657-8975C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022550 | ||||||
| chr9:89022663
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1657-9088C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022663 | ||||||
| chr9:89022678
|
G | A | 1 | a0001c0002t0039g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1657-9103C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022678 | ||||||
| chr9:89022718
|
A | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1657-9143T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022718 | ||||||
| chr9:89022921
|
C | G | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1657-9346G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022921 | ||||||
| chr9:89022996
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1657-9421A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89022996 | ||||||
| chr9:89023063
|
C | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1657-9488G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023063 | ||||||
| chr9:89023106
|
C | A | 3 | a0001c0001t0017g0076a0001c0001t0033g0037a0001c0002t0017g0031 | 3 | HG01891.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1657-9531G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023106 | ||||||
| chr9:89023297
|
C | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1657-9722G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023297 | ||||||
| chr9:89023705
|
G | A | 3 | a0001c0001t0026g0172a0001c0002t0015g0043a0001c0007t0015g0176 | 3 | HG02647.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1657-10130C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023705 | ||||||
| chr9:89023833
|
C | T | 9 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(6): Show | 9 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1657-10258G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023833 | ||||||
| chr9:89023923
|
T | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0030g0122 | 4 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1657-10348A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023923 | ||||||
| chr9:89023956
|
C | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 67 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1657-10381G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89023956 | ||||||
| chr9:89024007
|
C | G | 1 | a0001c0003t0004g0013 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1657-10432G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024007 | ||||||
| chr9:89024436
|
C | A | 9 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(6): Show | 9 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1657-10861G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024436 | ||||||
| chr9:89024570
|
C | T | 2 | a0001c0001t0004g0066a0001c0001t0004g0069 | 2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1657-10995G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024570 | ||||||
| chr9:89024592
|
C | T | 1 | a0001c0003t0001g0016 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1657-11017G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024592 | ||||||
| chr9:89024612
|
C | T | 2 | a0001c0001t0016g0098a0001c0001t0016g0160 | 2 | HG00738.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1657-11037G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024612 | ||||||
| chr9:89024661
|
G | A | 1 | a0001c0006t0004g0169 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1657-11086C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024661 | ||||||
| chr9:89024873
|
G | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 66 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1657-11298C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024873 | ||||||
| chr9:89024995
|
C | T | 4 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0023g0023others(1): Show | 4 | HG01255.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-11420G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89024995 | ||||||
| chr9:89025112
|
A | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1657-11537T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025112 | ||||||
| chr9:89025143
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(46): Show | 52 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1657-11568G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025143 | ||||||
| chr9:89025169
|
A | G | 12 | a0001c0001t0008g0108a0001c0001t0008g0109a0001c0001t0008g0132others(9): Show | 12 | HG01943.hp2 HG02486.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1657-11594T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025169 | ||||||
| chr9:89025194
|
TCA | T | 176 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1657-11621_1657-11 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025194 | ||||||
| chr9:89025411
|
C | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1657-11836G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025411 | ||||||
| chr9:89025484
|
T | C | 2 | a0001c0001t0014g0025a0001c0001t0014g0106 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1657-11909A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025484 | ||||||
| chr9:89025588
|
TG | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 53 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1657-12014delC | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025588 | ||||||
| chr9:89025598
|
T | A | 1 | a0001c0001t0037g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1657-12023A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025598 | ||||||
| chr9:89025628
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 53 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1657-12053G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025628 | ||||||
| chr9:89025959
|
A | G | 14 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(11): Show | 14 | HG00099.hp2 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1656+12034T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025959 | ||||||
| chr9:89025981
|
C | T | 3 | a0001c0001t0028g0139a0001c0002t0003g0091a0001c0002t0009g0082 | 3 | HG02486.hp1 HG03130.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1656+12012G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89025981 | ||||||
| chr9:89026018
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1656+11975G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026018 | ||||||
| chr9:89026235
|
CAA | C | 3 | a0001c0001t0014g0025a0001c0001t0014g0106a0001c0001t0043g0077 | 3 | HG01884.hp2 HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1656+11756_1656+11 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026235 | ||||||
| chr9:89026254
|
CA | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 82 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1656+11738delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026254 | ||||||
| chr9:89026254
|
CAA | C | 50 | a0001c0001t0002g0068a0001c0001t0002g0103a0001c0001t0002g0116others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1656+11737_1656+11 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026254 | ||||||
| chr9:89026254
|
CAAA | C | 11 | a0001c0001t0002g0130a0001c0001t0006g0060a0001c0001t0009g0096others(8): Show | 12 | HG00280.hp1 HG00735.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1656+11736_1656+11 others(9): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026254 | ||||||
| chr9:89026254
|
CAAAA | C | 8 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(5): Show | 9 | HG00741.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1656+11735_1656+11 others(10): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026254 | ||||||
| chr9:89026603
|
C | T | 6 | a0001c0001t0004g0038a0001c0001t0005g0145a0001c0001t0005g0171others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+11390G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026603 | ||||||
| chr9:89026648
|
C | T | 21 | a0001c0001t0004g0038a0001c0001t0005g0145a0001c0001t0005g0171others(18): Show | 22 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1656+11345G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026648 | ||||||
| chr9:89026972
|
T | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(54): Show | 59 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1656+11021A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89026972 | ||||||
| chr9:89027162
|
G | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(6): Show | 10 | HG00741.hp2 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1656+10831C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027162 | ||||||
| chr9:89027251
|
G | A | 8 | a0001c0001t0002g0065a0001c0001t0004g0069a0001c0003t0001g0016others(5): Show | 8 | HG00741.hp1 HG01258.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1656+10742C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027251 | ||||||
| chr9:89027327
|
A | ATTTTTTT others(3): Show |
10 | a0001c0001t0004g0069a0001c0001t0026g0172a0001c0001t0033g0037others(7): Show | 10 | HG00741.hp1 HG01358.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1656+10656_1656+10 others(16): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027327 | ||||||
| chr9:89027327
|
A | ATTTTTTT others(4): Show |
29 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(26): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1656+10655_1656+10 others(17): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027327 | ||||||
| chr9:89027327
|
A | ATTTTTTT others(5): Show |
13 | a0001c0001t0001g0062a0001c0001t0008g0109a0001c0001t0009g0161others(10): Show | 13 | HG01109.hp2 HG01169.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1656+10654_1656+10 others(18): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027327 | ||||||
| chr9:89027327
|
A | ATTTTTTT others(6): Show |
29 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(26): Show | 29 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1656+10665_1656+10 others(19): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027327 | ||||||
| chr9:89027327
|
A | ATTTTTTT others(7): Show |
9 | a0001c0001t0003g0075a0001c0001t0012g0040a0001c0001t0012g0041others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+10665_1656+10 others(20): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027327 | ||||||
| chr9:89027327
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0007g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1656+10665_1656+10 others(21): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027327 | ||||||
| chr9:89027462
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1656+10531T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027462 | ||||||
| chr9:89027550
|
T | C | 8 | a0001c0001t0001g0062a0001c0001t0002g0004a0001c0001t0002g0121others(5): Show | 9 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+10443A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027550 | ||||||
| chr9:89027567
|
A | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1656+10426T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027567 | ||||||
| chr9:89027568
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1656+10425C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027568 | ||||||
| chr9:89027594
|
GCATAAGC | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1656+10392_1656+10 others(13): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027594 | ||||||
| chr9:89027703
|
G | A | 8 | a0001c0001t0001g0062a0001c0001t0002g0004a0001c0001t0002g0121others(5): Show | 9 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+10290C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027703 | ||||||
| chr9:89027844
|
G | A | 1 | a0001c0002t0015g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1656+10149C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89027844 | ||||||
| chr9:89028067
|
C | T | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+9926G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028067 | ||||||
| chr9:89028178
|
C | T | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+9815G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028178 | ||||||
| chr9:89028244
|
T | C | 2 | a0001c0002t0002g0094a0001c0002t0002g0118 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1656+9749A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028244 | ||||||
| chr9:89028251
|
G | T | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+9742C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028251 | ||||||
| chr9:89028280
|
T | C | 1 | a0001c0002t0003g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1656+9713A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028280 | ||||||
| chr9:89028431
|
T | C | 1 | a0001c0002t0002g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1656+9562A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028431 | ||||||
| chr9:89028459
|
T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(39): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1656+9534A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028459 | ||||||
| chr9:89028471
|
GATATAGA others(24): Show |
G | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1656+9491_1656+952 others(35): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028471 | ||||||
| chr9:89028610
|
C | CTATA | 42 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(39): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1656+9379_1656+938 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028610 | ||||||
| chr9:89028689
|
CTATATCT others(42): Show |
C | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+9255_1656+930 others(53): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028689 | ||||||
| chr9:89028730
|
T | G | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1656+9263A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028730 | ||||||
| chr9:89028731
|
ATTC | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1656+9259_1656+926 others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028731 | ||||||
| chr9:89028736
|
C | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1656+9257G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028736 | ||||||
| chr9:89028745
|
T | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1656+9248A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028745 | ||||||
| chr9:89028759
|
A | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(56): Show | 62 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1656+9234T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028759 | ||||||
| chr9:89028821
|
C | CAT | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1656+9170_1656+917 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028821 | ||||||
| chr9:89028931
|
CT | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0164others(5): Show | 9 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+9061delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028931 | ||||||
| chr9:89028965
|
C | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(54): Show | 59 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1656+9028G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89028965 | ||||||
| chr9:89029006
|
TAG | T | 11 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(8): Show | 11 | HG00741.hp2 HG02258.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1656+8985_1656+898 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029006 | ||||||
| chr9:89029199
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1656+8794A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029199 | ||||||
| chr9:89029275
|
G | C | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+8718C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029275 | ||||||
| chr9:89029380
|
T | A | 1 | a0001c0001t0002g0116 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1656+8613A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029380 | ||||||
| chr9:89029391
|
A | T | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1656+8602T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029391 | ||||||
| chr9:89029482
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0162 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1656+8511G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029482 | ||||||
| chr9:89029532
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1656+8461A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029532 | ||||||
| chr9:89029552
|
A | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1656+8441T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029552 | ||||||
| chr9:89029596
|
C | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1656+8397G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029596 | ||||||
| chr9:89029641
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1656+8352C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029641 | ||||||
| chr9:89029750
|
C | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1656+8243G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029750 | ||||||
| chr9:89029999
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1656+7994G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89029999 | ||||||
| chr9:89030160
|
G | T | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+7833C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89030160 | ||||||
| chr9:89030201
|
C | T | 6 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+7792G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89030201 | ||||||
| chr9:89030462
|
C | T | 2 | a0001c0002t0002g0119a0001c0002t0038g0095 | 2 | HG01167.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1656+7531G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89030462 | ||||||
| chr9:89030660
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1656+7333A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89030660 | ||||||
| chr9:89030790
|
G | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(75): Show | 82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1656+7203C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89030790 | ||||||
| chr9:89030882
|
A | G | 1 | a0001c0002t0015g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1656+7111T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89030882 | ||||||
| chr9:89031529
|
A | G | 6 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1656+6464T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031529 | ||||||
| chr9:89031530
|
T | C | 1 | a0001c0002t0004g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1656+6463A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031530 | ||||||
| chr9:89031664
|
C | A | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+6329G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031664 | ||||||
| chr9:89031666
|
T | A | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+6327A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031666 | ||||||
| chr9:89031674
|
A | G | 8 | a0001c0001t0001g0062a0001c0001t0002g0004a0001c0001t0002g0121others(5): Show | 9 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+6319T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031674 | ||||||
| chr9:89031747
|
TG | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1656+6245delC | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031747 | ||||||
| chr9:89031904
|
G | T | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1656+6089C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89031904 | ||||||
| chr9:89032006
|
C | T | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+5987G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032006 | ||||||
| chr9:89032041
|
G | A | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+5952C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032041 | ||||||
| chr9:89032093
|
C | A | 1 | a0001c0001t0014g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1656+5900G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032093 | ||||||
| chr9:89032392
|
A | G | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1656+5601T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032392 | ||||||
| chr9:89032674
|
C | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1656+5319G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032674 | ||||||
| chr9:89032703
|
T | G | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+5290A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032703 | ||||||
| chr9:89032914
|
T | C | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+5079A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032914 | ||||||
| chr9:89032968
|
C | T | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+5025G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89032968 | ||||||
| chr9:89033007
|
C | CA | 57 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(54): Show | 59 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1656+4985dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033007 | ||||||
| chr9:89033024
|
CA | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0164others(19): Show | 24 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1656+4968delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033024 | ||||||
| chr9:89033025
|
A | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1656+4968T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033025 | ||||||
| chr9:89033277
|
A | T | 1 | a0001c0001t0041g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1656+4716T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033277 | ||||||
| chr9:89033578
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1656+4415C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033578 | ||||||
| chr9:89033717
|
C | A | 6 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+4276G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033717 | ||||||
| chr9:89033784
|
A | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1656+4209T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033784 | ||||||
| chr9:89033865
|
T | C | 1 | a0001c0001t0023g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1656+4128A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89033865 | ||||||
| chr9:89034076
|
T | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(51): Show | 56 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1656+3917A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034076 | ||||||
| chr9:89034346
|
A | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1656+3647T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034346 | ||||||
| chr9:89034426
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0104a0001c0001t0013g0105others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+3567A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034426 | ||||||
| chr9:89034636
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1656+3357G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034636 | ||||||
| chr9:89034702
|
C | G | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+3291G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034702 | ||||||
| chr9:89034757
|
A | C | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+3236T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034757 | ||||||
| chr9:89034797
|
C | T | 2 | a0001c0001t0002g0065a0001c0001t0004g0123 | 2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1656+3196G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034797 | ||||||
| chr9:89034880
|
G | A | 8 | a0001c0001t0001g0062a0001c0001t0002g0004a0001c0001t0002g0121others(5): Show | 9 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+3113C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034880 | ||||||
| chr9:89034982
|
C | T | 1 | a0001c0001t0008g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1656+3011G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89034982 | ||||||
| chr9:89035056
|
C | T | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+2937G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035056 | ||||||
| chr9:89035086
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1656+2907C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035086 | ||||||
| chr9:89035113
|
C | T | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+2880G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035113 | ||||||
| chr9:89035121
|
A | G | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1656+2872T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035121 | ||||||
| chr9:89035128
|
T | C | 2 | a0001c0001t0041g0174a0001c0001t0042g0079 | 2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1656+2865A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035128 | ||||||
| chr9:89035376
|
AT | A | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+2616delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035376 | ||||||
| chr9:89035413
|
G | A | 1 | a0001c0002t0008g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1656+2580C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035413 | ||||||
| chr9:89035477
|
A | C | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+2516T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035477 | ||||||
| chr9:89035662
|
C | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1656+2331G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035662 | ||||||
| chr9:89035764
|
C | T | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+2229G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035764 | ||||||
| chr9:89035771
|
A | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1656+2222T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035771 | ||||||
| chr9:89035830
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1656+2149_1656+216 others(18): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035830 | ||||||
| chr9:89035830
|
A | AATATATA others(9): Show |
1 | a0001c0001t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1656+2147_1656+216 others(20): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035830 | ||||||
| chr9:89035830
|
A | AATATATA others(11): Show |
1 | a0001c0001t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1656+2145_1656+216 others(22): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035830 | ||||||
| chr9:89035830
|
A | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0110 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1656+2163T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035830 | ||||||
| chr9:89035848
|
TAG | T | 2 | a0001c0001t0003g0149a0001c0001t0028g0139 | 2 | HG01168.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1656+2143_1656+214 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035848 | ||||||
| chr9:89035849
|
AGATG | A | 26 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(23): Show | 26 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1656+2140_1656+214 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035849 | ||||||
| chr9:89035850
|
G | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1656+2143C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035850 | ||||||
| chr9:89035851
|
A | ATG | 6 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(3): Show | 6 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+2140_1656+214 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035851 | ||||||
| chr9:89035851
|
ATG | A | 35 | a0001c0001t0001g0163a0001c0001t0004g0069a0001c0001t0033g0037others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1656+2140_1656+214 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035851 | ||||||
| chr9:89035851
|
ATGTG | A | 8 | a0001c0001t0004g0038a0001c0002t0002g0039a0001c0002t0003g0056others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1656+2138_1656+214 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035851 | ||||||
| chr9:89035851
|
ATGTGTG | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0007g0150others(4): Show | 8 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1656+2136_1656+214 others(10): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035851 | ||||||
| chr9:89035851
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1656+2132_1656+214 others(14): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035851 | ||||||
| chr9:89035851
|
ATGTGTGT others(5): Show |
A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0002g0130 | 3 | HG00639.hp2 HG01243.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1656+2130_1656+214 others(16): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035851 | ||||||
| chr9:89035853
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1656+2140C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035853 | ||||||
| chr9:89035854
|
T | TATATATA others(5): Show |
1 | a0001c0006t0024g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1656+2138_1656+213 others(16): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035854 | ||||||
| chr9:89035855
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1656+2138C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035855 | ||||||
| chr9:89035856
|
T | G | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+2137A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035856 | ||||||
| chr9:89035856
|
T | TATATATA others(5): Show |
4 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0016g0160others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+2136_1656+213 others(16): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035856 | ||||||
| chr9:89035856
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0162 | 3 | HG03491.hp2 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1656+2136_1656+213 others(18): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035856 | ||||||
| chr9:89035857
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1656+2136C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035857 | ||||||
| chr9:89035858
|
T | TATAG | 4 | a0001c0004t0001g0034a0001c0004t0010g0180a0001c0004t0010g0181others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+2134_1656+213 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035858 | ||||||
| chr9:89035859
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(87): Show | 92 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1656+2134C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035859 | ||||||
| chr9:89035860
|
T | G | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1656+2133A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035860 | ||||||
| chr9:89035861
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(82): Show | 87 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1656+2132C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035861 | ||||||
| chr9:89035862
|
T | G | 28 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(25): Show | 28 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1656+2131A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035862 | ||||||
| chr9:89035862
|
T | TAG | 24 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1656+2130_1656+213 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035862 | ||||||
| chr9:89035862
|
T | TATAG | 18 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 19 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1656+2130_1656+213 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035862 | ||||||
| chr9:89035862
|
T | TATATAG | 6 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0001g0170others(3): Show | 6 | HG01255.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1656+2130_1656+213 others(10): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035862 | ||||||
| chr9:89035862
|
T | TATATATA others(1): Show |
5 | a0001c0001t0001g0003a0001c0001t0003g0074a0001c0001t0009g0096others(2): Show | 6 | HG01943.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+2130_1656+213 others(12): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035862 | ||||||
| chr9:89035863
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(79): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1656+2130C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035863 | ||||||
| chr9:89035864
|
T | G | 1 | a0001c0001t0035g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1656+2129A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035864 | ||||||
| chr9:89035865
|
G | A | 1 | a0001c0001t0035g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1656+2128C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035865 | ||||||
| chr9:89035889
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1656+2104C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89035889 | ||||||
| chr9:89036223
|
A | G | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+1770T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036223 | ||||||
| chr9:89036377
|
G | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1656+1616C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036377 | ||||||
| chr9:89036506
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656+1487C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036506 | ||||||
| chr9:89036936
|
TA | T | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1656+1056delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036936 | ||||||
| chr9:89036963
|
T | TA | 66 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0099others(63): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1656+1029dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036963 | ||||||
| chr9:89036963
|
T | TAA | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(79): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1656+1028_1656+102 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036963 | ||||||
| chr9:89036963
|
T | TAAA | 7 | a0001c0001t0005g0145a0001c0001t0005g0171a0001c0004t0001g0034others(4): Show | 7 | HG02647.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1656+1027_1656+102 others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89036963 | ||||||
| chr9:89037188
|
C | A | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+805G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037188 | ||||||
| chr9:89037281
|
C | T | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1656+712G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037281 | ||||||
| chr9:89037320
|
A | G | 32 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(29): Show | 32 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1656+673T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037320 | ||||||
| chr9:89037499
|
A | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1656+494T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037499 | ||||||
| chr9:89037500
|
T | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1656+493A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037500 | ||||||
| chr9:89037501
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1656+492C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037501 | ||||||
| chr9:89037532
|
C | G | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1656+461G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037532 | ||||||
| chr9:89037623
|
C | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0004others(42): Show | 47 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1656+370G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037623 | ||||||
| chr9:89037822
|
C | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1656+171G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037822 | ||||||
| chr9:89037883
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0164others(5): Show | 9 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.1656+110C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037883 | ||||||
| chr9:89037892
|
G | A | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1656+101C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037892 | ||||||
| chr9:89037944
|
A | G | 1 | a0001c0002t0001g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1656+49T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 11/11 | chr9 | 89037944 | ||||||
| chr9:89038342
|
TA | T | 49 | a0001c0001t0001g0163a0001c0001t0003g0049a0001c0001t0043g0077others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1361-55delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038342 | ||||||
| chr9:89038342
|
TAAA | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(70): Show | 77 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1361-57_1361-55del others(3): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038342 | ||||||
| chr9:89038342
|
TAAAA | T | 9 | a0001c0001t0001g0089a0001c0001t0001g0099a0001c0001t0001g0100others(6): Show | 9 | HG00099.hp2 HG01175.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-58_1361-55del others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038342 | ||||||
| chr9:89038358
|
A | T | 1 | a0001c0002t0004g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1361-70T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038358 | ||||||
| chr9:89038372
|
G | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1361-84C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038372 | ||||||
| chr9:89038716
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1361-428G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038716 | ||||||
| chr9:89038776
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1361-488A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038776 | ||||||
| chr9:89038834
|
G | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1361-546C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038834 | ||||||
| chr9:89038893
|
A | T | 2 | a0001c0001t0003g0075a0001c0001t0003g0090 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1361-605T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89038893 | ||||||
| chr9:89039063
|
C | G | 1 | a0001c0001t0002g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1361-775G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89039063 | ||||||
| chr9:89039167
|
C | A | 1 | a0001c0001t0013g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1361-879G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89039167 | ||||||
| chr9:89039202
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(39): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1361-914C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89039202 | ||||||
| chr9:89039475
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0044others(39): Show | 43 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1361-1187G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89039475 | ||||||
| chr9:89039548
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1361-1260C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89039548 | ||||||
| chr9:89039623
|
G | A | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1361-1335C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89039623 | ||||||
| chr9:89040229
|
C | CATCATCA others(291): Show |
5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(302): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(291): Show |
13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(302): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(291): Show |
114 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(111): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(302): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(315): Show |
33 | a0001c0001t0001g0062a0001c0001t0002g0044a0001c0001t0002g0107others(30): Show | 33 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(326): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(291): Show |
2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(302): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(291): Show |
9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(302): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(291): Show |
4 | a0001c0001t0003g0120a0001c0001t0005g0145a0001c0001t0005g0171others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+1796_1360+179 others(302): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040229
|
C | CATCATCA others(288): Show |
1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1360+1796_1360+179 others(299): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040229 | ||||||
| chr9:89040288
|
T | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(65): Show | 70 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1360+1738A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040288 | ||||||
| chr9:89040325
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG01257.hp1 HG01258.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1360+1701A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040325 | ||||||
| chr9:89040499
|
A | T | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+1527T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040499 | ||||||
| chr9:89040527
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1360+1499G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040527 | ||||||
| chr9:89040664
|
A | G | 1 | a0001c0002t0021g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1360+1362T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040664 | ||||||
| chr9:89040678
|
G | T | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1360+1348C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040678 | ||||||
| chr9:89040731
|
G | A | 1 | a0001c0001t0043g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1360+1295C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040731 | ||||||
| chr9:89040756
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1360+1270T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040756 | ||||||
| chr9:89040929
|
C | T | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1360+1097G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040929 | ||||||
| chr9:89040952
|
A | T | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1360+1074T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040952 | ||||||
| chr9:89040962
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1360+1064G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89040962 | ||||||
| chr9:89041042
|
G | A | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1360+984C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89041042 | ||||||
| chr9:89041145
|
G | A | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1360+881C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89041145 | ||||||
| chr9:89041331
|
C | T | 2 | a0001c0001t0004g0061a0001c0001t0006g0060 | 2 | HG01106.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1360+695G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89041331 | ||||||
| chr9:89041489
|
T | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1360+537A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89041489 | ||||||
| chr9:89041642
|
G | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1360+384C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89041642 | ||||||
| chr9:89041928
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(20): Show | 25 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1360+98T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 10/11 | chr9 | 89041928 | ||||||
| chr9:89042268
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1202-84G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89042268 | ||||||
| chr9:89042507
|
C | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(57): Show | 63 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1202-323G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89042507 | ||||||
| chr9:89042785
|
G | C | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1202-601C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89042785 | ||||||
| chr9:89042959
|
C | G | 1 | a0001c0001t0044g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1202-775G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89042959 | ||||||
| chr9:89043000
|
G | A | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1202-816C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043000 | ||||||
| chr9:89043088
|
G | A | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-904C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043088 | ||||||
| chr9:89043360
|
C | T | 4 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-1176G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043360 | ||||||
| chr9:89043534
|
C | T | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0004g0061others(3): Show | 6 | HG01106.hp2 HG03017.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202-1350G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043534 | ||||||
| chr9:89043583
|
A | G | 67 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(64): Show | 70 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1202-1399T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043583 | ||||||
| chr9:89043596
|
G | T | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1202-1412C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043596 | ||||||
| chr9:89043656
|
T | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(143): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1202-1472A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043656 | ||||||
| chr9:89043657
|
T | A | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1202-1473A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043657 | ||||||
| chr9:89043660
|
T | A | 72 | a0001c0001t0001g0129a0001c0001t0002g0044a0001c0001t0002g0107others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1202-1476A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043660 | ||||||
| chr9:89043661
|
T | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1202-1477A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043661 | ||||||
| chr9:89043664
|
T | A | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1202-1480A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043664 | ||||||
| chr9:89043759
|
TCTC | T | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202-1578_1202-157 others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043759 | ||||||
| chr9:89043831
|
T | A | 2 | a0001c0001t0017g0076a0001c0001t0022g0042 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1202-1647A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043831 | ||||||
| chr9:89043866
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0145a0001c0001t0005g0171 | 3 | HG02647.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1202-1682G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043866 | ||||||
| chr9:89043871
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202-1687T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043871 | ||||||
| chr9:89043901
|
G | A | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1202-1717C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89043901 | ||||||
| chr9:89044086
|
G | A | 67 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(64): Show | 70 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1201+1660C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89044086 | ||||||
| chr9:89044146
|
G | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(20): Show | 25 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1201+1600C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89044146 | ||||||
| chr9:89044459
|
T | C | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201+1287A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89044459 | ||||||
| chr9:89044603
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0016g0160 | 2 | HG00738.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1201+1143C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89044603 | ||||||
| chr9:89044697
|
C | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1201+1049G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89044697 | ||||||
| chr9:89044872
|
C | G | 6 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(3): Show | 7 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1201+874G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89044872 | ||||||
| chr9:89045001
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1201+745C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045001 | ||||||
| chr9:89045153
|
T | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1201+593A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045153 | ||||||
| chr9:89045206
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1201+540C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045206 | ||||||
| chr9:89045223
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(58): Show | 63 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1201+523C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045223 | ||||||
| chr9:89045237
|
G | A | 1 | a0001c0002t0003g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1201+509C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045237 | ||||||
| chr9:89045243
|
T | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(64): Show | 70 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1201+503A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045243 | ||||||
| chr9:89045279
|
C | CT | 47 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(44): Show | 48 | HG00741.hp2 HG01070.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1201+466dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045279 | ||||||
| chr9:89045279
|
C | CTT | 15 | a0001c0001t0003g0149a0001c0001t0003g0151a0001c0003t0001g0009others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1201+465_1201+466d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045279 | ||||||
| chr9:89045279
|
CT | C | 6 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201+466delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045279 | ||||||
| chr9:89045565
|
G | A | 37 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(34): Show | 38 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1201+181C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045565 | ||||||
| chr9:89045567
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1201+179C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 9/11 | chr9 | 89045567 | ||||||
| chr9:89045916
|
G | A | 2 | a0001c0001t0012g0040a0001c0001t0012g0041 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1114-83C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89045916 | ||||||
| chr9:89045923
|
T | A | 1 | a0001c0002t0021g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1114-90A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89045923 | ||||||
| chr9:89046054
|
C | T | 1 | a0001c0002t0032g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1114-221G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89046054 | ||||||
| chr9:89046073
|
A | AC | 15 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0002g0164others(12): Show | 15 | HG00280.hp2 HG01106.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1114-241dupG | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89046073 | ||||||
| chr9:89046159
|
A | G | 29 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(26): Show | 29 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1114-326T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89046159 | ||||||
| chr9:89046271
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1114-438G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89046271 | ||||||
| chr9:89046527
|
T | C | 1 | a0001c0002t0038g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1113+317A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89046527 | ||||||
| chr9:89046831
|
C | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1113+13G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 8/11 | chr9 | 89046831 | ||||||
| chr9:89047339
|
C | A | 2 | a0001c0003t0001g0012a0001c0003t0002g0001 | 3 | HG01070.hp2 HG01071.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.963-345G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89047339 | ||||||
| chr9:89047536
|
G | A | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.963-542C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89047536 | ||||||
| chr9:89047610
|
T | C | 1 | a0001c0001t0017g0076 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.963-616A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89047610 | ||||||
| chr9:89047619
|
A | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.963-625T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89047619 | ||||||
| chr9:89047640
|
T | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.963-646A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89047640 | ||||||
| chr9:89047799
|
T | A | 5 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(2): Show | 5 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.963-805A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89047799 | ||||||
| chr9:89048016
|
C | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.963-1022G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048016 | ||||||
| chr9:89048021
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.963-1027T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048021 | ||||||
| chr9:89048047
|
C | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(2): Show | 6 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.963-1053G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048047 | ||||||
| chr9:89048241
|
T | TAA | 58 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.963-1249_963-1248d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048241 | ||||||
| chr9:89048241
|
T | TAAA | 20 | a0001c0001t0001g0129a0001c0001t0009g0096a0001c0001t0013g0112others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.963-1250_963-1248d others(5): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048241 | ||||||
| chr9:89048241
|
T | TAAAA | 5 | a0001c0002t0001g0158a0001c0002t0002g0159a0001c0002t0003g0056others(2): Show | 5 | HG01169.hp2 HG01243.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.963-1251_963-1248d others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048241 | ||||||
| chr9:89048241
|
TA | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(56): Show | 61 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.963-1248delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048241 | ||||||
| chr9:89048241
|
TAA | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(3): Show | 7 | HG01358.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.963-1249_963-1248d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048241 | ||||||
| chr9:89048258
|
G | T | 24 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.963-1264C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048258 | ||||||
| chr9:89048422
|
C | A | 1 | a0001c0002t0001g0141 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.963-1428G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048422 | ||||||
| chr9:89048765
|
T | C | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.963-1771A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048765 | ||||||
| chr9:89048984
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.963-1990C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89048984 | ||||||
| chr9:89049090
|
T | C | 2 | a0001c0001t0003g0075a0001c0001t0003g0090 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.963-2096A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049090 | ||||||
| chr9:89049261
|
A | AAAAAC | 13 | a0001c0001t0001g0062a0001c0001t0002g0136a0001c0001t0005g0026others(10): Show | 13 | HG00323.hp2 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.963-2272_963-2268d others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049261 | ||||||
| chr9:89049261
|
AAAAAC | A | 26 | a0001c0001t0029g0024a0001c0002t0001g0155a0001c0002t0001g0156others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.963-2272_963-2268d others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049261 | ||||||
| chr9:89049261
|
AAAAACAA others(3): Show |
A | 4 | a0001c0001t0001g0089a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG00099.hp2 HG01175.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.963-2277_963-2268d others(12): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049261 | ||||||
| chr9:89049291
|
C | CAAAAT | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.963-2298_963-2297i others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049291 | ||||||
| chr9:89049291
|
C | T | 55 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(52): Show | 57 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.963-2297G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049291 | ||||||
| chr9:89049343
|
A | G | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.963-2349T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049343 | ||||||
| chr9:89049402
|
C | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.963-2408G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049402 | ||||||
| chr9:89049449
|
A | G | 1 | a0001c0001t0013g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.963-2455T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049449 | ||||||
| chr9:89049550
|
T | A | 1 | a0001c0002t0031g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.962+2487A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049550 | ||||||
| chr9:89049798
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.962+2239A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049798 | ||||||
| chr9:89049901
|
G | T | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG00408.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.962+2136C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89049901 | ||||||
| chr9:89050058
|
G | A | 1 | a0001c0001t0036g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.962+1979C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050058 | ||||||
| chr9:89050072
|
T | C | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.962+1965A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050072 | ||||||
| chr9:89050177
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0162 | 3 | HG03491.hp2 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.962+1860C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050177 | ||||||
| chr9:89050355
|
A | G | 26 | a0001c0001t0029g0024a0001c0002t0001g0155a0001c0002t0001g0156others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.962+1682T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050355 | ||||||
| chr9:89050485
|
T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.962+1552A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050485 | ||||||
| chr9:89050549
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.962+1488C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050549 | ||||||
| chr9:89050726
|
T | C | 15 | a0001c0001t0004g0069a0001c0001t0026g0172a0001c0003t0001g0009others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.962+1311A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050726 | ||||||
| chr9:89050899
|
C | T | 5 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(2): Show | 5 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.962+1138G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050899 | ||||||
| chr9:89050903
|
C | CT | 54 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(51): Show | 56 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.962+1133dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050903 | ||||||
| chr9:89050903
|
C | CTT | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.962+1132_962+1133d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050903 | ||||||
| chr9:89050996
|
G | A | 1 | a0001c0001t0014g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.962+1041C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89050996 | ||||||
| chr9:89051470
|
T | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.962+567A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89051470 | ||||||
| chr9:89051505
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.962+532A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89051505 | ||||||
| chr9:89051572
|
A | G | 27 | a0001c0001t0026g0172a0001c0001t0029g0024a0001c0002t0001g0155others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.962+465T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89051572 | ||||||
| chr9:89051701
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.962+336T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89051701 | ||||||
| chr9:89051897
|
C | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(117): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.962+140G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 7/11 | chr9 | 89051897 | ||||||
| chr9:89052221
|
C | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(117): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.836-58G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89052221 | ||||||
| chr9:89052515
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(2): Show | 6 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-352G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89052515 | ||||||
| chr9:89052664
|
G | A | 1 | a0001c0002t0039g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.836-501C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89052664 | ||||||
| chr9:89052769
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-606C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89052769 | ||||||
| chr9:89052855
|
G | A | 1 | a0001c0001t0008g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.836-692C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89052855 | ||||||
| chr9:89052879
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.836-716C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89052879 | ||||||
| chr9:89053025
|
T | G | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.836-862A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053025 | ||||||
| chr9:89053111
|
A | G | 1 | a0001c0001t0008g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.836-948T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053111 | ||||||
| chr9:89053364
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-1201G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053364 | ||||||
| chr9:89053368
|
A | G | 7 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.836-1205T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053368 | ||||||
| chr9:89053369
|
T | C | 1 | a0001c0006t0024g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.836-1206A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053369 | ||||||
| chr9:89053870
|
G | T | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-1707C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053870 | ||||||
| chr9:89053926
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-1763G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053926 | ||||||
| chr9:89053933
|
C | T | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-1770G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89053933 | ||||||
| chr9:89054174
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.836-2011C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89054174 | ||||||
| chr9:89054263
|
C | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.836-2100G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89054263 | ||||||
| chr9:89054447
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.836-2284T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89054447 | ||||||
| chr9:89054455
|
A | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.836-2292T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89054455 | ||||||
| chr9:89054967
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-2804C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89054967 | ||||||
| chr9:89055032
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-2869C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055032 | ||||||
| chr9:89055346
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-3183C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055346 | ||||||
| chr9:89055358
|
T | C | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-3195A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055358 | ||||||
| chr9:89055401
|
C | A | 3 | a0001c0001t0003g0120a0001c0001t0005g0145a0001c0001t0005g0171 | 3 | HG02647.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.836-3238G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055401 | ||||||
| chr9:89055450
|
G | A | 4 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-3287C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055450 | ||||||
| chr9:89055484
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.836-3321A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055484 | ||||||
| chr9:89055890
|
C | A | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-3727G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89055890 | ||||||
| chr9:89056269
|
G | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(99): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.836-4106C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056269 | ||||||
| chr9:89056310
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0030g0122 | 4 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.836-4147C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056310 | ||||||
| chr9:89056363
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-4200G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056363 | ||||||
| chr9:89056371
|
C | T | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.836-4208G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056371 | ||||||
| chr9:89056627
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.836-4464G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056627 | ||||||
| chr9:89056698
|
G | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.836-4535C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056698 | ||||||
| chr9:89056710
|
T | G | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.836-4547A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056710 | ||||||
| chr9:89056859
|
C | T | 4 | a0001c0002t0006g0002a0001c0002t0006g0059a0001c0002t0006g0173others(1): Show | 5 | HG00280.hp1 HG00642.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-4696G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056859 | ||||||
| chr9:89056880
|
G | A | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-4717C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056880 | ||||||
| chr9:89056891
|
A | T | 2 | a0001c0004t0010g0179a0001c0004t0010g0180 | 2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.836-4728T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89056891 | ||||||
| chr9:89057061
|
G | A | 1 | a0001c0001t0007g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.836-4898C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057061 | ||||||
| chr9:89057202
|
C | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.836-5039G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057202 | ||||||
| chr9:89057286
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(17): Show | 21 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.836-5123G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057286 | ||||||
| chr9:89057315
|
CT | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(60): Show | 65 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.836-5153delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057315 | ||||||
| chr9:89057315
|
CTT | C | 53 | a0001c0001t0002g0004a0001c0001t0002g0044a0001c0001t0002g0107others(50): Show | 55 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.836-5154_836-5153d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057315 | ||||||
| chr9:89057315
|
CTTT | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0002g0164others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.836-5155_836-5153d others(5): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057315 | ||||||
| chr9:89057322
|
T | C | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.836-5159A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057322 | ||||||
| chr9:89057348
|
G | GT | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.836-5186dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057348 | ||||||
| chr9:89057357
|
C | T | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.836-5194G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057357 | ||||||
| chr9:89057455
|
T | C | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-5292A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057455 | ||||||
| chr9:89057492
|
T | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.836-5329A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057492 | ||||||
| chr9:89057503
|
A | G | 2 | a0001c0001t0026g0172a0001c0003t0045g0008 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.836-5340T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057503 | ||||||
| chr9:89057689
|
A | G | 1 | a0001c0003t0004g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.836-5526T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057689 | ||||||
| chr9:89057994
|
C | T | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.836-5831G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89057994 | ||||||
| chr9:89058141
|
T | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(2): Show | 6 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-5978A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058141 | ||||||
| chr9:89058176
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0004g0038others(2): Show | 6 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-6013T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058176 | ||||||
| chr9:89058336
|
G | A | 1 | a0001c0003t0004g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.836-6173C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058336 | ||||||
| chr9:89058355
|
G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(17): Show | 21 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.836-6192C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058355 | ||||||
| chr9:89058361
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(63): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.836-6198G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058361 | ||||||
| chr9:89058538
|
TTACATGG others(8): Show |
T | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.836-6390_836-6376d others(17): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058538 | ||||||
| chr9:89058556
|
C | T | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-6393G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058556 | ||||||
| chr9:89058674
|
T | A | 1 | a0001c0002t0031g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.836-6511A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058674 | ||||||
| chr9:89058708
|
TGGA | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(17): Show | 21 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.836-6548_836-6546d others(5): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058708 | ||||||
| chr9:89058819
|
A | G | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.836-6656T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058819 | ||||||
| chr9:89058869
|
C | T | 1 | a0001c0001t0007g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.835+6660G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058869 | ||||||
| chr9:89058945
|
G | A | 2 | a0001c0001t0026g0172a0001c0003t0045g0008 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.835+6584C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89058945 | ||||||
| chr9:89059031
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.835+6498G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059031 | ||||||
| chr9:89059069
|
G | A | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.835+6460C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059069 | ||||||
| chr9:89059084
|
ATGGAGGA others(6): Show |
A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.835+6432_835+6444d others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059084 | ||||||
| chr9:89059132
|
G | A | 24 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.835+6397C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059132 | ||||||
| chr9:89059170
|
G | A | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.835+6359C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059170 | ||||||
| chr9:89059309
|
GGTGGAGG others(5): Show |
G | 102 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(99): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.835+6208_835+6219d others(14): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059309 | ||||||
| chr9:89059319
|
G | A | 9 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(6): Show | 9 | HG01884.hp1 HG02451.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+6210C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059319 | ||||||
| chr9:89059321
|
TGTGGAGG others(6): Show |
T | 2 | a0001c0002t0002g0140a0001c0002t0002g0166 | 2 | HG01255.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.835+6195_835+6207d others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059321 | ||||||
| chr9:89059336
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0002g0130a0001c0001t0019g0057 | 3 | HG01243.hp2 HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.835+6193A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059336 | ||||||
| chr9:89059347
|
GGTGGAGG others(5): Show |
G | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.835+6170_835+6181d others(14): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059347 | ||||||
| chr9:89059568
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(99): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.835+5961G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059568 | ||||||
| chr9:89059751
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.835+5778C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059751 | ||||||
| chr9:89059755
|
G | GGTGGTGG others(103): Show |
5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+5773_835+5774i others(112): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059755 | ||||||
| chr9:89059755
|
G | GGTGGTGG others(103): Show |
117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.835+5773_835+5774i others(112): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059755 | ||||||
| chr9:89059755
|
G | GGTGGTGG others(91): Show |
15 | a0001c0001t0004g0069a0001c0001t0029g0024a0001c0003t0001g0009others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.835+5773_835+5774i others(100): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059755 | ||||||
| chr9:89059843
|
T | TGTGGTGG others(6): Show |
1 | a0001c0001t0007g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.835+5673_835+5685d others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059843 | ||||||
| chr9:89059843
|
TGTGGTGG others(6): Show |
T | 13 | a0001c0001t0004g0069a0001c0003t0001g0009a0001c0003t0001g0012others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.835+5673_835+5685d others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89059843 | ||||||
| chr9:89060062
|
G | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.835+5467C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060062 | ||||||
| chr9:89060095
|
G | GTGGTGGA others(18): Show |
1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.835+5409_835+5433d others(27): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060095 | ||||||
| chr9:89060131
|
CGTGGTGG others(6): Show |
C | 2 | a0001c0001t0003g0115a0001c0002t0031g0064 | 2 | HG01952.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.835+5385_835+5397d others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060131 | ||||||
| chr9:89060179
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(94): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.835+5350C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060179 | ||||||
| chr9:89060259
|
G | A | 1 | a0001c0001t0007g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.835+5270C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060259 | ||||||
| chr9:89060333
|
C | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.835+5196G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060333 | ||||||
| chr9:89060416
|
A | G | 2 | a0001c0001t0004g0061a0001c0001t0006g0060 | 2 | HG01106.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.835+5113T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060416 | ||||||
| chr9:89060617
|
C | T | 2 | a0001c0001t0001g0062a0001c0007t0015g0176 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.835+4912G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060617 | ||||||
| chr9:89060633
|
T | A | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.835+4896A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060633 | ||||||
| chr9:89060645
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.835+4884T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060645 | ||||||
| chr9:89060740
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.835+4789T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060740 | ||||||
| chr9:89060755
|
T | C | 1 | a0001c0001t0002g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.835+4774A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060755 | ||||||
| chr9:89060771
|
G | A | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.835+4758C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89060771 | ||||||
| chr9:89061073
|
A | G | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.835+4456T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061073 | ||||||
| chr9:89061091
|
A | T | 1 | a0001c0003t0004g0021 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.835+4438T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061091 | ||||||
| chr9:89061117
|
C | T | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.835+4412G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061117 | ||||||
| chr9:89061410
|
T | C | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+4119A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061410 | ||||||
| chr9:89061465
|
T | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(17): Show | 21 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.835+4064A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061465 | ||||||
| chr9:89061555
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0002g0130a0001c0001t0019g0057 | 3 | HG01243.hp2 HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.835+3974C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061555 | ||||||
| chr9:89061589
|
T | C | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.835+3940A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061589 | ||||||
| chr9:89061699
|
T | A | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+3830A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061699 | ||||||
| chr9:89061889
|
A | C | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+3640T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89061889 | ||||||
| chr9:89062029
|
C | T | 1 | a0002c0005t0011g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.835+3500G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062029 | ||||||
| chr9:89062088
|
C | T | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+3441G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062088 | ||||||
| chr9:89062092
|
C | T | 24 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.835+3437G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062092 | ||||||
| chr9:89062459
|
T | C | 3 | a0002c0005t0007g0032a0002c0005t0011g0033a0002c0005t0011g0048 | 3 | HG02572.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.835+3070A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062459 | ||||||
| chr9:89062574
|
A | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.835+2955T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062574 | ||||||
| chr9:89062592
|
G | A | 24 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.835+2937C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062592 | ||||||
| chr9:89062804
|
C | A | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.835+2725G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062804 | ||||||
| chr9:89062823
|
C | T | 1 | a0001c0001t0016g0098 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.835+2706G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062823 | ||||||
| chr9:89062826
|
T | C | 2 | a0001c0001t0029g0024a0001c0003t0046g0007 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.835+2703A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062826 | ||||||
| chr9:89062895
|
A | C | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+2634T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062895 | ||||||
| chr9:89062958
|
T | A | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.835+2571A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89062958 | ||||||
| chr9:89063026
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.835+2503G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063026 | ||||||
| chr9:89063084
|
C | T | 31 | a0001c0001t0002g0044a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.835+2445G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063084 | ||||||
| chr9:89063097
|
A | T | 2 | a0001c0001t0026g0172a0001c0003t0045g0008 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.835+2432T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063097 | ||||||
| chr9:89063170
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.835+2359C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063170 | ||||||
| chr9:89063242
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(63): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.835+2287C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063242 | ||||||
| chr9:89063318
|
T | G | 5 | a0001c0004t0001g0034a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+2211A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063318 | ||||||
| chr9:89063334
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.835+2195G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063334 | ||||||
| chr9:89063404
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.835+2125T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063404 | ||||||
| chr9:89063655
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.835+1874C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063655 | ||||||
| chr9:89063925
|
G | C | 1 | a0001c0001t0016g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.835+1604C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89063925 | ||||||
| chr9:89064203
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.835+1326C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064203 | ||||||
| chr9:89064252
|
A | G | 5 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(2): Show | 5 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+1277T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064252 | ||||||
| chr9:89064629
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.835+900G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064629 | ||||||
| chr9:89064808
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.835+721G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064808 | ||||||
| chr9:89064860
|
A | AG | 11 | a0001c0001t0004g0069a0001c0002t0002g0166a0001c0003t0001g0012others(8): Show | 12 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.835+668dupC | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064860 | ||||||
| chr9:89064861
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.835+668C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064861 | ||||||
| chr9:89064862
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.835+667C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064862 | ||||||
| chr9:89064903
|
T | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.835+626A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89064903 | ||||||
| chr9:89065050
|
C | T | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+479G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89065050 | ||||||
| chr9:89065109
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.835+420G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89065109 | ||||||
| chr9:89065185
|
G | A | 2 | a0001c0001t0042g0079a0001c0002t0039g0078 | 2 | HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.835+344C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89065185 | ||||||
| chr9:89065309
|
C | A | 8 | a0001c0001t0003g0049a0001c0001t0018g0046a0001c0002t0003g0052others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.835+220G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89065309 | ||||||
| chr9:89065330
|
T | C | 1 | a0001c0002t0031g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.835+199A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 6/11 | chr9 | 89065330 | ||||||
| chr9:89065616
|
C | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(91): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.784-36G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89065616 | ||||||
| chr9:89065685
|
A | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(78): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.784-105T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89065685 | ||||||
| chr9:89065874
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.784-294G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89065874 | ||||||
| chr9:89066023
|
G | A | 4 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(1): Show | 4 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-443C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066023 | ||||||
| chr9:89066034
|
C | T | 7 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-454G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066034 | ||||||
| chr9:89066053
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784-473C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066053 | ||||||
| chr9:89066388
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784-808G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066388 | ||||||
| chr9:89066491
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.784-911T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066491 | ||||||
| chr9:89066516
|
C | T | 1 | a0001c0001t0013g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.784-936G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066516 | ||||||
| chr9:89066631
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.784-1051G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066631 | ||||||
| chr9:89066633
|
C | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.784-1053G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066633 | ||||||
| chr9:89066634
|
T | A | 1 | a0001c0001t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.784-1054A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066634 | ||||||
| chr9:89066634
|
T | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.784-1054A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066634 | ||||||
| chr9:89066733
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.784-1153G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066733 | ||||||
| chr9:89066797
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.784-1217G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066797 | ||||||
| chr9:89066958
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784-1378G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89066958 | ||||||
| chr9:89067026
|
G | A | 1 | a0001c0003t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.784-1446C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067026 | ||||||
| chr9:89067042
|
G | A | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1462C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067042 | ||||||
| chr9:89067044
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.784-1464C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067044 | ||||||
| chr9:89067104
|
T | A | 1 | a0001c0001t0035g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.784-1524A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067104 | ||||||
| chr9:89067121
|
T | C | 1 | a0001c0001t0002g0004 | 2 | HG02723.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.784-1541A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067121 | ||||||
| chr9:89067130
|
G | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784-1550C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067130 | ||||||
| chr9:89067200
|
C | T | 1 | a0001c0001t0009g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784-1620G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067200 | ||||||
| chr9:89067441
|
G | A | 10 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.784-1861C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067441 | ||||||
| chr9:89067738
|
T | A | 5 | a0001c0003t0046g0007a0001c0004t0010g0179a0001c0004t0010g0180others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-2158A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067738 | ||||||
| chr9:89067790
|
T | G | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784-2210A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89067790 | ||||||
| chr9:89068062
|
C | T | 3 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0021g0051 | 3 | HG01884.hp1 HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.784-2482G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068062 | ||||||
| chr9:89068292
|
G | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(60): Show | 64 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.784-2712C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068292 | ||||||
| chr9:89068297
|
T | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(79): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.784-2717A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068297 | ||||||
| chr9:89068336
|
G | A | 23 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(20): Show | 23 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.784-2756C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068336 | ||||||
| chr9:89068458
|
C | T | 4 | a0001c0001t0002g0044a0001c0001t0012g0040a0001c0001t0012g0041others(1): Show | 4 | HG02258.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+2741G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068458 | ||||||
| chr9:89068502
|
T | G | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.783+2697A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068502 | ||||||
| chr9:89068660
|
A | AT | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0062others(3): Show | 6 | HG00639.hp2 HG01975.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+2538dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068660 | ||||||
| chr9:89068667
|
T | A | 1 | a0001c0002t0021g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.783+2532A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068667 | ||||||
| chr9:89068667
|
T | TA | 3 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031 | 3 | HG01884.hp1 HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.783+2531_783+2532i others(3): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068667 | ||||||
| chr9:89068668
|
T | A | 8 | a0001c0001t0029g0024a0001c0001t0043g0077a0001c0002t0002g0039others(5): Show | 8 | HG01884.hp1 HG02451.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.783+2531A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068668 | ||||||
| chr9:89068669
|
A | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.783+2530T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068669 | ||||||
| chr9:89068699
|
GA | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(14): Show | 18 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.783+2499delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89068699 | ||||||
| chr9:89069087
|
C | T | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+2112G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89069087 | ||||||
| chr9:89069176
|
G | A | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0002g0044others(14): Show | 17 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.783+2023C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89069176 | ||||||
| chr9:89069322
|
G | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.783+1877C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89069322 | ||||||
| chr9:89069428
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.783+1771T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89069428 | ||||||
| chr9:89069554
|
T | TG | 7 | a0001c0001t0042g0079a0001c0002t0002g0085a0001c0002t0002g0086others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+1644dupC | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89069554 | ||||||
| chr9:89069915
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+1284G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89069915 | ||||||
| chr9:89070008
|
C | T | 10 | a0001c0003t0001g0012a0001c0003t0001g0016a0001c0003t0001g0017others(7): Show | 11 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1191G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070008 | ||||||
| chr9:89070289
|
G | A | 13 | a0001c0001t0002g0044a0001c0001t0003g0049a0001c0001t0003g0055others(10): Show | 13 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.783+910C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070289 | ||||||
| chr9:89070321
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.783+878C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070321 | ||||||
| chr9:89070326
|
C | A | 1 | a0001c0001t0044g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.783+873G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070326 | ||||||
| chr9:89070390
|
A | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(92): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.783+809T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070390 | ||||||
| chr9:89070861
|
C | A | 3 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0021g0051 | 3 | HG01884.hp1 HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.783+338G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070861 | ||||||
| chr9:89070879
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.783+320G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070879 | ||||||
| chr9:89070915
|
G | T | 1 | a0001c0001t0003g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.783+284C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070915 | ||||||
| chr9:89070916
|
G | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.783+283C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89070916 | ||||||
| chr9:89071182
|
AC | A | 8 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0002t0003g0052others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+16delG | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 5/11 | chr9 | 89071182 | ||||||
| chr9:89071461
|
C | T | 5 | a0001c0001t0002g0044a0001c0001t0004g0038a0001c0001t0012g0040others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-209G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071461 | ||||||
| chr9:89071462
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.730-210C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071462 | ||||||
| chr9:89071581
|
A | G | 1 | a0001c0002t0009g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.730-329T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071581 | ||||||
| chr9:89071586
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.730-334G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071586 | ||||||
| chr9:89071600
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(79): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.730-348C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071600 | ||||||
| chr9:89071603
|
G | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(55): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.730-351C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071603 | ||||||
| chr9:89071703
|
TA | T | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.730-452delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071703 | ||||||
| chr9:89071708
|
A | T | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.730-456T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071708 | ||||||
| chr9:89071709
|
A | C | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.730-457T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071709 | ||||||
| chr9:89071710
|
G | C | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.730-458C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071710 | ||||||
| chr9:89071711
|
A | T | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.730-459T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071711 | ||||||
| chr9:89071802
|
C | T | 1 | a0002c0005t0011g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730-550G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071802 | ||||||
| chr9:89071922
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.730-670G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89071922 | ||||||
| chr9:89072194
|
C | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.730-942G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072194 | ||||||
| chr9:89072194
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-942G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072194 | ||||||
| chr9:89072286
|
C | A | 1 | a0001c0002t0031g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.730-1034G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072286 | ||||||
| chr9:89072330
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.730-1078C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072330 | ||||||
| chr9:89072443
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.730-1191T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072443 | ||||||
| chr9:89072535
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-1283G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072535 | ||||||
| chr9:89072631
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0002g0044a0001c0001t0012g0040others(1): Show | 4 | HG02818.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-1379G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072631 | ||||||
| chr9:89072688
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.730-1436A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072688 | ||||||
| chr9:89072693
|
T | C | 23 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(20): Show | 23 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.730-1441A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072693 | ||||||
| chr9:89072752
|
A | G | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.730-1500T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072752 | ||||||
| chr9:89072758
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.730-1506T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072758 | ||||||
| chr9:89072790
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-1538G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072790 | ||||||
| chr9:89072791
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.730-1539C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89072791 | ||||||
| chr9:89073362
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.729+1747T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89073362 | ||||||
| chr9:89073506
|
A | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0063others(79): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.729+1603T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89073506 | ||||||
| chr9:89073626
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.729+1483G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89073626 | ||||||
| chr9:89073674
|
G | A | 2 | a0001c0002t0001g0141a0001c0002t0002g0143 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.729+1435C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89073674 | ||||||
| chr9:89073798
|
C | T | 1 | a0001c0002t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.729+1311G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89073798 | ||||||
| chr9:89073838
|
C | T | 9 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0018g0046others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.729+1271G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89073838 | ||||||
| chr9:89074029
|
A | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.729+1080T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074029 | ||||||
| chr9:89074169
|
A | G | 2 | a0001c0004t0010g0179a0001c0004t0010g0180 | 2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.729+940T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074169 | ||||||
| chr9:89074231
|
C | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038 | 3 | HG02622.hp1 HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.729+878G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074231 | ||||||
| chr9:89074244
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0153 | 2 | HG03041.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.729+865A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074244 | ||||||
| chr9:89074304
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.729+805C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074304 | ||||||
| chr9:89074307
|
A | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038others(6): Show | 9 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+802T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074307 | ||||||
| chr9:89074431
|
G | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.729+678C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074431 | ||||||
| chr9:89074456
|
C | G | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.729+653G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074456 | ||||||
| chr9:89074456
|
C | T | 5 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+653G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074456 | ||||||
| chr9:89074527
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.729+582G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074527 | ||||||
| chr9:89074691
|
C | CA | 7 | a0001c0001t0018g0144a0001c0001t0028g0139a0001c0001t0042g0079others(4): Show | 7 | HG00642.hp1 HG00735.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.729+417dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074691 | ||||||
| chr9:89074691
|
CA | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0070others(106): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.729+417delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074691 | ||||||
| chr9:89074691
|
CAA | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0035others(13): Show | 18 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.729+416_729+417del others(2): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074691 | ||||||
| chr9:89074894
|
A | G | 5 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(2): Show | 5 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+215T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074894 | ||||||
| chr9:89074907
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.729+202C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 4/11 | chr9 | 89074907 | ||||||
| chr9:89075433
|
A | G | 5 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-205T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89075433 | ||||||
| chr9:89075461
|
A | G | 10 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-233T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89075461 | ||||||
| chr9:89075544
|
A | G | 10 | a0001c0001t0001g0062a0001c0001t0001g0153a0001c0001t0004g0038others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-316T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89075544 | ||||||
| chr9:89075557
|
G | A | 9 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0018g0046others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-329C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89075557 | ||||||
| chr9:89075688
|
T | A | 5 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-460A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89075688 | ||||||
| chr9:89076021
|
A | G | 1 | a0001c0002t0002g0085 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.610-793T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076021 | ||||||
| chr9:89076176
|
C | T | 22 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(19): Show | 22 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.610-948G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076176 | ||||||
| chr9:89076182
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.610-954G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076182 | ||||||
| chr9:89076196
|
G | A | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-968C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076196 | ||||||
| chr9:89076259
|
T | C | 31 | a0001c0001t0001g0153a0001c0001t0002g0107a0001c0001t0002g0110others(28): Show | 31 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.610-1031A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076259 | ||||||
| chr9:89076704
|
C | T | 1 | a0001c0001t0028g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.609+1136G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076704 | ||||||
| chr9:89076800
|
G | T | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.609+1040C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076800 | ||||||
| chr9:89076901
|
G | A | 1 | a0001c0001t0005g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.609+939C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076901 | ||||||
| chr9:89076949
|
C | T | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+891G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076949 | ||||||
| chr9:89076974
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(21): Show | 25 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.609+866G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89076974 | ||||||
| chr9:89077069
|
C | T | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.609+771G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077069 | ||||||
| chr9:89077106
|
G | A | 3 | a0001c0003t0001g0009a0001c0003t0003g0020a0001c0003t0011g0010 | 3 | HG02559.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.609+734C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077106 | ||||||
| chr9:89077139
|
T | C | 4 | a0001c0004t0010g0179a0001c0004t0010g0180a0001c0004t0010g0181others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+701A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077139 | ||||||
| chr9:89077176
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0033g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.609+652_609+663del others(12): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077176 | ||||||
| chr9:89077184
|
C | CA | 12 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(9): Show | 12 | HG00408.hp2 HG00639.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.609+655dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077184 | ||||||
| chr9:89077195
|
A | C | 21 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(18): Show | 21 | HG00741.hp2 HG01070.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.609+645T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077195 | ||||||
| chr9:89077400
|
G | A | 3 | a0001c0001t0003g0149a0001c0001t0003g0151a0001c0001t0007g0150 | 3 | HG01109.hp1 HG01168.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.609+440C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077400 | ||||||
| chr9:89077407
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.609+433G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077407 | ||||||
| chr9:89077778
|
C | T | 1 | a0001c0002t0002g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.609+62G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077778 | ||||||
| chr9:89077779
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.609+61C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 3/11 | chr9 | 89077779 | ||||||
| chr9:89078079
|
C | T | 1 | a0001c0001t0043g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.546-176G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078079 | ||||||
| chr9:89078080
|
GC | G | 20 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.546-178delG | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078080 | ||||||
| chr9:89078175
|
C | CT | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.546-273dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078175 | ||||||
| chr9:89078324
|
G | C | 6 | a0001c0003t0003g0022a0001c0003t0046g0007a0001c0004t0010g0179others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.546-421C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078324 | ||||||
| chr9:89078426
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.546-523A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078426 | ||||||
| chr9:89078511
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.546-608C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078511 | ||||||
| chr9:89078626
|
G | C | 1 | a0001c0001t0004g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.546-723C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078626 | ||||||
| chr9:89078629
|
G | A | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-726C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078629 | ||||||
| chr9:89078747
|
G | A | 3 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111 | 3 | HG00741.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.546-844C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078747 | ||||||
| chr9:89078885
|
T | A | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.546-982A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078885 | ||||||
| chr9:89078930
|
G | A | 21 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(18): Show | 22 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.546-1027C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89078930 | ||||||
| chr9:89079132
|
A | G | 4 | a0001c0004t0010g0179a0001c0004t0010g0180a0001c0004t0010g0181others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-1229T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079132 | ||||||
| chr9:89079205
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(76): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.546-1302A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079205 | ||||||
| chr9:89079336
|
A | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-1433T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079336 | ||||||
| chr9:89079542
|
G | GA | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-1640dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079542 | ||||||
| chr9:89079648
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.546-1745A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079648 | ||||||
| chr9:89079666
|
G | A | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.546-1763C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079666 | ||||||
| chr9:89079984
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-2081C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89079984 | ||||||
| chr9:89080325
|
G | A | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0120others(17): Show | 21 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.546-2422C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080325 | ||||||
| chr9:89080469
|
T | C | 1 | a0001c0001t0003g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.546-2566A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080469 | ||||||
| chr9:89080499
|
C | CT | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-2597dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080499 | ||||||
| chr9:89080725
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.546-2822T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080725 | ||||||
| chr9:89080734
|
A | AAT | 11 | a0001c0001t0002g0167a0001c0001t0003g0090a0001c0001t0012g0040others(8): Show | 11 | HG00323.hp1 HG01255.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.546-2833_546-2832d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080734 | ||||||
| chr9:89080734
|
A | AATAT | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG01952.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2835_546-2832d others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080734 | ||||||
| chr9:89080734
|
AAT | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(89): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.546-2833_546-2832d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080734 | ||||||
| chr9:89080734
|
AATATAT | A | 22 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(19): Show | 23 | HG00408.hp2 HG00639.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.546-2837_546-2832d others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080734 | ||||||
| chr9:89080755
|
A | ATATATAT others(23): Show |
1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-2853_546-2852i others(32): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080755 | ||||||
| chr9:89080768
|
C | CT | 42 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0162others(39): Show | 44 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.546-2866dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080768 | ||||||
| chr9:89080768
|
CT | C | 6 | a0001c0001t0001g0062a0001c0001t0003g0104a0001c0001t0004g0038others(3): Show | 6 | HG00323.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.546-2866delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080768 | ||||||
| chr9:89080914
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-3011G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89080914 | ||||||
| chr9:89081017
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.546-3114G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89081017 | ||||||
| chr9:89081163
|
T | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(76): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.546-3260A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89081163 | ||||||
| chr9:89081257
|
G | A | 1 | a0001c0001t0041g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.546-3354C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89081257 | ||||||
| chr9:89081590
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.546-3687C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89081590 | ||||||
| chr9:89081613
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.546-3710G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89081613 | ||||||
| chr9:89081670
|
G | T | 1 | a0001c0002t0019g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.546-3767C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89081670 | ||||||
| chr9:89082006
|
A | G | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-4103T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89082006 | ||||||
| chr9:89082427
|
CACAGCCA others(12): Show |
C | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-4543_546-4525d others(21): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89082427 | ||||||
| chr9:89082470
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-4567G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89082470 | ||||||
| chr9:89082479
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.546-4576C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89082479 | ||||||
| chr9:89082779
|
G | A | 1 | a0001c0001t0033g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546-4876C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89082779 | ||||||
| chr9:89082904
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-5001A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89082904 | ||||||
| chr9:89083037
|
C | T | 164 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.546-5134G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083037 | ||||||
| chr9:89083044
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.546-5141G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083044 | ||||||
| chr9:89083060
|
C | T | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.546-5157G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083060 | ||||||
| chr9:89083114
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-5211G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083114 | ||||||
| chr9:89083401
|
A | G | 3 | a0001c0001t0008g0108a0001c0001t0008g0109a0001c0009t0027g0178 | 3 | HG02809.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.546-5498T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083401 | ||||||
| chr9:89083467
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.546-5564A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083467 | ||||||
| chr9:89083654
|
G | A | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.546-5751C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083654 | ||||||
| chr9:89083661
|
A | G | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0120others(17): Show | 21 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.546-5758T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083661 | ||||||
| chr9:89083756
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-5853C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89083756 | ||||||
| chr9:89084024
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.546-6121C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084024 | ||||||
| chr9:89084084
|
A | C | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-6181T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084084 | ||||||
| chr9:89084430
|
G | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(21): Show | 25 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.546-6527C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084430 | ||||||
| chr9:89084588
|
T | G | 1 | a0001c0001t0029g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.546-6685A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084588 | ||||||
| chr9:89084790
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.546-6887A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084790 | ||||||
| chr9:89084900
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546-6997C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084900 | ||||||
| chr9:89084914
|
G | C | 1 | a0001c0001t0003g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.546-7011C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89084914 | ||||||
| chr9:89085289
|
C | T | 10 | a0001c0003t0001g0012a0001c0003t0001g0016a0001c0003t0001g0017others(7): Show | 11 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.546-7386G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085289 | ||||||
| chr9:89085333
|
T | A | 1 | a0001c0001t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.546-7430A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085333 | ||||||
| chr9:89085460
|
C | G | 1 | a0001c0001t0016g0098 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.546-7557G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085460 | ||||||
| chr9:89085647
|
G | A | 1 | a0001c0001t0007g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.546-7744C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085647 | ||||||
| chr9:89085786
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.546-7883G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085786 | ||||||
| chr9:89085874
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.546-7971G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085874 | ||||||
| chr9:89085875
|
G | A | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0120others(17): Show | 21 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.546-7972C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085875 | ||||||
| chr9:89085998
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-8095G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89085998 | ||||||
| chr9:89086249
|
A | T | 1 | a0001c0001t0002g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.546-8346T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89086249 | ||||||
| chr9:89086374
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-8471G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89086374 | ||||||
| chr9:89086528
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-8625G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89086528 | ||||||
| chr9:89086643
|
A | G | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-8740T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89086643 | ||||||
| chr9:89087167
|
A | G | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.546-9264T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087167 | ||||||
| chr9:89087403
|
C | A | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546-9500G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087403 | ||||||
| chr9:89087437
|
A | G | 1 | a0001c0002t0009g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.546-9534T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087437 | ||||||
| chr9:89087687
|
T | C | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-9784A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087687 | ||||||
| chr9:89087868
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-9965A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087868 | ||||||
| chr9:89087888
|
T | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.546-9985A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087888 | ||||||
| chr9:89087921
|
C | A | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-10018G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89087921 | ||||||
| chr9:89088160
|
A | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.546-10257T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89088160 | ||||||
| chr9:89088242
|
T | C | 11 | a0001c0001t0001g0154a0001c0001t0004g0061a0001c0001t0006g0060others(8): Show | 12 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.546-10339A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89088242 | ||||||
| chr9:89088327
|
C | T | 1 | a0001c0001t0005g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.546-10424G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89088327 | ||||||
| chr9:89088960
|
G | A | 2 | a0001c0001t0003g0120a0001c0001t0005g0171 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.546-11057C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89088960 | ||||||
| chr9:89089046
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.546-11143G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089046 | ||||||
| chr9:89089132
|
T | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.546-11229A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089132 | ||||||
| chr9:89089187
|
A | T | 7 | a0001c0001t0003g0045a0001c0001t0003g0104a0001c0001t0003g0149others(4): Show | 7 | HG01109.hp1 HG01168.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-11284T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089187 | ||||||
| chr9:89089259
|
T | C | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-11356A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089259 | ||||||
| chr9:89089392
|
C | T | 2 | a0001c0001t0003g0104a0001c0001t0013g0105 | 2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.546-11489G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089392 | ||||||
| chr9:89089514
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-11611G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089514 | ||||||
| chr9:89089552
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-11649C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089552 | ||||||
| chr9:89089644
|
G | T | 28 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(25): Show | 29 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.546-11741C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089644 | ||||||
| chr9:89089907
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-12004G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089907 | ||||||
| chr9:89089931
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-12028C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89089931 | ||||||
| chr9:89090051
|
T | C | 2 | a0001c0002t0002g0094a0001c0002t0002g0118 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.546-12148A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090051 | ||||||
| chr9:89090124
|
C | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0118 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.546-12221G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090124 | ||||||
| chr9:89090189
|
A | G | 1 | a0001c0001t0042g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546-12286T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090189 | ||||||
| chr9:89090586
|
G | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-12683C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090586 | ||||||
| chr9:89090662
|
C | T | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.546-12759G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090662 | ||||||
| chr9:89090701
|
G | C | 2 | a0001c0001t0001g0072a0001c0001t0008g0132 | 2 | NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.546-12798C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090701 | ||||||
| chr9:89090702
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.546-12799C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090702 | ||||||
| chr9:89090874
|
A | T | 3 | a0002c0005t0007g0032a0002c0005t0011g0033a0002c0005t0011g0048 | 3 | HG02572.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.546-12971T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090874 | ||||||
| chr9:89090962
|
A | G | 4 | a0001c0002t0006g0002a0001c0002t0006g0059a0001c0002t0006g0173others(1): Show | 5 | HG00280.hp1 HG00642.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.546-13059T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89090962 | ||||||
| chr9:89091461
|
A | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-13558T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89091461 | ||||||
| chr9:89091472
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.546-13569G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89091472 | ||||||
| chr9:89091932
|
TA | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.546-14030delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89091932 | ||||||
| chr9:89092291
|
A | G | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.546-14388T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092291 | ||||||
| chr9:89092348
|
C | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-14445G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092348 | ||||||
| chr9:89092355
|
C | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-14452G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092355 | ||||||
| chr9:89092425
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.546-14522C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092425 | ||||||
| chr9:89092477
|
C | T | 2 | a0001c0001t0003g0115a0001c0001t0018g0144 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.546-14574G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092477 | ||||||
| chr9:89092510
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-14607C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092510 | ||||||
| chr9:89092546
|
A | G | 24 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(21): Show | 25 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.546-14643T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092546 | ||||||
| chr9:89092610
|
T | C | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.546-14707A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092610 | ||||||
| chr9:89092615
|
C | CA | 17 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0162others(14): Show | 18 | HG00323.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.546-14713dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092615 | ||||||
| chr9:89092615
|
C | CAA | 6 | a0001c0001t0001g0153a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-14714_546-1471 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092615 | ||||||
| chr9:89092615
|
CA | C | 8 | a0001c0001t0002g0116a0001c0001t0003g0115a0001c0001t0009g0096others(5): Show | 8 | HG01261.hp1 HG01517.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-14713delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092615 | ||||||
| chr9:89092615
|
CAA | C | 19 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0120others(16): Show | 20 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.546-14714_546-1471 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092615 | ||||||
| chr9:89092652
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-14749G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092652 | ||||||
| chr9:89092739
|
G | GGT | 26 | a0001c0001t0002g0110a0001c0001t0003g0049a0001c0001t0003g0055others(23): Show | 26 | HG01106.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.546-14838_546-1483 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092739 | ||||||
| chr9:89092739
|
G | GGTGT | 11 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 12 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.546-14840_546-1483 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092739 | ||||||
| chr9:89092739
|
GGT | G | 15 | a0001c0001t0002g0044a0001c0001t0022g0042a0001c0003t0001g0009others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.546-14838_546-1483 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092739 | ||||||
| chr9:89092762
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.546-14859T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092762 | ||||||
| chr9:89092816
|
T | G | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-14913A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092816 | ||||||
| chr9:89092842
|
C | A | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-14939G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092842 | ||||||
| chr9:89092868
|
C | G | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-14965G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092868 | ||||||
| chr9:89092975
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.546-15072A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092975 | ||||||
| chr9:89092994
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.546-15091C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89092994 | ||||||
| chr9:89093031
|
T | C | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.546-15128A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093031 | ||||||
| chr9:89093281
|
A | G | 3 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111 | 3 | HG00741.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.546-15378T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093281 | ||||||
| chr9:89093289
|
T | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.546-15386A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093289 | ||||||
| chr9:89093515
|
CA | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.546-15613delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093515 | ||||||
| chr9:89093521
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.546-15618C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093521 | ||||||
| chr9:89093553
|
CA | C | 6 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0001t0033g0037others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.546-15651delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093553 | ||||||
| chr9:89093826
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-15923C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093826 | ||||||
| chr9:89093829
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.546-15926G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093829 | ||||||
| chr9:89093873
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-15970C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89093873 | ||||||
| chr9:89094103
|
C | CA | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0045others(3): Show | 6 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-16201dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094103 | ||||||
| chr9:89094103
|
CA | C | 11 | a0001c0001t0001g0154a0001c0001t0006g0060a0001c0002t0001g0155others(8): Show | 11 | HG00099.hp1 HG01081.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.546-16201delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094103 | ||||||
| chr9:89094113
|
A | AG | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.546-16211_546-1621 others(5): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094113 | ||||||
| chr9:89094116
|
A | AG | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-16214_546-1621 others(5): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094116 | ||||||
| chr9:89094426
|
A | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.546-16523T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094426 | ||||||
| chr9:89094452
|
G | C | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546-16549C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094452 | ||||||
| chr9:89094498
|
A | G | 1 | a0001c0001t0003g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.546-16595T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094498 | ||||||
| chr9:89094534
|
A | T | 1 | a0001c0002t0002g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.546-16631T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094534 | ||||||
| chr9:89094886
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.546-16983G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094886 | ||||||
| chr9:89094937
|
C | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-17034G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094937 | ||||||
| chr9:89094946
|
C | A | 9 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.546-17043G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094946 | ||||||
| chr9:89094950
|
CCAAA | C | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.546-17051_546-1704 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89094950 | ||||||
| chr9:89095016
|
T | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.546-17113A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095016 | ||||||
| chr9:89095045
|
G | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546-17142C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095045 | ||||||
| chr9:89095067
|
A | C | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.546-17164T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095067 | ||||||
| chr9:89095423
|
C | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(57): Show | 62 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.545+17133G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095423 | ||||||
| chr9:89095549
|
C | T | 1 | a0001c0001t0005g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.545+17007G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095549 | ||||||
| chr9:89095664
|
A | C | 1 | a0001c0001t0009g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.545+16892T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095664 | ||||||
| chr9:89095707
|
A | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.545+16849T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89095707 | ||||||
| chr9:89096010
|
C | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+16546G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096010 | ||||||
| chr9:89096273
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.545+16283A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096273 | ||||||
| chr9:89096523
|
C | T | 7 | a0001c0001t0003g0045a0001c0001t0003g0104a0001c0001t0003g0149others(4): Show | 7 | HG01109.hp1 HG01168.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+16033G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096523 | ||||||
| chr9:89096554
|
A | T | 9 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0001t0005g0026others(6): Show | 9 | HG01891.hp1 HG02622.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.545+16002T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096554 | ||||||
| chr9:89096646
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0002g0103a0001c0002t0002g0128 | 3 | HG00140.hp2 HG00323.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.545+15910T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096646 | ||||||
| chr9:89096691
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.545+15865C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096691 | ||||||
| chr9:89096711
|
C | T | 5 | a0001c0001t0003g0055a0001c0002t0003g0052a0001c0002t0003g0056others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+15845G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096711 | ||||||
| chr9:89096749
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.545+15807C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89096749 | ||||||
| chr9:89097098
|
G | A | 1 | a0001c0002t0015g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.545+15458C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097098 | ||||||
| chr9:89097106
|
GAAAAAA | G | 14 | a0001c0001t0001g0063a0001c0001t0003g0055a0001c0001t0005g0026others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.545+15444_545+1544 others(10): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097106 | ||||||
| chr9:89097106
|
GAAAAAAA | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.545+15443_545+1544 others(11): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097106 | ||||||
| chr9:89097106
|
GAAAAAAA others(1): Show |
G | 6 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0002g0103others(3): Show | 6 | HG00140.hp2 HG01167.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.545+15442_545+1544 others(12): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097106 | ||||||
| chr9:89097106
|
GAAAAAAA others(8): Show |
G | 1 | a0001c0003t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.545+15435_545+1544 others(19): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097106 | ||||||
| chr9:89097114
|
A | G | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.545+15442T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097114 | ||||||
| chr9:89097146
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.545+15410C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097146 | ||||||
| chr9:89097544
|
G | A | 11 | a0001c0001t0001g0154a0001c0001t0004g0061a0001c0001t0006g0060others(8): Show | 12 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.545+15012C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097544 | ||||||
| chr9:89097702
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+14854A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097702 | ||||||
| chr9:89097776
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+14780G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097776 | ||||||
| chr9:89097811
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+14745C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89097811 | ||||||
| chr9:89098056
|
T | G | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0002g0004others(17): Show | 22 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.545+14500A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098056 | ||||||
| chr9:89098137
|
T | G | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+14419A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098137 | ||||||
| chr9:89098328
|
C | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+14228G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098328 | ||||||
| chr9:89098472
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(57): Show | 62 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.545+14084A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098472 | ||||||
| chr9:89098481
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.545+14075C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098481 | ||||||
| chr9:89098529
|
G | C | 1 | a0001c0004t0001g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.545+14027C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098529 | ||||||
| chr9:89098546
|
C | T | 18 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0003g0120others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+14010G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098546 | ||||||
| chr9:89098547
|
G | A | 1 | a0001c0002t0008g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.545+14009C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098547 | ||||||
| chr9:89098626
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.545+13930G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098626 | ||||||
| chr9:89098637
|
G | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.545+13919C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098637 | ||||||
| chr9:89098668
|
G | A | 5 | a0001c0001t0002g0116a0001c0002t0002g0119a0001c0002t0005g0117others(2): Show | 5 | HG01167.hp1 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+13888C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098668 | ||||||
| chr9:89098683
|
C | A | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+13873G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098683 | ||||||
| chr9:89098727
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545+13829G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098727 | ||||||
| chr9:89098808
|
C | CA | 28 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(25): Show | 30 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.545+13747dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098808 | ||||||
| chr9:89098921
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.545+13635C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098921 | ||||||
| chr9:89098932
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0162 | 3 | HG03491.hp2 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.545+13624T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098932 | ||||||
| chr9:89098985
|
AAATT | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545+13567_545+1357 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098985 | ||||||
| chr9:89098989
|
T | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(110): Show | 117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.545+13567A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098989 | ||||||
| chr9:89098993
|
T | A | 6 | a0001c0001t0002g0103a0001c0001t0003g0045a0001c0001t0003g0149others(3): Show | 6 | HG00140.hp2 HG01109.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+13563A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89098993 | ||||||
| chr9:89099110
|
C | T | 4 | a0001c0001t0003g0115a0001c0001t0018g0144a0001c0001t0037g0113others(1): Show | 4 | HG03540.hp1 HG03834.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+13446G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099110 | ||||||
| chr9:89099151
|
GATT | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+13402_545+1340 others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099151 | ||||||
| chr9:89099167
|
T | A | 1 | a0001c0002t0002g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.545+13389A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099167 | ||||||
| chr9:89099250
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+13306C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099250 | ||||||
| chr9:89099408
|
G | A | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+13148C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099408 | ||||||
| chr9:89099484
|
T | C | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545+13072A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099484 | ||||||
| chr9:89099542
|
A | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+13014T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099542 | ||||||
| chr9:89099619
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+12937A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099619 | ||||||
| chr9:89099646
|
G | A | 1 | a0001c0002t0009g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.545+12910C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099646 | ||||||
| chr9:89099675
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+12881G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099675 | ||||||
| chr9:89099937
|
A | G | 2 | a0001c0003t0001g0012a0001c0003t0002g0001 | 3 | HG01070.hp2 HG01071.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.545+12619T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099937 | ||||||
| chr9:89099946
|
T | G | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545+12610A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89099946 | ||||||
| chr9:89100223
|
T | C | 1 | a0001c0001t0005g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.545+12333A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100223 | ||||||
| chr9:89100319
|
A | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+12237T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100319 | ||||||
| chr9:89100338
|
A | C | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+12218T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100338 | ||||||
| chr9:89100360
|
T | A | 9 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.545+12196A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100360 | ||||||
| chr9:89100445
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.545+12111G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100445 | ||||||
| chr9:89100512
|
C | T | 1 | a0001c0008t0001g0015 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.545+12044G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100512 | ||||||
| chr9:89100578
|
A | G | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+11978T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100578 | ||||||
| chr9:89100856
|
T | C | 2 | a0001c0004t0010g0181a0001c0004t0010g0182 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.545+11700A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100856 | ||||||
| chr9:89100875
|
A | T | 2 | a0001c0001t0003g0090a0001c0002t0003g0091 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.545+11681T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89100875 | ||||||
| chr9:89101238
|
T | C | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.545+11318A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101238 | ||||||
| chr9:89101466
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545+11090C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101466 | ||||||
| chr9:89101604
|
C | CAT | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+10950_545+1095 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101604 | ||||||
| chr9:89101604
|
CAT | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545+10950_545+1095 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101604 | ||||||
| chr9:89101617
|
A | T | 1 | a0001c0001t0005g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.545+10939T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101617 | ||||||
| chr9:89101619
|
A | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(89): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.545+10937T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101619 | ||||||
| chr9:89101621
|
T | A | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+10935A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89101621 | ||||||
| chr9:89102125
|
C | T | 2 | a0001c0006t0004g0169a0001c0006t0024g0168 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.545+10431G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102125 | ||||||
| chr9:89102306
|
T | G | 1 | a0001c0002t0040g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.545+10250A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102306 | ||||||
| chr9:89102401
|
A | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.545+10155T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102401 | ||||||
| chr9:89102407
|
T | C | 18 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(15): Show | 19 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.545+10149A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102407 | ||||||
| chr9:89102498
|
T | C | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+10058A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102498 | ||||||
| chr9:89102893
|
C | A | 1 | a0001c0001t0033g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.545+9663G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102893 | ||||||
| chr9:89102912
|
C | T | 1 | a0001c0001t0036g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.545+9644G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102912 | ||||||
| chr9:89102913
|
G | A | 2 | a0001c0001t0001g0153a0001c0003t0046g0007 | 2 | HG03225.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.545+9643C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89102913 | ||||||
| chr9:89103085
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.545+9471G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103085 | ||||||
| chr9:89103097
|
C | A | 1 | a0001c0001t0033g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.545+9459G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103097 | ||||||
| chr9:89103118
|
A | G | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545+9438T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103118 | ||||||
| chr9:89103166
|
A | C | 18 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0003g0120others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+9390T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103166 | ||||||
| chr9:89103245
|
A | AAG | 60 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(57): Show | 62 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.545+9309_545+9310d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103245 | ||||||
| chr9:89103295
|
T | C | 2 | a0001c0001t0003g0090a0001c0002t0003g0091 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.545+9261A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103295 | ||||||
| chr9:89103352
|
A | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.545+9204T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103352 | ||||||
| chr9:89103623
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(27): Show | 31 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.545+8933C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103623 | ||||||
| chr9:89103657
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+8899A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103657 | ||||||
| chr9:89103823
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.545+8733T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103823 | ||||||
| chr9:89103944
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+8612C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103944 | ||||||
| chr9:89103992
|
T | C | 1 | a0001c0001t0014g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.545+8564A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89103992 | ||||||
| chr9:89104171
|
G | GA | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+8384dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89104171 | ||||||
| chr9:89104374
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+8182C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89104374 | ||||||
| chr9:89104420
|
T | C | 4 | a0001c0001t0003g0115a0001c0001t0018g0144a0001c0001t0037g0113others(1): Show | 4 | HG03540.hp1 HG03834.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+8136A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89104420 | ||||||
| chr9:89104510
|
C | G | 1 | a0001c0001t0003g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.545+8046G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89104510 | ||||||
| chr9:89104630
|
A | T | 21 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(18): Show | 22 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.545+7926T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89104630 | ||||||
| chr9:89104755
|
T | C | 6 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+7801A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89104755 | ||||||
| chr9:89105061
|
G | A | 5 | a0001c0001t0003g0055a0001c0002t0003g0052a0001c0002t0003g0056others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+7495C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105061 | ||||||
| chr9:89105148
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0041g0174 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.545+7408A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105148 | ||||||
| chr9:89105435
|
G | A | 1 | a0001c0001t0037g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.545+7121C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105435 | ||||||
| chr9:89105451
|
G | A | 2 | a0001c0002t0002g0140a0001c0002t0040g0142 | 2 | HG01255.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.545+7105C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105451 | ||||||
| chr9:89105704
|
T | C | 17 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(14): Show | 18 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+6852A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105704 | ||||||
| chr9:89105730
|
C | T | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.545+6826G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105730 | ||||||
| chr9:89105829
|
G | C | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+6727C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105829 | ||||||
| chr9:89105900
|
A | C | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+6656T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89105900 | ||||||
| chr9:89106081
|
G | A | 1 | a0001c0001t0037g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.545+6475C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89106081 | ||||||
| chr9:89106108
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+6448G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89106108 | ||||||
| chr9:89106418
|
C | T | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+6138G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89106418 | ||||||
| chr9:89106516
|
G | A | 1 | a0001c0001t0005g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.545+6040C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89106516 | ||||||
| chr9:89106589
|
C | T | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+5967G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89106589 | ||||||
| chr9:89106991
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.545+5565G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89106991 | ||||||
| chr9:89107703
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.545+4853G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89107703 | ||||||
| chr9:89107782
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.545+4774G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89107782 | ||||||
| chr9:89107783
|
G | A | 1 | a0001c0002t0002g0143 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.545+4773C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89107783 | ||||||
| chr9:89108023
|
G | A | 3 | a0002c0005t0007g0032a0002c0005t0011g0033a0002c0005t0011g0048 | 3 | HG02572.hp2 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.545+4533C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108023 | ||||||
| chr9:89108029
|
T | A | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+4527A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108029 | ||||||
| chr9:89108091
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.545+4465C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108091 | ||||||
| chr9:89108116
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.545+4440C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108116 | ||||||
| chr9:89108168
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.545+4388C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108168 | ||||||
| chr9:89108209
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.545+4347G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108209 | ||||||
| chr9:89108227
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.545+4329G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108227 | ||||||
| chr9:89108287
|
T | C | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.545+4269A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108287 | ||||||
| chr9:89108350
|
C | CA | 53 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(50): Show | 55 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.545+4205dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108350 | ||||||
| chr9:89108375
|
G | A | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.545+4181C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108375 | ||||||
| chr9:89108467
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+4089T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108467 | ||||||
| chr9:89108499
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.545+4057G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108499 | ||||||
| chr9:89108540
|
T | TAC | 12 | a0001c0002t0002g0119a0001c0002t0004g0135a0001c0003t0001g0012others(9): Show | 13 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+4014_545+4015d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108540 | ||||||
| chr9:89108540
|
TAC | T | 4 | a0001c0001t0003g0115a0001c0001t0018g0144a0001c0001t0037g0113others(1): Show | 4 | HG03540.hp1 HG03834.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+4014_545+4015d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108540 | ||||||
| chr9:89108562
|
T | C | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.545+3994A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108562 | ||||||
| chr9:89108638
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.545+3918C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108638 | ||||||
| chr9:89108781
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+3775C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108781 | ||||||
| chr9:89108787
|
A | G | 6 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(3): Show | 6 | HG00099.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+3769T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108787 | ||||||
| chr9:89108797
|
C | T | 1 | a0001c0002t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.545+3759G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108797 | ||||||
| chr9:89108882
|
C | T | 2 | a0001c0001t0013g0093a0001c0001t0035g0092 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.545+3674G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89108882 | ||||||
| chr9:89109101
|
G | A | 3 | a0001c0003t0001g0016a0001c0003t0004g0013a0001c0003t0004g0014 | 3 | HG02148.hp2 HG02300.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.545+3455C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89109101 | ||||||
| chr9:89109354
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+3202G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89109354 | ||||||
| chr9:89109410
|
C | T | 4 | a0001c0001t0003g0049a0001c0001t0012g0040a0001c0001t0012g0041others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+3146G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89109410 | ||||||
| chr9:89109467
|
T | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+3089A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89109467 | ||||||
| chr9:89109547
|
T | C | 1 | a0001c0001t0004g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.545+3009A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89109547 | ||||||
| chr9:89109578
|
G | C | 1 | a0001c0002t0008g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.545+2978C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89109578 | ||||||
| chr9:89110053
|
C | A | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545+2503G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110053 | ||||||
| chr9:89110383
|
T | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+2173A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110383 | ||||||
| chr9:89110395
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+2161T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110395 | ||||||
| chr9:89110407
|
A | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.545+2149T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110407 | ||||||
| chr9:89110472
|
G | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(55): Show | 60 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.545+2084C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110472 | ||||||
| chr9:89110587
|
A | G | 1 | a0001c0002t0004g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.545+1969T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110587 | ||||||
| chr9:89110682
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.545+1874C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110682 | ||||||
| chr9:89110991
|
C | A | 1 | a0001c0001t0004g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.545+1565G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89110991 | ||||||
| chr9:89111097
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.545+1459C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111097 | ||||||
| chr9:89111344
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.545+1212A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111344 | ||||||
| chr9:89111379
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+1177C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111379 | ||||||
| chr9:89111480
|
G | T | 18 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0003g0120others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+1076C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111480 | ||||||
| chr9:89111522
|
A | C | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.545+1034T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111522 | ||||||
| chr9:89111592
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+964T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111592 | ||||||
| chr9:89111645
|
A | G | 1 | a0001c0001t0009g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.545+911T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111645 | ||||||
| chr9:89111759
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 6 | HG00323.hp1 HG00738.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+797A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111759 | ||||||
| chr9:89111962
|
G | A | 23 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(20): Show | 24 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.545+594C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89111962 | ||||||
| chr9:89112221
|
T | C | 1 | a0001c0001t0003g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.545+335A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89112221 | ||||||
| chr9:89112307
|
T | C | 1 | a0001c0001t0014g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.545+249A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89112307 | ||||||
| chr9:89112381
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0162 | 3 | HG03491.hp2 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.545+175G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89112381 | ||||||
| chr9:89112548
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
splice_region_variant&intron_variant | LOW | c.545+8C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 2/11 | chr9 | 89112548 | ||||||
| chr9:89112893
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-267C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89112893 | ||||||
| chr9:89113088
|
T | TC | 20 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.475-463dupG | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113088 | ||||||
| chr9:89113146
|
C | T | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.475-520G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113146 | ||||||
| chr9:89113253
|
A | T | 4 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(1): Show | 4 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-627T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113253 | ||||||
| chr9:89113438
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-812G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113438 | ||||||
| chr9:89113501
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-875T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113501 | ||||||
| chr9:89113589
|
C | A | 1 | a0001c0001t0043g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.475-963G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113589 | ||||||
| chr9:89113641
|
C | A | 1 | a0001c0001t0004g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.475-1015G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113641 | ||||||
| chr9:89113702
|
T | C | 1 | a0001c0001t0029g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-1076A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113702 | ||||||
| chr9:89113750
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-1124T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89113750 | ||||||
| chr9:89114074
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.475-1448T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114074 | ||||||
| chr9:89114090
|
C | G | 1 | a0001c0001t0003g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.475-1464G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114090 | ||||||
| chr9:89114098
|
T | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-1472A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114098 | ||||||
| chr9:89114224
|
G | A | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475-1598C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114224 | ||||||
| chr9:89114252
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-1626G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114252 | ||||||
| chr9:89114276
|
G | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-1650C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114276 | ||||||
| chr9:89114435
|
G | GA | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-1810dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114435 | ||||||
| chr9:89114567
|
A | G | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475-1941T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114567 | ||||||
| chr9:89114569
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-1943C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114569 | ||||||
| chr9:89114809
|
C | T | 2 | a0001c0001t0003g0090a0001c0002t0003g0091 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.475-2183G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114809 | ||||||
| chr9:89114817
|
C | A | 23 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(20): Show | 24 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.475-2191G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89114817 | ||||||
| chr9:89115011
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.475-2385A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89115011 | ||||||
| chr9:89115031
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0003t0001g0009others(12): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.475-2405G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89115031 | ||||||
| chr9:89115083
|
T | C | 1 | a0001c0002t0032g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.475-2457A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89115083 | ||||||
| chr9:89115214
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-2588G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89115214 | ||||||
| chr9:89115879
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.475-3253G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89115879 | ||||||
| chr9:89116294
|
C | T | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.475-3668G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116294 | ||||||
| chr9:89116357
|
T | C | 4 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(1): Show | 4 | HG02965.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-3731A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116357 | ||||||
| chr9:89116395
|
C | G | 1 | a0001c0001t0019g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.475-3769G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116395 | ||||||
| chr9:89116435
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-3809G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116435 | ||||||
| chr9:89116478
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-3852C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116478 | ||||||
| chr9:89116739
|
C | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-4113G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116739 | ||||||
| chr9:89116820
|
T | C | 9 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.475-4194A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116820 | ||||||
| chr9:89116833
|
G | A | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-4207C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116833 | ||||||
| chr9:89116880
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.475-4254G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89116880 | ||||||
| chr9:89117044
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-4418A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117044 | ||||||
| chr9:89117171
|
C | T | 3 | a0001c0003t0001g0009a0001c0003t0003g0020a0001c0003t0011g0010 | 3 | HG02559.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.475-4545G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117171 | ||||||
| chr9:89117172
|
C | G | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-4546G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117172 | ||||||
| chr9:89117271
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-4645G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117271 | ||||||
| chr9:89117722
|
A | T | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475-5096T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117722 | ||||||
| chr9:89117723
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-5097G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117723 | ||||||
| chr9:89117765
|
A | T | 6 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(3): Show | 6 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-5139T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117765 | ||||||
| chr9:89117794
|
T | C | 6 | a0001c0001t0004g0061a0001c0001t0006g0060a0001c0002t0006g0002others(3): Show | 7 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-5168A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117794 | ||||||
| chr9:89117817
|
G | A | 1 | a0001c0001t0035g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.475-5191C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89117817 | ||||||
| chr9:89118153
|
C | CT | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0005g0026others(10): Show | 13 | HG00639.hp2 HG01891.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.475-5528dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118153 | ||||||
| chr9:89118166
|
G | A | 4 | a0001c0002t0002g0085a0001c0002t0002g0086a0001c0002t0002g0087others(1): Show | 4 | HG00140.hp1 HG01109.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-5540C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118166 | ||||||
| chr9:89118220
|
A | AT | 30 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0162others(27): Show | 31 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.475-5595dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118220 | ||||||
| chr9:89118361
|
A | G | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.475-5735T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118361 | ||||||
| chr9:89118400
|
T | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-5774A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118400 | ||||||
| chr9:89118469
|
A | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0005g0026others(9): Show | 12 | HG00639.hp2 HG01891.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.475-5843T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118469 | ||||||
| chr9:89118594
|
A | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-5968T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118594 | ||||||
| chr9:89118753
|
A | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-6127T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118753 | ||||||
| chr9:89118941
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-6315C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118941 | ||||||
| chr9:89118960
|
C | T | 14 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(11): Show | 14 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-6334G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89118960 | ||||||
| chr9:89119159
|
T | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-6533A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89119159 | ||||||
| chr9:89119313
|
C | T | 4 | a0001c0002t0002g0039a0001c0002t0005g0050a0001c0002t0017g0031others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-6687G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89119313 | ||||||
| chr9:89119397
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-6771C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89119397 | ||||||
| chr9:89119409
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.475-6783A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89119409 | ||||||
| chr9:89119413
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-6787C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89119413 | ||||||
| chr9:89119941
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-7315T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89119941 | ||||||
| chr9:89120020
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-7394G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89120020 | ||||||
| chr9:89120117
|
G | A | 19 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(16): Show | 19 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.475-7491C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89120117 | ||||||
| chr9:89120331
|
A | C | 4 | a0001c0001t0003g0049a0001c0001t0012g0040a0001c0001t0012g0041others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-7705T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89120331 | ||||||
| chr9:89120538
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-7912C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89120538 | ||||||
| chr9:89120603
|
T | A | 1 | a0001c0001t0004g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.475-7977A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89120603 | ||||||
| chr9:89120998
|
C | T | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-8372G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89120998 | ||||||
| chr9:89121132
|
T | A | 1 | a0001c0006t0004g0169 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-8506A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121132 | ||||||
| chr9:89121238
|
G | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-8612C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121238 | ||||||
| chr9:89121264
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-8638G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121264 | ||||||
| chr9:89121415
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-8789G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121415 | ||||||
| chr9:89121499
|
A | G | 1 | a0001c0001t0044g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.475-8873T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121499 | ||||||
| chr9:89121517
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.475-8891G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121517 | ||||||
| chr9:89121528
|
G | C | 1 | a0001c0006t0004g0169 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-8902C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121528 | ||||||
| chr9:89121545
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-8919G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121545 | ||||||
| chr9:89121920
|
G | A | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-9294C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121920 | ||||||
| chr9:89121954
|
C | G | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-9328G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89121954 | ||||||
| chr9:89122139
|
A | T | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-9513T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89122139 | ||||||
| chr9:89122470
|
T | G | 1 | a0001c0002t0003g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.475-9844A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89122470 | ||||||
| chr9:89122477
|
T | C | 3 | a0001c0001t0017g0076a0001c0001t0020g0152a0001c0001t0043g0077 | 3 | HG02970.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.475-9851A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89122477 | ||||||
| chr9:89122700
|
A | G | 3 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111 | 3 | HG00741.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.475-10074T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89122700 | ||||||
| chr9:89122783
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-10157A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89122783 | ||||||
| chr9:89122801
|
G | C | 1 | a0001c0001t0002g0167 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.475-10175C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89122801 | ||||||
| chr9:89123043
|
A | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-10417T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89123043 | ||||||
| chr9:89123070
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-10444G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89123070 | ||||||
| chr9:89123130
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-10504A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89123130 | ||||||
| chr9:89123442
|
G | A | 2 | a0001c0001t0002g0116a0001c0002t0005g0117 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.475-10816C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89123442 | ||||||
| chr9:89124167
|
T | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.475-11541A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124167 | ||||||
| chr9:89124281
|
G | A | 4 | a0001c0004t0010g0179a0001c0004t0010g0180a0001c0004t0010g0181others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-11655C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124281 | ||||||
| chr9:89124301
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(3): Show | 6 | HG00639.hp2 HG01975.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-11675G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124301 | ||||||
| chr9:89124382
|
T | A | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.475-11756A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124382 | ||||||
| chr9:89124407
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.475-11781A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124407 | ||||||
| chr9:89124487
|
A | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(57): Show | 62 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.475-11861T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124487 | ||||||
| chr9:89124637
|
C | G | 1 | a0001c0001t0014g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.475-12011G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124637 | ||||||
| chr9:89124854
|
T | TA | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-12229dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124854 | ||||||
| chr9:89124900
|
T | G | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-12274A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124900 | ||||||
| chr9:89124989
|
G | A | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-12363C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89124989 | ||||||
| chr9:89125007
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-12381G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125007 | ||||||
| chr9:89125310
|
A | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.475-12684T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125310 | ||||||
| chr9:89125320
|
T | C | 1 | a0001c0001t0016g0098 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.475-12694A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125320 | ||||||
| chr9:89125442
|
T | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-12816A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125442 | ||||||
| chr9:89125574
|
T | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.475-12948A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125574 | ||||||
| chr9:89125756
|
G | A | 1 | a0001c0003t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475-13130C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125756 | ||||||
| chr9:89125930
|
G | T | 3 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0025g0028 | 3 | HG02965.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475-13304C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89125930 | ||||||
| chr9:89126015
|
T | C | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-13389A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126015 | ||||||
| chr9:89126035
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-13409T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126035 | ||||||
| chr9:89126114
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.475-13488T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126114 | ||||||
| chr9:89126179
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | NA18974.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.475-13553C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126179 | ||||||
| chr9:89126191
|
A | G | 1 | a0001c0002t0007g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.475-13565T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126191 | ||||||
| chr9:89126255
|
C | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-13629G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126255 | ||||||
| chr9:89126257
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-13631T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126257 | ||||||
| chr9:89126341
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-13715C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126341 | ||||||
| chr9:89126357
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.475-13731G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126357 | ||||||
| chr9:89126517
|
G | T | 4 | a0001c0001t0003g0049a0001c0001t0012g0040a0001c0001t0012g0041others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-13891C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126517 | ||||||
| chr9:89126552
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0005g0124 | 3 | HG00099.hp2 HG02300.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.475-13926C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126552 | ||||||
| chr9:89126560
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-13934G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126560 | ||||||
| chr9:89126758
|
T | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-14132A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126758 | ||||||
| chr9:89126777
|
G | T | 2 | a0001c0001t0002g0121a0001c0001t0030g0122 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.475-14151C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126777 | ||||||
| chr9:89126910
|
C | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(77): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.475-14284G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126910 | ||||||
| chr9:89126926
|
T | A | 4 | a0001c0001t0003g0045a0001c0001t0003g0149a0001c0001t0003g0151others(1): Show | 4 | HG01109.hp1 HG01168.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-14300A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126926 | ||||||
| chr9:89126993
|
A | G | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.475-14367T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89126993 | ||||||
| chr9:89127039
|
C | G | 1 | a0001c0001t0028g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.475-14413G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127039 | ||||||
| chr9:89127111
|
T | C | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.475-14485A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127111 | ||||||
| chr9:89127667
|
T | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-15041A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127667 | ||||||
| chr9:89127772
|
C | T | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.475-15146G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127772 | ||||||
| chr9:89127779
|
A | AC | 28 | a0001c0001t0001g0153a0001c0001t0003g0049a0001c0001t0003g0055others(25): Show | 28 | HG00099.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.475-15154dupG | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127779 | ||||||
| chr9:89127782
|
C | CT | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.475-15157_475-1515 others(5): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127782 | ||||||
| chr9:89127871
|
C | A | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.475-15245G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127871 | ||||||
| chr9:89127871
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-15245G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89127871 | ||||||
| chr9:89128077
|
A | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-15451T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128077 | ||||||
| chr9:89128131
|
A | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-15505T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128131 | ||||||
| chr9:89128141
|
GA | G | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.475-15516delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128141 | ||||||
| chr9:89128240
|
T | G | 1 | a0001c0001t0014g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.475-15614A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128240 | ||||||
| chr9:89128253
|
C | T | 3 | a0001c0001t0009g0096a0001c0001t0009g0097a0001c0001t0013g0112 | 3 | HG01943.hp2 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.475-15627G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128253 | ||||||
| chr9:89128416
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.475-15790C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128416 | ||||||
| chr9:89128530
|
G | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-15904C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128530 | ||||||
| chr9:89128614
|
C | T | 31 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0003g0120others(28): Show | 32 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.475-15988G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128614 | ||||||
| chr9:89128681
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.475-16055C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128681 | ||||||
| chr9:89128732
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.475-16106G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128732 | ||||||
| chr9:89128791
|
A | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-16165T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128791 | ||||||
| chr9:89128805
|
G | C | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-16179C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128805 | ||||||
| chr9:89128889
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0041g0174 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.475-16263G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128889 | ||||||
| chr9:89128894
|
C | T | 7 | a0001c0001t0042g0079a0001c0002t0002g0085a0001c0002t0002g0086others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-16268G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128894 | ||||||
| chr9:89128898
|
G | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-16272C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89128898 | ||||||
| chr9:89129049
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-16423C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129049 | ||||||
| chr9:89129385
|
C | A | 7 | a0001c0001t0042g0079a0001c0002t0002g0085a0001c0002t0002g0086others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-16759G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129385 | ||||||
| chr9:89129426
|
G | A | 1 | a0001c0001t0009g0097 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.475-16800C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129426 | ||||||
| chr9:89129455
|
T | C | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-16829A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129455 | ||||||
| chr9:89129486
|
T | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-16860A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129486 | ||||||
| chr9:89129505
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-16879C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129505 | ||||||
| chr9:89129552
|
A | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-16926T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129552 | ||||||
| chr9:89129568
|
A | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0005g0026others(10): Show | 13 | HG00639.hp2 HG01891.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.475-16942T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129568 | ||||||
| chr9:89129635
|
G | A | 3 | a0001c0001t0002g0044a0001c0001t0022g0042a0001c0002t0002g0088 | 3 | HG00140.hp1 HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-17009C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129635 | ||||||
| chr9:89129647
|
C | T | 4 | a0001c0001t0003g0055a0001c0002t0003g0052a0001c0002t0005g0054others(1): Show | 4 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-17021G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129647 | ||||||
| chr9:89129777
|
C | A | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-17151G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129777 | ||||||
| chr9:89129853
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-17227G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129853 | ||||||
| chr9:89129989
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.475-17363G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89129989 | ||||||
| chr9:89130161
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-17535C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89130161 | ||||||
| chr9:89130269
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0004g0038a0001c0007t0003g0177others(1): Show | 4 | HG02622.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-17643C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89130269 | ||||||
| chr9:89130610
|
C | T | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-17984G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89130610 | ||||||
| chr9:89130729
|
C | T | 3 | a0001c0003t0045g0008a0001c0007t0003g0177a0001c0007t0015g0176 | 3 | HG02055.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-18103G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89130729 | ||||||
| chr9:89130791
|
C | T | 2 | a0001c0001t0003g0090a0001c0002t0003g0091 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.475-18165G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89130791 | ||||||
| chr9:89131049
|
G | C | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.475-18423C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131049 | ||||||
| chr9:89131154
|
C | A | 4 | a0001c0001t0003g0115a0001c0001t0018g0144a0001c0001t0037g0113others(1): Show | 4 | HG03540.hp1 HG03834.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-18528G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131154 | ||||||
| chr9:89131163
|
A | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-18537T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131163 | ||||||
| chr9:89131607
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(93): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.475-18981G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131607 | ||||||
| chr9:89131657
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-19031G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131657 | ||||||
| chr9:89131710
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-19084C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131710 | ||||||
| chr9:89131758
|
T | G | 1 | a0001c0001t0029g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-19132A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89131758 | ||||||
| chr9:89132020
|
A | C | 1 | a0001c0001t0006g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.475-19394T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132020 | ||||||
| chr9:89132162
|
G | C | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-19536C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132162 | ||||||
| chr9:89132204
|
T | G | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.475-19578A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132204 | ||||||
| chr9:89132215
|
C | T | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-19589G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132215 | ||||||
| chr9:89132294
|
T | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-19668A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132294 | ||||||
| chr9:89132379
|
C | T | 15 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.475-19753G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132379 | ||||||
| chr9:89132551
|
T | C | 1 | a0001c0001t0003g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.475-19925A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132551 | ||||||
| chr9:89132569
|
C | T | 6 | a0001c0001t0004g0061a0001c0001t0006g0060a0001c0002t0006g0002others(3): Show | 7 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-19943G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132569 | ||||||
| chr9:89132603
|
C | A | 1 | a0001c0001t0008g0132 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.475-19977G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132603 | ||||||
| chr9:89132967
|
C | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-20341G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89132967 | ||||||
| chr9:89133000
|
A | C | 13 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-20374T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133000 | ||||||
| chr9:89133203
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.475-20577C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133203 | ||||||
| chr9:89133224
|
C | T | 1 | a0001c0003t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475-20598G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133224 | ||||||
| chr9:89133238
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-20612C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133238 | ||||||
| chr9:89133249
|
A | T | 1 | a0001c0002t0015g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.475-20623T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133249 | ||||||
| chr9:89133418
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-20792G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133418 | ||||||
| chr9:89133471
|
C | T | 30 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(27): Show | 31 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.475-20845G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133471 | ||||||
| chr9:89133643
|
G | C | 1 | a0001c0002t0002g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.475-21017C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133643 | ||||||
| chr9:89133655
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-21029C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133655 | ||||||
| chr9:89133720
|
T | C | 2 | a0001c0001t0003g0115a0001c0001t0018g0144 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.475-21094A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89133720 | ||||||
| chr9:89134155
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-21529A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134155 | ||||||
| chr9:89134242
|
G | A | 164 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.475-21616C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134242 | ||||||
| chr9:89134253
|
G | A | 1 | a0001c0007t0003g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.475-21627C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134253 | ||||||
| chr9:89134472
|
GT | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(57): Show | 62 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.475-21847delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134472 | ||||||
| chr9:89134582
|
T | C | 19 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(16): Show | 19 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.475-21956A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134582 | ||||||
| chr9:89134627
|
C | T | 2 | a0001c0001t0017g0076a0001c0001t0043g0077 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.475-22001G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134627 | ||||||
| chr9:89134727
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.475-22101G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134727 | ||||||
| chr9:89134827
|
C | G | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.475-22201G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89134827 | ||||||
| chr9:89135172
|
C | T | 12 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(9): Show | 12 | HG00408.hp1 HG01081.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.475-22546G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135172 | ||||||
| chr9:89135331
|
G | C | 1 | a0001c0001t0014g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.475-22705C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135331 | ||||||
| chr9:89135692
|
C | T | 4 | a0001c0002t0006g0002a0001c0002t0006g0059a0001c0002t0006g0173others(1): Show | 5 | HG00280.hp1 HG00642.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-23066G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135692 | ||||||
| chr9:89135701
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0002t0002g0166 | 3 | HG00280.hp2 HG00639.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.475-23075G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135701 | ||||||
| chr9:89135714
|
T | C | 1 | a0001c0001t0007g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.475-23088A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135714 | ||||||
| chr9:89135751
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG00639.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.475-23125T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135751 | ||||||
| chr9:89135822
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-23196T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89135822 | ||||||
| chr9:89136008
|
T | G | 1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475-23382A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136008 | ||||||
| chr9:89136010
|
A | C | 15 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0012g0040others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-23384T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136010 | ||||||
| chr9:89136202
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475-23576C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136202 | ||||||
| chr9:89136443
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-23817G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136443 | ||||||
| chr9:89136606
|
A | G | 5 | a0001c0001t0003g0055a0001c0002t0003g0052a0001c0002t0003g0056others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-23980T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136606 | ||||||
| chr9:89136681
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.475-24055G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136681 | ||||||
| chr9:89136741
|
T | C | 1 | a0001c0002t0021g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.475-24115A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136741 | ||||||
| chr9:89136752
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-24126G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136752 | ||||||
| chr9:89136798
|
G | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(55): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.475-24172C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89136798 | ||||||
| chr9:89137002
|
T | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-24376A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137002 | ||||||
| chr9:89137028
|
A | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-24402T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137028 | ||||||
| chr9:89137119
|
C | T | 2 | a0001c0001t0002g0121a0001c0001t0030g0122 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.475-24493G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137119 | ||||||
| chr9:89137507
|
T | A | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475-24881A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137507 | ||||||
| chr9:89137659
|
G | A | 1 | a0001c0002t0002g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.475-25033C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137659 | ||||||
| chr9:89137735
|
A | G | 1 | a0001c0002t0002g0118 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.475-25109T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137735 | ||||||
| chr9:89137900
|
T | C | 1 | a0001c0002t0004g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.475-25274A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89137900 | ||||||
| chr9:89138083
|
C | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-25457G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89138083 | ||||||
| chr9:89138447
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-25821T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89138447 | ||||||
| chr9:89138554
|
G | A | 1 | a0001c0001t0016g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.475-25928C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89138554 | ||||||
| chr9:89138721
|
C | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(96): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.475-26095G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89138721 | ||||||
| chr9:89138751
|
G | A | 2 | a0001c0006t0004g0169a0001c0006t0024g0168 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475-26125C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89138751 | ||||||
| chr9:89138885
|
G | C | 53 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(50): Show | 55 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.475-26259C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89138885 | ||||||
| chr9:89139232
|
A | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475-26606T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89139232 | ||||||
| chr9:89139918
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.475-27292G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89139918 | ||||||
| chr9:89140148
|
A | C | 12 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(9): Show | 12 | HG00408.hp1 HG01081.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.475-27522T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140148 | ||||||
| chr9:89140280
|
G | A | 2 | a0001c0001t0017g0076a0001c0001t0043g0077 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.475-27654C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140280 | ||||||
| chr9:89140337
|
C | T | 13 | a0001c0001t0003g0049a0001c0001t0003g0120a0001c0001t0005g0171others(10): Show | 13 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.475-27711G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140337 | ||||||
| chr9:89140344
|
C | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(27): Show | 31 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.475-27718G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140344 | ||||||
| chr9:89140454
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-27828C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140454 | ||||||
| chr9:89140614
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0016g0160 | 2 | HG00738.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.475-27988G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140614 | ||||||
| chr9:89140724
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-28098C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140724 | ||||||
| chr9:89140810
|
T | G | 1 | a0001c0001t0004g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.475-28184A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140810 | ||||||
| chr9:89140813
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-28187C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89140813 | ||||||
| chr9:89141214
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-28588T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89141214 | ||||||
| chr9:89141290
|
A | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0036others(36): Show | 41 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.475-28664T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89141290 | ||||||
| chr9:89141344
|
GA | G | 2 | a0001c0001t0001g0153a0001c0001t0004g0038 | 2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.475-28719delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89141344 | ||||||
| chr9:89141565
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0012g0040a0001c0001t0012g0041others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-28939A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89141565 | ||||||
| chr9:89141858
|
G | A | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.475-29232C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89141858 | ||||||
| chr9:89141988
|
T | A | 1 | a0001c0002t0006g0127 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.475-29362A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89141988 | ||||||
| chr9:89142102
|
A | T | 4 | a0001c0001t0003g0055a0001c0002t0003g0052a0001c0002t0005g0054others(1): Show | 4 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-29476T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142102 | ||||||
| chr9:89142183
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.475-29557G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142183 | ||||||
| chr9:89142242
|
C | T | 2 | a0001c0002t0006g0127a0001c0002t0019g0126 | 2 | HG00735.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.475-29616G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142242 | ||||||
| chr9:89142427
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-29801C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142427 | ||||||
| chr9:89142556
|
G | A | 1 | a0001c0003t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475-29930C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142556 | ||||||
| chr9:89142580
|
C | T | 1 | a0001c0001t0004g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.475-29954G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142580 | ||||||
| chr9:89142673
|
C | CA | 6 | a0001c0001t0002g0136a0001c0001t0003g0151a0001c0001t0009g0161others(3): Show | 6 | HG00280.hp1 HG00735.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-30048dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142673 | ||||||
| chr9:89142673
|
C | CAA | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0163others(8): Show | 13 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.475-30049_475-3004 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142673 | ||||||
| chr9:89142673
|
CAA | C | 30 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0002g0044others(27): Show | 31 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.475-30049_475-3004 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142673 | ||||||
| chr9:89142699
|
G | T | 3 | a0001c0001t0008g0108a0001c0001t0008g0109a0001c0009t0027g0178 | 3 | HG02809.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.475-30073C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142699 | ||||||
| chr9:89142746
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-30120C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142746 | ||||||
| chr9:89142797
|
G | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(55): Show | 61 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.475-30171C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142797 | ||||||
| chr9:89142944
|
AGTATT | A | 4 | a0001c0004t0010g0179a0001c0004t0010g0180a0001c0004t0010g0181others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-30323_475-3031 others(9): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142944 | ||||||
| chr9:89142990
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.475-30364C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89142990 | ||||||
| chr9:89143120
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0041g0174 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.475-30494G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143120 | ||||||
| chr9:89143181
|
A | G | 14 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(11): Show | 15 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.475-30555T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143181 | ||||||
| chr9:89143563
|
G | T | 1 | a0001c0001t0003g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.475-30937C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143563 | ||||||
| chr9:89143575
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0022g0042 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.475-30949G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143575 | ||||||
| chr9:89143663
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.475-31037A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143663 | ||||||
| chr9:89143706
|
T | C | 16 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-31080A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143706 | ||||||
| chr9:89143962
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.475-31336T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89143962 | ||||||
| chr9:89144051
|
A | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0030g0122 | 4 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-31425T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144051 | ||||||
| chr9:89144056
|
G | T | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0004g0066 | 3 | HG01081.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.475-31430C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144056 | ||||||
| chr9:89144145
|
G | A | 19 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(16): Show | 19 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.475-31519C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144145 | ||||||
| chr9:89144434
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.475-31808G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144434 | ||||||
| chr9:89144666
|
T | C | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.475-32040A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144666 | ||||||
| chr9:89144793
|
CT | C | 12 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0005g0026others(9): Show | 12 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.475-32168delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144793 | ||||||
| chr9:89144892
|
C | A | 1 | a0001c0001t0029g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-32266G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89144892 | ||||||
| chr9:89145103
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.475-32477G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145103 | ||||||
| chr9:89145188
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0162others(9): Show | 14 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.475-32562T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145188 | ||||||
| chr9:89145247
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-32621A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145247 | ||||||
| chr9:89145268
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.475-32642C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145268 | ||||||
| chr9:89145282
|
A | T | 1 | a0001c0001t0009g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.475-32656T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145282 | ||||||
| chr9:89145322
|
C | T | 1 | a0001c0001t0004g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474+32665G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145322 | ||||||
| chr9:89145356
|
C | T | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+32631G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145356 | ||||||
| chr9:89145417
|
A | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG01891.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+32570T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145417 | ||||||
| chr9:89145560
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.474+32427C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145560 | ||||||
| chr9:89145582
|
T | A | 3 | a0001c0001t0003g0120a0001c0001t0005g0171a0001c0001t0026g0172 | 3 | HG02723.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+32405A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145582 | ||||||
| chr9:89145783
|
T | C | 14 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(11): Show | 15 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.474+32204A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89145783 | ||||||
| chr9:89146049
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.474+31938G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146049 | ||||||
| chr9:89146165
|
G | A | 3 | a0001c0001t0001g0153a0001c0007t0003g0177a0001c0007t0015g0176 | 3 | HG03486.hp2 HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.474+31822C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146165 | ||||||
| chr9:89146198
|
AATACAAA others(4): Show |
A | 12 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0005g0026others(9): Show | 12 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+31778_474+3178 others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146198 | ||||||
| chr9:89146211
|
G | C | 12 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0005g0026others(9): Show | 12 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+31776C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146211 | ||||||
| chr9:89146212
|
C | G | 12 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0005g0026others(9): Show | 12 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+31775G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146212 | ||||||
| chr9:89146216
|
G | T | 12 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0005g0026others(9): Show | 12 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+31771C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146216 | ||||||
| chr9:89146275
|
G | T | 16 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0153others(13): Show | 16 | HG00639.hp2 HG01891.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.474+31712C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146275 | ||||||
| chr9:89146358
|
AAAAAC | A | 30 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0003g0120others(27): Show | 31 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.474+31624_474+3162 others(9): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146358 | ||||||
| chr9:89146374
|
AAAAC | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0029g0024others(1): Show | 4 | HG00639.hp2 HG01975.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+31609_474+3161 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146374 | ||||||
| chr9:89146523
|
A | T | 14 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(11): Show | 15 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.474+31464T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89146523 | ||||||
| chr9:89147164
|
TA | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.474+30822delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147164 | ||||||
| chr9:89147177
|
A | T | 2 | a0001c0001t0028g0139a0001c0001t0035g0092 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.474+30810T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147177 | ||||||
| chr9:89147401
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474+30586G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147401 | ||||||
| chr9:89147492
|
T | G | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+30495A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147492 | ||||||
| chr9:89147511
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+30476G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147511 | ||||||
| chr9:89147713
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.474+30274G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147713 | ||||||
| chr9:89147773
|
G | T | 1 | a0001c0001t0002g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474+30214C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147773 | ||||||
| chr9:89147809
|
T | C | 15 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0111others(12): Show | 15 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.474+30178A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147809 | ||||||
| chr9:89147834
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.474+30153C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89147834 | ||||||
| chr9:89148290
|
G | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.474+29697C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89148290 | ||||||
| chr9:89148547
|
T | C | 14 | a0001c0001t0001g0153a0001c0001t0002g0044a0001c0001t0005g0026others(11): Show | 14 | HG01891.hp1 HG02258.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.474+29440A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89148547 | ||||||
| chr9:89148982
|
C | G | 2 | a0001c0003t0003g0022a0001c0003t0045g0008 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.474+29005G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89148982 | ||||||
| chr9:89149080
|
G | A | 1 | a0001c0001t0023g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.474+28907C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149080 | ||||||
| chr9:89149146
|
C | A | 4 | a0001c0001t0002g0116a0001c0002t0002g0118a0001c0002t0002g0119others(1): Show | 4 | HG01167.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+28841G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149146 | ||||||
| chr9:89149212
|
T | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.474+28775A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149212 | ||||||
| chr9:89149349
|
T | C | 1 | a0001c0002t0032g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.474+28638A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149349 | ||||||
| chr9:89149495
|
A | C | 1 | a0001c0001t0002g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.474+28492T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149495 | ||||||
| chr9:89149519
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.474+28468C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149519 | ||||||
| chr9:89149564
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.474+28423A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149564 | ||||||
| chr9:89149582
|
A | C | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+28405T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149582 | ||||||
| chr9:89149738
|
A | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(63): Show | 69 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.474+28249T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149738 | ||||||
| chr9:89149852
|
A | T | 11 | a0001c0001t0002g0044a0001c0001t0005g0026a0001c0001t0005g0027others(8): Show | 11 | HG01891.hp1 HG02258.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+28135T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149852 | ||||||
| chr9:89149862
|
G | C | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+28125C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89149862 | ||||||
| chr9:89150317
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.474+27670A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150317 | ||||||
| chr9:89150403
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+27584G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150403 | ||||||
| chr9:89150497
|
T | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+27490A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150497 | ||||||
| chr9:89150562
|
C | T | 2 | a0001c0001t0042g0079a0001c0002t0039g0078 | 2 | HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.474+27425G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150562 | ||||||
| chr9:89150717
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0162others(9): Show | 14 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+27270T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150717 | ||||||
| chr9:89150796
|
C | T | 1 | a0001c0001t0005g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+27191G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150796 | ||||||
| chr9:89150888
|
T | A | 5 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(2): Show | 5 | HG02886.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+27099A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89150888 | ||||||
| chr9:89151016
|
CT | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(106): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.474+26970delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151016 | ||||||
| chr9:89151070
|
G | A | 1 | a0001c0001t0036g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.474+26917C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151070 | ||||||
| chr9:89151081
|
T | G | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+26906A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151081 | ||||||
| chr9:89151107
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+26880G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151107 | ||||||
| chr9:89151172
|
C | T | 1 | a0001c0002t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.474+26815G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151172 | ||||||
| chr9:89151391
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0162others(9): Show | 14 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+26596A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151391 | ||||||
| chr9:89151420
|
GA | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0162others(9): Show | 14 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+26566delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151420 | ||||||
| chr9:89151550
|
G | A | 1 | a0001c0001t0028g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.474+26437C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151550 | ||||||
| chr9:89151791
|
A | G | 101 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.474+26196T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151791 | ||||||
| chr9:89151818
|
A | G | 16 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(13): Show | 17 | HG00408.hp1 HG01081.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+26169T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151818 | ||||||
| chr9:89151828
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034 | 3 | HG00639.hp2 HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.474+26159T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89151828 | ||||||
| chr9:89152192
|
G | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+25795C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152192 | ||||||
| chr9:89152307
|
C | A | 1 | a0001c0003t0001g0016 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.474+25680G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152307 | ||||||
| chr9:89152371
|
A | G | 1 | a0001c0003t0004g0021 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.474+25616T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152371 | ||||||
| chr9:89152493
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+25494G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152493 | ||||||
| chr9:89152618
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+25369C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152618 | ||||||
| chr9:89152627
|
T | C | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+25360A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152627 | ||||||
| chr9:89152745
|
T | G | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+25242A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152745 | ||||||
| chr9:89152932
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+25055C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152932 | ||||||
| chr9:89152956
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0162others(9): Show | 14 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+25031C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89152956 | ||||||
| chr9:89153084
|
G | A | 1 | a0001c0001t0044g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.474+24903C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153084 | ||||||
| chr9:89153306
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+24681C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153306 | ||||||
| chr9:89153339
|
T | C | 2 | a0001c0001t0013g0093a0001c0001t0035g0092 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.474+24648A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153339 | ||||||
| chr9:89153374
|
C | T | 1 | a0001c0001t0005g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.474+24613G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153374 | ||||||
| chr9:89153503
|
C | G | 1 | a0001c0002t0002g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.474+24484G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153503 | ||||||
| chr9:89153692
|
C | G | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+24295G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153692 | ||||||
| chr9:89153733
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.474+24254G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153733 | ||||||
| chr9:89153748
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.474+24239A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153748 | ||||||
| chr9:89153902
|
C | T | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+24085G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153902 | ||||||
| chr9:89153909
|
G | A | 1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474+24078C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153909 | ||||||
| chr9:89153916
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(91): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.474+24071C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153916 | ||||||
| chr9:89153943
|
G | A | 1 | a0001c0001t0002g0004 | 2 | HG02723.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.474+24044C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153943 | ||||||
| chr9:89153960
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.474+24027A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89153960 | ||||||
| chr9:89154106
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.474+23881C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154106 | ||||||
| chr9:89154205
|
C | CT | 15 | a0001c0001t0002g0044a0001c0001t0002g0067a0001c0001t0002g0068others(12): Show | 15 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.474+23781dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154205 | ||||||
| chr9:89154289
|
C | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(73): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.474+23698G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154289 | ||||||
| chr9:89154318
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474+23669C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154318 | ||||||
| chr9:89154396
|
C | T | 4 | a0001c0001t0002g0116a0001c0002t0005g0117a0001c0007t0003g0177others(1): Show | 4 | HG01515.hp1 HG01517.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+23591G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154396 | ||||||
| chr9:89154844
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(17): Show | 21 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.474+23143C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154844 | ||||||
| chr9:89154848
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(90): Show | 96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.474+23139T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154848 | ||||||
| chr9:89154916
|
C | T | 3 | a0001c0003t0001g0012a0001c0003t0002g0001a0001c0003t0004g0011 | 4 | HG01070.hp2 HG01071.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+23071G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89154916 | ||||||
| chr9:89155080
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0003g0045 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+22907G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89155080 | ||||||
| chr9:89155481
|
G | A | 1 | a0001c0002t0004g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.474+22506C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89155481 | ||||||
| chr9:89155978
|
A | G | 1 | a0001c0001t0028g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.474+22009T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89155978 | ||||||
| chr9:89155986
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+22001G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89155986 | ||||||
| chr9:89156084
|
A | C | 1 | a0001c0001t0016g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.474+21903T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156084 | ||||||
| chr9:89156202
|
C | T | 2 | a0001c0002t0002g0094a0001c0002t0038g0095 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.474+21785G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156202 | ||||||
| chr9:89156233
|
G | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.474+21754C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156233 | ||||||
| chr9:89156251
|
C | T | 16 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.474+21736G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156251 | ||||||
| chr9:89156377
|
CCTGAACT others(4): Show |
C | 1 | a0001c0001t0004g0066 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.474+21599_474+2160 others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156377 | ||||||
| chr9:89156488
|
T | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+21499A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156488 | ||||||
| chr9:89156624
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.474+21363A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156624 | ||||||
| chr9:89156675
|
A | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+21312T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156675 | ||||||
| chr9:89156727
|
G | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(65): Show | 71 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.474+21260C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156727 | ||||||
| chr9:89156830
|
G | A | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+21157C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89156830 | ||||||
| chr9:89157073
|
C | T | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+20914G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157073 | ||||||
| chr9:89157265
|
G | C | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+20722C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157265 | ||||||
| chr9:89157457
|
C | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(64): Show | 69 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.474+20530G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157457 | ||||||
| chr9:89157489
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+20498C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157489 | ||||||
| chr9:89157543
|
T | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0062others(74): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.474+20444A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157543 | ||||||
| chr9:89157596
|
A | T | 3 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0009g0161 | 3 | HG03225.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+20391T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157596 | ||||||
| chr9:89157794
|
A | T | 5 | a0001c0001t0002g0116a0001c0001t0028g0139a0001c0002t0002g0118others(2): Show | 5 | HG01167.hp2 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+20193T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157794 | ||||||
| chr9:89157806
|
G | A | 3 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0009g0161 | 3 | HG03225.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+20181C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157806 | ||||||
| chr9:89157828
|
C | A | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+20159G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157828 | ||||||
| chr9:89157970
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.474+20017G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89157970 | ||||||
| chr9:89158058
|
T | C | 1 | a0001c0002t0003g0091 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.474+19929A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89158058 | ||||||
| chr9:89158337
|
T | C | 16 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+19650A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89158337 | ||||||
| chr9:89158337
|
T | G | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+19650A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89158337 | ||||||
| chr9:89158590
|
T | C | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+19397A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89158590 | ||||||
| chr9:89158636
|
G | A | 1 | a0001c0001t0014g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.474+19351C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89158636 | ||||||
| chr9:89159071
|
G | A | 1 | a0001c0002t0005g0147 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.474+18916C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159071 | ||||||
| chr9:89159080
|
T | TGAAAACC others(6085): Show |
1 | a0001c0001t0026g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474+18906_474+1890 others(6096): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159080 | ||||||
| chr9:89159080
|
T | TGAAAACC others(6086): Show |
1 | a0001c0001t0005g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.474+18906_474+1890 others(6097): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159080 | ||||||
| chr9:89159194
|
G | A | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+18793C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159194 | ||||||
| chr9:89159449
|
T | C | 1 | a0001c0001t0005g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474+18538A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159449 | ||||||
| chr9:89159546
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.474+18441C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159546 | ||||||
| chr9:89159619
|
C | T | 1 | a0001c0001t0016g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.474+18368G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159619 | ||||||
| chr9:89159828
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0023g0023 | 4 | HG01255.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+18159T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159828 | ||||||
| chr9:89159900
|
C | G | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.474+18087G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89159900 | ||||||
| chr9:89160010
|
C | T | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+17977G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160010 | ||||||
| chr9:89160418
|
T | C | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+17569A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160418 | ||||||
| chr9:89160430
|
C | T | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+17557G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160430 | ||||||
| chr9:89160514
|
C | T | 1 | a0001c0001t0037g0113 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.474+17473G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160514 | ||||||
| chr9:89160747
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.474+17240A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160747 | ||||||
| chr9:89160851
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+17136T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160851 | ||||||
| chr9:89160854
|
T | C | 1 | a0001c0001t0002g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.474+17133A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160854 | ||||||
| chr9:89160945
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.474+17042C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160945 | ||||||
| chr9:89160966
|
C | T | 11 | a0001c0001t0001g0154a0001c0001t0004g0061a0001c0001t0006g0060others(8): Show | 12 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+17021G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160966 | ||||||
| chr9:89160967
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.474+17020T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89160967 | ||||||
| chr9:89161023
|
C | G | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+16964G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161023 | ||||||
| chr9:89161063
|
C | T | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+16924G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161063 | ||||||
| chr9:89161216
|
G | A | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+16771C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161216 | ||||||
| chr9:89161260
|
C | T | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+16727G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161260 | ||||||
| chr9:89161279
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474+16708C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161279 | ||||||
| chr9:89161419
|
G | A | 1 | a0001c0003t0002g0019 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.474+16568C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161419 | ||||||
| chr9:89161568
|
G | T | 4 | a0001c0002t0006g0002a0001c0002t0006g0059a0001c0002t0006g0173others(1): Show | 5 | HG00280.hp1 HG00642.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+16419C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161568 | ||||||
| chr9:89161590
|
A | T | 1 | a0001c0004t0001g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.474+16397T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161590 | ||||||
| chr9:89161817
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.474+16170G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161817 | ||||||
| chr9:89161959
|
G | C | 1 | a0001c0001t0014g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.474+16028C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89161959 | ||||||
| chr9:89162037
|
T | G | 70 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.474+15950A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162037 | ||||||
| chr9:89162280
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.474+15707C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162280 | ||||||
| chr9:89162324
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 12 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+15663T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162324 | ||||||
| chr9:89162438
|
G | A | 1 | a0001c0001t0028g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.474+15549C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162438 | ||||||
| chr9:89162451
|
T | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 12 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+15536A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162451 | ||||||
| chr9:89162456
|
G | A | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+15531C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162456 | ||||||
| chr9:89162484
|
C | A | 3 | a0001c0003t0001g0009a0001c0003t0003g0020a0001c0003t0011g0010 | 3 | HG02559.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.474+15503G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162484 | ||||||
| chr9:89162574
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.474+15413G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162574 | ||||||
| chr9:89162639
|
C | T | 1 | a0001c0001t0013g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.474+15348G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162639 | ||||||
| chr9:89162683
|
T | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(64): Show | 69 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.474+15304A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162683 | ||||||
| chr9:89162716
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474+15271A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162716 | ||||||
| chr9:89162942
|
C | G | 4 | a0001c0004t0010g0179a0001c0004t0010g0180a0001c0004t0010g0181others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+15045G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89162942 | ||||||
| chr9:89163298
|
T | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+14689A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163298 | ||||||
| chr9:89163341
|
A | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 12 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+14646T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163341 | ||||||
| chr9:89163487
|
C | T | 1 | a0001c0001t0019g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.474+14500G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163487 | ||||||
| chr9:89163612
|
G | T | 4 | a0001c0001t0003g0049a0001c0002t0005g0050a0001c0002t0021g0051others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+14375C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163612 | ||||||
| chr9:89163668
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.474+14319C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163668 | ||||||
| chr9:89163746
|
A | T | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+14241T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163746 | ||||||
| chr9:89163872
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+14115C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89163872 | ||||||
| chr9:89164213
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.474+13774C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89164213 | ||||||
| chr9:89164633
|
A | T | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+13354T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89164633 | ||||||
| chr9:89164698
|
T | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 12 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+13289A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89164698 | ||||||
| chr9:89165260
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0022g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.474+12726_474+1272 others(15): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165260 | ||||||
| chr9:89165260
|
T | TTG | 27 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0162others(24): Show | 29 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.474+12725_474+1272 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165260 | ||||||
| chr9:89165260
|
T | TTGTG | 9 | a0001c0001t0001g0153a0001c0001t0033g0037a0001c0003t0001g0009others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+12723_474+1272 others(8): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165260 | ||||||
| chr9:89165260
|
T | TTGTGTG | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG02886.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+12721_474+1272 others(10): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165260 | ||||||
| chr9:89165260
|
T | TTGTGTGT others(5): Show |
17 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0003g0055others(14): Show | 17 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+12715_474+1272 others(16): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165260 | ||||||
| chr9:89165260
|
T | TTGTGTGT others(7): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0049others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+12713_474+1272 others(18): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165260 | ||||||
| chr9:89165291
|
C | T | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+12696G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165291 | ||||||
| chr9:89165323
|
T | C | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+12664A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165323 | ||||||
| chr9:89165343
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.474+12644C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165343 | ||||||
| chr9:89165526
|
C | CA | 45 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0100others(42): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+12460dupT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165526 | ||||||
| chr9:89165526
|
C | CAA | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0062others(74): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.474+12459_474+1246 others(6): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165526 | ||||||
| chr9:89165526
|
C | CAAA | 13 | a0001c0001t0005g0145a0001c0001t0007g0030a0001c0001t0014g0025others(10): Show | 14 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.474+12458_474+1246 others(7): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165526 | ||||||
| chr9:89165526
|
CA | C | 5 | a0001c0001t0003g0090a0001c0002t0003g0091a0001c0007t0003g0177others(2): Show | 5 | HG03130.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+12460delT | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165526 | ||||||
| chr9:89165551
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+12436C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165551 | ||||||
| chr9:89165675
|
G | C | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+12312C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165675 | ||||||
| chr9:89165705
|
C | G | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+12282G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165705 | ||||||
| chr9:89165899
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.474+12088A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165899 | ||||||
| chr9:89165941
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.474+12046C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165941 | ||||||
| chr9:89165962
|
G | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(62): Show | 67 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.474+12025C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89165962 | ||||||
| chr9:89166046
|
C | T | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+11941G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166046 | ||||||
| chr9:89166094
|
G | A | 3 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0009g0161 | 3 | HG03225.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+11893C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166094 | ||||||
| chr9:89166106
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474+11881A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166106 | ||||||
| chr9:89166699
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474+11288T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166699 | ||||||
| chr9:89166738
|
G | T | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+11249C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166738 | ||||||
| chr9:89166742
|
G | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(8): Show | 12 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+11245C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166742 | ||||||
| chr9:89166933
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.474+11054G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89166933 | ||||||
| chr9:89167101
|
G | T | 1 | a0001c0001t0016g0098 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.474+10886C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89167101 | ||||||
| chr9:89167144
|
G | T | 2 | a0001c0001t0009g0096a0001c0001t0009g0097 | 2 | HG01943.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.474+10843C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89167144 | ||||||
| chr9:89167736
|
A | G | 2 | a0001c0002t0002g0094a0001c0002t0038g0095 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.474+10251T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89167736 | ||||||
| chr9:89167846
|
C | T | 1 | a0001c0002t0017g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474+10141G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89167846 | ||||||
| chr9:89168013
|
G | A | 3 | a0001c0001t0013g0093a0001c0001t0035g0092a0001c0002t0017g0031 | 3 | HG02615.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.474+9974C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89168013 | ||||||
| chr9:89168295
|
T | C | 1 | a0001c0002t0005g0147 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.474+9692A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89168295 | ||||||
| chr9:89168929
|
A | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(64): Show | 69 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.474+9058T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89168929 | ||||||
| chr9:89169007
|
G | A | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+8980C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169007 | ||||||
| chr9:89169028
|
C | A | 1 | a0001c0001t0003g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.474+8959G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169028 | ||||||
| chr9:89169098
|
A | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.474+8889T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169098 | ||||||
| chr9:89169113
|
G | A | 1 | a0001c0003t0003g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.474+8874C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169113 | ||||||
| chr9:89169514
|
A | G | 2 | a0001c0001t0013g0093a0001c0001t0035g0092 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.474+8473T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169514 | ||||||
| chr9:89169552
|
C | A | 1 | a0001c0002t0008g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.474+8435G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169552 | ||||||
| chr9:89169552
|
C | T | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+8435G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169552 | ||||||
| chr9:89169629
|
C | T | 2 | a0001c0001t0003g0090a0001c0002t0003g0091 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.474+8358G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89169629 | ||||||
| chr9:89170070
|
T | C | 3 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0009g0161 | 3 | HG03225.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+7917A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170070 | ||||||
| chr9:89170104
|
G | A | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+7883C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170104 | ||||||
| chr9:89170212
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.474+7775G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170212 | ||||||
| chr9:89170309
|
T | G | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+7678A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170309 | ||||||
| chr9:89170324
|
C | A | 1 | a0001c0001t0003g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.474+7663G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170324 | ||||||
| chr9:89170325
|
C | T | 1 | a0001c0001t0003g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.474+7662G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170325 | ||||||
| chr9:89170363
|
C | T | 1 | a0001c0001t0014g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.474+7624G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170363 | ||||||
| chr9:89170530
|
A | G | 6 | a0001c0001t0003g0055a0001c0001t0018g0046a0001c0002t0003g0052others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+7457T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170530 | ||||||
| chr9:89170623
|
C | T | 4 | a0001c0001t0003g0049a0001c0002t0005g0050a0001c0002t0021g0051others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+7364G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170623 | ||||||
| chr9:89170640
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0003g0045 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+7347T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170640 | ||||||
| chr9:89170741
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474+7246A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170741 | ||||||
| chr9:89170821
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0004t0001g0034others(2): Show | 5 | HG00639.hp2 HG01975.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+7166C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170821 | ||||||
| chr9:89170923
|
G | A | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+7064C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89170923 | ||||||
| chr9:89171102
|
T | A | 16 | a0001c0003t0001g0009a0001c0003t0001g0012a0001c0003t0001g0016others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+6885A>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171102 | ||||||
| chr9:89171198
|
T | C | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+6789A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171198 | ||||||
| chr9:89171221
|
G | A | 1 | a0001c0003t0004g0021 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.474+6766C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171221 | ||||||
| chr9:89171234
|
A | AT | 32 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(29): Show | 34 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.474+6752dupA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171234 | ||||||
| chr9:89171234
|
AT | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0062others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.474+6752delA | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171234 | ||||||
| chr9:89171495
|
C | A | 2 | a0001c0001t0002g0044a0001c0001t0003g0045 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+6492G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171495 | ||||||
| chr9:89171737
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(33): Show | 38 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.474+6250T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171737 | ||||||
| chr9:89171750
|
G | A | 1 | a0001c0002t0006g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.474+6237C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171750 | ||||||
| chr9:89171885
|
A | C | 1 | a0001c0003t0045g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.474+6102T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89171885 | ||||||
| chr9:89172160
|
C | G | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+5827G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172160 | ||||||
| chr9:89172201
|
G | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(59): Show | 64 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.474+5786C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172201 | ||||||
| chr9:89172232
|
T | C | 3 | a0001c0001t0003g0149a0001c0001t0003g0151a0001c0001t0007g0150 | 3 | HG01109.hp1 HG01168.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.474+5755A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172232 | ||||||
| chr9:89172241
|
G | A | 57 | a0001c0001t0001g0006a0001c0001t0001g0162a0001c0001t0001g0163others(54): Show | 59 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.474+5746C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172241 | ||||||
| chr9:89172351
|
C | T | 1 | a0001c0003t0046g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+5636G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172351 | ||||||
| chr9:89172363
|
T | G | 1 | a0001c0001t0020g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.474+5624A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172363 | ||||||
| chr9:89172422
|
A | C | 12 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071others(9): Show | 12 | HG00408.hp1 HG01081.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+5565T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172422 | ||||||
| chr9:89172528
|
G | GAC | 3 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0009g0161 | 3 | HG03225.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+5457_474+5458d others(4): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172528 | ||||||
| chr9:89172552
|
GACACACA others(7): Show |
G | 26 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(23): Show | 27 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.474+5421_474+5434d others(16): Show |
SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172552 | ||||||
| chr9:89172862
|
T | C | 2 | a0001c0007t0003g0177a0001c0007t0015g0176 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.474+5125A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89172862 | ||||||
| chr9:89173038
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474+4949G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173038 | ||||||
| chr9:89173173
|
C | T | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+4814G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173173 | ||||||
| chr9:89173200
|
C | T | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+4787G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173200 | ||||||
| chr9:89173252
|
C | T | 1 | a0001c0001t0029g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.474+4735G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173252 | ||||||
| chr9:89173352
|
C | T | 6 | a0001c0001t0004g0061a0001c0001t0006g0060a0001c0002t0006g0002others(3): Show | 7 | HG00280.hp1 HG00642.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+4635G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173352 | ||||||
| chr9:89173442
|
C | T | 8 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(5): Show | 8 | HG01891.hp1 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+4545G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173442 | ||||||
| chr9:89173690
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474+4297C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173690 | ||||||
| chr9:89173713
|
G | A | 2 | a0001c0001t0005g0171a0001c0001t0026g0172 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+4274C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173713 | ||||||
| chr9:89173896
|
G | A | 30 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0005g0026others(27): Show | 31 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.474+4091C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89173896 | ||||||
| chr9:89174363
|
G | A | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+3624C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89174363 | ||||||
| chr9:89174461
|
G | A | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+3526C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89174461 | ||||||
| chr9:89174528
|
G | A | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+3459C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89174528 | ||||||
| chr9:89174720
|
T | C | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+3267A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89174720 | ||||||
| chr9:89175018
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.474+2969A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175018 | ||||||
| chr9:89175219
|
G | T | 1 | a0001c0001t0019g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.474+2768C>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175219 | ||||||
| chr9:89175324
|
A | G | 1 | a0001c0001t0016g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.474+2663T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175324 | ||||||
| chr9:89175418
|
A | G | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+2569T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175418 | ||||||
| chr9:89175466
|
T | C | 5 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(2): Show | 5 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+2521A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175466 | ||||||
| chr9:89175602
|
T | C | 25 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(22): Show | 26 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.474+2385A>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175602 | ||||||
| chr9:89175711
|
T | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(63): Show | 68 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.474+2276A>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175711 | ||||||
| chr9:89175909
|
A | C | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+2078T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175909 | ||||||
| chr9:89175959
|
C | T | 17 | a0001c0001t0003g0049a0001c0001t0003g0055a0001c0001t0004g0038others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.474+2028G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175959 | ||||||
| chr9:89175972
|
G | A | 1 | a0001c0003t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.474+2015C>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89175972 | ||||||
| chr9:89176129
|
C | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0027a0001c0001t0005g0029others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+1858G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89176129 | ||||||
| chr9:89176412
|
A | C | 1 | a0001c0002t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.474+1575T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89176412 | ||||||
| chr9:89176444
|
C | T | 1 | a0001c0001t0018g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.474+1543G>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89176444 | ||||||
| chr9:89176465
|
G | C | 1 | a0001c0002t0006g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.474+1522C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89176465 | ||||||
| chr9:89176466
|
A | C | 2 | a0001c0001t0002g0044a0001c0001t0003g0045 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.474+1521T>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89176466 | ||||||
| chr9:89177437
|
A | G | 6 | a0001c0001t0004g0038a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+550T>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89177437 | ||||||
| chr9:89177521
|
G | C | 1 | a0001c0001t0041g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.474+466C>G | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89177521 | ||||||
| chr9:89177613
|
C | G | 31 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0005g0026others(28): Show | 32 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.474+374G>C | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89177613 | ||||||
| chr9:89177623
|
C | A | 1 | a0001c0002t0003g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.474+364G>T | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89177623 | ||||||
| chr9:89177664
|
A | T | 1 | a0001c0001t0023g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.474+323T>A | SHC3 | ENSG00000148082.10 | transcript | ENST00000375835.9 | protein_coding | 1/11 | chr9 | 89177664 |