Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10019 |
| ensemblid | ENSG00000111252.11 |
| hgncid | 29605 |
| symbol | SH2B3 |
| name | SH2B adaptor protein 3 |
| refseq_nuc | NM_005475.3 |
| refseq_prot | NP_005466.1 |
| ensembl_nuc | ENST00000341259.7 |
| ensembl_prot | ENSP00000345492.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 111405923 |
| end | 111451623 |
| strand | + |
| ver | v1.2 |
| region | chr12:111405923-111451623 |
| region5000 | chr12:111400923-111456623 |
| regionname0 | SH2B3_chr12_111405923_111451623 |
| regionname5000 | SH2B3_chr12_111400923_111456623 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 575 | 250 | 39 | 31 | 143 | 3 | 33 | 117 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0002 | 0/0 | 575 | 42 | 38 | 4 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0003 | 1/0 | 575 | 17 | 3 | 10 | 0 | 3 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0004 | 0/0 | 575 | 8 | 0 | 0 | 8 | 0 | 0 | 2 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0005 | 0/0 | 575 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0006 | 0/0 | 575 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0007 | 0/0 | 575 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0008 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0009 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(570): Show |
chr12 | 111400923 | 111456623 |
| a0010 | 0/0 | 567 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | MNGPA others(562): Show |
chr12 | 111400923 | 111456623 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1725 | 244 | 36 | 29 | 142 | 3 | 33 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0001c0005 | 0/0 | 1725 | 3 | 3 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0001c0011 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0001c0013 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0001c0014 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0002c0002 | 0/0 | 1725 | 40 | 36 | 4 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0002c0008 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0003c0003 | 1/0 | 1725 | 17 | 3 | 10 | 0 | 3 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0004c0004 | 0/0 | 1725 | 8 | 0 | 0 | 8 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0005c0006 | 0/0 | 1725 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0006c0009 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0007c0007 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0008c0015 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0009c0010 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1720): Show |
chr12 | 111400923 | 111456623 | ||
| a0010c0012 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | ATGAA others(1696): Show |
chr12 | 111400923 | 111456623 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5431 | 66 | 10 | 10 | 26 | 1 | 18 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0002 | 0/0 | 5431 | 71 | 13 | 4 | 45 | 2 | 7 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0003 | 0/0 | 5431 | 61 | 1 | 6 | 52 | 0 | 2 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0006 | 0/0 | 5431 | 16 | 0 | 1 | 9 | 0 | 6 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0007 | 0/0 | 5431 | 11 | 10 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0008 | 0/0 | 5431 | 4 | 0 | 4 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0009 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0011 | 0/0 | 5431 | 3 | 0 | 3 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0012 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0015 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0016 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0017 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0018 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0019 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0020 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0021 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0001t0022 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0005t0010 | 0/0 | 5431 | 3 | 3 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0011t0001 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0013t0001 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0001c0014t0003 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0002c0002t0004 | 0/0 | 5431 | 21 | 17 | 4 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0002c0002t0005 | 0/0 | 5431 | 17 | 17 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0002c0002t0013 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0002c0002t0014 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0002c0008t0004 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0003c0003t0001 | 1/0 | 5431 | 17 | 3 | 10 | 0 | 3 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0004c0004t0002 | 0/0 | 5431 | 8 | 0 | 0 | 8 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0005c0006t0009 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0006c0009t0007 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0007c0007t0002 | 0/0 | 5431 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0008c0015t0002 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0009c0010t0001 | 0/0 | 5431 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5426): Show |
chr12 | 111400923 | 111456623 |
| a0010c0012t0002 | 0/0 | 5407 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | ACATA others(5402): Show |
chr12 | 111400923 | 111456623 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0008g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0011g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0011g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0016g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0017g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0018g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0019g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0020g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0021g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0001t0022g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0005t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0005t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0005t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0011t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0013t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0001c0014t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0013g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0002t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0008t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0002c0008t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0003 | 1/0 | 7 | 2 | 2 | 0 | 2 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0004c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0005c0006t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0005c0006t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0006c0009t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0006c0009t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0007c0007t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0007c0007t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0008c0015t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0009c0010t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| a0010c0012t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0228 | EUR | GBR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | GBR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | GBR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00558 | hp2 | a0004 | c0004 | t0002 | g0165 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0246 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0012 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0025 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01168 | hp1 | a0002 | c0002 | t0004 | g0117 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0222 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01169 | hp1 | a0002 | c0002 | t0004 | g0118 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0098 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0200 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0027 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0058 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0227 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0103 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0113 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01891 | hp2 | a0002 | c0002 | t0005 | g0101 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01943 | hp1 | a0002 | c0002 | t0004 | g0096 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0025 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01975 | hp2 | a0001 | c0001 | t0011 | g0012 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0226 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01993 | hp1 | a0001 | c0001 | t0006 | g0239 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0099 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02055 | hp2 | a0002 | c0002 | t0005 | g0107 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02056 | hp2 | a0001 | c0001 | t0019 | g0229 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02074 | hp1 | a0005 | c0006 | t0009 | g0076 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02080 | hp2 | a0001 | c0001 | t0020 | g0215 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02132 | hp2 | a0004 | c0004 | t0002 | g0021 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02135 | hp1 | a0004 | c0004 | t0002 | g0002 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0247 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02145 | hp2 | a0001 | c0001 | t0021 | g0130 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02155 | hp1 | a0004 | c0004 | t0002 | g0153 | EAS | CDX | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | CDX | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02165 | hp2 | a0008 | c0015 | t0002 | g0128 | EAS | CDX | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0097 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02293 | hp1 | a0009 | c0010 | t0001 | g0029 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02293 | hp2 | a0001 | c0011 | t0001 | g0231 | AMR | PEL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0224 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02451 | hp2 | a0006 | c0009 | t0007 | g0043 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02523 | hp1 | a0004 | c0004 | t0002 | g0125 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02622 | hp1 | a0001 | c0005 | t0010 | g0178 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02630 | hp1 | a0002 | c0002 | t0004 | g0022 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0095 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02717 | hp2 | a0007 | c0007 | t0002 | g0147 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0237 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02738 | hp1 | a0010 | c0012 | t0002 | g0161 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02809 | hp1 | a0007 | c0007 | t0002 | g0007 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02809 | hp2 | a0002 | c0008 | t0004 | g0092 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0114 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0115 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02897 | hp2 | a0001 | c0005 | t0010 | g0179 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0129 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02965 | hp2 | a0002 | c0002 | t0005 | g0104 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02970 | hp2 | a0002 | c0002 | t0005 | g0015 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02976 | hp1 | a0002 | c0002 | t0005 | g0110 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02976 | hp2 | a0002 | c0002 | t0013 | g0122 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03098 | hp1 | a0002 | c0002 | t0005 | g0120 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0253 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03209 | hp2 | a0002 | c0002 | t0005 | g0005 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03225 | hp1 | a0001 | c0005 | t0010 | g0180 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03225 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03453 | hp1 | a0002 | c0002 | t0005 | g0106 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03453 | hp2 | a0002 | c0002 | t0004 | g0100 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0112 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0241 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0221 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0240 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03516 | hp2 | a0002 | c0002 | t0005 | g0015 | AFR | ESN | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03540 | hp1 | a0002 | c0002 | t0014 | g0091 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | GWD | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03579 | hp1 | a0002 | c0002 | t0004 | g0116 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0259 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0203 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18612 | hp1 | a0004 | c0004 | t0002 | g0173 | EAS | CHB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0119 | AFR | YRI | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18950 | hp1 | a0005 | c0006 | t0009 | g0051 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18969 | hp1 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0263 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0209 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19030 | hp1 | a0002 | c0002 | t0004 | g0094 | AFR | LWK | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0102 | AFR | LWK | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | LWK | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19055 | hp2 | a0004 | c0004 | t0002 | g0020 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19057 | hp1 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19066 | hp1 | a0001 | c0001 | t0017 | g0017 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19066 | hp2 | a0001 | c0001 | t0009 | g0046 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19074 | hp1 | a0001 | c0001 | t0018 | g0181 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19084 | hp1 | a0001 | c0001 | t0016 | g0054 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19085 | hp1 | a0001 | c0013 | t0001 | g0252 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19086 | hp2 | a0001 | c0001 | t0012 | g0077 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19088 | hp1 | a0001 | c0001 | t0022 | g0086 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19088 | hp2 | a0004 | c0004 | t0002 | g0020 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0264 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19240 | hp1 | a0002 | c0002 | t0004 | g0016 | AFR | YRI | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA19240 | hp2 | a0006 | c0009 | t0007 | g0044 | AFR | YRI | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20129 | hp1 | a0002 | c0002 | t0005 | g0005 | AFR | ASW | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20129 | hp2 | a0002 | c0002 | t0004 | g0111 | AFR | ASW | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | TSI | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | TSI | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | GIH | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | GIH | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG01123 | hp2 | a0001 | c0014 | t0003 | g0001 | AMR | CLM | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02109 | hp2 | a0002 | c0002 | t0004 | g0016 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02486 | hp1 | a0002 | c0008 | t0004 | g0093 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02486 | hp2 | a0002 | c0002 | t0005 | g0105 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG02559 | hp2 | a0002 | c0002 | t0005 | g0108 | AFR | ACB | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03471 | hp1 | a0002 | c0002 | t0005 | g0109 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | USA | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20300 | hp1 | a0002 | c0002 | t0005 | g0005 | AFR | USA | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | USA | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| NA21309 | hp2 | a0002 | c0002 | t0005 | g0090 | AFR | LWK | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0234 | REF | REF | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0003 | REF | REF | SH2B3_chr12_111400923_111456623 | SH2B3 | chr12 | 111400923 | 111456623 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111418201 | C | G | 1 | a0008 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.56C>G | p.Pro19Arg | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 438/5431 | 56/1728 | 19/575 | chr12 | 111418201 | |||
| chr12:111418383 | C | T | 1 | a0006 | 2 | HG02451.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.238C>T | p.Arg80Cys | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 620/5431 | 238/1728 | 80/575 | chr12 | 111418383 | |||
| chr12:111418639 | C | G | 1 | a0002 | 42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
missense_variant | MODERATE | c.494C>G | p.Thr165Ser | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 876/5431 | 494/1728 | 165/575 | chr12 | 111418639 | |||
| chr12:111418689 | T | C | 1 | a0002 | 42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
missense_variant | MODERATE | c.544T>C | p.Phe182Leu | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 926/5431 | 544/1728 | 182/575 | chr12 | 111418689 | |||
| chr12:111418869 | C | T | 1 | a0004 | 8 | HG00558.hp2 HG02132.hp2 HG02135.hp1 others(5): Show |
missense_variant | MODERATE | c.724C>T | p.Pro242Ser | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 1106/5431 | 724/1728 | 242/575 | chr12 | 111418869 | |||
| chr12:111446804 | T | C | 9 | a0001 a0002 a0004 others(6): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): Show |
missense_variant | MODERATE | c.784T>C | p.Trp262Arg | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 3/8 | 1166/5431 | 784/1728 | 262/575 | chr12 | 111446804 | |||
| chr12:111447339 | C | T | 1 | a0007 | 2 | HG02717.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.1031C>T | p.Pro344Leu | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 6/8 | 1413/5431 | 1031/1728 | 344/575 | chr12 | 111447339 | |||
| chr12:111447506 | G | A | 1 | a0009 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.1198G>A | p.Glu400Lys | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 6/8 | 1580/5431 | 1198/1728 | 400/575 | chr12 | 111447506 | |||
| chr12:111448011 | CTCCCTTC others(17): Show |
C | 1 | a0010 | 1 | HG02738.hp1 | disruptive_inframe_deletion | MODERATE | c.1454_1477delATTCAG others(18): Show |
p.Asp485_Trp492del | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1836/5431 | 1454/1728 | 485/575 | INFO_REALIGN_3_PRIME | chr12 | 111448011 | ||
| chr12:111448180 | G | A | 1 | a0005 | 2 | HG02074.hp1 NA18950.hp1 |
missense_variant | MODERATE | c.1606G>A | p.Ala536Thr | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1988/5431 | 1606/1728 | 536/575 | chr12 | 111448180 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111418535 | C | T | 1 | a0001c0014 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.390C>T | p.Pro130Pro | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 772/5431 | 390/1728 | 130/575 | chr12 | 111418535 | |||
| chr12:111418685 | G | A | 1 | a0001c0005 | 3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.540G>A | p.Lys180Lys | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 922/5431 | 540/1728 | 180/575 | chr12 | 111418685 | |||
| chr12:111418874 | C | T | 1 | a0002c0008 | 2 | HG02486.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.729C>T | p.Pro243Pro | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/8 | 1111/5431 | 729/1728 | 243/575 | chr12 | 111418874 | |||
| chr12:111446815 | G | A | 1 | a0002c0008 | 2 | HG02486.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.795G>A | p.Arg265Arg | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 3/8 | 1177/5431 | 795/1728 | 265/575 | chr12 | 111446815 | |||
| chr12:111447703 | C | T | 1 | a0001c0013 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1284C>T | p.His428His | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 7/8 | 1666/5431 | 1284/1728 | 428/575 | chr12 | 111447703 | |||
| chr12:111448270 | C | A | 1 | a0001c0011 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.1696C>A | p.Arg566Arg | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 2078/5431 | 1696/1728 | 566/575 | chr12 | 111448270 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111405980 | C | T | 1 | a0001c0001t0022 | 1 | NA19088.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-325C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/8 | chr12 | 111405980 | |||||||
| chr12:111406007 | G | A | 1 | a0001c0001t0008 | 4 | HG00735.hp2 HG01081.hp2 HG01934.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-298G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/8 | 12139 | chr12 | 111406007 | ||||||
| chr12:111406050 | G | T | 1 | a0001c0001t0021 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-255G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/8 | 12096 | chr12 | 111406050 | ||||||
| chr12:111406160 | G | T | 1 | a0001c0001t0020 | 1 | HG02080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/8 | 11986 | chr12 | 111406160 | ||||||
| chr12:111406220 | A | G | 1 | a0002c0002t0005 | 17 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-85A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/8 | 11926 | chr12 | 111406220 | ||||||
| chr12:111448480 | G | A | 5 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0013 others(2): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*178G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 178 | chr12 | 111448480 | ||||||
| chr12:111448727 | G | A | 1 | a0001c0001t0015 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 425 | chr12 | 111448727 | ||||||
| chr12:111449163 | T | A | 9 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(6): Show |
76 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*861T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 861 | chr12 | 111449163 | ||||||
| chr12:111449247 | A | G | 1 | a0001c0001t0019 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*945A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 945 | chr12 | 111449247 | ||||||
| chr12:111449299 | C | A | 1 | a0001c0001t0017 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*997C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 997 | chr12 | 111449299 | ||||||
| chr12:111449768 | G | T | 5 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0013 others(2): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1466G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1466 | chr12 | 111449768 | ||||||
| chr12:111449855 | A | G | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(16): Show |
173 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1553A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1553 | chr12 | 111449855 | ||||||
| chr12:111450029 | C | T | 1 | a0002c0002t0014 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1727C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1727 | chr12 | 111450029 | ||||||
| chr12:111450142 | C | T | 2 | a0001c0001t0007 a0006c0009t0007 |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1840C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1840 | chr12 | 111450142 | ||||||
| chr12:111450170 | G | A | 9 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(6): Show |
84 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1868G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1868 | chr12 | 111450170 | ||||||
| chr12:111450202 | C | A | 1 | a0001c0001t0011 | 3 | HG01071.hp2 HG01433.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1900C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1900 | chr12 | 111450202 | ||||||
| chr12:111450204 | C | T | 1 | a0002c0002t0013 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1902C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1902 | chr12 | 111450204 | ||||||
| chr12:111450260 | A | G | 1 | a0001c0001t0018 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1958A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 1958 | chr12 | 111450260 | ||||||
| chr12:111450752 | A | C | 4 | a0002c0002t0004 a0002c0002t0013 a0002c0002t0014 others(1): Show |
25 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2450A>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 2450 | chr12 | 111450752 | ||||||
| chr12:111450809 | G | A | 1 | a0001c0005t0010 | 3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2507G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 2507 | chr12 | 111450809 | ||||||
| chr12:111451028 | C | G | 1 | a0001c0005t0010 | 3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2726C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 2726 | chr12 | 111451028 | ||||||
| chr12:111451098 | C | A | 1 | a0001c0001t0006 | 16 | HG01993.hp1 HG02135.hp2 HG02735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2796C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 2796 | chr12 | 111451098 | ||||||
| chr12:111451280 | G | A | 1 | a0001c0001t0016 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2978G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 2978 | chr12 | 111451280 | ||||||
| chr12:111451428 | T | C | 2 | a0001c0001t0009 a0005c0006t0009 |
4 | HG02074.hp1 NA18950.hp1 NA18969.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3126T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 3126 | chr12 | 111451428 | ||||||
| chr12:111451512 | A | T | 5 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0013 others(2): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3210A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 8/8 | 3210 | chr12 | 111451512 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111406282 | G | A | 1 | a0009c0010t0001g0029 | 1 | HG02293.hp1 | splice_region_variant&intron_variant | LOW | c.-28+5G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111406282 | |||||||
| chr12:111406288 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-28+11G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111406288 | |||||||
| chr12:111406399 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-28+122C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111406399 | |||||||
| chr12:111406414 | G | A | 177 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0002 others(174): Show |
217 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.-28+137G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111406414 | |||||||
| chr12:111406429 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-28+152G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111406429 | |||||||
| chr12:111406566 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-28+289G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111406566 | |||||||
| chr12:111407017 | C | T | 5 | a0001c0001t0006g0260 a0001c0001t0006g0261 a0001c0001t0006g0262 others(2): Show |
5 | NA18952.hp1 NA18973.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+740C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407017 | |||||||
| chr12:111407350 | C | T | 1 | a0001c0001t0006g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-28+1073C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407350 | |||||||
| chr12:111407373 | G | A | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+1096G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407373 | |||||||
| chr12:111407587 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
8 | HG01928.hp1 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+1310G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407587 | |||||||
| chr12:111407596 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-28+1319A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407596 | |||||||
| chr12:111407721 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-28+1444T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407721 | |||||||
| chr12:111407766 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-28+1489T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111407766 | |||||||
| chr12:111408029 | G | GGTGGTA | 5 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
5 | NA18948.hp2 NA19002.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+1758_-28+1763d others(8): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111408029 | ||||||
| chr12:111408074 | A | T | 1 | a0002c0002t0004g0022 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-28+1797A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111408074 | |||||||
| chr12:111408224 | C | T | 77 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0002 others(74): Show |
90 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.-28+1947C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111408224 | |||||||
| chr12:111408245 | C | T | 1 | a0002c0002t0013g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+1968C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111408245 | |||||||
| chr12:111408920 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-28+2643C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111408920 | |||||||
| chr12:111409139 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-28+2862C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409139 | |||||||
| chr12:111409269 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | NA18965.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-28+2992G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409269 | |||||||
| chr12:111409283 | G | C | 1 | a0003c0003t0001g0200 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-28+3006G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409283 | |||||||
| chr12:111409316 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-28+3039A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409316 | |||||||
| chr12:111409411 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28+3134C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409411 | |||||||
| chr12:111409432 | C | T | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+3155C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409432 | |||||||
| chr12:111409499 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-28+3222C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409499 | |||||||
| chr12:111409682 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-28+3405G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409682 | |||||||
| chr12:111409936 | A | G | 180 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0002 others(177): Show |
220 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.-28+3659A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409936 | |||||||
| chr12:111409960 | C | A | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+3683C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111409960 | |||||||
| chr12:111410041 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-28+3764G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410041 | |||||||
| chr12:111410430 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-28+4153C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410430 | |||||||
| chr12:111410478 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-28+4201C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410478 | |||||||
| chr12:111410623 | G | A | 1 | a0001c0001t0009g0046 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-28+4346G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410623 | |||||||
| chr12:111410645 | C | T | 1 | a0002c0002t0005g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-28+4368C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410645 | |||||||
| chr12:111410667 | A | C | 1 | a0001c0001t0018g0181 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-28+4390A>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410667 | |||||||
| chr12:111410813 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-28+4536G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111410813 | |||||||
| chr12:111411030 | C | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-28+4753C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411030 | |||||||
| chr12:111411175 | G | A | 5 | a0002c0002t0005g0015 a0002c0002t0005g0102 a0002c0002t0005g0103 others(2): Show |
6 | HG01884.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+4898G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411175 | |||||||
| chr12:111411203 | C | CA | 89 | a0001c0001t0001g0185 a0001c0001t0001g0197 a0001c0001t0001g0202 others(86): Show |
116 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.-28+4944dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111411203 | ||||||
| chr12:111411203 | C | CAA | 16 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(13): Show |
16 | HG01167.hp1 HG02148.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28+4943_-28+4944d others(4): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111411203 | ||||||
| chr12:111411283 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 |
3 | NA18959.hp2 NA18974.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-28+5006G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411283 | |||||||
| chr12:111411358 | G | GA | 6 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0003g0050 others(3): Show |
6 | HG02523.hp1 NA18948.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+5096dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111411358 | ||||||
| chr12:111411358 | GA | G | 13 | a0001c0001t0001g0184 a0001c0001t0001g0204 a0001c0001t0007g0036 others(10): Show |
14 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-28+5096delA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111411358 | ||||||
| chr12:111411396 | G | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0206 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-28+5119G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411396 | |||||||
| chr12:111411466 | C | T | 4 | a0002c0002t0004g0116 a0002c0002t0004g0117 a0002c0002t0004g0118 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+5189C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411466 | |||||||
| chr12:111411467 | G | A | 73 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0002 others(70): Show |
86 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-28+5190G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411467 | |||||||
| chr12:111411549 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-28+5272C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411549 | |||||||
| chr12:111411622 | G | T | 1 | a0001c0013t0001g0252 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-28+5345G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411622 | |||||||
| chr12:111411678 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-28+5401A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411678 | |||||||
| chr12:111411700 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-28+5423T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411700 | |||||||
| chr12:111411711 | G | T | 179 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0002 others(176): Show |
219 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.-28+5434G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411711 | |||||||
| chr12:111411848 | A | G | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+5571A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111411848 | |||||||
| chr12:111412360 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
2 | HG02071.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-27-5759C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412360 | |||||||
| chr12:111412375 | A | T | 1 | a0009c0010t0001g0029 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-27-5744A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412375 | |||||||
| chr12:111412378 | C | T | 1 | a0009c0010t0001g0029 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-27-5741C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412378 | |||||||
| chr12:111412421 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-27-5698G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412421 | |||||||
| chr12:111412426 | G | A | 76 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0002 others(73): Show |
89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.-27-5693G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412426 | |||||||
| chr12:111412443 | C | T | 1 | a0002c0002t0004g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-27-5676C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412443 | |||||||
| chr12:111412722 | C | T | 2 | a0002c0002t0005g0109 a0002c0002t0005g0110 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-27-5397C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111412722 | |||||||
| chr12:111413283 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-27-4836A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111413283 | |||||||
| chr12:111413461 | T | A | 23 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(20): Show |
25 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-27-4658T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111413461 | |||||||
| chr12:111414126 | C | A | 3 | a0001c0005t0010g0178 a0001c0005t0010g0179 a0001c0005t0010g0180 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-27-3993C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414126 | |||||||
| chr12:111414129 | T | C | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-27-3990T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414129 | |||||||
| chr12:111414363 | G | C | 1 | a0001c0001t0006g0209 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-27-3756G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414363 | |||||||
| chr12:111414448 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-27-3671C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414448 | |||||||
| chr12:111414456 | G | A | 2 | a0001c0001t0007g0037 a0001c0001t0007g0038 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-27-3663G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414456 | |||||||
| chr12:111414538 | C | T | 1 | a0001c0005t0010g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27-3581C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414538 | |||||||
| chr12:111414589 | C | CA | 9 | a0001c0001t0001g0210 a0001c0001t0001g0255 a0001c0001t0002g0126 others(6): Show |
9 | HG00597.hp2 HG01891.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-27-3515dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111414589 | ||||||
| chr12:111414745 | C | T | 1 | a0002c0002t0005g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-27-3374C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414745 | |||||||
| chr12:111414902 | T | A | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-27-3217T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111414902 | |||||||
| chr12:111415001 | G | A | 2 | a0001c0001t0001g0211 a0002c0002t0005g0101 |
2 | HG01891.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.-27-3118G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415001 | |||||||
| chr12:111415151 | C | T | 1 | a0001c0001t0003g0049 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-27-2968C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415151 | |||||||
| chr12:111415219 | A | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0249 a0001c0001t0001g0250 others(2): Show |
5 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-2900A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415219 | |||||||
| chr12:111415246 | CCTGAGTA others(242): Show |
C | 2 | a0001c0001t0006g0261 a0001c0001t0006g0264 |
2 | NA18992.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-27-2869_-27-2621d others(2): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111415246 | ||||||
| chr12:111415619 | A | AT | 47 | a0001c0001t0001g0207 a0001c0001t0001g0248 a0001c0001t0002g0174 others(44): Show |
52 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.-27-2482dupT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111415619 | ||||||
| chr12:111415639 | C | T | 1 | a0001c0001t0008g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-27-2480C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415639 | |||||||
| chr12:111415684 | T | C | 1 | a0001c0001t0007g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-27-2435T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415684 | |||||||
| chr12:111415729 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-27-2390C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415729 | |||||||
| chr12:111415941 | T | G | 4 | a0001c0001t0001g0212 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG00597.hp2 HG02165.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-2178T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111415941 | |||||||
| chr12:111416040 | C | T | 2 | a0001c0001t0007g0037 a0001c0001t0007g0038 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-27-2079C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416040 | |||||||
| chr12:111416130 | G | A | 1 | a0002c0002t0005g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-27-1989G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416130 | |||||||
| chr12:111416178 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-27-1941G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416178 | |||||||
| chr12:111416244 | A | T | 1 | a0001c0001t0006g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-27-1875A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416244 | |||||||
| chr12:111416280 | C | T | 1 | a0006c0009t0007g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-27-1839C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416280 | |||||||
| chr12:111416481 | GT | G | 135 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(132): Show |
170 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.-27-1628delT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111416481 | ||||||
| chr12:111416696 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0197 a0001c0001t0001g0198 others(7): Show |
11 | HG02080.hp2 NA18955.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-1423G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416696 | |||||||
| chr12:111416788 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-27-1331G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111416788 | |||||||
| chr12:111417050 | GGT | G | 6 | a0002c0002t0004g0094 a0002c0002t0004g0095 a0002c0002t0004g0096 others(3): Show |
6 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-1066_-27-1065d others(4): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417050 | ||||||
| chr12:111417184 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0168 a0001c0001t0002g0169 |
5 | HG01081.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-935C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417184 | |||||||
| chr12:111417275 | T | C | 1 | a0001c0001t0015g0129 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-27-844T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417275 | |||||||
| chr12:111417460 | T | TTTTA | 5 | a0001c0001t0001g0208 a0001c0001t0006g0203 a0002c0002t0004g0016 others(2): Show |
6 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-631_-27-628dup others(4): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | T | TTTTATTT others(1): Show |
9 | a0002c0002t0005g0005 a0002c0002t0005g0101 a0002c0002t0005g0105 others(6): Show |
11 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-635_-27-628dup others(8): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | T | TTTTATTT others(5): Show |
21 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0169 others(18): Show |
22 | HG01884.hp2 HG01891.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.-27-639_-27-628dup others(12): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | T | TTTTATTT others(9): Show |
17 | a0001c0001t0002g0021 a0001c0001t0002g0126 a0001c0001t0002g0160 others(14): Show |
18 | HG00558.hp2 HG00597.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-27-643_-27-628dup others(16): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | T | TTTTATTT others(13): Show |
52 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(49): Show |
65 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-27-647_-27-628dup others(20): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | T | TTTTATTT others(17): Show |
7 | a0001c0001t0002g0017 a0001c0001t0002g0123 a0001c0001t0002g0131 others(4): Show |
7 | HG00558.hp1 HG02145.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27-651_-27-628dup others(24): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | T | TTTTATTT others(21): Show |
1 | a0001c0001t0002g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-27-655_-27-628dup others(28): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417460 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0003g0079 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-27-639_-27-628del others(12): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417460 | ||||||
| chr12:111417492 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-27-627T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417492 | |||||||
| chr12:111417584 | A | C | 3 | a0001c0005t0010g0178 a0001c0005t0010g0179 a0001c0005t0010g0180 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-27-535A>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417584 | |||||||
| chr12:111417624 | G | A | 1 | a0005c0006t0009g0051 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27-495G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417624 | |||||||
| chr12:111417630 | G | GT | 4 | a0001c0001t0001g0205 a0001c0001t0001g0217 a0001c0001t0001g0255 others(1): Show |
4 | NA18941.hp1 NA18975.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-482dupT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 111417630 | ||||||
| chr12:111417657 | A | T | 74 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(71): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-27-462A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417657 | |||||||
| chr12:111417874 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-27-245A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417874 | |||||||
| chr12:111417884 | T | C | 2 | a0002c0008t0004g0092 a0002c0008t0004g0093 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-27-235T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 1/7 | chr12 | 111417884 | |||||||
| chr12:111418934 | T | A | 72 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(69): Show |
85 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.732+57T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111418934 | |||||||
| chr12:111419171 | T | C | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+294T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111419171 | |||||||
| chr12:111419421 | G | GAGGCCAG others(12): Show |
1 | a0001c0001t0002g0134 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.732+547_732+565dup others(19): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111419421 | ||||||
| chr12:111419540 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.732+663A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111419540 | |||||||
| chr12:111419636 | C | CA | 41 | a0001c0001t0002g0006 a0001c0001t0002g0018 a0001c0001t0002g0135 others(38): Show |
49 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.732+773dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111419636 | ||||||
| chr12:111419636 | CA | C | 6 | a0001c0001t0001g0216 a0001c0001t0002g0127 a0001c0001t0002g0175 others(3): Show |
6 | HG02896.hp2 NA18955.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+773delA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111419636 | ||||||
| chr12:111419683 | T | C | 66 | a0001c0001t0002g0062 a0001c0001t0002g0069 a0001c0001t0003g0001 others(63): Show |
88 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(85): Show |
intron_variant | MODIFIER | c.732+806T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111419683 | |||||||
| chr12:111420282 | C | T | 72 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(69): Show |
85 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.732+1405C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111420282 | |||||||
| chr12:111420283 | G | A | 1 | a0002c0002t0005g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.732+1406G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111420283 | |||||||
| chr12:111420367 | C | CA | 74 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0193 others(71): Show |
87 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.732+1514dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111420367 | ||||||
| chr12:111420367 | C | CAA | 98 | a0001c0001t0001g0186 a0001c0001t0002g0062 a0001c0001t0002g0069 others(95): Show |
123 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(120): Show |
intron_variant | MODIFIER | c.732+1513_732+1514d others(4): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111420367 | ||||||
| chr12:111420367 | C | CAAA | 11 | a0001c0001t0002g0124 a0001c0001t0003g0011 a0001c0001t0003g0052 others(8): Show |
13 | HG00544.hp2 HG00642.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+1512_732+1514d others(5): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111420367 | ||||||
| chr12:111420391 | A | G | 9 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0191 others(6): Show |
12 | HG01081.hp2 HG01934.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.732+1514A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111420391 | |||||||
| chr12:111420584 | G | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
8 | HG01928.hp1 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+1707G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111420584 | |||||||
| chr12:111420649 | C | A | 1 | a0001c0001t0011g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.732+1772C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111420649 | |||||||
| chr12:111421093 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.732+2216G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421093 | |||||||
| chr12:111421103 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+2226A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421103 | |||||||
| chr12:111421125 | GT | G | 6 | a0002c0002t0004g0099 a0002c0002t0004g0100 a0002c0002t0004g0116 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+2249delT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421125 | |||||||
| chr12:111421381 | T | G | 1 | a0001c0001t0006g0221 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.732+2504T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421381 | |||||||
| chr12:111421401 | C | CT | 21 | a0001c0001t0001g0172 a0001c0001t0001g0186 a0001c0001t0001g0196 others(18): Show |
23 | HG01169.hp2 HG01361.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.732+2550dupT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111421401 | ||||||
| chr12:111421401 | CT | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
103 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.732+2550delT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111421401 | ||||||
| chr12:111421401 | CTT | C | 7 | a0001c0001t0002g0143 a0001c0005t0010g0178 a0001c0005t0010g0179 others(4): Show |
7 | HG01168.hp1 HG02027.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+2549_732+2550d others(4): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111421401 | ||||||
| chr12:111421441 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.732+2564G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421441 | |||||||
| chr12:111421564 | G | T | 1 | a0001c0005t0010g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.732+2687G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421564 | |||||||
| chr12:111421636 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.732+2759C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421636 | |||||||
| chr12:111421655 | G | C | 1 | a0001c0001t0003g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.732+2778G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421655 | |||||||
| chr12:111421744 | G | T | 1 | a0001c0001t0001g0024 | 2 | NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.732+2867G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111421744 | |||||||
| chr12:111422067 | G | GT | 4 | a0001c0001t0002g0142 a0001c0001t0002g0154 a0001c0001t0002g0257 others(1): Show |
4 | NA18989.hp2 NA18992.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+3197dupT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111422067 | ||||||
| chr12:111422175 | G | A | 1 | a0002c0008t0004g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.732+3298G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422175 | |||||||
| chr12:111422226 | G | A | 2 | a0002c0002t0004g0112 a0002c0002t0004g0113 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.732+3349G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422226 | |||||||
| chr12:111422227 | C | T | 3 | a0001c0005t0010g0178 a0001c0005t0010g0179 a0001c0005t0010g0180 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.732+3350C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422227 | |||||||
| chr12:111422423 | T | A | 1 | a0002c0002t0005g0103 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3546T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422423 | |||||||
| chr12:111422563 | G | T | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+3686G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422563 | |||||||
| chr12:111422566 | T | G | 1 | a0001c0001t0006g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.732+3689T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422566 | |||||||
| chr12:111422568 | T | G | 1 | a0001c0001t0003g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.732+3691T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422568 | |||||||
| chr12:111422575 | T | C | 36 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(33): Show |
41 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.732+3698T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422575 | |||||||
| chr12:111422710 | G | A | 7 | a0001c0001t0007g0037 a0001c0001t0007g0038 a0001c0001t0007g0040 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+3833G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422710 | |||||||
| chr12:111422749 | A | T | 1 | a0001c0001t0002g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.732+3872A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422749 | |||||||
| chr12:111422981 | G | A | 1 | a0004c0004t0002g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.732+4104G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111422981 | |||||||
| chr12:111423244 | G | A | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+4367G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111423244 | |||||||
| chr12:111423366 | T | C | 1 | a0001c0001t0006g0219 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.732+4489T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111423366 | |||||||
| chr12:111423581 | C | A | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+4704C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111423581 | |||||||
| chr12:111423632 | A | G | 52 | a0001c0001t0002g0069 a0001c0001t0003g0001 a0001c0001t0003g0004 others(49): Show |
74 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.732+4755A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111423632 | |||||||
| chr12:111423652 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.732+4775G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111423652 | |||||||
| chr12:111423786 | C | T | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+4909C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111423786 | |||||||
| chr12:111424294 | C | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0191 others(5): Show |
9 | HG02735.hp1 HG03017.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.732+5417C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424294 | |||||||
| chr12:111424415 | G | A | 38 | a0001c0001t0001g0201 a0002c0002t0004g0016 a0002c0002t0004g0022 others(35): Show |
43 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.732+5538G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424415 | |||||||
| chr12:111424572 | C | T | 3 | a0002c0002t0005g0015 a0002c0002t0005g0102 a0002c0002t0005g0120 |
4 | HG02970.hp2 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+5695C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424572 | |||||||
| chr12:111424574 | G | A | 1 | a0002c0002t0004g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.732+5697G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424574 | |||||||
| chr12:111424621 | G | A | 1 | a0001c0001t0006g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.732+5744G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424621 | |||||||
| chr12:111424771 | C | T | 73 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(70): Show |
86 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.732+5894C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424771 | |||||||
| chr12:111424782 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.732+5905G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424782 | |||||||
| chr12:111424889 | C | T | 8 | a0001c0001t0003g0013 a0001c0001t0003g0056 a0001c0001t0003g0074 others(5): Show |
10 | HG01071.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+6012C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424889 | |||||||
| chr12:111424932 | A | C | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+6055A>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111424932 | |||||||
| chr12:111425750 | C | T | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6873C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425750 | |||||||
| chr12:111425751 | T | C | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6874T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425751 | |||||||
| chr12:111425752 | C | A | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6875C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425752 | |||||||
| chr12:111425776 | C | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6899C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425776 | |||||||
| chr12:111425777 | A | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6900A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425777 | |||||||
| chr12:111425778 | T | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6901T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425778 | |||||||
| chr12:111425780 | A | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6903A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425780 | |||||||
| chr12:111425782 | T | C | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6905T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425782 | |||||||
| chr12:111425785 | C | T | 36 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(33): Show |
41 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.732+6908C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425785 | |||||||
| chr12:111425787 | C | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6910C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425787 | |||||||
| chr12:111425788 | T | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6911T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425788 | |||||||
| chr12:111425789 | A | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6912A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425789 | |||||||
| chr12:111425798 | C | A | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6921C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425798 | |||||||
| chr12:111425811 | C | G | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6934C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425811 | |||||||
| chr12:111425819 | C | A | 1 | a0001c0001t0022g0086 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.732+6942C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425819 | |||||||
| chr12:111425842 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.732+6965G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111425842 | |||||||
| chr12:111426164 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.732+7287T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426164 | |||||||
| chr12:111426229 | G | A | 1 | a0002c0002t0014g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732+7352G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426229 | |||||||
| chr12:111426381 | T | G | 2 | a0002c0002t0004g0112 a0002c0002t0004g0113 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.732+7504T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426381 | |||||||
| chr12:111426385 | CT | C | 54 | a0001c0001t0001g0214 a0001c0001t0002g0168 a0001c0001t0003g0055 others(51): Show |
59 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.732+7525delT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111426385 | ||||||
| chr12:111426397 | T | G | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+7520T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426397 | |||||||
| chr12:111426400 | T | G | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+7523T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426400 | |||||||
| chr12:111426652 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.732+7775G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426652 | |||||||
| chr12:111426664 | A | G | 2 | a0002c0002t0004g0117 a0002c0002t0004g0118 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.732+7787A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426664 | |||||||
| chr12:111426880 | T | C | 177 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(174): Show |
217 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.732+8003T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426880 | |||||||
| chr12:111426904 | C | A | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+8027C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426904 | |||||||
| chr12:111426920 | C | T | 1 | a0004c0004t0002g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.732+8043C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111426920 | |||||||
| chr12:111427045 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.732+8168A>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427045 | |||||||
| chr12:111427049 | T | C | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+8172T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427049 | |||||||
| chr12:111427108 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0194 |
2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.732+8231G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427108 | |||||||
| chr12:111427151 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.732+8274G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427151 | |||||||
| chr12:111427245 | C | G | 260 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(257): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.732+8368C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427245 | |||||||
| chr12:111427346 | G | A | 1 | a0002c0002t0004g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.732+8469G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427346 | |||||||
| chr12:111427388 | G | GA | 22 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0196 others(19): Show |
22 | HG01123.hp1 HG01167.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.732+8541dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | G | GAA | 8 | a0001c0001t0001g0186 a0001c0001t0001g0230 a0001c0001t0003g0053 others(5): Show |
8 | HG01981.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.732+8540_732+8541d others(4): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | G | GAAA | 32 | a0001c0001t0002g0069 a0001c0001t0003g0001 a0001c0001t0003g0013 others(29): Show |
50 | HG01071.hp2 HG01123.hp2 HG01256.hp2 others(47): Show |
intron_variant | MODIFIER | c.732+8539_732+8541d others(5): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | G | GAAAA | 22 | a0001c0001t0002g0137 a0001c0001t0003g0004 a0001c0001t0003g0011 others(19): Show |
26 | HG00544.hp2 HG00597.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.732+8538_732+8541d others(6): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | GAAAAAA | G | 7 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0249 others(4): Show |
7 | HG02135.hp2 HG03098.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+8536_732+8541d others(8): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | GAAAAAAA | G | 34 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0171 others(31): Show |
35 | HG01361.hp1 HG01993.hp1 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.732+8535_732+8541d others(9): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | GAAAAAAA others(1): Show |
G | 61 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
72 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.732+8534_732+8541d others(10): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | GAAAAAAA others(2): Show |
G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0135 a0001c0001t0002g0152 others(8): Show |
14 | HG01081.hp1 HG02109.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.732+8533_732+8541d others(11): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | GAAAAAAA others(3): Show |
G | 31 | a0002c0002t0004g0022 a0002c0002t0004g0095 a0002c0002t0004g0096 others(28): Show |
35 | HG01168.hp1 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.732+8532_732+8541d others(12): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427388 | GAAAAAAA others(4): Show |
G | 2 | a0002c0002t0004g0118 a0002c0008t0004g0093 |
2 | HG01169.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.732+8531_732+8541d others(13): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427388 | ||||||
| chr12:111427452 | A | AG | 7 | a0001c0001t0003g0081 a0002c0002t0004g0099 a0002c0002t0004g0100 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+8580dupG | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111427452 | ||||||
| chr12:111427570 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0135 a0001c0001t0002g0136 |
5 | NA18946.hp1 NA18950.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+8693G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427570 | |||||||
| chr12:111427590 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.732+8713G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427590 | |||||||
| chr12:111427635 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0206 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.732+8758C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427635 | |||||||
| chr12:111427644 | G | A | 1 | a0002c0002t0005g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.732+8767G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427644 | |||||||
| chr12:111427761 | C | T | 74 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(71): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.732+8884C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427761 | |||||||
| chr12:111427857 | A | G | 2 | a0001c0001t0007g0040 a0001c0001t0007g0042 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.732+8980A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427857 | |||||||
| chr12:111427887 | C | T | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+9010C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427887 | |||||||
| chr12:111427977 | G | T | 1 | a0001c0001t0006g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.732+9100G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111427977 | |||||||
| chr12:111428262 | G | A | 1 | a0001c0001t0006g0259 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.732+9385G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428262 | |||||||
| chr12:111428283 | G | A | 76 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(73): Show |
89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.732+9406G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428283 | |||||||
| chr12:111428658 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.732+9781G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428658 | |||||||
| chr12:111428678 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.732+9801A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428678 | |||||||
| chr12:111428734 | A | G | 101 | a0001c0001t0002g0069 a0001c0001t0002g0137 a0001c0001t0003g0001 others(98): Show |
128 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(125): Show |
intron_variant | MODIFIER | c.732+9857A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428734 | |||||||
| chr12:111428796 | G | A | 1 | a0002c0002t0004g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.732+9919G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428796 | |||||||
| chr12:111428832 | C | T | 2 | a0002c0002t0005g0101 a0002c0002t0005g0108 |
2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.732+9955C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428832 | |||||||
| chr12:111428952 | G | A | 1 | a0004c0004t0002g0125 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.732+10075G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111428952 | |||||||
| chr12:111429015 | C | CGAG | 11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0206 others(8): Show |
11 | HG02055.hp2 HG02630.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+10168_732+1017 others(7): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111429015 | ||||||
| chr12:111429015 | CGAG | C | 61 | a0001c0001t0001g0256 a0001c0001t0002g0069 a0001c0001t0002g0137 others(58): Show |
83 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.732+10168_732+1017 others(7): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111429015 | ||||||
| chr12:111429015 | CGAGGAG | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0265 a0003c0003t0001g0228 |
3 | HG00099.hp1 HG04204.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.732+10165_732+1017 others(10): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111429015 | ||||||
| chr12:111429015 | CGAGGAGG others(5): Show |
C | 1 | a0001c0001t0003g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.732+10159_732+1017 others(16): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111429015 | ||||||
| chr12:111429015 | CGAGGAGG others(26): Show |
C | 1 | a0001c0001t0003g0121 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.732+10161_732+1019 others(37): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111429015 | ||||||
| chr12:111429027 | GGAGGAGG others(14): Show |
G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0246 |
4 | HG00735.hp2 HG01081.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+10171_732+1019 others(25): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111429027 | ||||||
| chr12:111429051 | G | A | 1 | a0001c0001t0003g0053 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.732+10174G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429051 | |||||||
| chr12:111429144 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.732+10267G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429144 | |||||||
| chr12:111429405 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.732+10528C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429405 | |||||||
| chr12:111429406 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.732+10529A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429406 | |||||||
| chr12:111429456 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0233 |
2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.732+10579C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429456 | |||||||
| chr12:111429489 | A | C | 1 | a0003c0003t0001g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.732+10612A>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429489 | |||||||
| chr12:111429626 | G | A | 1 | a0001c0001t0006g0221 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.732+10749G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429626 | |||||||
| chr12:111429683 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(68): Show |
84 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.732+10806C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111429683 | |||||||
| chr12:111430018 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.732+11141G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430018 | |||||||
| chr12:111430142 | G | A | 1 | a0002c0002t0005g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.732+11265G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430142 | |||||||
| chr12:111430176 | G | T | 23 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(20): Show |
25 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.732+11299G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430176 | |||||||
| chr12:111430299 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.732+11422C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430299 | |||||||
| chr12:111430333 | C | T | 2 | a0004c0004t0002g0020 a0004c0004t0002g0165 |
3 | HG00558.hp2 NA19055.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.732+11456C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430333 | |||||||
| chr12:111430378 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0205 a0001c0001t0001g0248 |
4 | HG00408.hp2 NA18979.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+11501C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430378 | |||||||
| chr12:111430417 | G | T | 2 | a0001c0001t0002g0137 a0001c0001t0003g0059 |
2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.732+11540G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430417 | |||||||
| chr12:111430710 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.732+11833G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430710 | |||||||
| chr12:111430752 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.732+11875C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430752 | |||||||
| chr12:111430879 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.732+12002C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430879 | |||||||
| chr12:111430928 | C | G | 1 | a0001c0001t0003g0065 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.732+12051C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430928 | |||||||
| chr12:111430991 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0144 a0001c0001t0002g0157 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+12114G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111430991 | |||||||
| chr12:111431410 | G | A | 14 | a0002c0002t0005g0005 a0002c0002t0005g0015 a0002c0002t0005g0090 others(11): Show |
17 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.732+12533G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111431410 | |||||||
| chr12:111431490 | G | GA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0205 a0001c0001t0001g0248 others(4): Show |
8 | HG00408.hp2 HG02622.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.732+12624dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111431490 | ||||||
| chr12:111431845 | G | A | 1 | a0002c0002t0005g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.732+12968G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111431845 | |||||||
| chr12:111431891 | GC | G | 6 | a0002c0002t0004g0094 a0002c0002t0004g0095 a0002c0002t0004g0096 others(3): Show |
6 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+13016delC | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111431891 | ||||||
| chr12:111432119 | CT | C | 173 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0006 others(170): Show |
213 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(210): Show |
intron_variant | MODIFIER | c.732+13258delT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111432119 | ||||||
| chr12:111432162 | G | A | 1 | a0001c0001t0009g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.732+13285G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432162 | |||||||
| chr12:111432337 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0020g0215 |
3 | HG02080.hp2 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.732+13460G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432337 | |||||||
| chr12:111432487 | G | A | 4 | a0001c0001t0007g0033 a0001c0001t0007g0034 a0001c0001t0007g0035 others(1): Show |
4 | HG01167.hp1 HG02818.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+13610G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432487 | |||||||
| chr12:111432819 | G | A | 1 | a0002c0002t0004g0022 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.733-13934G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432819 | |||||||
| chr12:111432951 | A | G | 1 | a0002c0002t0004g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733-13802A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432951 | |||||||
| chr12:111432966 | T | C | 6 | a0002c0002t0004g0094 a0002c0002t0004g0095 a0002c0002t0004g0096 others(3): Show |
6 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-13787T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432966 | |||||||
| chr12:111432969 | G | A | 6 | a0002c0002t0004g0099 a0002c0002t0004g0100 a0002c0002t0004g0116 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-13784G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432969 | |||||||
| chr12:111432986 | T | A | 20 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0195 others(17): Show |
20 | HG01993.hp1 HG02135.hp2 HG02735.hp2 others(17): Show |
intron_variant | MODIFIER | c.733-13767T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111432986 | |||||||
| chr12:111433027 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.733-13726G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433027 | |||||||
| chr12:111433098 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.733-13655T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433098 | |||||||
| chr12:111433154 | C | T | 13 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(10): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.733-13599C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433154 | |||||||
| chr12:111433337 | A | T | 178 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0006 others(175): Show |
218 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.733-13416A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433337 | |||||||
| chr12:111433679 | C | G | 1 | a0001c0001t0016g0054 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.733-13074C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433679 | |||||||
| chr12:111433751 | C | T | 1 | a0002c0002t0005g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.733-13002C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433751 | |||||||
| chr12:111433851 | C | T | 2 | a0001c0001t0009g0046 a0001c0001t0009g0078 |
2 | NA18969.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.733-12902C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433851 | |||||||
| chr12:111433903 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0002g0150 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.733-12850C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433903 | |||||||
| chr12:111433930 | A | T | 1 | a0001c0001t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.733-12823A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111433930 | |||||||
| chr12:111434188 | C | G | 1 | a0001c0001t0002g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.733-12565C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434188 | |||||||
| chr12:111434422 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.733-12331A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434422 | |||||||
| chr12:111434484 | G | C | 2 | a0001c0001t0012g0073 a0001c0001t0012g0077 |
2 | NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733-12269G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434484 | |||||||
| chr12:111434491 | A | G | 1 | a0002c0008t0004g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.733-12262A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434491 | |||||||
| chr12:111434872 | G | C | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-11881G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434872 | |||||||
| chr12:111434883 | G | A | 1 | a0002c0002t0013g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733-11870G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434883 | |||||||
| chr12:111434918 | T | C | 1 | a0003c0003t0001g0200 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.733-11835T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111434918 | |||||||
| chr12:111435152 | C | T | 1 | a0001c0001t0018g0181 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.733-11601C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435152 | |||||||
| chr12:111435321 | C | T | 1 | a0007c0007t0002g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.733-11432C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435321 | |||||||
| chr12:111435363 | G | A | 29 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0184 others(26): Show |
30 | HG01993.hp1 HG02135.hp2 HG02735.hp1 others(27): Show |
intron_variant | MODIFIER | c.733-11390G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435363 | |||||||
| chr12:111435430 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.733-11323G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435430 | |||||||
| chr12:111435471 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.733-11282G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435471 | |||||||
| chr12:111435784 | G | T | 1 | a0001c0001t0002g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.733-10969G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435784 | |||||||
| chr12:111435859 | G | T | 19 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0195 others(16): Show |
19 | HG01993.hp1 HG02135.hp2 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.733-10894G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435859 | |||||||
| chr12:111435904 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.733-10849G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111435904 | |||||||
| chr12:111436050 | A | T | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.733-10703A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436050 | |||||||
| chr12:111436068 | C | T | 1 | a0002c0008t0004g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.733-10685C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436068 | |||||||
| chr12:111436098 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0159 a0001c0001t0002g0176 others(1): Show |
5 | HG02071.hp1 NA18964.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-10655C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436098 | |||||||
| chr12:111436129 | G | A | 2 | a0002c0002t0005g0015 a0002c0002t0005g0102 |
3 | HG02970.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.733-10624G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436129 | |||||||
| chr12:111436356 | G | T | 1 | a0001c0001t0002g0152 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.733-10397G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436356 | |||||||
| chr12:111436465 | C | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-10288C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436465 | |||||||
| chr12:111436668 | C | T | 6 | a0002c0002t0004g0094 a0002c0002t0004g0095 a0002c0002t0004g0096 others(3): Show |
6 | HG01943.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-10085C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436668 | |||||||
| chr12:111436742 | T | C | 2 | a0002c0008t0004g0092 a0002c0008t0004g0093 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.733-10011T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436742 | |||||||
| chr12:111436982 | T | G | 1 | a0002c0002t0005g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733-9771T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111436982 | |||||||
| chr12:111437064 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.733-9689G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437064 | |||||||
| chr12:111437297 | T | C | 1 | a0002c0002t0004g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.733-9456T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437297 | |||||||
| chr12:111437309 | T | G | 2 | a0001c0001t0008g0010 a0001c0001t0008g0246 |
4 | HG00735.hp2 HG01081.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-9444T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437309 | |||||||
| chr12:111437425 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.733-9328G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437425 | |||||||
| chr12:111437606 | A | G | 176 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0006 others(173): Show |
216 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.733-9147A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437606 | |||||||
| chr12:111437660 | G | T | 1 | a0002c0002t0005g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733-9093G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437660 | |||||||
| chr12:111437661 | G | C | 1 | a0001c0001t0006g0262 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.733-9092G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437661 | |||||||
| chr12:111437748 | C | A | 1 | a0001c0001t0007g0033 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.733-9005C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437748 | |||||||
| chr12:111437840 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.733-8913T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111437840 | |||||||
| chr12:111438156 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.733-8597G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111438156 | |||||||
| chr12:111438463 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.733-8290A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111438463 | |||||||
| chr12:111438469 | A | G | 2 | a0001c0001t0003g0071 a0001c0001t0003g0089 |
2 | NA18948.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.733-8284A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111438469 | |||||||
| chr12:111438531 | C | T | 1 | a0006c0009t0007g0044 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.733-8222C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111438531 | |||||||
| chr12:111438968 | TTTTG | T | 2 | a0001c0001t0008g0010 a0001c0001t0008g0246 |
4 | HG00735.hp2 HG01081.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-7768_733-7765d others(6): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111438968 | ||||||
| chr12:111439179 | C | T | 1 | a0002c0002t0004g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.733-7574C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439179 | |||||||
| chr12:111439231 | C | T | 1 | a0001c0001t0011g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733-7522C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439231 | |||||||
| chr12:111439336 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.733-7417A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439336 | |||||||
| chr12:111439498 | C | A | 31 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0171 others(28): Show |
32 | HG01993.hp1 HG02135.hp2 HG02735.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-7255C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439498 | |||||||
| chr12:111439535 | C | T | 3 | a0002c0002t0004g0022 a0002c0002t0004g0098 a0002c0002t0013g0122 |
4 | HG01243.hp1 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-7218C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439535 | |||||||
| chr12:111439536 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.733-7217G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439536 | |||||||
| chr12:111439772 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.733-6981C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439772 | |||||||
| chr12:111439933 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-6820A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111439933 | |||||||
| chr12:111440130 | G | A | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-6623G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440130 | |||||||
| chr12:111440175 | A | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0191 others(5): Show |
9 | HG02735.hp1 HG03017.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-6578A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440175 | |||||||
| chr12:111440319 | C | T | 2 | a0001c0001t0006g0240 a0001c0001t0006g0241 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733-6434C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440319 | |||||||
| chr12:111440488 | T | G | 1 | a0001c0013t0001g0252 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.733-6265T>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440488 | |||||||
| chr12:111440553 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.733-6200G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440553 | |||||||
| chr12:111440584 | A | G | 3 | a0001c0001t0002g0069 a0001c0001t0003g0070 a0001c0001t0003g0072 |
3 | HG03017.hp1 HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.733-6169A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440584 | |||||||
| chr12:111440722 | T | C | 166 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0006 others(163): Show |
206 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.733-6031T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111440722 | |||||||
| chr12:111441170 | G | GT | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-5580dupT | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111441170 | ||||||
| chr12:111441350 | C | T | 1 | a0002c0002t0005g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.733-5403C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111441350 | |||||||
| chr12:111441360 | T | TA | 72 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(69): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.733-5375dupA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111441360 | ||||||
| chr12:111441360 | TA | T | 22 | a0001c0001t0001g0184 a0001c0001t0001g0216 a0001c0001t0001g0217 others(19): Show |
24 | HG01167.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.733-5375delA | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111441360 | ||||||
| chr12:111441589 | C | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-5164C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111441589 | |||||||
| chr12:111441614 | G | A | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-5139G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111441614 | |||||||
| chr12:111441957 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.733-4796G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111441957 | |||||||
| chr12:111442022 | C | T | 3 | a0002c0002t0004g0016 a0002c0002t0004g0114 a0002c0002t0004g0115 |
4 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-4731C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111442022 | |||||||
| chr12:111442032 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | NA19056.hp2 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.733-4721A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111442032 | |||||||
| chr12:111442424 | G | GTGGCTGG others(3): Show |
3 | a0001c0001t0002g0163 a0001c0001t0012g0073 a0001c0001t0012g0077 |
3 | HG03195.hp1 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733-4325_733-4316d others(12): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111442424 | ||||||
| chr12:111442474 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.733-4279C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111442474 | |||||||
| chr12:111442510 | AGACCACC others(3): Show |
A | 1 | a0001c0001t0002g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.733-4240_733-4231d others(12): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111442510 | ||||||
| chr12:111442519 | G | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0020g0215 |
3 | HG02080.hp2 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.733-4234G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111442519 | |||||||
| chr12:111442530 | T | A | 2 | a0001c0001t0002g0137 a0001c0001t0003g0059 |
2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.733-4223T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111442530 | |||||||
| chr12:111443476 | T | C | 1 | a0001c0001t0006g0237 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.733-3277T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443476 | |||||||
| chr12:111443504 | C | T | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-3249C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443504 | |||||||
| chr12:111443505 | G | T | 73 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(70): Show |
86 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.733-3248G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443505 | |||||||
| chr12:111443523 | G | A | 1 | a0009c0010t0001g0029 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.733-3230G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443523 | |||||||
| chr12:111443527 | G | T | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-3226G>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443527 | |||||||
| chr12:111443631 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.733-3122T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443631 | |||||||
| chr12:111443913 | C | T | 1 | a0002c0002t0005g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733-2840C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443913 | |||||||
| chr12:111443955 | C | G | 1 | a0009c0010t0001g0029 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.733-2798C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111443955 | |||||||
| chr12:111444092 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-2661A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444092 | |||||||
| chr12:111444313 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-2440A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444313 | |||||||
| chr12:111444315 | G | A | 50 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(47): Show |
55 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.733-2438G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444315 | |||||||
| chr12:111444331 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.733-2422T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444331 | |||||||
| chr12:111444550 | A | G | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-2203A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444550 | |||||||
| chr12:111444681 | C | A | 177 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(174): Show |
217 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.733-2072C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444681 | |||||||
| chr12:111444687 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.733-2066C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444687 | |||||||
| chr12:111444913 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.733-1840G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444913 | |||||||
| chr12:111444918 | A | AGGCCTGG others(9): Show |
1 | a0001c0001t0003g0056 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.733-1834_733-1819d others(18): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 111444918 | ||||||
| chr12:111444927 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.733-1826C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111444927 | |||||||
| chr12:111445248 | G | A | 3 | a0001c0005t0010g0178 a0001c0005t0010g0179 a0001c0005t0010g0180 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.733-1505G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445248 | |||||||
| chr12:111445527 | C | T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-1226C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445527 | |||||||
| chr12:111445667 | T | A | 3 | a0002c0002t0004g0016 a0002c0002t0004g0114 a0002c0002t0004g0115 |
4 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-1086T>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445667 | |||||||
| chr12:111445770 | C | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0183 a0001c0001t0021g0130 |
3 | HG01243.hp2 HG02145.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.733-983C>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445770 | |||||||
| chr12:111445832 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.733-921G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445832 | |||||||
| chr12:111445915 | C | G | 1 | a0002c0002t0014g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.733-838C>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445915 | |||||||
| chr12:111445975 | C | T | 55 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0017 others(52): Show |
65 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.733-778C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111445975 | |||||||
| chr12:111446268 | A | T | 2 | a0001c0001t0007g0032 a0001c0001t0007g0039 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.733-485A>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111446268 | |||||||
| chr12:111446309 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.733-444G>A | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111446309 | |||||||
| chr12:111446485 | G | C | 37 | a0002c0002t0004g0016 a0002c0002t0004g0022 a0002c0002t0004g0094 others(34): Show |
42 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.733-268G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111446485 | |||||||
| chr12:111446611 | T | C | 74 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(71): Show |
85 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.733-142T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111446611 | |||||||
| chr12:111446743 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.733-10G>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 2/7 | chr12 | 111446743 | |||||||
| chr12:111447105 | C | T | 2 | a0001c0001t0011g0012 a0001c0001t0011g0058 |
3 | HG01071.hp2 HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.927-20C>T | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 4/7 | chr12 | 111447105 | |||||||
| chr12:111447547 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01071.hp1 | splice_region_variant&intron_variant | LOW | c.1236+3A>G | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 6/7 | chr12 | 111447547 | |||||||
| chr12:111447547 | ATGGGG | A | 170 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(167): Show |
208 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.1236+24_1236+28del others(5): Show |
SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 111447547 | ||||||
| chr12:111447977 | T | C | 1 | a0001c0005t0010g0179 | 1 | HG02897.hp2 | splice_region_variant&intron_variant | LOW | c.1409-6T>C | SH2B3 | ENSG00000111252.11 | transcript | ENST00000341259.7 | protein_coding | 7/7 | chr12 | 111447977 |