Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6452 |
| ensemblid | ENSG00000087266.17 |
| hgncid | 10825 |
| symbol | SH3BP2 |
| name | SH3 domain binding protein 2 |
| refseq_nuc | NM_001122681.2 |
| refseq_prot | NP_001116153.1 |
| ensembl_nuc | ENST00000503393.8 |
| ensembl_prot | ENSP00000422168.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 2793085 |
| end | 2841096 |
| strand | + |
| ver | v1.2 |
| region | chr4:2793085-2841096 |
| region5000 | chr4:2788085-2846096 |
| regionname0 | SH3BP2_chr4_2793085_2841096 |
| regionname5000 | SH3BP2_chr4_2788085_2846096 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 561 | 374 | 92 | 82 | 140 | 14 | 44 | 95 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | MAAEE others(556): Show |
chr4 | 2788085 | 2846096 |
| a0002 | 0/0 | 561 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | MAAEE others(556): Show |
chr4 | 2788085 | 2846096 |
| a0003 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | MAAEE others(556): Show |
chr4 | 2788085 | 2846096 |
| a0004 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | MAAEE others(556): Show |
chr4 | 2788085 | 2846096 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1683 | 129 | 7 | 35 | 64 | 5 | 17 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0002 | 1/0 | 1683 | 88 | 2 | 17 | 56 | 3 | 9 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0003 | 0/0 | 1683 | 60 | 26 | 10 | 11 | 1 | 12 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0004 | 0/0 | 1683 | 54 | 26 | 18 | 2 | 3 | 5 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0005 | 0/0 | 1683 | 29 | 19 | 1 | 6 | 2 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0006 | 0/0 | 1683 | 5 | 5 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0007 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0009 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0010 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0011 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0012 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0001c0015 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0002c0008 | 0/0 | 1683 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0003c0014 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 | ||
| a0004c0013 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | ATGGC others(1678): Show |
chr4 | 2788085 | 2846096 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9007 | 57 | 2 | 10 | 34 | 2 | 9 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0002 | 0/0 | 9006 | 8 | 0 | 1 | 6 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0003 | 0/0 | 9006 | 4 | 0 | 0 | 4 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0004 | 0/1 | 9007 | 6 | 0 | 1 | 1 | 0 | 3 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0009 | 0/0 | 9006 | 6 | 0 | 0 | 6 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0010 | 0/0 | 9007 | 6 | 0 | 6 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0011 | 0/0 | 9006 | 5 | 0 | 5 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0012 | 0/0 | 9007 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0013 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0018 | 0/0 | 9007 | 3 | 0 | 3 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0022 | 0/0 | 9008 | 2 | 0 | 1 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0023 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0024 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0025 | 0/0 | 9007 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0026 | 0/0 | 9007 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0029 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0030 | 0/0 | 9007 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0032 | 0/0 | 9005 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0041 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0044 | 0/0 | 9007 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0045 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0046 | 0/0 | 9007 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0047 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0048 | 0/0 | 8992 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(8987): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0049 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0050 | 0/0 | 9007 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0052 | 0/0 | 9005 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0054 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0055 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0056 | 0/0 | 9007 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0063 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0064 | 0/0 | 9008 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0066 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0067 | 0/0 | 9006 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0068 | 0/0 | 9006 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0072 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0073 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0085 | 0/0 | 9008 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0001t0093 | 0/0 | 9007 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0001 | 0/0 | 9007 | 9 | 0 | 2 | 4 | 2 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0002 | 1/0 | 9006 | 18 | 1 | 5 | 8 | 0 | 3 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0003 | 0/0 | 9006 | 32 | 0 | 0 | 32 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0004 | 0/0 | 9007 | 3 | 0 | 1 | 0 | 1 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0007 | 0/0 | 9006 | 5 | 0 | 3 | 1 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0012 | 0/0 | 9007 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0017 | 0/0 | 9006 | 4 | 1 | 2 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0024 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0028 | 0/0 | 9005 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0029 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0032 | 0/0 | 9005 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0034 | 0/0 | 9005 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0051 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0057 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0060 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9024): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0061 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0071 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0076 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0084 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0087 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0090 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0002t0091 | 0/0 | 9006 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0001 | 0/0 | 9007 | 2 | 0 | 1 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0002 | 0/0 | 9006 | 7 | 0 | 1 | 2 | 0 | 4 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0006 | 0/0 | 9006 | 8 | 8 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0008 | 0/0 | 9007 | 7 | 0 | 0 | 6 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0009 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0012 | 0/0 | 9007 | 3 | 0 | 0 | 0 | 0 | 3 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0013 | 0/0 | 9007 | 4 | 0 | 4 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0014 | 0/0 | 9005 | 5 | 4 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0015 | 0/0 | 9005 | 3 | 3 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0016 | 0/0 | 9014 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9009): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0019 | 0/0 | 9003 | 3 | 3 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(8998): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0021 | 0/0 | 9006 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0023 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0033 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0034 | 0/0 | 9005 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0037 | 0/0 | 9006 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0059 | 0/0 | 9008 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0069 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0074 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0075 | 0/0 | 9007 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0080 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0081 | 0/0 | 9006 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0082 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0088 | 0/0 | 9006 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0003t0092 | 0/0 | 9006 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0001 | 0/0 | 9007 | 3 | 0 | 3 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0002 | 0/0 | 9006 | 5 | 1 | 4 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0004 | 0/0 | 9007 | 8 | 3 | 3 | 0 | 2 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0005 | 0/0 | 9005 | 12 | 10 | 1 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0007 | 0/0 | 9006 | 6 | 1 | 4 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0008 | 0/0 | 9007 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0015 | 0/0 | 9005 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0020 | 0/0 | 9008 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0026 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0035 | 0/0 | 9006 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0036 | 0/0 | 9019 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9014): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0038 | 0/0 | 9006 | 2 | 1 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0039 | 0/0 | 9007 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0043 | 0/0 | 9005 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0065 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0070 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0078 | 0/0 | 9004 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(8999): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0083 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0086 | 0/0 | 9008 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0089 | 0/0 | 9003 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(8998): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0094 | 0/0 | 9006 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0004t0096 | 0/0 | 9014 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9009): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0002 | 0/0 | 9006 | 15 | 7 | 1 | 5 | 1 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0004 | 0/0 | 9007 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0006 | 0/0 | 9006 | 3 | 3 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0016 | 0/0 | 9014 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9009): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0031 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0033 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0036 | 0/0 | 9019 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9014): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0042 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0058 | 0/0 | 9008 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0062 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0077 | 0/0 | 9019 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9014): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0079 | 0/0 | 9003 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(8998): Show |
chr4 | 2788085 | 2846096 |
| a0001c0005t0095 | 0/0 | 9013 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9008): Show |
chr4 | 2788085 | 2846096 |
| a0001c0006t0016 | 0/0 | 9014 | 3 | 3 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9009): Show |
chr4 | 2788085 | 2846096 |
| a0001c0006t0040 | 0/0 | 9013 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9008): Show |
chr4 | 2788085 | 2846096 |
| a0001c0007t0015 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0007t0027 | 0/0 | 9006 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0007t0031 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0009t0021 | 0/0 | 9006 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0010t0005 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0001c0011t0003 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0001c0012t0008 | 0/0 | 9007 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9002): Show |
chr4 | 2788085 | 2846096 |
| a0001c0015t0005 | 0/0 | 9005 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9000): Show |
chr4 | 2788085 | 2846096 |
| a0002c0008t0020 | 0/0 | 9008 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9003): Show |
chr4 | 2788085 | 2846096 |
| a0003c0014t0002 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| a0004c0013t0053 | 0/0 | 9006 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | GAGTC others(9001): Show |
chr4 | 2788085 | 2846096 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0004g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0010g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0010g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0010g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0010g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0011g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0018g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0022g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0022g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0023g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0024g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0025g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0025g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0026g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0029g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0030g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0032g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0041g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0044g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0045g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0046g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0047g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0048g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0049g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0050g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0052g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0054g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0055g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0056g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0063g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0064g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0066g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0067g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0068g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0072g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0073g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0085g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0001t0093g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0001 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0004g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0007g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0012g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0017g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0017g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0024g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0028g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0029g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0032g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0034g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0051g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0057g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0060g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0061g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0071g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0076g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0084g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0087g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0090g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0002t0091g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0006g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0008g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0008g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0012g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0012g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0013g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0013g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0013g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0013g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0014g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0014g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0015g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0015g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0019g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0021g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0021g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0023g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0033g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0034g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0037g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0037g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0059g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0069g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0074g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0075g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0080g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0081g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0082g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0088g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0003t0092g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0004g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0007g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0007g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0008g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0015g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0020g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0026g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0035g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0035g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0036g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0038g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0038g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0039g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0043g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0065g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0070g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0078g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0083g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0086g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0089g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0094g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0004t0096g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0031g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0033g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0036g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0042g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0058g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0062g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0077g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0079g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0005t0095g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0006t0016g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0006t0016g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0006t0016g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0006t0040g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0006t0040g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0007t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0007t0027g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0007t0027g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0007t0031g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0009t0021g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0010t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0011t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0012t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0001c0015t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0002c0008t0020g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0003c0014t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| a0004c0013t0053g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0150 | EUR | GBR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00099 | hp2 | a0001 | c0001 | t0067 | g0199 | EUR | GBR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00140 | hp1 | a0001 | c0004 | t0007 | g0022 | EUR | GBR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00280 | hp1 | a0001 | c0004 | t0004 | g0036 | EUR | FIN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0164 | EUR | FIN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00323 | hp1 | a0001 | c0003 | t0092 | g0086 | EUR | FIN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00323 | hp2 | a0001 | c0004 | t0004 | g0036 | EUR | FIN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0166 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00558 | hp1 | a0001 | c0002 | t0029 | g0172 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00597 | hp1 | a0001 | c0001 | t0024 | g0211 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00609 | hp1 | a0001 | c0002 | t0057 | g0165 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00609 | hp2 | a0003 | c0014 | t0002 | g0271 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00639 | hp2 | a0001 | c0004 | t0026 | g0153 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0031 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00733 | hp1 | a0001 | c0004 | t0004 | g0015 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00733 | hp2 | a0001 | c0001 | t0010 | g0223 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00735 | hp1 | a0001 | c0003 | t0023 | g0019 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00735 | hp2 | a0001 | c0001 | t0045 | g0263 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00738 | hp1 | a0001 | c0001 | t0022 | g0216 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00741 | hp1 | a0001 | c0002 | t0076 | g0162 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG00741 | hp2 | a0001 | c0004 | t0020 | g0068 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01069 | hp1 | a0001 | c0012 | t0008 | g0133 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01069 | hp2 | a0001 | c0004 | t0007 | g0034 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01070 | hp1 | a0001 | c0002 | t0007 | g0069 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01070 | hp2 | a0001 | c0001 | t0018 | g0016 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01071 | hp1 | a0001 | c0001 | t0018 | g0016 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01071 | hp2 | a0001 | c0004 | t0007 | g0034 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0003 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0028 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01081 | hp2 | a0001 | c0002 | t0007 | g0151 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01099 | hp1 | a0001 | c0001 | t0085 | g0266 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0029 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01106 | hp1 | a0001 | c0001 | t0064 | g0269 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01106 | hp2 | a0001 | c0004 | t0007 | g0161 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01109 | hp1 | a0001 | c0001 | t0018 | g0016 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01109 | hp2 | a0001 | c0004 | t0005 | g0008 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01167 | hp1 | a0001 | c0001 | t0023 | g0043 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01167 | hp2 | a0001 | c0005 | t0002 | g0100 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01168 | hp1 | a0001 | c0002 | t0034 | g0168 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01168 | hp2 | a0001 | c0004 | t0004 | g0015 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01169 | hp2 | a0001 | c0004 | t0004 | g0015 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01175 | hp2 | a0001 | c0002 | t0007 | g0160 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0062 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01192 | hp2 | a0001 | c0002 | t0087 | g0167 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01243 | hp1 | a0001 | c0003 | t0074 | g0057 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01243 | hp2 | a0001 | c0003 | t0088 | g0137 | AMR | PUR | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01255 | hp1 | a0001 | c0004 | t0015 | g0081 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01255 | hp2 | a0001 | c0001 | t0073 | g0200 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01256 | hp1 | a0001 | c0002 | t0017 | g0014 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01256 | hp2 | a0001 | c0001 | t0041 | g0213 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01257 | hp1 | a0001 | c0001 | t0011 | g0003 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01258 | hp1 | a0001 | c0002 | t0017 | g0014 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0003 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0154 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01261 | hp2 | a0001 | c0004 | t0007 | g0022 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0220 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01358 | hp1 | a0001 | c0002 | t0084 | g0159 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0037 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0073 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0037 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01515 | hp2 | a0001 | c0005 | t0002 | g0187 | EUR | IBS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01516 | hp1 | a0002 | c0008 | t0020 | g0020 | EUR | IBS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01516 | hp2 | a0001 | c0005 | t0004 | g0195 | EUR | IBS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01517 | hp1 | a0001 | c0001 | t0032 | g0046 | EUR | IBS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01517 | hp2 | a0002 | c0008 | t0020 | g0020 | EUR | IBS | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01884 | hp1 | a0001 | c0003 | t0015 | g0112 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01884 | hp2 | a0001 | c0005 | t0002 | g0093 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01928 | hp2 | a0001 | c0001 | t0011 | g0003 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01934 | hp1 | a0001 | c0003 | t0013 | g0128 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01952 | hp2 | a0001 | c0001 | t0010 | g0201 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01975 | hp1 | a0001 | c0003 | t0014 | g0189 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01975 | hp2 | a0001 | c0003 | t0013 | g0124 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01978 | hp1 | a0001 | c0004 | t0002 | g0028 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01978 | hp2 | a0001 | c0001 | t0010 | g0247 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02004 | hp2 | a0001 | c0004 | t0002 | g0071 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02027 | hp1 | a0001 | c0001 | t0029 | g0157 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02040 | hp1 | a0001 | c0001 | t0054 | g0224 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02055 | hp1 | a0001 | c0004 | t0035 | g0105 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02055 | hp2 | a0001 | c0009 | t0021 | g0056 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0222 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02071 | hp1 | a0001 | c0004 | t0005 | g0136 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02083 | hp1 | a0001 | c0001 | t0009 | g0262 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02145 | hp1 | a0001 | c0003 | t0019 | g0051 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02145 | hp2 | a0001 | c0003 | t0021 | g0082 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02148 | hp1 | a0001 | c0001 | t0011 | g0210 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | CDX | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02155 | hp2 | a0001 | c0003 | t0008 | g0040 | EAS | CDX | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02165 | hp1 | a0001 | c0003 | t0008 | g0234 | EAS | CDX | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | CDX | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02257 | hp1 | a0001 | c0005 | t0002 | g0090 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02257 | hp2 | a0001 | c0003 | t0037 | g0035 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02258 | hp1 | a0001 | c0005 | t0002 | g0196 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02258 | hp2 | a0001 | c0007 | t0031 | g0111 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02273 | hp1 | a0001 | c0003 | t0013 | g0125 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02273 | hp2 | a0001 | c0001 | t0049 | g0245 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02280 | hp1 | a0001 | c0006 | t0016 | g0205 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02280 | hp2 | a0001 | c0003 | t0014 | g0035 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02293 | hp1 | a0001 | c0003 | t0013 | g0135 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0074 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0047 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02451 | hp1 | a0001 | c0003 | t0006 | g0099 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02451 | hp2 | a0001 | c0010 | t0005 | g0142 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02523 | hp1 | a0001 | c0002 | t0007 | g0113 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02572 | hp1 | a0001 | c0007 | t0027 | g0055 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02572 | hp2 | a0001 | c0003 | t0015 | g0048 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02602 | hp1 | a0001 | c0004 | t0039 | g0033 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02602 | hp2 | a0001 | c0003 | t0012 | g0024 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02615 | hp1 | a0001 | c0005 | t0002 | g0192 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02615 | hp2 | a0001 | c0003 | t0014 | g0191 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02622 | hp1 | a0001 | c0002 | t0017 | g0152 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02622 | hp2 | a0001 | c0003 | t0016 | g0053 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02630 | hp1 | a0001 | c0001 | t0056 | g0253 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02630 | hp2 | a0001 | c0004 | t0078 | g0076 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02647 | hp1 | a0001 | c0007 | t0015 | g0049 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02647 | hp2 | a0001 | c0004 | t0005 | g0106 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02698 | hp2 | a0001 | c0001 | t0044 | g0215 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02717 | hp1 | a0001 | c0003 | t0069 | g0117 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02717 | hp2 | a0001 | c0005 | t0031 | g0101 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02723 | hp1 | a0001 | c0007 | t0027 | g0054 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02723 | hp2 | a0001 | c0005 | t0016 | g0098 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02735 | hp1 | a0001 | c0004 | t0039 | g0033 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0011 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02738 | hp1 | a0001 | c0003 | t0012 | g0024 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02809 | hp1 | a0001 | c0001 | t0046 | g0254 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02809 | hp2 | a0001 | c0004 | t0035 | g0107 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02886 | hp1 | a0001 | c0004 | t0007 | g0156 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02886 | hp2 | a0001 | c0006 | t0016 | g0207 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02895 | hp1 | a0001 | c0006 | t0016 | g0203 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02895 | hp2 | a0001 | c0004 | t0070 | g0021 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02896 | hp1 | a0001 | c0004 | t0038 | g0202 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02896 | hp2 | a0001 | c0005 | t0033 | g0025 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02897 | hp1 | a0001 | c0005 | t0006 | g0025 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02897 | hp2 | a0001 | c0006 | t0040 | g0206 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02922 | hp1 | a0001 | c0003 | t0006 | g0002 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02922 | hp2 | a0001 | c0004 | t0005 | g0088 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02965 | hp1 | a0001 | c0006 | t0040 | g0204 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02965 | hp2 | a0001 | c0003 | t0006 | g0002 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02970 | hp1 | a0001 | c0004 | t0004 | g0064 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02970 | hp2 | a0001 | c0003 | t0006 | g0002 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02976 | hp1 | a0001 | c0005 | t0095 | g0091 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02976 | hp2 | a0001 | c0003 | t0033 | g0002 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0031 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03017 | hp2 | a0001 | c0001 | t0022 | g0219 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03041 | hp1 | a0001 | c0005 | t0002 | g0096 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03041 | hp2 | a0001 | c0005 | t0079 | g0063 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03130 | hp1 | a0001 | c0005 | t0077 | g0084 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03130 | hp2 | a0001 | c0004 | t0065 | g0066 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03139 | hp1 | a0001 | c0003 | t0021 | g0058 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03139 | hp2 | a0001 | c0004 | t0096 | g0138 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03195 | hp1 | a0001 | c0003 | t0006 | g0002 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03195 | hp2 | a0001 | c0004 | t0005 | g0141 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03209 | hp1 | a0001 | c0005 | t0036 | g0097 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03209 | hp2 | a0001 | c0003 | t0014 | g0188 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03225 | hp1 | a0001 | c0004 | t0005 | g0008 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03225 | hp2 | a0001 | c0003 | t0015 | g0103 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03239 | hp1 | a0001 | c0004 | t0043 | g0075 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03239 | hp2 | a0001 | c0005 | t0002 | g0194 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03453 | hp1 | a0001 | c0003 | t0019 | g0050 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03453 | hp2 | a0001 | c0003 | t0006 | g0115 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03486 | hp1 | a0001 | c0003 | t0014 | g0190 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03486 | hp2 | a0001 | c0004 | t0036 | g0067 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03492 | hp1 | a0001 | c0003 | t0081 | g0127 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03516 | hp1 | a0001 | c0004 | t0004 | g0065 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03516 | hp2 | a0001 | c0004 | t0005 | g0023 | AFR | ESN | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03540 | hp1 | a0001 | c0004 | t0005 | g0139 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03540 | hp2 | a0001 | c0005 | t0006 | g0094 | AFR | GWD | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03669 | hp1 | a0001 | c0003 | t0075 | g0118 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03688 | hp2 | a0001 | c0003 | t0008 | g0131 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03704 | hp1 | a0001 | c0004 | t0038 | g0072 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03704 | hp2 | a0001 | c0003 | t0034 | g0120 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03710 | hp1 | a0001 | c0001 | t0026 | g0221 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03710 | hp2 | a0001 | c0002 | t0007 | g0185 | SAS | PJL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0087 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03834 | hp1 | a0001 | c0002 | t0017 | g0014 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03927 | hp1 | a0001 | c0002 | t0091 | g0175 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0123 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03942 | hp1 | a0001 | c0002 | t0012 | g0149 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03942 | hp2 | a0001 | c0003 | t0012 | g0011 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0275 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04115 | hp2 | a0001 | c0001 | t0093 | g0231 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0267 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0011 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04204 | hp1 | a0001 | c0004 | t0094 | g0070 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0013 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0122 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG04228 | hp2 | a0001 | c0001 | t0068 | g0217 | SAS | STU | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18522 | hp1 | a0001 | c0004 | t0005 | g0008 | AFR | YRI | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18522 | hp2 | a0001 | c0004 | t0083 | g0060 | AFR | YRI | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18612 | hp1 | a0001 | c0001 | t0055 | g0061 | EAS | CHB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0252 | EAS | CHB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18747 | hp2 | a0001 | c0005 | t0058 | g0148 | EAS | CHB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18906 | hp1 | a0001 | c0004 | t0005 | g0023 | AFR | YRI | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18906 | hp2 | a0001 | c0003 | t0006 | g0116 | AFR | YRI | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18940 | hp1 | a0001 | c0001 | t0072 | g0038 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18940 | hp2 | a0001 | c0002 | t0024 | g0027 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18942 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18944 | hp2 | a0001 | c0001 | t0066 | g0257 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18946 | hp1 | a0001 | c0001 | t0048 | g0240 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18948 | hp2 | a0001 | c0003 | t0080 | g0134 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18952 | hp2 | a0001 | c0001 | t0063 | g0038 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18957 | hp2 | a0001 | c0003 | t0082 | g0233 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18959 | hp2 | a0001 | c0005 | t0002 | g0007 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18961 | hp1 | a0001 | c0001 | t0025 | g0208 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0178 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18962 | hp2 | a0001 | c0001 | t0025 | g0250 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18964 | hp1 | a0001 | c0002 | t0051 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18964 | hp2 | a0001 | c0005 | t0002 | g0007 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18969 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18971 | hp1 | a0001 | c0005 | t0002 | g0007 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18981 | hp1 | a0001 | c0011 | t0003 | g0130 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18982 | hp2 | a0001 | c0001 | t0052 | g0283 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18984 | hp2 | a0001 | c0003 | t0002 | g0114 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18994 | hp1 | a0001 | c0002 | t0090 | g0032 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18999 | hp1 | a0001 | c0002 | t0032 | g0182 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19004 | hp1 | a0001 | c0001 | t0030 | g0041 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19004 | hp2 | a0001 | c0003 | t0008 | g0126 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19005 | hp1 | a0001 | c0002 | t0071 | g0282 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19007 | hp2 | a0001 | c0001 | t0030 | g0045 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19010 | hp1 | a0001 | c0003 | t0059 | g0236 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19010 | hp2 | a0001 | c0002 | t0061 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19011 | hp1 | a0001 | c0003 | t0008 | g0235 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0108 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19012 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19030 | hp1 | a0001 | c0003 | t0006 | g0002 | AFR | LWK | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19030 | hp2 | a0001 | c0004 | t0086 | g0083 | AFR | LWK | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19043 | hp1 | a0001 | c0004 | t0004 | g0078 | AFR | LWK | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19043 | hp2 | a0001 | c0005 | t0042 | g0193 | AFR | LWK | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19055 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19056 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19056 | hp2 | a0001 | c0002 | t0028 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19063 | hp1 | a0001 | c0005 | t0002 | g0059 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19063 | hp2 | a0004 | c0013 | t0053 | g0258 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19066 | hp2 | a0001 | c0005 | t0002 | g0007 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19076 | hp2 | a0001 | c0002 | t0060 | g0176 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19079 | hp1 | a0001 | c0003 | t0008 | g0040 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19080 | hp2 | a0001 | c0003 | t0008 | g0132 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19086 | hp1 | a0001 | c0002 | t0028 | g0129 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19088 | hp1 | a0001 | c0004 | t0008 | g0265 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA20129 | hp1 | a0001 | c0005 | t0062 | g0102 | AFR | ASW | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | ASW | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0170 | EUR | TSI | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02109 | hp2 | a0001 | c0003 | t0037 | g0092 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02486 | hp1 | a0001 | c0005 | t0006 | g0085 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0109 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02559 | hp1 | a0001 | c0005 | t0002 | g0104 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG02559 | hp2 | a0001 | c0015 | t0005 | g0256 | AFR | ACB | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03471 | hp1 | a0001 | c0004 | t0005 | g0008 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG03471 | hp2 | a0001 | c0005 | t0002 | g0089 | AFR | MSL | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG06807 | hp1 | a0001 | c0003 | t0009 | g0119 | AFR | USA | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| HG06807 | hp2 | a0001 | c0003 | t0019 | g0052 | AFR | USA | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA20300 | hp1 | a0001 | c0004 | t0089 | g0080 | AFR | USA | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA20300 | hp2 | a0001 | c0001 | t0050 | g0242 | AFR | USA | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA21309 | hp1 | a0001 | c0001 | t0047 | g0110 | AFR | LWK | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| NA21309 | hp2 | a0001 | c0004 | t0005 | g0140 | AFR | LWK | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0197 | REF | REF | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0181 | REF | REF | SH3BP2_chr4_2788085_2846096 | SH3BP2 | chr4 | 2788085 | 2846096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2832353 | C | T | 1 | a0002 | 2 | HG01516.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.1429C>T | p.Arg477Trp | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/13 | 1487/9006 | 1429/1686 | 477/561 | chr4 | 2832353 | |||
| chr4:2832401 | A | C | 1 | a0004 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.1477A>C | p.Lys493Gln | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/13 | 1535/9006 | 1477/1686 | 493/561 | chr4 | 2832401 | |||
| chr4:2833772 | G | A | 1 | a0003 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1624G>A | p.Val542Met | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1682/9006 | 1624/1686 | 542/561 | chr4 | 2833772 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2820740 | G | T | 4 | a0001c0001 a0001c0015 a0003c0014 others(1): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(128): Show |
synonymous_variant | LOW | c.123G>T | p.Leu41Leu | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/13 | 181/9006 | 123/1686 | 41/561 | chr4 | 2820740 | |||
| chr4:2822969 | C | T | 1 | a0001c0007 | 4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
synonymous_variant | LOW | c.171C>T | p.Cys57Cys | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/13 | 229/9006 | 171/1686 | 57/561 | chr4 | 2822969 | |||
| chr4:2824649 | C | T | 1 | a0001c0012 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.276C>T | p.Asn92Asn | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/13 | 334/9006 | 276/1686 | 92/561 | chr4 | 2824649 | |||
| chr4:2824673 | T | C | 13 | a0001c0001 a0001c0003 a0001c0004 others(10): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
synonymous_variant | LOW | c.300T>C | p.His100His | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/13 | 358/9006 | 300/1686 | 100/561 | chr4 | 2824673 | |||
| chr4:2825185 | C | G | 4 | a0001c0003 a0001c0009 a0001c0010 others(1): Show |
63 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(60): Show |
synonymous_variant | LOW | c.417C>G | p.Pro139Pro | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/13 | 475/9006 | 417/1686 | 139/561 | chr4 | 2825185 | |||
| chr4:2829596 | C | G | 1 | a0001c0011 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.690C>G | p.Gly230Gly | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/13 | 748/9006 | 690/1686 | 230/561 | chr4 | 2829596 | |||
| chr4:2829656 | T | G | 4 | a0001c0001 a0001c0005 a0001c0006 others(1): Show |
163 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(160): Show |
synonymous_variant | LOW | c.750T>G | p.Ala250Ala | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/13 | 808/9006 | 750/1686 | 250/561 | chr4 | 2829656 | |||
| chr4:2829707 | C | T | 1 | a0001c0006 | 5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.801C>T | p.Cys267Cys | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/13 | 859/9006 | 801/1686 | 267/561 | chr4 | 2829707 | |||
| chr4:2829995 | T | C | 1 | a0001c0009 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1089T>C | p.Ala363Ala | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/13 | 1147/9006 | 1089/1686 | 363/561 | chr4 | 2829995 | |||
| chr4:2831661 | G | A | 1 | a0001c0010 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1332G>A | p.Ser444Ser | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 9/13 | 1390/9006 | 1332/1686 | 444/561 | chr4 | 2831661 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2793134 | G | C | 2 | a0001c0001t0011 a0001c0001t0041 |
6 | HG01074.hp2 HG01256.hp2 HG01257.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-9G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/13 | 27484 | chr4 | 2793134 | ||||||
| chr4:2833876 | C | T | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*42C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 42 | chr4 | 2833876 | ||||||
| chr4:2833898 | C | T | 1 | a0001c0004t0094 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 64 | chr4 | 2833898 | ||||||
| chr4:2833917 | G | C | 1 | a0001c0005t0042 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 83 | chr4 | 2833917 | ||||||
| chr4:2834018 | A | G | 1 | a0001c0001t0093 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 184 | chr4 | 2834018 | ||||||
| chr4:2834139 | C | T | 1 | a0001c0002t0017 | 4 | HG01256.hp1 HG01258.hp1 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*305C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 305 | chr4 | 2834139 | ||||||
| chr4:2834206 | G | A | 1 | a0001c0004t0043 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 372 | chr4 | 2834206 | ||||||
| chr4:2834468 | C | A | 32 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(29): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*634C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 634 | chr4 | 2834468 | ||||||
| chr4:2834523 | C | T | 1 | a0001c0003t0092 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*689C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 689 | chr4 | 2834523 | ||||||
| chr4:2834637 | G | A | 1 | a0001c0001t0044 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 803 | chr4 | 2834637 | ||||||
| chr4:2834716 | C | T | 1 | a0001c0002t0091 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*882C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 882 | chr4 | 2834716 | ||||||
| chr4:2834751 | C | T | 1 | a0001c0002t0090 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 917 | chr4 | 2834751 | ||||||
| chr4:2834822 | T | C | 1 | a0001c0007t0027 | 2 | HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*988T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 988 | chr4 | 2834822 | ||||||
| chr4:2834901 | C | T | 76 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(73): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1067C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1067 | chr4 | 2834901 | ||||||
| chr4:2835152 | T | C | 11 | a0001c0001t0003 a0001c0001t0029 a0001c0002t0003 others(8): Show |
46 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1318T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1318 | chr4 | 2835152 | ||||||
| chr4:2835254 | C | T | 5 | a0001c0003t0015 a0001c0003t0021 a0001c0004t0015 others(2): Show |
8 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1420 | chr4 | 2835254 | ||||||
| chr4:2835490 | T | C | 3 | a0001c0004t0036 a0001c0005t0036 a0001c0005t0077 |
3 | HG03130.hp1 HG03209.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1656T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1656 | chr4 | 2835490 | ||||||
| chr4:2835513 | C | T | 1 | a0001c0002t0076 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1679 | chr4 | 2835513 | ||||||
| chr4:2835632 | T | C | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1798T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1798 | chr4 | 2835632 | ||||||
| chr4:2835645 | G | A | 1 | a0001c0005t0062 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1811G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1811 | chr4 | 2835645 | ||||||
| chr4:2835663 | C | T | 1 | a0001c0003t0075 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1829C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1829 | chr4 | 2835663 | ||||||
| chr4:2835694 | C | T | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1860C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1860 | chr4 | 2835694 | ||||||
| chr4:2835769 | C | T | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1935C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 1935 | chr4 | 2835769 | ||||||
| chr4:2835846 | G | A | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2012G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2012 | chr4 | 2835846 | ||||||
| chr4:2835873 | A | T | 1 | a0001c0004t0089 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2039A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2039 | chr4 | 2835873 | ||||||
| chr4:2835894 | G | C | 1 | a0001c0001t0046 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2060G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2060 | chr4 | 2835894 | ||||||
| chr4:2835900 | A | C | 1 | a0001c0002t0061 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2066A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2066 | chr4 | 2835900 | ||||||
| chr4:2835997 | A | T | 5 | a0001c0003t0074 a0001c0004t0005 a0001c0004t0035 others(2): Show |
17 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2163A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2163 | chr4 | 2835997 | ||||||
| chr4:2836028 | T | TGCTTTAT others(16): Show |
1 | a0001c0002t0060 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2195_*2217dupGCTT others(19): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2218 | INFO_REALIGN_3_PRIME | chr4 | 2836028 | |||||
| chr4:2836036 | G | C | 79 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(76): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*2202G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2202 | chr4 | 2836036 | ||||||
| chr4:2836176 | C | T | 7 | a0001c0002t0057 a0001c0003t0016 a0001c0004t0096 others(4): Show |
10 | HG00609.hp1 HG02280.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2342C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2342 | chr4 | 2836176 | ||||||
| chr4:2836344 | A | G | 1 | a0001c0001t0073 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2510A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2510 | chr4 | 2836344 | ||||||
| chr4:2836413 | C | T | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2579C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2579 | chr4 | 2836413 | ||||||
| chr4:2836457 | G | T | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2623G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2623 | chr4 | 2836457 | ||||||
| chr4:2836638 | G | A | 2 | a0001c0004t0078 a0001c0005t0079 |
2 | HG02630.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2804G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2804 | chr4 | 2836638 | ||||||
| chr4:2836746 | C | T | 13 | a0001c0001t0004 a0001c0001t0064 a0001c0001t0085 others(10): Show |
29 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2912C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2912 | chr4 | 2836746 | ||||||
| chr4:2836785 | C | G | 2 | a0001c0004t0020 a0002c0008t0020 |
3 | HG00741.hp2 HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2951C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 2951 | chr4 | 2836785 | ||||||
| chr4:2836849 | G | A | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3015G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3015 | chr4 | 2836849 | ||||||
| chr4:2836912 | G | A | 2 | a0001c0004t0078 a0001c0005t0079 |
2 | HG02630.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3078G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3078 | chr4 | 2836912 | ||||||
| chr4:2837053 | CT | C | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3229delT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3229 | INFO_REALIGN_3_PRIME | chr4 | 2837053 | |||||
| chr4:2837184 | C | G | 7 | a0001c0003t0016 a0001c0004t0089 a0001c0004t0096 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3350C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3350 | chr4 | 2837184 | ||||||
| chr4:2837472 | A | G | 11 | a0001c0003t0015 a0001c0003t0016 a0001c0003t0021 others(8): Show |
17 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3638A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3638 | chr4 | 2837472 | ||||||
| chr4:2837577 | G | A | 3 | a0001c0004t0043 a0001c0004t0065 a0001c0005t0062 |
3 | HG03130.hp2 HG03239.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3743G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3743 | chr4 | 2837577 | ||||||
| chr4:2837711 | G | C | 45 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(42): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3877G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3877 | chr4 | 2837711 | ||||||
| chr4:2837782 | C | T | 2 | a0001c0001t0029 a0001c0002t0029 |
2 | HG00558.hp1 HG02027.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3948C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3948 | chr4 | 2837782 | ||||||
| chr4:2837808 | G | T | 11 | a0001c0003t0016 a0001c0004t0036 a0001c0004t0078 others(8): Show |
14 | HG02280.hp1 HG02622.hp2 HG02630.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3974G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 3974 | chr4 | 2837808 | ||||||
| chr4:2837932 | G | A | 81 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(78): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*4098G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4098 | chr4 | 2837932 | ||||||
| chr4:2838013 | C | T | 2 | a0001c0001t0026 a0001c0004t0026 |
2 | HG00639.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4179C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4179 | chr4 | 2838013 | ||||||
| chr4:2838279 | C | G | 1 | a0001c0007t0027 | 2 | HG02572.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4445C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4445 | chr4 | 2838279 | ||||||
| chr4:2838341 | G | A | 1 | a0001c0004t0065 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4507G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4507 | chr4 | 2838341 | ||||||
| chr4:2838397 | A | C | 6 | a0001c0003t0016 a0001c0004t0096 a0001c0005t0016 others(3): Show |
9 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4563A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4563 | chr4 | 2838397 | ||||||
| chr4:2838641 | A | AT | 62 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(59): Show |
175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*4818dupT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4819 | INFO_REALIGN_3_PRIME | chr4 | 2838641 | |||||
| chr4:2838641 | A | ATTTTTTT others(5): Show |
1 | a0001c0005t0095 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4818_*4819insTTTT others(8): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4819 | INFO_REALIGN_3_PRIME | chr4 | 2838641 | |||||
| chr4:2838641 | A | ATTTTTTT others(6): Show |
8 | a0001c0003t0016 a0001c0004t0036 a0001c0004t0096 others(5): Show |
11 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4818_*4819insTTTT others(9): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4819 | INFO_REALIGN_3_PRIME | chr4 | 2838641 | |||||
| chr4:2838715 | A | G | 1 | a0001c0001t0025 | 2 | NA18961.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4881A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4881 | chr4 | 2838715 | ||||||
| chr4:2838826 | C | A | 2 | a0001c0005t0031 a0001c0007t0031 |
2 | HG02258.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4992C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 4992 | chr4 | 2838826 | ||||||
| chr4:2838996 | A | G | 5 | a0001c0003t0015 a0001c0003t0021 a0001c0004t0015 others(2): Show |
8 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5162A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5162 | chr4 | 2838996 | ||||||
| chr4:2839106 | TTGTCTCC others(7): Show |
T | 1 | a0001c0001t0048 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5278_*5291delCCTG others(10): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5278 | INFO_REALIGN_3_PRIME | chr4 | 2839106 | |||||
| chr4:2839163 | C | A | 1 | a0001c0001t0067 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5329C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5329 | chr4 | 2839163 | ||||||
| chr4:2839314 | CCA | C | 1 | a0001c0003t0019 | 3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5484_*5485delAC | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5484 | INFO_REALIGN_3_PRIME | chr4 | 2839314 | |||||
| chr4:2839363 | T | A | 1 | a0001c0003t0075 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5529T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5529 | chr4 | 2839363 | ||||||
| chr4:2839477 | T | G | 1 | a0001c0001t0018 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5643T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5643 | chr4 | 2839477 | ||||||
| chr4:2839513 | T | C | 90 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(87): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*5679T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5679 | chr4 | 2839513 | ||||||
| chr4:2839551 | G | A | 1 | a0001c0001t0030 | 2 | NA19004.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5717G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5717 | chr4 | 2839551 | ||||||
| chr4:2839572 | T | G | 11 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0049 others(8): Show |
21 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5738T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5738 | chr4 | 2839572 | ||||||
| chr4:2839581 | T | G | 1 | a0001c0001t0050 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5747T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5747 | chr4 | 2839581 | ||||||
| chr4:2839619 | A | T | 1 | a0001c0001t0056 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5785A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5785 | chr4 | 2839619 | ||||||
| chr4:2839674 | C | T | 1 | a0001c0001t0055 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5840C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5840 | chr4 | 2839674 | ||||||
| chr4:2839732 | T | A | 3 | a0001c0001t0013 a0001c0003t0013 a0001c0003t0080 |
6 | HG01934.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5898T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5898 | chr4 | 2839732 | ||||||
| chr4:2839734 | AT | A | 11 | a0001c0001t0049 a0001c0001t0052 a0001c0002t0051 others(8): Show |
13 | HG01243.hp2 HG02145.hp1 HG02273.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5916delT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5916 | INFO_REALIGN_3_PRIME | chr4 | 2839734 | |||||
| chr4:2839734 | ATTT | A | 7 | a0001c0003t0016 a0001c0004t0089 a0001c0004t0096 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5914_*5916delTTT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5914 | INFO_REALIGN_3_PRIME | chr4 | 2839734 | |||||
| chr4:2839806 | C | T | 4 | a0001c0001t0024 a0001c0001t0052 a0001c0002t0024 others(1): Show |
4 | HG00597.hp1 NA18940.hp2 NA18964.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5972C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5972 | chr4 | 2839806 | ||||||
| chr4:2839826 | A | G | 1 | a0001c0004t0039 | 2 | HG02602.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5992A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5992 | chr4 | 2839826 | ||||||
| chr4:2839830 | C | T | 1 | a0001c0005t0077 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5996C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 5996 | chr4 | 2839830 | ||||||
| chr4:2839910 | T | C | 8 | a0001c0001t0013 a0001c0003t0008 a0001c0003t0013 others(5): Show |
17 | HG01069.hp1 HG01934.hp1 HG01975.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6076T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6076 | chr4 | 2839910 | ||||||
| chr4:2839942 | C | T | 1 | a0001c0002t0087 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6108C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6108 | chr4 | 2839942 | ||||||
| chr4:2839943 | A | G | 7 | a0001c0003t0016 a0001c0004t0089 a0001c0004t0096 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6109A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6109 | chr4 | 2839943 | ||||||
| chr4:2839970 | A | C | 1 | a0001c0001t0054 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6136A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6136 | chr4 | 2839970 | ||||||
| chr4:2840045 | C | T | 4 | a0001c0002t0007 a0001c0002t0084 a0001c0004t0007 others(1): Show |
13 | HG00140.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6211C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6211 | chr4 | 2840045 | ||||||
| chr4:2840233 | C | A | 3 | a0001c0004t0043 a0001c0004t0065 a0001c0005t0062 |
3 | HG03130.hp2 HG03239.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6399C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6399 | chr4 | 2840233 | ||||||
| chr4:2840234 | C | A | 1 | a0004c0013t0053 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6400C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6400 | chr4 | 2840234 | ||||||
| chr4:2840234 | C | CA | 45 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(42): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*6420dupA | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6421 | INFO_REALIGN_3_PRIME | chr4 | 2840234 | |||||
| chr4:2840234 | CA | C | 8 | a0001c0002t0028 a0001c0002t0034 a0001c0003t0033 others(5): Show |
11 | HG01168.hp1 HG02896.hp1 HG02896.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6420delA | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6420 | INFO_REALIGN_3_PRIME | chr4 | 2840234 | |||||
| chr4:2840360 | C | T | 1 | a0001c0001t0093 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6526C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6526 | chr4 | 2840360 | ||||||
| chr4:2840426 | G | C | 1 | a0001c0001t0054 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6592G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6592 | chr4 | 2840426 | ||||||
| chr4:2840426 | G | T | 7 | a0001c0003t0016 a0001c0004t0089 a0001c0004t0096 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6592G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6592 | chr4 | 2840426 | ||||||
| chr4:2840437 | G | A | 7 | a0001c0003t0016 a0001c0004t0089 a0001c0004t0096 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6603G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6603 | chr4 | 2840437 | ||||||
| chr4:2840452 | G | A | 7 | a0001c0003t0016 a0001c0004t0089 a0001c0004t0096 others(4): Show |
10 | HG02280.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6618G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6618 | chr4 | 2840452 | ||||||
| chr4:2840813 | A | G | 3 | a0001c0004t0036 a0001c0005t0036 a0001c0005t0077 |
3 | HG03130.hp1 HG03209.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6979A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 6979 | chr4 | 2840813 | ||||||
| chr4:2840872 | T | A | 1 | a0001c0001t0072 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7038T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7038 | chr4 | 2840872 | ||||||
| chr4:2840990 | A | AT | 4 | a0001c0001t0012 a0001c0002t0012 a0001c0003t0012 others(1): Show |
6 | HG02486.hp2 HG02602.hp2 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7167dupT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7168 | INFO_REALIGN_3_PRIME | chr4 | 2840990 | |||||
| chr4:2840990 | AT | A | 58 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(55): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*7167delT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7167 | INFO_REALIGN_3_PRIME | chr4 | 2840990 | |||||
| chr4:2840990 | ATT | A | 5 | a0001c0001t0054 a0001c0003t0014 a0001c0003t0037 others(2): Show |
10 | HG01975.hp1 HG02040.hp1 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7166_*7167delTT | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7166 | INFO_REALIGN_3_PRIME | chr4 | 2840990 | |||||
| chr4:2840999 | T | G | 5 | a0001c0003t0006 a0001c0003t0033 a0001c0003t0069 others(2): Show |
14 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7165T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7165 | chr4 | 2840999 | ||||||
| chr4:2841015 | A | G | 3 | a0001c0004t0036 a0001c0005t0036 a0001c0005t0077 |
3 | HG03130.hp1 HG03209.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7181A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7181 | chr4 | 2841015 | ||||||
| chr4:2841018 | A | G | 1 | a0001c0003t0019 | 3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7184A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7184 | chr4 | 2841018 | ||||||
| chr4:2841049 | T | C | 1 | a0001c0004t0096 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7215T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 13/13 | 7215 | chr4 | 2841049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2793182 | G | C | 3 | a0001c0003t0001g0019 a0001c0003t0002g0047 a0001c0003t0023g0019 |
3 | HG00642.hp1 HG00735.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-5+44G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793182 | |||||||
| chr4:2793227 | G | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-5+89G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793227 | |||||||
| chr4:2793237 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0032g0046 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-5+99C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793237 | |||||||
| chr4:2793710 | C | T | 12 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(9): Show |
12 | HG01515.hp2 HG01516.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+572C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793710 | |||||||
| chr4:2793747 | C | G | 1 | a0001c0002t0002g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-5+609C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793747 | |||||||
| chr4:2793862 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0009g0018 |
3 | NA18999.hp2 NA19012.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-5+724C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793862 | |||||||
| chr4:2793923 | G | C | 1 | a0001c0003t0015g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-5+785G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793923 | |||||||
| chr4:2793927 | T | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(245): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-5+789T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2793927 | |||||||
| chr4:2794067 | T | G | 1 | a0001c0007t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-5+929T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794067 | |||||||
| chr4:2794135 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0198 |
5 | HG00673.hp2 HG02080.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+997C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794135 | |||||||
| chr4:2794234 | T | A | 6 | a0001c0003t0016g0053 a0001c0003t0019g0050 a0001c0003t0019g0051 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+1096T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794234 | |||||||
| chr4:2794349 | C | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+1211C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794349 | |||||||
| chr4:2794369 | C | G | 3 | a0001c0004t0005g0139 a0001c0004t0005g0140 a0001c0004t0005g0141 |
3 | HG03195.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-5+1231C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794369 | |||||||
| chr4:2794371 | A | G | 16 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(13): Show |
20 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.-5+1233A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794371 | |||||||
| chr4:2794390 | C | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+1252C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794390 | |||||||
| chr4:2794393 | C | G | 1 | a0001c0003t0002g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-5+1255C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794393 | |||||||
| chr4:2794405 | C | T | 1 | a0001c0005t0002g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-5+1267C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794405 | |||||||
| chr4:2794407 | AAGGGCCC others(17): Show |
A | 35 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0055g0061 others(32): Show |
40 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-5+1277_-5+1300del others(24): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2794407 | ||||||
| chr4:2794464 | G | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+1326G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794464 | |||||||
| chr4:2794466 | A | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+1328A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794466 | |||||||
| chr4:2794655 | G | T | 22 | a0001c0001t0001g0121 a0001c0002t0007g0113 a0001c0003t0001g0011 others(19): Show |
27 | HG00642.hp1 HG00735.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-5+1517G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794655 | |||||||
| chr4:2794773 | T | C | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+1635T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794773 | |||||||
| chr4:2794809 | G | A | 1 | a0001c0003t0013g0124 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-5+1671G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794809 | |||||||
| chr4:2794938 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
143 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-5+1800C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2794938 | |||||||
| chr4:2795031 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0276 others(11): Show |
17 | HG00438.hp1 HG01123.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.-5+1893C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795031 | |||||||
| chr4:2795243 | A | G | 106 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0095 others(103): Show |
120 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-5+2105A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795243 | |||||||
| chr4:2795345 | C | T | 3 | a0001c0004t0007g0034 a0001c0005t0006g0085 a0001c0005t0077g0084 |
4 | HG01069.hp2 HG01071.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+2207C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795345 | |||||||
| chr4:2795410 | TCCTCTCT others(3): Show |
T | 1 | a0001c0007t0031g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-5+2277_-5+2286del others(10): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2795410 | ||||||
| chr4:2795475 | G | C | 1 | a0001c0001t0010g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-5+2337G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795475 | |||||||
| chr4:2795505 | C | T | 1 | a0001c0003t0088g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5+2367C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795505 | |||||||
| chr4:2795562 | G | A | 6 | a0001c0004t0038g0202 a0001c0006t0016g0203 a0001c0006t0016g0205 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+2424G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795562 | |||||||
| chr4:2795573 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0276 others(10): Show |
16 | HG00438.hp1 HG01123.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+2435G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795573 | |||||||
| chr4:2795582 | G | A | 1 | a0001c0003t0019g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-5+2444G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795582 | |||||||
| chr4:2795661 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-5+2523G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795661 | |||||||
| chr4:2795661 | G | C | 23 | a0001c0001t0001g0121 a0001c0002t0007g0113 a0001c0003t0001g0011 others(20): Show |
28 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-5+2523G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795661 | |||||||
| chr4:2795682 | C | T | 16 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(13): Show |
20 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.-5+2544C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795682 | |||||||
| chr4:2795756 | C | T | 36 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0055g0061 others(33): Show |
41 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-5+2618C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795756 | |||||||
| chr4:2795900 | G | T | 2 | a0001c0001t0001g0274 a0001c0002t0002g0275 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-5+2762G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2795900 | |||||||
| chr4:2796021 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-5+2883C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796021 | |||||||
| chr4:2796150 | A | T | 121 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0095 others(118): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-5+3012A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796150 | |||||||
| chr4:2796260 | C | T | 5 | a0001c0001t0002g0045 a0001c0001t0002g0270 a0001c0001t0002g0272 others(2): Show |
5 | HG00609.hp2 HG00673.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+3122C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796260 | |||||||
| chr4:2796330 | A | C | 1 | a0001c0001t0047g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-5+3192A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796330 | |||||||
| chr4:2796374 | G | A | 1 | a0001c0004t0005g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-5+3236G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796374 | |||||||
| chr4:2796443 | G | A | 119 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0095 others(116): Show |
137 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.-5+3305G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796443 | |||||||
| chr4:2796647 | G | A | 5 | a0001c0003t0015g0048 a0001c0003t0021g0058 a0001c0003t0074g0057 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+3509G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796647 | |||||||
| chr4:2796781 | A | G | 130 | a0001c0001t0001g0043 a0001c0001t0001g0077 a0001c0001t0001g0079 others(127): Show |
149 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-5+3643A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796781 | |||||||
| chr4:2796856 | C | T | 40 | a0001c0001t0001g0095 a0001c0003t0006g0099 a0001c0003t0014g0035 others(37): Show |
44 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+3718C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796856 | |||||||
| chr4:2796869 | G | A | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+3731G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796869 | |||||||
| chr4:2796948 | G | A | 1 | a0001c0005t0002g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-5+3810G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796948 | |||||||
| chr4:2796994 | C | G | 3 | a0001c0004t0005g0106 a0001c0004t0035g0105 a0001c0004t0035g0107 |
3 | HG02055.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-5+3856C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2796994 | |||||||
| chr4:2797019 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-5+3881G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797019 | |||||||
| chr4:2797068 | TG | T | 4 | a0001c0001t0025g0208 a0001c0002t0001g0144 a0001c0002t0003g0143 others(1): Show |
4 | HG01515.hp2 NA18946.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+3935delG | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2797068 | ||||||
| chr4:2797085 | C | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+3947C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797085 | |||||||
| chr4:2797098 | G | T | 23 | a0001c0001t0001g0121 a0001c0002t0007g0113 a0001c0003t0001g0011 others(20): Show |
28 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-5+3960G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797098 | |||||||
| chr4:2797269 | C | T | 23 | a0001c0001t0001g0121 a0001c0002t0007g0113 a0001c0003t0001g0011 others(20): Show |
28 | HG00642.hp1 HG00735.hp1 HG02300.hp1 others(25): Show |
intron_variant | MODIFIER | c.-5+4131C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797269 | |||||||
| chr4:2797298 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-5+4160G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797298 | |||||||
| chr4:2797305 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0023g0043 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-5+4167G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797305 | |||||||
| chr4:2797318 | T | G | 1 | a0001c0002t0002g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-5+4180T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797318 | |||||||
| chr4:2797348 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-5+4210G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797348 | |||||||
| chr4:2797364 | C | T | 1 | a0001c0002t0007g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-5+4226C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797364 | |||||||
| chr4:2797711 | C | T | 5 | a0001c0003t0015g0048 a0001c0003t0021g0058 a0001c0003t0074g0057 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+4573C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797711 | |||||||
| chr4:2797738 | C | T | 4 | a0001c0003t0021g0082 a0001c0004t0015g0081 a0001c0004t0086g0083 others(1): Show |
4 | HG01255.hp1 HG02145.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+4600C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797738 | |||||||
| chr4:2797745 | G | A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+4607G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797745 | |||||||
| chr4:2797836 | T | C | 3 | a0001c0002t0002g0146 a0001c0002t0002g0147 a0001c0005t0058g0148 |
3 | NA18747.hp2 NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-5+4698T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797836 | |||||||
| chr4:2797934 | G | A | 1 | a0001c0004t0083g0060 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-5+4796G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797934 | |||||||
| chr4:2797936 | G | A | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+4798G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2797936 | |||||||
| chr4:2798157 | G | A | 1 | a0001c0001t0011g0210 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-5+5019G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798157 | |||||||
| chr4:2798198 | G | A | 1 | a0001c0004t0005g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-5+5060G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798198 | |||||||
| chr4:2798201 | C | T | 3 | a0001c0004t0005g0106 a0001c0004t0035g0105 a0001c0004t0035g0107 |
3 | HG02055.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-5+5063C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798201 | |||||||
| chr4:2798202 | G | T | 58 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(55): Show |
68 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-5+5064G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798202 | |||||||
| chr4:2798221 | C | A | 23 | a0001c0001t0001g0121 a0001c0002t0007g0113 a0001c0003t0001g0011 others(20): Show |
28 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-5+5083C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798221 | |||||||
| chr4:2798522 | C | T | 1 | a0001c0004t0008g0265 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-5+5384C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798522 | |||||||
| chr4:2798529 | G | A | 57 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(54): Show |
67 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-5+5391G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798529 | |||||||
| chr4:2798529 | G | C | 1 | a0001c0003t0015g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-5+5391G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798529 | |||||||
| chr4:2798567 | C | T | 22 | a0001c0001t0001g0121 a0001c0002t0007g0113 a0001c0003t0001g0011 others(19): Show |
27 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-5+5429C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798567 | |||||||
| chr4:2798671 | G | T | 1 | a0001c0005t0002g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-5+5533G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798671 | |||||||
| chr4:2798718 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-5+5580A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798718 | |||||||
| chr4:2798788 | G | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+5650G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798788 | |||||||
| chr4:2798802 | A | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(123): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+5664A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798802 | |||||||
| chr4:2798815 | C | A | 1 | a0001c0001t0024g0211 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-5+5677C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798815 | |||||||
| chr4:2798927 | G | A | 58 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(55): Show |
68 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-5+5789G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798927 | |||||||
| chr4:2798958 | C | G | 3 | a0001c0005t0002g0187 a0001c0005t0002g0194 a0001c0005t0004g0195 |
3 | HG01515.hp2 HG01516.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-5+5820C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2798958 | |||||||
| chr4:2799022 | C | T | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+5884C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799022 | |||||||
| chr4:2799045 | C | T | 2 | a0001c0007t0027g0054 a0001c0007t0027g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-5+5907C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799045 | |||||||
| chr4:2799060 | T | C | 1 | a0001c0003t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-5+5922T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799060 | |||||||
| chr4:2799099 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-5+5961A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799099 | |||||||
| chr4:2799102 | C | T | 5 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+5964C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799102 | |||||||
| chr4:2799117 | T | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+5979T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799117 | |||||||
| chr4:2799185 | G | A | 1 | a0001c0003t0016g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+6047G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799185 | |||||||
| chr4:2799203 | C | G | 1 | a0001c0004t0008g0265 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-5+6065C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799203 | |||||||
| chr4:2799242 | C | T | 1 | a0001c0005t0002g0187 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-5+6104C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799242 | |||||||
| chr4:2799300 | A | G | 1 | a0001c0005t0002g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-5+6162A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799300 | |||||||
| chr4:2799487 | G | A | 1 | a0001c0002t0012g0149 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5+6349G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799487 | |||||||
| chr4:2799487 | G | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+6349G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799487 | |||||||
| chr4:2799526 | G | A | 2 | a0001c0005t0006g0025 a0001c0005t0033g0025 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+6388G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799526 | |||||||
| chr4:2799611 | G | A | 2 | a0001c0002t0001g0150 a0001c0004t0001g0062 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-5+6473G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799611 | |||||||
| chr4:2799633 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.-5+6495A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799633 | |||||||
| chr4:2799644 | G | A | 1 | a0001c0002t0002g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-5+6506G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799644 | |||||||
| chr4:2799646 | T | G | 123 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0095 others(120): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-5+6508T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799646 | |||||||
| chr4:2799981 | C | T | 1 | a0001c0004t0004g0015 | 3 | HG00733.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-5+6843C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799981 | |||||||
| chr4:2799990 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+6852C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2799990 | |||||||
| chr4:2800386 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.-5+7248A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800386 | |||||||
| chr4:2800404 | T | G | 1 | a0001c0002t0007g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-5+7266T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800404 | |||||||
| chr4:2800457 | G | A | 7 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(4): Show |
7 | HG01243.hp2 HG01975.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5+7319G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800457 | |||||||
| chr4:2800477 | G | T | 24 | a0001c0001t0001g0041 a0001c0001t0001g0255 a0001c0001t0001g0259 others(21): Show |
28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+7339G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800477 | |||||||
| chr4:2800526 | G | A | 1 | a0001c0002t0003g0143 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-5+7388G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800526 | |||||||
| chr4:2800549 | G | A | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+7411G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800549 | |||||||
| chr4:2800549 | G | GC | 136 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(133): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-5+7421dupC | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2800549 | ||||||
| chr4:2800549 | G | GCC | 28 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0017 others(25): Show |
31 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-5+7420_-5+7421dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2800549 | ||||||
| chr4:2800549 | GC | G | 87 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0002t0003g0005 others(84): Show |
100 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.-5+7421delC | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2800549 | ||||||
| chr4:2800550 | C | A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+7412C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800550 | |||||||
| chr4:2800551 | C | CG | 3 | a0001c0005t0006g0025 a0001c0005t0033g0025 a0001c0010t0005g0142 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+7413_-5+7414ins others(1): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800551 | |||||||
| chr4:2800606 | G | A | 3 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 |
3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5+7468G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800606 | |||||||
| chr4:2800682 | C | T | 28 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0002t0007g0069 others(25): Show |
34 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5+7544C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800682 | |||||||
| chr4:2800760 | A | G | 19 | a0001c0001t0001g0041 a0001c0001t0001g0259 a0001c0001t0001g0260 others(16): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5+7622A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800760 | |||||||
| chr4:2800885 | C | T | 1 | a0001c0001t0047g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-5+7747C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800885 | |||||||
| chr4:2800933 | T | C | 13 | a0001c0002t0017g0152 a0001c0003t0014g0035 a0001c0003t0014g0188 others(10): Show |
13 | HG01243.hp2 HG01975.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-5+7795T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800933 | |||||||
| chr4:2800981 | AGGCTGGC others(72): Show |
A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0214 others(30): Show |
42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-5+7847_-5+7925del others(79): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2800981 | ||||||
| chr4:2800991 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-5+7853C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2800991 | |||||||
| chr4:2801098 | T | C | 25 | a0001c0003t0006g0099 a0001c0003t0014g0035 a0001c0003t0014g0188 others(22): Show |
26 | HG01884.hp1 HG01975.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-5+7960T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801098 | |||||||
| chr4:2801100 | C | T | 1 | a0001c0001t0004g0044 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-5+7962C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801100 | |||||||
| chr4:2801111 | C | CGCGGAGG others(43): Show |
1 | a0001c0005t0077g0084 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-5+8010_-5+8011ins others(50): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2801111 | ||||||
| chr4:2801112 | G | T | 1 | a0001c0004t0005g0136 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-5+7974G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801112 | |||||||
| chr4:2801147 | G | C | 2 | a0001c0004t0005g0023 a0001c0007t0015g0049 |
3 | HG02647.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-5+8009G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801147 | |||||||
| chr4:2801149 | G | T | 4 | a0001c0001t0067g0199 a0001c0001t0073g0200 a0001c0004t0004g0015 others(1): Show |
7 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5+8011G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801149 | |||||||
| chr4:2801150 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(233): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-5+8012G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801150 | |||||||
| chr4:2801155 | G | A | 1 | a0001c0005t0002g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-5+8017G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801155 | |||||||
| chr4:2801184 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-5+8046C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801184 | |||||||
| chr4:2801185 | G | A | 1 | a0001c0001t0056g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5+8047G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801185 | |||||||
| chr4:2801192 | C | T | 1 | a0001c0004t0008g0265 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-5+8054C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801192 | |||||||
| chr4:2801216 | C | T | 1 | a0001c0001t0049g0245 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-5+8078C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801216 | |||||||
| chr4:2801278 | G | C | 1 | a0001c0004t0007g0156 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5+8140G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801278 | |||||||
| chr4:2801346 | C | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-5+8208C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801346 | |||||||
| chr4:2801353 | C | T | 1 | a0001c0003t0015g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-5+8215C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801353 | |||||||
| chr4:2801395 | T | C | 2 | a0001c0004t0020g0068 a0002c0008t0020g0020 |
3 | HG00741.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-5+8257T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801395 | |||||||
| chr4:2801429 | C | G | 35 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0002t0007g0069 others(32): Show |
41 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-5+8291C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801429 | |||||||
| chr4:2801572 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+8434C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801572 | |||||||
| chr4:2801621 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-5+8483T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801621 | |||||||
| chr4:2801653 | G | A | 1 | a0001c0005t0002g0093 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-5+8515G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801653 | |||||||
| chr4:2801698 | C | T | 4 | a0001c0003t0015g0103 a0001c0003t0019g0050 a0001c0003t0019g0051 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8560C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801698 | |||||||
| chr4:2801776 | G | A | 1 | a0001c0001t0022g0219 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-5+8638G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801776 | |||||||
| chr4:2801800 | A | G | 1 | a0001c0001t0050g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-5+8662A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801800 | |||||||
| chr4:2801852 | A | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-5+8714A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801852 | |||||||
| chr4:2801889 | G | C | 3 | a0001c0004t0096g0138 a0001c0005t0006g0085 a0001c0005t0077g0084 |
3 | HG02486.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-5+8751G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801889 | |||||||
| chr4:2801963 | C | G | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+8825C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2801963 | |||||||
| chr4:2802258 | G | A | 1 | a0001c0002t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+9120G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802258 | |||||||
| chr4:2802319 | A | G | 68 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(65): Show |
79 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-5+9181A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802319 | |||||||
| chr4:2802388 | T | C | 68 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(65): Show |
79 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-5+9250T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802388 | |||||||
| chr4:2802394 | A | C | 1 | a0001c0003t0080g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-5+9256A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802394 | |||||||
| chr4:2802402 | ATATG | A | 5 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(2): Show |
5 | HG01975.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+9266_-5+9269del others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802402 | ||||||
| chr4:2802402 | ATATGTG | A | 6 | a0001c0003t0013g0125 a0001c0003t0015g0048 a0001c0003t0015g0112 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+9266_-5+9271del others(6): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802402 | ||||||
| chr4:2802402 | ATATGTGT others(1): Show |
A | 13 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(10): Show |
17 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-5+9266_-5+9273del others(8): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802402 | ||||||
| chr4:2802402 | ATATGTGT others(7): Show |
A | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-5+9266_-5+9279del others(14): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802402 | ||||||
| chr4:2802402 | ATATGTGT others(17): Show |
A | 1 | a0001c0009t0021g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-5+9266_-5+9289del others(24): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802402 | ||||||
| chr4:2802404 | A | ATG | 13 | a0001c0001t0001g0230 a0001c0001t0022g0216 a0001c0001t0026g0221 others(10): Show |
14 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-5+9304_-5+9305dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTG | 13 | a0001c0001t0004g0044 a0001c0004t0004g0036 a0001c0004t0005g0008 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5+9302_-5+9305dup others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTG | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0039 others(27): Show |
33 | HG00673.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-5+9300_-5+9305dup others(6): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTGT others(1): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0218 others(36): Show |
42 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-5+9298_-5+9305dup others(8): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTGT others(3): Show |
40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(37): Show |
47 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-5+9296_-5+9305dup others(10): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTGT others(5): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0225 others(5): Show |
11 | HG01099.hp1 HG02015.hp2 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+9294_-5+9305dup others(12): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0237 a0001c0001t0041g0213 |
2 | HG01256.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-5+9292_-5+9305dup others(14): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0006 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-5+9290_-5+9305dup others(16): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | A | ATGTGTGT others(11): Show |
1 | a0001c0001t0054g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-5+9288_-5+9305dup others(18): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | ATG | A | 27 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0050g0242 others(24): Show |
33 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.-5+9304_-5+9305del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | ATGTG | A | 32 | a0001c0001t0001g0121 a0001c0002t0003g0001 a0001c0002t0003g0177 others(29): Show |
37 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-5+9302_-5+9305del others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | ATGTGTG | A | 3 | a0001c0003t0016g0053 a0001c0007t0015g0049 a0001c0007t0031g0111 |
3 | HG02258.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-5+9300_-5+9305del others(6): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | ATGTGTGT others(3): Show |
A | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-5+9296_-5+9305del others(10): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802404 | ATGTGTGT others(11): Show |
A | 2 | a0001c0007t0027g0054 a0001c0007t0027g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-5+9288_-5+9305del others(18): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802404 | ||||||
| chr4:2802444 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-5+9306A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802444 | |||||||
| chr4:2802460 | G | A | 3 | a0001c0003t0014g0035 a0001c0003t0014g0190 a0001c0003t0037g0035 |
3 | HG02257.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-5+9322G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802460 | |||||||
| chr4:2802478 | A | C | 68 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(65): Show |
79 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-5+9340A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802478 | |||||||
| chr4:2802518 | GTA | G | 24 | a0001c0001t0001g0121 a0001c0001t0012g0109 a0001c0003t0001g0011 others(21): Show |
29 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-5+9390_-5+9391del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802518 | ||||||
| chr4:2802528 | A | G | 4 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 others(1): Show |
4 | HG02145.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+9390A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802528 | |||||||
| chr4:2802530 | G | A | 9 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+9392G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802530 | |||||||
| chr4:2802532 | A | ATG | 24 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0131 others(21): Show |
28 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+9406_-5+9407dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802532 | ||||||
| chr4:2802532 | A | G | 4 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 others(1): Show |
4 | HG02145.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+9394A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802532 | |||||||
| chr4:2802532 | ATG | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-5+9406_-5+9407del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802532 | ||||||
| chr4:2802544 | G | A | 31 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(28): Show |
36 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-5+9406G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802544 | |||||||
| chr4:2802544 | G | GTA | 35 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0002t0007g0069 others(32): Show |
41 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-5+9414_-5+9415dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802544 | ||||||
| chr4:2802548 | ATATATGT others(67): Show |
A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+9412_-5+9485del others(74): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802548 | ||||||
| chr4:2802562 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0004g0264 a0001c0003t0015g0103 |
3 | HG03225.hp2 NA18984.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-5+9424A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802562 | |||||||
| chr4:2802580 | G | GTA | 62 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(59): Show |
73 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.-5+9450_-5+9451dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802580 | ||||||
| chr4:2802586 | ATATGTTT others(1): Show |
A | 5 | a0001c0003t0002g0122 a0001c0007t0015g0049 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+9452_-5+9459del others(8): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802586 | ||||||
| chr4:2802592 | TTGTATAT others(3): Show |
T | 11 | a0001c0001t0009g0108 a0001c0002t0003g0143 a0001c0002t0007g0151 others(8): Show |
12 | HG01081.hp2 HG02071.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+9480_-5+9489del others(10): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802592 | ||||||
| chr4:2802600 | A | G | 5 | a0001c0003t0002g0122 a0001c0007t0015g0049 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+9462A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802600 | |||||||
| chr4:2802601 | T | C | 6 | a0001c0001t0010g0037 a0001c0001t0010g0201 a0001c0001t0010g0220 others(3): Show |
9 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+9463T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802601 | |||||||
| chr4:2802602 | G | T | 5 | a0001c0003t0002g0122 a0001c0007t0015g0049 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+9464G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802602 | |||||||
| chr4:2802616 | A | ATATACGT others(46): Show |
1 | a0001c0003t0013g0135 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-5+9482_-5+9483ins others(53): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802616 | ||||||
| chr4:2802616 | A | ATGTATGT others(36): Show |
1 | a0001c0012t0008g0133 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-5+9479_-5+9480ins others(43): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802616 | ||||||
| chr4:2802618 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-5+9480A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802618 | |||||||
| chr4:2802622 | G | A | 2 | a0001c0003t0013g0135 a0001c0012t0008g0133 |
2 | HG01069.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-5+9484G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802622 | |||||||
| chr4:2802622 | G | GTGTATGT others(46): Show |
17 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(14): Show |
21 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-5+9532_-5+9533ins others(53): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802622 | ||||||
| chr4:2802622 | GTGTA | G | 27 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(24): Show |
32 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.-5+9492_-5+9495del others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802622 | ||||||
| chr4:2802634 | G | GGTGTGTG others(25): Show |
1 | a0001c0002t0002g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-5+9521_-5+9552dup others(32): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802634 | ||||||
| chr4:2802657 | A | ATG | 7 | a0001c0001t0001g0281 a0001c0001t0048g0240 a0001c0002t0071g0282 others(4): Show |
7 | HG01255.hp1 HG02145.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+9535_-5+9536dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802657 | ||||||
| chr4:2802657 | ATG | A | 5 | a0001c0003t0006g0002 a0001c0003t0006g0115 a0001c0003t0006g0116 others(2): Show |
9 | HG02717.hp1 HG02922.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+9535_-5+9536del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802657 | ||||||
| chr4:2802659 | G | GTGTGTGT others(42): Show |
5 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0190 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+9530_-5+9531ins others(49): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802659 | ||||||
| chr4:2802659 | G | GTGTGTGT others(44): Show |
1 | a0001c0003t0014g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-5+9532_-5+9533ins others(51): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2802659 | ||||||
| chr4:2802673 | G | A | 1 | a0001c0001t0050g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-5+9535G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802673 | |||||||
| chr4:2802675 | A | G | 3 | a0001c0002t0002g0146 a0001c0002t0002g0147 a0001c0002t0002g0184 |
3 | NA18944.hp1 NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-5+9537A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802675 | |||||||
| chr4:2802749 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-5+9611A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802749 | |||||||
| chr4:2802822 | G | A | 1 | a0001c0001t0029g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-5+9684G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802822 | |||||||
| chr4:2802824 | T | C | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-5+9686T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2802824 | |||||||
| chr4:2803045 | G | T | 95 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(92): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+9907G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803045 | |||||||
| chr4:2803074 | G | A | 25 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(22): Show |
29 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-5+9936G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803074 | |||||||
| chr4:2803127 | C | T | 95 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(92): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+9989C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803127 | |||||||
| chr4:2803136 | G | A | 70 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(67): Show |
81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-5+9998G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803136 | |||||||
| chr4:2803141 | C | T | 26 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(23): Show |
31 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+10003C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803141 | |||||||
| chr4:2803235 | G | C | 70 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(67): Show |
81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-5+10097G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803235 | |||||||
| chr4:2803241 | G | A | 1 | a0001c0003t0081g0127 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-5+10103G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803241 | |||||||
| chr4:2803258 | G | A | 95 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(92): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+10120G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803258 | |||||||
| chr4:2803259 | T | C | 95 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(92): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+10121T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803259 | |||||||
| chr4:2803301 | C | T | 1 | a0001c0004t0004g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+10163C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803301 | |||||||
| chr4:2803354 | G | T | 1 | a0001c0001t0049g0245 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-5+10216G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803354 | |||||||
| chr4:2803380 | C | T | 1 | a0001c0004t0005g0023 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-5+10242C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803380 | |||||||
| chr4:2803403 | C | G | 21 | a0001c0001t0001g0095 a0001c0003t0006g0099 a0001c0003t0037g0092 others(18): Show |
21 | HG01167.hp2 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.-5+10265C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803403 | |||||||
| chr4:2803488 | A | G | 1 | a0001c0003t0016g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+10350A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803488 | |||||||
| chr4:2803542 | G | C | 1 | a0001c0003t0016g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+10404G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803542 | |||||||
| chr4:2803652 | C | T | 67 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(64): Show |
78 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-5+10514C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803652 | |||||||
| chr4:2803728 | C | T | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+10590C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803728 | |||||||
| chr4:2803766 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-5+10628A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803766 | |||||||
| chr4:2803794 | T | A | 1 | a0001c0001t0049g0245 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-5+10656T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803794 | |||||||
| chr4:2803813 | C | T | 21 | a0001c0001t0001g0077 a0001c0002t0003g0005 a0001c0002t0028g0129 others(18): Show |
28 | HG00408.hp2 HG01069.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+10675C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803813 | |||||||
| chr4:2803932 | G | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+10794G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803932 | |||||||
| chr4:2803950 | T | C | 3 | a0001c0005t0006g0025 a0001c0005t0006g0094 a0001c0005t0033g0025 |
3 | HG02896.hp2 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5+10812T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2803950 | |||||||
| chr4:2804010 | C | T | 27 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0002g0087 others(24): Show |
31 | HG00323.hp1 HG01069.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+10872C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804010 | |||||||
| chr4:2804113 | T | A | 26 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(23): Show |
31 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+10975T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804113 | |||||||
| chr4:2804198 | C | T | 1 | a0001c0005t0002g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-5+11060C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804198 | |||||||
| chr4:2804245 | G | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0259 a0001c0001t0001g0260 others(6): Show |
9 | NA18944.hp2 NA18947.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+11107G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804245 | |||||||
| chr4:2804339 | C | T | 21 | a0001c0001t0001g0095 a0001c0003t0006g0099 a0001c0003t0037g0092 others(18): Show |
21 | HG01167.hp2 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.-5+11201C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804339 | |||||||
| chr4:2804459 | A | G | 1 | a0001c0003t0014g0191 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5+11321A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804459 | |||||||
| chr4:2804537 | C | G | 26 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(23): Show |
31 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+11399C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804537 | |||||||
| chr4:2804621 | C | T | 69 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(66): Show |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-5+11483C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804621 | |||||||
| chr4:2804733 | C | T | 1 | a0001c0001t0004g0264 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5+11595C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804733 | |||||||
| chr4:2804843 | G | C | 1 | a0001c0005t0042g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-5+11705G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804843 | |||||||
| chr4:2804882 | C | T | 1 | a0001c0005t0079g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-5+11744C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804882 | |||||||
| chr4:2804887 | C | G | 1 | a0001c0002t0032g0182 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-5+11749C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2804887 | |||||||
| chr4:2805000 | T | C | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-5+11862T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805000 | |||||||
| chr4:2805065 | C | T | 1 | a0001c0015t0005g0256 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5+11927C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805065 | |||||||
| chr4:2805140 | C | G | 94 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0121 others(91): Show |
109 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+12002C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805140 | |||||||
| chr4:2805182 | A | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-5+12044A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805182 | |||||||
| chr4:2805315 | C | T | 3 | a0001c0004t0004g0064 a0001c0004t0004g0065 a0001c0004t0038g0202 |
3 | HG02896.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5+12177C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805315 | |||||||
| chr4:2805364 | C | T | 25 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(22): Show |
29 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-5+12226C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805364 | |||||||
| chr4:2805437 | G | T | 1 | a0001c0002t0032g0182 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-5+12299G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805437 | |||||||
| chr4:2805842 | G | A | 26 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(23): Show |
31 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+12704G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805842 | |||||||
| chr4:2805932 | G | A | 3 | a0001c0001t0001g0259 a0001c0001t0066g0257 a0004c0013t0053g0258 |
3 | NA18944.hp2 NA19063.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-5+12794G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805932 | |||||||
| chr4:2805979 | G | T | 1 | a0001c0003t0008g0132 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-5+12841G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2805979 | |||||||
| chr4:2806002 | C | T | 3 | a0001c0001t0001g0077 a0001c0005t0002g0007 a0001c0005t0002g0059 |
6 | HG00408.hp2 NA18959.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+12864C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806002 | |||||||
| chr4:2806183 | A | C | 11 | a0001c0001t0001g0079 a0001c0002t0007g0069 a0001c0004t0001g0073 others(8): Show |
14 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5+13045A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806183 | |||||||
| chr4:2806193 | C | T | 1 | a0001c0003t0080g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-5+13055C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806193 | |||||||
| chr4:2806234 | C | T | 1 | a0001c0003t0014g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-5+13096C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806234 | |||||||
| chr4:2806262 | G | A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-5+13124G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806262 | |||||||
| chr4:2806309 | C | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0259 a0001c0001t0001g0260 others(6): Show |
9 | NA18944.hp2 NA18947.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+13171C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806309 | |||||||
| chr4:2806356 | T | A | 1 | a0001c0003t0002g0114 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-5+13218T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806356 | |||||||
| chr4:2806485 | C | T | 1 | a0001c0003t0014g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-5+13347C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806485 | |||||||
| chr4:2806575 | C | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0272 a0001c0001t0030g0045 others(1): Show |
4 | HG00609.hp2 HG02083.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+13437C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806575 | |||||||
| chr4:2806588 | TTCACTGT others(13): Show |
T | 1 | a0001c0007t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-5+13455_-5+13474d others(22): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2806588 | ||||||
| chr4:2806593 | T | C | 5 | a0001c0004t0083g0060 a0001c0005t0079g0063 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+13455T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806593 | |||||||
| chr4:2806722 | G | A | 18 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(15): Show |
22 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-5+13584G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806722 | |||||||
| chr4:2806752 | C | T | 22 | a0001c0003t0006g0099 a0001c0003t0037g0092 a0001c0005t0002g0089 others(19): Show |
22 | HG01167.hp2 HG01515.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5+13614C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806752 | |||||||
| chr4:2806833 | G | A | 4 | a0001c0002t0001g0150 a0001c0002t0001g0164 a0001c0002t0002g0163 others(1): Show |
4 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+13695G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806833 | |||||||
| chr4:2806901 | C | G | 1 | a0001c0005t0042g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4-13713C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2806901 | |||||||
| chr4:2807070 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-13544C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807070 | |||||||
| chr4:2807085 | G | A | 1 | a0001c0001t0026g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-4-13529G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807085 | |||||||
| chr4:2807154 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-13460C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807154 | |||||||
| chr4:2807172 | G | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-4-13442G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807172 | |||||||
| chr4:2807228 | G | A | 1 | a0001c0003t0012g0024 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-4-13386G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807228 | |||||||
| chr4:2807393 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-4-13221C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807393 | |||||||
| chr4:2807644 | T | C | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4-12970T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807644 | |||||||
| chr4:2807712 | G | A | 1 | a0001c0001t0047g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-4-12902G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807712 | |||||||
| chr4:2807758 | C | G | 1 | a0001c0002t0002g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12856C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807758 | |||||||
| chr4:2807772 | C | A | 1 | a0001c0001t0002g0270 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-4-12842C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807772 | |||||||
| chr4:2807773 | G | C | 1 | a0001c0001t0012g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-4-12841G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807773 | |||||||
| chr4:2807881 | A | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-4-12733A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807881 | |||||||
| chr4:2807885 | G | A | 1 | a0001c0001t0009g0222 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-4-12729G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807885 | |||||||
| chr4:2807900 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-12714C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2807900 | |||||||
| chr4:2808111 | A | ACT | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-4-12499_-4-12498d others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2808111 | ||||||
| chr4:2808413 | G | A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-12201G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808413 | |||||||
| chr4:2808426 | G | T | 26 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(23): Show |
31 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-4-12188G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808426 | |||||||
| chr4:2808742 | GGTGCCCG others(287): Show |
G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(148): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-4-11816_-4-11523d others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2808742 | ||||||
| chr4:2808762 | C | A | 1 | a0001c0003t0008g0132 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-4-11852C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808762 | |||||||
| chr4:2808798 | ACCTTCCC others(287): Show |
A | 1 | a0001c0001t0001g0241 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-4-11767_-4-11474d others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2808798 | ||||||
| chr4:2808847 | A | G | 35 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(32): Show |
40 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-4-11767A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808847 | |||||||
| chr4:2808896 | A | G | 45 | a0001c0001t0001g0077 a0001c0002t0002g0027 a0001c0002t0002g0145 others(42): Show |
51 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-11718A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808896 | |||||||
| chr4:2808945 | A | G | 155 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0002t0001g0030 others(152): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.-4-11669A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808945 | |||||||
| chr4:2808994 | G | A | 2 | a0001c0002t0001g0158 a0001c0002t0004g0031 |
2 | HG00642.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-4-11620G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2808994 | |||||||
| chr4:2809029 | A | AGGGCTCA others(42): Show |
2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-11538_-4-11537i others(51): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809029 | ||||||
| chr4:2809077 | T | C | 91 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0002t0003g0005 others(88): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-4-11537T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809077 | |||||||
| chr4:2809078 | A | AGGGCTCA others(42): Show |
1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4-11489_-4-11488i others(51): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809078 | ||||||
| chr4:2809078 | A | C | 92 | a0001c0001t0001g0077 a0001c0001t0001g0121 a0001c0002t0003g0005 others(89): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-4-11536A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809078 | |||||||
| chr4:2809097 | C | T | 1 | a0001c0004t0078g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-4-11517C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809097 | |||||||
| chr4:2809126 | T | C | 6 | a0001c0002t0002g0027 a0001c0002t0002g0145 a0001c0002t0024g0027 others(3): Show |
7 | HG00621.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-11488T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809126 | |||||||
| chr4:2809127 | A | AGGGCTCA others(42): Show |
59 | a0001c0002t0001g0030 a0001c0002t0001g0144 a0001c0002t0001g0150 others(56): Show |
81 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-4-11440_-4-11439i others(51): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809127 | ||||||
| chr4:2809127 | A | C | 6 | a0001c0002t0002g0027 a0001c0002t0002g0145 a0001c0002t0024g0027 others(3): Show |
7 | HG00621.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-11487A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809127 | |||||||
| chr4:2809175 | T | C | 67 | a0001c0001t0001g0077 a0001c0002t0003g0005 a0001c0002t0028g0129 others(64): Show |
77 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.-4-11439T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809175 | |||||||
| chr4:2809176 | A | AGGGCTCA others(140): Show |
1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-11425_-4-11424i others(149): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809176 | ||||||
| chr4:2809176 | A | AGGGCTCA others(287): Show |
24 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(21): Show |
29 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-4-11425_-4-11424i others(296): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809176 | ||||||
| chr4:2809176 | A | AGGGCTCA others(287): Show |
1 | a0001c0003t0069g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-4-11425_-4-11424i others(296): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809176 | ||||||
| chr4:2809176 | A | AGGGCTCA others(287): Show |
1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-11425_-4-11424i others(296): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2809176 | ||||||
| chr4:2809176 | A | C | 67 | a0001c0001t0001g0077 a0001c0002t0003g0005 a0001c0002t0028g0129 others(64): Show |
77 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.-4-11438A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809176 | |||||||
| chr4:2809190 | A | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(243): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-4-11424A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809190 | |||||||
| chr4:2809328 | T | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0259 a0001c0001t0001g0260 others(6): Show |
9 | NA18944.hp2 NA18947.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-11286T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809328 | |||||||
| chr4:2809335 | C | T | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-11279C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809335 | |||||||
| chr4:2809436 | C | G | 2 | a0001c0003t0002g0087 a0001c0003t0092g0086 |
2 | HG00323.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-4-11178C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809436 | |||||||
| chr4:2809499 | A | G | 7 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(4): Show |
7 | HG01975.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-11115A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809499 | |||||||
| chr4:2809537 | G | T | 1 | a0001c0001t0001g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-4-11077G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809537 | |||||||
| chr4:2809576 | C | T | 1 | a0001c0003t0006g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4-11038C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809576 | |||||||
| chr4:2809639 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-10975C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809639 | |||||||
| chr4:2809710 | T | C | 1 | a0001c0001t0026g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-4-10904T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809710 | |||||||
| chr4:2809806 | G | A | 1 | a0001c0002t0003g0243 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-4-10808G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809806 | |||||||
| chr4:2809974 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-10640C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2809974 | |||||||
| chr4:2810027 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-10587C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810027 | |||||||
| chr4:2810114 | C | T | 29 | a0001c0001t0001g0121 a0001c0001t0001g0238 a0001c0003t0001g0011 others(26): Show |
34 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4-10500C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810114 | |||||||
| chr4:2810321 | C | T | 3 | a0001c0002t0001g0144 a0001c0002t0001g0179 a0001c0002t0001g0180 |
3 | NA18957.hp1 NA18975.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-4-10293C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810321 | |||||||
| chr4:2810452 | C | T | 1 | a0001c0005t0079g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-4-10162C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810452 | |||||||
| chr4:2810489 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-10125C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810489 | |||||||
| chr4:2810538 | G | A | 1 | a0001c0003t0021g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-4-10076G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810538 | |||||||
| chr4:2810618 | C | T | 1 | a0001c0003t0034g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-4-9996C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810618 | |||||||
| chr4:2810743 | A | C | 26 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(23): Show |
30 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-4-9871A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2810743 | |||||||
| chr4:2810957 | GCTGAAGG others(6): Show |
G | 2 | a0001c0002t0003g0012 a0001c0002t0003g0155 |
4 | NA18945.hp1 NA18983.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-9653_-4-9641del others(13): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2810957 | ||||||
| chr4:2811019 | C | A | 26 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0126 others(23): Show |
30 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-4-9595C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811019 | |||||||
| chr4:2811023 | G | C | 1 | a0001c0007t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-9591G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811023 | |||||||
| chr4:2811024 | G | A | 1 | a0001c0004t0086g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4-9590G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811024 | |||||||
| chr4:2811043 | G | A | 34 | a0001c0001t0001g0077 a0001c0003t0016g0053 a0001c0003t0021g0082 others(31): Show |
40 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-4-9571G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811043 | |||||||
| chr4:2811118 | C | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(147): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-4-9496C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811118 | |||||||
| chr4:2811160 | T | A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-9454T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811160 | |||||||
| chr4:2811180 | G | A | 1 | a0001c0001t0009g0262 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-4-9434G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811180 | |||||||
| chr4:2811290 | C | T | 4 | a0001c0001t0001g0237 a0001c0002t0001g0144 a0001c0002t0001g0179 others(1): Show |
4 | HG04199.hp1 NA18957.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-9324C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811290 | |||||||
| chr4:2811302 | C | A | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-9312C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811302 | |||||||
| chr4:2811322 | A | G | 1 | a0001c0005t0062g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4-9292A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811322 | |||||||
| chr4:2811530 | T | C | 1 | a0001c0001t0010g0223 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-4-9084T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811530 | |||||||
| chr4:2811570 | G | A | 22 | a0001c0001t0001g0121 a0001c0003t0001g0011 a0001c0003t0001g0019 others(19): Show |
27 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-4-9044G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811570 | |||||||
| chr4:2811661 | T | C | 2 | a0001c0001t0004g0044 a0001c0001t0085g0266 |
3 | HG01099.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-4-8953T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811661 | |||||||
| chr4:2811703 | G | A | 1 | a0001c0005t0042g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4-8911G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811703 | |||||||
| chr4:2811776 | C | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(207): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-4-8838C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811776 | |||||||
| chr4:2811780 | G | T | 1 | a0001c0002t0002g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-8834G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811780 | |||||||
| chr4:2811953 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-4-8661G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2811953 | |||||||
| chr4:2812141 | G | A | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-8473G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812141 | |||||||
| chr4:2812263 | G | A | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-8351G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812263 | |||||||
| chr4:2812340 | G | A | 1 | a0001c0002t0003g0166 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-4-8274G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812340 | |||||||
| chr4:2812421 | A | G | 41 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0040 others(38): Show |
50 | HG01069.hp1 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-4-8193A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812421 | |||||||
| chr4:2812528 | C | G | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-8086C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812528 | |||||||
| chr4:2812577 | C | T | 1 | a0001c0004t0038g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-4-8037C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812577 | |||||||
| chr4:2812654 | G | A | 2 | a0001c0004t0020g0068 a0002c0008t0020g0020 |
3 | HG00741.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-4-7960G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812654 | |||||||
| chr4:2812673 | C | G | 4 | a0001c0003t0015g0103 a0001c0003t0019g0050 a0001c0003t0019g0051 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-7941C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812673 | |||||||
| chr4:2812702 | G | A | 1 | a0001c0005t0062g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4-7912G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812702 | |||||||
| chr4:2812731 | A | AC | 80 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0041 others(77): Show |
107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-4-7876dupC | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2812731 | ||||||
| chr4:2812731 | A | C | 4 | a0001c0002t0002g0183 a0001c0002t0003g0177 a0001c0002t0003g0178 others(1): Show |
4 | HG01192.hp1 HG02027.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-7883A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812731 | |||||||
| chr4:2812737 | C | G | 19 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0040 others(16): Show |
24 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.-4-7877C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812737 | |||||||
| chr4:2812795 | C | T | 1 | a0001c0003t0002g0047 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-4-7819C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812795 | |||||||
| chr4:2812855 | C | CAT | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(243): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-4-7759_-4-7758ins others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812855 | |||||||
| chr4:2812887 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(237): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.-4-7727G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812887 | |||||||
| chr4:2812936 | G | T | 1 | a0001c0003t0008g0131 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-4-7678G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812936 | |||||||
| chr4:2812971 | G | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-4-7643G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2812971 | |||||||
| chr4:2813036 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-4-7578C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813036 | |||||||
| chr4:2813083 | G | A | 1 | a0001c0001t0054g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-4-7531G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813083 | |||||||
| chr4:2813089 | A | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(241): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.-4-7525A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813089 | |||||||
| chr4:2813256 | C | T | 1 | a0001c0004t0083g0060 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4-7358C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813256 | |||||||
| chr4:2813257 | G | A | 1 | a0001c0002t0004g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-4-7357G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813257 | |||||||
| chr4:2813529 | T | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(243): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-4-7085T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813529 | |||||||
| chr4:2813530 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-4-7084C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813530 | |||||||
| chr4:2813637 | G | A | 2 | a0001c0005t0002g0093 a0001c0005t0002g0096 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-4-6977G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813637 | |||||||
| chr4:2813725 | A | G | 29 | a0001c0003t0016g0053 a0001c0003t0021g0082 a0001c0004t0001g0062 others(26): Show |
35 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-4-6889A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813725 | |||||||
| chr4:2813737 | A | G | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4-6877A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813737 | |||||||
| chr4:2813745 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-4-6869G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813745 | |||||||
| chr4:2813782 | T | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-6832T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813782 | |||||||
| chr4:2813905 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(240): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.-4-6709G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2813905 | |||||||
| chr4:2813954 | TC | T | 2 | a0001c0005t0002g0007 a0001c0005t0002g0059 |
5 | NA18959.hp2 NA18964.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-6656delC | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2813954 | ||||||
| chr4:2814079 | C | T | 59 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(56): Show |
70 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-4-6535C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814079 | |||||||
| chr4:2814143 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-4-6471C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814143 | |||||||
| chr4:2814224 | T | G | 3 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 |
3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4-6390T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814224 | |||||||
| chr4:2814253 | C | T | 1 | a0001c0002t0002g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-4-6361C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814253 | |||||||
| chr4:2814261 | G | A | 29 | a0001c0003t0016g0053 a0001c0003t0021g0082 a0001c0004t0001g0062 others(26): Show |
35 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-4-6353G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814261 | |||||||
| chr4:2814285 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-4-6329G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814285 | |||||||
| chr4:2814336 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0218 |
2 | HG01952.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-4-6278C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814336 | |||||||
| chr4:2814498 | G | GCA | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-6100_-4-6099dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2814498 | ||||||
| chr4:2814498 | GCA | G | 43 | a0001c0003t0006g0099 a0001c0004t0002g0028 a0001c0004t0002g0154 others(40): Show |
51 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-4-6100_-4-6099del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2814498 | ||||||
| chr4:2814515 | C | T | 2 | a0001c0001t0025g0208 a0001c0001t0025g0250 |
2 | NA18961.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-4-6099C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814515 | |||||||
| chr4:2814523 | C | T | 1 | a0001c0004t0038g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-4-6091C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814523 | |||||||
| chr4:2814573 | A | G | 41 | a0001c0003t0006g0099 a0001c0004t0002g0028 a0001c0004t0002g0154 others(38): Show |
49 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-4-6041A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814573 | |||||||
| chr4:2814588 | C | A | 1 | a0001c0005t0058g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-4-6026C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814588 | |||||||
| chr4:2814632 | G | A | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(242): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-4-5982G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814632 | |||||||
| chr4:2814802 | C | A | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-5812C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2814802 | |||||||
| chr4:2815455 | G | T | 7 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(4): Show |
7 | HG01975.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-5159G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2815455 | |||||||
| chr4:2815626 | C | G | 1 | a0001c0005t0002g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-4-4988C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2815626 | |||||||
| chr4:2815801 | C | A | 1 | a0001c0002t0007g0069 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-4-4813C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2815801 | |||||||
| chr4:2816069 | T | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0268 a0001c0001t0004g0267 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-4545T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816069 | |||||||
| chr4:2816133 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0009g0017 |
3 | NA18951.hp2 NA18969.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-4-4481C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816133 | |||||||
| chr4:2816252 | G | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-4362G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816252 | |||||||
| chr4:2816320 | C | T | 1 | a0001c0001t0093g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-4-4294C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816320 | |||||||
| chr4:2816424 | T | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-4190T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816424 | |||||||
| chr4:2816558 | C | G | 2 | a0001c0003t0002g0087 a0001c0003t0092g0086 |
2 | HG00323.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-4-4056C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816558 | |||||||
| chr4:2816575 | G | T | 1 | a0001c0003t0002g0252 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-4-4039G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816575 | |||||||
| chr4:2816593 | T | C | 1 | a0001c0004t0038g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-4-4021T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816593 | |||||||
| chr4:2816638 | C | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-4-3976C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816638 | |||||||
| chr4:2816638 | C | T | 1 | a0001c0011t0003g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-4-3976C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816638 | |||||||
| chr4:2816684 | C | T | 1 | a0001c0002t0007g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-4-3930C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816684 | |||||||
| chr4:2816757 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-4-3857A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816757 | |||||||
| chr4:2816801 | A | C | 1 | a0001c0002t0002g0147 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-4-3813A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816801 | |||||||
| chr4:2816854 | G | GTTTA | 41 | a0001c0003t0006g0099 a0001c0004t0002g0028 a0001c0004t0002g0154 others(38): Show |
49 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-4-3758_-4-3755dup others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2816854 | ||||||
| chr4:2816922 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0079 others(25): Show |
34 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4-3692A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2816922 | |||||||
| chr4:2817301 | T | C | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-3313T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817301 | |||||||
| chr4:2817336 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
135 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-4-3278G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817336 | |||||||
| chr4:2817688 | G | A | 1 | a0001c0002t0002g0029 | 2 | HG01099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-4-2926G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817688 | |||||||
| chr4:2817721 | A | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-2893A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817721 | |||||||
| chr4:2817730 | T | G | 76 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(73): Show |
89 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.-4-2884T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817730 | |||||||
| chr4:2817806 | G | A | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4-2808G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817806 | |||||||
| chr4:2817990 | G | A | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-2624G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2817990 | |||||||
| chr4:2818029 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-2585C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818029 | |||||||
| chr4:2818151 | G | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-2463G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818151 | |||||||
| chr4:2818219 | C | T | 5 | a0001c0003t0015g0048 a0001c0003t0015g0112 a0001c0003t0021g0058 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-2395C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818219 | |||||||
| chr4:2818426 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-2188C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818426 | |||||||
| chr4:2818442 | C | G | 23 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(20): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4-2172C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818442 | |||||||
| chr4:2818534 | G | A | 23 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(20): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4-2080G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818534 | |||||||
| chr4:2818641 | A | C | 5 | a0001c0003t0021g0082 a0001c0004t0004g0078 a0001c0004t0015g0081 others(2): Show |
5 | HG01255.hp1 HG02145.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-1973A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818641 | |||||||
| chr4:2818648 | C | A | 1 | a0001c0003t0016g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-4-1966C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818648 | |||||||
| chr4:2818648 | C | G | 23 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(20): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4-1966C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818648 | |||||||
| chr4:2818660 | T | C | 76 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(73): Show |
89 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.-4-1954T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818660 | |||||||
| chr4:2818677 | T | A | 76 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(73): Show |
89 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.-4-1937T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818677 | |||||||
| chr4:2818716 | C | G | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-1898C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818716 | |||||||
| chr4:2818726 | T | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-1888T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818726 | |||||||
| chr4:2818833 | G | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-1781G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818833 | |||||||
| chr4:2818834 | A | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-1780A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818834 | |||||||
| chr4:2818925 | T | C | 1 | a0004c0013t0053g0258 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-4-1689T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818925 | |||||||
| chr4:2818976 | C | T | 20 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0040 others(17): Show |
25 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4-1638C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2818976 | |||||||
| chr4:2819164 | C | T | 5 | a0001c0003t0015g0048 a0001c0003t0015g0112 a0001c0003t0021g0058 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-1450C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819164 | |||||||
| chr4:2819201 | C | T | 25 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(22): Show |
30 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-4-1413C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819201 | |||||||
| chr4:2819304 | C | T | 1 | a0001c0005t0062g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4-1310C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819304 | |||||||
| chr4:2819373 | A | C | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1241A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819373 | |||||||
| chr4:2819389 | TA | T | 32 | a0001c0003t0016g0053 a0001c0003t0021g0082 a0001c0004t0001g0062 others(29): Show |
38 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-4-1216delA | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2819389 | ||||||
| chr4:2819399 | T | A | 42 | a0001c0003t0006g0099 a0001c0003t0014g0189 a0001c0004t0002g0028 others(39): Show |
50 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.-4-1215T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819399 | |||||||
| chr4:2819596 | T | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.-4-1018T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819596 | |||||||
| chr4:2819654 | G | T | 1 | a0001c0003t0008g0131 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-4-960G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819654 | |||||||
| chr4:2819657 | C | A | 1 | a0001c0001t0003g0042 | 2 | HG02015.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-4-957C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819657 | |||||||
| chr4:2819729 | GA | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-4-884delA | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819729 | |||||||
| chr4:2819752 | G | A | 1 | a0001c0004t0005g0023 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-4-862G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819752 | |||||||
| chr4:2819772 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0009g0017 |
3 | NA18951.hp2 NA18969.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-4-842A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819772 | |||||||
| chr4:2819773 | T | A | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-841T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819773 | |||||||
| chr4:2819906 | C | G | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-708C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819906 | |||||||
| chr4:2819920 | A | G | 13 | a0001c0002t0001g0158 a0001c0004t0002g0028 a0001c0004t0002g0154 others(10): Show |
14 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.-4-694A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819920 | |||||||
| chr4:2819926 | TCACTGGT others(4): Show |
T | 1 | a0001c0011t0003g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-4-682_-4-672delGT others(9): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 2819926 | ||||||
| chr4:2819935 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0009g0108 |
2 | NA18948.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-4-679C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819935 | |||||||
| chr4:2819956 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0009g0108 |
2 | NA18948.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-4-658C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819956 | |||||||
| chr4:2819986 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4-628T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819986 | |||||||
| chr4:2819988 | C | G | 31 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(28): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-4-626C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819988 | |||||||
| chr4:2819999 | G | A | 20 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0003t0008g0040 others(17): Show |
25 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4-615G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2819999 | |||||||
| chr4:2820108 | A | C | 6 | a0001c0003t0016g0053 a0001c0007t0015g0049 a0001c0007t0027g0054 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-506A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820108 | |||||||
| chr4:2820117 | A | C | 1 | a0001c0003t0002g0114 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-4-497A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820117 | |||||||
| chr4:2820117 | A | G | 1 | a0001c0001t0024g0211 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-4-497A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820117 | |||||||
| chr4:2820148 | T | C | 1 | a0001c0003t0008g0234 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-4-466T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820148 | |||||||
| chr4:2820435 | G | A | 40 | a0001c0004t0002g0028 a0001c0004t0002g0154 a0001c0004t0005g0008 others(37): Show |
48 | HG00639.hp2 HG01081.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-4-179G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820435 | |||||||
| chr4:2820474 | A | T | 1 | a0001c0001t0001g0261 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-4-140A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820474 | |||||||
| chr4:2820497 | C | T | 1 | a0001c0001t0068g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-4-117C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820497 | |||||||
| chr4:2820562 | C | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
184 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.-4-52C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820562 | |||||||
| chr4:2820580 | T | C | 23 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(20): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-4-34T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 1/12 | chr4 | 2820580 | |||||||
| chr4:2820921 | C | T | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+168C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2820921 | |||||||
| chr4:2820948 | C | T | 23 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(20): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.136+195C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2820948 | |||||||
| chr4:2821360 | G | T | 1 | a0001c0004t0005g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136+607G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821360 | |||||||
| chr4:2821521 | G | A | 2 | a0001c0001t0001g0259 a0004c0013t0053g0258 |
2 | NA19063.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.136+768G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821521 | |||||||
| chr4:2821578 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.136+825G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821578 | |||||||
| chr4:2821614 | T | C | 1 | a0001c0001t0003g0042 | 2 | HG02015.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.136+861T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821614 | |||||||
| chr4:2821760 | G | A | 1 | a0001c0001t0026g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136+1007G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821760 | |||||||
| chr4:2821791 | C | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136+1038C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821791 | |||||||
| chr4:2821834 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.136+1081C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821834 | |||||||
| chr4:2821837 | A | G | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136+1084A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821837 | |||||||
| chr4:2821950 | GTCCACC | G | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-981_137-976del others(6): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 2821950 | ||||||
| chr4:2821976 | T | G | 17 | a0001c0003t0008g0040 a0001c0003t0008g0126 a0001c0003t0008g0131 others(14): Show |
18 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.137-959T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2821976 | |||||||
| chr4:2822009 | A | G | 1 | a0001c0002t0060g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.137-926A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822009 | |||||||
| chr4:2822011 | G | A | 1 | a0001c0002t0060g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.137-924G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822011 | |||||||
| chr4:2822012 | A | G | 1 | a0001c0002t0060g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.137-923A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822012 | |||||||
| chr4:2822040 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.137-895G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822040 | |||||||
| chr4:2822131 | C | G | 2 | a0001c0003t0002g0087 a0001c0003t0092g0086 |
2 | HG00323.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.137-804C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822131 | |||||||
| chr4:2822154 | C | T | 1 | a0001c0005t0062g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.137-781C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822154 | |||||||
| chr4:2822157 | G | A | 1 | a0001c0007t0031g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137-778G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822157 | |||||||
| chr4:2822269 | C | T | 1 | a0001c0003t0002g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.137-666C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822269 | |||||||
| chr4:2822301 | G | C | 1 | a0001c0002t0002g0147 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137-634G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822301 | |||||||
| chr4:2822303 | A | T | 1 | a0001c0002t0002g0147 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137-632A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822303 | |||||||
| chr4:2822387 | T | C | 67 | a0001c0002t0001g0030 a0001c0002t0001g0144 a0001c0002t0001g0150 others(64): Show |
93 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.137-548T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822387 | |||||||
| chr4:2822425 | A | G | 2 | a0001c0004t0001g0062 a0001c0004t0001g0074 |
2 | HG01192.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.137-510A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822425 | |||||||
| chr4:2822462 | C | T | 25 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(22): Show |
31 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-473C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822462 | |||||||
| chr4:2822477 | C | T | 1 | a0001c0002t0091g0175 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.137-458C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822477 | |||||||
| chr4:2822615 | T | C | 1 | a0001c0004t0038g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.137-320T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822615 | |||||||
| chr4:2822698 | G | A | 1 | a0001c0003t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-237G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822698 | |||||||
| chr4:2822782 | G | C | 1 | a0001c0002t0001g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.137-153G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822782 | |||||||
| chr4:2822784 | G | A | 2 | a0001c0001t0063g0038 a0001c0001t0072g0038 |
2 | NA18940.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.137-151G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 2/12 | chr4 | 2822784 | |||||||
| chr4:2823121 | T | A | 23 | a0001c0003t0021g0082 a0001c0004t0001g0062 a0001c0004t0001g0073 others(20): Show |
29 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.239+84T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823121 | |||||||
| chr4:2823128 | G | A | 2 | a0001c0004t0015g0081 a0001c0004t0086g0083 |
2 | HG01255.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.239+91G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823128 | |||||||
| chr4:2823278 | G | C | 1 | a0001c0003t0021g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.239+241G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823278 | |||||||
| chr4:2823289 | C | T | 5 | a0001c0001t0002g0045 a0001c0001t0002g0270 a0001c0001t0002g0272 others(2): Show |
5 | HG00609.hp2 HG00673.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+252C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823289 | |||||||
| chr4:2823359 | C | T | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+322C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823359 | |||||||
| chr4:2823445 | C | T | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.239+408C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823445 | |||||||
| chr4:2823749 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.239+712C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823749 | |||||||
| chr4:2823826 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.240-787G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823826 | |||||||
| chr4:2823844 | A | C | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.240-769A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823844 | |||||||
| chr4:2823892 | C | T | 1 | a0001c0001t0050g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.240-721C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823892 | |||||||
| chr4:2823933 | G | A | 57 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(54): Show |
63 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.240-680G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2823933 | |||||||
| chr4:2824044 | C | G | 3 | a0001c0005t0016g0098 a0001c0005t0031g0101 a0001c0005t0095g0091 |
3 | HG02717.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.240-569C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2824044 | |||||||
| chr4:2824198 | A | G | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-415A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2824198 | |||||||
| chr4:2824348 | C | T | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-265C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2824348 | |||||||
| chr4:2824386 | C | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.240-227C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2824386 | |||||||
| chr4:2824491 | C | CA | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(241): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.240-122_240-121ins others(1): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2824491 | |||||||
| chr4:2824533 | C | T | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-80C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 3/12 | chr4 | 2824533 | |||||||
| chr4:2824745 | G | T | 22 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(19): Show |
27 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.357+15G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/12 | chr4 | 2824745 | |||||||
| chr4:2824944 | C | T | 7 | a0001c0003t0015g0048 a0001c0003t0015g0103 a0001c0003t0015g0112 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-182C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/12 | chr4 | 2824944 | |||||||
| chr4:2824998 | G | T | 1 | a0001c0001t0054g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.358-128G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/12 | chr4 | 2824998 | |||||||
| chr4:2825028 | G | C | 1 | a0001c0007t0031g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.358-98G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/12 | chr4 | 2825028 | |||||||
| chr4:2825029 | G | T | 1 | a0001c0007t0031g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.358-97G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/12 | chr4 | 2825029 | |||||||
| chr4:2825080 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.358-46C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 4/12 | chr4 | 2825080 | |||||||
| chr4:2825220 | C | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428+24C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825220 | |||||||
| chr4:2825266 | G | A | 1 | a0001c0004t0005g0023 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.428+70G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825266 | |||||||
| chr4:2825270 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.428+74C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825270 | |||||||
| chr4:2825294 | T | G | 1 | a0001c0005t0079g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.428+98T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825294 | |||||||
| chr4:2825417 | GCACA | G | 58 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(55): Show |
64 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.428+226_428+229del others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2825417 | ||||||
| chr4:2825447 | TGCACACA others(23): Show |
T | 3 | a0001c0002t0004g0031 a0001c0002t0004g0170 a0001c0002t0087g0167 |
4 | HG00642.hp2 HG01192.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+282_428+311del others(30): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2825447 | ||||||
| chr4:2825475 | TGC | T | 58 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(55): Show |
64 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.428+282_428+283del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2825475 | ||||||
| chr4:2825477 | C | CACACACA others(19): Show |
1 | a0001c0003t0088g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.428+281_428+282ins others(26): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825477 | |||||||
| chr4:2825478 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.428+282G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825478 | |||||||
| chr4:2825489 | G | C | 60 | a0001c0001t0001g0230 a0001c0003t0001g0011 a0001c0003t0001g0019 others(57): Show |
66 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.428+293G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825489 | |||||||
| chr4:2825489 | GAGCAACA others(21): Show |
G | 1 | a0001c0002t0002g0171 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.428+331_428+358del others(28): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2825489 | ||||||
| chr4:2825528 | G | A | 17 | a0001c0003t0008g0040 a0001c0003t0008g0126 a0001c0003t0008g0131 others(14): Show |
18 | HG01069.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.428+332G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825528 | |||||||
| chr4:2825534 | GCACA | G | 5 | a0001c0001t0056g0253 a0001c0007t0015g0049 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+347_428+350del others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2825534 | ||||||
| chr4:2825594 | GCA | G | 22 | a0001c0004t0001g0062 a0001c0004t0001g0073 a0001c0004t0001g0074 others(19): Show |
28 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.428+409_428+410del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2825594 | ||||||
| chr4:2825622 | T | C | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+426T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825622 | |||||||
| chr4:2825748 | G | A | 1 | a0001c0002t0034g0168 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.428+552G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825748 | |||||||
| chr4:2825886 | C | T | 1 | a0001c0002t0003g0174 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.428+690C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825886 | |||||||
| chr4:2825889 | C | T | 22 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(19): Show |
27 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.428+693C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825889 | |||||||
| chr4:2825919 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(240): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.428+723T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2825919 | |||||||
| chr4:2826044 | C | T | 57 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(54): Show |
63 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.428+848C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826044 | |||||||
| chr4:2826187 | C | A | 7 | a0001c0003t0015g0048 a0001c0003t0015g0103 a0001c0003t0015g0112 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.428+991C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826187 | |||||||
| chr4:2826242 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.429-988C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826242 | |||||||
| chr4:2826247 | G | A | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-983G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826247 | |||||||
| chr4:2826271 | GTGTGTGT others(19): Show |
G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
133 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.429-950_429-925del others(26): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826271 | ||||||
| chr4:2826287 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.429-943G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826287 | |||||||
| chr4:2826311 | G | GT | 72 | a0001c0004t0001g0062 a0001c0004t0001g0073 a0001c0004t0001g0074 others(69): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.429-919_429-918ins others(1): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826311 | |||||||
| chr4:2826312 | C | G | 72 | a0001c0004t0001g0062 a0001c0004t0001g0073 a0001c0004t0001g0074 others(69): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.429-918C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826312 | |||||||
| chr4:2826312 | CA | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.429-916delA | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826312 | ||||||
| chr4:2826313 | A | C | 72 | a0001c0004t0001g0062 a0001c0004t0001g0073 a0001c0004t0001g0074 others(69): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.429-917A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826313 | |||||||
| chr4:2826362 | CTG | C | 4 | a0001c0007t0015g0049 a0001c0007t0027g0054 a0001c0007t0027g0055 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-864_429-863del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826362 | ||||||
| chr4:2826396 | G | A | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-834G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826396 | |||||||
| chr4:2826411 | C | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429-819C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826411 | |||||||
| chr4:2826412 | A | G | 130 | a0001c0002t0001g0030 a0001c0002t0001g0144 a0001c0002t0001g0150 others(127): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.429-818A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826412 | |||||||
| chr4:2826498 | C | T | 10 | a0001c0004t0001g0073 a0001c0004t0002g0071 a0001c0004t0004g0015 others(7): Show |
16 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.429-732C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826498 | |||||||
| chr4:2826509 | T | C | 1 | a0001c0007t0031g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-721T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826509 | |||||||
| chr4:2826530 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0023g0043 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.429-700G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826530 | |||||||
| chr4:2826540 | C | CTG | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-675_429-674dup others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826540 | ||||||
| chr4:2826540 | CTG | C | 96 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0227 others(93): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.429-675_429-674del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826540 | ||||||
| chr4:2826566 | A | G | 1 | a0001c0004t0089g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.429-664A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826566 | |||||||
| chr4:2826578 | GTGTGTGT others(25): Show |
G | 1 | a0001c0003t0092g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.429-635_429-604del others(32): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826578 | ||||||
| chr4:2826592 | CTG | C | 3 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 |
3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.429-632_429-631del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826592 | ||||||
| chr4:2826604 | CTG | C | 57 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(54): Show |
63 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.429-622_429-621del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826604 | ||||||
| chr4:2826628 | G | A | 1 | a0001c0003t0016g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.429-602G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826628 | |||||||
| chr4:2826656 | A | G | 4 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-574A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826656 | |||||||
| chr4:2826658 | G | GTGTTGCT others(21): Show |
1 | a0001c0001t0001g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.429-553_429-526dup others(28): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826658 | ||||||
| chr4:2826666 | C | CTGTGTGT others(23): Show |
1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.429-547_429-546ins others(30): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826666 | ||||||
| chr4:2826676 | G | C | 21 | a0001c0004t0001g0062 a0001c0004t0001g0073 a0001c0004t0001g0074 others(18): Show |
27 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.429-554G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826676 | |||||||
| chr4:2826684 | T | G | 59 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(56): Show |
65 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.429-546T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826684 | |||||||
| chr4:2826714 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.429-516G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826714 | |||||||
| chr4:2826723 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.429-507T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826723 | |||||||
| chr4:2826757 | TTGTG | T | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-468_429-465del others(4): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826757 | ||||||
| chr4:2826800 | G | C | 129 | a0001c0002t0001g0030 a0001c0002t0001g0144 a0001c0002t0001g0150 others(126): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.429-430G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826800 | |||||||
| chr4:2826884 | C | T | 2 | a0001c0003t0016g0053 a0001c0010t0005g0142 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.429-346C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826884 | |||||||
| chr4:2826903 | G | T | 66 | a0001c0002t0001g0030 a0001c0002t0001g0144 a0001c0002t0001g0150 others(63): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.429-327G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826903 | |||||||
| chr4:2826958 | C | T | 5 | a0001c0004t0083g0060 a0001c0007t0015g0049 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-272C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826958 | |||||||
| chr4:2826989 | G | A | 7 | a0001c0003t0015g0048 a0001c0003t0015g0103 a0001c0003t0015g0112 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.429-241G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2826989 | |||||||
| chr4:2826993 | ATG | A | 7 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(4): Show |
7 | HG01975.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.429-229_429-228del others(2): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 2826993 | ||||||
| chr4:2827011 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.429-219G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2827011 | |||||||
| chr4:2827044 | T | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
172 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.429-186T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2827044 | |||||||
| chr4:2827108 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.429-122C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2827108 | |||||||
| chr4:2827134 | T | G | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.429-96T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2827134 | |||||||
| chr4:2827140 | C | T | 3 | a0001c0004t0002g0028 a0001c0004t0002g0154 a0001c0004t0026g0153 |
4 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-90C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2827140 | |||||||
| chr4:2827206 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.429-24G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 5/12 | chr4 | 2827206 | |||||||
| chr4:2827346 | C | T | 1 | a0001c0003t0006g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.517+28C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827346 | |||||||
| chr4:2827347 | G | A | 1 | a0001c0003t0015g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517+29G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827347 | |||||||
| chr4:2827350 | T | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(235): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.517+32T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827350 | |||||||
| chr4:2827379 | C | T | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+61C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827379 | |||||||
| chr4:2827440 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.517+122G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827440 | |||||||
| chr4:2827455 | G | A | 1 | a0001c0001t0018g0016 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.517+137G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827455 | |||||||
| chr4:2827511 | C | T | 1 | a0001c0004t0020g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.518-95C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827511 | |||||||
| chr4:2827588 | C | A | 7 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(4): Show |
7 | HG01975.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.518-18C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827588 | |||||||
| chr4:2827591 | C | G | 3 | a0001c0002t0003g0005 a0001c0002t0028g0129 a0001c0011t0003g0130 |
7 | NA18945.hp2 NA18959.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-15C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 6/12 | chr4 | 2827591 | |||||||
| chr4:2827682 | G | A | 59 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(56): Show |
65 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(62): Show |
splice_region_variant&intron_variant | LOW | c.586+8G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827682 | |||||||
| chr4:2827711 | T | C | 1 | a0001c0002t0084g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.586+37T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827711 | |||||||
| chr4:2827751 | G | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(236): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.586+77G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827751 | |||||||
| chr4:2827778 | G | A | 1 | a0001c0002t0029g0172 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.586+104G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827778 | |||||||
| chr4:2827805 | G | A | 1 | a0001c0003t0088g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.586+131G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827805 | |||||||
| chr4:2827974 | C | T | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.586+300C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827974 | |||||||
| chr4:2827976 | C | T | 3 | a0001c0003t0014g0189 a0001c0003t0014g0191 a0001c0003t0037g0092 |
3 | HG01975.hp1 HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.586+302C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827976 | |||||||
| chr4:2827989 | C | G | 1 | a0001c0011t0003g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.586+315C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2827989 | |||||||
| chr4:2828193 | CGCCTCCC others(5): Show |
C | 6 | a0001c0004t0002g0154 a0001c0004t0026g0153 a0001c0004t0036g0067 others(3): Show |
6 | HG00639.hp2 HG01261.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+520_586+531del others(12): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828193 | |||||||
| chr4:2828194 | G | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(228): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.586+520G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828194 | |||||||
| chr4:2828206 | T | C | 6 | a0001c0004t0002g0154 a0001c0004t0026g0153 a0001c0004t0036g0067 others(3): Show |
6 | HG00639.hp2 HG01261.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+532T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828206 | |||||||
| chr4:2828320 | C | T | 7 | a0001c0005t0002g0089 a0001c0005t0002g0090 a0001c0005t0002g0104 others(4): Show |
7 | HG02257.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+646C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828320 | |||||||
| chr4:2828349 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
160 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.586+675C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828349 | |||||||
| chr4:2828391 | A | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(235): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.586+717A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828391 | |||||||
| chr4:2828403 | A | G | 56 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(53): Show |
62 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.586+729A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828403 | |||||||
| chr4:2828473 | A | C | 22 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(19): Show |
27 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.586+799A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828473 | |||||||
| chr4:2828488 | G | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(235): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.586+814G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828488 | |||||||
| chr4:2828503 | G | A | 12 | a0001c0003t0008g0040 a0001c0003t0008g0126 a0001c0003t0008g0131 others(9): Show |
13 | HG01069.hp1 HG01243.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+829G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828503 | |||||||
| chr4:2828569 | C | G | 1 | a0001c0005t0004g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.586+895C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828569 | |||||||
| chr4:2828587 | C | T | 1 | a0001c0002t0003g0155 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.587-906C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828587 | |||||||
| chr4:2828628 | C | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.587-865C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828628 | |||||||
| chr4:2828750 | G | A | 55 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(52): Show |
61 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.587-743G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828750 | |||||||
| chr4:2828798 | C | T | 1 | a0001c0010t0005g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-695C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828798 | |||||||
| chr4:2828817 | C | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.587-676C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828817 | |||||||
| chr4:2828847 | G | A | 3 | a0001c0004t0002g0028 a0001c0004t0002g0154 a0001c0004t0026g0153 |
4 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-646G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828847 | |||||||
| chr4:2828850 | C | T | 1 | a0001c0002t0071g0282 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.587-643C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828850 | |||||||
| chr4:2828875 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
163 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.587-618G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828875 | |||||||
| chr4:2828892 | C | T | 1 | a0001c0002t0007g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.587-601C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828892 | |||||||
| chr4:2828924 | G | A | 2 | a0001c0004t0004g0015 a0001c0004t0004g0036 |
5 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-569G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828924 | |||||||
| chr4:2828958 | G | T | 3 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 |
3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.587-535G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2828958 | |||||||
| chr4:2829095 | G | C | 1 | a0001c0011t0003g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.587-398G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829095 | |||||||
| chr4:2829096 | C | G | 1 | a0001c0011t0003g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.587-397C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829096 | |||||||
| chr4:2829183 | T | G | 5 | a0001c0003t0015g0103 a0001c0007t0015g0049 a0001c0007t0027g0054 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-310T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829183 | |||||||
| chr4:2829237 | G | A | 7 | a0001c0004t0002g0028 a0001c0004t0002g0154 a0001c0004t0026g0153 others(4): Show |
8 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-256G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829237 | |||||||
| chr4:2829333 | G | T | 2 | a0001c0005t0006g0085 a0001c0005t0077g0084 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.587-160G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829333 | |||||||
| chr4:2829377 | G | A | 1 | a0001c0007t0027g0054 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.587-116G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829377 | |||||||
| chr4:2829417 | G | C | 2 | a0001c0007t0027g0054 a0001c0007t0027g0055 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.587-76G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829417 | |||||||
| chr4:2829455 | C | G | 40 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(37): Show |
45 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.587-38C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 7/12 | chr4 | 2829455 | |||||||
| chr4:2830187 | C | G | 22 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(19): Show |
27 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1241+40C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830187 | |||||||
| chr4:2830191 | G | A | 2 | a0001c0001t0044g0215 a0001c0003t0006g0099 |
2 | HG02451.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1241+44G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830191 | |||||||
| chr4:2830240 | C | T | 1 | a0001c0003t0016g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1241+93C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830240 | |||||||
| chr4:2830256 | C | CG | 12 | a0001c0001t0001g0276 a0001c0001t0004g0267 a0001c0002t0001g0179 others(9): Show |
12 | HG00741.hp1 HG02027.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241+113dupG | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 2830256 | ||||||
| chr4:2830304 | G | A | 1 | a0001c0004t0015g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1241+157G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830304 | |||||||
| chr4:2830367 | TTTTTTTC | T | 11 | a0001c0004t0005g0008 a0001c0004t0005g0023 a0001c0004t0005g0088 others(8): Show |
15 | HG01109.hp2 HG02055.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241+226_1241+232d others(9): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 2830367 | ||||||
| chr4:2830462 | G | A | 96 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(93): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1241+315G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830462 | |||||||
| chr4:2830518 | C | T | 7 | a0001c0004t0002g0028 a0001c0004t0002g0154 a0001c0004t0026g0153 others(4): Show |
8 | HG00639.hp2 HG01081.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241+371C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830518 | |||||||
| chr4:2830654 | C | T | 5 | a0001c0006t0016g0203 a0001c0006t0016g0205 a0001c0006t0016g0207 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241+507C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830654 | |||||||
| chr4:2830718 | T | G | 2 | a0001c0003t0014g0035 a0001c0003t0037g0035 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1241+571T>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830718 | |||||||
| chr4:2830849 | C | T | 25 | a0001c0003t0001g0011 a0001c0003t0001g0019 a0001c0003t0002g0011 others(22): Show |
30 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1241+702C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2830849 | |||||||
| chr4:2831000 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(80): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1242-571C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831000 | |||||||
| chr4:2831007 | C | T | 6 | a0001c0003t0006g0002 a0001c0003t0006g0099 a0001c0003t0006g0115 others(3): Show |
10 | HG02451.hp1 HG02717.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1242-564C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831007 | |||||||
| chr4:2831130 | C | T | 1 | a0001c0002t0002g0169 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1242-441C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831130 | |||||||
| chr4:2831253 | C | T | 1 | a0001c0004t0004g0036 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1242-318C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831253 | |||||||
| chr4:2831332 | T | C | 1 | a0001c0003t0059g0236 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1242-239T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831332 | |||||||
| chr4:2831362 | A | C | 26 | a0001c0003t0008g0040 a0001c0003t0008g0126 a0001c0003t0008g0131 others(23): Show |
27 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1242-209A>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831362 | |||||||
| chr4:2831401 | G | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(228): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1242-170G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831401 | |||||||
| chr4:2831473 | C | T | 4 | a0001c0002t0002g0029 a0001c0002t0017g0014 a0001c0002t0017g0152 others(1): Show |
7 | HG01099.hp2 HG01168.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1242-98C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831473 | |||||||
| chr4:2831487 | G | T | 1 | a0001c0004t0096g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1242-84G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831487 | |||||||
| chr4:2831499 | G | C | 58 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0249 others(55): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1242-72G>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 8/12 | chr4 | 2831499 | |||||||
| chr4:2831773 | T | C | 17 | a0001c0001t0001g0241 a0001c0002t0007g0151 a0001c0004t0002g0028 others(14): Show |
22 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1350+94T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 9/12 | chr4 | 2831773 | |||||||
| chr4:2831796 | C | T | 1 | a0001c0012t0008g0133 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1350+117C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 9/12 | chr4 | 2831796 | |||||||
| chr4:2831860 | C | T | 1 | a0001c0006t0040g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1351-63C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 9/12 | chr4 | 2831860 | |||||||
| chr4:2831872 | G | T | 1 | a0001c0002t0060g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1351-51G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 9/12 | chr4 | 2831872 | |||||||
| chr4:2831907 | C | T | 1 | a0001c0003t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1351-16C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 9/12 | chr4 | 2831907 | |||||||
| chr4:2832078 | A | G | 3 | a0001c0003t0019g0050 a0001c0003t0019g0051 a0001c0003t0019g0052 |
3 | HG02145.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1406+100A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 10/12 | chr4 | 2832078 | |||||||
| chr4:2832239 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(93): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1407-92G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 10/12 | chr4 | 2832239 | |||||||
| chr4:2832261 | C | T | 1 | a0001c0005t0079g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1407-70C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 10/12 | chr4 | 2832261 | |||||||
| chr4:2832320 | T | A | 3 | a0001c0001t0022g0216 a0001c0001t0022g0219 a0001c0005t0002g0187 |
3 | HG00738.hp1 HG01515.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1407-11T>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 10/12 | chr4 | 2832320 | |||||||
| chr4:2832503 | A | G | 17 | a0001c0001t0046g0254 a0001c0002t0007g0151 a0001c0003t0015g0048 others(14): Show |
18 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1488+91A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832503 | |||||||
| chr4:2832576 | AATAG | A | 6 | a0001c0003t0015g0048 a0001c0003t0015g0112 a0001c0003t0021g0058 others(3): Show |
6 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1488+167_1488+170d others(6): Show |
SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 2832576 | ||||||
| chr4:2832596 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1488+184T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832596 | |||||||
| chr4:2832802 | G | A | 4 | a0001c0001t0001g0121 a0001c0002t0001g0030 a0001c0002t0007g0160 others(1): Show |
5 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-188G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832802 | |||||||
| chr4:2832827 | C | T | 31 | a0001c0001t0001g0121 a0001c0001t0001g0228 a0001c0001t0001g0241 others(28): Show |
33 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1489-163C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832827 | |||||||
| chr4:2832867 | G | A | 1 | a0001c0007t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1489-123G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832867 | |||||||
| chr4:2832910 | C | G | 2 | a0001c0002t0003g0173 a0001c0007t0015g0049 |
2 | HG02071.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1489-80C>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832910 | |||||||
| chr4:2832924 | A | G | 1 | a0001c0004t0035g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1489-66A>G | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832924 | |||||||
| chr4:2832974 | C | T | 1 | a0001c0002t0003g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1489-16C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 11/12 | chr4 | 2832974 | |||||||
| chr4:2833072 | G | A | 1 | a0001c0005t0016g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1548+23G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833072 | |||||||
| chr4:2833203 | C | A | 1 | a0001c0002t0002g0146 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1548+154C>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833203 | |||||||
| chr4:2833422 | G | A | 17 | a0001c0001t0045g0263 a0001c0001t0067g0199 a0001c0001t0073g0200 others(14): Show |
21 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1549-275G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833422 | |||||||
| chr4:2833489 | A | T | 7 | a0001c0003t0014g0035 a0001c0003t0014g0188 a0001c0003t0014g0189 others(4): Show |
7 | HG01975.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1549-208A>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833489 | |||||||
| chr4:2833499 | C | T | 2 | a0001c0005t0031g0101 a0001c0007t0031g0111 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1549-198C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833499 | |||||||
| chr4:2833500 | G | A | 1 | a0001c0006t0016g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1549-197G>A | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833500 | |||||||
| chr4:2833514 | G | T | 1 | a0001c0001t0001g0260 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1549-183G>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833514 | |||||||
| chr4:2833523 | T | C | 1 | a0001c0003t0008g0234 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1549-174T>C | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833523 | |||||||
| chr4:2833543 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1549-154C>T | SH3BP2 | ENSG00000087266.17 | transcript | ENST00000503393.8 | protein_coding | 12/12 | chr4 | 2833543 |