Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 128954 |
| ensemblid | ENSG00000215568.9 |
| hgncid | 18325 |
| symbol | GAB4 |
| name | GRB2 associated binding protein family member 4 |
| refseq_nuc | NM_001037814.1 |
| refseq_prot | NP_001032903.1 |
| ensembl_nuc | ENST00000400588.5 |
| ensembl_prot | ENSP00000383431.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 16961936 |
| end | 17008222 |
| strand | - |
| ver | v1.2 |
| region | chr22:16961936-17008222 |
| region5000 | chr22:16956936-17013222 |
| regionname0 | GAB4_chr22_16961936_17008222 |
| regionname5000 | GAB4_chr22_16956936_17013222 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 574 | 256 | 67 | 41 | 116 | 14 | 17 | 85 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(569): Show |
chr22 | 16956936 | 17013222 |
| a0002 | 0/1 | 162 | 146 | 16 | 31 | 75 | 2 | 21 | 62 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(157): Show |
chr22 | 16956936 | 17013222 |
| a0003 | 0/0 | 574 | 12 | 0 | 6 | 0 | 0 | 6 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(569): Show |
chr22 | 16956936 | 17013222 |
| a0004 | 0/0 | 574 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(569): Show |
chr22 | 16956936 | 17013222 |
| a0005 | 0/0 | 162 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(157): Show |
chr22 | 16956936 | 17013222 |
| a0006 | 0/0 | 574 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | MSLSS others(569): Show |
chr22 | 16956936 | 17013222 |
| a0007 | 0/0 | 574 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(569): Show |
chr22 | 16956936 | 17013222 |
| a0008 | 0/0 | 574 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | MSLPS others(569): Show |
chr22 | 16956936 | 17013222 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1722 | 172 | 44 | 31 | 83 | 9 | 5 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0003 | 1/0 | 1722 | 58 | 4 | 8 | 29 | 4 | 12 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0005 | 0/0 | 1722 | 11 | 11 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0007 | 0/0 | 1722 | 4 | 4 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0009 | 0/0 | 1722 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0010 | 0/0 | 1722 | 3 | 2 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0012 | 0/0 | 1722 | 2 | 0 | 1 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0018 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0023 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0001c0024 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0002 | 0/1 | 1722 | 135 | 14 | 31 | 69 | 2 | 18 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0008 | 0/0 | 1722 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0013 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0014 | 0/0 | 1722 | 2 | 0 | 0 | 1 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0017 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0021 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0002c0022 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0003c0004 | 0/0 | 1722 | 11 | 0 | 5 | 0 | 0 | 6 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0003c0020 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0004c0006 | 0/0 | 1722 | 10 | 9 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0005c0011 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0006c0015 | 0/0 | 1722 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0007c0019 | 0/0 | 1722 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 | ||
| a0008c0016 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | ATGTC others(1717): Show |
chr22 | 16956936 | 17013222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2630 | 9 | 1 | 1 | 5 | 0 | 2 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0001t0002 | 0/0 | 2630 | 102 | 23 | 8 | 65 | 4 | 2 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0001t0003 | 0/0 | 2630 | 12 | 10 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0001t0004 | 0/0 | 2630 | 45 | 9 | 22 | 8 | 5 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0001t0010 | 0/0 | 2630 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0001t0011 | 0/0 | 2630 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0001t0012 | 0/0 | 2630 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0003t0003 | 1/0 | 2630 | 52 | 2 | 8 | 26 | 3 | 12 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0003t0008 | 0/0 | 2630 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0003t0009 | 0/0 | 2630 | 3 | 2 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0005t0005 | 0/0 | 2630 | 11 | 11 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0007t0004 | 0/0 | 2630 | 4 | 4 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0009t0003 | 0/0 | 2630 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0010t0004 | 0/0 | 2630 | 3 | 2 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0012t0003 | 0/0 | 2630 | 2 | 0 | 1 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0018t0002 | 0/0 | 2630 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0023t0003 | 0/0 | 2630 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0001c0024t0005 | 0/0 | 2630 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0002t0001 | 0/1 | 2630 | 122 | 10 | 26 | 66 | 2 | 17 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0002t0002 | 0/0 | 2630 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0002t0004 | 0/0 | 2630 | 5 | 4 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0002t0007 | 0/0 | 2630 | 6 | 0 | 5 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0008t0001 | 0/0 | 2630 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0013t0005 | 0/0 | 2630 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0014t0001 | 0/0 | 2630 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0014t0003 | 0/0 | 2630 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0017t0001 | 0/0 | 2630 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0021t0001 | 0/0 | 2630 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0002c0022t0001 | 0/0 | 2630 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0003c0004t0003 | 0/0 | 2630 | 11 | 0 | 5 | 0 | 0 | 6 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0003c0020t0003 | 0/0 | 2630 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0004c0006t0006 | 0/0 | 2630 | 10 | 9 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0005c0011t0001 | 0/0 | 2630 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0006c0015t0006 | 0/0 | 2630 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0007c0019t0002 | 0/0 | 2630 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| a0008c0016t0003 | 0/0 | 2630 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | GCTTT others(2625): Show |
chr22 | 16956936 | 17013222 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0001g0072 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0001 | 0/0 | 15 | 4 | 1 | 9 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0004 | 0/0 | 9 | 2 | 5 | 0 | 2 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0012 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0013 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0042 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0069 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0001t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0002 | 1/0 | 11 | 1 | 1 | 4 | 1 | 3 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0043 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0070 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0071 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0074 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0008g0044 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0003t0009g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0005t0005g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0005t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0005t0005g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0005t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0005t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0005t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0007t0004g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0009t0003g0073 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0009t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0010t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0010t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0010t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0012t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0012t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0018t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0023t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0001c0024t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0003 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0005 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0008 | 0/0 | 7 | 0 | 0 | 1 | 1 | 5 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0036 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0037 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0038 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0039 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0041 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0062 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0066 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0068 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0007g0040 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0007g0065 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0002t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0008t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0008t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0013t0005g0067 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0014t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0014t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0017t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0021t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0002c0022t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0003c0020t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0004c0006t0006g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0004c0006t0006g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0004c0006t0006g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0004c0006t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0004c0006t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0005c0011t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0005c0011t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0006c0015t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0006c0015t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0007c0019t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| a0008c0016t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | GBR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | GBR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00140 | hp1 | a0001 | c0012 | t0003 | g0224 | EUR | GBR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | GBR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0002 | EUR | FIN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0197 | EUR | FIN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0014 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00597 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00673 | hp2 | a0001 | c0003 | t0003 | g0234 | EAS | CHS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00733 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0228 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00741 | hp1 | a0003 | c0004 | t0003 | g0024 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0070 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01070 | hp1 | a0003 | c0004 | t0003 | g0025 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01074 | hp1 | a0002 | c0002 | t0007 | g0040 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0225 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0211 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01109 | hp2 | a0001 | c0010 | t0004 | g0208 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01167 | hp1 | a0001 | c0012 | t0003 | g0223 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01167 | hp2 | a0002 | c0002 | t0007 | g0040 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01168 | hp2 | a0002 | c0002 | t0007 | g0168 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01192 | hp1 | a0004 | c0006 | t0006 | g0018 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01243 | hp1 | a0007 | c0019 | t0002 | g0131 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01256 | hp2 | a0003 | c0004 | t0003 | g0025 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01258 | hp1 | a0003 | c0004 | t0003 | g0025 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01358 | hp2 | a0001 | c0003 | t0003 | g0217 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0219 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01361 | hp2 | a0003 | c0004 | t0003 | g0024 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0206 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0069 | EUR | IBS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0074 | EUR | IBS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | IBS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01517 | hp2 | a0001 | c0003 | t0003 | g0074 | EUR | IBS | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01884 | hp1 | a0004 | c0006 | t0006 | g0057 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01884 | hp2 | a0001 | c0003 | t0003 | g0002 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01934 | hp2 | a0002 | c0002 | t0007 | g0065 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01981 | hp1 | a0002 | c0002 | t0007 | g0065 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02055 | hp2 | a0001 | c0005 | t0005 | g0021 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0231 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02083 | hp1 | a0002 | c0014 | t0003 | g0167 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0114 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02129 | hp1 | a0001 | c0001 | t0010 | g0154 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02135 | hp1 | a0002 | c0021 | t0001 | g0177 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0155 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CDX | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CDX | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02165 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | CDX | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02257 | hp1 | a0001 | c0005 | t0005 | g0021 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02258 | hp1 | a0005 | c0011 | t0001 | g0077 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02280 | hp2 | a0001 | c0007 | t0004 | g0022 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0159 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0156 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0216 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02602 | hp2 | a0002 | c0002 | t0007 | g0040 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02615 | hp1 | a0001 | c0005 | t0005 | g0097 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02615 | hp2 | a0004 | c0006 | t0006 | g0056 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02622 | hp1 | a0001 | c0007 | t0004 | g0022 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02630 | hp2 | a0001 | c0005 | t0005 | g0047 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02683 | hp1 | a0003 | c0004 | t0003 | g0024 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02683 | hp2 | a0002 | c0017 | t0001 | g0076 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02698 | hp2 | a0003 | c0004 | t0003 | g0088 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02717 | hp2 | a0001 | c0005 | t0005 | g0079 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02723 | hp1 | a0001 | c0005 | t0005 | g0091 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0215 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02735 | hp2 | a0001 | c0003 | t0003 | g0221 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02738 | hp2 | a0001 | c0003 | t0003 | g0229 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0070 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02886 | hp1 | a0001 | c0003 | t0009 | g0238 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02895 | hp1 | a0004 | c0006 | t0006 | g0056 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02896 | hp2 | a0001 | c0003 | t0009 | g0239 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02897 | hp2 | a0004 | c0006 | t0006 | g0142 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02922 | hp2 | a0001 | c0005 | t0005 | g0046 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02965 | hp1 | a0004 | c0006 | t0006 | g0018 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02970 | hp2 | a0004 | c0006 | t0006 | g0144 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03017 | hp1 | a0001 | c0003 | t0003 | g0226 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03041 | hp1 | a0006 | c0015 | t0006 | g0236 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03098 | hp1 | a0002 | c0002 | t0004 | g0184 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03139 | hp1 | a0002 | c0013 | t0005 | g0067 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03139 | hp2 | a0001 | c0005 | t0005 | g0021 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03209 | hp1 | a0004 | c0006 | t0006 | g0057 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03225 | hp2 | a0001 | c0007 | t0004 | g0022 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0043 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03486 | hp1 | a0006 | c0015 | t0006 | g0237 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0002 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03492 | hp1 | a0003 | c0004 | t0003 | g0093 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0002 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03579 | hp1 | a0001 | c0024 | t0005 | g0235 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0096 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03688 | hp2 | a0002 | c0014 | t0001 | g0160 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0218 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0011 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03834 | hp1 | a0003 | c0004 | t0003 | g0089 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0227 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0036 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0043 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04115 | hp2 | a0003 | c0004 | t0003 | g0090 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04199 | hp2 | a0001 | c0003 | t0003 | g0002 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0149 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04228 | hp1 | a0003 | c0004 | t0003 | g0087 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG04228 | hp2 | a0002 | c0022 | t0001 | g0179 | SAS | STU | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18522 | hp1 | a0005 | c0011 | t0001 | g0078 | AFR | YRI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18522 | hp2 | a0001 | c0023 | t0003 | g0104 | AFR | YRI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18612 | hp2 | a0001 | c0003 | t0003 | g0232 | EAS | CHB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | CHB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0014 | EAS | CHB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18906 | hp1 | a0001 | c0005 | t0005 | g0046 | AFR | YRI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18941 | hp2 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18948 | hp2 | a0001 | c0003 | t0003 | g0213 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18950 | hp1 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18954 | hp2 | a0008 | c0016 | t0003 | g0075 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18961 | hp2 | a0001 | c0009 | t0003 | g0222 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18963 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18965 | hp1 | a0002 | c0008 | t0001 | g0085 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18966 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0043 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0212 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18973 | hp1 | a0002 | c0002 | t0004 | g0202 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18977 | hp2 | a0001 | c0001 | t0010 | g0117 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18981 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18984 | hp1 | a0002 | c0008 | t0001 | g0045 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18988 | hp1 | a0001 | c0018 | t0002 | g0134 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18990 | hp1 | a0001 | c0003 | t0008 | g0044 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18993 | hp1 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18999 | hp1 | a0001 | c0003 | t0008 | g0044 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19003 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19005 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19007 | hp2 | a0001 | c0003 | t0008 | g0044 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | LWK | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19043 | hp1 | a0001 | c0010 | t0004 | g0209 | AFR | LWK | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19043 | hp2 | a0001 | c0005 | t0005 | g0021 | AFR | LWK | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19063 | hp1 | a0002 | c0008 | t0001 | g0084 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19066 | hp1 | a0001 | c0009 | t0003 | g0073 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19068 | hp1 | a0002 | c0008 | t0001 | g0045 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19076 | hp1 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19088 | hp2 | a0001 | c0009 | t0003 | g0073 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19091 | hp2 | a0001 | c0003 | t0003 | g0220 | EAS | JPT | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | YRI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ASW | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA20129 | hp2 | a0001 | c0007 | t0004 | g0022 | AFR | ASW | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0187 | EUR | TSI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | TSI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | TSI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA20805 | hp2 | a0001 | c0003 | t0009 | g0240 | EUR | TSI | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG01123 | hp2 | a0003 | c0020 | t0003 | g0092 | AMR | CLM | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02109 | hp2 | a0004 | c0006 | t0006 | g0018 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02486 | hp2 | a0002 | c0013 | t0005 | g0067 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02559 | hp1 | a0004 | c0006 | t0006 | g0018 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG02559 | hp2 | a0001 | c0005 | t0005 | g0047 | AFR | ACB | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | MSL | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | USA | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | USA | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | LWK | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| NA21309 | hp2 | a0001 | c0010 | t0004 | g0207 | AFR | LWK | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0157 | REF | REF | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0002 | REF | REF | GAB4_chr22_16956936_17013222 | GAB4 | chr22 | 16956936 | 17013222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:16965233 | C | A | 1 | a0002 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1324G>T | p.Val442Phe | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 7/10 | 1432/2630 | 1324/1725 | 442/574 | chr22 | 16965233 | |||
| chr22:16966146 | C | G | 2 | a0004 a0006 |
12 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
missense_variant | MODERATE | c.1242G>C | p.Glu414Asp | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/10 | 1350/2630 | 1242/1725 | 414/574 | chr22 | 16966146 | |||
| chr22:16966248 | C | G | 1 | a0002 | 4 | NA18965.hp1 NA18984.hp1 NA19063.hp1 others(1): Show |
missense_variant | MODERATE | c.1140G>C | p.Gln380His | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/10 | 1248/2630 | 1140/1725 | 380/574 | chr22 | 16966248 | |||
| chr22:16970039 | C | T | 3 | a0003 a0004 a0006 |
24 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(21): Show |
missense_variant | MODERATE | c.841G>A | p.Ala281Thr | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/10 | 949/2630 | 841/1725 | 281/574 | chr22 | 16970039 | |||
| chr22:16970062 | A | G | 1 | a0003 | 12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
missense_variant | MODERATE | c.818T>C | p.Leu273Pro | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/10 | 926/2630 | 818/1725 | 273/574 | chr22 | 16970062 | |||
| chr22:16987996 | G | A | 1 | a0007 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.650C>T | p.Ser217Leu | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/10 | 758/2630 | 650/1725 | 217/574 | chr22 | 16987996 | |||
| chr22:16988028 | C | A | 1 | a0002 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.618G>T | p.Trp206Cys | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/10 | 726/2630 | 618/1725 | 206/574 | chr22 | 16988028 | |||
| chr22:16988159 | C | A | 2 | a0002 a0005 |
147 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
stop_gained | HIGH | c.487G>T | p.Gly163* | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/10 | 595/2630 | 487/1725 | 163/574 | chr22 | 16988159 | |||
| chr22:17008048 | A | G | 1 | a0005 | 2 | HG02258.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.67T>C | p.Ser23Pro | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/10 | 175/2630 | 67/1725 | 23/574 | chr22 | 17008048 | |||
| chr22:17008084 | C | T | 1 | a0008 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.31G>A | p.Glu11Lys | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/10 | 139/2630 | 31/1725 | 11/574 | chr22 | 17008084 | |||
| chr22:17008105 | G | A | 1 | a0006 | 2 | HG03041.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.10C>T | p.Pro4Ser | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/10 | 118/2630 | 10/1725 | 4/574 | chr22 | 17008105 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:16963785 | T | A | 1 | a0001c0018 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.1521A>T | p.Ser507Ser | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/10 | 1629/2630 | 1521/1725 | 507/574 | chr22 | 16963785 | |||
| chr22:16964820 | C | T | 4 | a0001c0005 a0001c0023 a0001c0024 others(1): Show |
15 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(12): Show |
synonymous_variant | LOW | c.1422G>A | p.Thr474Thr | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/10 | 1530/2630 | 1422/1725 | 474/574 | chr22 | 16964820 | |||
| chr22:16965267 | G | T | 3 | a0001c0012 a0003c0004 a0003c0020 |
14 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.1290C>A | p.Ala430Ala | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 7/10 | 1398/2630 | 1290/1725 | 430/574 | chr22 | 16965267 | |||
| chr22:16966101 | C | T | 19 | a0001c0001 a0001c0005 a0001c0007 others(16): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
splice_region_variant&synonymous_variant | LOW | c.1287G>A | p.Lys429Lys | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/10 | 1395/2630 | 1287/1725 | 429/574 | chr22 | 16966101 | |||
| chr22:16966218 | A | G | 1 | a0003c0020 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1170T>C | p.Leu390Leu | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/10 | 1278/2630 | 1170/1725 | 390/574 | chr22 | 16966218 | |||
| chr22:16966347 | C | G | 1 | a0001c0007 | 4 | HG02280.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.1041G>C | p.Val347Val | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/10 | 1149/2630 | 1041/1725 | 347/574 | chr22 | 16966347 | |||
| chr22:16987983 | G | A | 2 | a0001c0009 a0008c0016 |
4 | NA18954.hp2 NA18961.hp2 NA19066.hp1 others(1): Show |
synonymous_variant | LOW | c.663C>T | p.Ala221Ala | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/10 | 771/2630 | 663/1725 | 221/574 | chr22 | 16987983 | |||
| chr22:16988136 | G | A | 14 | a0001c0005 a0001c0007 a0001c0010 others(11): Show |
178 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(175): Show |
synonymous_variant | LOW | c.510C>T | p.His170His | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/10 | 618/2630 | 510/1725 | 170/574 | chr22 | 16988136 | |||
| chr22:16991895 | G | A | 1 | a0001c0023 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.456C>T | p.Gly152Gly | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/10 | 564/2630 | 456/1725 | 152/574 | chr22 | 16991895 | |||
| chr22:17007962 | G | C | 1 | a0001c0024 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.153C>G | p.Pro51Pro | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/10 | 261/2630 | 153/1725 | 51/574 | chr22 | 17007962 | |||
| chr22:17008055 | C | T | 1 | a0002c0017 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.60G>A | p.Ala20Ala | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/10 | 168/2630 | 60/1725 | 20/574 | chr22 | 17008055 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:16962097 | C | T | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0018t0002 others(2): Show |
107 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*636G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 636 | chr22 | 16962097 | ||||||
| chr22:16962163 | A | C | 1 | a0001c0001t0012 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 570 | chr22 | 16962163 | ||||||
| chr22:16962241 | T | C | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0018t0002 others(2): Show |
107 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*492A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 492 | chr22 | 16962241 | ||||||
| chr22:16962289 | A | G | 1 | a0002c0002t0007 | 6 | HG01074.hp1 HG01167.hp2 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*444T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 444 | chr22 | 16962289 | ||||||
| chr22:16962332 | G | A | 1 | a0001c0003t0008 | 3 | NA18990.hp1 NA18999.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*401C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 401 | chr22 | 16962332 | ||||||
| chr22:16962348 | T | A | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(14): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*385A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 385 | chr22 | 16962348 | ||||||
| chr22:16962373 | T | A | 10 | a0001c0001t0001 a0001c0001t0010 a0002c0002t0001 others(7): Show |
148 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*360A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 360 | chr22 | 16962373 | ||||||
| chr22:16962491 | G | A | 11 | a0001c0001t0001 a0002c0002t0001 a0002c0002t0007 others(8): Show |
158 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*242C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 242 | chr22 | 16962491 | ||||||
| chr22:16962677 | T | C | 3 | a0001c0005t0005 a0001c0024t0005 a0002c0013t0005 |
14 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 56 | chr22 | 16962677 | ||||||
| chr22:16962680 | C | T | 1 | a0001c0001t0011 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 10/10 | 53 | chr22 | 16962680 | ||||||
| chr22:17008195 | G | A | 1 | a0001c0003t0009 | 3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-81C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/10 | chr22 | 17008195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:16963010 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0133 a0002c0002t0002g0171 |
6 | HG02027.hp2 NA18954.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-134C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963010 | |||||||
| chr22:16963153 | C | A | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1582-277G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963153 | |||||||
| chr22:16963154 | T | A | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1582-278A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963154 | |||||||
| chr22:16963341 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0031 others(8): Show |
24 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.1581+384A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963341 | |||||||
| chr22:16963517 | C | T | 2 | a0001c0003t0003g0219 a0002c0002t0001g0187 |
2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1581+208G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963517 | |||||||
| chr22:16963530 | T | G | 1 | a0002c0002t0001g0174 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1581+195A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963530 | |||||||
| chr22:16963566 | C | T | 7 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(4): Show |
12 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+159G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963566 | |||||||
| chr22:16963632 | C | CAGCCCAG others(1): Show |
8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+85_1581+92dup others(8): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 9/9 | chr22 | 16963632 | |||||||
| chr22:16963858 | A | G | 7 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(4): Show |
12 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477-29T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16963858 | |||||||
| chr22:16964081 | C | A | 1 | a0001c0001t0004g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1477-252G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964081 | |||||||
| chr22:16964197 | G | A | 7 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(4): Show |
12 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477-368C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964197 | |||||||
| chr22:16964223 | C | T | 1 | a0001c0003t0003g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1477-394G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964223 | |||||||
| chr22:16964425 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1476+341G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964425 | |||||||
| chr22:16964461 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1476+305G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964461 | |||||||
| chr22:16964517 | G | A | 8 | a0001c0001t0002g0017 a0001c0001t0002g0033 a0001c0001t0002g0055 others(5): Show |
14 | HG00408.hp1 HG00597.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1476+249C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964517 | |||||||
| chr22:16964524 | G | A | 8 | a0001c0005t0005g0021 a0001c0005t0005g0046 a0001c0005t0005g0047 others(5): Show |
14 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1476+242C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964524 | |||||||
| chr22:16964599 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1476+167C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964599 | |||||||
| chr22:16964612 | A | C | 114 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0098 others(111): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1476+154T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964612 | |||||||
| chr22:16964750 | AC | A | 8 | a0001c0001t0004g0059 a0001c0001t0004g0101 a0001c0001t0004g0102 others(5): Show |
9 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1476+15delG | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 8/9 | chr22 | 16964750 | |||||||
| chr22:16964943 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1380-81A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 7/9 | chr22 | 16964943 | |||||||
| chr22:16965009 | T | A | 1 | a0004c0006t0006g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1380-147A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 7/9 | chr22 | 16965009 | |||||||
| chr22:16965010 | C | T | 1 | a0001c0003t0003g0218 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1380-148G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 7/9 | chr22 | 16965010 | |||||||
| chr22:16965033 | G | A | 1 | a0001c0010t0004g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1379+145C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 7/9 | chr22 | 16965033 | |||||||
| chr22:16965279 | A | G | 1 | a0002c0014t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1289-11T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965279 | |||||||
| chr22:16965362 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1289-94G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965362 | |||||||
| chr22:16965366 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0002g0112 a0001c0001t0002g0125 others(1): Show |
9 | HG00408.hp2 HG00423.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289-98C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965366 | |||||||
| chr22:16965381 | C | G | 1 | a0002c0002t0004g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1289-113G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965381 | |||||||
| chr22:16965694 | C | T | 4 | a0002c0002t0001g0061 a0002c0002t0001g0170 a0002c0002t0001g0172 others(1): Show |
5 | HG00558.hp2 HG00621.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+406G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965694 | |||||||
| chr22:16965733 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0107 |
5 | HG02258.hp2 HG02572.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288+367T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965733 | |||||||
| chr22:16965742 | C | A | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288+358G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965742 | |||||||
| chr22:16965762 | C | A | 1 | a0002c0002t0001g0038 | 3 | NA19002.hp1 NA19057.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1288+338G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965762 | |||||||
| chr22:16965810 | C | A | 1 | a0005c0011t0001g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1288+290G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965810 | |||||||
| chr22:16965825 | G | A | 19 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0031 others(16): Show |
33 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1288+275C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965825 | |||||||
| chr22:16965935 | G | A | 5 | a0001c0001t0003g0026 a0001c0001t0003g0035 a0001c0001t0003g0048 others(2): Show |
10 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1288+165C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16965935 | |||||||
| chr22:16966016 | G | A | 19 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0031 others(16): Show |
33 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1288+84C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16966016 | |||||||
| chr22:16966024 | T | G | 63 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0015 others(60): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1288+76A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 6/9 | chr22 | 16966024 | |||||||
| chr22:16966460 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1024-96C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16966460 | |||||||
| chr22:16966548 | G | A | 174 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0098 others(171): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1024-184C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16966548 | |||||||
| chr22:16967228 | C | T | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1024-864G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967228 | |||||||
| chr22:16967253 | G | A | 197 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0098 others(194): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.1024-889C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967253 | |||||||
| chr22:16967353 | G | A | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1023+945C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967353 | |||||||
| chr22:16967377 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1023+921C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967377 | |||||||
| chr22:16967388 | G | A | 1 | a0001c0003t0003g0071 | 2 | NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1023+910C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967388 | |||||||
| chr22:16967419 | G | A | 7 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(4): Show |
12 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1023+879C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967419 | |||||||
| chr22:16967470 | G | A | 1 | a0002c0002t0001g0193 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1023+828C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967470 | |||||||
| chr22:16967514 | C | T | 8 | a0001c0001t0004g0059 a0001c0001t0004g0101 a0001c0001t0004g0102 others(5): Show |
9 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1023+784G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967514 | |||||||
| chr22:16967528 | A | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1023+770T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967528 | |||||||
| chr22:16967539 | C | G | 1 | a0001c0001t0004g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1023+759G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967539 | |||||||
| chr22:16967571 | G | T | 1 | a0002c0002t0001g0058 | 2 | NA19004.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1023+727C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967571 | |||||||
| chr22:16967715 | C | T | 1 | a0001c0001t0004g0148 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1023+583G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967715 | |||||||
| chr22:16967853 | T | C | 1 | a0001c0001t0004g0199 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1023+445A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967853 | |||||||
| chr22:16967926 | C | T | 3 | a0001c0007t0004g0022 a0001c0010t0004g0208 a0001c0010t0004g0209 |
6 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+372G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967926 | |||||||
| chr22:16967996 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1023+302G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16967996 | |||||||
| chr22:16968104 | T | A | 1 | a0002c0002t0001g0165 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1023+194A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16968104 | |||||||
| chr22:16968186 | C | G | 199 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0098 others(196): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1023+112G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16968186 | |||||||
| chr22:16968225 | G | C | 47 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0010g0154 others(44): Show |
91 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1023+73C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 5/9 | chr22 | 16968225 | |||||||
| chr22:16968490 | A | C | 1 | a0001c0001t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.938-107T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16968490 | |||||||
| chr22:16968608 | T | C | 15 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(12): Show |
24 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.938-225A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16968608 | |||||||
| chr22:16968838 | A | C | 1 | a0001c0003t0003g0233 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.938-455T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16968838 | |||||||
| chr22:16968901 | C | T | 1 | a0002c0002t0001g0169 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.938-518G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16968901 | |||||||
| chr22:16968926 | A | G | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.938-543T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16968926 | |||||||
| chr22:16968957 | G | A | 5 | a0001c0001t0002g0015 a0001c0001t0002g0049 a0001c0001t0002g0107 others(2): Show |
9 | HG01243.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.938-574C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16968957 | |||||||
| chr22:16969063 | T | A | 1 | a0001c0001t0004g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.938-680A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969063 | |||||||
| chr22:16969167 | C | T | 2 | a0002c0002t0001g0189 a0002c0002t0001g0191 |
2 | HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.937+776G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969167 | |||||||
| chr22:16969250 | T | C | 1 | a0001c0001t0004g0042 | 3 | NA19057.hp2 NA19070.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.937+693A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969250 | |||||||
| chr22:16969255 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.937+688G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969255 | |||||||
| chr22:16969346 | C | G | 1 | a0001c0003t0003g0071 | 2 | NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.937+597G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969346 | |||||||
| chr22:16969357 | T | C | 3 | a0002c0002t0001g0010 a0002c0002t0001g0180 a0002c0017t0001g0076 |
7 | HG01358.hp1 HG02683.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+586A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969357 | |||||||
| chr22:16969625 | G | A | 73 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0122 others(70): Show |
145 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.937+318C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969625 | |||||||
| chr22:16969648 | G | A | 6 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0035 others(3): Show |
11 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.937+295C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969648 | |||||||
| chr22:16969655 | G | A | 4 | a0001c0001t0004g0059 a0001c0001t0012g0096 a0002c0002t0004g0155 others(1): Show |
5 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+288C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969655 | |||||||
| chr22:16969776 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.937+167C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969776 | |||||||
| chr22:16969875 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.937+68T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 4/9 | chr22 | 16969875 | |||||||
| chr22:16970261 | G | A | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-68C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970261 | |||||||
| chr22:16970295 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-102A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970295 | |||||||
| chr22:16970344 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.687-151A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970344 | |||||||
| chr22:16970510 | T | C | 1 | a0001c0003t0003g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.687-317A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970510 | |||||||
| chr22:16970511 | G | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0112 others(2): Show |
10 | NA18945.hp1 NA18953.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.687-318C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970511 | |||||||
| chr22:16970566 | G | C | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-373C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970566 | |||||||
| chr22:16970638 | G | A | 3 | a0001c0003t0003g0211 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG01099.hp1 HG01109.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.687-445C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970638 | |||||||
| chr22:16970723 | C | T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0145 a0001c0001t0004g0146 others(8): Show |
19 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.687-530G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970723 | |||||||
| chr22:16970820 | T | C | 25 | a0001c0001t0004g0004 a0001c0001t0004g0012 a0001c0001t0004g0013 others(22): Show |
49 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.687-627A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970820 | |||||||
| chr22:16970826 | G | A | 5 | a0001c0001t0001g0028 a0002c0002t0001g0039 a0002c0002t0001g0066 others(2): Show |
10 | HG00438.hp2 HG00544.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.687-633C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970826 | |||||||
| chr22:16970916 | C | T | 1 | a0001c0001t0004g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.687-723G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970916 | |||||||
| chr22:16970923 | C | T | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.687-730G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970923 | |||||||
| chr22:16970957 | A | G | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-764T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970957 | |||||||
| chr22:16970964 | G | C | 34 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0035 others(31): Show |
59 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.687-771C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970964 | |||||||
| chr22:16970993 | C | A | 11 | a0001c0001t0004g0004 a0001c0001t0004g0145 a0001c0001t0004g0146 others(8): Show |
19 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.687-800G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16970993 | |||||||
| chr22:16971016 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-823G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971016 | |||||||
| chr22:16971033 | C | CA | 10 | a0001c0001t0003g0099 a0001c0003t0003g0043 a0001c0003t0003g0215 others(7): Show |
17 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.687-841dupT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971033 | |||||||
| chr22:16971033 | CAAA | C | 7 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(4): Show |
11 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-843_687-841del others(3): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971033 | |||||||
| chr22:16971055 | G | A | 1 | a0002c0022t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.687-862C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971055 | |||||||
| chr22:16971072 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.687-879G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971072 | |||||||
| chr22:16971076 | G | A | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
9 | HG02486.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.687-883C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971076 | |||||||
| chr22:16971103 | A | C | 1 | a0001c0005t0005g0021 | 4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-910T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971103 | |||||||
| chr22:16971190 | C | T | 1 | a0001c0003t0003g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.687-997G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971190 | |||||||
| chr22:16971272 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0030 a0001c0001t0002g0051 others(2): Show |
14 | HG02027.hp1 NA18943.hp2 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.687-1079C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971272 | |||||||
| chr22:16971291 | T | G | 9 | a0001c0001t0004g0197 a0003c0004t0003g0024 a0003c0004t0003g0025 others(6): Show |
13 | HG00323.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.687-1098A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971291 | |||||||
| chr22:16971402 | C | T | 1 | a0001c0007t0004g0022 | 4 | HG02280.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-1209G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971402 | |||||||
| chr22:16971410 | T | G | 12 | a0001c0001t0002g0123 a0001c0001t0004g0012 a0001c0001t0004g0013 others(9): Show |
25 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.687-1217A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971410 | |||||||
| chr22:16971421 | T | C | 3 | a0001c0005t0005g0021 a0001c0005t0005g0097 a0001c0023t0003g0104 |
6 | HG02055.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-1228A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971421 | |||||||
| chr22:16971551 | A | G | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.687-1358T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971551 | |||||||
| chr22:16971578 | G | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-1385C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971578 | |||||||
| chr22:16971686 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.687-1493G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971686 | |||||||
| chr22:16971704 | G | A | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-1511C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971704 | |||||||
| chr22:16971830 | G | A | 1 | a0001c0001t0003g0128 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.687-1637C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971830 | |||||||
| chr22:16971854 | T | C | 5 | a0001c0001t0001g0098 a0001c0001t0002g0135 a0002c0002t0001g0060 others(2): Show |
7 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-1661A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971854 | |||||||
| chr22:16971882 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.687-1689G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971882 | |||||||
| chr22:16971955 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0100 |
3 | HG03209.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.687-1762T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16971955 | |||||||
| chr22:16972000 | A | G | 1 | a0002c0002t0004g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.687-1807T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972000 | |||||||
| chr22:16972012 | G | A | 1 | a0001c0003t0003g0220 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.687-1819C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972012 | |||||||
| chr22:16972035 | G | A | 199 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(196): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.687-1842C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972035 | |||||||
| chr22:16972062 | G | A | 1 | a0001c0010t0004g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.687-1869C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972062 | |||||||
| chr22:16972076 | T | C | 206 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(203): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(367): Show |
intron_variant | MODIFIER | c.687-1883A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972076 | |||||||
| chr22:16972129 | G | A | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.687-1936C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972129 | |||||||
| chr22:16972169 | G | A | 1 | a0001c0003t0003g0230 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.687-1976C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972169 | |||||||
| chr22:16972225 | A | C | 10 | a0001c0001t0004g0059 a0001c0005t0005g0021 a0001c0005t0005g0046 others(7): Show |
16 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.687-2032T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972225 | |||||||
| chr22:16972306 | G | C | 1 | a0001c0001t0004g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.687-2113C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972306 | |||||||
| chr22:16972341 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.687-2148G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972341 | |||||||
| chr22:16972564 | T | C | 1 | a0001c0003t0009g0239 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.687-2371A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972564 | |||||||
| chr22:16972578 | G | A | 8 | a0001c0001t0001g0028 a0001c0001t0002g0016 a0001c0001t0002g0029 others(5): Show |
19 | HG00438.hp2 HG01952.hp2 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.687-2385C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972578 | |||||||
| chr22:16972694 | C | T | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-2501G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972694 | |||||||
| chr22:16972698 | A | C | 172 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0098 others(169): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.687-2505T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972698 | |||||||
| chr22:16972778 | G | A | 1 | a0001c0001t0002g0051 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.687-2585C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972778 | |||||||
| chr22:16972940 | C | T | 7 | a0001c0010t0004g0207 a0001c0023t0003g0104 a0004c0006t0006g0018 others(4): Show |
12 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-2747G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972940 | |||||||
| chr22:16972949 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-2756G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972949 | |||||||
| chr22:16972954 | A | T | 65 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(62): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.687-2761T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16972954 | |||||||
| chr22:16973006 | C | G | 2 | a0002c0002t0001g0170 a0002c0002t0001g0172 |
2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.687-2813G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973006 | |||||||
| chr22:16973012 | G | A | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.687-2819C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973012 | |||||||
| chr22:16973066 | G | A | 5 | a0002c0002t0001g0039 a0002c0002t0001g0066 a0002c0002t0001g0175 others(2): Show |
8 | HG00544.hp2 HG01928.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-2873C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973066 | |||||||
| chr22:16973188 | T | C | 78 | a0001c0001t0001g0098 a0001c0001t0001g0205 a0001c0001t0010g0154 others(75): Show |
148 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.687-2995A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973188 | |||||||
| chr22:16973343 | C | T | 1 | a0002c0014t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.687-3150G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973343 | |||||||
| chr22:16973492 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-3299G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973492 | |||||||
| chr22:16973494 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-3301G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973494 | |||||||
| chr22:16973527 | G | A | 1 | a0002c0002t0004g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.687-3334C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973527 | |||||||
| chr22:16973561 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-3368A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973561 | |||||||
| chr22:16973596 | T | C | 70 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(67): Show |
127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.687-3403A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973596 | |||||||
| chr22:16973697 | C | T | 1 | a0001c0001t0004g0147 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.687-3504G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973697 | |||||||
| chr22:16973701 | T | C | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-3508A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973701 | |||||||
| chr22:16973711 | G | T | 1 | a0002c0014t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.687-3518C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973711 | |||||||
| chr22:16973766 | C | A | 1 | a0001c0001t0004g0059 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.687-3573G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973766 | |||||||
| chr22:16973805 | C | T | 64 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(61): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.687-3612G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973805 | |||||||
| chr22:16973833 | T | C | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-3640A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973833 | |||||||
| chr22:16973901 | C | T | 2 | a0001c0003t0009g0238 a0001c0003t0009g0239 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.687-3708G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16973901 | |||||||
| chr22:16974055 | G | A | 63 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(60): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.687-3862C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974055 | |||||||
| chr22:16974056 | CCAA | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-3866_687-3864d others(5): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974056 | |||||||
| chr22:16974153 | C | A | 3 | a0003c0004t0003g0088 a0003c0004t0003g0089 a0003c0004t0003g0090 |
3 | HG02698.hp2 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.687-3960G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974153 | |||||||
| chr22:16974279 | T | C | 1 | a0001c0005t0005g0021 | 4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-4086A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974279 | |||||||
| chr22:16974410 | C | A | 2 | a0002c0002t0004g0155 a0002c0002t0004g0156 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.687-4217G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974410 | |||||||
| chr22:16974501 | G | A | 9 | a0001c0005t0005g0021 a0001c0005t0005g0046 a0001c0005t0005g0047 others(6): Show |
14 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.687-4308C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974501 | |||||||
| chr22:16974700 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-4507G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974700 | |||||||
| chr22:16974740 | C | A | 202 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(199): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.687-4547G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974740 | |||||||
| chr22:16974771 | C | T | 7 | a0001c0001t0003g0026 a0001c0001t0003g0048 a0001c0001t0003g0099 others(4): Show |
10 | HG02647.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-4578G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974771 | |||||||
| chr22:16974776 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-4583T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974776 | |||||||
| chr22:16974791 | C | T | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-4598G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974791 | |||||||
| chr22:16974845 | G | A | 63 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(60): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.687-4652C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974845 | |||||||
| chr22:16974915 | G | A | 1 | a0001c0001t0012g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.687-4722C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16974915 | |||||||
| chr22:16975043 | C | T | 1 | a0001c0001t0004g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.687-4850G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975043 | |||||||
| chr22:16975074 | T | C | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-4881A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975074 | |||||||
| chr22:16975169 | C | A | 1 | a0001c0010t0004g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.687-4976G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975169 | |||||||
| chr22:16975336 | G | A | 4 | a0001c0007t0004g0022 a0001c0010t0004g0207 a0001c0010t0004g0208 others(1): Show |
7 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-5143C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975336 | |||||||
| chr22:16975480 | A | G | 203 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(200): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.687-5287T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975480 | |||||||
| chr22:16975489 | A | G | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-5296T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975489 | |||||||
| chr22:16975737 | G | A | 4 | a0002c0002t0001g0038 a0002c0002t0001g0064 a0002c0002t0001g0068 others(1): Show |
8 | HG02080.hp1 NA18939.hp2 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-5544C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975737 | |||||||
| chr22:16975752 | C | A | 191 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(188): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.687-5559G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975752 | |||||||
| chr22:16975876 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-5683G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975876 | |||||||
| chr22:16975877 | G | A | 1 | a0001c0001t0002g0034 | 3 | NA18948.hp1 NA19055.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.687-5684C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975877 | |||||||
| chr22:16975883 | A | C | 80 | a0001c0001t0001g0205 a0001c0001t0002g0116 a0001c0001t0010g0154 others(77): Show |
150 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.687-5690T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975883 | |||||||
| chr22:16975979 | TCAA | T | 1 | a0001c0007t0004g0022 | 4 | HG02280.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-5789_687-5787d others(5): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975979 | |||||||
| chr22:16975983 | C | A | 2 | a0001c0009t0003g0073 a0008c0016t0003g0075 |
3 | NA18954.hp2 NA19066.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.687-5790G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975983 | |||||||
| chr22:16975989 | C | A | 1 | a0001c0003t0003g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.687-5796G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975989 | |||||||
| chr22:16975989 | C | CA | 21 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0002g0123 others(18): Show |
35 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.687-5797dupT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16975989 | |||||||
| chr22:16976204 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-6011T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976204 | |||||||
| chr22:16976246 | T | C | 203 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(200): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.687-6053A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976246 | |||||||
| chr22:16976334 | T | C | 1 | a0001c0001t0002g0052 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.687-6141A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976334 | |||||||
| chr22:16976336 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.687-6143C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976336 | |||||||
| chr22:16976386 | C | T | 203 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(200): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.687-6193G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976386 | |||||||
| chr22:16976453 | G | C | 3 | a0001c0007t0004g0022 a0001c0010t0004g0208 a0001c0010t0004g0209 |
6 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-6260C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976453 | |||||||
| chr22:16976459 | G | A | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-6266C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976459 | |||||||
| chr22:16976548 | G | A | 2 | a0001c0010t0004g0208 a0001c0010t0004g0209 |
2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.687-6355C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976548 | |||||||
| chr22:16976682 | C | T | 4 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-6489G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976682 | |||||||
| chr22:16976871 | T | C | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.687-6678A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976871 | |||||||
| chr22:16976959 | C | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-6766G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16976959 | |||||||
| chr22:16977089 | A | G | 203 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(200): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.687-6896T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977089 | |||||||
| chr22:16977106 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.687-6913C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977106 | |||||||
| chr22:16977193 | G | T | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.687-7000C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977193 | |||||||
| chr22:16977204 | G | A | 1 | a0001c0001t0004g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.687-7011C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977204 | |||||||
| chr22:16977254 | G | A | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-7061C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977254 | |||||||
| chr22:16977348 | C | CA | 6 | a0001c0001t0002g0015 a0001c0001t0002g0049 a0001c0001t0002g0107 others(3): Show |
10 | HG02056.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-7156dupT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977348 | |||||||
| chr22:16977348 | C | CAA | 68 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(65): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.687-7157_687-7156d others(4): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977348 | |||||||
| chr22:16977428 | G | C | 1 | a0003c0004t0003g0093 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.687-7235C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977428 | |||||||
| chr22:16977455 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-7262A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977455 | |||||||
| chr22:16977685 | T | A | 1 | a0001c0003t0003g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.687-7492A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977685 | |||||||
| chr22:16977799 | T | A | 1 | a0002c0002t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.687-7606A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977799 | |||||||
| chr22:16977864 | G | C | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.687-7671C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977864 | |||||||
| chr22:16977889 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0010g0117 |
4 | HG00438.hp2 NA18612.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-7696T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977889 | |||||||
| chr22:16977923 | A | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-7730T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977923 | |||||||
| chr22:16977992 | A | AGACAC | 108 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0001g0205 others(105): Show |
202 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.687-7804_687-7800d others(7): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16977992 | |||||||
| chr22:16978072 | GA | G | 192 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(189): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.687-7880delT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978072 | |||||||
| chr22:16978126 | C | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-7933G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978126 | |||||||
| chr22:16978137 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.687-7944G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978137 | |||||||
| chr22:16978175 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-7982G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978175 | |||||||
| chr22:16978227 | A | T | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-8034T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978227 | |||||||
| chr22:16978230 | G | A | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.687-8037C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978230 | |||||||
| chr22:16978392 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-8199A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978392 | |||||||
| chr22:16978542 | C | T | 9 | a0001c0001t0002g0111 a0001c0001t0003g0026 a0001c0001t0003g0048 others(6): Show |
12 | HG01109.hp1 HG02647.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-8349G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978542 | |||||||
| chr22:16978656 | G | C | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.687-8463C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978656 | |||||||
| chr22:16978679 | TTG | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-8488_687-8487d others(4): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978679 | |||||||
| chr22:16978805 | T | C | 2 | a0002c0002t0007g0065 a0002c0002t0007g0168 |
3 | HG01168.hp2 HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.687-8612A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978805 | |||||||
| chr22:16978878 | T | C | 11 | a0001c0001t0001g0198 a0001c0001t0004g0012 a0001c0001t0004g0013 others(8): Show |
22 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.687-8685A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978878 | |||||||
| chr22:16978901 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.687-8708G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978901 | |||||||
| chr22:16978941 | T | A | 1 | a0001c0001t0002g0030 | 3 | NA18990.hp2 NA19012.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.687-8748A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978941 | |||||||
| chr22:16978947 | T | C | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.687-8754A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16978947 | |||||||
| chr22:16979229 | G | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0100 |
3 | HG03209.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.686+8731C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16979229 | |||||||
| chr22:16979571 | A | G | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.686+8389T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16979571 | |||||||
| chr22:16979573 | C | T | 1 | a0001c0003t0003g0071 | 2 | NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.686+8387G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16979573 | |||||||
| chr22:16979750 | C | T | 1 | a0002c0002t0001g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.686+8210G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16979750 | |||||||
| chr22:16979989 | C | T | 1 | a0001c0003t0003g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.686+7971G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16979989 | |||||||
| chr22:16980019 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+7941A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980019 | |||||||
| chr22:16980240 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+7720T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980240 | |||||||
| chr22:16980391 | C | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+7569G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980391 | |||||||
| chr22:16980728 | T | C | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+7232A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980728 | |||||||
| chr22:16980751 | C | A | 1 | a0002c0002t0001g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.686+7209G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980751 | |||||||
| chr22:16980808 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.686+7152G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980808 | |||||||
| chr22:16980809 | G | A | 7 | a0001c0005t0005g0021 a0001c0005t0005g0046 a0001c0005t0005g0047 others(4): Show |
12 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+7151C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980809 | |||||||
| chr22:16980885 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.686+7075A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980885 | |||||||
| chr22:16980910 | G | A | 1 | a0002c0002t0004g0202 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.686+7050C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980910 | |||||||
| chr22:16980923 | C | G | 1 | a0001c0001t0002g0125 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.686+7037G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980923 | |||||||
| chr22:16980993 | A | T | 4 | a0001c0001t0004g0012 a0001c0001t0004g0069 a0001c0001t0004g0197 others(1): Show |
9 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.686+6967T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980993 | |||||||
| chr22:16980995 | C | T | 4 | a0001c0007t0004g0022 a0001c0010t0004g0207 a0001c0010t0004g0208 others(1): Show |
7 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.686+6965G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16980995 | |||||||
| chr22:16981024 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+6936C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981024 | |||||||
| chr22:16981171 | A | G | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.686+6789T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981171 | |||||||
| chr22:16981222 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0115 |
4 | NA18948.hp1 NA19054.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+6738G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981222 | |||||||
| chr22:16981224 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+6736A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981224 | |||||||
| chr22:16981295 | C | A | 201 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(198): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.686+6665G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981295 | |||||||
| chr22:16981555 | A | C | 1 | a0002c0002t0001g0060 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.686+6405T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981555 | |||||||
| chr22:16981590 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.686+6370G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981590 | |||||||
| chr22:16981767 | G | T | 1 | a0001c0001t0004g0146 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.686+6193C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981767 | |||||||
| chr22:16981857 | T | G | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.686+6103A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981857 | |||||||
| chr22:16981946 | T | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | NA18952.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.686+6014A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16981946 | |||||||
| chr22:16982005 | C | T | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.686+5955G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982005 | |||||||
| chr22:16982084 | C | A | 1 | a0002c0008t0001g0084 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.686+5876G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982084 | |||||||
| chr22:16982196 | G | T | 1 | a0001c0001t0002g0027 | 3 | HG00621.hp2 HG02165.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.686+5764C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982196 | |||||||
| chr22:16982242 | C | T | 1 | a0002c0022t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.686+5718G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982242 | |||||||
| chr22:16982248 | T | C | 1 | a0002c0002t0001g0182 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.686+5712A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982248 | |||||||
| chr22:16982284 | A | G | 1 | a0003c0004t0003g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.686+5676T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982284 | |||||||
| chr22:16982286 | A | T | 1 | a0002c0002t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.686+5674T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982286 | |||||||
| chr22:16982287 | A | T | 1 | a0002c0002t0001g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.686+5673T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982287 | |||||||
| chr22:16982297 | G | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+5663C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982297 | |||||||
| chr22:16982299 | T | C | 19 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0003g0026 others(16): Show |
33 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.686+5661A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982299 | |||||||
| chr22:16982300 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+5660C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982300 | |||||||
| chr22:16982349 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+5611T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982349 | |||||||
| chr22:16982373 | T | C | 1 | a0001c0001t0004g0199 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.686+5587A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982373 | |||||||
| chr22:16982475 | TCAA | T | 6 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0064 others(3): Show |
12 | HG01928.hp2 HG01943.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+5482_686+5484d others(5): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982475 | |||||||
| chr22:16982730 | A | C | 19 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0003g0026 others(16): Show |
33 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.686+5230T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982730 | |||||||
| chr22:16982854 | C | G | 2 | a0004c0006t0006g0056 a0004c0006t0006g0142 |
3 | HG02615.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.686+5106G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982854 | |||||||
| chr22:16982890 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+5070C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982890 | |||||||
| chr22:16982910 | G | A | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.686+5050C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982910 | |||||||
| chr22:16982950 | G | A | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.686+5010C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982950 | |||||||
| chr22:16982955 | T | C | 1 | a0005c0011t0001g0078 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.686+5005A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16982955 | |||||||
| chr22:16983018 | C | T | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+4942G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983018 | |||||||
| chr22:16983137 | G | A | 5 | a0002c0002t0001g0036 a0002c0002t0001g0173 a0002c0002t0001g0187 others(2): Show |
7 | HG01106.hp1 HG01496.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.686+4823C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983137 | |||||||
| chr22:16983139 | C | G | 3 | a0002c0002t0001g0039 a0002c0002t0001g0175 a0002c0002t0002g0176 |
5 | HG00544.hp2 HG01928.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.686+4821G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983139 | |||||||
| chr22:16983147 | T | C | 1 | a0001c0001t0004g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.686+4813A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983147 | |||||||
| chr22:16983157 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+4803C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983157 | |||||||
| chr22:16983178 | C | T | 1 | a0002c0002t0001g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.686+4782G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983178 | |||||||
| chr22:16983327 | C | T | 2 | a0002c0002t0007g0065 a0002c0002t0007g0168 |
3 | HG01168.hp2 HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.686+4633G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983327 | |||||||
| chr22:16983773 | CCTAT | C | 1 | a0002c0002t0001g0019 | 4 | NA18967.hp2 NA19010.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+4183_686+4186d others(6): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983773 | |||||||
| chr22:16983814 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+4146C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983814 | |||||||
| chr22:16983949 | A | G | 78 | a0001c0001t0001g0205 a0001c0005t0005g0021 a0002c0002t0001g0003 others(75): Show |
151 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.686+4011T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16983949 | |||||||
| chr22:16984034 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+3926T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984034 | |||||||
| chr22:16984078 | T | C | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.686+3882A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984078 | |||||||
| chr22:16984174 | T | C | 1 | a0001c0001t0004g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.686+3786A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984174 | |||||||
| chr22:16984218 | G | A | 77 | a0001c0005t0005g0021 a0002c0002t0001g0003 a0002c0002t0001g0005 others(74): Show |
150 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.686+3742C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984218 | |||||||
| chr22:16984221 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+3739T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984221 | |||||||
| chr22:16984285 | A | G | 78 | a0001c0001t0001g0205 a0001c0005t0005g0021 a0002c0002t0001g0003 others(75): Show |
151 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.686+3675T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984285 | |||||||
| chr22:16984318 | G | C | 1 | a0006c0015t0006g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.686+3642C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984318 | |||||||
| chr22:16984346 | T | C | 3 | a0002c0002t0001g0007 a0002c0002t0001g0009 a0002c0002t0001g0166 |
13 | NA18945.hp2 NA18962.hp1 NA18978.hp1 others(10): Show |
intron_variant | MODIFIER | c.686+3614A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984346 | |||||||
| chr22:16984459 | A | G | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+3501T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984459 | |||||||
| chr22:16984724 | G | A | 1 | a0001c0001t0004g0031 | 3 | HG00408.hp2 HG00423.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.686+3236C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984724 | |||||||
| chr22:16984775 | G | C | 1 | a0001c0001t0002g0032 | 3 | NA18969.hp1 NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.686+3185C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984775 | |||||||
| chr22:16984789 | C | T | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+3171G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984789 | |||||||
| chr22:16984949 | G | A | 4 | a0001c0007t0004g0022 a0001c0010t0004g0207 a0001c0010t0004g0208 others(1): Show |
7 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.686+3011C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984949 | |||||||
| chr22:16984958 | C | A | 1 | a0001c0001t0002g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.686+3002G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16984958 | |||||||
| chr22:16985009 | T | C | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+2951A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985009 | |||||||
| chr22:16985046 | G | A | 1 | a0002c0022t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.686+2914C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985046 | |||||||
| chr22:16985109 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.686+2851A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985109 | |||||||
| chr22:16985118 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+2842C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985118 | |||||||
| chr22:16985359 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+2601T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985359 | |||||||
| chr22:16985489 | G | T | 1 | a0001c0001t0004g0145 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.686+2471C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985489 | |||||||
| chr22:16985601 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+2359A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985601 | |||||||
| chr22:16985787 | G | T | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.686+2173C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985787 | |||||||
| chr22:16985893 | A | T | 4 | a0001c0007t0004g0022 a0001c0010t0004g0207 a0001c0010t0004g0208 others(1): Show |
7 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.686+2067T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985893 | |||||||
| chr22:16985900 | G | T | 1 | a0001c0001t0002g0133 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.686+2060C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16985900 | |||||||
| chr22:16986028 | G | A | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+1932C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986028 | |||||||
| chr22:16986183 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+1777T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986183 | |||||||
| chr22:16986253 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(1): Show |
7 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.686+1707G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986253 | |||||||
| chr22:16986254 | C | A | 4 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(1): Show |
7 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.686+1706G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986254 | |||||||
| chr22:16986267 | T | A | 1 | a0002c0002t0001g0174 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.686+1693A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986267 | |||||||
| chr22:16986305 | C | T | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+1655G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986305 | |||||||
| chr22:16986337 | G | A | 1 | a0001c0001t0002g0055 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.686+1623C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986337 | |||||||
| chr22:16986514 | G | A | 1 | a0001c0001t0004g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.686+1446C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986514 | |||||||
| chr22:16986521 | G | A | 11 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(8): Show |
21 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.686+1439C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986521 | |||||||
| chr22:16986545 | T | C | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.686+1415A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986545 | |||||||
| chr22:16986584 | C | A | 202 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(199): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.686+1376G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986584 | |||||||
| chr22:16986643 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.686+1317A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986643 | |||||||
| chr22:16986794 | G | A | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.686+1166C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986794 | |||||||
| chr22:16986876 | G | A | 1 | a0001c0001t0003g0128 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.686+1084C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986876 | |||||||
| chr22:16986933 | G | A | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+1027C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16986933 | |||||||
| chr22:16987003 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.686+957C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987003 | |||||||
| chr22:16987077 | A | G | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.686+883T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987077 | |||||||
| chr22:16987085 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+875A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987085 | |||||||
| chr22:16987106 | C | T | 1 | a0002c0014t0003g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.686+854G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987106 | |||||||
| chr22:16987494 | G | T | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.686+466C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987494 | |||||||
| chr22:16987801 | G | C | 2 | a0001c0003t0003g0213 a0001c0003t0003g0214 |
2 | NA18948.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.686+159C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987801 | |||||||
| chr22:16987925 | G | A | 8 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(5): Show |
11 | HG02280.hp1 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.686+35C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 3/9 | chr22 | 16987925 | |||||||
| chr22:16988280 | C | T | 1 | a0001c0001t0002g0050 | 2 | HG02155.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.479-113G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988280 | |||||||
| chr22:16988418 | G | T | 1 | a0001c0003t0003g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.479-251C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988418 | |||||||
| chr22:16988420 | C | T | 76 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(73): Show |
146 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.479-253G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988420 | |||||||
| chr22:16988423 | C | G | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-256G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988423 | |||||||
| chr22:16988486 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.479-319C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988486 | |||||||
| chr22:16988621 | T | C | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.479-454A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988621 | |||||||
| chr22:16988668 | T | C | 5 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0138 others(2): Show |
5 | HG00099.hp2 HG01243.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-501A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988668 | |||||||
| chr22:16988774 | G | A | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.479-607C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988774 | |||||||
| chr22:16988802 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.479-635G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988802 | |||||||
| chr22:16988884 | C | T | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.479-717G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16988884 | |||||||
| chr22:16989119 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.479-952T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989119 | |||||||
| chr22:16989431 | G | C | 5 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0064 others(2): Show |
11 | HG01928.hp2 HG01943.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.479-1264C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989431 | |||||||
| chr22:16989558 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.479-1391C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989558 | |||||||
| chr22:16989716 | G | A | 1 | a0001c0012t0003g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.479-1549C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989716 | |||||||
| chr22:16989721 | T | C | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-1554A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989721 | |||||||
| chr22:16989806 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.479-1639C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989806 | |||||||
| chr22:16989837 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.479-1670G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989837 | |||||||
| chr22:16989889 | C | A | 53 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(50): Show |
95 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.479-1722G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16989889 | |||||||
| chr22:16990071 | C | G | 2 | a0001c0005t0005g0079 a0001c0005t0005g0091 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.478+1802G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990071 | |||||||
| chr22:16990097 | C | G | 1 | a0001c0001t0002g0113 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.478+1776G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990097 | |||||||
| chr22:16990253 | G | A | 1 | a0002c0002t0001g0020 | 4 | NA18953.hp2 NA18968.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+1620C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990253 | |||||||
| chr22:16990263 | T | A | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+1610A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990263 | |||||||
| chr22:16990464 | C | T | 64 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(61): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.478+1409G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990464 | |||||||
| chr22:16990468 | T | C | 1 | a0002c0002t0001g0081 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.478+1405A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990468 | |||||||
| chr22:16990479 | A | G | 3 | a0001c0007t0004g0022 a0001c0010t0004g0208 a0001c0010t0004g0209 |
6 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+1394T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990479 | |||||||
| chr22:16990547 | AC | A | 3 | a0001c0007t0004g0022 a0001c0010t0004g0208 a0001c0010t0004g0209 |
6 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.478+1325delG | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990547 | |||||||
| chr22:16990699 | T | C | 4 | a0001c0007t0004g0022 a0001c0010t0004g0207 a0001c0010t0004g0208 others(1): Show |
7 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+1174A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990699 | |||||||
| chr22:16990724 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478+1149G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990724 | |||||||
| chr22:16990739 | C | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478+1134G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990739 | |||||||
| chr22:16990897 | A | G | 1 | a0002c0002t0001g0174 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.478+976T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990897 | |||||||
| chr22:16990961 | T | C | 9 | a0001c0001t0010g0154 a0002c0002t0001g0080 a0002c0002t0001g0081 others(6): Show |
10 | HG02129.hp1 HG02698.hp1 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+912A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16990961 | |||||||
| chr22:16991020 | T | C | 1 | a0003c0004t0003g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.478+853A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991020 | |||||||
| chr22:16991024 | G | C | 6 | a0001c0001t0002g0017 a0001c0001t0002g0033 a0001c0001t0002g0055 others(3): Show |
12 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.478+849C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991024 | |||||||
| chr22:16991134 | A | G | 1 | a0001c0003t0003g0215 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.478+739T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991134 | |||||||
| chr22:16991142 | A | T | 53 | a0001c0001t0010g0154 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
100 | HG00558.hp2 HG00621.hp1 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.478+731T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991142 | |||||||
| chr22:16991181 | A | G | 203 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(200): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.478+692T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991181 | |||||||
| chr22:16991243 | A | G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0049 a0001c0001t0002g0107 others(2): Show |
9 | HG01243.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.478+630T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991243 | |||||||
| chr22:16991244 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.478+629A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991244 | |||||||
| chr22:16991301 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478+572A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991301 | |||||||
| chr22:16991313 | G | GA | 8 | a0001c0001t0002g0111 a0001c0001t0004g0059 a0001c0003t0009g0238 others(5): Show |
9 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.478+559dupT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991313 | |||||||
| chr22:16991313 | G | GAA | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478+558_478+559dup others(2): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991313 | |||||||
| chr22:16991313 | GA | G | 12 | a0001c0001t0002g0107 a0001c0001t0004g0196 a0002c0002t0001g0005 others(9): Show |
26 | HG00741.hp2 HG01081.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.478+559delT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991313 | |||||||
| chr22:16991349 | A | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.478+524T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 2/9 | chr22 | 16991349 | |||||||
| chr22:16992181 | G | C | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.175-5C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992181 | |||||||
| chr22:16992267 | C | T | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-91G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992267 | |||||||
| chr22:16992306 | CCA | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-132_175-131del others(2): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992306 | |||||||
| chr22:16992339 | A | G | 15 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(12): Show |
48 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.175-163T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992339 | |||||||
| chr22:16992501 | G | A | 1 | a0001c0023t0003g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.175-325C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992501 | |||||||
| chr22:16992588 | C | G | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.175-412G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992588 | |||||||
| chr22:16992838 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-662G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992838 | |||||||
| chr22:16992854 | T | A | 1 | a0001c0001t0003g0035 | 3 | HG01891.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.175-678A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992854 | |||||||
| chr22:16992998 | G | C | 19 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0001t0003g0026 others(16): Show |
33 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.175-822C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16992998 | |||||||
| chr22:16993151 | A | G | 1 | a0001c0001t0004g0069 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.175-975T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993151 | |||||||
| chr22:16993166 | A | G | 1 | a0001c0005t0005g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.175-990T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993166 | |||||||
| chr22:16993290 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.175-1114C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993290 | |||||||
| chr22:16993347 | C | T | 1 | a0002c0014t0001g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.175-1171G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993347 | |||||||
| chr22:16993373 | C | T | 1 | a0002c0002t0004g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.175-1197G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993373 | |||||||
| chr22:16993436 | G | C | 1 | a0001c0001t0002g0054 | 2 | NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.175-1260C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993436 | |||||||
| chr22:16993683 | G | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-1507C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993683 | |||||||
| chr22:16993724 | A | C | 1 | a0001c0001t0002g0112 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.175-1548T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993724 | |||||||
| chr22:16993799 | C | A | 5 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(2): Show |
7 | HG02559.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-1623G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993799 | |||||||
| chr22:16993799 | C | G | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.175-1623G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993799 | |||||||
| chr22:16993801 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-1625A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993801 | |||||||
| chr22:16993843 | A | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-1667T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993843 | |||||||
| chr22:16993883 | C | T | 1 | a0002c0002t0001g0009 | 5 | NA18988.hp2 NA18993.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-1707G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993883 | |||||||
| chr22:16993922 | A | G | 206 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(203): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.175-1746T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16993922 | |||||||
| chr22:16994112 | C | T | 1 | a0001c0003t0003g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-1936G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994112 | |||||||
| chr22:16994124 | A | G | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-1948T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994124 | |||||||
| chr22:16994160 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-1984A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994160 | |||||||
| chr22:16994220 | C | T | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.175-2044G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994220 | |||||||
| chr22:16994301 | C | T | 1 | a0002c0002t0001g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175-2125G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994301 | |||||||
| chr22:16994343 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(1): Show |
7 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-2167A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994343 | |||||||
| chr22:16994423 | A | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-2247T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994423 | |||||||
| chr22:16994436 | C | G | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.175-2260G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994436 | |||||||
| chr22:16994446 | G | A | 1 | a0002c0002t0001g0182 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.175-2270C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994446 | |||||||
| chr22:16994516 | T | C | 1 | a0002c0002t0001g0011 | 5 | HG01952.hp1 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-2340A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994516 | |||||||
| chr22:16994764 | A | G | 5 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(2): Show |
7 | HG02559.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-2588T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994764 | |||||||
| chr22:16994896 | A | C | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-2720T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994896 | |||||||
| chr22:16994930 | C | T | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-2754G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16994930 | |||||||
| chr22:16995031 | T | C | 60 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(57): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.175-2855A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995031 | |||||||
| chr22:16995174 | T | C | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.175-2998A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995174 | |||||||
| chr22:16995186 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-3010C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995186 | |||||||
| chr22:16995256 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.175-3080G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995256 | |||||||
| chr22:16995257 | G | A | 6 | a0001c0001t0002g0017 a0001c0001t0002g0033 a0001c0001t0002g0055 others(3): Show |
12 | HG00408.hp1 HG00597.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.175-3081C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995257 | |||||||
| chr22:16995391 | T | A | 3 | a0001c0007t0004g0022 a0001c0010t0004g0208 a0001c0010t0004g0209 |
6 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-3215A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995391 | |||||||
| chr22:16995648 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-3472G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995648 | |||||||
| chr22:16995689 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(1): Show |
7 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-3513G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995689 | |||||||
| chr22:16995806 | T | C | 2 | a0001c0012t0003g0223 a0001c0012t0003g0224 |
2 | HG00140.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.175-3630A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995806 | |||||||
| chr22:16995812 | A | C | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.175-3636T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995812 | |||||||
| chr22:16995952 | A | G | 1 | a0001c0001t0004g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.175-3776T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16995952 | |||||||
| chr22:16996185 | G | C | 1 | a0001c0001t0004g0059 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.175-4009C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996185 | |||||||
| chr22:16996380 | T | C | 1 | a0001c0010t0004g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.175-4204A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996380 | |||||||
| chr22:16996452 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0003g0026 |
4 | HG02280.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-4276T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996452 | |||||||
| chr22:16996644 | G | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-4468C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996644 | |||||||
| chr22:16996681 | C | CT | 2 | a0002c0002t0001g0058 a0002c0002t0001g0193 |
3 | NA19004.hp1 NA19004.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.175-4506dupA | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996681 | |||||||
| chr22:16996699 | A | G | 94 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(91): Show |
165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.175-4523T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996699 | |||||||
| chr22:16996816 | T | C | 202 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(199): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.175-4640A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996816 | |||||||
| chr22:16996878 | T | C | 1 | a0001c0003t0003g0226 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.175-4702A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996878 | |||||||
| chr22:16996969 | T | C | 3 | a0001c0003t0003g0211 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG01099.hp1 HG01109.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.175-4793A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16996969 | |||||||
| chr22:16997041 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-4865A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997041 | |||||||
| chr22:16997114 | G | C | 1 | a0003c0004t0003g0025 | 3 | HG01070.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.175-4938C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997114 | |||||||
| chr22:16997167 | G | A | 1 | a0001c0001t0004g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.175-4991C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997167 | |||||||
| chr22:16997308 | G | A | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-5132C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997308 | |||||||
| chr22:16997458 | G | C | 1 | a0001c0001t0002g0136 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.175-5282C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997458 | |||||||
| chr22:16997479 | T | G | 1 | a0001c0001t0002g0137 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.175-5303A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997479 | |||||||
| chr22:16997678 | T | C | 1 | a0001c0001t0003g0105 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.175-5502A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997678 | |||||||
| chr22:16997699 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-5523A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997699 | |||||||
| chr22:16997781 | C | A | 9 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(6): Show |
13 | HG02280.hp1 HG02486.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.175-5605G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997781 | |||||||
| chr22:16997832 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-5656T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997832 | |||||||
| chr22:16997838 | G | A | 11 | a0001c0001t0001g0198 a0001c0001t0004g0012 a0001c0001t0004g0013 others(8): Show |
22 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.175-5662C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16997838 | |||||||
| chr22:16998126 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-5950G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998126 | |||||||
| chr22:16998162 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-5986A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998162 | |||||||
| chr22:16998171 | A | G | 2 | a0001c0003t0003g0070 a0001c0003t0003g0074 |
4 | HG01069.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-5995T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998171 | |||||||
| chr22:16998277 | G | T | 1 | a0001c0001t0004g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.175-6101C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998277 | |||||||
| chr22:16998278 | C | G | 1 | a0001c0001t0004g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.175-6102G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998278 | |||||||
| chr22:16998282 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-6106C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998282 | |||||||
| chr22:16998359 | C | A | 1 | a0001c0001t0004g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.175-6183G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998359 | |||||||
| chr22:16998360 | T | C | 1 | a0001c0001t0004g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.175-6184A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998360 | |||||||
| chr22:16998396 | T | C | 1 | a0002c0002t0004g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-6220A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998396 | |||||||
| chr22:16998510 | G | T | 64 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(61): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.175-6334C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998510 | |||||||
| chr22:16998837 | T | C | 1 | a0002c0002t0004g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.175-6661A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998837 | |||||||
| chr22:16998952 | G | GTA | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-6777_175-6776i others(4): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16998952 | |||||||
| chr22:16999000 | G | A | 1 | a0002c0002t0001g0185 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.175-6824C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999000 | |||||||
| chr22:16999057 | C | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-6881G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999057 | |||||||
| chr22:16999160 | G | A | 1 | a0001c0001t0003g0035 | 3 | HG01891.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.175-6984C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999160 | |||||||
| chr22:16999174 | T | A | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.175-6998A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999174 | |||||||
| chr22:16999241 | T | C | 4 | a0001c0007t0004g0022 a0001c0010t0004g0207 a0001c0010t0004g0208 others(1): Show |
7 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-7065A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999241 | |||||||
| chr22:16999308 | C | T | 77 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(74): Show |
147 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.175-7132G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999308 | |||||||
| chr22:16999397 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.175-7221T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999397 | |||||||
| chr22:16999437 | T | C | 1 | a0001c0003t0003g0227 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.175-7261A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999437 | |||||||
| chr22:16999568 | C | T | 2 | a0001c0003t0003g0232 a0001c0003t0008g0044 |
4 | NA18612.hp2 NA18990.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-7392G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999568 | |||||||
| chr22:16999605 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175-7429A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999605 | |||||||
| chr22:16999628 | G | A | 14 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(11): Show |
22 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.175-7452C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999628 | |||||||
| chr22:16999708 | G | T | 1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.175-7532C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999708 | |||||||
| chr22:16999740 | T | C | 11 | a0001c0001t0004g0059 a0003c0004t0003g0024 a0003c0004t0003g0025 others(8): Show |
16 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-7564A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999740 | |||||||
| chr22:16999840 | G | A | 1 | a0002c0002t0001g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.175-7664C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999840 | |||||||
| chr22:16999861 | A | G | 1 | a0001c0003t0003g0213 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.175-7685T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999861 | |||||||
| chr22:16999875 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-7699A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 16999875 | |||||||
| chr22:17000002 | G | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0049 a0001c0001t0002g0107 others(2): Show |
9 | HG01243.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-7826C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000002 | |||||||
| chr22:17000037 | G | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-7861C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000037 | |||||||
| chr22:17000039 | C | T | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.175-7863G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000039 | |||||||
| chr22:17000061 | C | T | 77 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(74): Show |
147 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.174+7880G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000061 | |||||||
| chr22:17000158 | T | C | 201 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(198): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.174+7783A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000158 | |||||||
| chr22:17000190 | T | A | 1 | a0006c0015t0006g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+7751A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000190 | |||||||
| chr22:17000391 | T | C | 1 | a0003c0004t0003g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.174+7550A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000391 | |||||||
| chr22:17000465 | C | CT | 13 | a0001c0001t0001g0198 a0001c0001t0002g0106 a0001c0001t0003g0105 others(10): Show |
24 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.174+7475dupA | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000465 | |||||||
| chr22:17000477 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.174+7464A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000477 | |||||||
| chr22:17000558 | A | G | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+7383T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000558 | |||||||
| chr22:17000706 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.174+7235C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000706 | |||||||
| chr22:17000918 | G | T | 3 | a0001c0007t0004g0022 a0001c0010t0004g0208 a0001c0010t0004g0209 |
6 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+7023C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17000918 | |||||||
| chr22:17001099 | A | T | 4 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+6842T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001099 | |||||||
| chr22:17001196 | G | T | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+6745C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001196 | |||||||
| chr22:17001291 | T | A | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+6650A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001291 | |||||||
| chr22:17001294 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.174+6647C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001294 | |||||||
| chr22:17001372 | G | A | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+6569C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001372 | |||||||
| chr22:17001483 | T | C | 6 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(3): Show |
8 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+6458A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001483 | |||||||
| chr22:17001512 | A | G | 1 | a0001c0001t0003g0105 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.174+6429T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001512 | |||||||
| chr22:17001605 | G | T | 6 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(3): Show |
11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+6336C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001605 | |||||||
| chr22:17001829 | C | A | 4 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+6112G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001829 | |||||||
| chr22:17001832 | C | T | 4 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+6109G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001832 | |||||||
| chr22:17001842 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.174+6099G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001842 | |||||||
| chr22:17001890 | AGCCTCGC others(69): Show |
A | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+5975_174+6050d others(78): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001890 | |||||||
| chr22:17001935 | A | G | 202 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(199): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.174+6006T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001935 | |||||||
| chr22:17001957 | C | T | 53 | a0001c0001t0001g0028 a0001c0001t0001g0122 a0001c0001t0002g0001 others(50): Show |
95 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.174+5984G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001957 | |||||||
| chr22:17001958 | G | A | 4 | a0001c0023t0003g0104 a0004c0006t0006g0018 a0004c0006t0006g0056 others(1): Show |
8 | HG01192.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+5983C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001958 | |||||||
| chr22:17001983 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.174+5958A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17001983 | |||||||
| chr22:17002107 | T | C | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+5834A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002107 | |||||||
| chr22:17002193 | T | C | 2 | a0001c0001t0003g0035 a0001c0001t0003g0152 |
4 | HG01891.hp2 HG02109.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+5748A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002193 | |||||||
| chr22:17002283 | G | A | 5 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(2): Show |
7 | HG02559.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+5658C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002283 | |||||||
| chr22:17002401 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.174+5540G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002401 | |||||||
| chr22:17002508 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.174+5433G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002508 | |||||||
| chr22:17002656 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+5285T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002656 | |||||||
| chr22:17002675 | G | C | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.174+5266C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002675 | |||||||
| chr22:17002732 | C | T | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+5209G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002732 | |||||||
| chr22:17002747 | A | G | 1 | a0001c0003t0009g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.174+5194T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002747 | |||||||
| chr22:17002829 | A | T | 1 | a0001c0001t0004g0059 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.174+5112T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002829 | |||||||
| chr22:17002832 | AAAATTAA others(32): Show |
A | 1 | a0001c0005t0005g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174+5070_174+5108d others(41): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002832 | |||||||
| chr22:17002912 | T | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+5029A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002912 | |||||||
| chr22:17002914 | AG | A | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+5026delC | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17002914 | |||||||
| chr22:17003052 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0003g0026 a0001c0001t0003g0048 others(1): Show |
7 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+4889G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003052 | |||||||
| chr22:17003063 | C | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+4878G>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003063 | |||||||
| chr22:17003076 | C | T | 1 | a0001c0003t0003g0212 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.174+4865G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003076 | |||||||
| chr22:17003081 | AG | A | 2 | a0002c0002t0001g0041 a0002c0002t0001g0058 |
5 | NA18947.hp2 NA18986.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+4859delC | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003081 | |||||||
| chr22:17003153 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+4788G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003153 | |||||||
| chr22:17003679 | A | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+4262T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003679 | |||||||
| chr22:17003688 | A | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+4253T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003688 | |||||||
| chr22:17003694 | A | G | 1 | a0003c0004t0003g0088 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.174+4247T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003694 | |||||||
| chr22:17003727 | G | C | 1 | a0001c0003t0003g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.174+4214C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003727 | |||||||
| chr22:17003760 | A | C | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+4181T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003760 | |||||||
| chr22:17003843 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0141 |
3 | HG01081.hp2 HG01261.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.174+4098A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003843 | |||||||
| chr22:17003851 | C | CA | 6 | a0001c0001t0002g0094 a0001c0001t0004g0059 a0001c0003t0003g0233 others(3): Show |
7 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+4089dupT | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17003851 | |||||||
| chr22:17004068 | T | C | 5 | a0004c0006t0006g0018 a0004c0006t0006g0056 a0004c0006t0006g0057 others(2): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+3873A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004068 | |||||||
| chr22:17004233 | G | T | 77 | a0001c0005t0005g0021 a0002c0002t0001g0003 a0002c0002t0001g0005 others(74): Show |
150 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.174+3708C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004233 | |||||||
| chr22:17004317 | A | G | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.174+3624T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004317 | |||||||
| chr22:17004385 | T | C | 3 | a0003c0004t0003g0088 a0003c0004t0003g0089 a0003c0004t0003g0090 |
3 | HG02698.hp2 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.174+3556A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004385 | |||||||
| chr22:17004446 | C | A | 2 | a0006c0015t0006g0236 a0006c0015t0006g0237 |
2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.174+3495G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004446 | |||||||
| chr22:17004447 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.174+3494C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004447 | |||||||
| chr22:17004474 | A | G | 1 | a0001c0001t0004g0059 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.174+3467T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004474 | |||||||
| chr22:17004539 | C | T | 1 | a0001c0005t0005g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.174+3402G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004539 | |||||||
| chr22:17004544 | T | A | 78 | a0001c0005t0005g0021 a0002c0002t0001g0003 a0002c0002t0001g0005 others(75): Show |
151 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.174+3397A>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004544 | |||||||
| chr22:17004596 | T | C | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+3345A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004596 | |||||||
| chr22:17004630 | G | A | 1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.174+3311C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004630 | |||||||
| chr22:17004730 | A | T | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+3211T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17004730 | |||||||
| chr22:17005147 | G | A | 3 | a0001c0005t0005g0047 a0001c0005t0005g0079 a0001c0005t0005g0091 |
4 | HG02559.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+2794C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005147 | |||||||
| chr22:17005414 | C | T | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+2527G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005414 | |||||||
| chr22:17005428 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2513T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005428 | |||||||
| chr22:17005429 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2512T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005429 | |||||||
| chr22:17005430 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2511T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005430 | |||||||
| chr22:17005431 | G | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2510C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005431 | |||||||
| chr22:17005432 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2509A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005432 | |||||||
| chr22:17005433 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2508T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005433 | |||||||
| chr22:17005434 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2507T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005434 | |||||||
| chr22:17005435 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2506A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005435 | |||||||
| chr22:17005436 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2505A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005436 | |||||||
| chr22:17005437 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2504A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005437 | |||||||
| chr22:17005438 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2503T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005438 | |||||||
| chr22:17005440 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2501T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005440 | |||||||
| chr22:17005442 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2499T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005442 | |||||||
| chr22:17005443 | T | C | 80 | a0001c0001t0010g0154 a0001c0005t0005g0021 a0002c0002t0001g0003 others(77): Show |
154 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.174+2498A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005443 | |||||||
| chr22:17005444 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2497A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005444 | |||||||
| chr22:17005446 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2495T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005446 | |||||||
| chr22:17005453 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2488A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005453 | |||||||
| chr22:17005454 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2487A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005454 | |||||||
| chr22:17005457 | A | G | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2484T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005457 | |||||||
| chr22:17005458 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2483T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005458 | |||||||
| chr22:17005459 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2482A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005459 | |||||||
| chr22:17005461 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2480T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005461 | |||||||
| chr22:17005462 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2479T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005462 | |||||||
| chr22:17005462 | A | G | 8 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0087 others(5): Show |
12 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+2479T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005462 | |||||||
| chr22:17005463 | G | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2478C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005463 | |||||||
| chr22:17005466 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2475T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005466 | |||||||
| chr22:17005469 | A | T | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2472T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005469 | |||||||
| chr22:17005470 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2471A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005470 | |||||||
| chr22:17005472 | G | GCCCCTCC others(74): Show |
1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2468_174+2469i others(83): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005472 | |||||||
| chr22:17005473 | A | C | 1 | a0002c0002t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.174+2468T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005473 | |||||||
| chr22:17005483 | C | T | 1 | a0001c0010t0004g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+2458G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005483 | |||||||
| chr22:17005631 | T | C | 6 | a0002c0002t0001g0189 a0002c0002t0001g0190 a0002c0002t0001g0191 others(3): Show |
7 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+2310A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005631 | |||||||
| chr22:17005711 | T | C | 1 | a0001c0003t0003g0234 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.174+2230A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005711 | |||||||
| chr22:17005728 | G | A | 1 | a0001c0003t0003g0074 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.174+2213C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005728 | |||||||
| chr22:17005757 | C | A | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.174+2184G>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005757 | |||||||
| chr22:17005817 | C | T | 2 | a0002c0002t0004g0155 a0002c0002t0004g0156 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.174+2124G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005817 | |||||||
| chr22:17005869 | G | C | 1 | a0001c0003t0003g0229 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.174+2072C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005869 | |||||||
| chr22:17005894 | G | C | 1 | a0002c0002t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.174+2047C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17005894 | |||||||
| chr22:17006047 | T | C | 10 | a0001c0001t0003g0035 a0001c0001t0003g0152 a0001c0001t0004g0004 others(7): Show |
20 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+1894A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006047 | |||||||
| chr22:17006064 | T | G | 2 | a0002c0002t0001g0068 a0002c0002t0001g0193 |
3 | HG02080.hp1 NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.174+1877A>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006064 | |||||||
| chr22:17006074 | G | A | 81 | a0001c0001t0002g0153 a0001c0001t0004g0059 a0001c0005t0005g0021 others(78): Show |
155 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.174+1867C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006074 | |||||||
| chr22:17006092 | G | A | 3 | a0001c0001t0004g0059 a0006c0015t0006g0236 a0006c0015t0006g0237 |
4 | HG02922.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+1849C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006092 | |||||||
| chr22:17006431 | T | C | 1 | a0001c0003t0003g0230 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.174+1510A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006431 | |||||||
| chr22:17006448 | C | T | 1 | a0001c0001t0012g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.174+1493G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006448 | |||||||
| chr22:17006488 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.174+1453G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006488 | |||||||
| chr22:17006586 | G | A | 4 | a0003c0004t0003g0024 a0003c0004t0003g0025 a0003c0004t0003g0093 others(1): Show |
8 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+1355C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006586 | |||||||
| chr22:17006887 | A | G | 1 | a0001c0003t0003g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+1054T>C | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006887 | |||||||
| chr22:17006888 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.174+1053G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17006888 | |||||||
| chr22:17007136 | G | C | 78 | a0001c0001t0010g0154 a0001c0005t0005g0021 a0002c0002t0001g0003 others(75): Show |
150 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.174+805C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007136 | |||||||
| chr22:17007282 | C | T | 13 | a0001c0005t0005g0046 a0001c0005t0005g0047 a0001c0005t0005g0079 others(10): Show |
19 | HG00741.hp1 HG01070.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.174+659G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007282 | |||||||
| chr22:17007305 | G | A | 76 | a0001c0005t0005g0021 a0002c0002t0001g0003 a0002c0002t0001g0005 others(73): Show |
148 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.174+636C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007305 | |||||||
| chr22:17007319 | A | C | 1 | a0002c0002t0001g0086 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.174+622T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007319 | |||||||
| chr22:17007470 | G | T | 8 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 others(5): Show |
9 | HG02698.hp1 HG03710.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+471C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007470 | |||||||
| chr22:17007484 | G | T | 1 | a0001c0005t0005g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174+457C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007484 | |||||||
| chr22:17007487 | A | T | 1 | a0001c0005t0005g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174+454T>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007487 | |||||||
| chr22:17007488 | G | GTTATGGT others(32): Show |
1 | a0001c0005t0005g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174+452_174+453ins others(39): Show |
GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007488 | |||||||
| chr22:17007489 | G | T | 1 | a0001c0005t0005g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174+452C>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007489 | |||||||
| chr22:17007515 | G | A | 1 | a0002c0002t0001g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.174+426C>T | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007515 | |||||||
| chr22:17007538 | C | T | 3 | a0001c0003t0009g0238 a0001c0003t0009g0239 a0001c0003t0009g0240 |
3 | HG02886.hp1 HG02896.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.174+403G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007538 | |||||||
| chr22:17007540 | T | C | 15 | a0001c0001t0001g0198 a0001c0001t0004g0012 a0001c0001t0004g0013 others(12): Show |
29 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.174+401A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007540 | |||||||
| chr22:17007558 | G | C | 1 | a0001c0003t0003g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.174+383C>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007558 | |||||||
| chr22:17007603 | T | C | 5 | a0001c0003t0003g0014 a0001c0003t0003g0232 a0001c0003t0003g0233 others(2): Show |
11 | HG00544.hp1 HG00673.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+338A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007603 | |||||||
| chr22:17007732 | T | C | 2 | a0002c0002t0004g0202 a0005c0011t0001g0078 |
2 | NA18522.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.174+209A>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007732 | |||||||
| chr22:17007779 | C | T | 196 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(193): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.174+162G>A | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007779 | |||||||
| chr22:17007837 | A | C | 199 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(196): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.174+104T>G | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007837 | |||||||
| chr22:17007933 | C | CG | 203 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0122 others(200): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
splice_region_variant&intron_variant | LOW | c.174+7_174+8insC | GAB4 | ENSG00000215568.9 | transcript | ENST00000400588.5 | protein_coding | 1/9 | chr22 | 17007933 |