Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2572 |
| ensemblid | ENSG00000136750.13 |
| hgncid | 4093 |
| symbol | GAD2 |
| name | glutamate decarboxylase 2 |
| refseq_nuc | NM_001134366.2 |
| refseq_prot | NP_001127838.1 |
| ensembl_nuc | ENST00000376261.8 |
| ensembl_prot | ENSP00000365437.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 26216774 |
| end | 26304558 |
| strand | + |
| ver | v1.2 |
| region | chr10:26216774-26304558 |
| region5000 | chr10:26211774-26309558 |
| regionname0 | GAD2_chr10_26216774_26304558 |
| regionname5000 | GAD2_chr10_26211774_26309558 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 585 | 286 | 82 | 57 | 110 | 9 | 26 | 80 | GAD2_chr10_26211774_26309558 | GAD2 | MASPG others(580): Show |
chr10 | 26211774 | 26309558 |
| a0002 | 0/0 | 585 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | MASPG others(580): Show |
chr10 | 26211774 | 26309558 |
| a0003 | 0/0 | 585 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | MASPG others(580): Show |
chr10 | 26211774 | 26309558 |
| a0004 | 0/0 | 585 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | MASPG others(580): Show |
chr10 | 26211774 | 26309558 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1755 | 255 | 70 | 50 | 100 | 9 | 25 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0001c0002 | 0/1 | 1755 | 17 | 0 | 5 | 10 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0001c0003 | 0/0 | 1755 | 11 | 10 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0001c0007 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0001c0008 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0001c0009 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0002c0004 | 0/0 | 1755 | 5 | 0 | 3 | 0 | 2 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0003c0005 | 0/0 | 1755 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 | ||
| a0004c0006 | 0/0 | 1755 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | ATGGC others(1750): Show |
chr10 | 26211774 | 26309558 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5389 | 83 | 15 | 16 | 43 | 2 | 7 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5384): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0002 | 1/0 | 5391 | 67 | 10 | 17 | 25 | 2 | 12 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0003 | 0/0 | 5391 | 38 | 0 | 3 | 26 | 5 | 4 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0005 | 0/0 | 5394 | 10 | 9 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5389): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0006 | 0/0 | 5391 | 11 | 0 | 7 | 3 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0007 | 0/0 | 5432 | 8 | 7 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5427): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0008 | 0/0 | 5428 | 7 | 6 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5423): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0009 | 0/0 | 5395 | 5 | 4 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0011 | 0/0 | 5395 | 4 | 3 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0012 | 0/0 | 5391 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0013 | 0/0 | 5395 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0014 | 0/0 | 5438 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5433): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0015 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5384): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0016 | 0/0 | 5395 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0017 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5385): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0018 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0019 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0020 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5385): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0021 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0022 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0023 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0024 | 0/0 | 5389 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5384): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0025 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5398): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0026 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0027 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5320): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0028 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5385): Show |
chr10 | 26211774 | 26309558 |
| a0001c0001t0031 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0002t0004 | 0/0 | 5610 | 16 | 0 | 5 | 10 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5605): Show |
chr10 | 26211774 | 26309558 |
| a0001c0002t0030 | 0/1 | 5610 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5605): Show |
chr10 | 26211774 | 26309558 |
| a0001c0003t0002 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0003t0005 | 0/0 | 5394 | 4 | 4 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5389): Show |
chr10 | 26211774 | 26309558 |
| a0001c0003t0009 | 0/0 | 5395 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0003t0010 | 0/0 | 5395 | 4 | 4 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5390): Show |
chr10 | 26211774 | 26309558 |
| a0001c0003t0015 | 0/0 | 5389 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5384): Show |
chr10 | 26211774 | 26309558 |
| a0001c0007t0012 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0008t0003 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0001c0009t0032 | 0/0 | 5388 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5383): Show |
chr10 | 26211774 | 26309558 |
| a0002c0004t0002 | 0/0 | 5391 | 2 | 0 | 0 | 0 | 2 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0002c0004t0003 | 0/0 | 5391 | 3 | 0 | 3 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0003c0005t0002 | 0/0 | 5391 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5386): Show |
chr10 | 26211774 | 26309558 |
| a0004c0006t0029 | 0/0 | 5557 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | GCACT others(5552): Show |
chr10 | 26211774 | 26309558 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0008g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0009g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0016g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0018g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0019g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0021g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0022g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0023g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0024g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0025g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0026g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0027g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0028g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0001t0031g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0002t0030g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0003t0015g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0007t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0008t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0001c0009t0032g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0002c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0002c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0002c0004t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0002c0004t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0002c0004t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0003c0005t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0003c0005t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| a0004c0006t0029g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0169 | EUR | GBR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00323 | hp2 | a0004 | c0006 | t0029 | g0116 | EUR | FIN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00438 | hp2 | a0001 | c0001 | t0025 | g0198 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0238 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0117 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0108 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0103 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0012 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01070 | hp1 | a0002 | c0004 | t0003 | g0194 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01071 | hp2 | a0002 | c0004 | t0003 | g0195 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01168 | hp1 | a0001 | c0002 | t0004 | g0114 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0035 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0115 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0064 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0242 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01243 | hp2 | a0001 | c0003 | t0015 | g0266 | AMR | PUR | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0119 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01256 | hp1 | a0002 | c0004 | t0003 | g0213 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0221 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01516 | hp1 | a0002 | c0004 | t0002 | g0192 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0232 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0220 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01517 | hp2 | a0002 | c0004 | t0002 | g0193 | EUR | IBS | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01884 | hp1 | a0001 | c0009 | t0032 | g0264 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0105 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0156 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01952 | hp2 | a0003 | c0005 | t0002 | g0225 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0172 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01981 | hp1 | a0003 | c0005 | t0002 | g0227 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0118 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0171 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0239 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02083 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02148 | hp2 | a0001 | c0008 | t0003 | g0002 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02165 | hp2 | a0001 | c0002 | t0004 | g0236 | EAS | CDX | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0265 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02293 | hp2 | a0001 | c0001 | t0031 | g0146 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0202 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0061 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0104 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02572 | hp1 | a0001 | c0003 | t0010 | g0247 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02615 | hp2 | a0001 | c0003 | t0010 | g0245 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0111 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02630 | hp1 | a0001 | c0003 | t0009 | g0248 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0112 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02735 | hp2 | a0001 | c0001 | t0021 | g0197 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0276 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02886 | hp2 | a0001 | c0003 | t0010 | g0246 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0270 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0269 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02922 | hp2 | a0001 | c0003 | t0005 | g0263 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0257 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03195 | hp1 | a0001 | c0001 | t0019 | g0106 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0249 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0267 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03225 | hp1 | a0001 | c0001 | t0023 | g0250 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03225 | hp2 | a0001 | c0003 | t0010 | g0244 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03486 | hp1 | a0001 | c0007 | t0012 | g0258 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03486 | hp2 | a0001 | c0001 | t0028 | g0279 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03516 | hp1 | a0001 | c0001 | t0017 | g0015 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0253 | AFR | ESN | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03540 | hp1 | a0001 | c0001 | t0024 | g0071 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03831 | hp1 | a0001 | c0002 | t0004 | g0240 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0203 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0271 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0075 | EAS | CHB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0099 | AFR | YRI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18965 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18988 | hp1 | a0001 | c0002 | t0004 | g0235 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18995 | hp2 | a0001 | c0001 | t0022 | g0218 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19030 | hp2 | a0001 | c0003 | t0005 | g0241 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | LWK | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19074 | hp1 | a0001 | c0002 | t0004 | g0234 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19085 | hp2 | a0001 | c0001 | t0026 | g0097 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19087 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0100 | AFR | ASW | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ASW | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | TSI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | GIH | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0275 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0058 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0268 | AFR | MSL | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0280 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0201 | AFR | USA | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0030 | g0113 | REF | REF | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0150 | REF | REF | GAD2_chr10_26211774_26309558 | GAD2 | chr10 | 26211774 | 26309558 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:26224539 | G | A | 1 | a0004 | 1 | HG00323.hp2 | missense_variant&splice_region_variant | MODERATE | c.612G>A | p.Met204Ile | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/16 | 648/5391 | 612/1758 | 204/585 | chr10 | 26224539 | |||
| chr10:26224610 | T | C | 1 | a0003 | 2 | HG01952.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.683T>C | p.Ile228Thr | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/16 | 719/5391 | 683/1758 | 228/585 | chr10 | 26224610 | |||
| chr10:26224622 | G | A | 1 | a0002 | 5 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(2): Show |
missense_variant | MODERATE | c.695G>A | p.Gly232Glu | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/16 | 731/5391 | 695/1758 | 232/585 | chr10 | 26224622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:26216842 | C | T | 2 | a0001c0003 a0001c0009 |
12 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
synonymous_variant | LOW | c.33C>T | p.Phe11Phe | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/16 | 69/5391 | 33/1758 | 11/585 | chr10 | 26216842 | |||
| chr10:26217930 | C | T | 1 | a0001c0008 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.225C>T | p.Cys75Cys | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/16 | 261/5391 | 225/1758 | 75/585 | chr10 | 26217930 | |||
| chr10:26270642 | G | C | 2 | a0001c0002 a0004c0006 |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
splice_region_variant&synonymous_variant | LOW | c.978G>C | p.Gly326Gly | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/16 | 1014/5391 | 978/1758 | 326/585 | chr10 | 26270642 | |||
| chr10:26273650 | G | A | 1 | a0001c0009 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1107G>A | p.Gly369Gly | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/16 | 1143/5391 | 1107/1758 | 369/585 | chr10 | 26273650 | |||
| chr10:26281024 | G | A | 1 | a0001c0007 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1173G>A | p.Thr391Thr | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/16 | 1209/5391 | 1173/1758 | 391/585 | chr10 | 26281024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:26301147 | C | T | 1 | a0001c0009t0032 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 186 | chr10 | 26301147 | ||||||
| chr10:26301152 | C | G | 1 | a0001c0001t0031 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 191 | chr10 | 26301152 | ||||||
| chr10:26301387 | A | T | 2 | a0001c0002t0004 a0004c0006t0029 |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*426A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 426 | chr10 | 26301387 | ||||||
| chr10:26301517 | T | C | 1 | a0001c0001t0017 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 556 | chr10 | 26301517 | ||||||
| chr10:26301566 | AT | A | 2 | a0001c0002t0004 a0004c0006t0029 |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*614delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 614 | INFO_REALIGN_3_PRIME | chr10 | 26301566 | |||||
| chr10:26301670 | A | G | 1 | a0001c0001t0028 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*709A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 709 | chr10 | 26301670 | ||||||
| chr10:26301711 | A | C | 1 | a0001c0001t0008 | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 750 | chr10 | 26301711 | ||||||
| chr10:26301720 | A | G | 1 | a0001c0001t0008 | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*759A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 759 | chr10 | 26301720 | ||||||
| chr10:26301735 | G | A | 1 | a0001c0001t0018 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 774 | chr10 | 26301735 | ||||||
| chr10:26301852 | AGATTAAA others(59): Show |
A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893_*958delATTAAA others(60): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 893 | INFO_REALIGN_3_PRIME | chr10 | 26301852 | |||||
| chr10:26301920 | C | T | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*959C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 959 | chr10 | 26301920 | ||||||
| chr10:26302005 | C | G | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0025 others(4): Show |
56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1044C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1044 | chr10 | 26302005 | ||||||
| chr10:26302081 | A | G | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(4): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1120 | chr10 | 26302081 | ||||||
| chr10:26302228 | A | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1267 | chr10 | 26302228 | ||||||
| chr10:26302229 | C | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1268 | chr10 | 26302229 | ||||||
| chr10:26302232 | A | C | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1271 | chr10 | 26302232 | ||||||
| chr10:26302257 | G | C | 1 | a0001c0001t0024 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1296G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1296 | chr10 | 26302257 | ||||||
| chr10:26302341 | C | T | 2 | a0001c0002t0004 a0004c0006t0029 |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1380C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1380 | chr10 | 26302341 | ||||||
| chr10:26302352 | G | A | 2 | a0001c0001t0013 a0001c0003t0010 |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1391 | chr10 | 26302352 | ||||||
| chr10:26302459 | C | T | 1 | a0001c0001t0023 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1498 | chr10 | 26302459 | ||||||
| chr10:26302465 | T | C | 1 | a0001c0001t0013 | 2 | HG03209.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1504T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1504 | chr10 | 26302465 | ||||||
| chr10:26302650 | G | A | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(13): Show |
120 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1689G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1689 | chr10 | 26302650 | ||||||
| chr10:26302652 | C | T | 1 | a0001c0001t0026 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1691C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1691 | chr10 | 26302652 | ||||||
| chr10:26302942 | C | T | 1 | a0001c0001t0022 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1981C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 1981 | chr10 | 26302942 | ||||||
| chr10:26302994 | A | T | 2 | a0001c0001t0009 a0001c0003t0009 |
6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2033A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2033 | chr10 | 26302994 | ||||||
| chr10:26303059 | G | T | 12 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0014 others(9): Show |
100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2098G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2098 | chr10 | 26303059 | ||||||
| chr10:26303146 | T | C | 1 | a0001c0001t0014 | 2 | HG02451.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2185T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2185 | chr10 | 26303146 | ||||||
| chr10:26303261 | G | A | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(4): Show |
23 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2300G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2300 | chr10 | 26303261 | ||||||
| chr10:26303269 | AC | A | 6 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0020 others(3): Show |
18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2312delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2312 | INFO_REALIGN_3_PRIME | chr10 | 26303269 | |||||
| chr10:26303293 | T | C | 1 | a0001c0001t0014 | 2 | HG02451.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2332T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2332 | chr10 | 26303293 | ||||||
| chr10:26303432 | G | C | 2 | a0001c0001t0015 a0001c0003t0015 |
2 | HG01243.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2471G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2471 | chr10 | 26303432 | ||||||
| chr10:26303444 | A | AAGGGAGG others(5): Show |
1 | a0001c0001t0025 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2497_*2508dupGGGA others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2509 | INFO_REALIGN_3_PRIME | chr10 | 26303444 | |||||
| chr10:26303448 | G | GAGGGAGG others(38): Show |
1 | a0001c0001t0014 | 2 | HG02451.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(41): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303448 | |||||
| chr10:26303448 | G | GAGGGAGG others(148): Show |
1 | a0004c0006t0029 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(151): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303448 | |||||
| chr10:26303448 | G | GAGGGAGG others(201): Show |
1 | a0001c0002t0004 | 16 | HG00544.hp2 HG00639.hp2 HG01168.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(204): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303448 | |||||
| chr10:26303456 | G | GAGGA | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(12): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303456 | |||||
| chr10:26303456 | G | GAGGAAGG others(34): Show |
1 | a0001c0001t0007 | 8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2498_*2499insAAGG others(37): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | INFO_REALIGN_3_PRIME | chr10 | 26303456 | |||||
| chr10:26303460 | G | A | 4 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0020 others(1): Show |
10 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2499G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2499 | chr10 | 26303460 | ||||||
| chr10:26303462 | G | A | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(12): Show |
121 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2501G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2501 | chr10 | 26303462 | ||||||
| chr10:26303466 | G | A | 4 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0020 others(1): Show |
10 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2505G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2505 | chr10 | 26303466 | ||||||
| chr10:26303468 | G | A | 3 | a0001c0001t0014 a0001c0002t0004 a0004c0006t0029 |
19 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2507G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2507 | chr10 | 26303468 | ||||||
| chr10:26303470 | A | G | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
139 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2509A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2509 | chr10 | 26303470 | ||||||
| chr10:26303476 | G | A | 14 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(11): Show |
124 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2515 | chr10 | 26303476 | ||||||
| chr10:26303480 | G | A | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(16): Show |
132 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2519G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2519 | chr10 | 26303480 | ||||||
| chr10:26303480 | G | GAGGAAGG others(1): Show |
3 | a0001c0001t0014 a0001c0002t0004 a0004c0006t0029 |
19 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2521_*2528dupGGAA others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2529 | INFO_REALIGN_3_PRIME | chr10 | 26303480 | |||||
| chr10:26303480 | G | GAGGAAGG others(30): Show |
1 | a0001c0001t0008 | 7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2528_*2529insGGAA others(33): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2529 | INFO_REALIGN_3_PRIME | chr10 | 26303480 | |||||
| chr10:26303483 | G | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2522 | chr10 | 26303483 | ||||||
| chr10:26303491 | T | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2530 | chr10 | 26303491 | ||||||
| chr10:26303493 | A | AAGGG | 2 | a0001c0002t0004 a0004c0006t0029 |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2548_*2551dupGAGG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2552 | INFO_REALIGN_3_PRIME | chr10 | 26303493 | |||||
| chr10:26303499 | G | C | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2538G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2538 | chr10 | 26303499 | ||||||
| chr10:26303511 | G | A | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2550 | chr10 | 26303511 | ||||||
| chr10:26303513 | A | G | 2 | a0001c0001t0006 a0001c0001t0027 |
12 | HG01109.hp2 HG01168.hp2 HG01934.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2552A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2552 | chr10 | 26303513 | ||||||
| chr10:26303514 | A | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2553A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2553 | chr10 | 26303514 | ||||||
| chr10:26303541 | C | T | 1 | a0001c0001t0021 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2580C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2580 | chr10 | 26303541 | ||||||
| chr10:26303656 | T | C | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0019 others(2): Show |
10 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2695T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2695 | chr10 | 26303656 | ||||||
| chr10:26303689 | G | A | 2 | a0001c0001t0012 a0001c0007t0012 |
3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2728G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2728 | chr10 | 26303689 | ||||||
| chr10:26303931 | G | A | 1 | a0001c0001t0011 | 4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2970G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 2970 | chr10 | 26303931 | ||||||
| chr10:26303980 | TTCTCTC | T | 6 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0015 others(3): Show |
89 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3031_*3036delCTCT others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 3031 | INFO_REALIGN_3_PRIME | chr10 | 26303980 | |||||
| chr10:26304014 | C | G | 2 | a0001c0001t0020 a0001c0001t0028 |
2 | HG03486.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3053C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 3053 | chr10 | 26304014 | ||||||
| chr10:26304154 | T | C | 1 | a0001c0001t0021 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3193T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 16/16 | 3193 | chr10 | 26304154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:26216893 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
splice_region_variant&intron_variant | LOW | c.76+8G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26216893 | |||||||
| chr10:26216930 | G | A | 1 | a0001c0001t0007g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.76+45G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26216930 | |||||||
| chr10:26217001 | G | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 |
4 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.76+116G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217001 | |||||||
| chr10:26217230 | G | GA | 10 | a0001c0001t0001g0014 a0001c0001t0005g0107 a0001c0001t0011g0108 others(7): Show |
10 | HG00642.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.76+355dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr10 | 26217230 | ||||||
| chr10:26217253 | G | T | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77-357G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217253 | |||||||
| chr10:26217392 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0028g0279 |
3 | HG01106.hp1 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.77-218C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217392 | |||||||
| chr10:26217455 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.77-155C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 1/15 | chr10 | 26217455 | |||||||
| chr10:26217823 | G | T | 6 | a0001c0001t0005g0107 a0001c0001t0011g0108 a0001c0001t0011g0109 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-19G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 2/15 | chr10 | 26217823 | |||||||
| chr10:26218060 | C | A | 1 | a0001c0003t0005g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286+69C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218060 | |||||||
| chr10:26218070 | G | A | 6 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0117 others(3): Show |
6 | HG00323.hp2 HG00639.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+79G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218070 | |||||||
| chr10:26218070 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.286+79G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218070 | |||||||
| chr10:26218079 | C | G | 2 | a0001c0001t0015g0100 a0001c0001t0017g0015 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.286+88C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218079 | |||||||
| chr10:26218080 | G | A | 1 | a0001c0001t0006g0120 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.286+89G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218080 | |||||||
| chr10:26218101 | A | G | 68 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.286+110A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218101 | |||||||
| chr10:26218227 | C | G | 1 | a0001c0001t0002g0233 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.286+236C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218227 | |||||||
| chr10:26218233 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.286+242C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218233 | |||||||
| chr10:26218259 | C | T | 46 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(43): Show |
47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.286+268C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218259 | |||||||
| chr10:26218295 | G | T | 6 | a0001c0001t0005g0107 a0001c0001t0011g0108 a0001c0001t0011g0109 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+304G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218295 | |||||||
| chr10:26218535 | G | GCT | 14 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
15 | HG00735.hp1 HG01099.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-492_287-491dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | ||||||
| chr10:26218535 | G | GCTCT | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0007g0103 others(12): Show |
16 | HG00642.hp2 HG01346.hp1 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.287-494_287-491dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | ||||||
| chr10:26218535 | G | GCTCTCT | 3 | a0001c0001t0001g0052 a0001c0001t0012g0105 a0001c0001t0013g0267 |
3 | HG01884.hp2 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.287-496_287-491dup others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | ||||||
| chr10:26218535 | G | GCTCTCTC others(1): Show |
9 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(6): Show |
9 | HG02559.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-498_287-491dup others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218535 | ||||||
| chr10:26218544 | C | G | 1 | a0001c0001t0003g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.287-499C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218544 | |||||||
| chr10:26218551 | T | A | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0009g0099 |
3 | HG03831.hp2 HG04199.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.287-492T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218551 | |||||||
| chr10:26218551 | T | TCA | 4 | a0001c0001t0002g0006 a0001c0001t0002g0147 a0001c0001t0002g0148 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-456_287-455dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCACA | 3 | a0001c0001t0001g0145 a0001c0001t0002g0144 a0001c0001t0031g0146 |
3 | HG01169.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.287-458_287-455dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCACACA | 10 | a0001c0001t0001g0136 a0001c0001t0002g0134 a0001c0001t0002g0135 others(7): Show |
10 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.287-460_287-455dup others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCACACAC others(3): Show |
3 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0002t0004g0234 |
3 | NA18980.hp1 NA18997.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.287-464_287-455dup others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCACACAC others(5): Show |
5 | a0001c0001t0002g0131 a0001c0001t0003g0128 a0001c0001t0003g0129 others(2): Show |
5 | HG06807.hp1 NA18964.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-466_287-455dup others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCACACAC others(9): Show |
3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | HG02083.hp2 HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.287-470_287-455dup others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCACACAC others(11): Show |
1 | a0001c0001t0002g0123 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.287-472_287-455dup others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACA | 3 | a0001c0001t0003g0222 a0001c0001t0005g0243 a0001c0001t0018g0221 |
3 | HG01346.hp2 HG01358.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.287-491_287-490ins others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(1): Show |
8 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 others(5): Show |
8 | HG01243.hp1 HG01517.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(3): Show |
14 | a0001c0001t0001g0212 a0001c0001t0002g0210 a0001c0001t0002g0211 others(11): Show |
14 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(5): Show |
40 | a0001c0001t0002g0008 a0001c0001t0002g0176 a0001c0001t0002g0177 others(37): Show |
43 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(7): Show |
19 | a0001c0001t0001g0237 a0001c0001t0002g0163 a0001c0001t0002g0164 others(16): Show |
21 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(9): Show |
8 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(5): Show |
8 | HG00738.hp2 HG01934.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(11): Show |
2 | a0001c0001t0002g0154 a0001c0001t0003g0155 |
2 | HG00741.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCACAC others(13): Show |
2 | a0001c0001t0002g0153 a0001c0001t0006g0152 |
2 | HG01109.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(20): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCCACA others(10): Show |
1 | a0001c0001t0003g0224 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.287-491_287-490ins others(17): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCAC others(3): Show |
9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(6): Show |
9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCAC others(5): Show |
8 | a0001c0001t0002g0226 a0001c0001t0002g0228 a0001c0001t0003g0229 others(5): Show |
8 | HG01952.hp2 HG01981.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCTC others(3): Show |
1 | a0001c0001t0023g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCTC others(5): Show |
1 | a0001c0001t0003g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCTC others(3): Show |
4 | a0001c0001t0011g0108 a0001c0003t0002g0265 a0001c0003t0015g0266 others(1): Show |
4 | HG00642.hp1 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-491_287-490ins others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCTC others(5): Show |
1 | a0001c0003t0005g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.287-491_287-490ins others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCTC others(7): Show |
2 | a0001c0001t0005g0261 a0001c0001t0005g0262 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | T | TCTCTCTC others(11): Show |
2 | a0001c0001t0005g0259 a0001c0001t0005g0260 |
2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.287-491_287-490ins others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218551 | TCA | T | 18 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
18 | HG00597.hp2 HG01070.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.287-456_287-455del others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr10 | 26218551 | ||||||
| chr10:26218553 | A | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.287-490A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218553 | |||||||
| chr10:26218555 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.287-488A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218555 | |||||||
| chr10:26218557 | A | T | 56 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(53): Show |
56 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.287-486A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218557 | |||||||
| chr10:26218559 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0026g0097 |
2 | NA19085.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.287-484A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218559 | |||||||
| chr10:26218666 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.287-377A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218666 | |||||||
| chr10:26218721 | A | C | 1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.287-322A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218721 | |||||||
| chr10:26218722 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.287-321C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218722 | |||||||
| chr10:26218732 | C | T | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287-311C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218732 | |||||||
| chr10:26218844 | A | G | 46 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(43): Show |
47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.287-199A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218844 | |||||||
| chr10:26218918 | C | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
171 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.287-125C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26218918 | |||||||
| chr10:26219034 | A | G | 1 | a0001c0001t0003g0207 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.287-9A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 3/15 | chr10 | 26219034 | |||||||
| chr10:26219336 | T | C | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.520+60T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219336 | |||||||
| chr10:26219400 | C | T | 1 | a0001c0003t0010g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.520+124C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219400 | |||||||
| chr10:26219522 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.520+246G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219522 | |||||||
| chr10:26219537 | A | G | 1 | a0001c0001t0003g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.520+261A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219537 | |||||||
| chr10:26219721 | C | T | 1 | a0001c0001t0012g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520+445C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219721 | |||||||
| chr10:26219769 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.520+493A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219769 | |||||||
| chr10:26219779 | C | T | 1 | a0001c0001t0006g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.520+503C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219779 | |||||||
| chr10:26219931 | G | T | 2 | a0001c0001t0002g0208 a0001c0001t0005g0214 |
2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.520+655G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26219931 | |||||||
| chr10:26220029 | A | G | 46 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(43): Show |
47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.520+753A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220029 | |||||||
| chr10:26220062 | C | T | 1 | a0001c0001t0023g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520+786C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220062 | |||||||
| chr10:26220081 | A | G | 1 | a0001c0001t0003g0222 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.520+805A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220081 | |||||||
| chr10:26220115 | C | G | 1 | a0001c0003t0005g0249 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.520+839C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220115 | |||||||
| chr10:26220123 | C | A | 1 | a0001c0001t0002g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.520+847C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220123 | |||||||
| chr10:26220182 | G | A | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.520+906G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220182 | |||||||
| chr10:26220185 | A | C | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.520+909A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220185 | |||||||
| chr10:26220342 | TTTTGCTG others(5): Show |
T | 1 | a0001c0001t0003g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.520+1069_520+1080d others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26220342 | ||||||
| chr10:26220367 | C | T | 1 | a0001c0001t0003g0206 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.520+1091C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220367 | |||||||
| chr10:26220650 | G | A | 46 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(43): Show |
47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.520+1374G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220650 | |||||||
| chr10:26220656 | G | A | 1 | a0001c0001t0016g0271 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520+1380G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220656 | |||||||
| chr10:26220690 | C | A | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.520+1414C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220690 | |||||||
| chr10:26220690 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.520+1414C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220690 | |||||||
| chr10:26220886 | G | A | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.520+1610G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220886 | |||||||
| chr10:26220917 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.520+1641C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220917 | |||||||
| chr10:26220935 | A | G | 68 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.520+1659A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26220935 | |||||||
| chr10:26221123 | C | T | 2 | a0001c0003t0005g0241 a0001c0003t0005g0249 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.520+1847C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221123 | |||||||
| chr10:26221396 | T | G | 2 | a0001c0002t0004g0114 a0001c0002t0004g0115 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.520+2120T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221396 | |||||||
| chr10:26221547 | A | G | 46 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(43): Show |
47 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.520+2271A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221547 | |||||||
| chr10:26221790 | T | C | 68 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.521-2097T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221790 | |||||||
| chr10:26221928 | G | A | 1 | a0001c0001t0003g0132 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.521-1959G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221928 | |||||||
| chr10:26221987 | T | C | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-1900T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26221987 | |||||||
| chr10:26222157 | G | A | 2 | a0001c0001t0005g0107 a0001c0001t0023g0250 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.521-1730G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222157 | |||||||
| chr10:26222160 | G | A | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.521-1727G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222160 | |||||||
| chr10:26222303 | C | T | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.521-1584C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222303 | |||||||
| chr10:26222390 | C | T | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-1497C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222390 | |||||||
| chr10:26222452 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0028g0279 |
3 | HG01106.hp1 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.521-1435G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222452 | |||||||
| chr10:26222550 | A | G | 1 | a0001c0001t0023g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.521-1337A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222550 | |||||||
| chr10:26222822 | T | C | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.521-1065T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222822 | |||||||
| chr10:26222853 | A | G | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-1034A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26222853 | |||||||
| chr10:26222931 | ATCT | A | 3 | a0001c0001t0002g0037 a0001c0001t0003g0036 a0001c0001t0026g0097 |
3 | NA18942.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.521-952_521-950del others(3): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26222931 | ||||||
| chr10:26223115 | A | G | 46 | a0001c0001t0002g0173 a0001c0001t0002g0187 a0001c0001t0002g0190 others(43): Show |
48 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.521-772A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223115 | |||||||
| chr10:26223153 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0028g0279 |
3 | HG01106.hp1 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.521-734T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223153 | |||||||
| chr10:26223435 | G | A | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-452G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223435 | |||||||
| chr10:26223446 | C | T | 15 | a0001c0001t0001g0212 a0001c0001t0002g0008 a0001c0001t0002g0166 others(12): Show |
16 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.521-441C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223446 | |||||||
| chr10:26223677 | C | T | 1 | a0001c0001t0003g0174 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.521-210C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223677 | |||||||
| chr10:26223686 | GGT | G | 53 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(50): Show |
54 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.521-186_521-185del others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26223686 | ||||||
| chr10:26223709 | A | ATG | 7 | a0001c0001t0001g0136 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG01516.hp2 HG01981.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.521-160_521-159dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26223709 | ||||||
| chr10:26223709 | ATGTG | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-162_521-159del others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr10 | 26223709 | ||||||
| chr10:26223745 | G | A | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.521-142G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 4/15 | chr10 | 26223745 | |||||||
| chr10:26224018 | A | G | 2 | a0001c0002t0004g0235 a0001c0002t0004g0238 |
2 | HG00544.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.611+41A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224018 | |||||||
| chr10:26224187 | CAA | C | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.611+213_611+214del others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr10 | 26224187 | ||||||
| chr10:26224227 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.611+250A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224227 | |||||||
| chr10:26224253 | A | T | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.611+276A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224253 | |||||||
| chr10:26224331 | A | G | 6 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.612-208A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224331 | |||||||
| chr10:26224378 | T | C | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.612-161T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 5/15 | chr10 | 26224378 | |||||||
| chr10:26224661 | A | G | 1 | a0001c0002t0004g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.724+10A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26224661 | |||||||
| chr10:26224927 | G | A | 13 | a0001c0001t0014g0104 a0001c0003t0002g0265 a0001c0003t0005g0112 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.724+276G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26224927 | |||||||
| chr10:26224990 | T | A | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.724+339T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26224990 | |||||||
| chr10:26225065 | A | ATATC | 13 | a0001c0001t0014g0104 a0001c0003t0002g0265 a0001c0003t0005g0112 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.724+417_724+420dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26225065 | ||||||
| chr10:26225114 | C | A | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+463C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225114 | |||||||
| chr10:26225118 | A | T | 2 | a0001c0001t0002g0159 a0001c0001t0003g0232 |
2 | HG00738.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.724+467A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225118 | |||||||
| chr10:26225283 | A | C | 68 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.724+632A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225283 | |||||||
| chr10:26225294 | C | A | 8 | a0001c0001t0005g0107 a0001c0001t0005g0242 a0001c0001t0005g0243 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.724+643C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225294 | |||||||
| chr10:26225400 | G | C | 1 | a0001c0001t0006g0038 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.724+749G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225400 | |||||||
| chr10:26225520 | T | G | 8 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(5): Show |
10 | HG00544.hp2 HG02080.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.724+869T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225520 | |||||||
| chr10:26225670 | C | T | 1 | a0001c0001t0003g0230 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.724+1019C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225670 | |||||||
| chr10:26225676 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.724+1025T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225676 | |||||||
| chr10:26225679 | C | A | 2 | a0001c0001t0005g0107 a0001c0001t0023g0250 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.724+1028C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225679 | |||||||
| chr10:26225902 | G | A | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.724+1251G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225902 | |||||||
| chr10:26225991 | T | A | 1 | a0001c0001t0002g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.724+1340T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26225991 | |||||||
| chr10:26226079 | A | AT | 38 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(35): Show |
39 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.724+1437dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26226079 | ||||||
| chr10:26226148 | C | T | 31 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(28): Show |
32 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.724+1497C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226148 | |||||||
| chr10:26226181 | C | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG01099.hp2 HG01109.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.724+1530C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226181 | |||||||
| chr10:26226277 | T | G | 68 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.724+1626T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226277 | |||||||
| chr10:26226323 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.724+1672C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226323 | |||||||
| chr10:26226327 | C | T | 53 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(50): Show |
54 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.724+1676C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226327 | |||||||
| chr10:26226586 | C | T | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.724+1935C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226586 | |||||||
| chr10:26226727 | A | C | 1 | a0001c0002t0004g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.724+2076A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226727 | |||||||
| chr10:26226737 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
93 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.724+2086G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226737 | |||||||
| chr10:26226745 | G | C | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.724+2094G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226745 | |||||||
| chr10:26226993 | T | C | 6 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.724+2342T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26226993 | |||||||
| chr10:26227159 | A | G | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-2503A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227159 | |||||||
| chr10:26227311 | A | G | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-2351A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227311 | |||||||
| chr10:26227588 | C | T | 68 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(65): Show |
71 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.725-2074C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227588 | |||||||
| chr10:26227649 | A | G | 1 | a0001c0001t0015g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.725-2013A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227649 | |||||||
| chr10:26227710 | C | G | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-1952C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227710 | |||||||
| chr10:26227866 | T | G | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.725-1796T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227866 | |||||||
| chr10:26227881 | A | G | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-1781A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227881 | |||||||
| chr10:26227909 | G | A | 2 | a0001c0001t0005g0107 a0001c0001t0023g0250 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.725-1753G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26227909 | |||||||
| chr10:26228048 | C | T | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.725-1614C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228048 | |||||||
| chr10:26228124 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-1538G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228124 | |||||||
| chr10:26228256 | A | G | 47 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(44): Show |
48 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.725-1406A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228256 | |||||||
| chr10:26228370 | C | G | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.725-1292C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228370 | |||||||
| chr10:26228534 | C | T | 1 | a0001c0001t0015g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.725-1128C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228534 | |||||||
| chr10:26228541 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.725-1121C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228541 | |||||||
| chr10:26228553 | C | T | 7 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-1109C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228553 | |||||||
| chr10:26228554 | G | A | 2 | a0001c0001t0005g0107 a0001c0001t0023g0250 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.725-1108G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228554 | |||||||
| chr10:26228607 | G | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.725-1055G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228607 | |||||||
| chr10:26228680 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.725-982G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228680 | |||||||
| chr10:26228852 | C | T | 3 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-810C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26228852 | |||||||
| chr10:26229005 | T | C | 21 | a0001c0001t0001g0237 a0001c0001t0009g0099 a0001c0001t0011g0108 others(18): Show |
23 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.725-657T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229005 | |||||||
| chr10:26229172 | C | T | 6 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.725-490C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229172 | |||||||
| chr10:26229196 | GA | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
123 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.725-452delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26229196 | ||||||
| chr10:26229219 | G | A | 29 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(26): Show |
31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.725-443G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229219 | |||||||
| chr10:26229236 | C | T | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.725-426C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229236 | |||||||
| chr10:26229284 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.725-378G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229284 | |||||||
| chr10:26229284 | G | GA | 28 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.725-367dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr10 | 26229284 | ||||||
| chr10:26229318 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.725-344C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229318 | |||||||
| chr10:26229469 | A | G | 29 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(26): Show |
31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.725-193A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229469 | |||||||
| chr10:26229489 | C | A | 29 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(26): Show |
31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.725-173C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229489 | |||||||
| chr10:26229489 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.725-173C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229489 | |||||||
| chr10:26229550 | T | G | 29 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(26): Show |
31 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.725-112T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 6/15 | chr10 | 26229550 | |||||||
| chr10:26229876 | T | C | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+99T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26229876 | |||||||
| chr10:26229939 | T | A | 4 | a0001c0001t0003g0128 a0001c0001t0003g0132 a0001c0001t0003g0133 others(1): Show |
4 | NA18977.hp1 NA18980.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+162T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26229939 | |||||||
| chr10:26230048 | C | CACAA | 28 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.840+273_840+274ins others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230048 | ||||||
| chr10:26230066 | G | A | 2 | a0001c0001t0012g0105 a0001c0007t0012g0258 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.840+289G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230066 | |||||||
| chr10:26230107 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.840+330G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230107 | |||||||
| chr10:26230129 | C | T | 3 | a0001c0001t0005g0107 a0001c0001t0005g0260 a0001c0001t0023g0250 |
3 | HG02280.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.840+352C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230129 | |||||||
| chr10:26230131 | A | G | 69 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(66): Show |
72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.840+354A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230131 | |||||||
| chr10:26230310 | T | C | 12 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(9): Show |
12 | HG00642.hp1 HG00642.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.840+533T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230310 | |||||||
| chr10:26230425 | T | TTTTG | 6 | a0001c0001t0002g0131 a0001c0001t0002g0140 a0001c0001t0002g0141 others(3): Show |
6 | HG00741.hp1 HG01106.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+669_840+672dup others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230425 | ||||||
| chr10:26230425 | T | TTTTGTTT others(5): Show |
1 | a0001c0001t0005g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.840+661_840+672dup others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230425 | ||||||
| chr10:26230425 | TTTTGTTT others(1): Show |
T | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.840+665_840+672del others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26230425 | ||||||
| chr10:26230670 | G | A | 28 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.840+893G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230670 | |||||||
| chr10:26230815 | C | T | 1 | a0001c0001t0006g0034 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.840+1038C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230815 | |||||||
| chr10:26230964 | A | C | 28 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.840+1187A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230964 | |||||||
| chr10:26230995 | C | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+1218C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26230995 | |||||||
| chr10:26231023 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
168 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.840+1246A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231023 | |||||||
| chr10:26231044 | C | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1267C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231044 | |||||||
| chr10:26231223 | G | C | 2 | a0001c0001t0019g0106 a0001c0001t0020g0280 |
2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.840+1446G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231223 | |||||||
| chr10:26231303 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.840+1526C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231303 | |||||||
| chr10:26231475 | C | T | 1 | a0001c0001t0003g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.840+1698C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231475 | |||||||
| chr10:26231558 | G | A | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0137 others(1): Show |
4 | HG01981.hp2 HG03017.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+1781G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231558 | |||||||
| chr10:26231578 | A | G | 28 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.840+1801A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231578 | |||||||
| chr10:26231584 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
92 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.840+1807C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231584 | |||||||
| chr10:26231588 | C | G | 8 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+1811C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231588 | |||||||
| chr10:26231621 | T | A | 1 | a0001c0001t0003g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.840+1844T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26231621 | |||||||
| chr10:26232007 | A | T | 1 | a0001c0001t0002g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.840+2230A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232007 | |||||||
| chr10:26232012 | C | T | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.840+2235C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232012 | |||||||
| chr10:26232027 | G | A | 2 | a0001c0001t0005g0107 a0001c0001t0023g0250 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.840+2250G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232027 | |||||||
| chr10:26232170 | T | C | 1 | a0001c0001t0003g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.840+2393T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232170 | |||||||
| chr10:26232223 | T | C | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.840+2446T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232223 | |||||||
| chr10:26232245 | G | A | 28 | a0001c0001t0001g0237 a0001c0001t0007g0103 a0001c0001t0007g0251 others(25): Show |
30 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.840+2468G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232245 | |||||||
| chr10:26232405 | T | C | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | NA18979.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.840+2628T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232405 | |||||||
| chr10:26232447 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.840+2670C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232447 | |||||||
| chr10:26232468 | AC | A | 3 | a0001c0001t0011g0108 a0001c0001t0011g0111 a0001c0002t0004g0238 |
3 | HG00544.hp2 HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.840+2692delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232468 | |||||||
| chr10:26232468 | ACT | A | 16 | a0001c0001t0001g0237 a0001c0001t0009g0099 a0001c0001t0011g0109 others(13): Show |
18 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+2692_840+2693d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232468 | |||||||
| chr10:26232469 | C | CT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(16): Show |
22 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.840+2715dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26232469 | ||||||
| chr10:26232469 | C | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+2692C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232469 | |||||||
| chr10:26232469 | CT | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0083 a0001c0001t0001g0087 others(23): Show |
26 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.840+2715delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26232469 | ||||||
| chr10:26232469 | CTT | C | 15 | a0001c0001t0008g0011 a0001c0001t0008g0270 a0001c0001t0015g0100 others(12): Show |
15 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+2714_840+2715d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26232469 | ||||||
| chr10:26232646 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2869G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232646 | |||||||
| chr10:26232649 | C | T | 1 | a0001c0001t0006g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.840+2872C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232649 | |||||||
| chr10:26232840 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+3063G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232840 | |||||||
| chr10:26232954 | T | G | 1 | a0001c0001t0005g0261 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.840+3177T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26232954 | |||||||
| chr10:26233031 | CT | C | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+3255delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233031 | |||||||
| chr10:26233361 | T | C | 2 | a0001c0003t0005g0241 a0001c0003t0005g0249 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.840+3584T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233361 | |||||||
| chr10:26233428 | C | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+3651C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233428 | |||||||
| chr10:26233456 | T | C | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+3679T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233456 | |||||||
| chr10:26233487 | C | T | 6 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+3710C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233487 | |||||||
| chr10:26233526 | C | T | 8 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+3749C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233526 | |||||||
| chr10:26233567 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+3790G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233567 | |||||||
| chr10:26233835 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.840+4058G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233835 | |||||||
| chr10:26233872 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.840+4095G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233872 | |||||||
| chr10:26233888 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+4111G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26233888 | |||||||
| chr10:26234046 | G | A | 8 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+4269G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234046 | |||||||
| chr10:26234052 | G | A | 1 | a0001c0001t0005g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.840+4275G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234052 | |||||||
| chr10:26234243 | G | A | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.840+4466G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234243 | |||||||
| chr10:26234278 | C | T | 8 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
8 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+4501C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234278 | |||||||
| chr10:26234335 | A | G | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+4558A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234335 | |||||||
| chr10:26234338 | C | CA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.840+4577dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | ||||||
| chr10:26234338 | C | CAA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+4576_840+4577d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | ||||||
| chr10:26234338 | CA | C | 47 | a0001c0001t0001g0212 a0001c0001t0002g0008 a0001c0001t0002g0123 others(44): Show |
48 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.840+4577delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | ||||||
| chr10:26234338 | CAA | C | 8 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0003g0175 others(5): Show |
8 | HG02559.hp1 HG02735.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+4576_840+4577d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234338 | ||||||
| chr10:26234442 | A | G | 48 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(45): Show |
50 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.840+4665A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234442 | |||||||
| chr10:26234594 | G | A | 21 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(18): Show |
21 | HG00642.hp1 HG00642.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.840+4817G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234594 | |||||||
| chr10:26234642 | A | T | 8 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(5): Show |
8 | HG02040.hp1 HG02083.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+4865A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234642 | |||||||
| chr10:26234736 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.840+4959A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234736 | |||||||
| chr10:26234772 | C | G | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+4995C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26234772 | |||||||
| chr10:26234880 | CT | C | 9 | a0001c0001t0001g0017 a0001c0001t0002g0272 a0001c0001t0002g0273 others(6): Show |
9 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.840+5113delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26234880 | ||||||
| chr10:26235089 | G | C | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | NA18979.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.840+5312G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235089 | |||||||
| chr10:26235128 | C | T | 1 | a0001c0001t0015g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.840+5351C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235128 | |||||||
| chr10:26235153 | C | T | 6 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+5376C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235153 | |||||||
| chr10:26235175 | C | T | 15 | a0001c0001t0001g0237 a0001c0002t0004g0009 a0001c0002t0004g0010 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.840+5398C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235175 | |||||||
| chr10:26235188 | T | C | 64 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(61): Show |
66 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.840+5411T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235188 | |||||||
| chr10:26235231 | C | A | 4 | a0001c0001t0005g0107 a0001c0001t0005g0260 a0001c0001t0019g0106 others(1): Show |
4 | HG02280.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+5454C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235231 | |||||||
| chr10:26235423 | T | G | 12 | a0001c0001t0014g0104 a0001c0003t0002g0265 a0001c0003t0005g0112 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.840+5646T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235423 | |||||||
| chr10:26235438 | C | G | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.840+5661C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235438 | |||||||
| chr10:26235445 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(78): Show |
83 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.840+5668G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235445 | |||||||
| chr10:26235457 | G | A | 69 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0278 others(66): Show |
72 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.840+5680G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235457 | |||||||
| chr10:26235551 | T | C | 3 | a0002c0004t0002g0192 a0002c0004t0002g0193 a0002c0004t0003g0213 |
3 | HG01256.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.840+5774T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235551 | |||||||
| chr10:26235608 | A | C | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840+5831A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235608 | |||||||
| chr10:26235684 | G | A | 17 | a0001c0001t0009g0099 a0001c0001t0011g0108 a0001c0001t0011g0109 others(14): Show |
17 | HG00642.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+5907G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235684 | |||||||
| chr10:26235877 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG01099.hp2 HG01109.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+6100C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235877 | |||||||
| chr10:26235911 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840+6134T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235911 | |||||||
| chr10:26235971 | G | A | 8 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0099 others(5): Show |
9 | HG00642.hp1 HG00735.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.840+6194G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235971 | |||||||
| chr10:26235982 | G | A | 42 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0002g0272 others(39): Show |
44 | HG00642.hp1 HG00735.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.840+6205G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26235982 | |||||||
| chr10:26236001 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
171 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.840+6224A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236001 | |||||||
| chr10:26236057 | C | T | 27 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(24): Show |
27 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.840+6280C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236057 | |||||||
| chr10:26236064 | G | A | 25 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(22): Show |
25 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.840+6287G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236064 | |||||||
| chr10:26236091 | A | G | 13 | a0001c0001t0001g0074 a0001c0001t0001g0277 a0001c0001t0001g0278 others(10): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+6314A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236091 | |||||||
| chr10:26236092 | T | G | 13 | a0001c0001t0005g0214 a0001c0001t0011g0108 a0001c0001t0011g0109 others(10): Show |
13 | HG00642.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.840+6315T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236092 | |||||||
| chr10:26236187 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.840+6410C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236187 | |||||||
| chr10:26236235 | C | G | 5 | a0001c0001t0001g0060 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG03139.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+6458C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236235 | |||||||
| chr10:26236301 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.840+6524T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236301 | |||||||
| chr10:26236302 | C | CT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
114 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.840+6540dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26236302 | ||||||
| chr10:26236302 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.840+6525C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236302 | |||||||
| chr10:26236307 | T | A | 1 | a0001c0001t0001g0017 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.840+6530T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236307 | |||||||
| chr10:26236347 | C | T | 1 | a0001c0001t0026g0097 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.840+6570C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236347 | |||||||
| chr10:26236354 | G | A | 6 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+6577G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236354 | |||||||
| chr10:26236383 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.840+6606C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236383 | |||||||
| chr10:26236394 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG00140.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.840+6617G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236394 | |||||||
| chr10:26236436 | A | G | 10 | a0001c0001t0001g0077 a0001c0001t0007g0103 a0001c0001t0007g0251 others(7): Show |
10 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+6659A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236436 | |||||||
| chr10:26236445 | C | T | 5 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(2): Show |
5 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+6668C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236445 | |||||||
| chr10:26236471 | C | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.840+6694C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236471 | |||||||
| chr10:26236490 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+6713G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236490 | |||||||
| chr10:26236590 | C | T | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.840+6813C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236590 | |||||||
| chr10:26236754 | C | G | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.840+6977C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236754 | |||||||
| chr10:26236815 | T | C | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+7038T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236815 | |||||||
| chr10:26236851 | A | G | 3 | a0001c0001t0012g0061 a0001c0001t0012g0105 a0001c0007t0012g0258 |
3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.840+7074A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236851 | |||||||
| chr10:26236991 | G | A | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.840+7214G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26236991 | |||||||
| chr10:26237009 | C | G | 62 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(59): Show |
65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.840+7232C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237009 | |||||||
| chr10:26237067 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.840+7290C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237067 | |||||||
| chr10:26237089 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.840+7312G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237089 | |||||||
| chr10:26237215 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840+7438G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237215 | |||||||
| chr10:26237268 | A | T | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.840+7491A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237268 | |||||||
| chr10:26237401 | T | C | 5 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+7624T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237401 | |||||||
| chr10:26237410 | C | T | 13 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(10): Show |
13 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+7633C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237410 | |||||||
| chr10:26237412 | C | T | 1 | a0001c0001t0005g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.840+7635C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237412 | |||||||
| chr10:26237423 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+7646G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237423 | |||||||
| chr10:26237449 | G | A | 1 | a0001c0001t0028g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.840+7672G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237449 | |||||||
| chr10:26237524 | A | G | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.840+7747A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237524 | |||||||
| chr10:26237601 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.840+7824C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237601 | |||||||
| chr10:26237729 | C | T | 17 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(14): Show |
17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.840+7952C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237729 | |||||||
| chr10:26237773 | T | C | 62 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(59): Show |
65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.840+7996T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237773 | |||||||
| chr10:26237774 | G | A | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.840+7997G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237774 | |||||||
| chr10:26237892 | A | G | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-8029A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237892 | |||||||
| chr10:26237913 | AGGAGAAT others(12): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.841-8004_841-7986d others(21): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237913 | ||||||
| chr10:26237932 | G | A | 5 | a0001c0001t0008g0016 a0001c0001t0009g0003 a0001c0001t0009g0012 others(2): Show |
6 | HG00735.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-7989G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26237932 | |||||||
| chr10:26237998 | TCACACAG others(1): Show |
T | 3 | a0001c0001t0005g0214 a0001c0002t0004g0117 a0001c0003t0015g0266 |
3 | HG00639.hp2 HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-7916_841-7909d others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | ||||||
| chr10:26237998 | TCACACAG others(3): Show |
T | 3 | a0001c0001t0011g0108 a0001c0001t0011g0110 a0001c0001t0011g0111 |
3 | HG00642.hp1 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.841-7916_841-7907d others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | ||||||
| chr10:26237998 | TCACACAG others(5): Show |
T | 3 | a0001c0001t0008g0269 a0001c0001t0008g0270 a0001c0001t0014g0104 |
3 | HG02451.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.841-7916_841-7905d others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | ||||||
| chr10:26237998 | TCACACAG others(7): Show |
T | 6 | a0001c0001t0008g0011 a0001c0001t0011g0109 a0001c0001t0019g0106 others(3): Show |
7 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.841-7916_841-7903d others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237998 | ||||||
| chr10:26237999 | CACACAG | C | 15 | a0001c0001t0007g0252 a0001c0001t0013g0268 a0001c0002t0004g0009 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.841-7916_841-7911d others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26237999 | ||||||
| chr10:26238001 | CACAG | C | 12 | a0001c0001t0001g0278 a0001c0001t0005g0107 a0001c0001t0005g0242 others(9): Show |
12 | HG01106.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.841-7916_841-7913d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238001 | ||||||
| chr10:26238003 | CAG | C | 16 | a0001c0001t0001g0277 a0001c0001t0005g0260 a0001c0001t0007g0103 others(13): Show |
16 | HG00642.hp2 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.841-7916_841-7915d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238003 | ||||||
| chr10:26238005 | G | C | 4 | a0001c0003t0005g0112 a0001c0003t0005g0249 a0001c0003t0010g0246 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-7916G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238005 | |||||||
| chr10:26238005 | G | GAC | 22 | a0001c0001t0002g0008 a0001c0001t0002g0124 a0001c0001t0002g0137 others(19): Show |
23 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.841-7874_841-7873d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | ||||||
| chr10:26238005 | G | GACAC | 4 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0210 others(1): Show |
4 | HG01993.hp1 HG02145.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-7876_841-7873d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | ||||||
| chr10:26238005 | GAC | G | 52 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0079 others(49): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.841-7874_841-7873d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | ||||||
| chr10:26238005 | GACAC | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
71 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.841-7876_841-7873d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | ||||||
| chr10:26238005 | GACACAC | G | 14 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0041 others(11): Show |
14 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.841-7878_841-7873d others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238005 | ||||||
| chr10:26238118 | C | T | 17 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(14): Show |
17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-7803C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238118 | |||||||
| chr10:26238129 | T | C | 3 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-7792T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238129 | |||||||
| chr10:26238144 | A | G | 62 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(59): Show |
65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.841-7777A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238144 | |||||||
| chr10:26238254 | G | C | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-7667G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238254 | |||||||
| chr10:26238352 | T | G | 1 | a0001c0002t0004g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.841-7569T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238352 | |||||||
| chr10:26238461 | G | A | 34 | a0001c0001t0005g0214 a0001c0001t0005g0242 a0001c0001t0005g0243 others(31): Show |
37 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.841-7460G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238461 | |||||||
| chr10:26238632 | G | A | 1 | a0001c0001t0005g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.841-7289G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238632 | |||||||
| chr10:26238661 | G | A | 45 | a0001c0001t0002g0008 a0001c0001t0002g0123 a0001c0001t0002g0124 others(42): Show |
46 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.841-7260G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238661 | |||||||
| chr10:26238791 | TC | T | 7 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(4): Show |
8 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-7129delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238791 | |||||||
| chr10:26238797 | G | A | 17 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(14): Show |
17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-7124G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238797 | |||||||
| chr10:26238831 | G | A | 17 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(14): Show |
17 | HG00642.hp1 HG01106.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-7090G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238831 | |||||||
| chr10:26238902 | G | A | 1 | a0001c0001t0011g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.841-7019G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238902 | |||||||
| chr10:26238909 | G | A | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-7012G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238909 | |||||||
| chr10:26238921 | A | G | 35 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(32): Show |
35 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.841-7000A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26238921 | |||||||
| chr10:26238979 | TG | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-6940delG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26238979 | ||||||
| chr10:26239004 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.841-6917G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239004 | |||||||
| chr10:26239135 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.841-6786G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239135 | |||||||
| chr10:26239374 | G | A | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-6547G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239374 | |||||||
| chr10:26239420 | T | C | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-6501T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239420 | |||||||
| chr10:26239444 | C | T | 11 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(8): Show |
11 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.841-6477C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239444 | |||||||
| chr10:26239555 | T | G | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841-6366T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239555 | |||||||
| chr10:26239626 | G | C | 11 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(8): Show |
11 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.841-6295G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239626 | |||||||
| chr10:26239651 | T | A | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-6270T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239651 | |||||||
| chr10:26239906 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
167 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.841-6015A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26239906 | |||||||
| chr10:26240194 | A | G | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-5727A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240194 | |||||||
| chr10:26240250 | T | C | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.841-5671T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240250 | |||||||
| chr10:26240269 | C | T | 1 | a0001c0001t0016g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.841-5652C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240269 | |||||||
| chr10:26240347 | C | T | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-5574C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240347 | |||||||
| chr10:26240392 | C | T | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5529C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240392 | |||||||
| chr10:26240427 | A | G | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-5494A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240427 | |||||||
| chr10:26240432 | G | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-5489G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240432 | |||||||
| chr10:26240454 | A | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0003t0010g0244 others(3): Show |
6 | HG01106.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-5467A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240454 | |||||||
| chr10:26240474 | G | T | 1 | a0001c0001t0005g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.841-5447G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240474 | |||||||
| chr10:26240503 | G | T | 7 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(4): Show |
8 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-5418G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240503 | |||||||
| chr10:26240586 | G | A | 1 | a0001c0001t0019g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841-5335G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240586 | |||||||
| chr10:26240687 | A | G | 50 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(47): Show |
52 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.841-5234A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240687 | |||||||
| chr10:26240731 | C | CA | 26 | a0001c0001t0001g0083 a0001c0001t0002g0134 a0001c0001t0002g0191 others(23): Show |
28 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.841-5175dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26240731 | ||||||
| chr10:26240731 | C | CAA | 54 | a0001c0001t0002g0177 a0001c0001t0002g0190 a0001c0001t0003g0002 others(51): Show |
56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.841-5176_841-5175d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26240731 | ||||||
| chr10:26240733 | A | C | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5188A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240733 | |||||||
| chr10:26240735 | A | C | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5186A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240735 | |||||||
| chr10:26240737 | A | C | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5184A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240737 | |||||||
| chr10:26240739 | A | C | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.841-5182A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240739 | |||||||
| chr10:26240851 | G | A | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-5070G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240851 | |||||||
| chr10:26240967 | G | A | 6 | a0001c0001t0005g0260 a0001c0003t0005g0112 a0001c0003t0005g0241 others(3): Show |
6 | HG01884.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-4954G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240967 | |||||||
| chr10:26240984 | G | A | 1 | a0001c0001t0028g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.841-4937G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26240984 | |||||||
| chr10:26241006 | C | G | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-4915C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241006 | |||||||
| chr10:26241030 | A | G | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-4891A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241030 | |||||||
| chr10:26241066 | T | A | 27 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(24): Show |
27 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.841-4855T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241066 | |||||||
| chr10:26241086 | T | C | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.841-4835T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241086 | |||||||
| chr10:26241179 | G | A | 1 | a0001c0001t0003g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.841-4742G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241179 | |||||||
| chr10:26241287 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.841-4634G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241287 | |||||||
| chr10:26241330 | C | A | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-4591C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241330 | |||||||
| chr10:26241428 | A | G | 62 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(59): Show |
65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.841-4493A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241428 | |||||||
| chr10:26241476 | T | C | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-4445T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241476 | |||||||
| chr10:26241550 | C | CT | 22 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(19): Show |
22 | HG00642.hp1 HG01106.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.841-4357dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241550 | ||||||
| chr10:26241550 | C | CTT | 42 | a0001c0001t0005g0214 a0001c0001t0005g0242 a0001c0001t0005g0243 others(39): Show |
45 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.841-4358_841-4357d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241550 | ||||||
| chr10:26241554 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.841-4367T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241554 | |||||||
| chr10:26241638 | T | C | 20 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(17): Show |
22 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.841-4283T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241638 | |||||||
| chr10:26241652 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.841-4269T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241652 | |||||||
| chr10:26241673 | A | G | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.841-4248A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241673 | |||||||
| chr10:26241738 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-4183A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241738 | |||||||
| chr10:26241837 | C | T | 18 | a0001c0001t0005g0260 a0001c0001t0007g0103 a0001c0001t0007g0251 others(15): Show |
18 | HG00642.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.841-4084C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241837 | |||||||
| chr10:26241838 | G | A | 1 | a0001c0002t0004g0118 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.841-4083G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241838 | |||||||
| chr10:26241912 | A | C | 1 | a0001c0001t0003g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.841-4009A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26241912 | |||||||
| chr10:26241969 | A | ATTTG | 8 | a0001c0001t0005g0214 a0001c0001t0005g0260 a0001c0001t0014g0104 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-3928_841-3925d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241969 | ||||||
| chr10:26241969 | A | ATTTGTTT others(1): Show |
11 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(8): Show |
11 | HG00642.hp2 HG01243.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.841-3932_841-3925d others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26241969 | ||||||
| chr10:26242134 | C | T | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-3787C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242134 | |||||||
| chr10:26242135 | G | A | 2 | a0001c0001t0003g0204 a0001c0001t0003g0222 |
2 | HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.841-3786G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242135 | |||||||
| chr10:26242179 | A | G | 12 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(9): Show |
12 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-3742A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242179 | |||||||
| chr10:26242202 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-3719G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242202 | |||||||
| chr10:26242277 | C | T | 1 | a0001c0001t0017g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.841-3644C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242277 | |||||||
| chr10:26242301 | A | G | 2 | a0001c0001t0009g0099 a0001c0001t0014g0104 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.841-3620A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242301 | |||||||
| chr10:26242321 | C | A | 1 | a0001c0001t0002g0149 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.841-3600C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242321 | |||||||
| chr10:26242335 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.841-3586T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242335 | |||||||
| chr10:26242435 | A | G | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-3486A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242435 | |||||||
| chr10:26242468 | G | A | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.841-3453G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242468 | |||||||
| chr10:26242586 | G | A | 2 | a0001c0001t0009g0099 a0001c0001t0014g0104 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.841-3335G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242586 | |||||||
| chr10:26242631 | C | T | 12 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(9): Show |
12 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-3290C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242631 | |||||||
| chr10:26242741 | C | T | 14 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(11): Show |
14 | HG00642.hp1 HG00642.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-3180C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242741 | |||||||
| chr10:26242754 | C | A | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.841-3167C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242754 | |||||||
| chr10:26242930 | G | T | 16 | a0001c0001t0005g0214 a0001c0001t0005g0260 a0001c0001t0007g0103 others(13): Show |
16 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.841-2991G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26242930 | |||||||
| chr10:26243027 | C | A | 1 | a0001c0001t0003g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.841-2894C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243027 | |||||||
| chr10:26243040 | A | AAAG | 51 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(48): Show |
54 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.841-2879_841-2878i others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26243040 | ||||||
| chr10:26243041 | A | C | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.841-2880A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243041 | |||||||
| chr10:26243042 | A | AGAAC | 12 | a0001c0001t0007g0103 a0001c0001t0007g0252 a0001c0001t0007g0253 others(9): Show |
13 | HG00642.hp2 HG00735.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.841-2879_841-2878i others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243042 | |||||||
| chr10:26243042 | A | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG02040.hp1 HG02083.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.841-2879A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243042 | |||||||
| chr10:26243043 | C | T | 1 | a0001c0001t0005g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.841-2878C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243043 | |||||||
| chr10:26243044 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.841-2877C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243044 | |||||||
| chr10:26243383 | G | T | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-2538G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243383 | |||||||
| chr10:26243564 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.841-2357G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243564 | |||||||
| chr10:26243721 | C | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-2200C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243721 | |||||||
| chr10:26243832 | C | A | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-2089C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243832 | |||||||
| chr10:26243883 | A | G | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.841-2038A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243883 | |||||||
| chr10:26243898 | T | C | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-2023T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26243898 | |||||||
| chr10:26244000 | T | C | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1921T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244000 | |||||||
| chr10:26244015 | T | C | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1906T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244015 | |||||||
| chr10:26244169 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.841-1752C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244169 | |||||||
| chr10:26244320 | T | G | 3 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0003g0175 |
3 | HG00639.hp1 HG01192.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.841-1601T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244320 | |||||||
| chr10:26244437 | T | G | 19 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(16): Show |
19 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-1484T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244437 | |||||||
| chr10:26244479 | A | G | 1 | a0001c0001t0022g0218 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.841-1442A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244479 | |||||||
| chr10:26244536 | A | T | 1 | a0001c0001t0002g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.841-1385A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244536 | |||||||
| chr10:26244554 | A | G | 19 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(16): Show |
19 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-1367A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244554 | |||||||
| chr10:26244808 | A | T | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1113A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244808 | |||||||
| chr10:26244825 | A | G | 7 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(4): Show |
8 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-1096A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244825 | |||||||
| chr10:26244836 | A | G | 60 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(57): Show |
64 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.841-1085A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244836 | |||||||
| chr10:26244878 | A | G | 60 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(57): Show |
64 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.841-1043A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244878 | |||||||
| chr10:26244917 | T | C | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1004T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244917 | |||||||
| chr10:26244942 | A | G | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-979A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244942 | |||||||
| chr10:26244997 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.841-924C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26244997 | |||||||
| chr10:26245053 | T | C | 1 | a0001c0001t0028g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.841-868T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245053 | |||||||
| chr10:26245131 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.841-790C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245131 | |||||||
| chr10:26245146 | T | C | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-775T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245146 | |||||||
| chr10:26245153 | C | CAA | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0214 others(9): Show |
12 | HG01106.hp1 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-753_841-752dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245153 | ||||||
| chr10:26245153 | CA | C | 14 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0002g0219 others(11): Show |
14 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-752delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245153 | ||||||
| chr10:26245153 | CAAAAA | C | 6 | a0001c0001t0005g0107 a0001c0001t0012g0061 a0001c0001t0012g0105 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-756_841-752del others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245153 | ||||||
| chr10:26245163 | AAAAAAAG | A | 8 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
8 | HG01346.hp2 HG02293.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-743_841-737del others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245163 | ||||||
| chr10:26245193 | G | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.841-728G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245193 | |||||||
| chr10:26245230 | G | T | 5 | a0001c0001t0001g0136 a0001c0001t0009g0003 a0001c0001t0009g0012 others(2): Show |
6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-691G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245230 | |||||||
| chr10:26245231 | G | GC | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-690_841-689ins others(1): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245231 | |||||||
| chr10:26245354 | C | T | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.841-567C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245354 | |||||||
| chr10:26245355 | G | A | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-566G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245355 | |||||||
| chr10:26245383 | T | TA | 6 | a0001c0001t0002g0157 a0001c0001t0005g0242 a0001c0001t0005g0243 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-528dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245383 | ||||||
| chr10:26245383 | TA | T | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-528delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245383 | ||||||
| chr10:26245390 | A | AT | 4 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(1): Show |
5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-531_841-530ins others(1): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245390 | |||||||
| chr10:26245390 | A | T | 19 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(16): Show |
19 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.841-531A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245390 | |||||||
| chr10:26245404 | C | T | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-517C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245404 | |||||||
| chr10:26245418 | TTTAAG | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.841-499_841-495del others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245418 | ||||||
| chr10:26245442 | A | AT | 61 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0277 others(58): Show |
65 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.841-467dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245442 | ||||||
| chr10:26245442 | A | ATT | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
76 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.841-468_841-467dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245442 | ||||||
| chr10:26245442 | A | ATTT | 9 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0067 others(6): Show |
9 | HG02055.hp2 HG02922.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-469_841-467dup others(3): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245442 | ||||||
| chr10:26245524 | G | A | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-397G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245524 | |||||||
| chr10:26245604 | A | AT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0007g0103 others(9): Show |
14 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-306dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245604 | ||||||
| chr10:26245680 | G | T | 1 | a0001c0001t0018g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.841-241G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245680 | |||||||
| chr10:26245720 | G | A | 1 | a0003c0005t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.841-201G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245720 | |||||||
| chr10:26245725 | A | C | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.841-196A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245725 | |||||||
| chr10:26245827 | GAAAGGAA others(1): Show |
G | 4 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(1): Show |
5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-84_841-77delAA others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr10 | 26245827 | ||||||
| chr10:26245880 | G | T | 51 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(48): Show |
54 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.841-41G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245880 | |||||||
| chr10:26245882 | A | G | 1 | a0001c0001t0009g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841-39A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245882 | |||||||
| chr10:26245907 | TA | T | 11 | a0001c0001t0003g0224 a0001c0001t0007g0103 a0001c0001t0007g0251 others(8): Show |
11 | HG00642.hp2 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.841-13delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 7/15 | chr10 | 26245907 | |||||||
| chr10:26246008 | C | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.920+8C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246008 | |||||||
| chr10:26246021 | C | A | 2 | a0001c0002t0004g0235 a0001c0002t0004g0238 |
2 | HG00544.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.920+21C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246021 | |||||||
| chr10:26246094 | C | T | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+94C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246094 | |||||||
| chr10:26246251 | C | T | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+251C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246251 | |||||||
| chr10:26246348 | T | C | 9 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(6): Show |
9 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+348T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246348 | |||||||
| chr10:26246409 | A | C | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+409A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246409 | |||||||
| chr10:26246433 | A | G | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+433A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246433 | |||||||
| chr10:26246614 | A | G | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+614A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246614 | |||||||
| chr10:26246783 | C | T | 9 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(6): Show |
9 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+783C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246783 | |||||||
| chr10:26246812 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.920+812C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246812 | |||||||
| chr10:26246825 | A | G | 18 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(15): Show |
18 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+825A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246825 | |||||||
| chr10:26246909 | C | T | 51 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(48): Show |
54 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.920+909C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246909 | |||||||
| chr10:26246924 | G | A | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+924G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26246924 | |||||||
| chr10:26247154 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.920+1154T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247154 | |||||||
| chr10:26247215 | A | C | 1 | a0001c0001t0005g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.920+1215A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247215 | |||||||
| chr10:26247286 | G | A | 2 | a0001c0001t0003g0160 a0001c0001t0003g0161 |
2 | NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.920+1286G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247286 | |||||||
| chr10:26247379 | C | CATCTT | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1379_920+1380i others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247379 | |||||||
| chr10:26247568 | A | G | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1568A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247568 | |||||||
| chr10:26247595 | C | A | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+1595C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247595 | |||||||
| chr10:26247614 | G | A | 2 | a0002c0004t0003g0194 a0002c0004t0003g0195 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.920+1614G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247614 | |||||||
| chr10:26247622 | G | T | 18 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(15): Show |
18 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+1622G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247622 | |||||||
| chr10:26247731 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+1731A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247731 | |||||||
| chr10:26247768 | C | A | 5 | a0001c0001t0005g0260 a0001c0003t0005g0112 a0001c0003t0005g0241 others(2): Show |
5 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+1768C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247768 | |||||||
| chr10:26247790 | G | A | 6 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.920+1790G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247790 | |||||||
| chr10:26247895 | C | CA | 61 | a0001c0001t0001g0042 a0001c0001t0002g0178 a0001c0001t0002g0184 others(58): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.920+1912dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247895 | ||||||
| chr10:26247895 | CA | C | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+1912delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247895 | ||||||
| chr10:26247919 | G | GA | 133 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0037 others(130): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.920+1931dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247919 | ||||||
| chr10:26247919 | GA | G | 11 | a0001c0001t0001g0093 a0001c0001t0001g0277 a0001c0001t0001g0278 others(8): Show |
11 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.920+1931delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26247919 | ||||||
| chr10:26247970 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.920+1970G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26247970 | |||||||
| chr10:26248069 | C | G | 19 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(16): Show |
20 | HG00642.hp2 HG00735.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.920+2069C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248069 | |||||||
| chr10:26248112 | G | A | 12 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(9): Show |
12 | HG01106.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.920+2112G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248112 | |||||||
| chr10:26248155 | G | T | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+2155G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248155 | |||||||
| chr10:26248241 | A | G | 60 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(57): Show |
64 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.920+2241A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248241 | |||||||
| chr10:26248481 | G | C | 1 | a0001c0001t0002g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.920+2481G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248481 | |||||||
| chr10:26248701 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
87 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.920+2701A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248701 | |||||||
| chr10:26248810 | G | GA | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+2819dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26248810 | ||||||
| chr10:26248880 | C | T | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+2880C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248880 | |||||||
| chr10:26248934 | C | T | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+2934C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26248934 | |||||||
| chr10:26249008 | A | AT | 9 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(6): Show |
9 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.920+3010dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26249008 | ||||||
| chr10:26249008 | AT | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+3010delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26249008 | ||||||
| chr10:26249073 | C | T | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3073C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249073 | |||||||
| chr10:26249099 | G | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+3099G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249099 | |||||||
| chr10:26249127 | G | A | 28 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(25): Show |
28 | HG00642.hp1 HG00642.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.920+3127G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249127 | |||||||
| chr10:26249180 | A | C | 1 | a0001c0001t0007g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.920+3180A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249180 | |||||||
| chr10:26249214 | A | G | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3214A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249214 | |||||||
| chr10:26249219 | G | A | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3219G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249219 | |||||||
| chr10:26249308 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.920+3308C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249308 | |||||||
| chr10:26249411 | A | C | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+3411A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249411 | |||||||
| chr10:26249523 | C | T | 6 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(3): Show |
6 | HG00642.hp1 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+3523C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249523 | |||||||
| chr10:26249651 | G | A | 1 | a0001c0001t0009g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.920+3651G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249651 | |||||||
| chr10:26249690 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.920+3690G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249690 | |||||||
| chr10:26249723 | G | A | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+3723G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249723 | |||||||
| chr10:26249730 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.920+3730G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249730 | |||||||
| chr10:26249732 | C | G | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+3732C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249732 | |||||||
| chr10:26249747 | A | G | 8 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(5): Show |
9 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+3747A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249747 | |||||||
| chr10:26249868 | T | C | 2 | a0001c0003t0005g0241 a0001c0003t0005g0249 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.920+3868T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249868 | |||||||
| chr10:26249917 | A | C | 13 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(10): Show |
13 | HG00642.hp1 HG01106.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.920+3917A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249917 | |||||||
| chr10:26249962 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.920+3962G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26249962 | |||||||
| chr10:26250017 | T | G | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+4017T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250017 | |||||||
| chr10:26250081 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.920+4081G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250081 | |||||||
| chr10:26250144 | G | C | 2 | a0001c0001t0002g0177 a0001c0001t0002g0180 |
2 | NA18948.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.920+4144G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250144 | |||||||
| chr10:26250519 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.920+4519C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250519 | |||||||
| chr10:26250520 | G | A | 17 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(14): Show |
17 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+4520G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250520 | |||||||
| chr10:26250566 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
112 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.920+4566A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250566 | |||||||
| chr10:26250708 | A | G | 4 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(1): Show |
5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+4708A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250708 | |||||||
| chr10:26250754 | A | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
110 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.920+4754A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250754 | |||||||
| chr10:26250780 | A | G | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(6): Show |
9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+4780A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250780 | |||||||
| chr10:26250867 | G | T | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.920+4867G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250867 | |||||||
| chr10:26250875 | T | C | 1 | a0001c0001t0003g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.920+4875T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250875 | |||||||
| chr10:26250877 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.920+4897dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26250877 | ||||||
| chr10:26250877 | C | CTT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0049 others(7): Show |
10 | HG01255.hp1 HG01256.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+4896_920+4897d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26250877 | ||||||
| chr10:26250877 | C | T | 1 | a0001c0001t0003g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.920+4877C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250877 | |||||||
| chr10:26250877 | CT | C | 10 | a0001c0001t0005g0107 a0001c0001t0005g0242 a0001c0001t0005g0243 others(7): Show |
10 | HG01070.hp1 HG01168.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+4897delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26250877 | ||||||
| chr10:26250918 | C | T | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+4918C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250918 | |||||||
| chr10:26250930 | A | C | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+4930A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26250930 | |||||||
| chr10:26251040 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
118 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.920+5040C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251040 | |||||||
| chr10:26251044 | A | AT | 16 | a0001c0001t0002g0134 a0001c0002t0004g0009 a0001c0002t0004g0010 others(13): Show |
18 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.920+5054dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26251044 | ||||||
| chr10:26251055 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0005g0214 |
2 | NA18522.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.920+5055G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251055 | |||||||
| chr10:26251056 | C | CT | 6 | a0001c0001t0002g0178 a0001c0001t0003g0132 a0001c0001t0003g0161 others(3): Show |
6 | HG02027.hp1 HG03471.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+5072dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26251056 | ||||||
| chr10:26251056 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0005g0214 |
2 | NA18522.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.920+5056C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251056 | |||||||
| chr10:26251056 | CT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
105 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.920+5072delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26251056 | ||||||
| chr10:26251057 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0005g0214 |
2 | NA18522.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.920+5057T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251057 | |||||||
| chr10:26251242 | C | A | 5 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+5242C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251242 | |||||||
| chr10:26251266 | A | G | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+5266A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251266 | |||||||
| chr10:26251351 | G | A | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+5351G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251351 | |||||||
| chr10:26251451 | G | A | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(6): Show |
9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+5451G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251451 | |||||||
| chr10:26251510 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.920+5510A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251510 | |||||||
| chr10:26251585 | G | A | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+5585G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251585 | |||||||
| chr10:26251600 | C | T | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920+5600C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251600 | |||||||
| chr10:26251683 | T | G | 28 | a0001c0001t0008g0011 a0001c0001t0008g0016 a0001c0001t0008g0269 others(25): Show |
32 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.920+5683T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251683 | |||||||
| chr10:26251761 | G | A | 3 | a0001c0001t0012g0061 a0001c0001t0012g0105 a0001c0007t0012g0258 |
3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920+5761G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251761 | |||||||
| chr10:26251800 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
145 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.920+5800T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251800 | |||||||
| chr10:26251842 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
154 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.920+5842G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251842 | |||||||
| chr10:26251920 | G | A | 1 | a0001c0001t0003g0207 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.920+5920G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26251920 | |||||||
| chr10:26252347 | C | CTT | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+6353_920+6354d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26252347 | ||||||
| chr10:26252355 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
149 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.920+6355C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252355 | |||||||
| chr10:26252492 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.920+6492G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252492 | |||||||
| chr10:26252501 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.920+6501C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252501 | |||||||
| chr10:26252762 | G | A | 1 | a0001c0001t0009g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.920+6762G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252762 | |||||||
| chr10:26252883 | C | G | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(6): Show |
9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+6883C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252883 | |||||||
| chr10:26252896 | G | A | 1 | a0001c0001t0013g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920+6896G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26252896 | |||||||
| chr10:26253076 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+7076G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253076 | |||||||
| chr10:26253113 | T | C | 1 | a0001c0001t0017g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.920+7113T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253113 | |||||||
| chr10:26253238 | T | G | 9 | a0001c0001t0008g0011 a0001c0001t0008g0016 a0001c0001t0008g0269 others(6): Show |
10 | HG02145.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+7238T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253238 | |||||||
| chr10:26253316 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920+7316C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253316 | |||||||
| chr10:26253342 | G | A | 2 | a0001c0001t0020g0280 a0001c0001t0028g0279 |
2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.920+7342G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253342 | |||||||
| chr10:26253343 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.920+7343T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253343 | |||||||
| chr10:26253369 | A | G | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+7369A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253369 | |||||||
| chr10:26253456 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.920+7456G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253456 | |||||||
| chr10:26253489 | C | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+7489C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26253489 | |||||||
| chr10:26254041 | A | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+8041A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254041 | |||||||
| chr10:26254060 | C | T | 1 | a0001c0003t0005g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920+8060C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254060 | |||||||
| chr10:26254190 | G | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
149 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.920+8190G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254190 | |||||||
| chr10:26254198 | G | A | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0005g0107 others(6): Show |
9 | HG01106.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+8198G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254198 | |||||||
| chr10:26254210 | T | C | 1 | a0001c0001t0005g0261 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.920+8210T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254210 | |||||||
| chr10:26254439 | A | T | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+8439A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254439 | |||||||
| chr10:26254453 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920+8453G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254453 | |||||||
| chr10:26254455 | T | C | 3 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.920+8455T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254455 | |||||||
| chr10:26254463 | C | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.920+8463C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254463 | |||||||
| chr10:26254515 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
123 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.920+8515C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254515 | |||||||
| chr10:26254685 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920+8685G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254685 | |||||||
| chr10:26254805 | C | G | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920+8805C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254805 | |||||||
| chr10:26254884 | G | A | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+8884G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254884 | |||||||
| chr10:26254929 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
154 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.920+8929G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26254929 | |||||||
| chr10:26255064 | G | C | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+9064G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255064 | |||||||
| chr10:26255274 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.920+9274G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255274 | |||||||
| chr10:26255397 | G | A | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+9397G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255397 | |||||||
| chr10:26255424 | C | G | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.920+9424C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255424 | |||||||
| chr10:26255550 | T | TTTCGCTA others(8): Show |
1 | a0001c0001t0001g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.920+9551_920+9565d others(17): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255550 | ||||||
| chr10:26255600 | G | GGAAA | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
159 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.920+9604_920+9607d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255600 | ||||||
| chr10:26255608 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0005g0214 |
3 | HG01099.hp2 HG01346.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.920+9608G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255608 | |||||||
| chr10:26255646 | AGGGGAG | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
140 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.920+9652_920+9657d others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255646 | ||||||
| chr10:26255670 | G | T | 3 | a0001c0001t0005g0214 a0001c0001t0015g0100 a0001c0003t0015g0266 |
3 | HG01243.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+9670G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255670 | |||||||
| chr10:26255702 | AAAGG | A | 3 | a0001c0001t0005g0214 a0001c0001t0015g0100 a0001c0003t0015g0266 |
3 | HG01243.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+9717_920+9720d others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26255702 | ||||||
| chr10:26255741 | A | T | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.920+9741A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255741 | |||||||
| chr10:26255766 | C | T | 3 | a0001c0001t0012g0061 a0001c0001t0012g0105 a0001c0007t0012g0258 |
3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920+9766C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255766 | |||||||
| chr10:26255858 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
140 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.920+9858G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255858 | |||||||
| chr10:26255914 | A | T | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920+9914A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255914 | |||||||
| chr10:26255915 | T | C | 14 | a0001c0001t0006g0152 a0001c0001t0008g0011 a0001c0001t0008g0269 others(11): Show |
15 | HG00642.hp1 HG01109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.920+9915T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255915 | |||||||
| chr10:26255933 | G | T | 1 | a0001c0001t0001g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.920+9933G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255933 | |||||||
| chr10:26255939 | A | G | 3 | a0001c0001t0012g0061 a0001c0001t0012g0105 a0001c0007t0012g0258 |
3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920+9939A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26255939 | |||||||
| chr10:26256248 | T | TTA | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+10261_920+1026 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26256248 | ||||||
| chr10:26256257 | T | G | 16 | a0001c0001t0001g0084 a0001c0001t0007g0103 a0001c0001t0007g0251 others(13): Show |
17 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+10257T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256257 | |||||||
| chr10:26256259 | T | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(102): Show |
111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.920+10259T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256259 | |||||||
| chr10:26256261 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
174 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.920+10261T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256261 | |||||||
| chr10:26256435 | C | T | 2 | a0001c0001t0016g0271 a0001c0001t0016g0276 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.920+10435C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256435 | |||||||
| chr10:26256474 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
144 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.920+10474C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256474 | |||||||
| chr10:26256573 | A | G | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+10573A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256573 | |||||||
| chr10:26256750 | T | C | 11 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(8): Show |
11 | HG00642.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.920+10750T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256750 | |||||||
| chr10:26256760 | G | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.920+10760G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256760 | |||||||
| chr10:26256771 | G | A | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+10771G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256771 | |||||||
| chr10:26256862 | C | A | 4 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(1): Show |
5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+10862C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256862 | |||||||
| chr10:26256864 | C | T | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920+10864C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26256864 | |||||||
| chr10:26257095 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920+11095C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257095 | |||||||
| chr10:26257115 | T | G | 1 | a0001c0001t0001g0031 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.920+11115T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257115 | |||||||
| chr10:26257260 | C | T | 3 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0257 |
3 | HG00642.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.920+11260C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257260 | |||||||
| chr10:26257295 | T | C | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.920+11295T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257295 | |||||||
| chr10:26257301 | C | T | 1 | a0001c0001t0028g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.920+11301C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257301 | |||||||
| chr10:26257303 | G | T | 1 | a0001c0001t0003g0143 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.920+11303G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257303 | |||||||
| chr10:26257308 | C | A | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+11308C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257308 | |||||||
| chr10:26257342 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
143 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.920+11342C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257342 | |||||||
| chr10:26257433 | T | C | 1 | a0001c0002t0004g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.920+11433T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257433 | |||||||
| chr10:26257507 | A | G | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+11507A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257507 | |||||||
| chr10:26257580 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | NA18999.hp2 NA19060.hp2 NA19076.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-11539C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257580 | |||||||
| chr10:26257634 | AC | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
138 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.921-11483delC | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26257634 | ||||||
| chr10:26257832 | G | A | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-11287G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257832 | |||||||
| chr10:26257833 | C | T | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-11286C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257833 | |||||||
| chr10:26257908 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.921-11211C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26257908 | |||||||
| chr10:26258100 | T | TA | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-11018dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26258100 | ||||||
| chr10:26258213 | T | C | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-10906T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258213 | |||||||
| chr10:26258257 | C | A | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.921-10862C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258257 | |||||||
| chr10:26258578 | C | T | 1 | a0001c0001t0017g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921-10541C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258578 | |||||||
| chr10:26258605 | G | T | 3 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0002g0173 |
3 | HG03017.hp1 HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.921-10514G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258605 | |||||||
| chr10:26258684 | T | C | 2 | a0001c0001t0016g0271 a0001c0001t0016g0276 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.921-10435T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258684 | |||||||
| chr10:26258742 | C | T | 1 | a0001c0001t0005g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.921-10377C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258742 | |||||||
| chr10:26258787 | G | A | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.921-10332G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26258787 | |||||||
| chr10:26258812 | AT | A | 13 | a0001c0001t0001g0014 a0001c0001t0002g0163 a0001c0001t0005g0107 others(10): Show |
14 | HG00735.hp1 HG02165.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.921-10292delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26258812 | ||||||
| chr10:26258812 | ATT | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
137 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.921-10293_921-1029 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26258812 | ||||||
| chr10:26259023 | G | T | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.921-10096G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259023 | |||||||
| chr10:26259024 | G | A | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-10095G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259024 | |||||||
| chr10:26259106 | C | A | 1 | a0001c0001t0005g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.921-10013C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259106 | |||||||
| chr10:26259147 | C | T | 7 | a0001c0001t0005g0107 a0001c0001t0013g0267 a0001c0001t0013g0268 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-9972C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259147 | |||||||
| chr10:26259276 | C | T | 6 | a0001c0001t0005g0127 a0001c0001t0005g0260 a0001c0003t0005g0112 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-9843C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259276 | |||||||
| chr10:26259517 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
91 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.921-9602T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259517 | |||||||
| chr10:26259539 | C | G | 1 | a0001c0001t0002g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.921-9580C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259539 | |||||||
| chr10:26259546 | T | C | 4 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(1): Show |
5 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-9573T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259546 | |||||||
| chr10:26259696 | T | A | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-9423T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259696 | |||||||
| chr10:26259869 | A | G | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.921-9250A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26259869 | |||||||
| chr10:26260000 | T | A | 7 | a0001c0001t0005g0107 a0001c0001t0013g0267 a0001c0001t0013g0268 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-9119T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260000 | |||||||
| chr10:26260387 | G | A | 5 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-8732G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260387 | |||||||
| chr10:26260394 | C | T | 9 | a0001c0001t0006g0075 a0001c0001t0006g0120 a0001c0001t0006g0152 others(6): Show |
9 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.921-8725C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260394 | |||||||
| chr10:26260466 | T | G | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.921-8653T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260466 | |||||||
| chr10:26260496 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.921-8623C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260496 | |||||||
| chr10:26260497 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0134 a0001c0001t0002g0135 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-8622G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260497 | |||||||
| chr10:26260498 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.921-8621C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260498 | |||||||
| chr10:26260518 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.921-8601C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260518 | |||||||
| chr10:26260550 | C | T | 1 | a0001c0001t0015g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.921-8569C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260550 | |||||||
| chr10:26260647 | T | G | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-8472T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260647 | |||||||
| chr10:26260685 | G | A | 7 | a0001c0001t0005g0107 a0001c0001t0013g0267 a0001c0001t0013g0268 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-8434G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260685 | |||||||
| chr10:26260774 | C | G | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-8345C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260774 | |||||||
| chr10:26260824 | T | C | 1 | a0001c0001t0003g0230 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.921-8295T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260824 | |||||||
| chr10:26260936 | G | C | 1 | a0001c0001t0006g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.921-8183G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26260936 | |||||||
| chr10:26261075 | G | C | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-8044G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261075 | |||||||
| chr10:26261151 | C | A | 1 | a0001c0001t0012g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.921-7968C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261151 | |||||||
| chr10:26261214 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.921-7905T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261214 | |||||||
| chr10:26261433 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.921-7686C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261433 | |||||||
| chr10:26261529 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.921-7590C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261529 | |||||||
| chr10:26261548 | T | G | 7 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0069 others(4): Show |
7 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.921-7571T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261548 | |||||||
| chr10:26261629 | A | G | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.921-7490A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261629 | |||||||
| chr10:26261831 | A | G | 1 | a0001c0001t0002g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.921-7288A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26261831 | |||||||
| chr10:26262031 | T | C | 1 | a0001c0001t0014g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.921-7088T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262031 | |||||||
| chr10:26262145 | TA | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.921-6973delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262145 | |||||||
| chr10:26262269 | G | GT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
113 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.921-6837dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26262269 | ||||||
| chr10:26262308 | A | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0166 a0001c0001t0002g0184 |
4 | HG02080.hp2 NA18970.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-6811A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262308 | |||||||
| chr10:26262353 | C | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-6766C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262353 | |||||||
| chr10:26262501 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.921-6618T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262501 | |||||||
| chr10:26262850 | CT | C | 44 | a0001c0001t0001g0017 a0001c0001t0005g0107 a0001c0001t0005g0242 others(41): Show |
47 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.921-6257delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26262850 | ||||||
| chr10:26262858 | T | A | 5 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-6261T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262858 | |||||||
| chr10:26262860 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.921-6259T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262860 | |||||||
| chr10:26262870 | A | G | 1 | a0001c0001t0017g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921-6249A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262870 | |||||||
| chr10:26262894 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.921-6225C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26262894 | |||||||
| chr10:26263074 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.921-6045A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263074 | |||||||
| chr10:26263137 | T | C | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-5982T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263137 | |||||||
| chr10:26263185 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
89 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.921-5934C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263185 | |||||||
| chr10:26263337 | C | A | 1 | a0001c0001t0002g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.921-5782C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263337 | |||||||
| chr10:26263374 | C | T | 23 | a0001c0001t0005g0107 a0001c0001t0007g0103 a0001c0001t0007g0251 others(20): Show |
23 | HG00642.hp2 HG01884.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.921-5745C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263374 | |||||||
| chr10:26263478 | G | A | 2 | a0001c0001t0003g0206 a0001c0001t0017g0015 |
2 | HG03516.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.921-5641G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263478 | |||||||
| chr10:26263565 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.921-5554C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263565 | |||||||
| chr10:26263648 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.921-5471C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263648 | |||||||
| chr10:26263736 | G | A | 8 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG02559.hp2 HG02922.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.921-5383G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263736 | |||||||
| chr10:26263794 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.921-5325G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263794 | |||||||
| chr10:26263890 | G | T | 1 | a0001c0001t0002g0142 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.921-5229G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263890 | |||||||
| chr10:26263942 | C | T | 1 | a0001c0001t0003g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.921-5177C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26263942 | |||||||
| chr10:26264056 | A | G | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.921-5063A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264056 | |||||||
| chr10:26264160 | A | G | 1 | a0001c0003t0005g0249 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.921-4959A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264160 | |||||||
| chr10:26264161 | C | G | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-4958C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264161 | |||||||
| chr10:26264312 | C | CT | 9 | a0001c0001t0001g0277 a0001c0001t0005g0259 a0001c0001t0009g0003 others(6): Show |
10 | HG00735.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-4789dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264312 | ||||||
| chr10:26264312 | C | CTT | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.921-4790_921-4789d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264312 | ||||||
| chr10:26264312 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
85 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.921-4789delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264312 | ||||||
| chr10:26264336 | A | G | 6 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0003t0010g0244 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-4783A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264336 | |||||||
| chr10:26264344 | G | A | 26 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.921-4775G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264344 | |||||||
| chr10:26264465 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.921-4654C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264465 | |||||||
| chr10:26264467 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.921-4652C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264467 | |||||||
| chr10:26264474 | G | GATTTTTT others(2): Show |
15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.921-4637_921-4629d others(11): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26264474 | ||||||
| chr10:26264500 | C | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-4619C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264500 | |||||||
| chr10:26264606 | C | T | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.921-4513C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264606 | |||||||
| chr10:26264631 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.921-4488A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264631 | |||||||
| chr10:26264646 | T | G | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.921-4473T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264646 | |||||||
| chr10:26264786 | A | G | 3 | a0001c0001t0012g0061 a0001c0001t0012g0105 a0001c0007t0012g0258 |
3 | HG01884.hp2 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.921-4333A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264786 | |||||||
| chr10:26264817 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.921-4302C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264817 | |||||||
| chr10:26264849 | G | T | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-4270G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26264849 | |||||||
| chr10:26265038 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.921-4081T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265038 | |||||||
| chr10:26265040 | G | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-4079G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265040 | |||||||
| chr10:26265146 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.921-3973C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265146 | |||||||
| chr10:26265202 | C | T | 26 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.921-3917C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265202 | |||||||
| chr10:26265203 | G | A | 2 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.921-3916G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265203 | |||||||
| chr10:26265205 | C | CT | 6 | a0001c0001t0002g0141 a0001c0001t0002g0180 a0001c0001t0005g0242 others(3): Show |
6 | HG01106.hp2 HG01243.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-3896dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26265205 | ||||||
| chr10:26265205 | CT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
130 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.921-3896delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26265205 | ||||||
| chr10:26265205 | CTT | C | 14 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0005g0127 others(11): Show |
15 | HG00735.hp1 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.921-3897_921-3896d others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26265205 | ||||||
| chr10:26265326 | C | T | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-3793C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265326 | |||||||
| chr10:26265378 | C | T | 26 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(23): Show |
27 | HG00642.hp2 HG00735.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.921-3741C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265378 | |||||||
| chr10:26265439 | G | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.921-3680G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265439 | |||||||
| chr10:26265450 | G | A | 2 | a0001c0001t0005g0107 a0001c0001t0005g0214 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.921-3669G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265450 | |||||||
| chr10:26265493 | G | A | 1 | a0001c0001t0017g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.921-3626G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265493 | |||||||
| chr10:26265512 | C | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.921-3607C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265512 | |||||||
| chr10:26265699 | T | C | 1 | a0001c0001t0008g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.921-3420T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265699 | |||||||
| chr10:26265736 | A | G | 14 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(11): Show |
14 | HG00642.hp2 HG01884.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.921-3383A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265736 | |||||||
| chr10:26265926 | C | T | 3 | a0001c0001t0008g0011 a0001c0001t0008g0269 a0001c0001t0008g0270 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-3193C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26265926 | |||||||
| chr10:26266333 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.921-2786C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266333 | |||||||
| chr10:26266442 | G | A | 1 | a0003c0005t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.921-2677G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266442 | |||||||
| chr10:26266792 | A | C | 6 | a0001c0001t0005g0127 a0001c0001t0005g0260 a0001c0003t0005g0112 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-2327A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266792 | |||||||
| chr10:26266815 | T | G | 1 | a0001c0001t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.921-2304T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26266815 | |||||||
| chr10:26267188 | G | C | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.921-1931G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267188 | |||||||
| chr10:26267270 | C | A | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.921-1849C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267270 | |||||||
| chr10:26267489 | C | T | 1 | a0001c0001t0013g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.921-1630C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267489 | |||||||
| chr10:26267612 | G | A | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-1507G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267612 | |||||||
| chr10:26267631 | G | A | 29 | a0001c0001t0002g0037 a0001c0001t0002g0123 a0001c0001t0002g0124 others(26): Show |
29 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-1488G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267631 | |||||||
| chr10:26267758 | C | T | 2 | a0001c0001t0007g0253 a0001c0001t0007g0255 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.921-1361C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267758 | |||||||
| chr10:26267948 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.921-1171G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26267948 | |||||||
| chr10:26268038 | A | G | 54 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0007g0103 others(51): Show |
58 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.921-1081A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268038 | |||||||
| chr10:26268384 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
137 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.921-735T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268384 | |||||||
| chr10:26268417 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.921-702A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268417 | |||||||
| chr10:26268467 | C | CA | 41 | a0001c0001t0001g0068 a0001c0001t0001g0091 a0001c0001t0002g0124 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.921-634dupA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | ||||||
| chr10:26268467 | C | CAA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
75 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.921-635_921-634dup others(2): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | ||||||
| chr10:26268467 | C | CAAA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0043 others(11): Show |
14 | HG01106.hp1 HG01109.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.921-636_921-634dup others(3): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | ||||||
| chr10:26268467 | CA | C | 6 | a0001c0001t0003g0207 a0001c0001t0006g0075 a0001c0001t0012g0061 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-634delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr10 | 26268467 | ||||||
| chr10:26268549 | T | G | 1 | a0001c0001t0005g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.921-570T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268549 | |||||||
| chr10:26268681 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.921-438A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268681 | |||||||
| chr10:26268796 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
135 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.921-323A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268796 | |||||||
| chr10:26268841 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
87 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.921-278C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 8/15 | chr10 | 26268841 | |||||||
| chr10:26269418 | G | A | 1 | a0001c0001t0008g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.975+245G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269418 | |||||||
| chr10:26269440 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.975+267G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269440 | |||||||
| chr10:26269556 | G | A | 1 | a0001c0001t0016g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.975+383G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269556 | |||||||
| chr10:26269806 | T | G | 2 | a0001c0001t0005g0107 a0001c0001t0005g0214 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.975+633T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26269806 | |||||||
| chr10:26270049 | C | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.976-591C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270049 | |||||||
| chr10:26270106 | G | A | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-534G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270106 | |||||||
| chr10:26270338 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.976-302G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270338 | |||||||
| chr10:26270474 | A | T | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.976-166A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270474 | |||||||
| chr10:26270475 | G | C | 7 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.976-165G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270475 | |||||||
| chr10:26270510 | G | A | 5 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(2): Show |
6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-130G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270510 | |||||||
| chr10:26270622 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.976-18G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270622 | |||||||
| chr10:26270631 | T | C | 1 | a0001c0001t0016g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.976-9T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 9/15 | chr10 | 26270631 | |||||||
| chr10:26270798 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1092+42C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26270798 | |||||||
| chr10:26270934 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1092+178G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26270934 | |||||||
| chr10:26270941 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1092+185A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26270941 | |||||||
| chr10:26271001 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
84 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1092+245A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271001 | |||||||
| chr10:26271020 | A | G | 4 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0187 others(1): Show |
4 | HG00735.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+264A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271020 | |||||||
| chr10:26271028 | G | C | 5 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+272G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271028 | |||||||
| chr10:26271087 | G | T | 1 | a0001c0001t0005g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1092+331G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271087 | |||||||
| chr10:26271101 | A | G | 3 | a0001c0001t0016g0271 a0001c0001t0016g0276 a0001c0009t0032g0264 |
3 | HG01884.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1092+345A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271101 | |||||||
| chr10:26271104 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1092+348A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271104 | |||||||
| chr10:26271173 | G | A | 38 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0259 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1092+417G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271173 | |||||||
| chr10:26271228 | T | C | 5 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(2): Show |
6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+472T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271228 | |||||||
| chr10:26271283 | G | A | 1 | a0001c0001t0016g0276 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1092+527G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271283 | |||||||
| chr10:26271376 | GA | G | 6 | a0001c0001t0005g0259 a0001c0001t0011g0108 a0001c0001t0011g0109 others(3): Show |
6 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1092+628delA | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr10 | 26271376 | ||||||
| chr10:26271453 | G | T | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1092+697G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271453 | |||||||
| chr10:26271711 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1092+955G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271711 | |||||||
| chr10:26271846 | G | A | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+1090G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271846 | |||||||
| chr10:26271909 | G | A | 2 | a0001c0001t0002g0008 a0001c0001t0002g0184 |
3 | NA18970.hp2 NA18981.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1092+1153G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271909 | |||||||
| chr10:26271987 | T | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+1231T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26271987 | |||||||
| chr10:26272145 | G | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+1389G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272145 | |||||||
| chr10:26272173 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1092+1417G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272173 | |||||||
| chr10:26272292 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
160 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1093-1344T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272292 | |||||||
| chr10:26272310 | G | T | 8 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1093-1326G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272310 | |||||||
| chr10:26272333 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
130 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1093-1303C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272333 | |||||||
| chr10:26272554 | C | CAG | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1093-1081_1093-108 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr10 | 26272554 | ||||||
| chr10:26272698 | T | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0233 |
3 | HG00544.hp1 NA18941.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1093-938T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272698 | |||||||
| chr10:26272747 | C | A | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-889C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272747 | |||||||
| chr10:26272755 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1093-881T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272755 | |||||||
| chr10:26272790 | G | A | 1 | a0001c0001t0003g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1093-846G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272790 | |||||||
| chr10:26272920 | T | C | 45 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(42): Show |
48 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1093-716T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272920 | |||||||
| chr10:26272949 | C | T | 32 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(29): Show |
35 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1093-687C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272949 | |||||||
| chr10:26272950 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
160 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1093-686A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26272950 | |||||||
| chr10:26273092 | TAAG | T | 8 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1093-542_1093-540d others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr10 | 26273092 | ||||||
| chr10:26273249 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1093-387C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273249 | |||||||
| chr10:26273422 | C | T | 1 | a0001c0001t0028g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1093-214C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273422 | |||||||
| chr10:26273485 | G | A | 2 | a0001c0003t0005g0241 a0001c0003t0005g0249 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1093-151G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273485 | |||||||
| chr10:26273576 | A | G | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1093-60A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273576 | |||||||
| chr10:26273601 | A | G | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093-35A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273601 | |||||||
| chr10:26273622 | T | C | 1 | a0001c0001t0007g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1093-14T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 10/15 | chr10 | 26273622 | |||||||
| chr10:26273968 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1157+268G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26273968 | |||||||
| chr10:26274024 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1157+324C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274024 | |||||||
| chr10:26274041 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
160 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1157+341A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274041 | |||||||
| chr10:26274105 | T | A | 1 | a0001c0001t0006g0120 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1157+405T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274105 | |||||||
| chr10:26274168 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1157+468G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274168 | |||||||
| chr10:26274245 | T | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+545T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274245 | |||||||
| chr10:26274509 | C | T | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+809C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274509 | |||||||
| chr10:26274667 | G | A | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+967G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274667 | |||||||
| chr10:26274701 | C | A | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+1001C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274701 | |||||||
| chr10:26274716 | G | A | 3 | a0001c0001t0003g0207 a0001c0001t0003g0229 a0001c0001t0025g0198 |
3 | HG00438.hp2 NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1157+1016G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274716 | |||||||
| chr10:26274758 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1157+1058G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274758 | |||||||
| chr10:26274772 | G | T | 1 | a0001c0001t0005g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1157+1072G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274772 | |||||||
| chr10:26274844 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1157+1144C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26274844 | |||||||
| chr10:26275226 | G | A | 32 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(29): Show |
35 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1157+1526G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275226 | |||||||
| chr10:26275439 | G | A | 8 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+1739G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275439 | |||||||
| chr10:26275480 | C | A | 1 | a0001c0001t0003g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1157+1780C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275480 | |||||||
| chr10:26275504 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1157+1804T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275504 | |||||||
| chr10:26275598 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
160 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1157+1898T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275598 | |||||||
| chr10:26275650 | G | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157+1950G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275650 | |||||||
| chr10:26275907 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1157+2207G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275907 | |||||||
| chr10:26275922 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
110 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1157+2222A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275922 | |||||||
| chr10:26275927 | G | A | 24 | a0001c0001t0003g0155 a0001c0001t0005g0107 a0001c0001t0005g0127 others(21): Show |
26 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1157+2227G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275927 | |||||||
| chr10:26275993 | G | T | 9 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(6): Show |
9 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1157+2293G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26275993 | |||||||
| chr10:26276227 | C | T | 1 | a0001c0001t0007g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1157+2527C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276227 | |||||||
| chr10:26276309 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
110 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1157+2609G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276309 | |||||||
| chr10:26276345 | G | A | 1 | a0001c0003t0015g0266 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1157+2645G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276345 | |||||||
| chr10:26276391 | T | C | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1157+2691T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276391 | |||||||
| chr10:26276457 | C | CT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
120 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1157+2758dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr10 | 26276457 | ||||||
| chr10:26276506 | T | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+2806T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276506 | |||||||
| chr10:26276631 | G | A | 11 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(8): Show |
11 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1157+2931G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276631 | |||||||
| chr10:26276705 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
160 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1157+3005G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276705 | |||||||
| chr10:26276744 | G | A | 58 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0208 others(55): Show |
60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1157+3044G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276744 | |||||||
| chr10:26276893 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
86 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1157+3193A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26276893 | |||||||
| chr10:26277010 | T | C | 2 | a0001c0001t0008g0269 a0001c0001t0008g0270 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1157+3310T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277010 | |||||||
| chr10:26277030 | G | A | 1 | a0001c0001t0024g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1157+3330G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277030 | |||||||
| chr10:26277163 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0051 |
2 | NA18612.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1157+3463G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277163 | |||||||
| chr10:26277306 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
122 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1157+3606T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277306 | |||||||
| chr10:26277363 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1158-3646C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277363 | |||||||
| chr10:26277417 | C | G | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-3592C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277417 | |||||||
| chr10:26277418 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG02109.hp2 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1158-3591G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277418 | |||||||
| chr10:26277479 | G | A | 1 | a0001c0001t0005g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1158-3530G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277479 | |||||||
| chr10:26277498 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
161 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1158-3511A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277498 | |||||||
| chr10:26277527 | C | T | 29 | a0001c0001t0002g0037 a0001c0001t0002g0123 a0001c0001t0002g0124 others(26): Show |
29 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1158-3482C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277527 | |||||||
| chr10:26277606 | G | T | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-3403G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277606 | |||||||
| chr10:26277616 | G | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-3393G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277616 | |||||||
| chr10:26277678 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1158-3331G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277678 | |||||||
| chr10:26277704 | T | C | 2 | a0001c0001t0015g0100 a0001c0003t0015g0266 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1158-3305T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277704 | |||||||
| chr10:26277789 | A | G | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-3220A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277789 | |||||||
| chr10:26277860 | G | A | 9 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(6): Show |
9 | HG02280.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-3149G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277860 | |||||||
| chr10:26277920 | A | G | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-3089A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26277920 | |||||||
| chr10:26277989 | GT | G | 18 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(15): Show |
19 | HG00642.hp2 HG02145.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1158-3008delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr10 | 26277989 | ||||||
| chr10:26278252 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
132 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1158-2757C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278252 | |||||||
| chr10:26278291 | A | G | 2 | a0001c0001t0019g0106 a0001c0001t0023g0250 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1158-2718A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278291 | |||||||
| chr10:26278411 | C | T | 4 | a0001c0001t0008g0011 a0001c0001t0008g0016 a0001c0001t0008g0269 others(1): Show |
5 | HG02145.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-2598C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278411 | |||||||
| chr10:26278414 | C | T | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-2595C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278414 | |||||||
| chr10:26278473 | T | A | 1 | a0001c0001t0003g0132 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1158-2536T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278473 | |||||||
| chr10:26278523 | G | A | 9 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(6): Show |
9 | HG02280.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-2486G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278523 | |||||||
| chr10:26278716 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1158-2293T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278716 | |||||||
| chr10:26278759 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1158-2250T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278759 | |||||||
| chr10:26278897 | G | A | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1158-2112G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278897 | |||||||
| chr10:26278931 | C | A | 12 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(9): Show |
13 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1158-2078C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278931 | |||||||
| chr10:26278932 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
138 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1158-2077A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278932 | |||||||
| chr10:26278978 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01192.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-2031G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278978 | |||||||
| chr10:26278986 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1158-2023A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26278986 | |||||||
| chr10:26279330 | G | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1158-1679G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279330 | |||||||
| chr10:26279353 | C | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158-1656C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279353 | |||||||
| chr10:26279433 | C | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1158-1576C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279433 | |||||||
| chr10:26279604 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1158-1405C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279604 | |||||||
| chr10:26279605 | G | A | 1 | a0001c0001t0006g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1158-1404G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279605 | |||||||
| chr10:26279776 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
103 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1158-1233A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279776 | |||||||
| chr10:26279810 | T | C | 6 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0003t0010g0244 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-1199T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279810 | |||||||
| chr10:26279935 | T | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-1074T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26279935 | |||||||
| chr10:26280049 | A | G | 1 | a0001c0001t0002g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1158-960A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280049 | |||||||
| chr10:26280427 | C | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1158-582C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280427 | |||||||
| chr10:26280587 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1158-422G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280587 | |||||||
| chr10:26280675 | A | G | 1 | a0001c0001t0012g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1158-334A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280675 | |||||||
| chr10:26280698 | T | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0214 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1158-311T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280698 | |||||||
| chr10:26280826 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1158-183A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 11/15 | chr10 | 26280826 | |||||||
| chr10:26281267 | G | A | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1236+180G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281267 | |||||||
| chr10:26281394 | C | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1236+307C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281394 | |||||||
| chr10:26281504 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1236+417C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281504 | |||||||
| chr10:26281505 | A | C | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+418A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281505 | |||||||
| chr10:26281577 | G | T | 1 | a0001c0001t0003g0174 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1236+490G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281577 | |||||||
| chr10:26281749 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1236+662G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281749 | |||||||
| chr10:26281754 | C | T | 1 | a0001c0001t0003g0130 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1236+667C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281754 | |||||||
| chr10:26281778 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1236+691C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281778 | |||||||
| chr10:26281792 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1236+705G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281792 | |||||||
| chr10:26281996 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1236+909G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26281996 | |||||||
| chr10:26282044 | G | A | 6 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0003t0010g0244 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+957G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282044 | |||||||
| chr10:26282080 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1236+993A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282080 | |||||||
| chr10:26282135 | GT | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
141 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1236+1052delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26282135 | ||||||
| chr10:26282513 | T | C | 2 | a0001c0001t0019g0106 a0001c0001t0023g0250 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1236+1426T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282513 | |||||||
| chr10:26282593 | A | G | 30 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(27): Show |
30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1236+1506A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282593 | |||||||
| chr10:26282981 | C | T | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1236+1894C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282981 | |||||||
| chr10:26282997 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG00438.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1236+1910G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26282997 | |||||||
| chr10:26283023 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1236+1936A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283023 | |||||||
| chr10:26283077 | G | T | 1 | a0001c0001t0003g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1236+1990G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283077 | |||||||
| chr10:26283144 | C | A | 4 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0187 others(1): Show |
4 | HG00735.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+2057C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283144 | |||||||
| chr10:26283237 | A | G | 2 | a0001c0001t0016g0271 a0001c0001t0016g0276 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1236+2150A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283237 | |||||||
| chr10:26283253 | G | A | 1 | a0001c0001t0003g0128 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1236+2166G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283253 | |||||||
| chr10:26283851 | G | C | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237-2494G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283851 | |||||||
| chr10:26283913 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
141 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1237-2432A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26283913 | |||||||
| chr10:26284109 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237-2236C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284109 | |||||||
| chr10:26284147 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
68 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1237-2198G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284147 | |||||||
| chr10:26284478 | A | G | 5 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0117 others(2): Show |
5 | HG00323.hp2 HG00639.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-1867A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284478 | |||||||
| chr10:26284544 | A | G | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1237-1801A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284544 | |||||||
| chr10:26284564 | C | CT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
87 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1237-1758dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | ||||||
| chr10:26284564 | C | CTT | 37 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0077 others(34): Show |
40 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1237-1759_1237-175 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | ||||||
| chr10:26284564 | C | CTTT | 8 | a0001c0001t0008g0016 a0001c0001t0011g0108 a0001c0001t0011g0109 others(5): Show |
8 | HG00642.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-1760_1237-175 others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | ||||||
| chr10:26284564 | CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(17): Show |
20 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1237-1767_1237-175 others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26284564 | ||||||
| chr10:26284628 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237-1717G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284628 | |||||||
| chr10:26284700 | T | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0180 |
2 | NA18948.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1237-1645T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284700 | |||||||
| chr10:26284763 | G | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-1582G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284763 | |||||||
| chr10:26284808 | A | T | 14 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(11): Show |
14 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1237-1537A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284808 | |||||||
| chr10:26284820 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
86 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1237-1525C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284820 | |||||||
| chr10:26284862 | C | G | 2 | a0001c0001t0005g0107 a0001c0001t0005g0214 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1237-1483C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284862 | |||||||
| chr10:26284865 | G | A | 3 | a0001c0001t0017g0015 a0001c0001t0020g0280 a0001c0001t0028g0279 |
3 | HG03486.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1237-1480G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26284865 | |||||||
| chr10:26285001 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1237-1344T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285001 | |||||||
| chr10:26285020 | T | C | 2 | a0001c0001t0003g0207 a0001c0001t0003g0229 |
2 | NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1237-1325T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285020 | |||||||
| chr10:26285253 | C | T | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-1092C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285253 | |||||||
| chr10:26285330 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
138 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1237-1015G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285330 | |||||||
| chr10:26285365 | T | C | 1 | a0001c0001t0020g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1237-980T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285365 | |||||||
| chr10:26285366 | G | T | 1 | a0001c0003t0005g0249 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1237-979G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285366 | |||||||
| chr10:26285605 | T | G | 2 | a0001c0001t0016g0271 a0001c0001t0016g0276 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1237-740T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285605 | |||||||
| chr10:26285651 | C | G | 1 | a0001c0001t0003g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1237-694C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285651 | |||||||
| chr10:26285673 | C | T | 1 | a0001c0003t0009g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1237-672C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285673 | |||||||
| chr10:26285768 | GT | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
136 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.1237-563delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr10 | 26285768 | ||||||
| chr10:26285818 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237-527C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285818 | |||||||
| chr10:26285964 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
141 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.1237-381T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26285964 | |||||||
| chr10:26286119 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1237-226C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26286119 | |||||||
| chr10:26286292 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237-53A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 12/15 | chr10 | 26286292 | |||||||
| chr10:26286719 | T | C | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+225T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286719 | |||||||
| chr10:26286861 | G | A | 2 | a0001c0001t0019g0106 a0001c0001t0023g0250 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1386+367G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286861 | |||||||
| chr10:26286935 | T | C | 1 | a0001c0001t0009g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1386+441T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286935 | |||||||
| chr10:26286967 | CT | C | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1386+474delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26286967 | |||||||
| chr10:26287012 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1386+518A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287012 | |||||||
| chr10:26287097 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1386+603A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287097 | |||||||
| chr10:26287164 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1386+670G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287164 | |||||||
| chr10:26287321 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1386+827A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287321 | |||||||
| chr10:26287333 | G | A | 10 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(7): Show |
10 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386+839G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287333 | |||||||
| chr10:26287339 | G | C | 4 | a0001c0001t0003g0168 a0001c0001t0003g0199 a0001c0001t0003g0205 others(1): Show |
4 | HG00558.hp1 HG02523.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+845G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287339 | |||||||
| chr10:26287576 | G | A | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+1082G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287576 | |||||||
| chr10:26287696 | T | C | 6 | a0001c0001t0008g0011 a0001c0001t0008g0016 a0001c0001t0008g0063 others(3): Show |
7 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+1202T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287696 | |||||||
| chr10:26287704 | A | G | 1 | a0001c0001t0001g0005 | 2 | NA18962.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1386+1210A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287704 | |||||||
| chr10:26287853 | A | C | 36 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(33): Show |
37 | HG00642.hp1 HG01192.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1386+1359A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287853 | |||||||
| chr10:26287905 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1386+1411G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26287905 | |||||||
| chr10:26288097 | C | A | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1386+1603C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288097 | |||||||
| chr10:26288280 | C | T | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1386+1786C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288280 | |||||||
| chr10:26288355 | T | A | 1 | a0001c0001t0002g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1386+1861T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288355 | |||||||
| chr10:26288387 | T | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0214 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1386+1893T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288387 | |||||||
| chr10:26288532 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1386+2038C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288532 | |||||||
| chr10:26288563 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1386+2069C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288563 | |||||||
| chr10:26288656 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1386+2162C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288656 | |||||||
| chr10:26288706 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1386+2212C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288706 | |||||||
| chr10:26288742 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
70 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1386+2248G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288742 | |||||||
| chr10:26288881 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1386+2387T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26288881 | |||||||
| chr10:26289015 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1386+2521G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289015 | |||||||
| chr10:26289036 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1386+2542C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289036 | |||||||
| chr10:26289064 | C | T | 1 | a0001c0003t0002g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1386+2570C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289064 | |||||||
| chr10:26289078 | G | GT | 14 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(11): Show |
14 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1386+2593dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289078 | ||||||
| chr10:26289101 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1386+2607A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289101 | |||||||
| chr10:26289186 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1386+2692C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289186 | |||||||
| chr10:26289223 | C | T | 2 | a0001c0001t0002g0122 a0001c0001t0018g0221 |
2 | HG01358.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1386+2729C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289223 | |||||||
| chr10:26289408 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1386+2914C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289408 | |||||||
| chr10:26289534 | A | G | 36 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(33): Show |
37 | HG00642.hp1 HG01192.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1387-2931A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289534 | |||||||
| chr10:26289541 | A | T | 5 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-2924A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289541 | |||||||
| chr10:26289710 | A | G | 1 | a0001c0001t0028g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1387-2755A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289710 | |||||||
| chr10:26289727 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1387-2738C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26289727 | |||||||
| chr10:26289793 | C | CT | 24 | a0001c0001t0002g0166 a0001c0001t0002g0233 a0001c0001t0005g0107 others(21): Show |
25 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1387-2655dupT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289793 | ||||||
| chr10:26289793 | CT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1387-2655delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289793 | ||||||
| chr10:26289793 | CTTT | C | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1387-2657_1387-265 others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26289793 | ||||||
| chr10:26290038 | T | C | 1 | a0001c0001t0018g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1387-2427T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290038 | |||||||
| chr10:26290401 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1387-2064A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290401 | |||||||
| chr10:26290534 | C | T | 1 | a0001c0009t0032g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1387-1931C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290534 | |||||||
| chr10:26290601 | G | T | 1 | a0001c0002t0004g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1387-1864G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290601 | |||||||
| chr10:26290742 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1387-1723C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290742 | |||||||
| chr10:26290864 | A | G | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1387-1601A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26290864 | |||||||
| chr10:26291047 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1387-1418T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291047 | |||||||
| chr10:26291107 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1387-1358T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291107 | |||||||
| chr10:26291430 | A | AAGAAGTG others(8): Show |
20 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(17): Show |
20 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1387-1033_1387-101 others(19): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr10 | 26291430 | ||||||
| chr10:26291455 | G | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
86 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1387-1010G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291455 | |||||||
| chr10:26291644 | T | C | 3 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0143 |
3 | NA18980.hp1 NA18982.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1387-821T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291644 | |||||||
| chr10:26291655 | G | A | 1 | a0001c0001t0005g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1387-810G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291655 | |||||||
| chr10:26291813 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
8 | NA18941.hp1 NA18948.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1387-652T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291813 | |||||||
| chr10:26291997 | A | G | 30 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(27): Show |
30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1387-468A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26291997 | |||||||
| chr10:26292164 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
123 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1387-301T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26292164 | |||||||
| chr10:26292392 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
124 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1387-73G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 13/15 | chr10 | 26292392 | |||||||
| chr10:26292634 | A | G | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+62A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 14/15 | chr10 | 26292634 | |||||||
| chr10:26293049 | T | G | 2 | a0001c0001t0008g0269 a0001c0001t0008g0270 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1584+58T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293049 | |||||||
| chr10:26293172 | CT | C | 12 | a0001c0001t0002g0177 a0001c0001t0005g0127 a0001c0001t0005g0260 others(9): Show |
12 | HG01070.hp1 HG01256.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1584+204delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26293172 | ||||||
| chr10:26293193 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0016g0271 |
3 | HG01106.hp1 HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1584+202T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293193 | |||||||
| chr10:26293193 | T | TTC | 11 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0032 others(8): Show |
11 | HG01070.hp2 HG01255.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1584+203_1584+204i others(4): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26293193 | ||||||
| chr10:26293193 | T | TTTC | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
78 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1584+204_1584+205i others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26293193 | ||||||
| chr10:26293201 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1584+210G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293201 | |||||||
| chr10:26293456 | G | A | 2 | a0001c0001t0002g0159 a0002c0004t0002g0192 |
2 | HG00738.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1584+465G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293456 | |||||||
| chr10:26293648 | A | G | 1 | a0001c0001t0001g0005 | 2 | NA18962.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1584+657A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293648 | |||||||
| chr10:26293668 | G | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1584+677G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293668 | |||||||
| chr10:26293912 | G | A | 3 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 |
3 | HG02809.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1584+921G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26293912 | |||||||
| chr10:26294090 | T | C | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1584+1099T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294090 | |||||||
| chr10:26294102 | G | A | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+1111G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294102 | |||||||
| chr10:26294396 | A | G | 5 | a0001c0001t0014g0058 a0001c0001t0014g0104 a0001c0001t0017g0015 others(2): Show |
5 | HG02451.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+1405A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294396 | |||||||
| chr10:26294449 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1584+1458T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294449 | |||||||
| chr10:26294459 | G | T | 6 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0003t0010g0244 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+1468G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294459 | |||||||
| chr10:26294747 | G | C | 24 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(21): Show |
24 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1584+1756G>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294747 | |||||||
| chr10:26294779 | A | T | 1 | a0001c0001t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1584+1788A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294779 | |||||||
| chr10:26294802 | C | T | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1584+1811C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294802 | |||||||
| chr10:26294959 | T | G | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+1968T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26294959 | |||||||
| chr10:26295041 | TG | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1584+2053delG | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295041 | ||||||
| chr10:26295052 | A | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG00140.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1584+2061A>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295052 | |||||||
| chr10:26295073 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1584+2082G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295073 | |||||||
| chr10:26295082 | C | CA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1584+2091_1584+209 others(5): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295082 | |||||||
| chr10:26295092 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1584+2101T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295092 | |||||||
| chr10:26295124 | G | T | 2 | a0001c0001t0012g0105 a0001c0007t0012g0258 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1584+2133G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295124 | |||||||
| chr10:26295185 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1584+2194G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295185 | |||||||
| chr10:26295434 | T | A | 14 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(11): Show |
15 | HG00642.hp2 HG01192.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1584+2443T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295434 | |||||||
| chr10:26295503 | C | T | 5 | a0001c0001t0005g0127 a0001c0001t0005g0260 a0001c0003t0005g0112 others(2): Show |
5 | HG02647.hp1 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1584+2512C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295503 | |||||||
| chr10:26295505 | C | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1584+2514C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295505 | |||||||
| chr10:26295508 | G | GCA | 30 | a0001c0001t0002g0123 a0001c0001t0002g0137 a0001c0001t0002g0138 others(27): Show |
31 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1584+2556_1584+255 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACA | 15 | a0001c0001t0002g0126 a0001c0001t0003g0188 a0001c0001t0003g0229 others(12): Show |
15 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1584+2554_1584+255 others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
9 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1584+2552_1584+255 others(10): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0060 others(4): Show |
7 | HG01243.hp2 HG02027.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1584+2550_1584+255 others(12): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG03669.hp1 NA18522.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1584+2548_1584+255 others(14): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(5): Show |
25 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0042 others(22): Show |
26 | HG00597.hp2 HG00735.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1584+2546_1584+255 others(16): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(7): Show |
21 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0033 others(18): Show |
21 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1584+2544_1584+255 others(18): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(9): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(23): Show |
30 | HG00140.hp1 HG01099.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1584+2542_1584+255 others(20): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(11): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0005g0261 others(1): Show |
4 | HG01993.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+2540_1584+255 others(22): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(13): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+2538_1584+255 others(24): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(15): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0041 others(6): Show |
9 | HG00438.hp1 HG00642.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1584+2536_1584+255 others(26): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | G | GCACACAC others(17): Show |
2 | a0001c0001t0001g0021 a0001c0001t0011g0111 |
2 | HG01069.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1584+2534_1584+255 others(28): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | GCA | G | 19 | a0001c0001t0002g0008 a0001c0001t0002g0166 a0001c0001t0002g0182 others(16): Show |
20 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1584+2556_1584+255 others(6): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295508 | GCACA | G | 4 | a0001c0001t0002g0167 a0001c0001t0003g0204 a0001c0003t0005g0241 others(1): Show |
4 | HG02293.hp1 HG03195.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584+2554_1584+255 others(8): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26295508 | ||||||
| chr10:26295946 | G | A | 4 | a0001c0001t0011g0108 a0001c0001t0011g0109 a0001c0001t0011g0110 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+2955G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26295946 | |||||||
| chr10:26296060 | G | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1584+3069G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296060 | |||||||
| chr10:26296087 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1584+3096C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296087 | |||||||
| chr10:26296104 | C | G | 5 | a0001c0001t0014g0058 a0001c0001t0014g0104 a0001c0001t0017g0015 others(2): Show |
5 | HG02451.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+3113C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296104 | |||||||
| chr10:26296159 | G | T | 5 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(2): Show |
6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+3168G>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296159 | |||||||
| chr10:26296211 | C | T | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1584+3220C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296211 | |||||||
| chr10:26296248 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1584+3257T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296248 | |||||||
| chr10:26296425 | GTTA | G | 25 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(22): Show |
25 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1584+3438_1584+344 others(7): Show |
GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26296425 | ||||||
| chr10:26296432 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1584+3441A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296432 | |||||||
| chr10:26296576 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1584+3585A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296576 | |||||||
| chr10:26296589 | G | A | 25 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(22): Show |
25 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1584+3598G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296589 | |||||||
| chr10:26296673 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1584+3682A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296673 | |||||||
| chr10:26296882 | A | C | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1584+3891A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26296882 | |||||||
| chr10:26296920 | AT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1585-3856delT | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr10 | 26296920 | ||||||
| chr10:26297174 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1585-3614A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297174 | |||||||
| chr10:26297176 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1585-3612C>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297176 | |||||||
| chr10:26297281 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1585-3507C>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297281 | |||||||
| chr10:26297872 | T | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0104 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1585-2916T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297872 | |||||||
| chr10:26297997 | A | G | 1 | a0001c0001t0016g0271 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1585-2791A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26297997 | |||||||
| chr10:26298221 | C | T | 1 | a0001c0001t0017g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1585-2567C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298221 | |||||||
| chr10:26298225 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1585-2563G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298225 | |||||||
| chr10:26298239 | T | C | 1 | a0001c0002t0004g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1585-2549T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298239 | |||||||
| chr10:26298315 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1585-2473C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298315 | |||||||
| chr10:26298440 | C | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1585-2348C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298440 | |||||||
| chr10:26298457 | G | A | 1 | a0001c0001t0011g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1585-2331G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298457 | |||||||
| chr10:26298612 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
99 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1585-2176A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298612 | |||||||
| chr10:26298794 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1585-1994G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298794 | |||||||
| chr10:26298805 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1585-1983A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298805 | |||||||
| chr10:26298817 | C | T | 3 | a0001c0001t0002g0157 a0001c0001t0002g0178 a0001c0001t0002g0179 |
3 | HG03710.hp1 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1585-1971C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298817 | |||||||
| chr10:26298992 | G | A | 2 | a0001c0003t0005g0241 a0001c0003t0005g0249 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1585-1796G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26298992 | |||||||
| chr10:26299361 | T | G | 1 | a0001c0002t0004g0240 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1585-1427T>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299361 | |||||||
| chr10:26299434 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
124 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1585-1354A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299434 | |||||||
| chr10:26299664 | A | G | 15 | a0001c0002t0004g0009 a0001c0002t0004g0010 a0001c0002t0004g0019 others(12): Show |
17 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1585-1124A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299664 | |||||||
| chr10:26299926 | T | C | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1585-862T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299926 | |||||||
| chr10:26299962 | A | G | 1 | a0001c0001t0002g0226 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1585-826A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26299962 | |||||||
| chr10:26300203 | G | A | 18 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(15): Show |
18 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1585-585G>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300203 | |||||||
| chr10:26300318 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1585-470A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300318 | |||||||
| chr10:26300456 | T | C | 30 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(27): Show |
30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1585-332T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300456 | |||||||
| chr10:26300464 | A | C | 4 | a0001c0003t0010g0244 a0001c0003t0010g0245 a0001c0003t0010g0246 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1585-324A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300464 | |||||||
| chr10:26300498 | A | G | 30 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(27): Show |
30 | HG00642.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1585-290A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300498 | |||||||
| chr10:26300508 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0066 |
2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1585-280T>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300508 | |||||||
| chr10:26300528 | A | C | 1 | a0001c0003t0010g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1585-260A>C | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300528 | |||||||
| chr10:26300618 | C | T | 8 | a0001c0001t0007g0103 a0001c0001t0007g0251 a0001c0001t0007g0252 others(5): Show |
8 | HG00642.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1585-170C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300618 | |||||||
| chr10:26300675 | A | G | 24 | a0001c0001t0005g0107 a0001c0001t0005g0127 a0001c0001t0005g0214 others(21): Show |
24 | HG00642.hp1 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1585-113A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300675 | |||||||
| chr10:26300696 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1585-92T>A | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300696 | |||||||
| chr10:26300709 | C | T | 5 | a0001c0001t0009g0003 a0001c0001t0009g0012 a0001c0001t0009g0013 others(2): Show |
6 | HG00735.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-79C>T | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300709 | |||||||
| chr10:26300742 | A | G | 1 | a0001c0003t0005g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1585-46A>G | GAD2 | ENSG00000136750.13 | transcript | ENST00000376261.8 | protein_coding | 15/15 | chr10 | 26300742 |