Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 203102 |
| ensemblid | ENSG00000197140.15 |
| hgncid | 15479 |
| symbol | ADAM32 |
| name | ADAM metallopeptidase domain 32 |
| refseq_nuc | NM_145004.7 |
| refseq_prot | NP_659441.4 |
| ensembl_nuc | ENST00000379907.9 |
| ensembl_prot | ENSP00000369238.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 39107734 |
| end | 39284917 |
| strand | + |
| ver | v1.2 |
| region | chr8:39107734-39284917 |
| region5000 | chr8:39102734-39289917 |
| regionname0 | ADAM32_chr8_39107734_39284917 |
| regionname5000 | ADAM32_chr8_39102734_39289917 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 787 | 199 | 16 | 55 | 97 | 12 | 18 | 77 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0002 | 0/0 | 787 | 30 | 24 | 1 | 5 | 0 | 0 | 3 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0003 | 0/0 | 787 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0004 | 0/0 | 787 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0005 | 0/0 | 787 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0006 | 0/0 | 787 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0007 | 0/0 | 787 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0008 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0009 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0010 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0011 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| a0012 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | MFRLW others(782): Show |
chr8 | 39102734 | 39289917 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2361 | 130 | 15 | 41 | 53 | 9 | 12 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0001c0002 | 0/1 | 2361 | 69 | 1 | 14 | 44 | 3 | 6 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0002c0003 | 0/0 | 2361 | 23 | 19 | 1 | 3 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0002c0005 | 0/0 | 2361 | 7 | 5 | 0 | 2 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0003c0004 | 0/0 | 2361 | 10 | 10 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0004c0007 | 0/0 | 2361 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0005c0006 | 0/0 | 2361 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0006c0008 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0007c0009 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0008c0012 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0009c0014 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0010c0010 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0011c0011 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 | ||
| a0012c0013 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | ATGTT others(2356): Show |
chr8 | 39102734 | 39289917 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2524 | 62 | 9 | 24 | 17 | 3 | 9 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0001c0001t0002 | 0/0 | 2524 | 68 | 6 | 17 | 36 | 6 | 3 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0001c0002t0001 | 0/1 | 2524 | 24 | 0 | 2 | 19 | 0 | 2 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0001c0002t0002 | 0/0 | 2524 | 45 | 1 | 12 | 25 | 3 | 4 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0002c0003t0001 | 0/0 | 2524 | 20 | 16 | 1 | 3 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0002c0003t0002 | 0/0 | 2524 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0002c0005t0001 | 0/0 | 2524 | 4 | 2 | 0 | 2 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0002c0005t0002 | 0/0 | 2524 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0003c0004t0001 | 0/0 | 2524 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0003c0004t0002 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0004c0007t0001 | 0/0 | 2524 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0005c0006t0001 | 0/0 | 2524 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0006c0008t0001 | 0/0 | 2524 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0006c0008t0002 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0007c0009t0001 | 0/0 | 2524 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0008c0012t0002 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0009c0014t0002 | 0/0 | 2524 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0010c0010t0001 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0011c0011t0001 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| a0012c0013t0001 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | GACTT others(2519): Show |
chr8 | 39102734 | 39289917 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0002c0005t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0003c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0004c0007t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0004c0007t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0004c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0004c0007t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0005c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0005c0006t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0005c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0005c0006t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0006c0008t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0006c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0006c0008t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0007c0009t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0007c0009t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0008c0012t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0009c0014t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0010c0010t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0011c0011t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| a0012c0013t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0117 | EUR | GBR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0102 | EUR | FIN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00408 | hp2 | a0002 | c0005 | t0001 | g0249 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00621 | hp2 | a0002 | c0005 | t0001 | g0250 | EAS | CHS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00642 | hp2 | a0008 | c0012 | t0002 | g0119 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0214 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0086 | EUR | IBS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | IBS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0124 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01978 | hp1 | a0009 | c0014 | t0002 | g0106 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0103 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02055 | hp1 | a0010 | c0010 | t0001 | g0077 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02257 | hp2 | a0003 | c0004 | t0001 | g0136 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02258 | hp2 | a0003 | c0004 | t0001 | g0143 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0228 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02615 | hp2 | a0011 | c0011 | t0001 | g0138 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0246 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02647 | hp1 | a0002 | c0005 | t0001 | g0241 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0255 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0139 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02717 | hp2 | a0004 | c0007 | t0001 | g0244 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02723 | hp1 | a0005 | c0006 | t0001 | g0216 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02723 | hp2 | a0007 | c0009 | t0001 | g0152 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02809 | hp1 | a0007 | c0009 | t0001 | g0245 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0239 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02886 | hp2 | a0004 | c0007 | t0001 | g0154 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0135 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0151 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02896 | hp1 | a0002 | c0005 | t0002 | g0093 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0140 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02897 | hp2 | a0002 | c0005 | t0002 | g0095 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0137 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0229 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0254 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0230 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0242 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03041 | hp2 | a0003 | c0004 | t0002 | g0047 | AFR | GWD | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0253 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03209 | hp1 | a0005 | c0006 | t0001 | g0144 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03209 | hp2 | a0003 | c0004 | t0001 | g0142 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03225 | hp1 | a0005 | c0006 | t0001 | g0223 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0141 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0166 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0238 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03516 | hp1 | a0006 | c0008 | t0001 | g0068 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03579 | hp1 | a0012 | c0013 | t0001 | g0153 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0049 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0126 | SAS | STU | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0189 | SAS | BEB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | STU | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | STU | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | STU | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18522 | hp1 | a0005 | c0006 | t0001 | g0222 | AFR | YRI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18522 | hp2 | a0006 | c0008 | t0001 | g0069 | AFR | YRI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | CHB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18906 | hp1 | a0004 | c0007 | t0001 | g0155 | AFR | YRI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18906 | hp2 | a0002 | c0003 | t0002 | g0017 | AFR | YRI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19043 | hp1 | a0002 | c0005 | t0002 | g0115 | AFR | LWK | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0048 | AFR | YRI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0157 | AFR | YRI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0042 | EUR | TSI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | TSI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0247 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02559 | hp1 | a0006 | c0008 | t0002 | g0132 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | ACB | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG03471 | hp2 | a0004 | c0007 | t0001 | g0156 | AFR | MSL | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG06807 | hp1 | a0003 | c0004 | t0001 | g0134 | AFR | USA | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | USA | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA20300 | hp1 | a0002 | c0005 | t0001 | g0006 | AFR | USA | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0165 | AFR | USA | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0133 | REF | REF | ADAM32_chr8_39102734_39289917 | ADAM32 | chr8 | 39102734 | 39289917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39165073 | A | C | 1 | a0009 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.710A>C | p.Glu237Ala | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/25 | 752/2524 | 710/2364 | 237/787 | chr8 | 39165073 | |||
| chr8:39169989 | G | A | 1 | a0010 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.907G>A | p.Val303Ile | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/25 | 949/2524 | 907/2364 | 303/787 | chr8 | 39169989 | |||
| chr8:39223113 | C | G | 9 | a0001 a0002 a0004 others(6): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
missense_variant | MODERATE | c.1400C>G | p.Thr467Ser | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/25 | 1442/2524 | 1400/2364 | 467/787 | chr8 | 39223113 | |||
| chr8:39233940 | G | A | 1 | a0008 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1676G>A | p.Arg559Gln | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/25 | 1718/2524 | 1676/2364 | 559/787 | chr8 | 39233940 | |||
| chr8:39234027 | G | A | 1 | a0006 | 3 | HG02559.hp1 HG03516.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.1763G>A | p.Arg588Gln | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/25 | 1805/2524 | 1763/2364 | 588/787 | chr8 | 39234027 | |||
| chr8:39254514 | T | C | 5 | a0003 a0004 a0007 others(2): Show |
18 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(15): Show |
missense_variant&splice_region_variant | MODERATE | c.2003T>C | p.Met668Thr | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/25 | 2045/2524 | 2003/2364 | 668/787 | chr8 | 39254514 | |||
| chr8:39275845 | G | A | 1 | a0007 | 2 | HG02723.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.2258G>A | p.Ser753Asn | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/25 | 2300/2524 | 2258/2364 | 753/787 | chr8 | 39275845 | |||
| chr8:39283601 | C | A | 6 | a0002 a0005 a0006 others(3): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
missense_variant | MODERATE | c.2334C>A | p.Asp778Glu | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/25 | 2376/2524 | 2334/2364 | 778/787 | chr8 | 39283601 | |||
| chr8:39284793 | T | A | 1 | a0011 | 1 | HG02615.hp2 | missense_variant&splice_region_variant | MODERATE | c.2358T>A | p.Ser786Arg | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 25/25 | 2400/2524 | 2358/2364 | 786/787 | chr8 | 39284793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39234007 | T | C | 3 | a0001c0002 a0002c0005 a0009c0014 |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
synonymous_variant | LOW | c.1743T>C | p.Thr581Thr | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/25 | 1785/2524 | 1743/2364 | 581/787 | chr8 | 39234007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39107752 | C | T | 8 | a0001c0001t0002 a0001c0002t0002 a0002c0003t0002 others(5): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/25 | chr8 | 39107752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39108153 | T | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG00280.hp1 HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.58+320T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108153 | |||||||
| chr8:39108350 | T | C | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.58+517T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108350 | |||||||
| chr8:39108402 | A | G | 1 | a0002c0003t0001g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+569A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108402 | |||||||
| chr8:39108471 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0240 a0001c0001t0001g0243 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+638A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108471 | |||||||
| chr8:39108494 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
108 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.58+661A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108494 | |||||||
| chr8:39108601 | A | G | 5 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG00621.hp1 HG02083.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+768A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108601 | |||||||
| chr8:39108699 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58+866C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39108699 | |||||||
| chr8:39109343 | T | C | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+1510T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109343 | |||||||
| chr8:39109346 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.58+1513A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109346 | |||||||
| chr8:39109509 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+1676C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109509 | |||||||
| chr8:39109576 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58+1743T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109576 | |||||||
| chr8:39109787 | C | T | 1 | a0006c0008t0002g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+1954C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109787 | |||||||
| chr8:39109934 | T | G | 1 | a0001c0002t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58+2101T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109934 | |||||||
| chr8:39109939 | T | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0149 others(100): Show |
103 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+2106T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39109939 | |||||||
| chr8:39110000 | C | CT | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.58+2176dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39110000 | ||||||
| chr8:39110042 | C | G | 6 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(3): Show |
6 | HG01934.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+2209C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110042 | |||||||
| chr8:39110163 | G | A | 1 | a0002c0003t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58+2330G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110163 | |||||||
| chr8:39110380 | T | C | 24 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(21): Show |
24 | HG00438.hp1 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.58+2547T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110380 | |||||||
| chr8:39110543 | A | G | 1 | a0001c0002t0002g0131 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.58+2710A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110543 | |||||||
| chr8:39110548 | G | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(4): Show |
8 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+2715G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110548 | |||||||
| chr8:39110649 | A | T | 14 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(11): Show |
14 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.58+2816A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110649 | |||||||
| chr8:39110680 | T | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58+2847T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110680 | |||||||
| chr8:39110789 | T | C | 1 | a0002c0003t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58+2956T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39110789 | |||||||
| chr8:39111106 | T | A | 4 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(1): Show |
4 | HG02886.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+3273T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111106 | |||||||
| chr8:39111141 | A | G | 3 | a0006c0008t0001g0068 a0006c0008t0001g0069 a0006c0008t0002g0132 |
3 | HG02559.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.58+3308A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111141 | |||||||
| chr8:39111149 | G | A | 84 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0240 others(81): Show |
84 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.58+3316G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111149 | |||||||
| chr8:39111178 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58+3345T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111178 | |||||||
| chr8:39111203 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58+3370T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111203 | |||||||
| chr8:39111279 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
145 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.58+3446G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111279 | |||||||
| chr8:39111464 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58+3631G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111464 | |||||||
| chr8:39111714 | C | A | 6 | a0001c0001t0001g0240 a0001c0001t0001g0243 a0002c0003t0001g0238 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3881C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111714 | |||||||
| chr8:39111720 | CA | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0149 others(81): Show |
85 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.58+3909delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39111720 | ||||||
| chr8:39111720 | CAA | C | 13 | a0001c0001t0001g0160 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | HG01516.hp2 HG02056.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+3908_58+3909del others(2): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39111720 | ||||||
| chr8:39111720 | CAAA | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.58+3907_58+3909del others(3): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39111720 | ||||||
| chr8:39111720 | CAAAAA | C | 5 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG00438.hp2 NA18612.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+3905_58+3909del others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39111720 | ||||||
| chr8:39111742 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.58+3909A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111742 | |||||||
| chr8:39111744 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.58+3911G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111744 | |||||||
| chr8:39111753 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58+3920A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111753 | |||||||
| chr8:39111781 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.58+3948C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111781 | |||||||
| chr8:39111908 | T | C | 66 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(63): Show |
66 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.58+4075T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111908 | |||||||
| chr8:39111984 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58+4151A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39111984 | |||||||
| chr8:39112456 | T | G | 86 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0240 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.58+4623T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39112456 | |||||||
| chr8:39112519 | C | A | 72 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(69): Show |
72 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.58+4686C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39112519 | |||||||
| chr8:39112523 | G | A | 72 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(69): Show |
72 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.58+4690G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39112523 | |||||||
| chr8:39112535 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.58+4702T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39112535 | |||||||
| chr8:39112593 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.58+4760A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39112593 | |||||||
| chr8:39112629 | A | AATG | 72 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(69): Show |
72 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.58+4797_58+4798ins others(3): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39112629 | ||||||
| chr8:39112698 | A | G | 76 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(73): Show |
76 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+4865A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39112698 | |||||||
| chr8:39113002 | T | C | 2 | a0002c0005t0001g0249 a0002c0005t0001g0250 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.59-5084T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39113002 | |||||||
| chr8:39113230 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
100 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.59-4856C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39113230 | |||||||
| chr8:39113295 | G | A | 1 | a0001c0002t0002g0091 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.59-4791G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39113295 | |||||||
| chr8:39113338 | C | T | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59-4748C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39113338 | |||||||
| chr8:39113363 | TCTTGAA | T | 18 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(15): Show |
18 | HG02257.hp2 HG02258.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-4718_59-4713del others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39113363 | ||||||
| chr8:39113500 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-4586G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39113500 | |||||||
| chr8:39113998 | AT | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.59-4081delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39113998 | ||||||
| chr8:39114079 | A | C | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-4007A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39114079 | |||||||
| chr8:39114087 | C | T | 52 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(49): Show |
52 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.59-3999C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39114087 | |||||||
| chr8:39114366 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.59-3720C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39114366 | |||||||
| chr8:39114388 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-3698G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39114388 | |||||||
| chr8:39114641 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0058 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.59-3445C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39114641 | |||||||
| chr8:39114750 | A | C | 46 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.59-3336A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39114750 | |||||||
| chr8:39114847 | G | GT | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01261.hp1 NA18944.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3234dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39114847 | ||||||
| chr8:39115180 | C | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
120 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.59-2906C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115180 | |||||||
| chr8:39115260 | G | T | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.59-2826G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115260 | |||||||
| chr8:39115474 | T | C | 1 | a0001c0002t0002g0092 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.59-2612T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115474 | |||||||
| chr8:39115549 | T | C | 124 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.59-2537T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115549 | |||||||
| chr8:39115588 | G | GT | 13 | a0001c0001t0001g0176 a0001c0001t0001g0215 a0001c0001t0002g0053 others(10): Show |
13 | HG00544.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-2485dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39115588 | ||||||
| chr8:39115588 | G | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-2498G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115588 | |||||||
| chr8:39115628 | T | C | 124 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.59-2458T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115628 | |||||||
| chr8:39115804 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-2282A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115804 | |||||||
| chr8:39115808 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.59-2278C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115808 | |||||||
| chr8:39115861 | C | T | 124 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.59-2225C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115861 | |||||||
| chr8:39115887 | A | C | 1 | a0002c0005t0001g0250 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.59-2199A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115887 | |||||||
| chr8:39115924 | G | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0253 a0002c0003t0001g0254 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-2162G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115924 | |||||||
| chr8:39115937 | T | C | 1 | a0001c0001t0002g0011 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.59-2149T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115937 | |||||||
| chr8:39115991 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-2095A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39115991 | |||||||
| chr8:39116406 | T | C | 1 | a0002c0003t0001g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-1680T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116406 | |||||||
| chr8:39116466 | G | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-1620G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116466 | |||||||
| chr8:39116674 | G | A | 3 | a0001c0001t0001g0007 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.59-1412G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116674 | |||||||
| chr8:39116715 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-1371G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116715 | |||||||
| chr8:39116767 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.59-1319C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116767 | |||||||
| chr8:39116890 | C | CT | 74 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.59-1185dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39116890 | ||||||
| chr8:39116890 | CT | C | 6 | a0001c0001t0001g0149 a0001c0001t0002g0012 a0001c0001t0002g0013 others(3): Show |
6 | HG01243.hp2 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1185delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39116890 | ||||||
| chr8:39116914 | T | G | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-1172T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116914 | |||||||
| chr8:39116944 | T | C | 125 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.59-1142T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39116944 | |||||||
| chr8:39117007 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
121 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.59-1079C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39117007 | |||||||
| chr8:39117157 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-929C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39117157 | |||||||
| chr8:39117178 | G | C | 3 | a0001c0002t0002g0094 a0002c0005t0002g0093 a0002c0005t0002g0095 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.59-908G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39117178 | |||||||
| chr8:39117351 | A | AT | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-726dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39117351 | ||||||
| chr8:39117713 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-373A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39117713 | |||||||
| chr8:39117849 | C | T | 72 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.59-237C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39117849 | |||||||
| chr8:39118023 | T | A | 2 | a0001c0001t0002g0016 a0002c0003t0002g0017 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.59-63T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | chr8 | 39118023 | |||||||
| chr8:39118061 | CT | C | 7 | a0001c0001t0001g0007 a0001c0001t0002g0057 a0001c0001t0002g0078 others(4): Show |
7 | HG01069.hp1 HG01169.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-11delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | 39118061 | ||||||
| chr8:39118480 | A | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.138+315A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118480 | |||||||
| chr8:39118489 | C | A | 52 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(49): Show |
52 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.138+324C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118489 | |||||||
| chr8:39118525 | A | C | 46 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.138+360A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118525 | |||||||
| chr8:39118528 | C | T | 1 | a0002c0003t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.138+363C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118528 | |||||||
| chr8:39118659 | G | A | 46 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.138+494G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118659 | |||||||
| chr8:39118676 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138+511A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118676 | |||||||
| chr8:39118802 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02523.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.138+637C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118802 | |||||||
| chr8:39118937 | G | A | 1 | a0001c0002t0002g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.138+772G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39118937 | |||||||
| chr8:39119323 | T | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138+1158T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119323 | |||||||
| chr8:39119516 | G | C | 124 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.138+1351G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119516 | |||||||
| chr8:39119563 | T | C | 75 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.138+1398T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119563 | |||||||
| chr8:39119817 | C | A | 125 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.138+1652C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119817 | |||||||
| chr8:39119866 | G | T | 1 | a0002c0003t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.138+1701G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119866 | |||||||
| chr8:39119942 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+1777A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119942 | |||||||
| chr8:39119951 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+1786A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39119951 | |||||||
| chr8:39120017 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138+1852A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120017 | |||||||
| chr8:39120028 | G | A | 1 | a0001c0001t0002g0018 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.138+1863G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120028 | |||||||
| chr8:39120126 | A | G | 2 | a0001c0002t0001g0192 a0001c0002t0001g0193 |
2 | HG02523.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.138+1961A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120126 | |||||||
| chr8:39120245 | G | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138+2080G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120245 | |||||||
| chr8:39120287 | T | C | 125 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.138+2122T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120287 | |||||||
| chr8:39120391 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.138+2226T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120391 | |||||||
| chr8:39120484 | G | A | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+2319G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120484 | |||||||
| chr8:39120634 | C | T | 3 | a0006c0008t0001g0068 a0006c0008t0001g0069 a0006c0008t0002g0132 |
3 | HG02559.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138+2469C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120634 | |||||||
| chr8:39120655 | G | A | 125 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.138+2490G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120655 | |||||||
| chr8:39120701 | G | C | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+2536G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120701 | |||||||
| chr8:39120722 | A | G | 3 | a0005c0006t0001g0216 a0005c0006t0001g0222 a0005c0006t0001g0223 |
3 | HG02723.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.138+2557A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120722 | |||||||
| chr8:39120761 | C | CA | 79 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(76): Show |
80 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.138+2615dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39120761 | ||||||
| chr8:39120761 | C | CAA | 12 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0201 others(9): Show |
12 | HG02148.hp1 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+2614_138+2615d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39120761 | ||||||
| chr8:39120761 | C | CAAA | 69 | a0001c0001t0001g0221 a0001c0001t0002g0127 a0001c0001t0002g0128 others(66): Show |
70 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.138+2613_138+2615d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39120761 | ||||||
| chr8:39120761 | C | CAAAA | 6 | a0001c0001t0001g0220 a0001c0002t0001g0162 a0001c0002t0001g0194 others(3): Show |
6 | HG02896.hp1 NA18949.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+2612_138+2615d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39120761 | ||||||
| chr8:39120761 | CA | C | 13 | a0001c0001t0001g0007 a0001c0001t0002g0057 a0001c0001t0002g0075 others(10): Show |
13 | HG01934.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+2615delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39120761 | ||||||
| chr8:39120864 | G | T | 1 | a0001c0001t0002g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.138+2699G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120864 | |||||||
| chr8:39120908 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.138+2743T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120908 | |||||||
| chr8:39120925 | G | A | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+2760G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120925 | |||||||
| chr8:39120984 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.138+2819C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39120984 | |||||||
| chr8:39121130 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+2965A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121130 | |||||||
| chr8:39121273 | T | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0058 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.138+3108T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121273 | |||||||
| chr8:39121315 | T | C | 1 | a0005c0006t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+3150T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121315 | |||||||
| chr8:39121320 | C | T | 2 | a0002c0005t0001g0249 a0002c0005t0001g0250 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.138+3155C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121320 | |||||||
| chr8:39121344 | A | C | 1 | a0001c0002t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.138+3179A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121344 | |||||||
| chr8:39121367 | G | A | 2 | a0001c0001t0002g0016 a0002c0003t0002g0017 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.138+3202G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121367 | |||||||
| chr8:39121382 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.138+3217T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121382 | |||||||
| chr8:39121385 | G | A | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+3220G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121385 | |||||||
| chr8:39121451 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138+3286G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121451 | |||||||
| chr8:39121451 | G | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138+3286G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121451 | |||||||
| chr8:39121505 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138+3340C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121505 | |||||||
| chr8:39121508 | G | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+3343G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121508 | |||||||
| chr8:39121586 | A | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 |
3 | HG00735.hp2 HG01517.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.138+3421A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121586 | |||||||
| chr8:39121792 | G | A | 52 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(49): Show |
52 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.138+3627G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121792 | |||||||
| chr8:39121819 | G | A | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+3654G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39121819 | |||||||
| chr8:39122019 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.138+3854G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122019 | |||||||
| chr8:39122143 | C | T | 1 | a0007c0009t0001g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.138+3978C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122143 | |||||||
| chr8:39122349 | T | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.138+4184T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122349 | |||||||
| chr8:39122408 | A | G | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+4243A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122408 | |||||||
| chr8:39122487 | C | T | 3 | a0001c0001t0001g0007 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138+4322C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122487 | |||||||
| chr8:39122598 | A | T | 1 | a0001c0001t0002g0080 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.138+4433A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122598 | |||||||
| chr8:39122709 | T | G | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+4544T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122709 | |||||||
| chr8:39122745 | T | A | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+4580T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39122745 | |||||||
| chr8:39123191 | C | CT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+5029dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39123191 | ||||||
| chr8:39123235 | T | G | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+5070T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123235 | |||||||
| chr8:39123348 | A | G | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+5183A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123348 | |||||||
| chr8:39123350 | A | G | 46 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(43): Show |
46 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.138+5185A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123350 | |||||||
| chr8:39123393 | C | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+5228C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123393 | |||||||
| chr8:39123395 | C | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+5230C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123395 | |||||||
| chr8:39123552 | G | T | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.138+5387G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123552 | |||||||
| chr8:39123650 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.138+5485T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123650 | |||||||
| chr8:39123704 | C | CT | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.138+5555dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39123704 | ||||||
| chr8:39123704 | C | CTT | 14 | a0001c0001t0001g0233 a0001c0001t0002g0034 a0003c0004t0001g0134 others(11): Show |
14 | HG00621.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.138+5554_138+5555d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39123704 | ||||||
| chr8:39123704 | C | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+5539C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123704 | |||||||
| chr8:39123798 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0055 |
2 | HG02148.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.138+5633C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39123798 | |||||||
| chr8:39124060 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.138+5895G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124060 | |||||||
| chr8:39124199 | C | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138+6034C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124199 | |||||||
| chr8:39124203 | G | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+6038G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124203 | |||||||
| chr8:39124258 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+6093A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124258 | |||||||
| chr8:39124268 | G | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+6103G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124268 | |||||||
| chr8:39124329 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.138+6164T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124329 | |||||||
| chr8:39124396 | T | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.138+6231T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124396 | |||||||
| chr8:39124410 | T | A | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+6245T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124410 | |||||||
| chr8:39124414 | C | CT | 74 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.138+6264dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39124414 | ||||||
| chr8:39124414 | CT | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.138+6264delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39124414 | ||||||
| chr8:39124414 | CTT | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(53): Show |
57 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.138+6263_138+6264d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39124414 | ||||||
| chr8:39124510 | C | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0183 others(16): Show |
19 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.138+6345C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124510 | |||||||
| chr8:39124542 | C | T | 1 | a0001c0002t0001g0205 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.138+6377C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124542 | |||||||
| chr8:39124559 | A | G | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+6394A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124559 | |||||||
| chr8:39124573 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+6408A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124573 | |||||||
| chr8:39124602 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
181 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.138+6437A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124602 | |||||||
| chr8:39124627 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+6462A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124627 | |||||||
| chr8:39124662 | G | A | 3 | a0001c0002t0002g0099 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.138+6497G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124662 | |||||||
| chr8:39124762 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.138+6597G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124762 | |||||||
| chr8:39124797 | G | A | 1 | a0001c0002t0001g0185 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.138+6632G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124797 | |||||||
| chr8:39124840 | T | A | 1 | a0004c0007t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138+6675T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39124840 | |||||||
| chr8:39125034 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.138+6869A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125034 | |||||||
| chr8:39125046 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.138+6881A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125046 | |||||||
| chr8:39125081 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+6916C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125081 | |||||||
| chr8:39125211 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.138+7046A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125211 | |||||||
| chr8:39125288 | T | C | 75 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.138+7123T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125288 | |||||||
| chr8:39125434 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.138+7269A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125434 | |||||||
| chr8:39125476 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(46): Show |
50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+7311G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125476 | |||||||
| chr8:39125528 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.138+7363A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125528 | |||||||
| chr8:39125621 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.138+7456G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125621 | |||||||
| chr8:39125838 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.138+7673A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125838 | |||||||
| chr8:39125977 | T | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.138+7812T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125977 | |||||||
| chr8:39125982 | T | C | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.138+7817T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39125982 | |||||||
| chr8:39126086 | T | C | 75 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.138+7921T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126086 | |||||||
| chr8:39126416 | G | A | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+8251G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126416 | |||||||
| chr8:39126635 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.138+8470C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126635 | |||||||
| chr8:39126651 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.138+8486A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126651 | |||||||
| chr8:39126660 | T | A | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+8495T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126660 | |||||||
| chr8:39126849 | A | G | 1 | a0001c0002t0002g0125 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.138+8684A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126849 | |||||||
| chr8:39126864 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.138+8699G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126864 | |||||||
| chr8:39126916 | A | G | 1 | a0001c0002t0002g0124 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.138+8751A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39126916 | |||||||
| chr8:39127175 | T | A | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+9010T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127175 | |||||||
| chr8:39127179 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0032 a0001c0001t0002g0033 others(4): Show |
7 | HG02056.hp2 NA18943.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+9014C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127179 | |||||||
| chr8:39127263 | T | C | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+9098T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127263 | |||||||
| chr8:39127265 | C | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+9100C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127265 | |||||||
| chr8:39127266 | T | C | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138+9101T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127266 | |||||||
| chr8:39127331 | T | G | 3 | a0006c0008t0001g0068 a0006c0008t0001g0069 a0006c0008t0002g0132 |
3 | HG02559.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138+9166T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127331 | |||||||
| chr8:39127533 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.139-9124A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127533 | |||||||
| chr8:39127710 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.139-8947C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127710 | |||||||
| chr8:39127734 | T | C | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.139-8923T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127734 | |||||||
| chr8:39127820 | T | C | 1 | a0001c0002t0002g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.139-8837T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127820 | |||||||
| chr8:39127958 | G | T | 2 | a0002c0003t0002g0048 a0002c0003t0002g0049 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.139-8699G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39127958 | |||||||
| chr8:39128030 | C | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG00438.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.139-8627C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128030 | |||||||
| chr8:39128112 | A | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.139-8545A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128112 | |||||||
| chr8:39128199 | G | T | 1 | a0005c0006t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.139-8458G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128199 | |||||||
| chr8:39128289 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.139-8368T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128289 | |||||||
| chr8:39128496 | G | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.139-8161G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128496 | |||||||
| chr8:39128706 | C | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-7951C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128706 | |||||||
| chr8:39128710 | G | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0206 others(4): Show |
7 | HG00639.hp2 HG01175.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-7947G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128710 | |||||||
| chr8:39128780 | G | A | 1 | a0001c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.139-7877G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39128780 | |||||||
| chr8:39129044 | A | G | 1 | a0002c0003t0001g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.139-7613A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39129044 | |||||||
| chr8:39129125 | CT | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.139-7518delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39129125 | ||||||
| chr8:39129125 | CTT | C | 9 | a0001c0001t0002g0019 a0004c0007t0001g0154 a0004c0007t0001g0155 others(6): Show |
9 | HG01943.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-7519_139-7518d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39129125 | ||||||
| chr8:39129140 | G | A | 72 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.139-7517G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39129140 | |||||||
| chr8:39129350 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.139-7307A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39129350 | |||||||
| chr8:39129551 | T | C | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.139-7106T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39129551 | |||||||
| chr8:39129828 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.139-6829T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39129828 | |||||||
| chr8:39129955 | CT | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
114 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-6686delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39129955 | ||||||
| chr8:39130312 | T | C | 2 | a0001c0002t0002g0096 a0001c0002t0002g0101 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.139-6345T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130312 | |||||||
| chr8:39130359 | T | C | 25 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(22): Show |
25 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.139-6298T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130359 | |||||||
| chr8:39130654 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.139-6003G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130654 | |||||||
| chr8:39130788 | T | C | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-5869T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130788 | |||||||
| chr8:39130895 | A | T | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-5762A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130895 | |||||||
| chr8:39130917 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.139-5740A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130917 | |||||||
| chr8:39130925 | G | A | 1 | a0001c0002t0002g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.139-5732G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130925 | |||||||
| chr8:39130933 | G | A | 1 | a0002c0003t0001g0181 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.139-5724G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130933 | |||||||
| chr8:39130944 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.139-5713G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39130944 | |||||||
| chr8:39130956 | C | CTTT | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-5685_139-5683d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39130956 | ||||||
| chr8:39130956 | C | CTTTTT | 43 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(40): Show |
43 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.139-5687_139-5683d others(7): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39130956 | ||||||
| chr8:39130956 | C | CTTTTTT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0202 a0001c0001t0001g0251 others(1): Show |
5 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-5688_139-5683d others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39130956 | ||||||
| chr8:39131105 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.139-5552C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131105 | |||||||
| chr8:39131302 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.139-5355T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131302 | |||||||
| chr8:39131335 | T | G | 1 | a0001c0002t0001g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.139-5322T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131335 | |||||||
| chr8:39131423 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139-5234A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131423 | |||||||
| chr8:39131688 | A | T | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139-4969A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131688 | |||||||
| chr8:39131834 | A | C | 1 | a0002c0005t0001g0249 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.139-4823A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131834 | |||||||
| chr8:39131996 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.139-4661C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39131996 | |||||||
| chr8:39132004 | C | A | 2 | a0002c0005t0001g0249 a0002c0005t0001g0250 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.139-4653C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132004 | |||||||
| chr8:39132139 | C | T | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.139-4518C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132139 | |||||||
| chr8:39132140 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.139-4517A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132140 | |||||||
| chr8:39132176 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.139-4481C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132176 | |||||||
| chr8:39132294 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(46): Show |
50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-4363G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132294 | |||||||
| chr8:39132385 | A | G | 1 | a0001c0002t0002g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.139-4272A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132385 | |||||||
| chr8:39132752 | A | AT | 88 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0163 others(85): Show |
89 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.139-3894dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39132752 | ||||||
| chr8:39132752 | AT | A | 9 | a0001c0001t0001g0207 a0001c0001t0002g0036 a0002c0003t0001g0151 others(6): Show |
9 | HG01192.hp2 HG01358.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-3894delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39132752 | ||||||
| chr8:39132896 | C | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.139-3761C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132896 | |||||||
| chr8:39132929 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-3728G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132929 | |||||||
| chr8:39132968 | A | G | 1 | a0003c0004t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.139-3689A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39132968 | |||||||
| chr8:39133020 | A | T | 1 | a0001c0001t0002g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.139-3637A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39133020 | |||||||
| chr8:39133446 | C | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.139-3211C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39133446 | |||||||
| chr8:39133457 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.139-3200T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39133457 | |||||||
| chr8:39133668 | G | C | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-2989G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39133668 | |||||||
| chr8:39133762 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.139-2895C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39133762 | |||||||
| chr8:39133919 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139-2738G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39133919 | |||||||
| chr8:39134201 | A | G | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.139-2456A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39134201 | |||||||
| chr8:39134341 | AG | A | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-2312delG | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | 39134341 | ||||||
| chr8:39134564 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(55): Show |
59 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.139-2093A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39134564 | |||||||
| chr8:39134674 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.139-1983C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39134674 | |||||||
| chr8:39134675 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
83 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.139-1982A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39134675 | |||||||
| chr8:39134755 | C | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.139-1902C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39134755 | |||||||
| chr8:39134922 | G | A | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.139-1735G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39134922 | |||||||
| chr8:39135111 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.139-1546C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135111 | |||||||
| chr8:39135248 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.139-1409A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135248 | |||||||
| chr8:39135294 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139-1363G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135294 | |||||||
| chr8:39135458 | T | A | 1 | a0001c0002t0002g0105 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.139-1199T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135458 | |||||||
| chr8:39135556 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.139-1101C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135556 | |||||||
| chr8:39135572 | T | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.139-1085T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135572 | |||||||
| chr8:39135627 | G | A | 1 | a0009c0014t0002g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.139-1030G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135627 | |||||||
| chr8:39135752 | C | G | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.139-905C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39135752 | |||||||
| chr8:39136086 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.139-571C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39136086 | |||||||
| chr8:39136215 | A | C | 1 | a0001c0001t0002g0061 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.139-442A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39136215 | |||||||
| chr8:39136293 | T | C | 3 | a0001c0002t0002g0087 a0001c0002t0002g0107 a0001c0002t0002g0108 |
3 | HG00408.hp1 HG02056.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.139-364T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39136293 | |||||||
| chr8:39136373 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-284T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39136373 | |||||||
| chr8:39136440 | A | T | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.139-217A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | chr8 | 39136440 | |||||||
| chr8:39136825 | T | A | 1 | a0001c0002t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.200+107T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39136825 | |||||||
| chr8:39136859 | CTTAA | C | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.200+146_200+149del others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39136859 | ||||||
| chr8:39137044 | G | T | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.200+326G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39137044 | |||||||
| chr8:39137494 | G | A | 9 | a0001c0002t0002g0001 a0001c0002t0002g0084 a0001c0002t0002g0097 others(6): Show |
10 | HG01106.hp2 HG01934.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.200+776G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39137494 | |||||||
| chr8:39137737 | C | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0253 a0002c0003t0001g0254 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.200+1019C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39137737 | |||||||
| chr8:39137747 | G | A | 2 | a0002c0005t0001g0249 a0002c0005t0001g0250 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.200+1029G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39137747 | |||||||
| chr8:39137770 | C | CA | 130 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0145 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.200+1067dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39137770 | ||||||
| chr8:39137770 | CA | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
100 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.200+1067delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39137770 | ||||||
| chr8:39138027 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.200+1309C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138027 | |||||||
| chr8:39138267 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.200+1549G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138267 | |||||||
| chr8:39138475 | C | G | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.200+1757C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138475 | |||||||
| chr8:39138518 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.200+1800G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138518 | |||||||
| chr8:39138523 | A | G | 3 | a0001c0002t0002g0087 a0001c0002t0002g0107 a0001c0002t0002g0108 |
3 | HG00408.hp1 HG02056.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.200+1805A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138523 | |||||||
| chr8:39138697 | G | A | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.200+1979G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138697 | |||||||
| chr8:39138785 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.200+2067C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138785 | |||||||
| chr8:39138848 | C | T | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.200+2130C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138848 | |||||||
| chr8:39138855 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.200+2137A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138855 | |||||||
| chr8:39138894 | T | A | 1 | a0001c0001t0002g0020 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.200+2176T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138894 | |||||||
| chr8:39138918 | T | G | 1 | a0001c0001t0002g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.200+2200T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39138918 | |||||||
| chr8:39139251 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.200+2533A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139251 | |||||||
| chr8:39139297 | T | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.200+2579T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139297 | |||||||
| chr8:39139434 | C | T | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.200+2716C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139434 | |||||||
| chr8:39139484 | T | C | 44 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(41): Show |
44 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.200+2766T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139484 | |||||||
| chr8:39139513 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.200+2795C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139513 | |||||||
| chr8:39139605 | G | A | 1 | a0002c0003t0001g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.200+2887G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139605 | |||||||
| chr8:39139717 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.200+2999C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139717 | |||||||
| chr8:39139718 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.200+3000A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139718 | |||||||
| chr8:39139926 | C | T | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.200+3208C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139926 | |||||||
| chr8:39139929 | C | T | 1 | a0001c0002t0001g0205 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.200+3211C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39139929 | |||||||
| chr8:39140288 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.200+3570G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39140288 | |||||||
| chr8:39140542 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.200+3824G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39140542 | |||||||
| chr8:39140700 | A | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.200+3982A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39140700 | |||||||
| chr8:39140806 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.200+4088A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39140806 | |||||||
| chr8:39140999 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.200+4281T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39140999 | |||||||
| chr8:39141101 | C | A | 1 | a0005c0006t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.200+4383C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141101 | |||||||
| chr8:39141321 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.200+4603G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141321 | |||||||
| chr8:39141394 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.200+4676T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141394 | |||||||
| chr8:39141454 | A | G | 80 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.200+4736A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141454 | |||||||
| chr8:39141793 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(126): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.200+5075T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141793 | |||||||
| chr8:39141923 | A | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.200+5205A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141923 | |||||||
| chr8:39141960 | C | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(46): Show |
50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.201-5170C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39141960 | |||||||
| chr8:39142038 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201-5092C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142038 | |||||||
| chr8:39142102 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.201-5028G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142102 | |||||||
| chr8:39142110 | GA | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.201-5019delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142110 | |||||||
| chr8:39142342 | G | A | 72 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.201-4788G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142342 | |||||||
| chr8:39142361 | T | A | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG01975.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.201-4769T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142361 | |||||||
| chr8:39142437 | T | G | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-4693T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142437 | |||||||
| chr8:39142512 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.201-4618C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142512 | |||||||
| chr8:39142953 | T | C | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.201-4177T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39142953 | |||||||
| chr8:39143287 | A | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0231 |
2 | HG01243.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.201-3843A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39143287 | |||||||
| chr8:39143467 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.201-3663T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39143467 | |||||||
| chr8:39143539 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201-3591G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39143539 | |||||||
| chr8:39143875 | G | A | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.201-3255G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39143875 | |||||||
| chr8:39143959 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02523.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.201-3171G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39143959 | |||||||
| chr8:39144042 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.201-3088T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144042 | |||||||
| chr8:39144056 | C | A | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.201-3074C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144056 | |||||||
| chr8:39144178 | C | T | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.201-2952C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144178 | |||||||
| chr8:39144195 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(128): Show |
133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.201-2935T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144195 | |||||||
| chr8:39144278 | A | G | 2 | a0001c0002t0001g0190 a0001c0002t0001g0191 |
2 | NA18943.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.201-2852A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144278 | |||||||
| chr8:39144470 | C | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.201-2660C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144470 | |||||||
| chr8:39144606 | T | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.201-2524T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144606 | |||||||
| chr8:39144664 | A | AT | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.201-2466_201-2465i others(3): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144664 | |||||||
| chr8:39144668 | T | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(128): Show |
133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.201-2462T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144668 | |||||||
| chr8:39144684 | G | A | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.201-2446G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144684 | |||||||
| chr8:39144850 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201-2280G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144850 | |||||||
| chr8:39144866 | A | T | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.201-2264A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144866 | |||||||
| chr8:39144894 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.201-2236T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144894 | |||||||
| chr8:39144973 | G | C | 1 | a0001c0002t0001g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.201-2157G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144973 | |||||||
| chr8:39144974 | T | A | 1 | a0001c0002t0001g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.201-2156T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39144974 | |||||||
| chr8:39145005 | G | A | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.201-2125G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145005 | |||||||
| chr8:39145041 | GA | G | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.201-2086delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39145041 | ||||||
| chr8:39145132 | A | C | 1 | a0005c0006t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.201-1998A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145132 | |||||||
| chr8:39145166 | G | T | 1 | a0001c0002t0002g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.201-1964G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145166 | |||||||
| chr8:39145195 | G | A | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.201-1935G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145195 | |||||||
| chr8:39145234 | T | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.201-1896T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145234 | |||||||
| chr8:39145251 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(127): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.201-1879C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145251 | |||||||
| chr8:39145252 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.201-1878G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145252 | |||||||
| chr8:39145772 | C | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201-1358C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145772 | |||||||
| chr8:39145799 | T | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.201-1331T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145799 | |||||||
| chr8:39145800 | C | T | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.201-1330C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145800 | |||||||
| chr8:39145802 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.201-1328G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145802 | |||||||
| chr8:39145937 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201-1193C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39145937 | |||||||
| chr8:39146023 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.201-1107C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146023 | |||||||
| chr8:39146177 | A | C | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.201-953A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146177 | |||||||
| chr8:39146242 | G | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.201-888G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146242 | |||||||
| chr8:39146326 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.201-804A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146326 | |||||||
| chr8:39146381 | A | G | 9 | a0001c0002t0001g0224 a0001c0002t0002g0009 a0001c0002t0002g0086 others(6): Show |
9 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.201-749A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146381 | |||||||
| chr8:39146411 | A | AT | 11 | a0001c0001t0001g0007 a0001c0001t0002g0042 a0002c0003t0001g0157 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.201-702dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39146411 | ||||||
| chr8:39146411 | A | ATT | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
98 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.201-703_201-702dup others(2): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39146411 | ||||||
| chr8:39146411 | A | ATTT | 16 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0003c0004t0001g0134 others(13): Show |
16 | HG01106.hp1 HG01123.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.201-704_201-702dup others(3): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | 39146411 | ||||||
| chr8:39146462 | T | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.201-668T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146462 | |||||||
| chr8:39146480 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.201-650A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146480 | |||||||
| chr8:39146703 | G | A | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.201-427G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146703 | |||||||
| chr8:39146943 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.201-187T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39146943 | |||||||
| chr8:39147101 | A | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.201-29A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | 39147101 | |||||||
| chr8:39147509 | A | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(54): Show |
58 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.276+304A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39147509 | |||||||
| chr8:39148191 | A | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.276+986A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39148191 | |||||||
| chr8:39148424 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.276+1219G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39148424 | |||||||
| chr8:39148507 | G | T | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-1284G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39148507 | |||||||
| chr8:39148526 | T | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.277-1265T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39148526 | |||||||
| chr8:39148589 | C | T | 3 | a0001c0002t0002g0102 a0001c0002t0002g0103 a0001c0002t0002g0104 |
3 | HG00280.hp2 HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.277-1202C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39148589 | |||||||
| chr8:39148781 | A | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.277-1010A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39148781 | |||||||
| chr8:39149024 | T | C | 6 | a0002c0003t0001g0151 a0005c0006t0001g0144 a0005c0006t0001g0216 others(3): Show |
6 | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-767T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149024 | |||||||
| chr8:39149084 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.277-707G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149084 | |||||||
| chr8:39149093 | A | C | 4 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 others(1): Show |
4 | HG02723.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-698A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149093 | |||||||
| chr8:39149094 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.277-697C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149094 | |||||||
| chr8:39149129 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.277-662A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149129 | |||||||
| chr8:39149243 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.277-548A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149243 | |||||||
| chr8:39149364 | C | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
123 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.277-427C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149364 | |||||||
| chr8:39149377 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG00280.hp1 HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.277-414G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149377 | |||||||
| chr8:39149677 | A | G | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.277-114A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149677 | |||||||
| chr8:39149681 | C | T | 26 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(23): Show |
26 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.277-110C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | chr8 | 39149681 | |||||||
| chr8:39150113 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.353+246T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39150113 | |||||||
| chr8:39150150 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.353+283A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39150150 | |||||||
| chr8:39150204 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.353+337G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39150204 | |||||||
| chr8:39150837 | AATATTTC others(91): Show |
A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.354-440_354-343del others(98): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr8 | 39150837 | ||||||
| chr8:39151036 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.354-341A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39151036 | |||||||
| chr8:39151075 | TTTAA | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
131 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.354-299_354-296del others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr8 | 39151075 | ||||||
| chr8:39151161 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.354-216G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39151161 | |||||||
| chr8:39151171 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(26): Show |
30 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.354-206G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39151171 | |||||||
| chr8:39151287 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.354-90C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39151287 | |||||||
| chr8:39151331 | A | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.354-46A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 5/24 | chr8 | 39151331 | |||||||
| chr8:39151675 | C | CT | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.525+143dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39151675 | ||||||
| chr8:39151777 | C | T | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+229C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39151777 | |||||||
| chr8:39151808 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.525+260C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39151808 | |||||||
| chr8:39152390 | T | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+842T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39152390 | |||||||
| chr8:39152434 | A | T | 1 | a0001c0002t0002g0131 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.525+886A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39152434 | |||||||
| chr8:39152594 | C | T | 6 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(3): Show |
6 | HG02055.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+1046C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39152594 | |||||||
| chr8:39152637 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.525+1089T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39152637 | |||||||
| chr8:39152720 | CA | C | 19 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0240 others(16): Show |
19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.525+1201delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39152720 | ||||||
| chr8:39152720 | CAAAAAAA others(11): Show |
C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.525+1184_525+1201d others(20): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39152720 | ||||||
| chr8:39152978 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.525+1430G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39152978 | |||||||
| chr8:39153818 | A | G | 1 | a0001c0002t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+2270A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39153818 | |||||||
| chr8:39153819 | G | T | 1 | a0001c0002t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+2271G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39153819 | |||||||
| chr8:39153994 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.525+2446A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39153994 | |||||||
| chr8:39154033 | C | CATATAT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.525+2496_525+2501d others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(1): Show |
108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0145 others(105): Show |
108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.525+2494_525+2501d others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(16): Show |
1 | a0001c0002t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+2494_525+2495i others(25): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(3): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0207 a0001c0001t0001g0225 others(10): Show |
13 | HG01358.hp1 HG01978.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+2492_525+2501d others(12): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(5): Show |
1 | a0001c0001t0002g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.525+2490_525+2501d others(14): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(7): Show |
34 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.525+2488_525+2501d others(16): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(9): Show |
20 | a0001c0002t0001g0162 a0001c0002t0001g0224 a0001c0002t0002g0009 others(17): Show |
20 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.525+2486_525+2501d others(18): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(11): Show |
18 | a0001c0002t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0188 others(15): Show |
19 | HG01261.hp1 HG02523.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.525+2501_525+2502i others(20): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(13): Show |
4 | a0001c0002t0001g0178 a0001c0002t0001g0186 a0001c0002t0001g0187 others(1): Show |
4 | NA18972.hp1 NA18974.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+2501_525+2502i others(22): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(17): Show |
1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.525+2501_525+2502i others(26): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(21): Show |
1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.525+2501_525+2502i others(30): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(35): Show |
1 | a0002c0003t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.525+2501_525+2502i others(44): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154033 | C | CATATATA others(39): Show |
1 | a0002c0003t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.525+2501_525+2502i others(48): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154033 | ||||||
| chr8:39154088 | G | T | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.525+2540G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154088 | |||||||
| chr8:39154169 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.525+2621T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154169 | |||||||
| chr8:39154204 | G | A | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.525+2656G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154204 | |||||||
| chr8:39154313 | G | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.525+2765G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154313 | |||||||
| chr8:39154654 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.525+3106C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154654 | |||||||
| chr8:39154732 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.525+3184C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154732 | |||||||
| chr8:39154885 | G | GT | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
143 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.525+3347dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39154885 | ||||||
| chr8:39154885 | G | T | 2 | a0003c0004t0001g0142 a0003c0004t0001g0143 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525+3337G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154885 | |||||||
| chr8:39154927 | C | G | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.525+3379C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154927 | |||||||
| chr8:39154933 | A | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+3385A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154933 | |||||||
| chr8:39154949 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.525+3401A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39154949 | |||||||
| chr8:39155044 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+3496G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155044 | |||||||
| chr8:39155051 | A | T | 1 | a0001c0002t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+3503A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155051 | |||||||
| chr8:39155243 | A | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+3695A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155243 | |||||||
| chr8:39155328 | T | A | 1 | a0001c0002t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+3780T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155328 | |||||||
| chr8:39155329 | A | T | 1 | a0001c0002t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.525+3781A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155329 | |||||||
| chr8:39155668 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.525+4120G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155668 | |||||||
| chr8:39155948 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.525+4400C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155948 | |||||||
| chr8:39155955 | G | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.525+4407G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39155955 | |||||||
| chr8:39156105 | G | A | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.525+4557G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156105 | |||||||
| chr8:39156150 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.525+4602T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156150 | |||||||
| chr8:39156201 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.525+4653C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156201 | |||||||
| chr8:39156427 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-4470A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156427 | |||||||
| chr8:39156540 | T | C | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.526-4357T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156540 | |||||||
| chr8:39156862 | C | A | 2 | a0002c0005t0001g0249 a0002c0005t0001g0250 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.526-4035C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156862 | |||||||
| chr8:39156920 | T | A | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.526-3977T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156920 | |||||||
| chr8:39156935 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-3962T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39156935 | |||||||
| chr8:39157093 | C | T | 72 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.526-3804C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39157093 | |||||||
| chr8:39157347 | G | A | 2 | a0002c0003t0001g0246 a0002c0003t0001g0247 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.526-3550G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39157347 | |||||||
| chr8:39157597 | C | A | 2 | a0001c0001t0002g0073 a0001c0001t0002g0075 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.526-3300C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39157597 | |||||||
| chr8:39157613 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.526-3284C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39157613 | |||||||
| chr8:39157616 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526-3281C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39157616 | |||||||
| chr8:39158001 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
58 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.526-2896G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158001 | |||||||
| chr8:39158066 | G | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2831G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158066 | |||||||
| chr8:39158097 | C | T | 72 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.526-2800C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158097 | |||||||
| chr8:39158102 | GCTTCACA others(4): Show |
G | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2793_526-2783d others(13): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39158102 | ||||||
| chr8:39158153 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.526-2744C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158153 | |||||||
| chr8:39158156 | T | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.526-2741T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158156 | |||||||
| chr8:39158241 | C | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-2656C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158241 | |||||||
| chr8:39158243 | A | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-2654A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158243 | |||||||
| chr8:39158244 | G | GTGGATGA others(16): Show |
240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-2653_526-2652i others(25): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158244 | |||||||
| chr8:39158274 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
142 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.526-2623T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158274 | |||||||
| chr8:39158304 | A | G | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.526-2593A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158304 | |||||||
| chr8:39158330 | G | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-2567G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158330 | |||||||
| chr8:39158344 | C | T | 3 | a0001c0002t0002g0094 a0002c0005t0002g0093 a0002c0005t0002g0095 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.526-2553C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158344 | |||||||
| chr8:39158684 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.526-2213A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39158684 | |||||||
| chr8:39159029 | T | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.526-1868T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39159029 | |||||||
| chr8:39159496 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG00280.hp1 HG01361.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-1401G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39159496 | |||||||
| chr8:39159828 | A | G | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526-1069A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39159828 | |||||||
| chr8:39159874 | C | A | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526-1023C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39159874 | |||||||
| chr8:39159978 | C | T | 4 | a0004c0007t0001g0154 a0004c0007t0001g0156 a0004c0007t0001g0244 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-919C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39159978 | |||||||
| chr8:39160006 | G | C | 1 | a0001c0001t0002g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.526-891G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160006 | |||||||
| chr8:39160158 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.526-739A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160158 | |||||||
| chr8:39160232 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526-665G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160232 | |||||||
| chr8:39160266 | C | T | 1 | a0003c0004t0001g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.526-631C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160266 | |||||||
| chr8:39160303 | G | C | 1 | a0003c0004t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.526-594G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160303 | |||||||
| chr8:39160326 | G | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-571G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160326 | |||||||
| chr8:39160400 | C | T | 11 | a0001c0001t0001g0149 a0003c0004t0001g0134 a0003c0004t0001g0135 others(8): Show |
11 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-497C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160400 | |||||||
| chr8:39160445 | C | T | 1 | a0002c0003t0002g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.526-452C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160445 | |||||||
| chr8:39160494 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(26): Show |
30 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.526-403C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160494 | |||||||
| chr8:39160519 | G | A | 1 | a0001c0002t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.526-378G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160519 | |||||||
| chr8:39160539 | CA | C | 12 | a0001c0001t0001g0201 a0001c0001t0001g0215 a0001c0001t0001g0219 others(9): Show |
12 | HG00423.hp2 HG01175.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-327delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAA | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0161 others(47): Show |
50 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.526-328_526-327del others(2): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAA | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.526-329_526-327del others(3): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAAA | C | 29 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0159 others(26): Show |
29 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.526-330_526-327del others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAAAAAA | C | 5 | a0001c0001t0001g0007 a0002c0003t0001g0151 a0002c0003t0001g0157 others(2): Show |
5 | HG02559.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-333_526-327del others(7): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0002t0001g0186 others(10): Show |
13 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.526-334_526-327del others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAAAAAA others(2): Show |
C | 61 | a0001c0001t0002g0127 a0001c0002t0001g0146 a0001c0002t0001g0162 others(58): Show |
62 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.526-335_526-327del others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526-336_526-327del others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160539 | CAAAAAAA others(5): Show |
C | 1 | a0002c0003t0002g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.526-338_526-327del others(12): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | 39160539 | ||||||
| chr8:39160764 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.526-133A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160764 | |||||||
| chr8:39160832 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.526-65G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | chr8 | 39160832 | |||||||
| chr8:39161264 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.594+299G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39161264 | |||||||
| chr8:39161330 | G | A | 74 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.594+365G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39161330 | |||||||
| chr8:39161440 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0074 |
2 | NA19012.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.594+475C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39161440 | |||||||
| chr8:39161468 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.594+503C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39161468 | |||||||
| chr8:39161490 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.594+525C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39161490 | |||||||
| chr8:39161517 | G | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.594+552G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39161517 | |||||||
| chr8:39161997 | ATT | A | 3 | a0001c0001t0001g0233 a0001c0001t0002g0067 a0001c0001t0002g0089 |
3 | HG00423.hp2 HG00621.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.594+1035_594+1036d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | 39161997 | ||||||
| chr8:39161998 | TTTTA | T | 9 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(6): Show |
9 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.594+1035_594+1038d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | 39161998 | ||||||
| chr8:39162000 | TTA | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.594+1055_594+1056d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | 39162000 | ||||||
| chr8:39162000 | TTATA | T | 75 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(72): Show |
76 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.594+1053_594+1056d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | 39162000 | ||||||
| chr8:39162177 | T | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.594+1212T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162177 | |||||||
| chr8:39162222 | C | T | 1 | a0001c0002t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.594+1257C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162222 | |||||||
| chr8:39162240 | T | A | 1 | a0001c0001t0002g0019 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.594+1275T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162240 | |||||||
| chr8:39162325 | A | G | 1 | a0002c0003t0001g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.594+1360A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162325 | |||||||
| chr8:39162477 | G | T | 1 | a0001c0002t0002g0130 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.594+1512G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162477 | |||||||
| chr8:39162707 | TA | T | 77 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.594+1751delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | 39162707 | ||||||
| chr8:39162862 | G | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.594+1897G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162862 | |||||||
| chr8:39162928 | A | G | 78 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.595-1836A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39162928 | |||||||
| chr8:39163030 | C | T | 1 | a0002c0005t0001g0250 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.595-1734C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39163030 | |||||||
| chr8:39163439 | C | G | 80 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.595-1325C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39163439 | |||||||
| chr8:39163475 | AAAT | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.595-1288_595-1286d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39163475 | |||||||
| chr8:39163516 | G | T | 78 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.595-1248G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39163516 | |||||||
| chr8:39163753 | C | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.595-1011C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39163753 | |||||||
| chr8:39163875 | C | T | 4 | a0002c0003t0001g0008 a0002c0003t0001g0246 a0002c0003t0001g0247 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-889C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39163875 | |||||||
| chr8:39164101 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.595-663C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39164101 | |||||||
| chr8:39164315 | T | C | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-449T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39164315 | |||||||
| chr8:39164350 | C | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0206 others(2): Show |
5 | HG01358.hp1 HG02148.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-414C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39164350 | |||||||
| chr8:39164727 | A | G | 1 | a0002c0003t0001g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.595-37A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | chr8 | 39164727 | |||||||
| chr8:39164956 | A | C | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.667-74A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 8/24 | chr8 | 39164956 | |||||||
| chr8:39165003 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.667-27G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 8/24 | chr8 | 39165003 | |||||||
| chr8:39165005 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.667-25A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 8/24 | chr8 | 39165005 | |||||||
| chr8:39165234 | A | G | 1 | a0001c0002t0001g0162 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.833+38A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165234 | |||||||
| chr8:39165365 | T | A | 79 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.833+169T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165365 | |||||||
| chr8:39165424 | C | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.833+228C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165424 | |||||||
| chr8:39165438 | A | G | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.833+242A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165438 | |||||||
| chr8:39165445 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.833+249G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165445 | |||||||
| chr8:39165661 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.833+465A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165661 | |||||||
| chr8:39165684 | T | G | 1 | a0004c0007t0001g0156 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833+488T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165684 | |||||||
| chr8:39165948 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.833+752C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39165948 | |||||||
| chr8:39166290 | G | C | 1 | a0001c0001t0002g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.833+1094G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39166290 | |||||||
| chr8:39166352 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01071.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.833+1156G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39166352 | |||||||
| chr8:39166457 | G | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833+1261G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39166457 | |||||||
| chr8:39167011 | C | T | 77 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.833+1815C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39167011 | |||||||
| chr8:39167130 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.833+1934G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39167130 | |||||||
| chr8:39167138 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.833+1942T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39167138 | |||||||
| chr8:39167418 | C | A | 1 | a0001c0002t0002g0114 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.833+2222C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39167418 | |||||||
| chr8:39167430 | G | A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.833+2234G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39167430 | |||||||
| chr8:39167635 | T | TATG | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.834-2279_834-2278i others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr8 | 39167635 | ||||||
| chr8:39167851 | G | A | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.834-2065G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39167851 | |||||||
| chr8:39168109 | C | CT | 76 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.834-1799dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr8 | 39168109 | ||||||
| chr8:39168109 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.834-1807C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168109 | |||||||
| chr8:39168211 | G | T | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.834-1705G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168211 | |||||||
| chr8:39168213 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.834-1703T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168213 | |||||||
| chr8:39168289 | A | G | 3 | a0001c0002t0002g0094 a0002c0005t0002g0093 a0002c0005t0002g0095 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.834-1627A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168289 | |||||||
| chr8:39168316 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.834-1600T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168316 | |||||||
| chr8:39168868 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.834-1048G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168868 | |||||||
| chr8:39168886 | A | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.834-1030A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168886 | |||||||
| chr8:39168923 | T | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.834-993T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168923 | |||||||
| chr8:39168991 | T | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.834-925T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39168991 | |||||||
| chr8:39169084 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.834-832C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39169084 | |||||||
| chr8:39169104 | C | A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.834-812C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39169104 | |||||||
| chr8:39169157 | A | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.834-759A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39169157 | |||||||
| chr8:39169500 | G | A | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.834-416G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39169500 | |||||||
| chr8:39169753 | A | G | 79 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.834-163A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 9/24 | chr8 | 39169753 | |||||||
| chr8:39170022 | T | C | 16 | a0001c0001t0001g0150 a0001c0001t0002g0038 a0001c0001t0002g0042 others(13): Show |
16 | HG00738.hp2 HG01081.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.915+25T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39170022 | |||||||
| chr8:39170307 | A | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+310A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39170307 | |||||||
| chr8:39170620 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.915+623G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39170620 | |||||||
| chr8:39170628 | A | G | 1 | a0001c0002t0002g0001 | 2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.915+631A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39170628 | |||||||
| chr8:39170884 | G | C | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+887G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39170884 | |||||||
| chr8:39171024 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.915+1027C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171024 | |||||||
| chr8:39171262 | G | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.915+1265G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171262 | |||||||
| chr8:39171337 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.915+1340T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171337 | |||||||
| chr8:39171434 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.915+1437G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171434 | |||||||
| chr8:39171472 | A | C | 85 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(82): Show |
86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.915+1475A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171472 | |||||||
| chr8:39171733 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.915+1736C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171733 | |||||||
| chr8:39171757 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.915+1760C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171757 | |||||||
| chr8:39171862 | T | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.915+1865T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171862 | |||||||
| chr8:39171881 | T | G | 1 | a0001c0001t0002g0020 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.915+1884T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171881 | |||||||
| chr8:39171920 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.915+1923A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39171920 | |||||||
| chr8:39172072 | A | AATAAAT | 18 | a0001c0002t0001g0178 a0001c0002t0001g0184 a0001c0002t0001g0185 others(15): Show |
18 | HG01261.hp1 HG02523.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.915+2078_915+2083d others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39172072 | ||||||
| chr8:39172124 | A | G | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.915+2127A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39172124 | |||||||
| chr8:39172508 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.915+2511G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39172508 | |||||||
| chr8:39172634 | T | C | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.915+2637T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39172634 | |||||||
| chr8:39172795 | A | G | 2 | a0001c0001t0001g0007 a0002c0003t0001g0157 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.915+2798A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39172795 | |||||||
| chr8:39172804 | C | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+2807C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39172804 | |||||||
| chr8:39173089 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02523.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.915+3092C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173089 | |||||||
| chr8:39173157 | C | T | 26 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(23): Show |
26 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.915+3160C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173157 | |||||||
| chr8:39173297 | A | G | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.915+3300A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173297 | |||||||
| chr8:39173503 | C | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+3506C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173503 | |||||||
| chr8:39173696 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.915+3699A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173696 | |||||||
| chr8:39173780 | GT | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+3787delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39173780 | ||||||
| chr8:39173786 | A | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+3789A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173786 | |||||||
| chr8:39173970 | G | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.915+3973G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39173970 | |||||||
| chr8:39174001 | T | C | 14 | a0001c0001t0001g0150 a0001c0001t0002g0038 a0001c0001t0002g0042 others(11): Show |
14 | HG00738.hp2 HG01081.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.915+4004T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174001 | |||||||
| chr8:39174007 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.915+4010T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174007 | |||||||
| chr8:39174094 | G | A | 1 | a0001c0002t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.915+4097G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174094 | |||||||
| chr8:39174344 | G | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+4347G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174344 | |||||||
| chr8:39174449 | C | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+4452C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174449 | |||||||
| chr8:39174467 | AT | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.915+4480delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39174467 | ||||||
| chr8:39174489 | CTTAT | C | 2 | a0001c0002t0002g0086 a0001c0002t0002g0120 |
2 | HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.915+4507_915+4510d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39174489 | ||||||
| chr8:39174555 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0213 others(28): Show |
32 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.915+4558A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174555 | |||||||
| chr8:39174629 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.915+4632A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39174629 | |||||||
| chr8:39174695 | G | GT | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+4707dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39174695 | ||||||
| chr8:39174801 | ATTCT | A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+4809_915+4812d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39174801 | ||||||
| chr8:39175169 | C | T | 56 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0002t0001g0146 others(53): Show |
57 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.915+5172C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39175169 | |||||||
| chr8:39175169 | CTTTA | C | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+5176_915+5179d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39175169 | ||||||
| chr8:39175272 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.915+5275G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39175272 | |||||||
| chr8:39175382 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.915+5385G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39175382 | |||||||
| chr8:39175601 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.915+5604G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39175601 | |||||||
| chr8:39175743 | T | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+5746T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39175743 | |||||||
| chr8:39175798 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.915+5801T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39175798 | |||||||
| chr8:39176057 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.915+6060A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39176057 | |||||||
| chr8:39176141 | G | C | 1 | a0001c0002t0002g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.915+6144G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39176141 | |||||||
| chr8:39176240 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+6243G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39176240 | |||||||
| chr8:39176712 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.915+6715C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39176712 | |||||||
| chr8:39177039 | G | A | 73 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.915+7042G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39177039 | |||||||
| chr8:39177061 | CT | C | 76 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.915+7078delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39177061 | ||||||
| chr8:39177502 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.915+7505G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39177502 | |||||||
| chr8:39177761 | GT | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(26): Show |
30 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.915+7767delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39177761 | ||||||
| chr8:39178035 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.915+8038T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178035 | |||||||
| chr8:39178038 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.915+8041G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178038 | |||||||
| chr8:39178185 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.915+8188C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178185 | |||||||
| chr8:39178374 | A | G | 1 | a0001c0002t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.915+8377A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178374 | |||||||
| chr8:39178494 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.916-8415C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178494 | |||||||
| chr8:39178741 | G | A | 4 | a0001c0002t0002g0009 a0001c0002t0002g0092 a0001c0002t0002g0123 others(1): Show |
4 | HG00642.hp1 HG00642.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-8168G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178741 | |||||||
| chr8:39178890 | C | A | 72 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.916-8019C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39178890 | |||||||
| chr8:39179322 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.916-7587T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39179322 | |||||||
| chr8:39179403 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.916-7506G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39179403 | |||||||
| chr8:39179413 | C | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-7496C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39179413 | |||||||
| chr8:39179611 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.916-7298C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39179611 | |||||||
| chr8:39179793 | G | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.916-7116G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39179793 | |||||||
| chr8:39179980 | C | T | 1 | a0005c0006t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.916-6929C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39179980 | |||||||
| chr8:39180134 | C | G | 1 | a0001c0002t0002g0108 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.916-6775C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180134 | |||||||
| chr8:39180157 | G | A | 16 | a0001c0002t0001g0162 a0001c0002t0002g0001 a0001c0002t0002g0084 others(13): Show |
17 | HG00423.hp1 HG01106.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.916-6752G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180157 | |||||||
| chr8:39180182 | G | A | 1 | a0002c0003t0001g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.916-6727G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180182 | |||||||
| chr8:39180192 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0215 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.916-6717C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180192 | |||||||
| chr8:39180237 | C | T | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.916-6672C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180237 | |||||||
| chr8:39180240 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
162 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.916-6669T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180240 | |||||||
| chr8:39180255 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0177 |
2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.916-6654C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180255 | |||||||
| chr8:39180258 | G | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(26): Show |
30 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.916-6651G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180258 | |||||||
| chr8:39180326 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.916-6583C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180326 | |||||||
| chr8:39180447 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0002g0127 a0001c0001t0002g0128 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.916-6462C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180447 | |||||||
| chr8:39180475 | G | A | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916-6434G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180475 | |||||||
| chr8:39180487 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.916-6422C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180487 | |||||||
| chr8:39180511 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.916-6398C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180511 | |||||||
| chr8:39180815 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.916-6094G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39180815 | |||||||
| chr8:39181240 | A | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.916-5669A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39181240 | |||||||
| chr8:39181249 | T | C | 77 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.916-5660T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39181249 | |||||||
| chr8:39181298 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.916-5611C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39181298 | |||||||
| chr8:39181374 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.916-5535G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39181374 | |||||||
| chr8:39181801 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-5108G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39181801 | |||||||
| chr8:39181842 | C | A | 74 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.916-5067C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39181842 | |||||||
| chr8:39182221 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.916-4688A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39182221 | |||||||
| chr8:39182549 | T | C | 77 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0127 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.916-4360T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39182549 | |||||||
| chr8:39182758 | T | C | 3 | a0001c0001t0001g0233 a0001c0001t0002g0067 a0001c0001t0002g0089 |
3 | HG00423.hp2 HG00621.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.916-4151T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39182758 | |||||||
| chr8:39182785 | G | A | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.916-4124G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39182785 | |||||||
| chr8:39183007 | C | A | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916-3902C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183007 | |||||||
| chr8:39183024 | T | C | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-3885T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183024 | |||||||
| chr8:39183266 | C | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
59 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.916-3643C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183266 | |||||||
| chr8:39183269 | A | C | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.916-3640A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183269 | |||||||
| chr8:39183285 | T | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.916-3624T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183285 | |||||||
| chr8:39183359 | G | T | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.916-3550G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183359 | |||||||
| chr8:39183371 | A | T | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-3538A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183371 | |||||||
| chr8:39183455 | CTATTCCC others(9): Show |
C | 9 | a0001c0002t0002g0001 a0001c0002t0002g0084 a0001c0002t0002g0097 others(6): Show |
10 | HG01106.hp2 HG01934.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-3435_916-3420d others(18): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39183455 | ||||||
| chr8:39183743 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.916-3166G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183743 | |||||||
| chr8:39183811 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(18): Show |
21 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.916-3098T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183811 | |||||||
| chr8:39183871 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.916-3038C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183871 | |||||||
| chr8:39183881 | G | A | 1 | a0001c0002t0001g0185 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.916-3028G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183881 | |||||||
| chr8:39183954 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.916-2955C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39183954 | |||||||
| chr8:39184513 | A | C | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.916-2396A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39184513 | |||||||
| chr8:39184523 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.916-2386T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39184523 | |||||||
| chr8:39184814 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.916-2095A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39184814 | |||||||
| chr8:39184931 | T | G | 1 | a0001c0002t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.916-1978T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39184931 | |||||||
| chr8:39184972 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.916-1937T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39184972 | |||||||
| chr8:39185006 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.916-1903T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185006 | |||||||
| chr8:39185249 | G | A | 1 | a0003c0004t0001g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.916-1660G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185249 | |||||||
| chr8:39185265 | CA | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.916-1628delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39185265 | ||||||
| chr8:39185341 | A | C | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.916-1568A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185341 | |||||||
| chr8:39185346 | A | AAAAAAAA others(1): Show |
116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.916-1557_916-1556i others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39185346 | ||||||
| chr8:39185346 | A | AAAAAAAC | 134 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(131): Show |
136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.916-1552_916-1546d others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39185346 | ||||||
| chr8:39185356 | A | AAAACAAA others(4): Show |
1 | a0001c0001t0002g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.916-1546_916-1545i others(13): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39185356 | ||||||
| chr8:39185836 | C | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-1073C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185836 | |||||||
| chr8:39185842 | G | C | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.916-1067G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185842 | |||||||
| chr8:39185848 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.916-1061G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185848 | |||||||
| chr8:39185881 | C | CT | 80 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.916-1015dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | 39185881 | ||||||
| chr8:39185933 | TCTGCTGG others(6): Show |
T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-975_916-963del others(13): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39185933 | |||||||
| chr8:39186132 | G | A | 3 | a0004c0007t0001g0154 a0004c0007t0001g0244 a0012c0013t0001g0153 |
3 | HG02717.hp2 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.916-777G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39186132 | |||||||
| chr8:39186193 | C | G | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.916-716C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39186193 | |||||||
| chr8:39186319 | A | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.916-590A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39186319 | |||||||
| chr8:39186519 | G | A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.916-390G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39186519 | |||||||
| chr8:39186817 | A | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-92A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | chr8 | 39186817 | |||||||
| chr8:39187098 | A | G | 5 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG00438.hp2 NA18612.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052+53A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39187098 | |||||||
| chr8:39187254 | A | C | 76 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1052+209A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39187254 | |||||||
| chr8:39187281 | A | AT | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+244dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39187281 | ||||||
| chr8:39187399 | G | A | 1 | a0001c0002t0001g0190 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1052+354G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39187399 | |||||||
| chr8:39187536 | G | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052+491G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39187536 | |||||||
| chr8:39187563 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0168 |
2 | HG01361.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1052+518G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39187563 | |||||||
| chr8:39187665 | G | GA | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+627dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39187665 | ||||||
| chr8:39187808 | C | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1052+763C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39187808 | |||||||
| chr8:39188059 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1052+1014A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39188059 | |||||||
| chr8:39188089 | CAT | C | 75 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1052+1047_1052+104 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39188089 | ||||||
| chr8:39188270 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1052+1225T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39188270 | |||||||
| chr8:39188371 | A | ATCTG | 74 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1052+1342_1052+134 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39188371 | ||||||
| chr8:39188371 | A | G | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1052+1326A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39188371 | |||||||
| chr8:39188371 | ATCTG | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1052+1342_1052+134 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39188371 | ||||||
| chr8:39188474 | A | G | 1 | a0002c0003t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1052+1429A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39188474 | |||||||
| chr8:39188668 | TAA | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052+1624_1052+162 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39188668 | |||||||
| chr8:39188868 | C | G | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+1823C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39188868 | |||||||
| chr8:39189092 | G | A | 6 | a0001c0001t0001g0240 a0001c0001t0001g0243 a0002c0003t0001g0238 others(3): Show |
6 | HG02258.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052+2047G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189092 | |||||||
| chr8:39189346 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1052+2301C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189346 | |||||||
| chr8:39189422 | T | C | 1 | a0001c0001t0002g0018 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1052+2377T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189422 | |||||||
| chr8:39189426 | A | G | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+2381A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189426 | |||||||
| chr8:39189484 | A | G | 1 | a0001c0001t0002g0029 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1052+2439A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189484 | |||||||
| chr8:39189544 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1052+2499C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189544 | |||||||
| chr8:39189696 | A | G | 1 | a0001c0002t0002g0091 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1052+2651A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189696 | |||||||
| chr8:39189740 | C | A | 1 | a0001c0002t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1052+2695C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189740 | |||||||
| chr8:39189802 | T | C | 2 | a0001c0001t0001g0007 a0002c0003t0001g0157 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1052+2757T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189802 | |||||||
| chr8:39189829 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1052+2784G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189829 | |||||||
| chr8:39189915 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1052+2870C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189915 | |||||||
| chr8:39189940 | G | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1052+2895G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189940 | |||||||
| chr8:39189959 | C | T | 1 | a0001c0002t0002g0124 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1052+2914C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39189959 | |||||||
| chr8:39190215 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1052+3170T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39190215 | |||||||
| chr8:39190615 | G | A | 2 | a0001c0001t0001g0007 a0002c0003t0001g0157 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1052+3570G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39190615 | |||||||
| chr8:39190696 | A | T | 1 | a0001c0001t0002g0025 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1052+3651A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39190696 | |||||||
| chr8:39190793 | G | T | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+3748G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39190793 | |||||||
| chr8:39190816 | G | A | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+3771G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39190816 | |||||||
| chr8:39191016 | G | C | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1052+3971G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191016 | |||||||
| chr8:39191048 | T | TC | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(17): Show |
20 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1052+4005dupC | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39191048 | ||||||
| chr8:39191095 | A | G | 2 | a0001c0001t0001g0007 a0002c0003t0001g0157 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1052+4050A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191095 | |||||||
| chr8:39191163 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1052+4118T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191163 | |||||||
| chr8:39191222 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1052+4177G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191222 | |||||||
| chr8:39191271 | T | C | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+4226T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191271 | |||||||
| chr8:39191297 | G | A | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+4252G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191297 | |||||||
| chr8:39191465 | T | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1052+4420T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191465 | |||||||
| chr8:39191473 | T | C | 2 | a0001c0002t0002g0096 a0001c0002t0002g0101 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1052+4428T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191473 | |||||||
| chr8:39191503 | G | A | 68 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(65): Show |
69 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1052+4458G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191503 | |||||||
| chr8:39191600 | GT | G | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+4562delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39191600 | ||||||
| chr8:39191849 | A | G | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+4804A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191849 | |||||||
| chr8:39191940 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1052+4895A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191940 | |||||||
| chr8:39191964 | C | A | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+4919C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39191964 | |||||||
| chr8:39192126 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052+5081G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192126 | |||||||
| chr8:39192347 | T | G | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1052+5302T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192347 | |||||||
| chr8:39192407 | C | G | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1052+5362C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192407 | |||||||
| chr8:39192418 | A | G | 1 | a0007c0009t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1052+5373A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192418 | |||||||
| chr8:39192491 | T | C | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1052+5446T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192491 | |||||||
| chr8:39192652 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1052+5607C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192652 | |||||||
| chr8:39192653 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1052+5608G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192653 | |||||||
| chr8:39192765 | C | T | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1052+5720C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192765 | |||||||
| chr8:39192782 | T | C | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+5737T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39192782 | |||||||
| chr8:39193632 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1052+6587T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39193632 | |||||||
| chr8:39193754 | T | G | 1 | a0001c0002t0001g0190 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1052+6709T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39193754 | |||||||
| chr8:39194002 | C | T | 76 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1052+6957C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194002 | |||||||
| chr8:39194003 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1052+6958A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194003 | |||||||
| chr8:39194217 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1052+7172G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194217 | |||||||
| chr8:39194218 | C | A | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1052+7173C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194218 | |||||||
| chr8:39194222 | G | T | 2 | a0001c0002t0002g0113 a0001c0002t0002g0114 |
2 | NA18957.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1052+7177G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194222 | |||||||
| chr8:39194382 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1052+7337A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194382 | |||||||
| chr8:39194502 | G | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052+7457G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194502 | |||||||
| chr8:39194704 | T | G | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1052+7659T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194704 | |||||||
| chr8:39194729 | T | A | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1052+7684T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194729 | |||||||
| chr8:39194804 | C | T | 3 | a0001c0002t0002g0099 a0001c0002t0002g0110 a0001c0002t0002g0111 |
3 | NA18946.hp1 NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1052+7759C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39194804 | |||||||
| chr8:39195089 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+8044T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195089 | |||||||
| chr8:39195100 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+8055C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195100 | |||||||
| chr8:39195103 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+8058A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195103 | |||||||
| chr8:39195114 | C | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052+8069C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195114 | |||||||
| chr8:39195238 | G | A | 2 | a0004c0007t0001g0156 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1052+8193G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195238 | |||||||
| chr8:39195420 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1052+8375G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195420 | |||||||
| chr8:39195443 | T | C | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1052+8398T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195443 | |||||||
| chr8:39195447 | A | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052+8402A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195447 | |||||||
| chr8:39195450 | A | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1052+8405A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195450 | |||||||
| chr8:39195668 | A | T | 2 | a0001c0001t0001g0176 a0001c0001t0002g0076 |
2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1052+8623A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195668 | |||||||
| chr8:39195672 | A | AT | 76 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1052+8628dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39195672 | ||||||
| chr8:39195720 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0213 others(26): Show |
30 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1052+8675G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195720 | |||||||
| chr8:39195922 | C | T | 1 | a0001c0002t0001g0193 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1052+8877C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39195922 | |||||||
| chr8:39196128 | T | C | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1052+9083T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39196128 | |||||||
| chr8:39196387 | T | G | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1052+9342T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39196387 | |||||||
| chr8:39196681 | A | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052+9636A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39196681 | |||||||
| chr8:39196694 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1052+9649A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39196694 | |||||||
| chr8:39196837 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1052+9792G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39196837 | |||||||
| chr8:39197099 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+10054T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197099 | |||||||
| chr8:39197140 | A | G | 76 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1052+10095A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197140 | |||||||
| chr8:39197255 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1052+10210A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197255 | |||||||
| chr8:39197455 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+10410A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197455 | |||||||
| chr8:39197457 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+10412C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197457 | |||||||
| chr8:39197839 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0231 |
2 | HG01243.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1052+10794A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197839 | |||||||
| chr8:39197877 | G | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+10832G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39197877 | |||||||
| chr8:39198167 | A | AT | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+11130dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39198167 | ||||||
| chr8:39198418 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+11373C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198418 | |||||||
| chr8:39198437 | G | T | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1052+11392G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198437 | |||||||
| chr8:39198480 | C | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052+11435C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198480 | |||||||
| chr8:39198517 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1052+11472A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198517 | |||||||
| chr8:39198658 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0002g0031 |
2 | HG01069.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1052+11613G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198658 | |||||||
| chr8:39198739 | AT | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1052+11704delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39198739 | ||||||
| chr8:39198904 | T | G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1052+11859T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198904 | |||||||
| chr8:39198937 | A | T | 1 | a0001c0002t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1052+11892A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198937 | |||||||
| chr8:39198982 | G | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1052+11937G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39198982 | |||||||
| chr8:39199052 | A | G | 3 | a0001c0002t0002g0102 a0001c0002t0002g0103 a0001c0002t0002g0104 |
3 | HG00280.hp2 HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1052+12007A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199052 | |||||||
| chr8:39199247 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1053-11897A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199247 | |||||||
| chr8:39199251 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1053-11893C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199251 | |||||||
| chr8:39199334 | A | C | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-11810A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199334 | |||||||
| chr8:39199734 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1053-11410T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199734 | |||||||
| chr8:39199867 | C | T | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053-11277C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199867 | |||||||
| chr8:39199891 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1053-11253G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199891 | |||||||
| chr8:39199984 | G | T | 1 | a0002c0005t0001g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1053-11160G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39199984 | |||||||
| chr8:39200012 | A | G | 1 | a0001c0001t0002g0020 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1053-11132A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200012 | |||||||
| chr8:39200286 | A | G | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-10858A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200286 | |||||||
| chr8:39200408 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-10736G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200408 | |||||||
| chr8:39200443 | C | T | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1053-10701C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200443 | |||||||
| chr8:39200453 | CA | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1053-10690delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200453 | |||||||
| chr8:39200661 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1053-10483C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200661 | |||||||
| chr8:39200838 | A | G | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053-10306A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39200838 | |||||||
| chr8:39201087 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-10057A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201087 | |||||||
| chr8:39201153 | C | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-9991C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201153 | |||||||
| chr8:39201248 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1053-9896A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201248 | |||||||
| chr8:39201346 | C | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-9798C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201346 | |||||||
| chr8:39201424 | T | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-9720T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201424 | |||||||
| chr8:39201433 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-9711A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201433 | |||||||
| chr8:39201435 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-9709C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201435 | |||||||
| chr8:39201442 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-9702A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201442 | |||||||
| chr8:39201444 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-9700A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201444 | |||||||
| chr8:39201447 | G | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-9697G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201447 | |||||||
| chr8:39201523 | T | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-9621T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201523 | |||||||
| chr8:39201689 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053-9455C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201689 | |||||||
| chr8:39201735 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1053-9409G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201735 | |||||||
| chr8:39201785 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1053-9359A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201785 | |||||||
| chr8:39201812 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1053-9332A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39201812 | |||||||
| chr8:39202068 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1053-9076G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202068 | |||||||
| chr8:39202212 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-8932T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202212 | |||||||
| chr8:39202360 | G | T | 2 | a0005c0006t0001g0222 a0005c0006t0001g0223 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1053-8784G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202360 | |||||||
| chr8:39202544 | G | A | 76 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1053-8600G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202544 | |||||||
| chr8:39202563 | C | T | 1 | a0001c0002t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1053-8581C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202563 | |||||||
| chr8:39202623 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1053-8521C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202623 | |||||||
| chr8:39202685 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-8459G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202685 | |||||||
| chr8:39202761 | G | T | 1 | a0002c0003t0001g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1053-8383G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202761 | |||||||
| chr8:39202822 | G | T | 1 | a0001c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1053-8322G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202822 | |||||||
| chr8:39202831 | G | A | 1 | a0001c0002t0001g0205 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1053-8313G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202831 | |||||||
| chr8:39202840 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-8304T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202840 | |||||||
| chr8:39202937 | TG | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1053-8205delG | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39202937 | ||||||
| chr8:39202987 | G | A | 4 | a0002c0003t0001g0008 a0002c0003t0001g0246 a0002c0003t0001g0247 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053-8157G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39202987 | |||||||
| chr8:39203003 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG00280.hp1 HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1053-8141G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203003 | |||||||
| chr8:39203078 | T | C | 1 | a0001c0002t0002g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1053-8066T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203078 | |||||||
| chr8:39203188 | G | A | 1 | a0002c0003t0001g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1053-7956G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203188 | |||||||
| chr8:39203194 | T | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0206 others(4): Show |
7 | HG00639.hp2 HG01175.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053-7950T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203194 | |||||||
| chr8:39203353 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-7791T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203353 | |||||||
| chr8:39203425 | G | T | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1053-7719G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203425 | |||||||
| chr8:39203490 | C | G | 2 | a0001c0001t0001g0213 a0001c0001t0002g0064 |
2 | HG02027.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1053-7654C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203490 | |||||||
| chr8:39203538 | A | T | 1 | a0001c0002t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1053-7606A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203538 | |||||||
| chr8:39203544 | C | T | 1 | a0002c0003t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1053-7600C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203544 | |||||||
| chr8:39203830 | G | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 |
3 | HG02257.hp1 HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1053-7314G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203830 | |||||||
| chr8:39203866 | G | T | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-7278G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203866 | |||||||
| chr8:39203876 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1053-7268C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203876 | |||||||
| chr8:39203958 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1053-7186C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203958 | |||||||
| chr8:39203974 | G | C | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1053-7170G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39203974 | |||||||
| chr8:39204150 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1053-6994C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204150 | |||||||
| chr8:39204451 | G | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-6693G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204451 | |||||||
| chr8:39204486 | T | C | 1 | a0002c0003t0001g0208 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1053-6658T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204486 | |||||||
| chr8:39204526 | A | G | 1 | a0003c0004t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1053-6618A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204526 | |||||||
| chr8:39204625 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1053-6519A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204625 | |||||||
| chr8:39204638 | A | G | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-6506A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204638 | |||||||
| chr8:39204668 | C | T | 1 | a0002c0005t0001g0249 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1053-6476C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204668 | |||||||
| chr8:39204690 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1053-6454G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204690 | |||||||
| chr8:39204717 | T | G | 3 | a0001c0002t0001g0146 a0001c0002t0002g0100 a0001c0002t0002g0121 |
3 | HG03654.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1053-6427T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204717 | |||||||
| chr8:39204874 | G | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-6270G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39204874 | |||||||
| chr8:39205023 | G | T | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1053-6121G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205023 | |||||||
| chr8:39205067 | G | A | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053-6077G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205067 | |||||||
| chr8:39205332 | G | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0169 a0001c0001t0001g0177 others(4): Show |
7 | HG01243.hp2 HG01981.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053-5812G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205332 | |||||||
| chr8:39205403 | C | T | 1 | a0001c0002t0002g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1053-5741C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205403 | |||||||
| chr8:39205404 | G | A | 1 | a0009c0014t0002g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1053-5740G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205404 | |||||||
| chr8:39205410 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1053-5734G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205410 | |||||||
| chr8:39205431 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0002g0067 |
2 | HG00621.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1053-5713G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205431 | |||||||
| chr8:39205614 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-5530G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205614 | |||||||
| chr8:39205717 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1053-5427G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205717 | |||||||
| chr8:39205887 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(26): Show |
30 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1053-5257T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205887 | |||||||
| chr8:39205892 | G | C | 2 | a0001c0002t0002g0082 a0001c0002t0002g0131 |
2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1053-5252G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205892 | |||||||
| chr8:39205994 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1053-5150G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39205994 | |||||||
| chr8:39206134 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053-5010T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206134 | |||||||
| chr8:39206166 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1053-4978A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206166 | |||||||
| chr8:39206263 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053-4881C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206263 | |||||||
| chr8:39206264 | G | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-4880G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206264 | |||||||
| chr8:39206362 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1053-4782G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206362 | |||||||
| chr8:39206404 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1053-4740G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206404 | |||||||
| chr8:39206404 | GGGCCTGT others(11): Show |
G | 1 | a0001c0002t0001g0162 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1053-4739_1053-472 others(22): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206404 | |||||||
| chr8:39206533 | T | A | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053-4611T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206533 | |||||||
| chr8:39206642 | G | A | 10 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-4502G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206642 | |||||||
| chr8:39206717 | A | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-4427A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206717 | |||||||
| chr8:39206860 | T | A | 1 | a0001c0001t0002g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1053-4284T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206860 | |||||||
| chr8:39206988 | G | C | 2 | a0002c0003t0001g0246 a0002c0003t0001g0247 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1053-4156G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39206988 | |||||||
| chr8:39207000 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1053-4144A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207000 | |||||||
| chr8:39207029 | C | T | 1 | a0002c0003t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1053-4115C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207029 | |||||||
| chr8:39207030 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1053-4114A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207030 | |||||||
| chr8:39207128 | T | C | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-4016T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207128 | |||||||
| chr8:39207262 | T | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1053-3882T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207262 | |||||||
| chr8:39207419 | A | T | 1 | a0004c0007t0001g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1053-3725A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207419 | |||||||
| chr8:39207580 | T | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-3564T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207580 | |||||||
| chr8:39207585 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1053-3559G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207585 | |||||||
| chr8:39207751 | T | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-3393T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207751 | |||||||
| chr8:39207752 | C | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-3392C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207752 | |||||||
| chr8:39207806 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053-3338C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207806 | |||||||
| chr8:39207904 | G | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1053-3240G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39207904 | |||||||
| chr8:39208232 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1053-2912A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208232 | |||||||
| chr8:39208354 | A | G | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1053-2790A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208354 | |||||||
| chr8:39208619 | G | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1053-2525G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208619 | |||||||
| chr8:39208724 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1053-2420T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208724 | |||||||
| chr8:39208725 | G | A | 1 | a0002c0003t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1053-2419G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208725 | |||||||
| chr8:39208808 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053-2336C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208808 | |||||||
| chr8:39208855 | T | C | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1053-2289T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39208855 | |||||||
| chr8:39209031 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1053-2113A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209031 | |||||||
| chr8:39209083 | C | T | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-2061C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209083 | |||||||
| chr8:39209289 | A | G | 1 | a0001c0002t0002g0094 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1053-1855A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209289 | |||||||
| chr8:39209326 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1053-1818A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209326 | |||||||
| chr8:39209483 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1053-1661T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209483 | |||||||
| chr8:39209534 | G | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-1610G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209534 | |||||||
| chr8:39209538 | A | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1053-1606A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209538 | |||||||
| chr8:39209542 | A | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-1602A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209542 | |||||||
| chr8:39209712 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1053-1432G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209712 | |||||||
| chr8:39209938 | C | T | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1053-1206C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39209938 | |||||||
| chr8:39210326 | G | A | 2 | a0005c0006t0001g0222 a0005c0006t0001g0223 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1053-818G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210326 | |||||||
| chr8:39210345 | A | G | 2 | a0001c0002t0002g0116 a0001c0002t0002g0130 |
2 | HG00423.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1053-799A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210345 | |||||||
| chr8:39210419 | G | A | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1053-725G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210419 | |||||||
| chr8:39210657 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1053-487A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210657 | |||||||
| chr8:39210662 | C | T | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1053-482C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210662 | |||||||
| chr8:39210710 | C | T | 1 | a0001c0002t0002g0102 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1053-434C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210710 | |||||||
| chr8:39210743 | T | G | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1053-401T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | 39210743 | |||||||
| chr8:39210866 | GAAT | G | 10 | a0001c0001t0002g0018 a0001c0001t0002g0032 a0001c0001t0002g0059 others(7): Show |
10 | HG00438.hp2 NA18612.hp1 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053-273_1053-271d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | 39210866 | ||||||
| chr8:39211371 | A | G | 80 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1233+47A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39211371 | |||||||
| chr8:39211634 | G | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1233+310G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39211634 | |||||||
| chr8:39211836 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1233+512G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39211836 | |||||||
| chr8:39211888 | A | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1233+564A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39211888 | |||||||
| chr8:39212103 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(26): Show |
30 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1233+779G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212103 | |||||||
| chr8:39212120 | G | A | 2 | a0001c0002t0002g0065 a0001c0002t0002g0098 |
2 | NA18963.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1233+796G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212120 | |||||||
| chr8:39212173 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1233+849T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212173 | |||||||
| chr8:39212261 | G | A | 2 | a0001c0002t0002g0065 a0001c0002t0002g0098 |
2 | NA18963.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1233+937G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212261 | |||||||
| chr8:39212265 | C | T | 2 | a0001c0001t0001g0007 a0002c0003t0001g0157 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1233+941C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212265 | |||||||
| chr8:39212571 | TA | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+1248delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212571 | |||||||
| chr8:39212690 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1233+1366T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212690 | |||||||
| chr8:39212968 | T | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1233+1644T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39212968 | |||||||
| chr8:39213002 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1233+1678C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213002 | |||||||
| chr8:39213153 | T | A | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1233+1829T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213153 | |||||||
| chr8:39213164 | G | A | 1 | a0008c0012t0002g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1233+1840G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213164 | |||||||
| chr8:39213264 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1233+1940C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213264 | |||||||
| chr8:39213452 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1233+2128C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213452 | |||||||
| chr8:39213555 | A | T | 16 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(13): Show |
16 | HG00438.hp1 HG00544.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1233+2231A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213555 | |||||||
| chr8:39213613 | T | C | 1 | a0001c0002t0002g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1233+2289T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213613 | |||||||
| chr8:39213778 | G | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1233+2454G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39213778 | |||||||
| chr8:39214043 | C | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+2719C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39214043 | |||||||
| chr8:39214170 | C | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1233+2846C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39214170 | |||||||
| chr8:39214378 | T | A | 79 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1233+3054T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39214378 | |||||||
| chr8:39214520 | C | A | 1 | a0001c0002t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1233+3196C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39214520 | |||||||
| chr8:39214739 | G | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1233+3415G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39214739 | |||||||
| chr8:39214961 | T | C | 1 | a0001c0002t0002g0118 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1233+3637T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39214961 | |||||||
| chr8:39215021 | T | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1233+3697T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215021 | |||||||
| chr8:39215079 | C | A | 1 | a0001c0002t0002g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1233+3755C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215079 | |||||||
| chr8:39215269 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1233+3945G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215269 | |||||||
| chr8:39215357 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+4033G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215357 | |||||||
| chr8:39215473 | C | G | 1 | a0001c0002t0002g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1233+4149C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215473 | |||||||
| chr8:39215716 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1233+4392C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215716 | |||||||
| chr8:39215808 | A | G | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1233+4484A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215808 | |||||||
| chr8:39215851 | G | A | 73 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1233+4527G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39215851 | |||||||
| chr8:39216042 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1233+4718T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39216042 | |||||||
| chr8:39216114 | T | A | 26 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(23): Show |
26 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1233+4790T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39216114 | |||||||
| chr8:39216257 | T | C | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1233+4933T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39216257 | |||||||
| chr8:39216471 | C | T | 1 | a0001c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1234-5139C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39216471 | |||||||
| chr8:39216796 | TACTG | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-4810_1234-480 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39216796 | ||||||
| chr8:39216890 | T | TTAAAGTG others(9): Show |
239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1234-4710_1234-469 others(20): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39216890 | ||||||
| chr8:39216974 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-4636C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39216974 | |||||||
| chr8:39216981 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1234-4629G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39216981 | |||||||
| chr8:39217038 | G | T | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-4572G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39217038 | |||||||
| chr8:39217087 | C | T | 1 | a0006c0008t0001g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1234-4523C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39217087 | |||||||
| chr8:39217104 | A | AAT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1234-4493_1234-449 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39217104 | ||||||
| chr8:39217117 | A | AT | 74 | a0001c0001t0001g0007 a0001c0001t0002g0030 a0001c0001t0002g0127 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1234-4486dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39217117 | ||||||
| chr8:39217117 | A | ATAT | 6 | a0001c0001t0002g0033 a0004c0007t0001g0154 a0004c0007t0001g0155 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-4492_1234-449 others(7): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39217117 | ||||||
| chr8:39217117 | A | ATT | 19 | a0001c0001t0001g0149 a0001c0001t0001g0164 a0001c0001t0001g0177 others(16): Show |
19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1234-4487_1234-448 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39217117 | ||||||
| chr8:39217117 | A | T | 4 | a0002c0003t0001g0151 a0002c0003t0001g0253 a0002c0003t0001g0254 others(1): Show |
4 | HG02723.hp2 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-4493A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39217117 | |||||||
| chr8:39217119 | T | A | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1234-4491T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39217119 | |||||||
| chr8:39217677 | T | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1234-3933T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39217677 | |||||||
| chr8:39218226 | C | A | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1234-3384C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218226 | |||||||
| chr8:39218247 | G | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1234-3363G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218247 | |||||||
| chr8:39218261 | T | C | 16 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0158 others(13): Show |
16 | HG00438.hp1 HG00544.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1234-3349T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218261 | |||||||
| chr8:39218438 | G | C | 74 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1234-3172G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218438 | |||||||
| chr8:39218526 | A | C | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-3084A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218526 | |||||||
| chr8:39218847 | G | T | 9 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0202 others(6): Show |
9 | HG01258.hp1 HG02698.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-2763G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218847 | |||||||
| chr8:39218914 | A | G | 1 | a0002c0005t0001g0250 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1234-2696A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39218914 | |||||||
| chr8:39219039 | T | G | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1234-2571T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219039 | |||||||
| chr8:39219088 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1234-2522C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219088 | |||||||
| chr8:39219101 | C | T | 2 | a0001c0001t0001g0007 a0002c0003t0001g0157 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1234-2509C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219101 | |||||||
| chr8:39219128 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1234-2482C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219128 | |||||||
| chr8:39219378 | G | T | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1234-2232G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219378 | |||||||
| chr8:39219675 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1234-1935C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219675 | |||||||
| chr8:39219778 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1234-1832A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39219778 | |||||||
| chr8:39220007 | T | C | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1234-1603T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220007 | |||||||
| chr8:39220079 | G | C | 1 | a0005c0006t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1234-1531G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220079 | |||||||
| chr8:39220139 | A | G | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1234-1471A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220139 | |||||||
| chr8:39220192 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0213 others(27): Show |
31 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1234-1418G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220192 | |||||||
| chr8:39220304 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1234-1306A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220304 | |||||||
| chr8:39220431 | A | G | 1 | a0001c0002t0002g0084 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1234-1179A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220431 | |||||||
| chr8:39220758 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1234-852T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220758 | |||||||
| chr8:39220958 | A | AT | 14 | a0001c0001t0001g0219 a0001c0001t0001g0225 a0003c0004t0001g0134 others(11): Show |
14 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1234-646dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr8 | 39220958 | ||||||
| chr8:39220964 | TC | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1234-645delC | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220964 | |||||||
| chr8:39220965 | C | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1234-645C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39220965 | |||||||
| chr8:39221178 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0252 |
4 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-432T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39221178 | |||||||
| chr8:39221374 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1234-236A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39221374 | |||||||
| chr8:39221528 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1234-82A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39221528 | |||||||
| chr8:39221536 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1234-74C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | 39221536 | |||||||
| chr8:39221732 | A | G | 3 | a0001c0002t0001g0146 a0001c0002t0002g0100 a0001c0002t0002g0121 |
3 | HG03654.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1326+30A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 13/24 | chr8 | 39221732 | |||||||
| chr8:39221885 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1326+183A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 13/24 | chr8 | 39221885 | |||||||
| chr8:39222225 | A | G | 75 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1326+523A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 13/24 | chr8 | 39222225 | |||||||
| chr8:39222310 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1326+608G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 13/24 | chr8 | 39222310 | |||||||
| chr8:39222389 | G | A | 4 | a0001c0001t0001g0248 a0006c0008t0001g0068 a0006c0008t0001g0069 others(1): Show |
4 | HG02559.hp1 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327-651G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 13/24 | chr8 | 39222389 | |||||||
| chr8:39222916 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1327-124A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 13/24 | chr8 | 39222916 | |||||||
| chr8:39223272 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1525+34A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223272 | |||||||
| chr8:39223305 | T | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1525+67T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223305 | |||||||
| chr8:39223475 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+237G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223475 | |||||||
| chr8:39223632 | AT | A | 15 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1525+403delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr8 | 39223632 | ||||||
| chr8:39223635 | T | TTC | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1525+398_1525+399i others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr8 | 39223635 | ||||||
| chr8:39223742 | A | G | 35 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(32): Show |
35 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1525+504A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223742 | |||||||
| chr8:39223764 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1525+526A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223764 | |||||||
| chr8:39223850 | G | T | 1 | a0007c0009t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1525+612G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223850 | |||||||
| chr8:39223912 | T | C | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+674T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39223912 | |||||||
| chr8:39224241 | G | T | 72 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1525+1003G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224241 | |||||||
| chr8:39224280 | T | C | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525+1042T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224280 | |||||||
| chr8:39224302 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1525+1064T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224302 | |||||||
| chr8:39224386 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1525+1148C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224386 | |||||||
| chr8:39224389 | T | C | 86 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0030 others(83): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1525+1151T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224389 | |||||||
| chr8:39224392 | C | T | 72 | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1525+1154C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224392 | |||||||
| chr8:39224452 | T | G | 1 | a0001c0002t0002g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1525+1214T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224452 | |||||||
| chr8:39224532 | T | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1525+1294T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224532 | |||||||
| chr8:39224780 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1525+1542C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39224780 | |||||||
| chr8:39225113 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525+1875C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225113 | |||||||
| chr8:39225189 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525+1951C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225189 | |||||||
| chr8:39225217 | G | A | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525+1979G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225217 | |||||||
| chr8:39225318 | C | G | 2 | a0002c0003t0001g0151 a0007c0009t0001g0152 |
2 | HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1525+2080C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225318 | |||||||
| chr8:39225338 | C | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+2100C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225338 | |||||||
| chr8:39225422 | C | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+2184C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225422 | |||||||
| chr8:39225788 | A | AT | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
136 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1525+2561dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr8 | 39225788 | ||||||
| chr8:39225952 | A | C | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1525+2714A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225952 | |||||||
| chr8:39225959 | T | C | 22 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(19): Show |
22 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525+2721T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225959 | |||||||
| chr8:39225984 | A | G | 1 | a0001c0002t0002g0108 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1525+2746A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39225984 | |||||||
| chr8:39226163 | C | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1525+2925C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39226163 | |||||||
| chr8:39226166 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1525+2928A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39226166 | |||||||
| chr8:39226338 | C | T | 1 | a0005c0006t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1525+3100C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39226338 | |||||||
| chr8:39226424 | A | G | 86 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0221 others(83): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1525+3186A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39226424 | |||||||
| chr8:39226632 | G | GA | 7 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0004c0007t0001g0154 others(4): Show |
7 | HG01516.hp2 HG01517.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525+3405dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr8 | 39226632 | ||||||
| chr8:39226717 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1525+3479C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39226717 | |||||||
| chr8:39227007 | A | G | 1 | a0007c0009t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1525+3769A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227007 | |||||||
| chr8:39227359 | G | C | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525+4121G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227359 | |||||||
| chr8:39227369 | T | G | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525+4131T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227369 | |||||||
| chr8:39227409 | G | A | 4 | a0001c0001t0001g0007 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+4171G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227409 | |||||||
| chr8:39227548 | G | A | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1525+4310G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227548 | |||||||
| chr8:39227776 | C | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1526-4251C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227776 | |||||||
| chr8:39227823 | C | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0032 |
2 | NA18943.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1526-4204C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227823 | |||||||
| chr8:39227937 | G | A | 31 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(28): Show |
31 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1526-4090G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39227937 | |||||||
| chr8:39228023 | C | T | 3 | a0003c0004t0001g0135 a0003c0004t0001g0139 a0003c0004t0001g0140 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1526-4004C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228023 | |||||||
| chr8:39228051 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1526-3976G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228051 | |||||||
| chr8:39228126 | C | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1526-3901C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228126 | |||||||
| chr8:39228127 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-3900G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228127 | |||||||
| chr8:39228343 | C | T | 1 | a0001c0002t0002g0113 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1526-3684C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228343 | |||||||
| chr8:39228478 | A | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-3549A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228478 | |||||||
| chr8:39228763 | G | T | 20 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1526-3264G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228763 | |||||||
| chr8:39228834 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1526-3193C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39228834 | |||||||
| chr8:39229032 | T | C | 32 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(29): Show |
32 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1526-2995T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39229032 | |||||||
| chr8:39229480 | C | T | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1526-2547C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39229480 | |||||||
| chr8:39229927 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1526-2100A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39229927 | |||||||
| chr8:39230084 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1526-1943A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39230084 | |||||||
| chr8:39230239 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1526-1788A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39230239 | |||||||
| chr8:39230405 | G | A | 9 | a0001c0002t0001g0224 a0001c0002t0002g0009 a0001c0002t0002g0086 others(6): Show |
9 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1526-1622G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39230405 | |||||||
| chr8:39230426 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1526-1601G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39230426 | |||||||
| chr8:39230530 | T | C | 120 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1526-1497T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39230530 | |||||||
| chr8:39230939 | A | T | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1526-1088A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39230939 | |||||||
| chr8:39231231 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1526-796T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231231 | |||||||
| chr8:39231353 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1526-674C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231353 | |||||||
| chr8:39231356 | C | T | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1526-671C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231356 | |||||||
| chr8:39231357 | T | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1526-670T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231357 | |||||||
| chr8:39231435 | A | T | 1 | a0001c0002t0001g0205 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1526-592A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231435 | |||||||
| chr8:39231717 | G | T | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1526-310G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231717 | |||||||
| chr8:39231718 | G | T | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1526-309G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | chr8 | 39231718 | |||||||
| chr8:39232422 | C | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1634+287C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232422 | |||||||
| chr8:39232456 | A | G | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634+321A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232456 | |||||||
| chr8:39232485 | C | A | 1 | a0003c0004t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1634+350C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232485 | |||||||
| chr8:39232693 | A | T | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1634+558A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232693 | |||||||
| chr8:39232728 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1634+593G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232728 | |||||||
| chr8:39232836 | A | T | 1 | a0001c0001t0002g0070 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1634+701A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232836 | |||||||
| chr8:39232997 | A | T | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634+862A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39232997 | |||||||
| chr8:39233050 | G | A | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1635-849G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233050 | |||||||
| chr8:39233278 | A | G | 1 | a0003c0004t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1635-621A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233278 | |||||||
| chr8:39233326 | C | G | 1 | a0001c0001t0002g0022 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1635-573C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233326 | |||||||
| chr8:39233372 | T | C | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1635-527T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233372 | |||||||
| chr8:39233478 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1635-421G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233478 | |||||||
| chr8:39233490 | C | T | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1635-409C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233490 | |||||||
| chr8:39233688 | G | A | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1635-211G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233688 | |||||||
| chr8:39233797 | A | G | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1635-102A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 15/24 | chr8 | 39233797 | |||||||
| chr8:39234127 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1818+45G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234127 | |||||||
| chr8:39234167 | G | T | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+85G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234167 | |||||||
| chr8:39234212 | C | CT | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1818+132dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr8 | 39234212 | ||||||
| chr8:39234379 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG00280.hp1 HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1818+297G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234379 | |||||||
| chr8:39234476 | C | A | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818+394C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234476 | |||||||
| chr8:39234609 | ATAT | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1818+531_1818+533d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr8 | 39234609 | ||||||
| chr8:39234658 | C | T | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1818+576C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234658 | |||||||
| chr8:39234815 | C | A | 3 | a0001c0002t0002g0102 a0001c0002t0002g0103 a0001c0002t0002g0104 |
3 | HG00280.hp2 HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1818+733C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234815 | |||||||
| chr8:39234896 | G | T | 10 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0206 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1818+814G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39234896 | |||||||
| chr8:39235202 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1818+1120A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235202 | |||||||
| chr8:39235211 | A | G | 1 | a0002c0005t0002g0115 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1818+1129A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235211 | |||||||
| chr8:39235448 | A | G | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+1366A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235448 | |||||||
| chr8:39235515 | G | C | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818+1433G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235515 | |||||||
| chr8:39235571 | A | T | 2 | a0002c0005t0001g0249 a0002c0005t0001g0250 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1818+1489A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235571 | |||||||
| chr8:39235592 | A | G | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1818+1510A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235592 | |||||||
| chr8:39235621 | T | A | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1818+1539T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235621 | |||||||
| chr8:39235671 | A | G | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1818+1589A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235671 | |||||||
| chr8:39235807 | T | C | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+1725T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235807 | |||||||
| chr8:39235851 | G | T | 1 | a0001c0001t0002g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1818+1769G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39235851 | |||||||
| chr8:39236012 | T | A | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+1930T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236012 | |||||||
| chr8:39236120 | A | G | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+2038A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236120 | |||||||
| chr8:39236154 | G | A | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+2072G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236154 | |||||||
| chr8:39236188 | T | C | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818+2106T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236188 | |||||||
| chr8:39236337 | T | C | 13 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+2255T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236337 | |||||||
| chr8:39236594 | C | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+2512C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236594 | |||||||
| chr8:39236642 | T | C | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818+2560T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236642 | |||||||
| chr8:39236644 | G | A | 6 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0002g0012 others(3): Show |
6 | HG01243.hp2 HG02257.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1818+2562G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236644 | |||||||
| chr8:39236658 | G | A | 12 | a0001c0001t0001g0210 a0001c0001t0001g0240 a0001c0001t0001g0243 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1818+2576G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236658 | |||||||
| chr8:39236892 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1818+2810C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236892 | |||||||
| chr8:39236949 | G | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1818+2867G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236949 | |||||||
| chr8:39236998 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+2916A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39236998 | |||||||
| chr8:39237036 | A | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+2954A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237036 | |||||||
| chr8:39237154 | G | A | 4 | a0001c0001t0001g0164 a0002c0003t0001g0165 a0002c0003t0001g0166 others(1): Show |
4 | HG02615.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818+3072G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237154 | |||||||
| chr8:39237172 | G | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+3090G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237172 | |||||||
| chr8:39237182 | C | T | 4 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 others(1): Show |
4 | HG02723.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818+3100C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237182 | |||||||
| chr8:39237184 | G | A | 9 | a0001c0001t0001g0150 a0001c0001t0002g0038 a0001c0001t0002g0042 others(6): Show |
9 | HG00738.hp2 HG01081.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1818+3102G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237184 | |||||||
| chr8:39237258 | G | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+3176G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237258 | |||||||
| chr8:39237470 | G | T | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1818+3388G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237470 | |||||||
| chr8:39237605 | G | A | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+3523G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237605 | |||||||
| chr8:39237683 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+3601A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237683 | |||||||
| chr8:39237716 | G | A | 1 | a0001c0002t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1818+3634G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237716 | |||||||
| chr8:39237779 | G | T | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1818+3697G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237779 | |||||||
| chr8:39237932 | C | A | 1 | a0001c0002t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1818+3850C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237932 | |||||||
| chr8:39237951 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1818+3869T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237951 | |||||||
| chr8:39237952 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1818+3870C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237952 | |||||||
| chr8:39237956 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+3874G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39237956 | |||||||
| chr8:39238078 | G | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1818+3996G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238078 | |||||||
| chr8:39238296 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0215 |
2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1818+4214C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238296 | |||||||
| chr8:39238387 | A | C | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1818+4305A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238387 | |||||||
| chr8:39238495 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1818+4413A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238495 | |||||||
| chr8:39238517 | A | G | 1 | a0002c0003t0001g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1818+4435A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238517 | |||||||
| chr8:39238545 | C | T | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1818+4463C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238545 | |||||||
| chr8:39238598 | T | A | 119 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1818+4516T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238598 | |||||||
| chr8:39238788 | G | A | 1 | a0001c0002t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1818+4706G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238788 | |||||||
| chr8:39238855 | C | G | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1818+4773C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238855 | |||||||
| chr8:39238890 | C | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0145 others(195): Show |
200 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1818+4808C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238890 | |||||||
| chr8:39238895 | A | T | 1 | a0007c0009t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1818+4813A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238895 | |||||||
| chr8:39238918 | G | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1818+4836G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39238918 | |||||||
| chr8:39239064 | C | T | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1818+4982C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239064 | |||||||
| chr8:39239237 | C | T | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1818+5155C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239237 | |||||||
| chr8:39239293 | G | T | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1818+5211G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239293 | |||||||
| chr8:39239303 | T | G | 5 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0206 others(2): Show |
5 | HG01358.hp1 HG02148.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+5221T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239303 | |||||||
| chr8:39239363 | C | T | 1 | a0002c0003t0002g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1818+5281C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239363 | |||||||
| chr8:39239500 | A | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+5418A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239500 | |||||||
| chr8:39239637 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+5555A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39239637 | |||||||
| chr8:39240052 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1818+5970T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240052 | |||||||
| chr8:39240165 | C | G | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1819-5918C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240165 | |||||||
| chr8:39240193 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(27): Show |
31 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1819-5890A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240193 | |||||||
| chr8:39240407 | C | T | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0024 others(2): Show |
5 | HG02523.hp1 NA18944.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1819-5676C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240407 | |||||||
| chr8:39240426 | G | A | 1 | a0002c0003t0001g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1819-5657G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240426 | |||||||
| chr8:39240583 | T | C | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1819-5500T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240583 | |||||||
| chr8:39240675 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1819-5408C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240675 | |||||||
| chr8:39240696 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(25): Show |
29 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1819-5387T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240696 | |||||||
| chr8:39240768 | G | A | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1819-5315G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240768 | |||||||
| chr8:39240910 | C | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(24): Show |
28 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1819-5173C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240910 | |||||||
| chr8:39240966 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0002g0057 |
2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1819-5117G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39240966 | |||||||
| chr8:39241016 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-5067A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241016 | |||||||
| chr8:39241157 | A | G | 21 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(18): Show |
21 | HG02055.hp1 HG02257.hp2 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1819-4926A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241157 | |||||||
| chr8:39241330 | G | C | 2 | a0003c0004t0001g0142 a0003c0004t0001g0143 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1819-4753G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241330 | |||||||
| chr8:39241395 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1819-4688G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241395 | |||||||
| chr8:39241460 | A | G | 102 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(99): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1819-4623A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241460 | |||||||
| chr8:39241774 | G | A | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1819-4309G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241774 | |||||||
| chr8:39241821 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1819-4262A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241821 | |||||||
| chr8:39241839 | C | A | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1819-4244C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241839 | |||||||
| chr8:39241861 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1819-4222G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241861 | |||||||
| chr8:39241939 | C | T | 2 | a0005c0006t0001g0216 a0005c0006t0001g0222 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1819-4144C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241939 | |||||||
| chr8:39241978 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1819-4105A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241978 | |||||||
| chr8:39241979 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1819-4104A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39241979 | |||||||
| chr8:39242088 | G | A | 20 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1819-3995G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242088 | |||||||
| chr8:39242306 | C | A | 1 | a0001c0002t0002g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1819-3777C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242306 | |||||||
| chr8:39242317 | A | C | 1 | a0001c0001t0002g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1819-3766A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242317 | |||||||
| chr8:39242356 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1819-3727C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242356 | |||||||
| chr8:39242417 | T | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(27): Show |
31 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1819-3666T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242417 | |||||||
| chr8:39242623 | C | T | 1 | a0001c0002t0002g0094 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1819-3460C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242623 | |||||||
| chr8:39242644 | C | T | 1 | a0001c0002t0002g0118 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1819-3439C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242644 | |||||||
| chr8:39242652 | A | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-3431A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242652 | |||||||
| chr8:39242662 | A | C | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1819-3421A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242662 | |||||||
| chr8:39242733 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1819-3350A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242733 | |||||||
| chr8:39242790 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1819-3293C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242790 | |||||||
| chr8:39242938 | T | A | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-3145T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242938 | |||||||
| chr8:39242943 | T | C | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1819-3140T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39242943 | |||||||
| chr8:39243028 | C | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1819-3055C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243028 | |||||||
| chr8:39243173 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1819-2910G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243173 | |||||||
| chr8:39243249 | A | G | 1 | a0001c0002t0002g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1819-2834A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243249 | |||||||
| chr8:39243259 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1819-2824A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243259 | |||||||
| chr8:39243292 | A | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1819-2791A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243292 | |||||||
| chr8:39243454 | T | A | 1 | a0001c0002t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1819-2629T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243454 | |||||||
| chr8:39243476 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1819-2607T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243476 | |||||||
| chr8:39243581 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1819-2502G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243581 | |||||||
| chr8:39243793 | GAGAA | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(24): Show |
28 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1819-2274_1819-227 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr8 | 39243793 | ||||||
| chr8:39243858 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-2225A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243858 | |||||||
| chr8:39243867 | T | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1819-2216T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39243867 | |||||||
| chr8:39244224 | A | G | 1 | a0001c0002t0001g0191 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1819-1859A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39244224 | |||||||
| chr8:39244265 | G | A | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1819-1818G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39244265 | |||||||
| chr8:39244402 | T | A | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-1681T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39244402 | |||||||
| chr8:39244507 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1819-1576C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39244507 | |||||||
| chr8:39244641 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-1442T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39244641 | |||||||
| chr8:39244735 | T | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-1348T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39244735 | |||||||
| chr8:39244850 | T | TA | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1819-1225dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr8 | 39244850 | ||||||
| chr8:39245067 | C | CAGTGGCT others(4): Show |
3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1819-1015_1819-101 others(15): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr8 | 39245067 | ||||||
| chr8:39245071 | C | A | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1819-1012C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39245071 | |||||||
| chr8:39245077 | T | C | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1819-1006T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39245077 | |||||||
| chr8:39245222 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-861T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39245222 | |||||||
| chr8:39245505 | G | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-578G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39245505 | |||||||
| chr8:39245529 | T | TA | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-548dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr8 | 39245529 | ||||||
| chr8:39245752 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1819-331T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 16/24 | chr8 | 39245752 | |||||||
| chr8:39246343 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1902+177A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246343 | |||||||
| chr8:39246369 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1902+203C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246369 | |||||||
| chr8:39246390 | T | C | 19 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(16): Show |
19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1902+224T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246390 | |||||||
| chr8:39246407 | G | C | 1 | a0001c0002t0001g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1902+241G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246407 | |||||||
| chr8:39246413 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1902+247A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246413 | |||||||
| chr8:39246594 | A | C | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1902+428A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246594 | |||||||
| chr8:39246890 | T | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(147): Show |
152 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1902+724T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39246890 | |||||||
| chr8:39247011 | G | A | 3 | a0001c0002t0002g0094 a0002c0005t0002g0093 a0002c0005t0002g0095 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1902+845G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247011 | |||||||
| chr8:39247139 | T | C | 1 | a0001c0002t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1902+973T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247139 | |||||||
| chr8:39247174 | T | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1902+1008T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247174 | |||||||
| chr8:39247220 | C | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1902+1054C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247220 | |||||||
| chr8:39247469 | A | G | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1902+1303A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247469 | |||||||
| chr8:39247487 | T | TG | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1902+1321_1902+132 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247487 | |||||||
| chr8:39247488 | A | G | 76 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1902+1322A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247488 | |||||||
| chr8:39247488 | A | T | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1902+1322A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247488 | |||||||
| chr8:39247554 | G | A | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1902+1388G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247554 | |||||||
| chr8:39247778 | G | GT | 27 | a0001c0001t0002g0020 a0001c0001t0002g0060 a0002c0003t0001g0151 others(24): Show |
27 | HG00099.hp1 HG02055.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1902+1626dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39247778 | ||||||
| chr8:39247778 | GT | G | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0183 others(16): Show |
19 | HG00639.hp2 HG00735.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1902+1626delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39247778 | ||||||
| chr8:39247876 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1902+1710A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247876 | |||||||
| chr8:39247895 | CT | C | 20 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1902+1739delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39247895 | ||||||
| chr8:39247989 | C | G | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+1823C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39247989 | |||||||
| chr8:39248040 | T | C | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1902+1874T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248040 | |||||||
| chr8:39248118 | G | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1902+1952G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248118 | |||||||
| chr8:39248152 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1902+1986A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248152 | |||||||
| chr8:39248248 | G | C | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+2082G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248248 | |||||||
| chr8:39248297 | G | A | 102 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(99): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1902+2131G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248297 | |||||||
| chr8:39248404 | A | C | 12 | a0001c0001t0001g0210 a0001c0001t0001g0240 a0001c0001t0001g0243 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1902+2238A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248404 | |||||||
| chr8:39248753 | C | A | 1 | a0004c0007t0001g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1902+2587C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248753 | |||||||
| chr8:39248904 | C | CT | 72 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1902+2754dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39248904 | ||||||
| chr8:39248964 | A | G | 122 | a0001c0001t0001g0007 a0001c0001t0001g0149 a0001c0001t0001g0177 others(119): Show |
123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1902+2798A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39248964 | |||||||
| chr8:39249162 | C | G | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1902+2996C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249162 | |||||||
| chr8:39249202 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1902+3036C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249202 | |||||||
| chr8:39249288 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1902+3122G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249288 | |||||||
| chr8:39249443 | T | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1902+3277T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249443 | |||||||
| chr8:39249501 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1902+3335G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249501 | |||||||
| chr8:39249553 | G | A | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+3387G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249553 | |||||||
| chr8:39249601 | A | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(145): Show |
150 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1902+3435A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249601 | |||||||
| chr8:39249680 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(25): Show |
29 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1902+3514T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249680 | |||||||
| chr8:39249904 | T | C | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1902+3738T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249904 | |||||||
| chr8:39249910 | T | G | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1902+3744T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249910 | |||||||
| chr8:39249912 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1902+3746C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39249912 | |||||||
| chr8:39250193 | G | T | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1902+4027G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250193 | |||||||
| chr8:39250393 | G | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1903-4021G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250393 | |||||||
| chr8:39250613 | T | C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0206 others(2): Show |
5 | HG01358.hp1 HG02148.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-3801T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250613 | |||||||
| chr8:39250711 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0036 |
2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1903-3703A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250711 | |||||||
| chr8:39250725 | A | T | 1 | a0002c0003t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1903-3689A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250725 | |||||||
| chr8:39250763 | T | G | 1 | a0002c0005t0001g0250 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1903-3651T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250763 | |||||||
| chr8:39250766 | G | A | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1903-3648G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250766 | |||||||
| chr8:39250983 | A | G | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1903-3431A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39250983 | |||||||
| chr8:39251068 | A | G | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1903-3346A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251068 | |||||||
| chr8:39251081 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1903-3333C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251081 | |||||||
| chr8:39251108 | A | G | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1903-3306A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251108 | |||||||
| chr8:39251331 | C | A | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1903-3083C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251331 | |||||||
| chr8:39251342 | C | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1903-3072C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251342 | |||||||
| chr8:39251344 | ATCTTTTT others(15): Show |
A | 20 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1903-3062_1903-304 others(26): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39251344 | ||||||
| chr8:39251351 | T | TG | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1903-3063_1903-306 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251351 | |||||||
| chr8:39251378 | CA | C | 99 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(96): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1903-3026delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39251378 | ||||||
| chr8:39251476 | T | C | 1 | a0001c0002t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1903-2938T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251476 | |||||||
| chr8:39251700 | G | C | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1903-2714G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251700 | |||||||
| chr8:39251775 | T | G | 2 | a0002c0003t0001g0238 a0002c0003t0001g0239 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1903-2639T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39251775 | |||||||
| chr8:39252204 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0215 a0001c0001t0001g0219 |
3 | HG00639.hp2 HG01175.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1903-2210C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39252204 | |||||||
| chr8:39252405 | CA | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1903-2003delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39252405 | ||||||
| chr8:39252413 | G | GA | 12 | a0001c0001t0001g0212 a0003c0004t0001g0134 a0003c0004t0001g0135 others(9): Show |
12 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1903-1991dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39252413 | ||||||
| chr8:39252498 | A | C | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1903-1916A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39252498 | |||||||
| chr8:39252645 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1903-1769T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39252645 | |||||||
| chr8:39253010 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1903-1404G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253010 | |||||||
| chr8:39253057 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1903-1357C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253057 | |||||||
| chr8:39253081 | C | T | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1903-1333C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253081 | |||||||
| chr8:39253164 | A | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1903-1250A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253164 | |||||||
| chr8:39253193 | C | A | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1903-1221C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253193 | |||||||
| chr8:39253268 | T | G | 1 | a0001c0002t0001g0162 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1903-1146T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253268 | |||||||
| chr8:39253270 | C | T | 1 | a0001c0002t0002g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1903-1144C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253270 | |||||||
| chr8:39253404 | G | A | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1903-1010G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253404 | |||||||
| chr8:39253696 | G | A | 4 | a0001c0002t0001g0185 a0001c0002t0001g0190 a0001c0002t0001g0191 others(1): Show |
4 | NA18943.hp1 NA19002.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903-718G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253696 | |||||||
| chr8:39253753 | A | C | 1 | a0001c0002t0002g0118 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1903-661A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253753 | |||||||
| chr8:39253793 | C | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1903-621C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253793 | |||||||
| chr8:39253932 | C | T | 3 | a0001c0002t0002g0094 a0002c0005t0002g0093 a0002c0005t0002g0095 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1903-482C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39253932 | |||||||
| chr8:39254010 | G | T | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1903-404G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | chr8 | 39254010 | |||||||
| chr8:39254225 | CT | C | 86 | a0001c0001t0001g0248 a0001c0001t0002g0028 a0001c0002t0001g0146 others(83): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1903-173delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39254225 | ||||||
| chr8:39254298 | CTG | C | 18 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1903-114_1903-113d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | 39254298 | ||||||
| chr8:39254540 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2005+24C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39254540 | |||||||
| chr8:39254543 | A | G | 1 | a0005c0006t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2005+27A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39254543 | |||||||
| chr8:39254568 | A | G | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2005+52A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39254568 | |||||||
| chr8:39254815 | C | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0213 others(27): Show |
31 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2005+299C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39254815 | |||||||
| chr8:39254827 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2005+311A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39254827 | |||||||
| chr8:39255081 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(28): Show |
32 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.2005+565T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255081 | |||||||
| chr8:39255313 | CGTA | C | 9 | a0001c0002t0001g0224 a0001c0002t0002g0009 a0001c0002t0002g0086 others(6): Show |
9 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2005+800_2005+802d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr8 | 39255313 | ||||||
| chr8:39255357 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2005+841T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255357 | |||||||
| chr8:39255469 | C | T | 2 | a0001c0002t0002g0116 a0001c0002t0002g0130 |
2 | HG00423.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.2005+953C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255469 | |||||||
| chr8:39255520 | A | G | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2005+1004A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255520 | |||||||
| chr8:39255541 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0234 others(24): Show |
28 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2005+1025C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255541 | |||||||
| chr8:39255703 | T | G | 1 | a0001c0001t0002g0018 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2005+1187T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255703 | |||||||
| chr8:39255935 | T | C | 1 | a0004c0007t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2006-1252T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255935 | |||||||
| chr8:39255983 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2006-1204G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39255983 | |||||||
| chr8:39256038 | G | A | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2006-1149G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256038 | |||||||
| chr8:39256087 | G | T | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2006-1100G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256087 | |||||||
| chr8:39256316 | G | A | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2006-871G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256316 | |||||||
| chr8:39256358 | T | A | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2006-829T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256358 | |||||||
| chr8:39256403 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2006-784T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256403 | |||||||
| chr8:39256630 | A | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2006-557A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256630 | |||||||
| chr8:39256666 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0026 a0001c0001t0002g0083 |
3 | NA18944.hp1 NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2006-521A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39256666 | |||||||
| chr8:39257020 | T | C | 1 | a0006c0008t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2006-167T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39257020 | |||||||
| chr8:39257054 | C | G | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2006-133C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39257054 | |||||||
| chr8:39257072 | T | C | 23 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(20): Show |
23 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2006-115T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | chr8 | 39257072 | |||||||
| chr8:39257157 | GT | G | 78 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2006-17delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr8 | 39257157 | ||||||
| chr8:39257430 | C | T | 78 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2162+87C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39257430 | |||||||
| chr8:39257591 | TTTAC | T | 101 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(98): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2162+249_2162+252d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39257591 | |||||||
| chr8:39257906 | T | C | 4 | a0001c0002t0002g0084 a0001c0002t0002g0105 a0001c0002t0002g0109 others(1): Show |
4 | HG01106.hp2 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2162+563T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39257906 | |||||||
| chr8:39258018 | G | A | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2162+675G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39258018 | |||||||
| chr8:39258123 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(148): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.2162+780T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39258123 | |||||||
| chr8:39258193 | A | G | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2162+850A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39258193 | |||||||
| chr8:39258206 | T | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2162+863T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39258206 | |||||||
| chr8:39258395 | TA | T | 120 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2162+1054delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | 39258395 | ||||||
| chr8:39258410 | C | T | 120 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2162+1067C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39258410 | |||||||
| chr8:39258659 | T | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2162+1316T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39258659 | |||||||
| chr8:39259221 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0251 |
2 | HG02486.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2162+1878C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259221 | |||||||
| chr8:39259293 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2162+1950G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259293 | |||||||
| chr8:39259309 | C | T | 3 | a0002c0003t0001g0228 a0002c0003t0001g0229 a0002c0003t0001g0230 |
3 | HG02572.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2162+1966C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259309 | |||||||
| chr8:39259347 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2162+2004G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259347 | |||||||
| chr8:39259390 | T | G | 102 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(99): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2162+2047T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259390 | |||||||
| chr8:39259409 | A | G | 102 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(99): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2162+2066A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259409 | |||||||
| chr8:39259505 | G | A | 120 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2162+2162G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259505 | |||||||
| chr8:39259553 | A | G | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2162+2210A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259553 | |||||||
| chr8:39259930 | A | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(30): Show |
34 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2162+2587A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259930 | |||||||
| chr8:39259942 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2162+2599G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259942 | |||||||
| chr8:39259957 | T | C | 3 | a0001c0002t0002g0099 a0001c0002t0002g0110 a0001c0002t0002g0111 |
3 | NA18946.hp1 NA19081.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2162+2614T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39259957 | |||||||
| chr8:39260249 | G | A | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2162+2906G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39260249 | |||||||
| chr8:39260594 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2162+3251A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39260594 | |||||||
| chr8:39260694 | A | G | 1 | a0008c0012t0002g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2162+3351A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39260694 | |||||||
| chr8:39260883 | T | G | 1 | a0001c0001t0002g0057 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2162+3540T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39260883 | |||||||
| chr8:39261031 | C | G | 1 | a0004c0007t0001g0156 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2162+3688C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261031 | |||||||
| chr8:39261096 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2162+3753C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261096 | |||||||
| chr8:39261125 | A | G | 3 | a0001c0002t0002g0087 a0001c0002t0002g0107 a0001c0002t0002g0108 |
3 | HG00408.hp1 HG02056.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2162+3782A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261125 | |||||||
| chr8:39261253 | A | G | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2162+3910A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261253 | |||||||
| chr8:39261349 | T | C | 102 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(99): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2162+4006T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261349 | |||||||
| chr8:39261364 | G | T | 1 | a0004c0007t0001g0156 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2162+4021G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261364 | |||||||
| chr8:39261635 | G | C | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2162+4292G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261635 | |||||||
| chr8:39261647 | G | A | 15 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2162+4304G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261647 | |||||||
| chr8:39261683 | T | C | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2162+4340T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261683 | |||||||
| chr8:39261712 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2162+4369A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39261712 | |||||||
| chr8:39262010 | T | A | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2162+4667T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262010 | |||||||
| chr8:39262204 | GT | G | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2162+4874delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | 39262204 | ||||||
| chr8:39262257 | A | G | 15 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2162+4914A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262257 | |||||||
| chr8:39262426 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2162+5083A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262426 | |||||||
| chr8:39262521 | A | C | 102 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(99): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2162+5178A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262521 | |||||||
| chr8:39262641 | A | C | 117 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(114): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2162+5298A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262641 | |||||||
| chr8:39262728 | C | CT | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2162+5390dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | 39262728 | ||||||
| chr8:39262765 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0183 |
2 | NA19064.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.2162+5422T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262765 | |||||||
| chr8:39262943 | A | G | 4 | a0001c0001t0001g0248 a0005c0006t0001g0144 a0005c0006t0001g0216 others(1): Show |
4 | HG02723.hp1 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2162+5600A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39262943 | |||||||
| chr8:39263007 | G | A | 1 | a0001c0002t0002g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2162+5664G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263007 | |||||||
| chr8:39263145 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(148): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.2162+5802A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263145 | |||||||
| chr8:39263169 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2162+5826T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263169 | |||||||
| chr8:39263452 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2162+6109T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263452 | |||||||
| chr8:39263464 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2162+6121C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263464 | |||||||
| chr8:39263512 | ATCTTCTT others(4): Show |
A | 1 | a0001c0001t0001g0236 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2162+6172_2162+618 others(15): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | 39263512 | ||||||
| chr8:39263584 | T | C | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2162+6241T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263584 | |||||||
| chr8:39263824 | A | G | 78 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2162+6481A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263824 | |||||||
| chr8:39263993 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2162+6650G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39263993 | |||||||
| chr8:39264047 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2162+6704C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264047 | |||||||
| chr8:39264294 | G | A | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2163-6582G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264294 | |||||||
| chr8:39264299 | T | G | 1 | a0002c0005t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2163-6577T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264299 | |||||||
| chr8:39264322 | T | C | 1 | a0001c0002t0001g0193 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2163-6554T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264322 | |||||||
| chr8:39264341 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-6535G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264341 | |||||||
| chr8:39264506 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2163-6370T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264506 | |||||||
| chr8:39264641 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2163-6235G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264641 | |||||||
| chr8:39264798 | G | A | 97 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.2163-6078G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39264798 | |||||||
| chr8:39265165 | T | A | 1 | a0001c0002t0002g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2163-5711T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39265165 | |||||||
| chr8:39265252 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-5624G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39265252 | |||||||
| chr8:39265397 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2163-5479G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39265397 | |||||||
| chr8:39265767 | C | T | 8 | a0001c0002t0002g0001 a0001c0002t0002g0084 a0001c0002t0002g0099 others(5): Show |
9 | HG01106.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163-5109C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39265767 | |||||||
| chr8:39265848 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01071.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2163-5028G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39265848 | |||||||
| chr8:39265996 | C | G | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2163-4880C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39265996 | |||||||
| chr8:39266013 | G | T | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2163-4863G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39266013 | |||||||
| chr8:39266301 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0217 others(27): Show |
31 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2163-4575C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39266301 | |||||||
| chr8:39266350 | G | C | 3 | a0001c0002t0001g0178 a0001c0002t0001g0186 a0001c0002t0001g0187 |
3 | NA18972.hp1 NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2163-4526G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39266350 | |||||||
| chr8:39266449 | T | A | 20 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2163-4427T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39266449 | |||||||
| chr8:39266591 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0053 a0001c0002t0002g0082 |
3 | HG00544.hp1 NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2163-4285C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39266591 | |||||||
| chr8:39266946 | T | C | 77 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2163-3930T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39266946 | |||||||
| chr8:39267253 | G | C | 1 | a0002c0003t0001g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2163-3623G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267253 | |||||||
| chr8:39267324 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-3552A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267324 | |||||||
| chr8:39267394 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2163-3482A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267394 | |||||||
| chr8:39267480 | A | G | 1 | a0002c0003t0001g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2163-3396A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267480 | |||||||
| chr8:39267514 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-3362G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267514 | |||||||
| chr8:39267572 | G | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2163-3304G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267572 | |||||||
| chr8:39267653 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2163-3223G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267653 | |||||||
| chr8:39267743 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-3133C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267743 | |||||||
| chr8:39267840 | C | T | 77 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2163-3036C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267840 | |||||||
| chr8:39267885 | T | G | 116 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(113): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2163-2991T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39267885 | |||||||
| chr8:39268123 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2163-2753A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268123 | |||||||
| chr8:39268263 | C | T | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2163-2613C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268263 | |||||||
| chr8:39268455 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(141): Show |
146 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2163-2421C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268455 | |||||||
| chr8:39268566 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2163-2310G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268566 | |||||||
| chr8:39268679 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-2197C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268679 | |||||||
| chr8:39268803 | A | T | 2 | a0002c0003t0002g0048 a0002c0003t0002g0049 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2163-2073A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268803 | |||||||
| chr8:39268856 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-2020A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268856 | |||||||
| chr8:39268931 | C | G | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2163-1945C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39268931 | |||||||
| chr8:39269022 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2163-1854G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269022 | |||||||
| chr8:39269092 | C | T | 1 | a0001c0002t0001g0178 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2163-1784C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269092 | |||||||
| chr8:39269299 | G | C | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2163-1577G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269299 | |||||||
| chr8:39269594 | G | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2163-1282G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269594 | |||||||
| chr8:39269659 | G | A | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163-1217G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269659 | |||||||
| chr8:39269684 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(31): Show |
35 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2163-1192T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269684 | |||||||
| chr8:39269764 | G | T | 1 | a0005c0006t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2163-1112G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269764 | |||||||
| chr8:39269905 | C | T | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2163-971C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269905 | |||||||
| chr8:39269914 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2163-962A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269914 | |||||||
| chr8:39269925 | C | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163-951C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39269925 | |||||||
| chr8:39270029 | TTCACTA | T | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2163-842_2163-837d others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | 39270029 | ||||||
| chr8:39270549 | A | G | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2163-327A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39270549 | |||||||
| chr8:39270748 | C | T | 20 | a0002c0003t0001g0151 a0003c0004t0001g0134 a0003c0004t0001g0135 others(17): Show |
20 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2163-128C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39270748 | |||||||
| chr8:39270868 | C | T | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
splice_region_variant&intron_variant | LOW | c.2163-8C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | chr8 | 39270868 | |||||||
| chr8:39270991 | AT | A | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2201+86delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39270991 | ||||||
| chr8:39271020 | A | G | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2201+106A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39271020 | |||||||
| chr8:39271460 | C | CA | 18 | a0001c0001t0001g0212 a0001c0001t0001g0225 a0002c0003t0001g0151 others(15): Show |
18 | HG02055.hp1 HG02647.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.2201+559dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39271460 | ||||||
| chr8:39271460 | C | CAA | 77 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2201+558_2201+559d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39271460 | ||||||
| chr8:39271460 | C | CAAA | 5 | a0001c0002t0001g0189 a0001c0002t0001g0205 a0001c0002t0002g0121 others(2): Show |
5 | HG02717.hp1 HG03927.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.2201+557_2201+559d others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39271460 | ||||||
| chr8:39271460 | CA | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(47): Show |
51 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2201+559delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39271460 | ||||||
| chr8:39271504 | A | C | 1 | a0001c0001t0002g0033 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2201+590A>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39271504 | |||||||
| chr8:39271539 | CA | C | 90 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0183 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.2201+638delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39271539 | ||||||
| chr8:39271539 | CAA | C | 6 | a0001c0002t0002g0123 a0001c0002t0002g0130 a0002c0005t0002g0115 others(3): Show |
6 | HG02027.hp1 HG02683.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2201+637_2201+638d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39271539 | ||||||
| chr8:39271707 | C | T | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2201+793C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39271707 | |||||||
| chr8:39271793 | T | G | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2201+879T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39271793 | |||||||
| chr8:39271939 | A | T | 11 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2201+1025A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39271939 | |||||||
| chr8:39271941 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2201+1027G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39271941 | |||||||
| chr8:39272046 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0002g0057 |
2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2201+1132T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272046 | |||||||
| chr8:39272090 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2201+1176A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272090 | |||||||
| chr8:39272101 | GAA | G | 6 | a0001c0002t0001g0200 a0001c0002t0002g0096 a0001c0002t0002g0103 others(3): Show |
6 | HG01069.hp1 HG01943.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2201+1206_2201+120 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39272101 | ||||||
| chr8:39272118 | A | G | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2201+1204A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272118 | |||||||
| chr8:39272143 | A | G | 95 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(92): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2201+1229A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272143 | |||||||
| chr8:39272190 | G | A | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2201+1276G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272190 | |||||||
| chr8:39272229 | G | T | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2201+1315G>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272229 | |||||||
| chr8:39272353 | G | A | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2201+1439G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272353 | |||||||
| chr8:39272515 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2201+1601T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272515 | |||||||
| chr8:39272628 | A | G | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2202-1684A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272628 | |||||||
| chr8:39272804 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2202-1508G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272804 | |||||||
| chr8:39272873 | T | C | 116 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(113): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2202-1439T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39272873 | |||||||
| chr8:39273192 | C | T | 5 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2202-1120C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273192 | |||||||
| chr8:39273209 | A | G | 15 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2202-1103A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273209 | |||||||
| chr8:39273233 | C | T | 2 | a0002c0003t0002g0048 a0002c0003t0002g0049 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2202-1079C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273233 | |||||||
| chr8:39273265 | A | G | 116 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(113): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2202-1047A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273265 | |||||||
| chr8:39273353 | A | AAAAT | 4 | a0001c0001t0001g0248 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2202-939_2202-936d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39273353 | ||||||
| chr8:39273388 | G | A | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2202-924G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273388 | |||||||
| chr8:39273529 | A | AAAAACAA others(2): Show |
74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2202-780_2202-779i others(11): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39273529 | ||||||
| chr8:39273529 | A | AAAAC | 38 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(35): Show |
38 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.2202-763_2202-760d others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39273529 | ||||||
| chr8:39273630 | A | G | 16 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(13): Show |
16 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2202-682A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273630 | |||||||
| chr8:39273803 | AT | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2202-498delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39273803 | ||||||
| chr8:39273839 | G | A | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2202-473G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273839 | |||||||
| chr8:39273973 | T | A | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2202-339T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39273973 | |||||||
| chr8:39274018 | GT | G | 116 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(113): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2202-287delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | 39274018 | ||||||
| chr8:39274171 | G | A | 39 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(36): Show |
39 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.2202-141G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39274171 | |||||||
| chr8:39274194 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2202-118A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | chr8 | 39274194 | |||||||
| chr8:39274633 | G | A | 1 | a0003c0004t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2240+283G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39274633 | |||||||
| chr8:39274634 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2240+284G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39274634 | |||||||
| chr8:39274694 | G | A | 1 | a0010c0010t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2240+344G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39274694 | |||||||
| chr8:39274843 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG00280.hp1 HG01361.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2240+493A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39274843 | |||||||
| chr8:39275059 | T | C | 4 | a0001c0001t0001g0248 a0002c0003t0001g0157 a0002c0003t0001g0253 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2240+709T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275059 | |||||||
| chr8:39275068 | T | A | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2240+718T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275068 | |||||||
| chr8:39275073 | C | A | 2 | a0003c0004t0001g0137 a0003c0004t0002g0047 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2240+723C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275073 | |||||||
| chr8:39275089 | A | G | 75 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2240+739A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275089 | |||||||
| chr8:39275093 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2241-735C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275093 | |||||||
| chr8:39275398 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2241-430T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275398 | |||||||
| chr8:39275616 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2241-212G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275616 | |||||||
| chr8:39275687 | C | G | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2241-141C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 21/24 | chr8 | 39275687 | |||||||
| chr8:39275962 | A | T | 15 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2279+96A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39275962 | |||||||
| chr8:39276028 | C | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0036 |
2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.2279+162C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276028 | |||||||
| chr8:39276297 | GA | G | 77 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2279+443delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | 39276297 | ||||||
| chr8:39276334 | A | G | 35 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(32): Show |
35 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.2279+468A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276334 | |||||||
| chr8:39276346 | G | A | 3 | a0001c0002t0002g0091 a0001c0002t0002g0116 a0001c0002t0002g0130 |
3 | HG00423.hp1 HG02027.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.2279+480G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276346 | |||||||
| chr8:39276680 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0158 others(26): Show |
30 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2279+814C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276680 | |||||||
| chr8:39276729 | G | A | 35 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(32): Show |
35 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.2279+863G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276729 | |||||||
| chr8:39276777 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0177 |
2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2279+911C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276777 | |||||||
| chr8:39276932 | C | T | 2 | a0002c0003t0001g0151 a0010c0010t0001g0077 |
2 | HG02055.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2279+1066C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39276932 | |||||||
| chr8:39277043 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0002g0057 |
2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2279+1177C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277043 | |||||||
| chr8:39277054 | CTA | C | 109 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(106): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2279+1198_2279+119 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | 39277054 | ||||||
| chr8:39277296 | C | T | 2 | a0002c0003t0001g0253 a0002c0003t0001g0254 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2279+1430C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277296 | |||||||
| chr8:39277378 | T | A | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2279+1512T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277378 | |||||||
| chr8:39277545 | G | A | 74 | a0001c0002t0001g0146 a0001c0002t0001g0148 a0001c0002t0001g0162 others(71): Show |
75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2279+1679G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277545 | |||||||
| chr8:39277568 | C | T | 109 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(106): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2279+1702C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277568 | |||||||
| chr8:39277602 | G | A | 109 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(106): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2279+1736G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277602 | |||||||
| chr8:39277608 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0150 others(145): Show |
150 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.2279+1742A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277608 | |||||||
| chr8:39277656 | C | A | 75 | a0001c0001t0001g0207 a0001c0002t0001g0146 a0001c0002t0001g0148 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2279+1790C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277656 | |||||||
| chr8:39277766 | C | T | 2 | a0007c0009t0001g0152 a0007c0009t0001g0245 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2279+1900C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277766 | |||||||
| chr8:39277767 | G | A | 3 | a0005c0006t0001g0144 a0005c0006t0001g0216 a0005c0006t0001g0222 |
3 | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2279+1901G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277767 | |||||||
| chr8:39277888 | C | T | 34 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(31): Show |
34 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.2279+2022C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277888 | |||||||
| chr8:39277909 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2279+2043C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277909 | |||||||
| chr8:39277932 | C | T | 1 | a0001c0002t0002g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2279+2066C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277932 | |||||||
| chr8:39277950 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2279+2084G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39277950 | |||||||
| chr8:39278135 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2279+2269C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278135 | |||||||
| chr8:39278239 | G | A | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2279+2373G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278239 | |||||||
| chr8:39278257 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0203 |
2 | NA18972.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2279+2391T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278257 | |||||||
| chr8:39278309 | G | GAAAAGGC others(5): Show |
112 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(109): Show |
113 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2279+2443_2279+244 others(16): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278309 | |||||||
| chr8:39278359 | G | C | 1 | a0003c0004t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2279+2493G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278359 | |||||||
| chr8:39278366 | C | T | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2279+2500C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278366 | |||||||
| chr8:39278380 | C | T | 73 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0001g0148 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2279+2514C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278380 | |||||||
| chr8:39278463 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2279+2597A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278463 | |||||||
| chr8:39278528 | G | A | 1 | a0002c0005t0001g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2280-2608G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278528 | |||||||
| chr8:39278535 | C | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 |
3 | HG01243.hp2 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2280-2601C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278535 | |||||||
| chr8:39278603 | T | C | 2 | a0001c0002t0001g0194 a0001c0002t0001g0197 |
2 | NA18944.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2280-2533T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278603 | |||||||
| chr8:39278700 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0168 others(122): Show |
127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2280-2436C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278700 | |||||||
| chr8:39278712 | T | C | 82 | a0001c0001t0001g0243 a0001c0002t0001g0146 a0001c0002t0001g0148 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2280-2424T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278712 | |||||||
| chr8:39278807 | A | G | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2280-2329A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39278807 | |||||||
| chr8:39279032 | G | A | 12 | a0001c0001t0001g0164 a0001c0002t0002g0094 a0002c0003t0001g0165 others(9): Show |
12 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2280-2104G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279032 | |||||||
| chr8:39279207 | C | G | 1 | a0004c0007t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2280-1929C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279207 | |||||||
| chr8:39279385 | G | A | 57 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0231 others(54): Show |
58 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.2280-1751G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279385 | |||||||
| chr8:39279430 | C | T | 3 | a0001c0002t0002g0102 a0001c0002t0002g0103 a0001c0002t0002g0104 |
3 | HG00280.hp2 HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2280-1706C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279430 | |||||||
| chr8:39279532 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2280-1604T>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279532 | |||||||
| chr8:39279550 | G | A | 18 | a0002c0003t0001g0181 a0002c0003t0001g0182 a0002c0003t0001g0208 others(15): Show |
18 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2280-1586G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279550 | |||||||
| chr8:39279562 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2280-1574G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279562 | |||||||
| chr8:39279572 | A | G | 44 | a0001c0001t0001g0243 a0001c0001t0001g0248 a0001c0002t0002g0094 others(41): Show |
44 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.2280-1564A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279572 | |||||||
| chr8:39279739 | T | A | 1 | a0002c0003t0002g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2280-1397T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39279739 | |||||||
| chr8:39280139 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2280-997G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280139 | |||||||
| chr8:39280144 | C | T | 1 | a0002c0003t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2280-992C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280144 | |||||||
| chr8:39280279 | A | AT | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2280-848dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | 39280279 | ||||||
| chr8:39280289 | A | T | 1 | a0004c0007t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2280-847A>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280289 | |||||||
| chr8:39280543 | G | C | 1 | a0011c0011t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2280-593G>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280543 | |||||||
| chr8:39280724 | G | A | 10 | a0002c0003t0001g0008 a0002c0003t0001g0238 a0002c0003t0001g0239 others(7): Show |
10 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2280-412G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280724 | |||||||
| chr8:39280809 | G | A | 15 | a0001c0001t0001g0145 a0001c0001t0001g0218 a0002c0003t0001g0008 others(12): Show |
15 | HG01081.hp2 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2280-327G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280809 | |||||||
| chr8:39280981 | A | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0243 others(1): Show |
4 | HG01243.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280-155A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39280981 | |||||||
| chr8:39281013 | AC | A | 3 | a0002c0003t0001g0165 a0002c0003t0001g0166 a0005c0006t0001g0223 |
3 | HG03225.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2280-121delC | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | 39281013 | ||||||
| chr8:39281028 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2280-108C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39281028 | |||||||
| chr8:39281073 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2280-63C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | chr8 | 39281073 | |||||||
| chr8:39281194 | T | A | 1 | a0001c0002t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2318+20T>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281194 | |||||||
| chr8:39281235 | T | C | 11 | a0001c0001t0001g0164 a0001c0001t0002g0014 a0001c0001t0002g0016 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2318+61T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281235 | |||||||
| chr8:39281536 | C | T | 10 | a0002c0003t0001g0008 a0002c0003t0001g0238 a0002c0003t0001g0239 others(7): Show |
10 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2318+362C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281536 | |||||||
| chr8:39281651 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0055 |
2 | HG02148.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2318+477C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281651 | |||||||
| chr8:39281655 | A | G | 3 | a0002c0003t0001g0157 a0002c0003t0001g0253 a0002c0003t0001g0254 |
3 | HG02976.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2318+481A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281655 | |||||||
| chr8:39281679 | G | A | 33 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0201 others(30): Show |
33 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2318+505G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281679 | |||||||
| chr8:39281925 | C | T | 1 | a0006c0008t0001g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2318+751C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39281925 | |||||||
| chr8:39282027 | T | C | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2318+853T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282027 | |||||||
| chr8:39282116 | G | A | 4 | a0004c0007t0001g0154 a0004c0007t0001g0155 a0004c0007t0001g0156 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2318+942G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282116 | |||||||
| chr8:39282248 | C | T | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2318+1074C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282248 | |||||||
| chr8:39282425 | T | C | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2319-1161T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282425 | |||||||
| chr8:39282462 | A | G | 1 | a0005c0006t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2319-1124A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282462 | |||||||
| chr8:39282494 | C | T | 6 | a0002c0003t0001g0151 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2319-1092C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282494 | |||||||
| chr8:39282616 | G | A | 1 | a0007c0009t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2319-970G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282616 | |||||||
| chr8:39282860 | T | C | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2319-726T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282860 | |||||||
| chr8:39282891 | G | A | 22 | a0002c0003t0001g0181 a0002c0003t0001g0182 a0002c0003t0001g0208 others(19): Show |
22 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2319-695G>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282891 | |||||||
| chr8:39282951 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2319-635C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282951 | |||||||
| chr8:39282991 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2319-595C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39282991 | |||||||
| chr8:39283023 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0001t0001g0168 others(26): Show |
30 | HG00438.hp2 HG00738.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2319-563C>A | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39283023 | |||||||
| chr8:39283101 | A | G | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2319-485A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39283101 | |||||||
| chr8:39283298 | T | C | 2 | a0001c0002t0002g0009 a0001c0002t0002g0092 |
2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2319-288T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39283298 | |||||||
| chr8:39283310 | T | C | 19 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(16): Show |
19 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.2319-276T>C | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39283310 | |||||||
| chr8:39283393 | A | G | 1 | a0001c0001t0002g0034 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2319-193A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39283393 | |||||||
| chr8:39283411 | T | TA | 52 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0160 others(49): Show |
52 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.2319-150dupA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr8 | 39283411 | ||||||
| chr8:39283411 | TA | T | 5 | a0001c0001t0001g0158 a0001c0001t0002g0079 a0001c0001t0002g0080 others(2): Show |
5 | HG00280.hp2 HG02895.hp2 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319-150delA | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr8 | 39283411 | ||||||
| chr8:39283580 | C | G | 18 | a0002c0003t0001g0181 a0002c0003t0001g0182 a0002c0003t0001g0208 others(15): Show |
18 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.2319-6C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | chr8 | 39283580 | |||||||
| chr8:39283714 | C | T | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2357+90C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39283714 | |||||||
| chr8:39283771 | C | CT | 133 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0149 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.2357+167dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39283771 | ||||||
| chr8:39283771 | C | CTT | 5 | a0001c0001t0001g0210 a0001c0001t0002g0012 a0001c0001t0002g0013 others(2): Show |
5 | HG01934.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2357+166_2357+167d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39283771 | ||||||
| chr8:39283771 | CT | C | 8 | a0001c0002t0002g0090 a0002c0003t0001g0151 a0002c0003t0001g0157 others(5): Show |
8 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2357+167delT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39283771 | ||||||
| chr8:39283856 | C | T | 1 | a0005c0006t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2357+232C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39283856 | |||||||
| chr8:39283866 | C | T | 1 | a0002c0005t0001g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2357+242C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39283866 | |||||||
| chr8:39283876 | C | T | 41 | a0002c0003t0001g0008 a0002c0003t0001g0151 a0002c0003t0001g0157 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.2357+252C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39283876 | |||||||
| chr8:39283934 | C | T | 3 | a0002c0003t0001g0151 a0002c0005t0002g0093 a0002c0005t0002g0095 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2357+310C>T | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39283934 | |||||||
| chr8:39284020 | C | G | 31 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0201 others(28): Show |
31 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2357+396C>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39284020 | |||||||
| chr8:39284145 | G | GT | 4 | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0243 others(1): Show |
4 | HG01243.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2357+529dupT | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284145 | ||||||
| chr8:39284360 | T | TAC | 43 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0002c0003t0001g0008 others(40): Show |
43 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.2358-418_2358-417d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284360 | ||||||
| chr8:39284378 | T | TAC | 8 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0002g0037 others(5): Show |
8 | HG02015.hp1 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2358-394_2358-393d others(4): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284378 | ||||||
| chr8:39284378 | T | TACACAC | 18 | a0002c0003t0001g0008 a0002c0003t0001g0181 a0002c0003t0001g0182 others(15): Show |
18 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2358-398_2358-393d others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284378 | ||||||
| chr8:39284378 | T | TACACACA others(1): Show |
11 | a0002c0003t0001g0151 a0002c0003t0001g0238 a0002c0003t0001g0239 others(8): Show |
11 | HG02486.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2358-400_2358-393d others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284378 | ||||||
| chr8:39284378 | T | TACACACA others(3): Show |
1 | a0002c0003t0001g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2358-402_2358-393d others(12): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284378 | ||||||
| chr8:39284378 | T | TACACACA others(13): Show |
1 | a0002c0003t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2358-412_2358-393d others(22): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284378 | ||||||
| chr8:39284378 | T | TACACACA others(15): Show |
1 | a0002c0003t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2358-414_2358-393d others(24): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284378 | ||||||
| chr8:39284381 | A | ACACACAC others(5): Show |
3 | a0002c0003t0001g0165 a0002c0003t0001g0166 a0005c0006t0001g0223 |
3 | HG03225.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2358-401_2358-400i others(14): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | 39284381 | ||||||
| chr8:39284715 | A | G | 6 | a0002c0003t0001g0151 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2358-78A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39284715 | |||||||
| chr8:39284745 | A | G | 71 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0202 others(68): Show |
71 | HG00408.hp2 HG00621.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.2358-48A>G | ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | chr8 | 39284745 |