Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8756 |
| ensemblid | ENSG00000069206.15 |
| hgncid | 214 |
| symbol | ADAM7 |
| name | ADAM metallopeptidase domain 7 |
| refseq_nuc | NM_003817.4 |
| refseq_prot | NP_003808.2 |
| ensembl_nuc | ENST00000175238.10 |
| ensembl_prot | ENSP00000175238.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 24441026 |
| end | 24509565 |
| strand | + |
| ver | v1.2 |
| region | chr8:24441026-24509565 |
| region5000 | chr8:24436026-24514565 |
| regionname0 | ADAM7_chr8_24441026_24509565 |
| regionname5000 | ADAM7_chr8_24436026_24514565 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 754 | 234 | 60 | 49 | 93 | 10 | 21 | 69 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0002 | 0/1 | 754 | 77 | 5 | 16 | 39 | 3 | 13 | 31 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0003 | 0/0 | 754 | 16 | 12 | 2 | 1 | 0 | 1 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0004 | 0/0 | 754 | 10 | 0 | 5 | 5 | 0 | 0 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0005 | 0/0 | 754 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0006 | 0/0 | 754 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0007 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0008 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0009 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0010 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0011 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0012 | 0/0 | 754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0013 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0014 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0015 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0016 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| a0017 | 0/0 | 754 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | MLPGC others(749): Show |
chr8 | 24436026 | 24514565 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2262 | 218 | 58 | 40 | 93 | 9 | 17 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0001c0003 | 0/0 | 2262 | 15 | 1 | 9 | 0 | 1 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0001c0011 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0002c0002 | 0/1 | 2262 | 74 | 5 | 15 | 39 | 3 | 11 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0002c0007 | 0/0 | 2262 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0002c0014 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0003c0004 | 0/0 | 2262 | 15 | 12 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0003c0020 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0004c0005 | 0/0 | 2262 | 10 | 0 | 5 | 5 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0005c0006 | 0/0 | 2262 | 10 | 10 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0006c0008 | 0/0 | 2262 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0007c0022 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0008c0019 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0009c0010 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0010c0012 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0011c0009 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0012c0018 | 0/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0013c0013 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0014c0015 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0015c0016 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0016c0021 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 | ||
| a0017c0017 | 0/0 | 2262 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATGCT others(2257): Show |
chr8 | 24436026 | 24514565 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3367 | 77 | 31 | 17 | 20 | 3 | 6 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0002 | 0/0 | 3367 | 123 | 15 | 22 | 70 | 6 | 10 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0004 | 0/0 | 3365 | 8 | 7 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3360): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0006 | 1/0 | 3367 | 4 | 3 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0007 | 0/0 | 3367 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0009 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0010 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0011 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0001t0013 | 0/0 | 3367 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0003t0003 | 0/0 | 3367 | 15 | 1 | 9 | 0 | 1 | 4 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0001c0011t0003 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0002c0002t0001 | 0/1 | 3367 | 72 | 5 | 13 | 39 | 3 | 11 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0002c0002t0012 | 0/0 | 3367 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0002c0002t0015 | 0/0 | 3367 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0002c0007t0001 | 0/0 | 3367 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0002c0014t0001 | 0/0 | 3367 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0003c0004t0001 | 0/0 | 3367 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0003c0004t0004 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3360): Show |
chr8 | 24436026 | 24514565 |
| a0003c0004t0005 | 0/0 | 3367 | 7 | 5 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0003c0004t0008 | 0/0 | 3367 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0003c0004t0014 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0003c0020t0001 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0004c0005t0001 | 0/0 | 3367 | 10 | 0 | 5 | 5 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0005c0006t0001 | 0/0 | 3367 | 10 | 10 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0006c0008t0005 | 0/0 | 3367 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0007c0022t0002 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0008c0019t0007 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0009c0010t0008 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0010c0012t0002 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0011c0009t0004 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3360): Show |
chr8 | 24436026 | 24514565 |
| a0012c0018t0001 | 0/0 | 3367 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0013c0013t0001 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0014c0015t0001 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0015c0016t0001 | 0/0 | 3367 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0016c0021t0008 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| a0017c0017t0001 | 0/0 | 3367 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | ATCCC others(3362): Show |
chr8 | 24436026 | 24514565 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0006g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0009g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0001c0011t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0002t0015g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0007t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0002c0014t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0008g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0004t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0003c0020t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0004c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0005c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0006c0008t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0007c0022t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0008c0019t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0009c0010t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0010c0012t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0011c0009t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0012c0018t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0013c0013t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0014c0015t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0015c0016t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0016c0021t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| a0017c0017t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0252 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0115 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0150 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0090 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0104 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00438 | hp1 | a0007 | c0022 | t0002 | g0247 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | CHS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00733 | hp1 | a0003 | c0004 | t0005 | g0315 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00733 | hp2 | a0001 | c0003 | t0003 | g0060 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0058 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00738 | hp2 | a0003 | c0004 | t0005 | g0316 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01069 | hp1 | a0002 | c0002 | t0012 | g0103 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01081 | hp1 | a0004 | c0005 | t0001 | g0112 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0059 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01167 | hp2 | a0001 | c0003 | t0003 | g0063 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01168 | hp2 | a0001 | c0003 | t0003 | g0066 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01192 | hp1 | a0004 | c0005 | t0001 | g0002 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01256 | hp1 | a0002 | c0002 | t0015 | g0139 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01257 | hp1 | a0001 | c0003 | t0003 | g0011 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0011 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01261 | hp2 | a0002 | c0014 | t0001 | g0138 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01358 | hp1 | a0004 | c0005 | t0001 | g0002 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01358 | hp2 | a0001 | c0003 | t0003 | g0061 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | IBS | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01891 | hp2 | a0008 | c0019 | t0007 | g0148 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01978 | hp1 | a0001 | c0003 | t0003 | g0062 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0254 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02080 | hp2 | a0004 | c0005 | t0001 | g0088 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0243 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02145 | hp1 | a0003 | c0004 | t0005 | g0035 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02258 | hp1 | a0009 | c0010 | t0008 | g0057 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02258 | hp2 | a0005 | c0006 | t0001 | g0046 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02293 | hp1 | a0004 | c0005 | t0001 | g0135 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02300 | hp2 | a0004 | c0005 | t0001 | g0002 | AMR | PEL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02451 | hp2 | a0005 | c0006 | t0001 | g0045 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02602 | hp2 | a0001 | c0003 | t0003 | g0151 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02622 | hp1 | a0010 | c0012 | t0002 | g0219 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02622 | hp2 | a0003 | c0004 | t0004 | g0203 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02630 | hp2 | a0005 | c0006 | t0001 | g0047 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02647 | hp2 | a0006 | c0008 | t0005 | g0027 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02738 | hp1 | a0001 | c0003 | t0003 | g0152 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02738 | hp2 | a0003 | c0004 | t0008 | g0126 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02809 | hp1 | a0005 | c0006 | t0001 | g0041 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0209 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02886 | hp1 | a0003 | c0004 | t0001 | g0144 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02895 | hp2 | a0005 | c0006 | t0001 | g0009 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02897 | hp1 | a0005 | c0006 | t0001 | g0009 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02922 | hp1 | a0005 | c0006 | t0001 | g0042 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0065 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0075 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02976 | hp1 | a0005 | c0006 | t0001 | g0044 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03098 | hp2 | a0003 | c0004 | t0014 | g0187 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03139 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03209 | hp1 | a0001 | c0011 | t0003 | g0067 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03225 | hp2 | a0011 | c0009 | t0004 | g0056 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0064 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03453 | hp1 | a0003 | c0004 | t0005 | g0181 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03486 | hp1 | a0005 | c0006 | t0001 | g0040 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03490 | hp2 | a0002 | c0007 | t0001 | g0110 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | ESN | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0276 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0149 | SAS | PJL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03942 | hp2 | a0012 | c0018 | t0001 | g0180 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04184 | hp1 | a0002 | c0007 | t0001 | g0083 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0125 | SAS | BEB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | STU | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18906 | hp2 | a0003 | c0004 | t0005 | g0035 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18940 | hp2 | a0004 | c0005 | t0001 | g0117 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18952 | hp2 | a0013 | c0013 | t0001 | g0123 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0269 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18979 | hp1 | a0004 | c0005 | t0001 | g0118 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18980 | hp2 | a0004 | c0005 | t0001 | g0019 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18993 | hp1 | a0014 | c0015 | t0001 | g0124 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19043 | hp1 | a0003 | c0004 | t0005 | g0023 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19055 | hp2 | a0004 | c0005 | t0001 | g0102 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19068 | hp1 | a0015 | c0016 | t0001 | g0019 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19083 | hp1 | a0003 | c0020 | t0001 | g0289 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19240 | hp1 | a0006 | c0008 | t0005 | g0027 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | YRI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA20129 | hp1 | a0016 | c0021 | t0008 | g0039 | AFR | ASW | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0176 | EUR | TSI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA20805 | hp2 | a0017 | c0017 | t0001 | g0186 | EUR | TSI | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0179 | SAS | GIH | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG06807 | hp1 | a0005 | c0006 | t0001 | g0043 | AFR | USA | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | USA | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| NA21309 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | LWK | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0081 | REF | REF | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0211 | REF | REF | ADAM7_chr8_24436026_24514565 | ADAM7 | chr8 | 24436026 | 24514565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:24442493 | G | C | 2 | a0009 a0011 |
2 | HG02258.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.73G>C | p.Glu25Gln | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/22 | 156/3367 | 73/2265 | 25/754 | chr8 | 24442493 | |||
| chr8:24447190 | C | T | 1 | a0007 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.161C>T | p.Thr54Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/22 | 244/3367 | 161/2265 | 54/754 | chr8 | 24447190 | |||
| chr8:24447241 | T | C | 1 | a0010 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.212T>C | p.Val71Ala | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/22 | 295/3367 | 212/2265 | 71/754 | chr8 | 24447241 | |||
| chr8:24468800 | A | G | 2 | a0009 a0016 |
2 | HG02258.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.613A>G | p.Ile205Val | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/22 | 696/3367 | 613/2265 | 205/754 | chr8 | 24468800 | |||
| chr8:24482166 | G | A | 5 | a0002 a0004 a0013 others(2): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
missense_variant | MODERATE | c.730G>A | p.Val244Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/22 | 813/3367 | 730/2265 | 244/754 | chr8 | 24482166 | |||
| chr8:24482227 | T | C | 1 | a0017 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.791T>C | p.Ile264Thr | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/22 | 874/3367 | 791/2265 | 264/754 | chr8 | 24482227 | |||
| chr8:24487298 | G | A | 1 | a0012 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1072G>A | p.Val358Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/22 | 1155/3367 | 1072/2265 | 358/754 | chr8 | 24487298 | |||
| chr8:24487317 | G | A | 1 | a0013 | 1 | NA18952.hp2 | missense_variant&splice_region_variant | MODERATE | c.1091G>A | p.Ser364Asn | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/22 | 1174/3367 | 1091/2265 | 364/754 | chr8 | 24487317 | |||
| chr8:24490841 | A | G | 1 | a0015 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1309A>G | p.Lys437Glu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/22 | 1392/3367 | 1309/2265 | 437/754 | chr8 | 24490841 | |||
| chr8:24490842 | A | T | 1 | a0015 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1310A>T | p.Lys437Met | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/22 | 1393/3367 | 1310/2265 | 437/754 | chr8 | 24490842 | |||
| chr8:24491904 | T | C | 2 | a0004 a0015 |
11 | HG01081.hp1 HG01192.hp1 HG01358.hp1 others(8): Show |
missense_variant&splice_region_variant | MODERATE | c.1358T>C | p.Ile453Thr | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/22 | 1441/3367 | 1358/2265 | 453/754 | chr8 | 24491904 | |||
| chr8:24492049 | G | A | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1503G>A | p.Met501Ile | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/22 | 1586/3367 | 1503/2265 | 501/754 | chr8 | 24492049 | |||
| chr8:24499305 | A | C | 11 | a0002 a0003 a0004 others(8): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
missense_variant | MODERATE | c.1912A>C | p.Asn638His | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/22 | 1995/3367 | 1912/2265 | 638/754 | chr8 | 24499305 | |||
| chr8:24500837 | G | A | 1 | a0014 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.2050G>A | p.Gly684Arg | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/22 | 2133/3367 | 2050/2265 | 684/754 | chr8 | 24500837 | |||
| chr8:24501572 | T | C | 1 | a0005 | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.2204T>C | p.Leu735Pro | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/22 | 2287/3367 | 2204/2265 | 735/754 | chr8 | 24501572 | |||
| chr8:24507484 | C | T | 1 | a0006 | 2 | HG02647.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.2213C>T | p.Pro738Leu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/22 | 2296/3367 | 2213/2265 | 738/754 | chr8 | 24507484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:24442528 | T | C | 1 | a0002c0007 | 2 | HG03490.hp2 HG04184.hp1 |
synonymous_variant | LOW | c.108T>C | p.Pro36Pro | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/22 | 191/3367 | 108/2265 | 36/754 | chr8 | 24442528 | |||
| chr8:24442558 | C | A | 1 | a0001c0011 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.138C>A | p.Thr46Thr | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/22 | 221/3367 | 138/2265 | 46/754 | chr8 | 24442558 | |||
| chr8:24465731 | C | T | 1 | a0010c0012 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.345C>T | p.His115His | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/22 | 428/3367 | 345/2265 | 115/754 | chr8 | 24465731 | |||
| chr8:24489327 | T | C | 1 | a0002c0014 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1260T>C | p.Pro420Pro | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/22 | 1343/3367 | 1260/2265 | 420/754 | chr8 | 24489327 | |||
| chr8:24490849 | A | T | 1 | a0015c0016 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.1317A>T | p.Gly439Gly | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/22 | 1400/3367 | 1317/2265 | 439/754 | chr8 | 24490849 | |||
| chr8:24492592 | G | A | 1 | a0005c0006 | 10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
synonymous_variant | LOW | c.1650G>A | p.Glu550Glu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/22 | 1733/3367 | 1650/2265 | 550/754 | chr8 | 24492592 | |||
| chr8:24493202 | G | A | 2 | a0001c0003 a0001c0011 |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
synonymous_variant | LOW | c.1815G>A | p.Ala605Ala | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/22 | 1898/3367 | 1815/2265 | 605/754 | chr8 | 24493202 | |||
| chr8:24501555 | G | A | 8 | a0002c0002 a0002c0007 a0002c0014 others(5): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
synonymous_variant | LOW | c.2187G>A | p.Leu729Leu | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/22 | 2270/3367 | 2187/2265 | 729/754 | chr8 | 24501555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:24441058 | T | C | 1 | a0001c0001t0009 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/22 | 51 | chr8 | 24441058 | ||||||
| chr8:24441070 | C | T | 1 | a0002c0002t0015 | 1 | HG01256.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/22 | 39 | chr8 | 24441070 | ||||||
| chr8:24441079 | T | G | 2 | a0001c0001t0007 a0008c0019t0007 |
3 | HG01891.hp2 HG02109.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-30T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/22 | 30 | chr8 | 24441079 | ||||||
| chr8:24508703 | A | C | 3 | a0003c0004t0005 a0003c0004t0014 a0006c0008t0005 |
10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*157A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 157 | chr8 | 24508703 | ||||||
| chr8:24508824 | T | C | 2 | a0003c0004t0005 a0006c0008t0005 |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*278T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 278 | chr8 | 24508824 | ||||||
| chr8:24509016 | G | A | 2 | a0003c0004t0005 a0006c0008t0005 |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 470 | chr8 | 24509016 | ||||||
| chr8:24509042 | C | T | 2 | a0003c0004t0005 a0006c0008t0005 |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*496C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 496 | chr8 | 24509042 | ||||||
| chr8:24509107 | T | C | 1 | a0001c0001t0010 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*561T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 561 | chr8 | 24509107 | ||||||
| chr8:24509147 | T | C | 2 | a0001c0003t0003 a0001c0011t0003 |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 601 | chr8 | 24509147 | ||||||
| chr8:24509199 | CAG | C | 3 | a0001c0001t0004 a0003c0004t0004 a0011c0009t0004 |
10 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*658delGA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 657 | INFO_REALIGN_3_PRIME | chr8 | 24509199 | |||||
| chr8:24509367 | A | G | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(32): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*821A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 821 | chr8 | 24509367 | ||||||
| chr8:24509381 | G | T | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(21): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*835G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 835 | chr8 | 24509381 | ||||||
| chr8:24509498 | T | C | 1 | a0002c0002t0012 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 952 | chr8 | 24509498 | ||||||
| chr8:24509520 | A | G | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(26): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*974A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 974 | chr8 | 24509520 | ||||||
| chr8:24509529 | C | T | 1 | a0001c0001t0013 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 983 | chr8 | 24509529 | ||||||
| chr8:24509530 | G | A | 1 | a0001c0001t0011 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*984G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 984 | chr8 | 24509530 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:24441385 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.52+225A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441385 | |||||||
| chr8:24441494 | G | C | 2 | a0002c0002t0001g0036 a0002c0002t0001g0037 |
2 | NA18962.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.52+334G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441494 | |||||||
| chr8:24441756 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.52+596G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441756 | |||||||
| chr8:24441781 | A | G | 3 | a0003c0004t0005g0035 a0003c0004t0005g0315 a0003c0004t0005g0316 |
4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+621A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441781 | |||||||
| chr8:24441911 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(196): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.53-562T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441911 | |||||||
| chr8:24441917 | T | C | 2 | a0009c0010t0008g0057 a0011c0009t0004g0056 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.53-556T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24441917 | |||||||
| chr8:24442003 | G | A | 14 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(11): Show |
15 | HG00733.hp2 HG00735.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-470G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442003 | |||||||
| chr8:24442132 | C | CCACT | 3 | a0002c0002t0001g0071 a0002c0002t0001g0072 a0002c0002t0001g0073 |
3 | HG03710.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.53-340_53-337dupCA others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 24442132 | ||||||
| chr8:24442137 | A | G | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.53-336A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442137 | |||||||
| chr8:24442195 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.53-278A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442195 | |||||||
| chr8:24442261 | T | C | 1 | a0002c0002t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.53-212T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442261 | |||||||
| chr8:24442357 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG01106.hp1 HG01361.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-116C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442357 | |||||||
| chr8:24442470 | T | C | 2 | a0003c0004t0001g0012 a0003c0004t0001g0075 |
3 | HG02572.hp1 HG02970.hp1 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.53-3T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 1/21 | chr8 | 24442470 | |||||||
| chr8:24442639 | T | A | 1 | a0001c0001t0002g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.156+63T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442639 | |||||||
| chr8:24442821 | C | CT | 235 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.156+248dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24442821 | ||||||
| chr8:24442836 | A | G | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | NA18995.hp1 NA19002.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.156+260A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442836 | |||||||
| chr8:24442912 | T | C | 86 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0002g0092 others(83): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.156+336T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442912 | |||||||
| chr8:24442926 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.156+350T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24442926 | |||||||
| chr8:24443057 | C | T | 1 | a0001c0001t0002g0280 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.156+481C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443057 | |||||||
| chr8:24443209 | T | C | 1 | a0002c0002t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.156+633T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443209 | |||||||
| chr8:24443303 | C | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+727C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443303 | |||||||
| chr8:24443393 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.156+817T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443393 | |||||||
| chr8:24443443 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+867G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443443 | |||||||
| chr8:24443542 | C | A | 1 | a0001c0001t0002g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.156+966C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443542 | |||||||
| chr8:24443608 | A | G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+1032A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443608 | |||||||
| chr8:24443719 | C | T | 1 | a0003c0004t0004g0203 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.156+1143C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443719 | |||||||
| chr8:24443720 | G | A | 1 | a0002c0002t0001g0078 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.156+1144G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443720 | |||||||
| chr8:24443726 | C | T | 1 | a0006c0008t0005g0027 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156+1150C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443726 | |||||||
| chr8:24443852 | T | C | 1 | a0008c0019t0007g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.156+1276T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443852 | |||||||
| chr8:24443861 | G | C | 3 | a0002c0002t0001g0013 a0002c0002t0001g0079 a0002c0002t0001g0080 |
4 | HG00738.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+1285G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443861 | |||||||
| chr8:24443886 | A | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.156+1310A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443886 | |||||||
| chr8:24443939 | A | AAAAAT | 13 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
15 | HG00642.hp1 HG00741.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+1398_156+1402d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | ||||||
| chr8:24443939 | AAAAAT | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.156+1398_156+1402d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | ||||||
| chr8:24443939 | AAAAATAA others(3): Show |
A | 2 | a0001c0001t0002g0050 a0002c0002t0001g0099 |
2 | HG01106.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.156+1393_156+1402d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | ||||||
| chr8:24443939 | AAAAATAA others(13): Show |
A | 1 | a0001c0001t0001g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.156+1383_156+1402d others(22): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24443939 | ||||||
| chr8:24443954 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.156+1378T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24443954 | |||||||
| chr8:24444309 | G | T | 2 | a0002c0002t0001g0036 a0002c0002t0001g0037 |
2 | NA18962.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.156+1733G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444309 | |||||||
| chr8:24444365 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+1789G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444365 | |||||||
| chr8:24444548 | G | A | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+1972G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444548 | |||||||
| chr8:24444679 | C | T | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG00673.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.156+2103C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444679 | |||||||
| chr8:24444680 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0153 a0001c0001t0001g0154 |
5 | HG01192.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+2104G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444680 | |||||||
| chr8:24444691 | A | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(38): Show |
49 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+2115A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444691 | |||||||
| chr8:24444695 | C | CA | 4 | a0001c0001t0002g0048 a0001c0001t0002g0213 a0002c0002t0001g0077 others(1): Show |
4 | HG01934.hp2 HG02027.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+2126dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 24444695 | ||||||
| chr8:24444760 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.156+2184C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444760 | |||||||
| chr8:24444856 | A | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.156+2280A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444856 | |||||||
| chr8:24444861 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.156+2285G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444861 | |||||||
| chr8:24444913 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.157-2273A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24444913 | |||||||
| chr8:24445148 | C | T | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-2038C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445148 | |||||||
| chr8:24445229 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-1957A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445229 | |||||||
| chr8:24445262 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.157-1924C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445262 | |||||||
| chr8:24445281 | C | T | 1 | a0001c0001t0002g0275 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.157-1905C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445281 | |||||||
| chr8:24445282 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.157-1904G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445282 | |||||||
| chr8:24445310 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.157-1876C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445310 | |||||||
| chr8:24445367 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.157-1819A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445367 | |||||||
| chr8:24445433 | A | G | 1 | a0002c0002t0001g0143 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.157-1753A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445433 | |||||||
| chr8:24445479 | T | C | 1 | a0001c0001t0004g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.157-1707T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445479 | |||||||
| chr8:24445479 | T | G | 1 | a0001c0001t0002g0307 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.157-1707T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445479 | |||||||
| chr8:24445563 | G | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.157-1623G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445563 | |||||||
| chr8:24445574 | T | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1612T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445574 | |||||||
| chr8:24445657 | G | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0051 others(116): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.157-1529G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445657 | |||||||
| chr8:24445760 | T | A | 1 | a0002c0007t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.157-1426T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445760 | |||||||
| chr8:24445856 | T | C | 1 | a0001c0001t0013g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.157-1330T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24445856 | |||||||
| chr8:24446020 | G | A | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-1166G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446020 | |||||||
| chr8:24446049 | G | A | 1 | a0012c0018t0001g0180 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.157-1137G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446049 | |||||||
| chr8:24446070 | A | G | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.157-1116A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446070 | |||||||
| chr8:24446101 | T | C | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-1085T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446101 | |||||||
| chr8:24446187 | A | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(75): Show |
90 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.157-999A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446187 | |||||||
| chr8:24446652 | T | C | 1 | a0002c0002t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.157-534T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446652 | |||||||
| chr8:24446672 | C | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.157-514C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446672 | |||||||
| chr8:24446727 | GA | G | 2 | a0003c0004t0001g0012 a0003c0004t0001g0075 |
3 | HG02572.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.157-458delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446727 | |||||||
| chr8:24446756 | C | T | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG02135.hp2 NA18978.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-430C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | 24446756 | |||||||
| chr8:24447405 | A | C | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+143A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447405 | |||||||
| chr8:24447438 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.233+176G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447438 | |||||||
| chr8:24447444 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(30): Show |
38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+182C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447444 | |||||||
| chr8:24447450 | T | C | 5 | a0001c0001t0002g0008 a0001c0001t0002g0307 a0001c0001t0002g0308 others(2): Show |
7 | HG02015.hp1 NA18612.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+188T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447450 | |||||||
| chr8:24447457 | G | C | 1 | a0001c0001t0002g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.233+195G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447457 | |||||||
| chr8:24447464 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.233+202C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447464 | |||||||
| chr8:24447679 | G | A | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.233+417G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447679 | |||||||
| chr8:24447794 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.233+532C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447794 | |||||||
| chr8:24447840 | T | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02280.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.233+578T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447840 | |||||||
| chr8:24447840 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.233+578T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447840 | |||||||
| chr8:24447886 | A | G | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+624A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447886 | |||||||
| chr8:24447936 | A | C | 1 | a0002c0002t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.233+674A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24447936 | |||||||
| chr8:24447937 | A | AAC | 47 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0021 others(44): Show |
54 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.233+721_233+722dup others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | A | AACAC | 15 | a0001c0001t0002g0033 a0001c0001t0002g0175 a0001c0001t0002g0176 others(12): Show |
16 | HG01516.hp1 HG01517.hp1 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+719_233+722dup others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | A | AACACAC | 6 | a0001c0001t0001g0146 a0001c0001t0002g0022 a0001c0001t0002g0178 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+717_233+722dup others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AAC | A | 52 | a0001c0001t0001g0028 a0001c0001t0001g0119 a0001c0001t0001g0191 others(49): Show |
58 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.233+721_233+722del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACAC | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0153 others(52): Show |
66 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.233+719_233+722del others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACAC | A | 17 | a0001c0001t0001g0026 a0001c0001t0001g0183 a0001c0001t0001g0184 others(14): Show |
18 | HG01070.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.233+717_233+722del others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACACA others(1): Show |
A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0182 a0001c0001t0001g0185 others(6): Show |
10 | HG01243.hp1 HG02129.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+715_233+722del others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACACA others(3): Show |
A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.233+713_233+722del others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACACA others(5): Show |
A | 11 | a0002c0002t0001g0085 a0005c0006t0001g0009 a0005c0006t0001g0040 others(8): Show |
12 | HG02071.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.233+711_233+722del others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACACA others(7): Show |
A | 3 | a0001c0001t0001g0034 a0003c0004t0004g0203 a0011c0009t0004g0056 |
4 | HG01123.hp2 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+709_233+722del others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACACA others(9): Show |
A | 1 | a0001c0001t0002g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.233+707_233+722del others(16): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24447937 | AACACACA others(11): Show |
A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+705_233+722del others(18): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24447937 | ||||||
| chr8:24448352 | T | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1090T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448352 | |||||||
| chr8:24448364 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.233+1102C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448364 | |||||||
| chr8:24448397 | T | A | 1 | a0001c0001t0002g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.233+1135T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448397 | |||||||
| chr8:24448440 | A | G | 2 | a0003c0004t0005g0023 a0003c0004t0005g0181 |
3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.233+1178A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448440 | |||||||
| chr8:24448646 | C | T | 5 | a0002c0002t0001g0105 a0002c0002t0001g0106 a0002c0002t0001g0107 others(2): Show |
5 | NA18943.hp1 NA18944.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+1384C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448646 | |||||||
| chr8:24448657 | T | TTTA | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
37 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.233+1421_233+1423d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24448657 | ||||||
| chr8:24448657 | T | TTTATTA | 4 | a0001c0001t0001g0301 a0001c0001t0002g0311 a0001c0001t0002g0313 others(1): Show |
4 | HG01517.hp2 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1418_233+1423d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24448657 | ||||||
| chr8:24448657 | TTTA | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(168): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.233+1421_233+1423d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24448657 | ||||||
| chr8:24448735 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.233+1473G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448735 | |||||||
| chr8:24448815 | A | C | 1 | a0002c0002t0015g0139 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233+1553A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448815 | |||||||
| chr8:24448829 | T | C | 1 | a0005c0006t0001g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.233+1567T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448829 | |||||||
| chr8:24448861 | T | G | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1599T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448861 | |||||||
| chr8:24448899 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02257.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.233+1637G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24448899 | |||||||
| chr8:24449183 | C | G | 2 | a0001c0001t0002g0283 a0003c0004t0001g0276 |
2 | HG03579.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.233+1921C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449183 | |||||||
| chr8:24449256 | T | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1994T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449256 | |||||||
| chr8:24449275 | TAA | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+2016_233+2017d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24449275 | ||||||
| chr8:24449276 | A | G | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+2014A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449276 | |||||||
| chr8:24449407 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
37 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.233+2145C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449407 | |||||||
| chr8:24449471 | A | G | 1 | a0001c0001t0002g0236 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.233+2209A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449471 | |||||||
| chr8:24449474 | G | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.233+2212G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449474 | |||||||
| chr8:24449480 | G | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+2218G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449480 | |||||||
| chr8:24449534 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.233+2272A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449534 | |||||||
| chr8:24449573 | C | T | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+2311C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449573 | |||||||
| chr8:24449574 | G | A | 1 | a0003c0004t0014g0187 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.233+2312G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449574 | |||||||
| chr8:24449616 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233+2354A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449616 | |||||||
| chr8:24449660 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.233+2398C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449660 | |||||||
| chr8:24449677 | G | T | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+2415G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449677 | |||||||
| chr8:24449787 | A | G | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+2525A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449787 | |||||||
| chr8:24449789 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.233+2527A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449789 | |||||||
| chr8:24449830 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+2568G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449830 | |||||||
| chr8:24449833 | G | A | 6 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+2571G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449833 | |||||||
| chr8:24449926 | T | C | 5 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(2): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+2664T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449926 | |||||||
| chr8:24449937 | T | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+2675T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449937 | |||||||
| chr8:24449951 | G | A | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+2689G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24449951 | |||||||
| chr8:24450024 | T | C | 44 | a0001c0001t0002g0008 a0001c0001t0002g0021 a0001c0001t0002g0022 others(41): Show |
48 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.233+2762T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450024 | |||||||
| chr8:24450025 | G | C | 44 | a0001c0001t0002g0008 a0001c0001t0002g0021 a0001c0001t0002g0022 others(41): Show |
48 | HG00323.hp2 HG00558.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.233+2763G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450025 | |||||||
| chr8:24450082 | A | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+2820A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450082 | |||||||
| chr8:24450125 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+2863C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450125 | |||||||
| chr8:24450131 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+2869G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450131 | |||||||
| chr8:24450153 | C | G | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+2891C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450153 | |||||||
| chr8:24450257 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.233+2995C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450257 | |||||||
| chr8:24450307 | G | T | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+3045G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450307 | |||||||
| chr8:24450365 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
65 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.233+3103C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450365 | |||||||
| chr8:24450366 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0051 others(19): Show |
25 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.233+3104G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450366 | |||||||
| chr8:24450450 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.233+3188T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450450 | |||||||
| chr8:24450549 | G | A | 1 | a0009c0010t0008g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.233+3287G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450549 | |||||||
| chr8:24450583 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0051 others(19): Show |
25 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.233+3321G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450583 | |||||||
| chr8:24450601 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0090 |
3 | HG00280.hp2 HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.233+3339G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450601 | |||||||
| chr8:24450603 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+3341C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450603 | |||||||
| chr8:24450715 | C | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3453C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450715 | |||||||
| chr8:24450777 | G | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+3515G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450777 | |||||||
| chr8:24450793 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3531G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450793 | |||||||
| chr8:24450802 | T | C | 1 | a0001c0001t0002g0281 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.233+3540T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450802 | |||||||
| chr8:24450825 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+3563T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450825 | |||||||
| chr8:24450837 | G | A | 82 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0002g0092 others(79): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.233+3575G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450837 | |||||||
| chr8:24450853 | G | A | 5 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0268 others(2): Show |
5 | HG02040.hp2 NA18964.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+3591G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450853 | |||||||
| chr8:24450861 | G | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(171): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.233+3599G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450861 | |||||||
| chr8:24450862 | G | A | 1 | a0005c0006t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.233+3600G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450862 | |||||||
| chr8:24450883 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.233+3621C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450883 | |||||||
| chr8:24450948 | A | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+3686A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450948 | |||||||
| chr8:24450964 | G | A | 10 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0220 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3702G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450964 | |||||||
| chr8:24450964 | G | T | 2 | a0001c0003t0003g0058 a0001c0003t0003g0063 |
2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.233+3702G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24450964 | |||||||
| chr8:24451032 | T | C | 86 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0002g0092 others(83): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.233+3770T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451032 | |||||||
| chr8:24451044 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233+3782C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451044 | |||||||
| chr8:24451055 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233+3793C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451055 | |||||||
| chr8:24451080 | A | T | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+3818A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451080 | |||||||
| chr8:24451174 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.233+3912T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451174 | |||||||
| chr8:24451281 | C | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
15 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.233+4019C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451281 | |||||||
| chr8:24451282 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+4020G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451282 | |||||||
| chr8:24451304 | A | G | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.233+4042A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451304 | |||||||
| chr8:24451329 | C | T | 1 | a0006c0008t0005g0027 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.233+4067C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451329 | |||||||
| chr8:24451335 | A | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+4073A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451335 | |||||||
| chr8:24451366 | G | A | 1 | a0006c0008t0005g0027 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.233+4104G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451366 | |||||||
| chr8:24451382 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.233+4120G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451382 | |||||||
| chr8:24451435 | G | A | 83 | a0001c0001t0001g0028 a0001c0001t0001g0086 a0001c0001t0001g0119 others(80): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.233+4173G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451435 | |||||||
| chr8:24451486 | G | A | 1 | a0001c0001t0006g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.233+4224G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451486 | |||||||
| chr8:24451490 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG00673.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.233+4228G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451490 | |||||||
| chr8:24451518 | C | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(23): Show |
28 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.233+4256C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451518 | |||||||
| chr8:24451538 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
29 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.233+4276C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451538 | |||||||
| chr8:24451567 | T | C | 1 | a0009c0010t0008g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.233+4305T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451567 | |||||||
| chr8:24451569 | T | C | 1 | a0002c0002t0015g0139 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.233+4307T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451569 | |||||||
| chr8:24451699 | C | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0003t0003g0058 others(1): Show |
4 | HG00735.hp2 HG01167.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+4437C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451699 | |||||||
| chr8:24451761 | T | A | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+4499T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451761 | |||||||
| chr8:24451780 | G | A | 1 | a0002c0002t0001g0108 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.233+4518G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451780 | |||||||
| chr8:24451955 | C | T | 1 | a0002c0014t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.233+4693C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451955 | |||||||
| chr8:24451983 | G | C | 2 | a0001c0001t0002g0256 a0001c0001t0002g0257 |
2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.233+4721G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24451983 | |||||||
| chr8:24452013 | G | T | 1 | a0003c0004t0001g0075 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233+4751G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452013 | |||||||
| chr8:24452055 | G | A | 1 | a0001c0003t0003g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.233+4793G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452055 | |||||||
| chr8:24452198 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.233+4936G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452198 | |||||||
| chr8:24452209 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+4947A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452209 | |||||||
| chr8:24452222 | G | A | 1 | a0011c0009t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.233+4960G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452222 | |||||||
| chr8:24452296 | C | T | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.233+5034C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452296 | |||||||
| chr8:24452319 | C | T | 1 | a0002c0002t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233+5057C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452319 | |||||||
| chr8:24452338 | A | G | 2 | a0005c0006t0001g0046 a0005c0006t0001g0047 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.233+5076A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452338 | |||||||
| chr8:24452441 | C | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.233+5179C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452441 | |||||||
| chr8:24452455 | A | C | 82 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0002g0092 others(79): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.233+5193A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452455 | |||||||
| chr8:24452493 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+5231C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452493 | |||||||
| chr8:24452575 | G | C | 1 | a0005c0006t0001g0046 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.233+5313G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452575 | |||||||
| chr8:24452641 | T | C | 2 | a0005c0006t0001g0009 a0005c0006t0001g0041 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.233+5379T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452641 | |||||||
| chr8:24452717 | G | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+5455G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452717 | |||||||
| chr8:24452759 | A | G | 1 | a0001c0001t0013g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+5497A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452759 | |||||||
| chr8:24452810 | C | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0051 others(18): Show |
24 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.233+5548C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452810 | |||||||
| chr8:24452885 | G | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+5623G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452885 | |||||||
| chr8:24452921 | G | T | 2 | a0005c0006t0001g0009 a0005c0006t0001g0041 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.233+5659G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452921 | |||||||
| chr8:24452981 | C | T | 2 | a0003c0004t0005g0023 a0003c0004t0005g0181 |
3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.233+5719C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24452981 | |||||||
| chr8:24453010 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+5748C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453010 | |||||||
| chr8:24453011 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.233+5749G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453011 | |||||||
| chr8:24453033 | T | C | 1 | a0003c0004t0005g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+5771T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453033 | |||||||
| chr8:24453055 | C | T | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.233+5793C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453055 | |||||||
| chr8:24453128 | G | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0003c0004t0004g0203 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+5866G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453128 | |||||||
| chr8:24453164 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233+5902A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453164 | |||||||
| chr8:24453259 | TC | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+5999delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24453259 | ||||||
| chr8:24453292 | C | G | 87 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0002g0092 others(84): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.233+6030C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453292 | |||||||
| chr8:24453296 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.233+6034C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453296 | |||||||
| chr8:24453320 | T | C | 2 | a0001c0001t0002g0221 a0001c0001t0002g0228 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.233+6058T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453320 | |||||||
| chr8:24453384 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.233+6122G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453384 | |||||||
| chr8:24453479 | C | T | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.233+6217C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453479 | |||||||
| chr8:24453651 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.233+6389C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453651 | |||||||
| chr8:24453683 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+6421G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453683 | |||||||
| chr8:24453724 | G | A | 15 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(12): Show |
15 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.233+6462G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453724 | |||||||
| chr8:24453734 | A | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.233+6472A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453734 | |||||||
| chr8:24453815 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.233+6553A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453815 | |||||||
| chr8:24453942 | G | A | 1 | a0001c0001t0002g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.233+6680G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453942 | |||||||
| chr8:24453979 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0002g0038 a0001c0001t0002g0048 others(2): Show |
5 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+6717G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453979 | |||||||
| chr8:24453999 | A | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.233+6737A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24453999 | |||||||
| chr8:24454032 | C | T | 1 | a0010c0012t0002g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.233+6770C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454032 | |||||||
| chr8:24454230 | T | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+6968T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454230 | |||||||
| chr8:24454358 | C | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+7096C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454358 | |||||||
| chr8:24454362 | C | A | 1 | a0001c0001t0002g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.233+7100C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454362 | |||||||
| chr8:24454386 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+7124G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454386 | |||||||
| chr8:24454453 | G | A | 1 | a0001c0001t0006g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.233+7191G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454453 | |||||||
| chr8:24454459 | G | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+7197G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454459 | |||||||
| chr8:24454464 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(30): Show |
38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+7202G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454464 | |||||||
| chr8:24454470 | T | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+7208T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454470 | |||||||
| chr8:24454533 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.233+7271C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454533 | |||||||
| chr8:24454570 | A | G | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+7308A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454570 | |||||||
| chr8:24454573 | A | C | 1 | a0001c0003t0003g0066 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.233+7311A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454573 | |||||||
| chr8:24454624 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+7362C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454624 | |||||||
| chr8:24454651 | G | A | 1 | a0002c0002t0001g0085 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.233+7389G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454651 | |||||||
| chr8:24454677 | G | C | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.233+7415G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454677 | |||||||
| chr8:24454705 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+7443G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454705 | |||||||
| chr8:24454713 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.233+7451A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454713 | |||||||
| chr8:24454754 | G | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
34 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.233+7492G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454754 | |||||||
| chr8:24454770 | C | T | 1 | a0005c0006t0001g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.233+7508C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454770 | |||||||
| chr8:24454828 | T | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+7566T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454828 | |||||||
| chr8:24454838 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0153 others(5): Show |
11 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+7576T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454838 | |||||||
| chr8:24454949 | C | T | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+7687C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24454949 | |||||||
| chr8:24455042 | G | A | 1 | a0001c0001t0010g0254 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.233+7780G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455042 | |||||||
| chr8:24455111 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.233+7849T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455111 | |||||||
| chr8:24455193 | C | T | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | HG02129.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.233+7931C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455193 | |||||||
| chr8:24455392 | A | G | 1 | a0001c0001t0013g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+8130A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455392 | |||||||
| chr8:24455504 | G | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+8242G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455504 | |||||||
| chr8:24455597 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-8285T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455597 | |||||||
| chr8:24455643 | C | A | 1 | a0002c0002t0001g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.234-8239C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455643 | |||||||
| chr8:24455664 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.234-8218C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455664 | |||||||
| chr8:24455668 | A | T | 1 | a0001c0001t0002g0215 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.234-8214A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24455668 | |||||||
| chr8:24456011 | C | T | 2 | a0001c0001t0002g0252 a0001c0001t0002g0253 |
2 | HG00099.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.234-7871C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456011 | |||||||
| chr8:24456058 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.234-7824G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456058 | |||||||
| chr8:24456212 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.234-7670G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456212 | |||||||
| chr8:24456299 | A | C | 5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | NA18978.hp1 NA18999.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-7583A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456299 | |||||||
| chr8:24456383 | C | T | 1 | a0002c0002t0015g0139 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.234-7499C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456383 | |||||||
| chr8:24456480 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.234-7402C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456480 | |||||||
| chr8:24456503 | G | T | 1 | a0002c0002t0001g0017 | 2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.234-7379G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456503 | |||||||
| chr8:24456630 | G | T | 1 | a0001c0001t0002g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.234-7252G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456630 | |||||||
| chr8:24456632 | AT | A | 293 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(290): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.234-7232delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24456632 | ||||||
| chr8:24456721 | A | G | 4 | a0002c0002t0001g0109 a0002c0002t0001g0120 a0002c0002t0001g0121 others(1): Show |
4 | NA18947.hp2 NA18966.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-7161A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456721 | |||||||
| chr8:24456740 | A | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
29 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.234-7142A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456740 | |||||||
| chr8:24456759 | T | C | 1 | a0002c0002t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.234-7123T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456759 | |||||||
| chr8:24456884 | T | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01261.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.234-6998T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456884 | |||||||
| chr8:24456961 | A | G | 1 | a0001c0001t0002g0163 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.234-6921A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24456961 | |||||||
| chr8:24457123 | A | G | 1 | a0001c0003t0003g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.234-6759A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457123 | |||||||
| chr8:24457213 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-6669C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457213 | |||||||
| chr8:24457293 | A | AT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-6580dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457293 | ||||||
| chr8:24457310 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-6572C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457310 | |||||||
| chr8:24457389 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18999.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.234-6493C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457389 | |||||||
| chr8:24457475 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-6407C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457475 | |||||||
| chr8:24457550 | ACAGGC | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-6331_234-6327d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457550 | |||||||
| chr8:24457556 | A | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-6326A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457556 | |||||||
| chr8:24457606 | G | A | 1 | a0010c0012t0002g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234-6276G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457606 | |||||||
| chr8:24457780 | G | C | 1 | a0001c0001t0002g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.234-6102G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457780 | |||||||
| chr8:24457854 | A | ATG | 4 | a0002c0002t0001g0016 a0002c0002t0001g0074 a0002c0002t0001g0104 others(1): Show |
5 | HG00323.hp1 HG02683.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-6021_234-6020d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457854 | ||||||
| chr8:24457854 | A | ATGTG | 3 | a0001c0001t0002g0311 a0001c0001t0002g0313 a0001c0001t0002g0314 |
3 | NA18962.hp1 NA19005.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.234-6023_234-6020d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457854 | ||||||
| chr8:24457855 | T | TGTGTGTG others(1): Show |
16 | a0001c0001t0001g0024 a0001c0003t0003g0011 a0001c0003t0003g0058 others(13): Show |
18 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-6019_234-6012d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457855 | ||||||
| chr8:24457861 | TGA | T | 2 | a0002c0002t0001g0013 a0002c0002t0015g0139 |
3 | HG01256.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.234-6019_234-6018d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457861 | ||||||
| chr8:24457863 | A | AGT | 76 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0028 others(73): Show |
84 | HG00323.hp2 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.234-5992_234-5991d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | ||||||
| chr8:24457863 | A | AGTGT | 66 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(63): Show |
74 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.234-5994_234-5991d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | ||||||
| chr8:24457863 | A | AGTGTGT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG01074.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-5996_234-5991d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | ||||||
| chr8:24457863 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234-6002_234-5991d others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | ||||||
| chr8:24457863 | A | T | 40 | a0001c0001t0002g0092 a0001c0001t0002g0311 a0001c0001t0002g0313 others(37): Show |
47 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.234-6019A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24457863 | |||||||
| chr8:24457863 | AGT | A | 16 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(13): Show |
18 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-5992_234-5991d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24457863 | ||||||
| chr8:24458441 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-5441T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458441 | |||||||
| chr8:24458517 | A | G | 10 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
11 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-5365A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458517 | |||||||
| chr8:24458552 | G | A | 1 | a0001c0003t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.234-5330G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458552 | |||||||
| chr8:24458602 | C | T | 83 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0002g0092 others(80): Show |
93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.234-5280C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458602 | |||||||
| chr8:24458633 | T | A | 7 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0164 others(4): Show |
8 | NA18612.hp1 NA18747.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-5249T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458633 | |||||||
| chr8:24458817 | T | C | 3 | a0001c0003t0003g0060 a0001c0003t0003g0064 a0001c0003t0003g0150 |
3 | HG00140.hp1 HG00733.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.234-5065T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458817 | |||||||
| chr8:24458848 | T | A | 1 | a0002c0002t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.234-5034T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458848 | |||||||
| chr8:24458873 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-5009G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458873 | |||||||
| chr8:24458877 | A | C | 3 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0266 |
3 | HG03834.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.234-5005A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24458877 | |||||||
| chr8:24459045 | C | T | 2 | a0001c0001t0007g0025 a0008c0019t0007g0148 |
3 | HG01891.hp2 HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.234-4837C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459045 | |||||||
| chr8:24459199 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234-4683G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459199 | |||||||
| chr8:24459415 | G | C | 1 | a0002c0002t0001g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.234-4467G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459415 | |||||||
| chr8:24459429 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.234-4453C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459429 | |||||||
| chr8:24459434 | T | TTTTA | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-4432_234-4429d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24459434 | ||||||
| chr8:24459622 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0090 |
3 | HG00280.hp2 HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.234-4260G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459622 | |||||||
| chr8:24459814 | G | T | 1 | a0010c0012t0002g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234-4068G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459814 | |||||||
| chr8:24459952 | T | A | 2 | a0002c0002t0001g0074 a0002c0002t0001g0104 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.234-3930T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24459952 | |||||||
| chr8:24459970 | A | AT | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3904dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24459970 | ||||||
| chr8:24460009 | T | G | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.234-3873T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460009 | |||||||
| chr8:24460083 | AT | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-3792delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460083 | ||||||
| chr8:24460090 | T | A | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-3792T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460090 | |||||||
| chr8:24460167 | T | A | 1 | a0002c0002t0001g0087 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.234-3715T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460167 | |||||||
| chr8:24460263 | T | A | 1 | a0002c0014t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.234-3619T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460263 | |||||||
| chr8:24460385 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.234-3497C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460385 | |||||||
| chr8:24460386 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
22 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-3496G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460386 | |||||||
| chr8:24460583 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-3299T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460583 | |||||||
| chr8:24460648 | TAA | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-3230_234-3229d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460648 | ||||||
| chr8:24460650 | A | G | 3 | a0003c0004t0005g0035 a0003c0004t0005g0315 a0003c0004t0005g0316 |
4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-3232A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460650 | |||||||
| chr8:24460703 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG01123.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.234-3179A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460703 | |||||||
| chr8:24460751 | ATG | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.234-3115_234-3114d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460751 | ||||||
| chr8:24460753 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
11 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.234-3129G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460753 | |||||||
| chr8:24460765 | GTGTA | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0028 others(76): Show |
90 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.234-3115_234-3112d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460765 | ||||||
| chr8:24460767 | G | A | 1 | a0002c0002t0012g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.234-3115G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460767 | |||||||
| chr8:24460767 | G | GTA | 5 | a0001c0001t0002g0246 a0001c0001t0002g0281 a0001c0001t0002g0282 others(2): Show |
5 | HG02559.hp2 NA18995.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-3097_234-3096d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460767 | ||||||
| chr8:24460767 | GTATA | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0194 |
3 | HG02135.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.234-3099_234-3096d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24460767 | ||||||
| chr8:24460846 | T | C | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.234-3036T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460846 | |||||||
| chr8:24460869 | CTTCTT | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-3012_234-3008d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460869 | |||||||
| chr8:24460881 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3001C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24460881 | |||||||
| chr8:24461246 | C | A | 1 | a0001c0001t0002g0215 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.234-2636C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24461246 | |||||||
| chr8:24461337 | C | CCT | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.234-2542_234-2541d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24461337 | ||||||
| chr8:24461346 | G | A | 1 | a0001c0001t0002g0241 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.234-2536G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24461346 | |||||||
| chr8:24461580 | C | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0230 a0001c0001t0002g0231 |
4 | HG00609.hp2 HG02132.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-2302C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24461580 | |||||||
| chr8:24461788 | C | CTT | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.234-2093_234-2092d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 24461788 | ||||||
| chr8:24462032 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1850T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462032 | |||||||
| chr8:24462161 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.234-1721C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462161 | |||||||
| chr8:24462293 | A | C | 1 | a0002c0002t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.234-1589A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462293 | |||||||
| chr8:24462434 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.234-1448C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462434 | |||||||
| chr8:24462526 | C | A | 3 | a0003c0004t0005g0035 a0003c0004t0005g0315 a0003c0004t0005g0316 |
4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-1356C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462526 | |||||||
| chr8:24462597 | C | T | 2 | a0001c0001t0002g0263 a0001c0001t0002g0271 |
2 | NA18949.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.234-1285C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462597 | |||||||
| chr8:24462598 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.234-1284G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462598 | |||||||
| chr8:24462613 | G | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.234-1269G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462613 | |||||||
| chr8:24462692 | A | C | 1 | a0001c0001t0004g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234-1190A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462692 | |||||||
| chr8:24462812 | A | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(18): Show |
23 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-1070A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462812 | |||||||
| chr8:24462907 | T | C | 1 | a0001c0001t0002g0225 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234-975T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462907 | |||||||
| chr8:24462922 | A | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.234-960A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24462922 | |||||||
| chr8:24463050 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.234-832G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463050 | |||||||
| chr8:24463151 | C | A | 1 | a0001c0001t0002g0264 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.234-731C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463151 | |||||||
| chr8:24463481 | G | A | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.234-401G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463481 | |||||||
| chr8:24463518 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.234-364A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463518 | |||||||
| chr8:24463592 | A | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(18): Show |
23 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-290A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463592 | |||||||
| chr8:24463711 | G | C | 2 | a0002c0002t0001g0074 a0002c0002t0001g0104 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.234-171G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | chr8 | 24463711 | |||||||
| chr8:24463983 | G | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+23G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24463983 | |||||||
| chr8:24464010 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.312+50G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464010 | |||||||
| chr8:24464053 | G | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+93G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464053 | |||||||
| chr8:24464262 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.312+302A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464262 | |||||||
| chr8:24464263 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.312+303G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464263 | |||||||
| chr8:24464316 | AC | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.312+357delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464316 | |||||||
| chr8:24464370 | G | T | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG02135.hp2 NA18978.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+410G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464370 | |||||||
| chr8:24464418 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+458G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464418 | |||||||
| chr8:24464494 | A | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0033 a0001c0001t0002g0252 others(1): Show |
6 | HG00099.hp1 HG00140.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+534A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464494 | |||||||
| chr8:24464653 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.312+693C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464653 | |||||||
| chr8:24464699 | C | A | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.312+739C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464699 | |||||||
| chr8:24464749 | TGCCACCG others(179): Show |
T | 94 | a0001c0001t0002g0092 a0002c0002t0001g0001 a0002c0002t0001g0013 others(91): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.312+868_313-686del | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 24464749 | ||||||
| chr8:24464844 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-855C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464844 | |||||||
| chr8:24464872 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.313-827C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24464872 | |||||||
| chr8:24465085 | G | A | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.313-614G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465085 | |||||||
| chr8:24465085 | G | T | 1 | a0001c0001t0002g0248 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.313-614G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465085 | |||||||
| chr8:24465161 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.313-538C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465161 | |||||||
| chr8:24465291 | G | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-408G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465291 | |||||||
| chr8:24465612 | A | G | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-87A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | 24465612 | |||||||
| chr8:24465856 | A | T | 1 | a0001c0001t0002g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.389+81A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24465856 | |||||||
| chr8:24465884 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18999.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.389+109G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24465884 | |||||||
| chr8:24466127 | T | C | 1 | a0001c0001t0002g0032 | 2 | HG01433.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.389+352T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466127 | |||||||
| chr8:24466243 | C | T | 1 | a0001c0003t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.389+468C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466243 | |||||||
| chr8:24466375 | T | A | 2 | a0003c0004t0004g0203 a0011c0009t0004g0056 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.390-424T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466375 | |||||||
| chr8:24466441 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.390-358A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466441 | |||||||
| chr8:24466668 | C | T | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.390-131C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466668 | |||||||
| chr8:24466678 | T | C | 11 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(8): Show |
12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.390-121T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 5/21 | chr8 | 24466678 | |||||||
| chr8:24466989 | GTGAGTAC others(23): Show |
G | 1 | a0001c0001t0002g0264 | 1 | NA19090.hp2 | splice_region_variant&intron_variant | LOW | c.579+5_579+34delGTA others(27): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | 24466989 | ||||||
| chr8:24467128 | G | A | 3 | a0001c0003t0003g0060 a0001c0003t0003g0064 a0001c0003t0003g0150 |
3 | HG00140.hp1 HG00733.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.579+140G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467128 | |||||||
| chr8:24467145 | T | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+157T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467145 | |||||||
| chr8:24467289 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579+301A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467289 | |||||||
| chr8:24467318 | A | AT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.579+339dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | 24467318 | ||||||
| chr8:24467513 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.579+525T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467513 | |||||||
| chr8:24467588 | A | C | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.579+600A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467588 | |||||||
| chr8:24467640 | T | C | 40 | a0001c0001t0002g0092 a0002c0002t0001g0001 a0002c0002t0001g0013 others(37): Show |
48 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.579+652T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467640 | |||||||
| chr8:24467656 | C | A | 3 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 |
4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+668C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467656 | |||||||
| chr8:24467674 | A | G | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+686A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467674 | |||||||
| chr8:24467698 | A | G | 81 | a0001c0001t0002g0092 a0002c0002t0001g0001 a0002c0002t0001g0013 others(78): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.579+710A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24467698 | |||||||
| chr8:24468026 | A | C | 1 | a0002c0007t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.580-741A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468026 | |||||||
| chr8:24468093 | A | T | 1 | a0002c0002t0001g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.580-674A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468093 | |||||||
| chr8:24468264 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.580-503A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468264 | |||||||
| chr8:24468290 | GA | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
14 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-465delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | 24468290 | ||||||
| chr8:24468404 | A | T | 11 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(8): Show |
12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-363A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468404 | |||||||
| chr8:24468413 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.580-354T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468413 | |||||||
| chr8:24468592 | C | A | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.580-175C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468592 | |||||||
| chr8:24468644 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.580-123T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | chr8 | 24468644 | |||||||
| chr8:24469028 | T | C | 5 | a0001c0001t0002g0008 a0001c0001t0002g0307 a0001c0001t0002g0308 others(2): Show |
7 | HG02015.hp1 NA18612.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+208T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469028 | |||||||
| chr8:24469055 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.633+235C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469055 | |||||||
| chr8:24469117 | T | G | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.633+297T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469117 | |||||||
| chr8:24469235 | A | C | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
8 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.633+415A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469235 | |||||||
| chr8:24469380 | A | G | 2 | a0002c0002t0001g0014 a0002c0002t0001g0090 |
3 | HG00280.hp2 HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.633+560A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469380 | |||||||
| chr8:24469383 | G | C | 1 | a0001c0001t0002g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.633+563G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469383 | |||||||
| chr8:24469569 | T | C | 1 | a0002c0002t0001g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.633+749T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469569 | |||||||
| chr8:24469583 | A | G | 10 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(7): Show |
10 | HG02135.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.633+763A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469583 | |||||||
| chr8:24469643 | T | C | 11 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(8): Show |
12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.633+823T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469643 | |||||||
| chr8:24469686 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+866C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469686 | |||||||
| chr8:24469688 | C | T | 108 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.633+868C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24469688 | |||||||
| chr8:24470006 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.633+1186A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470006 | |||||||
| chr8:24470156 | T | C | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.633+1336T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470156 | |||||||
| chr8:24470181 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+1361G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470181 | |||||||
| chr8:24470449 | G | A | 7 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(4): Show |
8 | HG02451.hp2 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+1629G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470449 | |||||||
| chr8:24470711 | A | C | 1 | a0014c0015t0001g0124 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.633+1891A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470711 | |||||||
| chr8:24470875 | A | T | 1 | a0002c0002t0001g0017 | 2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.633+2055A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470875 | |||||||
| chr8:24470989 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.633+2169G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24470989 | |||||||
| chr8:24471228 | A | G | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.633+2408A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471228 | |||||||
| chr8:24471257 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0153 others(6): Show |
12 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.633+2437C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471257 | |||||||
| chr8:24471465 | G | GT | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.633+2657dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24471465 | ||||||
| chr8:24471465 | G | GTT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(50): Show |
62 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.633+2656_633+2657d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24471465 | ||||||
| chr8:24471465 | G | GTTT | 10 | a0001c0001t0001g0199 a0005c0006t0001g0009 a0005c0006t0001g0040 others(7): Show |
11 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.633+2655_633+2657d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24471465 | ||||||
| chr8:24471503 | C | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
36 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.633+2683C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471503 | |||||||
| chr8:24471575 | C | G | 1 | a0002c0002t0001g0099 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.633+2755C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471575 | |||||||
| chr8:24471656 | C | T | 5 | a0004c0005t0001g0019 a0004c0005t0001g0102 a0004c0005t0001g0117 others(2): Show |
5 | NA18940.hp2 NA18979.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.633+2836C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471656 | |||||||
| chr8:24471793 | A | G | 6 | a0002c0002t0001g0001 a0002c0002t0001g0078 a0002c0002t0001g0087 others(3): Show |
8 | HG01978.hp2 HG02080.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+2973A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471793 | |||||||
| chr8:24471933 | T | C | 4 | a0002c0002t0001g0109 a0002c0002t0001g0120 a0002c0002t0001g0121 others(1): Show |
4 | NA18947.hp2 NA18966.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+3113T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471933 | |||||||
| chr8:24471968 | C | T | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.633+3148C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24471968 | |||||||
| chr8:24472014 | T | A | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.633+3194T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472014 | |||||||
| chr8:24472019 | G | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(30): Show |
38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.633+3199G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472019 | |||||||
| chr8:24472122 | C | CA | 45 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(42): Show |
51 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.633+3318dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24472122 | ||||||
| chr8:24472122 | CA | C | 28 | a0001c0001t0001g0119 a0001c0001t0001g0298 a0001c0001t0002g0038 others(25): Show |
29 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.633+3318delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24472122 | ||||||
| chr8:24472122 | CAAA | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.633+3316_633+3318d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24472122 | ||||||
| chr8:24472124 | A | AC | 3 | a0001c0001t0001g0200 a0001c0001t0002g0190 a0017c0017t0001g0186 |
3 | HG00639.hp1 HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.633+3304_633+3305i others(3): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472124 | |||||||
| chr8:24472125 | A | C | 1 | a0001c0001t0002g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+3305A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472125 | |||||||
| chr8:24472255 | A | G | 1 | a0009c0010t0008g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.633+3435A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472255 | |||||||
| chr8:24472286 | A | T | 10 | a0002c0002t0001g0074 a0005c0006t0001g0009 a0005c0006t0001g0040 others(7): Show |
11 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.633+3466A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472286 | |||||||
| chr8:24472493 | C | T | 3 | a0001c0001t0001g0200 a0001c0001t0002g0190 a0017c0017t0001g0186 |
3 | HG00639.hp1 HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.633+3673C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472493 | |||||||
| chr8:24472793 | C | G | 1 | a0002c0002t0001g0122 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.634-3640C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472793 | |||||||
| chr8:24472882 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.634-3551A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24472882 | |||||||
| chr8:24473093 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-3340G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473093 | |||||||
| chr8:24473112 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.634-3321T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473112 | |||||||
| chr8:24473219 | C | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(61): Show |
74 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.634-3214C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473219 | |||||||
| chr8:24473235 | T | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.634-3198T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473235 | |||||||
| chr8:24473292 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0002g0255 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.634-3141G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473292 | |||||||
| chr8:24473304 | A | G | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.634-3129A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473304 | |||||||
| chr8:24473326 | T | C | 2 | a0001c0001t0002g0224 a0001c0001t0002g0240 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634-3107T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473326 | |||||||
| chr8:24473370 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.634-3063T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473370 | |||||||
| chr8:24473593 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.634-2840G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473593 | |||||||
| chr8:24473691 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.634-2742A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473691 | |||||||
| chr8:24473808 | G | A | 3 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 |
4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-2625G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24473808 | |||||||
| chr8:24474082 | C | T | 1 | a0006c0008t0005g0027 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.634-2351C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474082 | |||||||
| chr8:24474186 | A | G | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.634-2247A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474186 | |||||||
| chr8:24474245 | C | T | 5 | a0002c0002t0001g0085 a0002c0002t0001g0089 a0002c0002t0001g0108 others(2): Show |
5 | HG02071.hp2 HG02273.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-2188C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474245 | |||||||
| chr8:24474352 | G | A | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.634-2081G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474352 | |||||||
| chr8:24474517 | A | G | 41 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(38): Show |
49 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.634-1916A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474517 | |||||||
| chr8:24474530 | A | T | 3 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0001t0002g0265 |
3 | HG01993.hp2 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.634-1903A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474530 | |||||||
| chr8:24474577 | A | C | 10 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
11 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.634-1856A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474577 | |||||||
| chr8:24474670 | T | C | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.634-1763T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24474670 | |||||||
| chr8:24475118 | C | A | 1 | a0001c0001t0002g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.634-1315C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475118 | |||||||
| chr8:24475268 | T | A | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.634-1165T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475268 | |||||||
| chr8:24475372 | T | C | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.634-1061T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475372 | |||||||
| chr8:24475637 | G | A | 2 | a0001c0001t0002g0263 a0001c0001t0002g0271 |
2 | NA18949.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.634-796G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475637 | |||||||
| chr8:24475699 | T | C | 1 | a0002c0002t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.634-734T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475699 | |||||||
| chr8:24475719 | T | G | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-714T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24475719 | |||||||
| chr8:24476088 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.634-345G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24476088 | |||||||
| chr8:24476335 | A | AT | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
36 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.634-91dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 24476335 | ||||||
| chr8:24476387 | C | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-46C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | chr8 | 24476387 | |||||||
| chr8:24476587 | T | C | 1 | a0002c0002t0001g0085 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.705+83T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476587 | |||||||
| chr8:24476615 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.705+111G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476615 | |||||||
| chr8:24476756 | C | T | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.705+252C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476756 | |||||||
| chr8:24476758 | A | G | 1 | a0002c0014t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.705+254A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476758 | |||||||
| chr8:24476827 | C | A | 1 | a0006c0008t0005g0027 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.705+323C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24476827 | |||||||
| chr8:24477024 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.705+520T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477024 | |||||||
| chr8:24477104 | G | A | 1 | a0001c0003t0003g0066 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.705+600G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477104 | |||||||
| chr8:24477107 | A | G | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.705+603A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477107 | |||||||
| chr8:24477289 | C | T | 1 | a0001c0003t0003g0062 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.705+785C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477289 | |||||||
| chr8:24477297 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+793G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477297 | |||||||
| chr8:24477481 | T | C | 2 | a0003c0004t0004g0203 a0011c0009t0004g0056 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.705+977T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477481 | |||||||
| chr8:24477560 | AC | A | 80 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(77): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.705+1059delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477560 | ||||||
| chr8:24477569 | A | AGTGTGTG others(3): Show |
1 | a0003c0004t0004g0203 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.705+1072_705+1073i others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(5): Show |
10 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(7): Show |
11 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(7): Show |
15 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0145 others(12): Show |
17 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(16): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(9): Show |
111 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(108): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(18): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(11): Show |
49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
61 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(20): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(13): Show |
6 | a0001c0001t0001g0028 a0001c0001t0001g0119 a0001c0001t0001g0188 others(3): Show |
7 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(22): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(15): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0185 a0001c0001t0001g0191 others(4): Show |
8 | HG00280.hp1 HG02129.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.705+1072_705+1073i others(24): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477569 | A | AGTGTGTG others(17): Show |
1 | a0001c0001t0001g0287 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.705+1072_705+1073i others(26): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24477569 | ||||||
| chr8:24477584 | G | A | 4 | a0001c0001t0002g0242 a0001c0001t0002g0281 a0001c0001t0002g0282 others(1): Show |
4 | NA18995.hp1 NA19002.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+1080G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477584 | |||||||
| chr8:24477610 | G | T | 1 | a0002c0002t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.705+1106G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477610 | |||||||
| chr8:24477772 | C | T | 1 | a0002c0002t0001g0133 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.705+1268C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477772 | |||||||
| chr8:24477881 | C | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+1377C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477881 | |||||||
| chr8:24477914 | A | G | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.705+1410A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477914 | |||||||
| chr8:24477929 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
36 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.705+1425G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24477929 | |||||||
| chr8:24478004 | G | C | 3 | a0002c0002t0001g0105 a0002c0002t0001g0106 a0002c0002t0001g0107 |
3 | NA18943.hp1 NA18953.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.705+1500G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478004 | |||||||
| chr8:24478009 | T | TC | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+1506dupC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24478009 | ||||||
| chr8:24478032 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
31 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.705+1528C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478032 | |||||||
| chr8:24478157 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+1653G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478157 | |||||||
| chr8:24478204 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.705+1700T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478204 | |||||||
| chr8:24478310 | G | A | 1 | a0008c0019t0007g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.705+1806G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478310 | |||||||
| chr8:24478377 | C | G | 6 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0157 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.705+1873C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478377 | |||||||
| chr8:24478507 | T | A | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.705+2003T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478507 | |||||||
| chr8:24478616 | G | A | 1 | a0002c0002t0001g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.705+2112G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478616 | |||||||
| chr8:24478844 | T | G | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+2340T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478844 | |||||||
| chr8:24478889 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.705+2385C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478889 | |||||||
| chr8:24478906 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.705+2402G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478906 | |||||||
| chr8:24478919 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+2415T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24478919 | |||||||
| chr8:24479052 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.705+2548C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479052 | |||||||
| chr8:24479172 | C | T | 1 | a0002c0002t0001g0107 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.705+2668C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479172 | |||||||
| chr8:24479174 | T | A | 3 | a0002c0002t0001g0091 a0002c0002t0001g0093 a0002c0002t0001g0095 |
3 | HG00642.hp2 HG01257.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.705+2670T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479174 | |||||||
| chr8:24479193 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(29): Show |
37 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.705+2689C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479193 | |||||||
| chr8:24479247 | A | G | 7 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(4): Show |
10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.705+2743A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479247 | |||||||
| chr8:24479307 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+2803G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479307 | |||||||
| chr8:24479361 | T | TTTTTG | 5 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2756_706-2752d others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24479361 | ||||||
| chr8:24479469 | T | A | 1 | a0001c0001t0001g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-2673T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479469 | |||||||
| chr8:24479493 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.706-2649C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479493 | |||||||
| chr8:24479626 | C | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.706-2516C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479626 | |||||||
| chr8:24479668 | T | C | 7 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(4): Show |
10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.706-2474T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479668 | |||||||
| chr8:24479737 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.706-2405C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479737 | |||||||
| chr8:24479889 | A | T | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-2253A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479889 | |||||||
| chr8:24479978 | G | A | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-2164G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24479978 | |||||||
| chr8:24480019 | G | A | 1 | a0002c0007t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.706-2123G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480019 | |||||||
| chr8:24480103 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.706-2039C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480103 | |||||||
| chr8:24480125 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.706-2017G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480125 | |||||||
| chr8:24480334 | G | A | 1 | a0001c0001t0009g0269 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.706-1808G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480334 | |||||||
| chr8:24480393 | C | G | 3 | a0001c0003t0003g0011 a0001c0003t0003g0059 a0001c0003t0003g0061 |
4 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1749C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480393 | |||||||
| chr8:24480513 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.706-1629C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480513 | |||||||
| chr8:24480590 | A | T | 2 | a0002c0002t0001g0137 a0002c0002t0001g0141 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.706-1552A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480590 | |||||||
| chr8:24480622 | G | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1520G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480622 | |||||||
| chr8:24480626 | G | A | 2 | a0005c0006t0001g0046 a0005c0006t0001g0047 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.706-1516G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480626 | |||||||
| chr8:24480650 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.706-1492G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480650 | |||||||
| chr8:24480691 | G | A | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-1451G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480691 | |||||||
| chr8:24480698 | T | C | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.706-1444T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480698 | |||||||
| chr8:24480718 | T | C | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.706-1424T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480718 | |||||||
| chr8:24480736 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.706-1406C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480736 | |||||||
| chr8:24480776 | C | T | 5 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(2): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-1366C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480776 | |||||||
| chr8:24480870 | T | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.706-1272T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480870 | |||||||
| chr8:24480897 | G | T | 1 | a0002c0002t0001g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.706-1245G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24480897 | |||||||
| chr8:24481063 | A | AAAAC | 23 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0054 others(20): Show |
26 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.706-1048_706-1045d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | ||||||
| chr8:24481063 | A | AAAACAAA others(1): Show |
2 | a0001c0001t0001g0026 a0003c0004t0001g0075 |
3 | HG01167.hp1 HG01169.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.706-1052_706-1045d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | ||||||
| chr8:24481063 | AAAAC | A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.706-1048_706-1045d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | ||||||
| chr8:24481063 | AAAACAAA others(1): Show |
A | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01257.hp2 HG01261.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-1052_706-1045d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481063 | ||||||
| chr8:24481092 | AAAC | A | 10 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(7): Show |
10 | HG02135.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.706-1047_706-1045d others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 24481092 | ||||||
| chr8:24481199 | C | A | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.706-943C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481199 | |||||||
| chr8:24481275 | T | A | 1 | a0001c0001t0001g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-867T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481275 | |||||||
| chr8:24481313 | A | G | 2 | a0002c0002t0001g0100 a0002c0002t0001g0101 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.706-829A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481313 | |||||||
| chr8:24481346 | T | C | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.706-796T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481346 | |||||||
| chr8:24481559 | G | A | 1 | a0003c0004t0001g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.706-583G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481559 | |||||||
| chr8:24481585 | G | T | 2 | a0003c0004t0004g0203 a0011c0009t0004g0056 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.706-557G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481585 | |||||||
| chr8:24481823 | T | C | 1 | a0005c0006t0001g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.706-319T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481823 | |||||||
| chr8:24481897 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.706-245T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | chr8 | 24481897 | |||||||
| chr8:24482383 | GA | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.875+80delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24482383 | ||||||
| chr8:24482473 | A | C | 2 | a0002c0002t0001g0137 a0002c0002t0001g0141 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.875+162A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482473 | |||||||
| chr8:24482510 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0287 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.875+199G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482510 | |||||||
| chr8:24482543 | T | A | 1 | a0008c0019t0007g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.875+232T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482543 | |||||||
| chr8:24482952 | A | C | 1 | a0001c0001t0002g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.875+641A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482952 | |||||||
| chr8:24482955 | G | A | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.875+644G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24482955 | |||||||
| chr8:24483493 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.875+1182T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483493 | |||||||
| chr8:24483505 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
5 | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+1194C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483505 | |||||||
| chr8:24483600 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.875+1289C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483600 | |||||||
| chr8:24483650 | A | C | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.875+1339A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483650 | |||||||
| chr8:24483667 | G | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.875+1356G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483667 | |||||||
| chr8:24483724 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.875+1413G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483724 | |||||||
| chr8:24483779 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.875+1468T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483779 | |||||||
| chr8:24483823 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | NA18978.hp1 NA19004.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.876-1454A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483823 | |||||||
| chr8:24483835 | G | T | 2 | a0005c0006t0001g0046 a0005c0006t0001g0047 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.876-1442G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483835 | |||||||
| chr8:24483872 | G | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.876-1405G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24483872 | |||||||
| chr8:24484000 | C | T | 6 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0157 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-1277C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484000 | |||||||
| chr8:24484001 | C | T | 49 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0030 others(46): Show |
56 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.876-1276C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484001 | |||||||
| chr8:24484038 | G | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-1239G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484038 | |||||||
| chr8:24484081 | T | A | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-1196T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484081 | |||||||
| chr8:24484089 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.876-1188C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484089 | |||||||
| chr8:24484114 | G | A | 1 | a0001c0001t0002g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.876-1163G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484114 | |||||||
| chr8:24484177 | C | A | 6 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0157 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-1100C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484177 | |||||||
| chr8:24484195 | C | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0153 others(6): Show |
12 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-1082C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484195 | |||||||
| chr8:24484333 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.876-944C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484333 | |||||||
| chr8:24484427 | A | G | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.876-850A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484427 | |||||||
| chr8:24484530 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-747C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484530 | |||||||
| chr8:24484802 | C | CT | 18 | a0001c0001t0001g0026 a0001c0001t0002g0032 a0001c0001t0002g0217 others(15): Show |
23 | HG00733.hp1 HG00738.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.876-453dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | ||||||
| chr8:24484802 | CT | C | 46 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0054 others(43): Show |
49 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.876-453delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | ||||||
| chr8:24484802 | CTT | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.876-454_876-453del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | ||||||
| chr8:24484802 | CTTT | C | 6 | a0002c0002t0001g0073 a0002c0002t0001g0094 a0002c0002t0001g0113 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-455_876-453del others(3): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 24484802 | ||||||
| chr8:24484892 | G | T | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-385G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484892 | |||||||
| chr8:24484985 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(11): Show |
16 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.876-292C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484985 | |||||||
| chr8:24484986 | A | G | 1 | a0002c0002t0001g0078 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.876-291A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24484986 | |||||||
| chr8:24485055 | C | T | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | HG00735.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.876-222C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | chr8 | 24485055 | |||||||
| chr8:24485409 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02280.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.960+48G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485409 | |||||||
| chr8:24485461 | T | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0240 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.960+100T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485461 | |||||||
| chr8:24485588 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.960+227A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485588 | |||||||
| chr8:24485636 | T | TG | 12 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0220 others(9): Show |
12 | HG01891.hp1 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.960+276dupG | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 24485636 | ||||||
| chr8:24485672 | T | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(62): Show |
75 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.960+311T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485672 | |||||||
| chr8:24485856 | A | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.960+495A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485856 | |||||||
| chr8:24485858 | A | T | 1 | a0002c0002t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.960+497A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485858 | |||||||
| chr8:24485879 | C | T | 1 | a0008c0019t0007g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.960+518C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485879 | |||||||
| chr8:24485952 | T | G | 80 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(77): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.960+591T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24485952 | |||||||
| chr8:24486009 | T | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG02135.hp2 NA18978.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+648T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486009 | |||||||
| chr8:24486100 | T | C | 1 | a0002c0002t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.960+739T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486100 | |||||||
| chr8:24486239 | T | C | 1 | a0006c0008t0005g0027 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.960+878T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486239 | |||||||
| chr8:24486282 | A | G | 1 | a0002c0002t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.961-905A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486282 | |||||||
| chr8:24486291 | T | C | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.961-896T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486291 | |||||||
| chr8:24486303 | A | C | 2 | a0005c0006t0001g0009 a0005c0006t0001g0041 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.961-884A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486303 | |||||||
| chr8:24486362 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.961-825G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486362 | |||||||
| chr8:24486402 | G | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-785G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486402 | |||||||
| chr8:24486442 | A | G | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.961-745A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486442 | |||||||
| chr8:24486572 | G | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.961-615G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486572 | |||||||
| chr8:24486576 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.961-611A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486576 | |||||||
| chr8:24486639 | C | T | 83 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(80): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.961-548C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486639 | |||||||
| chr8:24486762 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-425G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486762 | |||||||
| chr8:24486773 | A | G | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.961-414A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486773 | |||||||
| chr8:24486859 | A | G | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.961-328A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486859 | |||||||
| chr8:24486870 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.961-317A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486870 | |||||||
| chr8:24486888 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.961-299A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24486888 | |||||||
| chr8:24487126 | G | T | 1 | a0001c0003t0003g0066 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.961-61G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 10/21 | chr8 | 24487126 | |||||||
| chr8:24487369 | G | GGTGCA | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+53_1091+54ins others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 24487369 | ||||||
| chr8:24487412 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1091+95C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487412 | |||||||
| chr8:24487520 | G | A | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1091+203G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487520 | |||||||
| chr8:24487584 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1091+267G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487584 | |||||||
| chr8:24487635 | C | CA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1091+329dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 24487635 | ||||||
| chr8:24487668 | A | T | 1 | a0001c0001t0002g0223 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1091+351A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487668 | |||||||
| chr8:24487762 | G | T | 1 | a0002c0002t0001g0105 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1091+445G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487762 | |||||||
| chr8:24487765 | G | A | 94 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(91): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1091+448G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487765 | |||||||
| chr8:24487807 | T | A | 1 | a0002c0002t0001g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1091+490T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487807 | |||||||
| chr8:24487827 | G | A | 5 | a0005c0006t0001g0040 a0005c0006t0001g0042 a0005c0006t0001g0043 others(2): Show |
5 | HG02451.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+510G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487827 | |||||||
| chr8:24487884 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | NA18978.hp1 NA18999.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091+567G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487884 | |||||||
| chr8:24487899 | A | C | 1 | a0001c0001t0001g0302 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1091+582A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24487899 | |||||||
| chr8:24488001 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1091+684C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488001 | |||||||
| chr8:24488043 | C | G | 1 | a0002c0002t0001g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1091+726C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488043 | |||||||
| chr8:24488063 | C | G | 11 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(8): Show |
12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091+746C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488063 | |||||||
| chr8:24488131 | C | T | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1091+814C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488131 | |||||||
| chr8:24488237 | C | T | 11 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(8): Show |
12 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1091+920C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488237 | |||||||
| chr8:24488412 | A | G | 2 | a0002c0002t0001g0115 a0002c0002t0001g0136 |
2 | HG00099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1092-747A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488412 | |||||||
| chr8:24488446 | A | G | 94 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(91): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1092-713A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488446 | |||||||
| chr8:24488452 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1092-707A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488452 | |||||||
| chr8:24488561 | C | T | 1 | a0001c0003t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1092-598C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488561 | |||||||
| chr8:24488564 | A | G | 2 | a0005c0006t0001g0043 a0005c0006t0001g0044 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1092-595A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488564 | |||||||
| chr8:24488599 | C | T | 94 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(91): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1092-560C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488599 | |||||||
| chr8:24488631 | G | A | 94 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(91): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1092-528G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 11/21 | chr8 | 24488631 | |||||||
| chr8:24489388 | T | C | 4 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0114 others(1): Show |
4 | HG00438.hp2 NA18962.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+55T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24489388 | |||||||
| chr8:24489467 | T | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1266+134T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24489467 | |||||||
| chr8:24490005 | G | C | 1 | a0001c0001t0004g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1266+672G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490005 | |||||||
| chr8:24490021 | G | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+688G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490021 | |||||||
| chr8:24490133 | T | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0153 others(7): Show |
13 | HG01192.hp2 HG02129.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1267-666T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490133 | |||||||
| chr8:24490163 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1267-636A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490163 | |||||||
| chr8:24490386 | T | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0272 |
3 | HG01433.hp1 HG01934.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1267-413T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490386 | |||||||
| chr8:24490608 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1267-191C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490608 | |||||||
| chr8:24490641 | C | T | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1267-158C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490641 | |||||||
| chr8:24490708 | T | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1267-91T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490708 | |||||||
| chr8:24490728 | A | G | 83 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(80): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1267-71A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490728 | |||||||
| chr8:24490756 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1267-43A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | chr8 | 24490756 | |||||||
| chr8:24490774 | ATC | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1267-19_1267-18del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 24490774 | ||||||
| chr8:24490912 | G | GT | 9 | a0001c0001t0001g0202 a0001c0001t0001g0294 a0001c0001t0002g0048 others(6): Show |
9 | HG01258.hp2 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1356+35dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 24490912 | ||||||
| chr8:24491116 | G | C | 1 | a0001c0003t0003g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1356+228G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491116 | |||||||
| chr8:24491192 | T | C | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1356+304T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491192 | |||||||
| chr8:24491217 | G | T | 1 | a0002c0002t0001g0037 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1356+329G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491217 | |||||||
| chr8:24491241 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1356+353G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491241 | |||||||
| chr8:24491277 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1356+389C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491277 | |||||||
| chr8:24491341 | A | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1356+453A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491341 | |||||||
| chr8:24491422 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1357-481T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491422 | |||||||
| chr8:24491447 | T | C | 1 | a0005c0006t0001g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1357-456T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491447 | |||||||
| chr8:24491466 | A | G | 1 | a0003c0004t0004g0203 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1357-437A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491466 | |||||||
| chr8:24491643 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1357-260G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491643 | |||||||
| chr8:24491747 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0288 a0001c0001t0001g0299 others(1): Show |
5 | HG01123.hp2 HG01175.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1357-156T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491747 | |||||||
| chr8:24491846 | G | A | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357-57G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491846 | |||||||
| chr8:24491867 | T | C | 1 | a0002c0002t0001g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1357-36T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491867 | |||||||
| chr8:24491882 | C | G | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1357-21C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 13/21 | chr8 | 24491882 | |||||||
| chr8:24492243 | C | T | 1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1552+145C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/21 | chr8 | 24492243 | |||||||
| chr8:24492265 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(29): Show |
37 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1552+167C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/21 | chr8 | 24492265 | |||||||
| chr8:24492408 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1553-87G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 14/21 | chr8 | 24492408 | |||||||
| chr8:24492638 | G | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1655+41G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492638 | |||||||
| chr8:24492660 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1655+63G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492660 | |||||||
| chr8:24492675 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1655+78C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492675 | |||||||
| chr8:24492694 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1655+97T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492694 | |||||||
| chr8:24492861 | C | T | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1656-182C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492861 | |||||||
| chr8:24492862 | G | A | 1 | a0002c0002t0012g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1656-181G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492862 | |||||||
| chr8:24492900 | T | A | 1 | a0004c0005t0001g0102 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1656-143T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492900 | |||||||
| chr8:24492960 | A | G | 1 | a0002c0007t0001g0110 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1656-83A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492960 | |||||||
| chr8:24492984 | G | T | 14 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0231 others(11): Show |
14 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.1656-59G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 15/21 | chr8 | 24492984 | |||||||
| chr8:24493483 | T | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1842+254T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493483 | |||||||
| chr8:24493484 | AGACATG | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1842+258_1842+263d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24493484 | ||||||
| chr8:24493491 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1842+262G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493491 | |||||||
| chr8:24493698 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1842+469T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493698 | |||||||
| chr8:24493837 | A | G | 3 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 |
4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+608A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24493837 | |||||||
| chr8:24494170 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(29): Show |
37 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1842+941A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494170 | |||||||
| chr8:24494300 | A | T | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1842+1071A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494300 | |||||||
| chr8:24494457 | T | A | 1 | a0001c0003t0003g0061 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1842+1228T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494457 | |||||||
| chr8:24494459 | C | G | 1 | a0001c0003t0003g0061 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1842+1230C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494459 | |||||||
| chr8:24494464 | T | TGCTTCCT others(322): Show |
1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1842+1247_1842+124 others(333): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24494464 | ||||||
| chr8:24494484 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1842+1255G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494484 | |||||||
| chr8:24494712 | GA | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1842+1492delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24494712 | ||||||
| chr8:24494721 | A | T | 102 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(99): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1842+1492A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494721 | |||||||
| chr8:24494722 | T | C | 102 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(99): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1842+1493T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494722 | |||||||
| chr8:24494723 | C | T | 102 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(99): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1842+1494C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494723 | |||||||
| chr8:24494839 | C | T | 1 | a0001c0001t0013g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1842+1610C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494839 | |||||||
| chr8:24494846 | G | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1842+1617G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494846 | |||||||
| chr8:24494872 | A | C | 5 | a0002c0002t0001g0105 a0002c0002t0001g0106 a0002c0002t0001g0107 others(2): Show |
5 | NA18943.hp1 NA18944.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+1643A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494872 | |||||||
| chr8:24494949 | C | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+1720C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494949 | |||||||
| chr8:24494986 | C | G | 1 | a0001c0001t0001g0026 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1842+1757C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24494986 | |||||||
| chr8:24495034 | C | A | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842+1805C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495034 | |||||||
| chr8:24495398 | G | GA | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2176dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24495398 | ||||||
| chr8:24495468 | G | A | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2239G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495468 | |||||||
| chr8:24495480 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1842+2251C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495480 | |||||||
| chr8:24495499 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1842+2270G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495499 | |||||||
| chr8:24495563 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(30): Show |
38 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1842+2334A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495563 | |||||||
| chr8:24495704 | T | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1842+2475T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495704 | |||||||
| chr8:24495722 | AAG | A | 2 | a0003c0004t0005g0023 a0003c0004t0005g0181 |
3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1842+2499_1842+250 others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24495722 | ||||||
| chr8:24495913 | G | A | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2684G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24495913 | |||||||
| chr8:24496033 | G | C | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1842+2804G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496033 | |||||||
| chr8:24496083 | T | C | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1842+2854T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496083 | |||||||
| chr8:24496089 | A | G | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1842+2860A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496089 | |||||||
| chr8:24496254 | G | A | 15 | a0001c0003t0003g0011 a0001c0003t0003g0058 a0001c0003t0003g0059 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1843-2982G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496254 | |||||||
| chr8:24496368 | C | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-2868C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496368 | |||||||
| chr8:24496393 | T | G | 2 | a0002c0002t0001g0137 a0002c0002t0001g0141 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1843-2843T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496393 | |||||||
| chr8:24496442 | C | T | 83 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(80): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1843-2794C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496442 | |||||||
| chr8:24496648 | T | G | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1843-2588T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496648 | |||||||
| chr8:24496668 | C | T | 3 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 |
4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843-2568C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496668 | |||||||
| chr8:24496767 | G | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(97): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1843-2469G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496767 | |||||||
| chr8:24496959 | C | T | 83 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(80): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1843-2277C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24496959 | |||||||
| chr8:24497049 | A | G | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1843-2187A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497049 | |||||||
| chr8:24497050 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1843-2186T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497050 | |||||||
| chr8:24497062 | C | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-2174C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497062 | |||||||
| chr8:24497080 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1843-2156T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497080 | |||||||
| chr8:24497102 | G | C | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1843-2134G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497102 | |||||||
| chr8:24497269 | G | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1967G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497269 | |||||||
| chr8:24497308 | G | A | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1928G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497308 | |||||||
| chr8:24497342 | T | C | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1843-1894T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497342 | |||||||
| chr8:24497456 | T | C | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1780T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497456 | |||||||
| chr8:24497571 | A | C | 1 | a0016c0021t0008g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1843-1665A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497571 | |||||||
| chr8:24497620 | G | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-1616G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497620 | |||||||
| chr8:24497830 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1843-1406C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24497830 | |||||||
| chr8:24498032 | T | C | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843-1204T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498032 | |||||||
| chr8:24498054 | A | C | 1 | a0001c0001t0002g0259 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1843-1182A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498054 | |||||||
| chr8:24498300 | G | A | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1843-936G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498300 | |||||||
| chr8:24498409 | T | C | 18 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(15): Show |
22 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1843-827T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498409 | |||||||
| chr8:24498543 | C | G | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1843-693C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498543 | |||||||
| chr8:24498549 | G | GTA | 4 | a0003c0004t0001g0012 a0003c0004t0001g0075 a0003c0004t0001g0144 others(1): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1843-673_1843-672d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24498549 | ||||||
| chr8:24498549 | G | GTATA | 80 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(77): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1843-675_1843-672d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 24498549 | ||||||
| chr8:24498552 | T | C | 3 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0266 |
3 | HG03834.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1843-684T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498552 | |||||||
| chr8:24498651 | T | A | 3 | a0003c0004t0005g0035 a0003c0004t0005g0315 a0003c0004t0005g0316 |
4 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843-585T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498651 | |||||||
| chr8:24498714 | C | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-522C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498714 | |||||||
| chr8:24498751 | G | C | 1 | a0001c0003t0003g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1843-485G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498751 | |||||||
| chr8:24498806 | T | C | 8 | a0001c0001t0002g0215 a0001c0001t0002g0231 a0001c0001t0002g0241 others(5): Show |
8 | HG00408.hp1 HG02132.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843-430T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498806 | |||||||
| chr8:24498848 | T | C | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1843-388T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24498848 | |||||||
| chr8:24499120 | A | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01261.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1843-116A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24499120 | |||||||
| chr8:24499212 | C | G | 1 | a0002c0002t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1843-24C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24499212 | |||||||
| chr8:24499233 | T | C | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1843-3T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | chr8 | 24499233 | |||||||
| chr8:24499414 | T | G | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1923+98T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499414 | |||||||
| chr8:24499650 | C | T | 80 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(77): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1923+334C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499650 | |||||||
| chr8:24499729 | A | G | 105 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(102): Show |
121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1923+413A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499729 | |||||||
| chr8:24499758 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
4 | HG00558.hp1 HG02027.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1924-420G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499758 | |||||||
| chr8:24499771 | G | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01261.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1924-407G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499771 | |||||||
| chr8:24499797 | T | TAC | 35 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0028 others(32): Show |
40 | HG00408.hp1 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1924-351_1924-350d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499797 | T | TACAC | 6 | a0001c0001t0001g0184 a0001c0001t0001g0196 a0001c0001t0001g0205 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1924-353_1924-350d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499797 | TAC | T | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 others(49): Show |
59 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1924-351_1924-350d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499797 | TACAC | T | 5 | a0001c0001t0001g0302 a0001c0001t0002g0227 a0001c0001t0002g0228 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-353_1924-350d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499797 | TACACACA others(1): Show |
T | 80 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(77): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1924-357_1924-350d others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499797 | TACACACA others(3): Show |
T | 3 | a0003c0004t0001g0276 a0005c0006t0001g0009 a0005c0006t0001g0041 |
4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-359_1924-350d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499797 | TACACACA others(5): Show |
T | 14 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(11): Show |
17 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1924-361_1924-350d others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499797 | ||||||
| chr8:24499822 | A | T | 1 | a0002c0002t0012g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1924-356A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499822 | |||||||
| chr8:24499827 | C | T | 3 | a0003c0004t0004g0203 a0009c0010t0008g0057 a0011c0009t0004g0056 |
3 | HG02258.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1924-351C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499827 | |||||||
| chr8:24499836 | TCA | T | 8 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(5): Show |
9 | HG02451.hp2 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1924-325_1924-324d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499836 | ||||||
| chr8:24499838 | A | T | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1924-340A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499838 | |||||||
| chr8:24499856 | A | G | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-322A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499856 | |||||||
| chr8:24499881 | T | C | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-297T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499881 | |||||||
| chr8:24499898 | C | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-280C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499898 | |||||||
| chr8:24499902 | G | GA | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1924-273dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 24499902 | ||||||
| chr8:24499953 | A | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-225A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499953 | |||||||
| chr8:24499997 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1924-181A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24499997 | |||||||
| chr8:24500047 | A | T | 16 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(13): Show |
20 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1924-131A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24500047 | |||||||
| chr8:24500137 | A | T | 1 | a0001c0001t0002g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1924-41A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | chr8 | 24500137 | |||||||
| chr8:24500311 | A | G | 2 | a0005c0006t0001g0009 a0005c0006t0001g0041 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2002+55A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500311 | |||||||
| chr8:24500404 | G | T | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2002+148G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500404 | |||||||
| chr8:24500557 | T | C | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2003-233T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500557 | |||||||
| chr8:24500706 | A | G | 86 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(83): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2003-84A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 18/21 | chr8 | 24500706 | |||||||
| chr8:24500977 | A | G | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108+82A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24500977 | |||||||
| chr8:24501117 | A | T | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2108+222A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501117 | |||||||
| chr8:24501161 | T | C | 1 | a0002c0002t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2108+266T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501161 | |||||||
| chr8:24501179 | T | C | 85 | a0001c0001t0001g0054 a0002c0002t0001g0001 a0002c0002t0001g0013 others(82): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2108+284T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501179 | |||||||
| chr8:24501337 | C | G | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2109-140C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 19/21 | chr8 | 24501337 | |||||||
| chr8:24501612 | A | AT | 14 | a0001c0001t0001g0292 a0003c0004t0005g0023 a0003c0004t0005g0035 others(11): Show |
18 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2208+48dupT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24501612 | ||||||
| chr8:24501612 | ATT | A | 83 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(80): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2208+47_2208+48del others(2): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24501612 | ||||||
| chr8:24501735 | A | G | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+159A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501735 | |||||||
| chr8:24501743 | G | A | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+167G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501743 | |||||||
| chr8:24501766 | G | A | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+190G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501766 | |||||||
| chr8:24501792 | T | C | 1 | a0002c0002t0001g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2208+216T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501792 | |||||||
| chr8:24501825 | C | T | 101 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(98): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2208+249C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501825 | |||||||
| chr8:24501827 | A | G | 1 | a0014c0015t0001g0124 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2208+251A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501827 | |||||||
| chr8:24501837 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2208+261C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501837 | |||||||
| chr8:24501856 | G | A | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+280G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501856 | |||||||
| chr8:24501857 | C | A | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+281C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501857 | |||||||
| chr8:24501896 | A | T | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2208+320A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501896 | |||||||
| chr8:24501930 | G | A | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2208+354G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501930 | |||||||
| chr8:24501958 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(56): Show |
66 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2208+382G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24501958 | |||||||
| chr8:24502028 | TAA | T | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+454_2208+455d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24502028 | ||||||
| chr8:24502159 | G | C | 1 | a0002c0007t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2208+583G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502159 | |||||||
| chr8:24502210 | A | G | 2 | a0003c0004t0004g0203 a0011c0009t0004g0056 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2208+634A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502210 | |||||||
| chr8:24502227 | GA | G | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+655delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24502227 | ||||||
| chr8:24502254 | T | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2208+678T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502254 | |||||||
| chr8:24502569 | A | T | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+993A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502569 | |||||||
| chr8:24502625 | T | A | 101 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(98): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2208+1049T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502625 | |||||||
| chr8:24502661 | T | C | 6 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0157 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2208+1085T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502661 | |||||||
| chr8:24502919 | GAA | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2208+1347_2208+134 others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24502919 | ||||||
| chr8:24502941 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2208+1365C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24502941 | |||||||
| chr8:24503028 | G | A | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+1452G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503028 | |||||||
| chr8:24503100 | G | T | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+1524G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503100 | |||||||
| chr8:24503129 | T | C | 1 | a0002c0014t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2208+1553T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503129 | |||||||
| chr8:24503146 | A | G | 1 | a0001c0001t0002g0239 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2208+1570A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503146 | |||||||
| chr8:24503208 | C | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0288 others(6): Show |
12 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2208+1632C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503208 | |||||||
| chr8:24503301 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2208+1725A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503301 | |||||||
| chr8:24503306 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
30 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2208+1730G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503306 | |||||||
| chr8:24503362 | A | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2208+1786A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503362 | |||||||
| chr8:24503431 | G | C | 3 | a0001c0001t0002g0029 a0001c0001t0002g0311 a0001c0001t0011g0243 |
4 | HG00609.hp2 HG02132.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.2208+1855G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503431 | |||||||
| chr8:24503550 | C | A | 84 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2208+1974C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503550 | |||||||
| chr8:24503577 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2208+2001G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503577 | |||||||
| chr8:24503581 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2208+2005G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503581 | |||||||
| chr8:24503587 | C | T | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2208+2011C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503587 | |||||||
| chr8:24503616 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2208+2040G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503616 | |||||||
| chr8:24503639 | A | G | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2208+2063A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503639 | |||||||
| chr8:24503850 | A | G | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2208+2274A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503850 | |||||||
| chr8:24503866 | A | G | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2208+2290A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24503866 | |||||||
| chr8:24504023 | A | AAAAAT | 12 | a0001c0001t0001g0195 a0001c0001t0002g0021 a0001c0001t0002g0076 others(9): Show |
13 | HG02630.hp1 NA18612.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.2208+2486_2208+249 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | ||||||
| chr8:24504023 | AAAAAT | A | 40 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(37): Show |
43 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.2208+2486_2208+249 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | ||||||
| chr8:24504023 | AAAAATAA others(3): Show |
A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG02109.hp2 HG02895.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2208+2481_2208+249 others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | ||||||
| chr8:24504023 | AAAAATAA others(8): Show |
A | 80 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(77): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2208+2476_2208+249 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504023 | ||||||
| chr8:24504062 | A | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2208+2486A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504062 | |||||||
| chr8:24504063 | T | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(25): Show |
35 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.2208+2487T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504063 | |||||||
| chr8:24504063 | T | TA | 12 | a0003c0004t0005g0023 a0003c0004t0005g0181 a0003c0004t0005g0315 others(9): Show |
13 | HG00733.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2208+2490dupA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504063 | ||||||
| chr8:24504063 | T | TAAAATA | 4 | a0001c0001t0002g0242 a0003c0004t0005g0035 a0003c0004t0005g0316 others(1): Show |
6 | HG00738.hp2 HG02145.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208+2490_2208+249 others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504063 | ||||||
| chr8:24504063 | T | TAAAATAA others(4): Show |
2 | a0005c0006t0001g0041 a0006c0008t0005g0027 |
3 | HG02647.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2208+2490_2208+249 others(15): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504063 | ||||||
| chr8:24504072 | T | A | 1 | a0001c0001t0002g0242 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2208+2496T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504072 | |||||||
| chr8:24504165 | C | G | 18 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(15): Show |
22 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2208+2589C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504165 | |||||||
| chr8:24504171 | C | T | 1 | a0002c0002t0001g0014 | 2 | HG01123.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2208+2595C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504171 | |||||||
| chr8:24504191 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2208+2615G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504191 | |||||||
| chr8:24504260 | G | A | 23 | a0001c0001t0001g0028 a0001c0001t0001g0182 a0001c0001t0001g0183 others(20): Show |
25 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2208+2684G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504260 | |||||||
| chr8:24504382 | T | A | 102 | a0001c0001t0001g0054 a0002c0002t0001g0001 a0002c0002t0001g0013 others(99): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2208+2806T>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504382 | |||||||
| chr8:24504389 | C | A | 102 | a0001c0001t0001g0054 a0002c0002t0001g0001 a0002c0002t0001g0013 others(99): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2208+2813C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504389 | |||||||
| chr8:24504443 | TA | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2208+2878delA | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504443 | ||||||
| chr8:24504547 | A | G | 1 | a0002c0002t0001g0107 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2209-2933A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504547 | |||||||
| chr8:24504572 | T | C | 8 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(5): Show |
11 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209-2908T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504572 | |||||||
| chr8:24504578 | G | A | 1 | a0001c0001t0002g0308 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2209-2902G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504578 | |||||||
| chr8:24504599 | C | T | 2 | a0005c0006t0001g0009 a0005c0006t0001g0041 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2209-2881C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504599 | |||||||
| chr8:24504700 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
4 | HG00558.hp1 HG02027.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2209-2780G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24504700 | |||||||
| chr8:24504755 | AC | A | 8 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(5): Show |
11 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209-2720delC | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24504755 | ||||||
| chr8:24505010 | C | T | 2 | a0003c0004t0004g0203 a0011c0009t0004g0056 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2209-2470C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505010 | |||||||
| chr8:24505013 | A | G | 8 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(5): Show |
11 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209-2467A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505013 | |||||||
| chr8:24505024 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2209-2456G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505024 | |||||||
| chr8:24505177 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2209-2303C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505177 | |||||||
| chr8:24505190 | G | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
104 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.2209-2290G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505190 | |||||||
| chr8:24505269 | G | A | 3 | a0004c0005t0001g0002 a0004c0005t0001g0112 a0004c0005t0001g0135 |
5 | HG01081.hp1 HG01192.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2209-2211G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505269 | |||||||
| chr8:24505276 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2209-2204A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505276 | |||||||
| chr8:24505297 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2209-2183C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505297 | |||||||
| chr8:24505358 | A | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2209-2122A>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505358 | |||||||
| chr8:24505383 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2209-2097G>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505383 | |||||||
| chr8:24505585 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2209-1895C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505585 | |||||||
| chr8:24505621 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2209-1859T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505621 | |||||||
| chr8:24505669 | T | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2209-1811T>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505669 | |||||||
| chr8:24505720 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2209-1760A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505720 | |||||||
| chr8:24505872 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-1608C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505872 | |||||||
| chr8:24505934 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2209-1546T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24505934 | |||||||
| chr8:24506086 | A | C | 1 | a0001c0001t0002g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2209-1394A>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506086 | |||||||
| chr8:24506161 | G | A | 17 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(14): Show |
21 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2209-1319G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506161 | |||||||
| chr8:24506230 | T | C | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2209-1250T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506230 | |||||||
| chr8:24506250 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2209-1230G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506250 | |||||||
| chr8:24506279 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.2209-1201G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506279 | |||||||
| chr8:24506353 | G | T | 1 | a0001c0001t0002g0235 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2209-1127G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506353 | |||||||
| chr8:24506404 | T | C | 1 | a0001c0003t0003g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2209-1076T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506404 | |||||||
| chr8:24506476 | C | T | 7 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(4): Show |
10 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2209-1004C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506476 | |||||||
| chr8:24506495 | T | C | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-985T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506495 | |||||||
| chr8:24506592 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
28 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2209-888A>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506592 | |||||||
| chr8:24506753 | G | GCA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0292 others(25): Show |
34 | HG00280.hp1 HG00558.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2209-690_2209-689d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | G | GCACA | 7 | a0001c0001t0001g0202 a0001c0001t0002g0230 a0001c0001t0002g0312 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2209-692_2209-689d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | G | GCACACAC others(3): Show |
1 | a0003c0004t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2209-698_2209-689d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | GCA | G | 140 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0183 others(137): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.2209-690_2209-689d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | GCACA | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(22): Show |
26 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.2209-692_2209-689d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | GCACACA | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0086 others(23): Show |
30 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2209-694_2209-689d others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | GCACACAC others(3): Show |
G | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2209-698_2209-689d others(12): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506753 | GCACACAC others(5): Show |
G | 1 | a0001c0001t0002g0239 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2209-700_2209-689d others(14): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24506753 | ||||||
| chr8:24506896 | C | T | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2209-584C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506896 | |||||||
| chr8:24506967 | C | T | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2209-513C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24506967 | |||||||
| chr8:24507021 | C | A | 9 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2209-459C>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24507021 | |||||||
| chr8:24507169 | C | G | 2 | a0009c0010t0008g0057 a0016c0021t0008g0039 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2209-311C>G | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24507169 | |||||||
| chr8:24507182 | T | TGAAAATC others(24): Show |
1 | a0013c0013t0001g0123 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2209-295_2209-265d others(33): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 24507182 | ||||||
| chr8:24507220 | C | T | 7 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-260C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | chr8 | 24507220 | |||||||
| chr8:24507644 | TCA | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2264+112_2264+113d others(4): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 24507644 | ||||||
| chr8:24507662 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2264+127G>A | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24507662 | |||||||
| chr8:24507668 | AT | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.2264+148delT | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 24507668 | ||||||
| chr8:24507668 | ATTTT | A | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2264+145_2264+148d others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 24507668 | ||||||
| chr8:24507878 | T | C | 6 | a0003c0004t0005g0023 a0003c0004t0005g0035 a0003c0004t0005g0181 others(3): Show |
9 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2264+343T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24507878 | |||||||
| chr8:24508450 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2265-96G>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24508450 | |||||||
| chr8:24508507 | T | C | 91 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(88): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2265-39T>C | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24508507 | |||||||
| chr8:24508514 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2265-32C>T | ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | chr8 | 24508514 |