Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2515 |
| ensemblid | ENSG00000104755.16 |
| hgncid | 198 |
| symbol | ADAM2 |
| name | ADAM metallopeptidase domain 2 |
| refseq_nuc | NM_001464.5 |
| refseq_prot | NP_001455.3 |
| ensembl_nuc | ENST00000265708.9 |
| ensembl_prot | ENSP00000265708.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 39743735 |
| end | 39838227 |
| strand | - |
| ver | v1.2 |
| region | chr8:39743735-39838227 |
| region5000 | chr8:39738735-39843227 |
| regionname0 | ADAM2_chr8_39743735_39838227 |
| regionname5000 | ADAM2_chr8_39738735_39843227 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 735 | 303 | 82 | 59 | 121 | 12 | 28 | 93 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0002 | 0/0 | 735 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0003 | 0/0 | 735 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0004 | 0/0 | 735 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0005 | 0/0 | 735 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0006 | 0/0 | 735 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0007 | 0/0 | 735 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0008 | 0/0 | 735 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0009 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0010 | 0/0 | 305 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(300): Show |
chr8 | 39738735 | 39843227 |
| a0011 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0012 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| a0013 | 0/0 | 735 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | MWRVL others(730): Show |
chr8 | 39738735 | 39843227 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2205 | 295 | 79 | 59 | 118 | 12 | 26 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0001c0006 | 0/0 | 2205 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0001c0007 | 0/0 | 2205 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0001c0014 | 0/0 | 2205 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0001c0015 | 0/0 | 2205 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0001c0018 | 0/0 | 2205 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0001c0020 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0002c0002 | 0/0 | 2205 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0003c0003 | 0/0 | 2205 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0004c0008 | 0/0 | 2205 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0005c0009 | 0/0 | 2205 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0006c0005 | 0/0 | 2205 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0007c0004 | 0/0 | 2205 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0008c0010 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0008c0011 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0009c0016 | 0/0 | 2205 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0010c0019 | 0/0 | 2068 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2063): Show |
chr8 | 39738735 | 39843227 | ||
| a0011c0012 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0012c0013 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 | ||
| a0013c0017 | 0/0 | 2205 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ATGTG others(2200): Show |
chr8 | 39738735 | 39843227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2610 | 293 | 79 | 58 | 118 | 12 | 25 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0001t0002 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0001t0003 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0006t0001 | 0/0 | 2610 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0007t0001 | 0/0 | 2610 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0014t0001 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0015t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0018t0001 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0001c0020t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0002c0002t0001 | 0/0 | 2610 | 7 | 7 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0003c0003t0001 | 0/0 | 2610 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0004c0008t0001 | 0/0 | 2610 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0005c0009t0001 | 0/0 | 2610 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0006c0005t0001 | 0/0 | 2610 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0007c0004t0001 | 0/0 | 2610 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0008c0010t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0008c0011t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0009c0016t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0010c0019t0001 | 0/0 | 2473 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2468): Show |
chr8 | 39738735 | 39843227 |
| a0011c0012t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0012c0013t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| a0013c0017t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | ACCAA others(2605): Show |
chr8 | 39738735 | 39843227 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0014t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0015t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0018t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0001c0020t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0004c0008t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0005c0009t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0006c0005t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0007c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0007c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0008c0010t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0008c0011t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0009c0016t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0010c0019t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0011c0012t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0012c0013t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| a0013c0017t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01070 | hp2 | a0004 | c0008 | t0001 | g0010 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01515 | hp2 | a0005 | c0009 | t0001 | g0009 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01517 | hp1 | a0005 | c0009 | t0001 | g0009 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01884 | hp1 | a0009 | c0016 | t0001 | g0289 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01891 | hp1 | a0006 | c0005 | t0001 | g0008 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0179 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02040 | hp2 | a0004 | c0008 | t0001 | g0010 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02080 | hp1 | a0010 | c0019 | t0001 | g0121 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0298 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02602 | hp1 | a0001 | c0014 | t0001 | g0046 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02615 | hp2 | a0006 | c0005 | t0001 | g0008 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0164 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02738 | hp1 | a0001 | c0018 | t0001 | g0230 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02886 | hp1 | a0007 | c0004 | t0001 | g0162 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03486 | hp1 | a0007 | c0004 | t0001 | g0163 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03486 | hp2 | a0001 | c0015 | t0001 | g0221 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18961 | hp2 | a0011 | c0012 | t0001 | g0024 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18992 | hp1 | a0008 | c0010 | t0001 | g0023 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA18999 | hp2 | a0012 | c0013 | t0001 | g0037 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19004 | hp2 | a0013 | c0017 | t0001 | g0123 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19012 | hp1 | a0001 | c0020 | t0001 | g0133 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19066 | hp1 | a0008 | c0011 | t0001 | g0022 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19068 | hp2 | a0001 | c0007 | t0001 | g0241 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19079 | hp1 | a0001 | c0007 | t0001 | g0066 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | GIH | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0301 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | USA | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0175 | REF | REF | ADAM2_chr8_39738735_39843227 | ADAM2 | chr8 | 39738735 | 39843227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39746584 | G | C | 1 | a0009 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2062C>G | p.Pro688Ala | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/21 | 2104/2610 | 2062/2208 | 688/735 | chr8 | 39746584 | |||
| chr8:39749416 | G | A | 1 | a0004 | 2 | HG01070.hp2 HG02040.hp2 |
missense_variant | MODERATE | c.1910C>T | p.Ala637Val | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/21 | 1952/2610 | 1910/2208 | 637/735 | chr8 | 39749416 | |||
| chr8:39755764 | C | A | 1 | a0006 | 2 | HG01891.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1761G>T | p.Met587Ile | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/21 | 1803/2610 | 1761/2208 | 587/735 | chr8 | 39755764 | |||
| chr8:39755887 | T | C | 1 | a0013 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.1638A>G | p.Ile546Met | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/21 | 1680/2610 | 1638/2208 | 546/735 | chr8 | 39755887 | |||
| chr8:39767202 | A | G | 1 | a0005 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.1262T>C | p.Phe421Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 13/21 | 1304/2610 | 1262/2208 | 421/735 | chr8 | 39767202 | |||
| chr8:39769403 | C | T | 1 | a0006 | 2 | HG01891.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1201G>A | p.Gly401Arg | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/21 | 1243/2610 | 1201/2208 | 401/735 | chr8 | 39769403 | |||
| chr8:39769462 | A | G | 1 | a0003 | 4 | NA18954.hp1 NA18998.hp2 NA19007.hp2 others(1): Show |
missense_variant | MODERATE | c.1142T>C | p.Phe381Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/21 | 1184/2610 | 1142/2208 | 381/735 | chr8 | 39769462 | |||
| chr8:39774918 | TACTCTAA others(11035): Show |
T | 1 | a0010 | 1 | HG02080.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.891+1014_1028+2106 others(3): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/21 | chr8 | 39774918 | |||||||
| chr8:39788707 | C | T | 1 | a0007 | 2 | HG02886.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.604G>A | p.Ala202Thr | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 8/21 | 646/2610 | 604/2208 | 202/735 | chr8 | 39788707 | |||
| chr8:39837167 | C | T | 1 | a0012 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.101G>A | p.Arg34Gln | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/21 | 143/2610 | 101/2208 | 34/735 | chr8 | 39837167 | |||
| chr8:39838152 | C | T | 1 | a0011 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.34G>A | p.Gly12Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/21 | 76/2610 | 34/2208 | 12/735 | chr8 | 39838152 | |||
| chr8:39838158 | C | A | 1 | a0002 | 7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
missense_variant | MODERATE | c.28G>T | p.Gly10Trp | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/21 | 70/2610 | 28/2208 | 10/735 | chr8 | 39838158 | |||
| chr8:39838168 | A | C | 1 | a0008 | 2 | NA18992.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.18T>G | p.Phe6Leu | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/21 | 60/2610 | 18/2208 | 6/735 | chr8 | 39838168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39746552 | A | G | 2 | a0001c0007 a0008c0010 |
3 | NA18992.hp1 NA19068.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.2094T>C | p.Ile698Ile | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/21 | 2136/2610 | 2094/2208 | 698/735 | chr8 | 39746552 | |||
| chr8:39755743 | A | G | 1 | a0001c0006 | 2 | HG01891.hp2 HG02622.hp2 |
synonymous_variant | LOW | c.1782T>C | p.Ser594Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/21 | 1824/2610 | 1782/2208 | 594/735 | chr8 | 39755743 | |||
| chr8:39766873 | T | C | 1 | a0001c0018 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1482A>G | p.Lys494Lys | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/21 | 1524/2610 | 1482/2208 | 494/735 | chr8 | 39766873 | |||
| chr8:39788702 | T | C | 1 | a0005c0009 | 2 | HG01515.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.609A>G | p.Gln203Gln | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 8/21 | 651/2610 | 609/2208 | 203/735 | chr8 | 39788702 | |||
| chr8:39821636 | A | G | 1 | a0001c0015 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.294T>C | p.Ile98Ile | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 5/21 | 336/2610 | 294/2208 | 98/735 | chr8 | 39821636 | |||
| chr8:39833967 | T | C | 1 | a0001c0020 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.165A>G | p.Pro55Pro | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/21 | 207/2610 | 165/2208 | 55/735 | chr8 | 39833967 | |||
| chr8:39837139 | C | T | 1 | a0001c0014 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.129G>A | p.Ser43Ser | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/21 | 171/2610 | 129/2208 | 43/735 | chr8 | 39837139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39743941 | A | G | 1 | a0001c0001t0003 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 21/21 | 919 | chr8 | 39743941 | ||||||
| chr8:39743968 | A | C | 1 | a0001c0001t0002 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 21/21 | 892 | chr8 | 39743968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39744075 | GA | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(121): Show |
128 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.*31-12delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744075 | |||||||
| chr8:39744245 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(122): Show |
129 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.*31-181T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744245 | |||||||
| chr8:39744287 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.*31-223A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744287 | |||||||
| chr8:39744469 | C | G | 2 | a0001c0001t0001g0291 a0002c0002t0001g0299 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*30+361G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744469 | |||||||
| chr8:39744528 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.*30+302T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744528 | |||||||
| chr8:39744685 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.*30+145C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744685 | |||||||
| chr8:39744708 | G | A | 8 | a0001c0001t0001g0106 a0001c0001t0001g0205 a0001c0001t0001g0235 others(5): Show |
8 | HG00738.hp1 HG01069.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.*30+122C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744708 | |||||||
| chr8:39744747 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*30+83G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744747 | |||||||
| chr8:39744809 | A | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0225 |
2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.*30+21T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 20/20 | chr8 | 39744809 | |||||||
| chr8:39744897 | C | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.2175-4G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39744897 | |||||||
| chr8:39745009 | C | A | 1 | a0001c0001t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2175-116G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745009 | |||||||
| chr8:39745126 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG00673.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2175-233C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745126 | |||||||
| chr8:39745263 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2175-370G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745263 | |||||||
| chr8:39745298 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2175-405G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745298 | |||||||
| chr8:39745402 | T | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175-509A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745402 | |||||||
| chr8:39745459 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2175-566T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745459 | |||||||
| chr8:39745532 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2175-639C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745532 | |||||||
| chr8:39745545 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.2175-652A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745545 | |||||||
| chr8:39745984 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 |
3 | HG01884.hp2 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2174+488A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39745984 | |||||||
| chr8:39746017 | G | GTA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2174+453_2174+454d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746017 | |||||||
| chr8:39746037 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
211 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.2174+435G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746037 | |||||||
| chr8:39746094 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2174+378G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746094 | |||||||
| chr8:39746157 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2174+315G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746157 | |||||||
| chr8:39746171 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2174+301C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746171 | |||||||
| chr8:39746226 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2174+246G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746226 | |||||||
| chr8:39746257 | C | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174+215G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746257 | |||||||
| chr8:39746289 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2174+183T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746289 | |||||||
| chr8:39746306 | C | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174+166G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746306 | |||||||
| chr8:39746335 | T | G | 1 | a0001c0001t0001g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2174+137A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746335 | |||||||
| chr8:39746376 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2174+96A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 19/20 | chr8 | 39746376 | |||||||
| chr8:39746650 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0193 |
2 | HG01175.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2015-19T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746650 | |||||||
| chr8:39746706 | G | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2015-75C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746706 | |||||||
| chr8:39746714 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2015-83T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746714 | |||||||
| chr8:39746855 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2015-224G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746855 | |||||||
| chr8:39746972 | G | A | 19 | a0001c0001t0001g0052 a0001c0001t0001g0146 a0001c0001t0001g0148 others(16): Show |
20 | HG00733.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2015-341C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746972 | |||||||
| chr8:39746980 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2015-349G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39746980 | |||||||
| chr8:39747073 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2015-442C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747073 | |||||||
| chr8:39747101 | A | T | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2015-470T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747101 | |||||||
| chr8:39747167 | C | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2015-536G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747167 | |||||||
| chr8:39747187 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2015-556G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747187 | |||||||
| chr8:39747384 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2015-753A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747384 | |||||||
| chr8:39747541 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2015-910C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747541 | |||||||
| chr8:39747561 | T | A | 1 | a0001c0001t0001g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2015-930A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747561 | |||||||
| chr8:39747594 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2015-963G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747594 | |||||||
| chr8:39747673 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2015-1042G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747673 | |||||||
| chr8:39747685 | T | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2015-1054A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747685 | |||||||
| chr8:39747905 | C | T | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2015-1274G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747905 | |||||||
| chr8:39747996 | T | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2014+1316A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39747996 | |||||||
| chr8:39748235 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
6 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2014+1077G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748235 | |||||||
| chr8:39748309 | G | C | 1 | a0007c0004t0001g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2014+1003C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748309 | |||||||
| chr8:39748437 | T | C | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2014+875A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748437 | |||||||
| chr8:39748669 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0229 |
3 | HG02818.hp1 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2014+643C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748669 | |||||||
| chr8:39748701 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0231 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2014+611C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39748701 | |||||||
| chr8:39749038 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.2014+274C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39749038 | |||||||
| chr8:39749176 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.2014+136G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39749176 | |||||||
| chr8:39749311 | C | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0141 |
2 | HG02922.hp1 NA19030.hp2 |
splice_donor_variant&intron_variant | HIGH | c.2014+1G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 18/20 | chr8 | 39749311 | |||||||
| chr8:39749584 | T | C | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1875+83A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749584 | |||||||
| chr8:39749585 | G | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1875+82C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749585 | |||||||
| chr8:39749586 | C | CATGT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
231 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1875+80_1875+81ins others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749586 | |||||||
| chr8:39749586 | C | T | 2 | a0001c0001t0001g0160 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1875+81G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749586 | |||||||
| chr8:39749608 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1875+59G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 17/20 | chr8 | 39749608 | |||||||
| chr8:39749778 | A | C | 3 | a0001c0007t0001g0066 a0001c0007t0001g0241 a0008c0010t0001g0023 |
3 | NA18992.hp1 NA19068.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1798-34T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39749778 | |||||||
| chr8:39749825 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1798-81T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39749825 | |||||||
| chr8:39750341 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1798-597A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750341 | |||||||
| chr8:39750424 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1798-680A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750424 | |||||||
| chr8:39750550 | T | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-806A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750550 | |||||||
| chr8:39750577 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1798-833G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750577 | |||||||
| chr8:39750755 | T | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0279 |
2 | HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1798-1011A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750755 | |||||||
| chr8:39750843 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
231 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1798-1099C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750843 | |||||||
| chr8:39750995 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1798-1251T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39750995 | |||||||
| chr8:39751112 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1798-1368G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751112 | |||||||
| chr8:39751203 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1798-1459A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751203 | |||||||
| chr8:39751291 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1798-1547A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751291 | |||||||
| chr8:39751423 | G | A | 14 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0051 others(11): Show |
14 | HG00621.hp1 HG02040.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1798-1679C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751423 | |||||||
| chr8:39751466 | G | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-1722C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751466 | |||||||
| chr8:39751497 | TTTTG | T | 9 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1798-1757_1798-175 others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751497 | |||||||
| chr8:39751513 | GT | G | 10 | a0001c0001t0001g0071 a0001c0001t0001g0106 a0001c0001t0001g0137 others(7): Show |
10 | HG00738.hp1 HG01069.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1798-1770delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751513 | |||||||
| chr8:39751620 | T | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
233 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1798-1876A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751620 | |||||||
| chr8:39751662 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1798-1918T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751662 | |||||||
| chr8:39751839 | CT | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-2096delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751839 | |||||||
| chr8:39751955 | C | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1798-2211G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39751955 | |||||||
| chr8:39752041 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
232 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1798-2297G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752041 | |||||||
| chr8:39752107 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02109.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1798-2363T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752107 | |||||||
| chr8:39752109 | T | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0236 a0001c0001t0001g0237 others(2): Show |
5 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1798-2365A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752109 | |||||||
| chr8:39752202 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1798-2458G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752202 | |||||||
| chr8:39752222 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0231 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1798-2478C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752222 | |||||||
| chr8:39752408 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1798-2664C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752408 | |||||||
| chr8:39752517 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0278 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1798-2773C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752517 | |||||||
| chr8:39752532 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1798-2788A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752532 | |||||||
| chr8:39752537 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1798-2793T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752537 | |||||||
| chr8:39752588 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1798-2844C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752588 | |||||||
| chr8:39752651 | G | C | 1 | a0001c0001t0001g0100 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1798-2907C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752651 | |||||||
| chr8:39752827 | T | C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797+2901A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39752827 | |||||||
| chr8:39753100 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1797+2628G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753100 | |||||||
| chr8:39753163 | G | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1797+2565C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753163 | |||||||
| chr8:39753196 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1797+2532C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753196 | |||||||
| chr8:39753286 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18961.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1797+2442G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753286 | |||||||
| chr8:39753426 | G | GA | 6 | a0001c0001t0001g0102 a0001c0001t0001g0125 a0001c0001t0001g0143 others(3): Show |
6 | HG01433.hp1 NA18906.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+2301dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753426 | |||||||
| chr8:39753426 | GA | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
33 | HG01255.hp1 HG01928.hp1 HG01978.hp2 others(30): Show |
intron_variant | MODIFIER | c.1797+2301delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753426 | |||||||
| chr8:39753439 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1797+2289G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753439 | |||||||
| chr8:39753662 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0155 others(8): Show |
12 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1797+2066A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753662 | |||||||
| chr8:39753752 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1797+1976C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753752 | |||||||
| chr8:39753812 | A | AAC | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1797+1914_1797+191 others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753812 | |||||||
| chr8:39753872 | A | T | 6 | a0001c0001t0001g0166 a0001c0001t0001g0177 a0001c0001t0001g0180 others(3): Show |
6 | HG00733.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+1856T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753872 | |||||||
| chr8:39753886 | G | A | 1 | a0006c0005t0001g0008 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1797+1842C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753886 | |||||||
| chr8:39753994 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1797+1734A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39753994 | |||||||
| chr8:39754034 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0035 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+1694T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754034 | |||||||
| chr8:39754464 | G | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
8 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1797+1264C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754464 | |||||||
| chr8:39754473 | C | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(147): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1797+1255G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754473 | |||||||
| chr8:39754484 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1797+1244T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754484 | |||||||
| chr8:39754664 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1797+1064T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754664 | |||||||
| chr8:39754804 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(147): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1797+924G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754804 | |||||||
| chr8:39754813 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(147): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1797+915T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754813 | |||||||
| chr8:39754897 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1797+831T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754897 | |||||||
| chr8:39754954 | A | C | 5 | a0001c0001t0001g0086 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | NA18949.hp2 NA19005.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797+774T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754954 | |||||||
| chr8:39754978 | G | A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0075 others(3): Show |
6 | HG00423.hp1 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797+750C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39754978 | |||||||
| chr8:39755013 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1797+715G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755013 | |||||||
| chr8:39755138 | T | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797+590A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755138 | |||||||
| chr8:39755249 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1797+479C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755249 | |||||||
| chr8:39755337 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1797+391A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755337 | |||||||
| chr8:39755448 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1797+280C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755448 | |||||||
| chr8:39755458 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1797+270G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755458 | |||||||
| chr8:39755524 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1797+204T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 16/20 | chr8 | 39755524 | |||||||
| chr8:39756032 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1614-121G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756032 | |||||||
| chr8:39756069 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1614-158C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756069 | |||||||
| chr8:39756134 | T | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(13): Show |
19 | HG02040.hp1 HG02080.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.1614-223A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756134 | |||||||
| chr8:39756142 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1614-231T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756142 | |||||||
| chr8:39756364 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1614-453A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756364 | |||||||
| chr8:39756366 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1614-455G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756366 | |||||||
| chr8:39756420 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614-509C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756420 | |||||||
| chr8:39756501 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1614-590G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756501 | |||||||
| chr8:39756659 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1614-748T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756659 | |||||||
| chr8:39756800 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
273 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1614-889T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756800 | |||||||
| chr8:39756902 | A | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
266 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1614-991T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756902 | |||||||
| chr8:39756924 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1614-1013G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39756924 | |||||||
| chr8:39757075 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1614-1164A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757075 | |||||||
| chr8:39757295 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614-1384T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757295 | |||||||
| chr8:39757352 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1614-1441A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757352 | |||||||
| chr8:39757646 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1614-1735T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757646 | |||||||
| chr8:39757777 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1614-1866C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39757777 | |||||||
| chr8:39758316 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1614-2405T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758316 | |||||||
| chr8:39758370 | T | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1614-2459A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758370 | |||||||
| chr8:39758573 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1613+2603A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758573 | |||||||
| chr8:39758575 | T | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(74): Show |
87 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1613+2601A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758575 | |||||||
| chr8:39758694 | A | C | 2 | a0002c0002t0001g0300 a0002c0002t0001g0301 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1613+2482T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758694 | |||||||
| chr8:39758784 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1613+2392C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39758784 | |||||||
| chr8:39759274 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1613+1902T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39759274 | |||||||
| chr8:39759933 | C | T | 1 | a0002c0002t0001g0298 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1613+1243G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39759933 | |||||||
| chr8:39760055 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1613+1121G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760055 | |||||||
| chr8:39760162 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1613+1014G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760162 | |||||||
| chr8:39760361 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0229 |
3 | HG02818.hp1 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1613+815G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760361 | |||||||
| chr8:39760363 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1613+813T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760363 | |||||||
| chr8:39760450 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1613+726C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760450 | |||||||
| chr8:39760549 | G | T | 1 | a0001c0001t0001g0268 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1613+627C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760549 | |||||||
| chr8:39760582 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1613+594C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760582 | |||||||
| chr8:39760698 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1613+478C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760698 | |||||||
| chr8:39760739 | T | TA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1613+436dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760739 | |||||||
| chr8:39760838 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1613+338C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760838 | |||||||
| chr8:39760846 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1613+330C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760846 | |||||||
| chr8:39760882 | C | CA | 35 | a0001c0001t0001g0011 a0001c0001t0001g0148 a0001c0001t0001g0149 others(32): Show |
37 | HG00544.hp2 HG01175.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1613+293dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | C | CAA | 10 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG00733.hp2 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1613+292_1613+293d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1613+284_1613+293d others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0015t0001g0221 |
3 | HG02145.hp2 HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1613+283_1613+293d others(13): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1613+279_1613+293d others(17): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | CA | C | 13 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0198 others(10): Show |
14 | HG01167.hp1 HG01167.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1613+293delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | CAA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0109 others(3): Show |
7 | HG01175.hp1 HG01952.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613+292_1613+293d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | CAAA | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1613+291_1613+293d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | CAAAA | C | 63 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 others(60): Show |
65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1613+290_1613+293d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | CAAAAA | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0043 others(4): Show |
9 | HG00323.hp1 HG02080.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1613+289_1613+293d others(7): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39760882 | CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613+282_1613+293d others(14): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39760882 | |||||||
| chr8:39761031 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1613+145C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39761031 | |||||||
| chr8:39761118 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1613+58C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | 39761118 | |||||||
| chr8:39761346 | C | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-65G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761346 | |||||||
| chr8:39761365 | G | T | 1 | a0002c0002t0001g0299 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1508-84C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761365 | |||||||
| chr8:39761402 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1508-121A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761402 | |||||||
| chr8:39761429 | A | G | 2 | a0001c0001t0001g0228 a0001c0001t0001g0231 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1508-148T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761429 | |||||||
| chr8:39761641 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-360A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761641 | |||||||
| chr8:39761927 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1508-646T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39761927 | |||||||
| chr8:39762058 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1508-777A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762058 | |||||||
| chr8:39762104 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-823G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762104 | |||||||
| chr8:39762496 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1508-1215T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762496 | |||||||
| chr8:39762568 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1508-1287A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762568 | |||||||
| chr8:39762759 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1508-1478C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762759 | |||||||
| chr8:39762910 | T | A | 1 | a0001c0001t0001g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1508-1629A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762910 | |||||||
| chr8:39762990 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0285 others(3): Show |
6 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1508-1709C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39762990 | |||||||
| chr8:39763099 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-1818C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763099 | |||||||
| chr8:39763142 | A | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1508-1861T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763142 | |||||||
| chr8:39763274 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1508-1993A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763274 | |||||||
| chr8:39763457 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1508-2176G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763457 | |||||||
| chr8:39763568 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1508-2287C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763568 | |||||||
| chr8:39763571 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1508-2290T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763571 | |||||||
| chr8:39763610 | C | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1508-2329G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763610 | |||||||
| chr8:39763791 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1508-2510C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763791 | |||||||
| chr8:39763881 | CAA | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1508-2602_1508-260 others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763881 | |||||||
| chr8:39763892 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(73): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1508-2611A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763892 | |||||||
| chr8:39763955 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1508-2674T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763955 | |||||||
| chr8:39763998 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1508-2717G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39763998 | |||||||
| chr8:39764042 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1508-2761A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764042 | |||||||
| chr8:39764045 | G | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(26): Show |
30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1508-2764C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764045 | |||||||
| chr8:39764130 | A | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | NA18959.hp2 NA19005.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507+2718T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764130 | |||||||
| chr8:39764148 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507+2700A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764148 | |||||||
| chr8:39764400 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+2448A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764400 | |||||||
| chr8:39764416 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0210 |
3 | HG01361.hp1 HG01433.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1507+2432T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764416 | |||||||
| chr8:39764456 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1507+2392G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764456 | |||||||
| chr8:39764655 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1507+2193C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764655 | |||||||
| chr8:39764754 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1507+2094C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764754 | |||||||
| chr8:39764921 | G | A | 1 | a0007c0004t0001g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1507+1927C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764921 | |||||||
| chr8:39764921 | G | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0144 |
2 | HG00408.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1507+1927C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764921 | |||||||
| chr8:39764992 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+1856G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764992 | |||||||
| chr8:39764998 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1507+1850C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39764998 | |||||||
| chr8:39765026 | A | AAAAT | 18 | a0001c0001t0001g0201 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
18 | HG00544.hp2 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1507+1818_1507+182 others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | |||||||
| chr8:39765026 | AAAAT | A | 37 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0027 others(34): Show |
38 | HG00621.hp1 HG00733.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1507+1818_1507+182 others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | |||||||
| chr8:39765026 | AAAATAAA others(1): Show |
A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1507+1814_1507+182 others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | |||||||
| chr8:39765026 | AAAATAAA others(5): Show |
A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(71): Show |
83 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1507+1810_1507+182 others(16): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | |||||||
| chr8:39765026 | AAAATAAA others(9): Show |
A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0074 a0001c0001t0001g0098 others(1): Show |
4 | HG02258.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507+1806_1507+182 others(20): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765026 | |||||||
| chr8:39765033 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1507+1815T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765033 | |||||||
| chr8:39765079 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1507+1769T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765079 | |||||||
| chr8:39765148 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1507+1700C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765148 | |||||||
| chr8:39765207 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1507+1641G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765207 | |||||||
| chr8:39765214 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
273 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1507+1634A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765214 | |||||||
| chr8:39765231 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(83): Show |
96 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1507+1617A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765231 | |||||||
| chr8:39765385 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1507+1463C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765385 | |||||||
| chr8:39765400 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1507+1448C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765400 | |||||||
| chr8:39765475 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1507+1373A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765475 | |||||||
| chr8:39765504 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1507+1344C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765504 | |||||||
| chr8:39765541 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1507+1307T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765541 | |||||||
| chr8:39765551 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(14): Show |
20 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1507+1297G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765551 | |||||||
| chr8:39765564 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1507+1284G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765564 | |||||||
| chr8:39765826 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1507+1022T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765826 | |||||||
| chr8:39765920 | GT | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+927delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39765920 | |||||||
| chr8:39766052 | C | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1507+796G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766052 | |||||||
| chr8:39766107 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0278 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1507+741A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766107 | |||||||
| chr8:39766268 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1507+580C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766268 | |||||||
| chr8:39766438 | CT | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(7): Show |
10 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1507+409delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766438 | |||||||
| chr8:39766490 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1507+358T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766490 | |||||||
| chr8:39766494 | C | A | 1 | a0002c0002t0001g0301 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1507+354G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766494 | |||||||
| chr8:39766551 | G | T | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1507+297C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766551 | |||||||
| chr8:39766805 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1507+43G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766805 | |||||||
| chr8:39766806 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1507+42T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766806 | |||||||
| chr8:39766807 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1507+41C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | 39766807 | |||||||
| chr8:39767133 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1311+20T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 13/20 | chr8 | 39767133 | |||||||
| chr8:39767328 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1213-77T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767328 | |||||||
| chr8:39767341 | T | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1213-90A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767341 | |||||||
| chr8:39767458 | G | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1213-207C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767458 | |||||||
| chr8:39767891 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1213-640A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767891 | |||||||
| chr8:39767896 | T | TCA | 12 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0138 others(9): Show |
14 | HG00423.hp1 HG01433.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1213-647_1213-646d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767896 | T | TCACA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(98): Show |
109 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1213-649_1213-646d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767896 | T | TCACACA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0029 others(30): Show |
35 | HG00140.hp2 HG00673.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1213-651_1213-646d others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767896 | T | TCACACAC others(1): Show |
13 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0155 others(10): Show |
13 | HG00621.hp1 HG00733.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1213-653_1213-646d others(10): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767896 | T | TCACACAC others(3): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0222 others(1): Show |
4 | HG00323.hp2 HG03453.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213-655_1213-646d others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767896 | T | TCACACAC others(7): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0176 a0001c0001t0001g0232 others(1): Show |
4 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-659_1213-646d others(16): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767896 | TCA | T | 37 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(34): Show |
37 | HG00733.hp2 HG01192.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1213-647_1213-646d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767896 | |||||||
| chr8:39767914 | A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1213-664_1213-663i others(12): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39767914 | |||||||
| chr8:39768020 | T | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-769A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768020 | |||||||
| chr8:39768161 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1213-910A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768161 | |||||||
| chr8:39768260 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-1009G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768260 | |||||||
| chr8:39768320 | G | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1213-1069C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768320 | |||||||
| chr8:39768560 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1212+832C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768560 | |||||||
| chr8:39768787 | A | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+605T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768787 | |||||||
| chr8:39768900 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1212+492T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39768900 | |||||||
| chr8:39769072 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0294 |
2 | HG03540.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1212+320C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39769072 | |||||||
| chr8:39769135 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1212+257T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39769135 | |||||||
| chr8:39769300 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1212+92A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | 39769300 | |||||||
| chr8:39769624 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1029-49A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769624 | |||||||
| chr8:39769722 | T | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029-147A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769722 | |||||||
| chr8:39769848 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1029-273C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769848 | |||||||
| chr8:39769943 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0165 others(3): Show |
8 | HG00738.hp2 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-368G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769943 | |||||||
| chr8:39769950 | C | CT | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
234 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1029-376dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39769950 | |||||||
| chr8:39770040 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(26): Show |
30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1029-465C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770040 | |||||||
| chr8:39770094 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-519G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770094 | |||||||
| chr8:39770190 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1029-615C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770190 | |||||||
| chr8:39770356 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029-781G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770356 | |||||||
| chr8:39770361 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1029-786A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770361 | |||||||
| chr8:39770372 | C | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1029-797G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770372 | |||||||
| chr8:39770638 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1063C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770638 | |||||||
| chr8:39770670 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1029-1095G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770670 | |||||||
| chr8:39770687 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1029-1112T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770687 | |||||||
| chr8:39770855 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1280G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39770855 | |||||||
| chr8:39771062 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1029-1487C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771062 | |||||||
| chr8:39771171 | G | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
244 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1029-1596C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771171 | |||||||
| chr8:39771182 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-1607G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771182 | |||||||
| chr8:39771219 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0285 others(3): Show |
6 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029-1644C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771219 | |||||||
| chr8:39771344 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-1769C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771344 | |||||||
| chr8:39771467 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1029-1892A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771467 | |||||||
| chr8:39771537 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1029-1962A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771537 | |||||||
| chr8:39771549 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1029-1974A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771549 | |||||||
| chr8:39771648 | G | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1029-2073C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39771648 | |||||||
| chr8:39772039 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1029-2464C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772039 | |||||||
| chr8:39772109 | T | TA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1029-2535dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772109 | |||||||
| chr8:39772220 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0205 |
2 | HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1029-2645G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772220 | |||||||
| chr8:39772231 | C | CT | 15 | a0001c0001t0001g0025 a0001c0001t0001g0149 a0001c0001t0001g0150 others(12): Show |
15 | HG01167.hp1 HG02040.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029-2657dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772231 | |||||||
| chr8:39772239 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1029-2664A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772239 | |||||||
| chr8:39772291 | T | C | 17 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(14): Show |
17 | HG00733.hp2 HG01891.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1029-2716A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772291 | |||||||
| chr8:39772324 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1029-2749G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772324 | |||||||
| chr8:39772530 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029-2955C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772530 | |||||||
| chr8:39772732 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1029-3157C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772732 | |||||||
| chr8:39772741 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1029-3166A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772741 | |||||||
| chr8:39772754 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1029-3179A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772754 | |||||||
| chr8:39772777 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1029-3202C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772777 | |||||||
| chr8:39772980 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1029-3405C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39772980 | |||||||
| chr8:39773031 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1029-3456G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773031 | |||||||
| chr8:39773043 | C | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-3468G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773043 | |||||||
| chr8:39773091 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1029-3516C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773091 | |||||||
| chr8:39773263 | C | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1029-3688G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773263 | |||||||
| chr8:39773484 | A | C | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028+3541T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773484 | |||||||
| chr8:39773859 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1028+3166G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773859 | |||||||
| chr8:39773884 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1028+3141A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39773884 | |||||||
| chr8:39774047 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1028+2978G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774047 | |||||||
| chr8:39774430 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1028+2595C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774430 | |||||||
| chr8:39774446 | T | C | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01243.hp2 HG03491.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1028+2579A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774446 | |||||||
| chr8:39774493 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1028+2532T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774493 | |||||||
| chr8:39774496 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0124 |
2 | NA18953.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1028+2529A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774496 | |||||||
| chr8:39774529 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1028+2496T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774529 | |||||||
| chr8:39774693 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1028+2332T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774693 | |||||||
| chr8:39774789 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1028+2236T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774789 | |||||||
| chr8:39774831 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028+2194T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774831 | |||||||
| chr8:39774923 | T | G | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1028+2102A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39774923 | |||||||
| chr8:39775007 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0271 |
3 | HG00738.hp1 HG01361.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1028+2018C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775007 | |||||||
| chr8:39775021 | C | G | 8 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0105 others(5): Show |
8 | HG02135.hp1 NA18969.hp2 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+2004G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775021 | |||||||
| chr8:39775138 | C | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(26): Show |
30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1028+1887G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775138 | |||||||
| chr8:39775249 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0165 others(3): Show |
8 | HG00738.hp2 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+1776G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775249 | |||||||
| chr8:39775576 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1028+1449T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775576 | |||||||
| chr8:39775803 | T | C | 1 | a0007c0004t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1028+1222A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775803 | |||||||
| chr8:39775990 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(143): Show |
155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1028+1035T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39775990 | |||||||
| chr8:39776346 | A | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0114 a0005c0009t0001g0009 |
4 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028+679T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776346 | |||||||
| chr8:39776438 | A | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1028+587T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776438 | |||||||
| chr8:39776446 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1028+579G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776446 | |||||||
| chr8:39776448 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1028+577C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776448 | |||||||
| chr8:39776449 | G | T | 6 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0002c0002t0001g0298 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028+576C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776449 | |||||||
| chr8:39776495 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1028+530C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776495 | |||||||
| chr8:39776511 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1028+514A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776511 | |||||||
| chr8:39776727 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1028+298C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776727 | |||||||
| chr8:39776744 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1028+281C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 11/20 | chr8 | 39776744 | |||||||
| chr8:39777240 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0231 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.892-79G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777240 | |||||||
| chr8:39777362 | A | T | 1 | a0002c0002t0001g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.892-201T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777362 | |||||||
| chr8:39777398 | T | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-237A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777398 | |||||||
| chr8:39777490 | A | G | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.892-329T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777490 | |||||||
| chr8:39777643 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.892-482T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777643 | |||||||
| chr8:39777659 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.892-498T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777659 | |||||||
| chr8:39777771 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.892-610C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777771 | |||||||
| chr8:39777988 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.892-827C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39777988 | |||||||
| chr8:39778030 | A | G | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-869T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778030 | |||||||
| chr8:39778189 | T | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.892-1028A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778189 | |||||||
| chr8:39778403 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.892-1242T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778403 | |||||||
| chr8:39778655 | G | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1494C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778655 | |||||||
| chr8:39778686 | A | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.892-1525T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778686 | |||||||
| chr8:39778766 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.892-1605T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778766 | |||||||
| chr8:39778802 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.892-1641T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778802 | |||||||
| chr8:39778822 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.892-1661A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778822 | |||||||
| chr8:39778949 | A | T | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.892-1788T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778949 | |||||||
| chr8:39778989 | G | A | 1 | a0002c0002t0001g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.892-1828C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39778989 | |||||||
| chr8:39779068 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.892-1907A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779068 | |||||||
| chr8:39779204 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.892-2043G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779204 | |||||||
| chr8:39779297 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.892-2136G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779297 | |||||||
| chr8:39779344 | C | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.892-2183G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779344 | |||||||
| chr8:39779578 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.892-2417C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779578 | |||||||
| chr8:39779895 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0196 |
3 | HG01261.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.892-2734G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39779895 | |||||||
| chr8:39780160 | C | T | 2 | a0001c0001t0001g0081 a0009c0016t0001g0289 |
2 | HG01884.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.892-2999G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780160 | |||||||
| chr8:39780194 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.892-3033C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780194 | |||||||
| chr8:39780276 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.892-3115G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780276 | |||||||
| chr8:39780547 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0144 |
2 | HG00408.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.892-3386G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780547 | |||||||
| chr8:39780783 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.892-3622G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780783 | |||||||
| chr8:39780898 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.892-3737G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780898 | |||||||
| chr8:39780927 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.892-3766C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780927 | |||||||
| chr8:39780988 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(3): Show |
9 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-3827A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780988 | |||||||
| chr8:39780996 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.892-3835G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39780996 | |||||||
| chr8:39781012 | CT | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0134 others(5): Show |
8 | HG02451.hp1 HG02886.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-3852delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781012 | |||||||
| chr8:39781069 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.892-3908G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781069 | |||||||
| chr8:39781190 | T | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-4029A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781190 | |||||||
| chr8:39781225 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(117): Show |
129 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.892-4064A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781225 | |||||||
| chr8:39781269 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.892-4108C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781269 | |||||||
| chr8:39781278 | TGTG | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-4120_892-4118d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781278 | |||||||
| chr8:39781288 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.892-4127A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781288 | |||||||
| chr8:39781290 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.892-4129G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781290 | |||||||
| chr8:39781291 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-4130C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781291 | |||||||
| chr8:39781506 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.892-4345C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781506 | |||||||
| chr8:39781637 | T | A | 1 | a0001c0001t0001g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.892-4476A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781637 | |||||||
| chr8:39781892 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(147): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.892-4731T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781892 | |||||||
| chr8:39781923 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.892-4762C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39781923 | |||||||
| chr8:39782186 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG00735.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.891+4788C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782186 | |||||||
| chr8:39782305 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.891+4669A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782305 | |||||||
| chr8:39782369 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.891+4605T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782369 | |||||||
| chr8:39782705 | G | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+4269C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782705 | |||||||
| chr8:39782805 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.891+4169A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782805 | |||||||
| chr8:39782958 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(3): Show |
9 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+4016T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39782958 | |||||||
| chr8:39783332 | A | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(61): Show |
68 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.891+3642T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783332 | |||||||
| chr8:39783349 | T | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0034 others(3): Show |
6 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+3625A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783349 | |||||||
| chr8:39783389 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.891+3585A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783389 | |||||||
| chr8:39783670 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.891+3304C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783670 | |||||||
| chr8:39783701 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+3273G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783701 | |||||||
| chr8:39783820 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+3154G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783820 | |||||||
| chr8:39783899 | C | T | 2 | a0001c0001t0001g0068 a0005c0009t0001g0009 |
3 | HG00735.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.891+3075G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783899 | |||||||
| chr8:39783931 | C | T | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.891+3043G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783931 | |||||||
| chr8:39783950 | G | GA | 77 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(74): Show |
87 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.891+3023dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39783950 | |||||||
| chr8:39784101 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): Show |
18 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.891+2873G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784101 | |||||||
| chr8:39784401 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.891+2573C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784401 | |||||||
| chr8:39784600 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.891+2374C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784600 | |||||||
| chr8:39784848 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.891+2126A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784848 | |||||||
| chr8:39784925 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.891+2049A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39784925 | |||||||
| chr8:39785003 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.891+1971C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785003 | |||||||
| chr8:39785159 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.891+1815G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785159 | |||||||
| chr8:39785165 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.891+1809C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785165 | |||||||
| chr8:39785206 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0202 a0001c0001t0001g0215 others(1): Show |
5 | HG00544.hp1 NA19003.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1768G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785206 | |||||||
| chr8:39785289 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.891+1685C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785289 | |||||||
| chr8:39785380 | G | A | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+1594C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785380 | |||||||
| chr8:39785405 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+1569A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785405 | |||||||
| chr8:39785426 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.891+1548T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785426 | |||||||
| chr8:39785443 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.891+1531C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785443 | |||||||
| chr8:39785449 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.891+1525G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785449 | |||||||
| chr8:39785745 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.891+1229G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785745 | |||||||
| chr8:39785754 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.891+1220C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785754 | |||||||
| chr8:39785796 | T | TAAA | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+1175_891+1177d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785796 | |||||||
| chr8:39785796 | TA | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(142): Show |
153 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.891+1177delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785796 | |||||||
| chr8:39785796 | TAAA | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0155 others(7): Show |
11 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1175_891+1177d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785796 | |||||||
| chr8:39785920 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.891+1054G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785920 | |||||||
| chr8:39785935 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.891+1039C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785935 | |||||||
| chr8:39785983 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.891+991A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39785983 | |||||||
| chr8:39786133 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.891+841T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786133 | |||||||
| chr8:39786230 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.891+744G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786230 | |||||||
| chr8:39786287 | A | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0170 a0001c0001t0001g0185 others(1): Show |
4 | HG00423.hp2 HG00673.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+687T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786287 | |||||||
| chr8:39786301 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+673C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786301 | |||||||
| chr8:39786341 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.891+633A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786341 | |||||||
| chr8:39786348 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.891+626A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786348 | |||||||
| chr8:39786526 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.891+448G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786526 | |||||||
| chr8:39786564 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0074 a0001c0001t0001g0098 others(1): Show |
4 | HG02258.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+410G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786564 | |||||||
| chr8:39786583 | C | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0271 |
3 | HG00738.hp1 HG01361.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.891+391G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786583 | |||||||
| chr8:39786595 | T | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.891+379A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786595 | |||||||
| chr8:39786673 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0297 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.891+301G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786673 | |||||||
| chr8:39786712 | A | G | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.891+262T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786712 | |||||||
| chr8:39786716 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.891+258G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786716 | |||||||
| chr8:39786753 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.891+221G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 10/20 | chr8 | 39786753 | |||||||
| chr8:39787172 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.810-117G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787172 | |||||||
| chr8:39787264 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.810-209T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787264 | |||||||
| chr8:39787295 | A | T | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.810-240T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787295 | |||||||
| chr8:39787387 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.810-332C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787387 | |||||||
| chr8:39787414 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.810-359A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787414 | |||||||
| chr8:39787436 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.810-381T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787436 | |||||||
| chr8:39787453 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.810-398C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787453 | |||||||
| chr8:39787531 | A | ACT | 3 | a0001c0001t0001g0065 a0001c0001t0001g0291 a0001c0015t0001g0221 |
3 | HG01978.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.810-478_810-477dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787531 | |||||||
| chr8:39787542 | C | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0176 others(8): Show |
12 | HG00408.hp2 HG01070.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.810-487G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787542 | |||||||
| chr8:39787542 | C | CTA | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-489_810-488dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787542 | |||||||
| chr8:39787542 | CTA | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.810-489_810-488del others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787542 | |||||||
| chr8:39787544 | A | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(163): Show |
177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.810-489T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787544 | |||||||
| chr8:39787546 | A | C | 8 | a0001c0001t0001g0087 a0001c0001t0001g0120 a0001c0001t0001g0225 others(5): Show |
8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.810-491T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787546 | |||||||
| chr8:39787557 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810-502G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787557 | |||||||
| chr8:39787581 | ATG | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
262 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.809+502_809+503del others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787581 | |||||||
| chr8:39787583 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.809+502C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787583 | |||||||
| chr8:39787732 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0292 |
2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.809+353T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787732 | |||||||
| chr8:39787870 | G | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.809+215C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787870 | |||||||
| chr8:39787925 | A | G | 1 | a0002c0002t0001g0298 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.809+160T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787925 | |||||||
| chr8:39787944 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.809+141G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787944 | |||||||
| chr8:39787975 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.809+110C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787975 | |||||||
| chr8:39787977 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.809+108C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39787977 | |||||||
| chr8:39788036 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.809+49C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39788036 | |||||||
| chr8:39788053 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.809+32T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | 39788053 | |||||||
| chr8:39788567 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.642+102G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 8/20 | chr8 | 39788567 | |||||||
| chr8:39788742 | T | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0200 a0001c0001t0001g0205 |
3 | HG03239.hp2 NA19030.hp1 NA21309.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.571-2A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39788742 | |||||||
| chr8:39789049 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-309C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789049 | |||||||
| chr8:39789410 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0176 a0001c0001t0001g0232 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-670G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789410 | |||||||
| chr8:39789462 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0200 a0001c0001t0001g0205 |
3 | HG03239.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.571-722C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789462 | |||||||
| chr8:39789808 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.571-1068C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789808 | |||||||
| chr8:39789889 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-1149T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789889 | |||||||
| chr8:39789926 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.571-1186G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789926 | |||||||
| chr8:39789927 | A | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-1187T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39789927 | |||||||
| chr8:39790133 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-1393G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790133 | |||||||
| chr8:39790317 | T | G | 1 | a0001c0001t0002g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.571-1577A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790317 | |||||||
| chr8:39790320 | G | A | 1 | a0012c0013t0001g0037 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.571-1580C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790320 | |||||||
| chr8:39790369 | C | T | 1 | a0006c0005t0001g0008 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.571-1629G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790369 | |||||||
| chr8:39790399 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571-1659G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790399 | |||||||
| chr8:39790400 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18961.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.571-1660C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790400 | |||||||
| chr8:39790483 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.571-1743A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790483 | |||||||
| chr8:39790544 | G | A | 2 | a0002c0002t0001g0300 a0002c0002t0001g0301 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.571-1804C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790544 | |||||||
| chr8:39790549 | T | A | 1 | a0001c0001t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.571-1809A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790549 | |||||||
| chr8:39790549 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.571-1809A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790549 | |||||||
| chr8:39790586 | T | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0204 |
2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.571-1846A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790586 | |||||||
| chr8:39790698 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-1958G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790698 | |||||||
| chr8:39790789 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18949.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.571-2049A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790789 | |||||||
| chr8:39790923 | C | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-2183G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39790923 | |||||||
| chr8:39791085 | C | T | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.571-2345G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791085 | |||||||
| chr8:39791352 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.571-2612A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791352 | |||||||
| chr8:39791518 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-2778T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791518 | |||||||
| chr8:39791665 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.571-2925C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791665 | |||||||
| chr8:39791866 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.571-3126C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791866 | |||||||
| chr8:39791928 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3188G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39791928 | |||||||
| chr8:39792112 | C | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-3372G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792112 | |||||||
| chr8:39792143 | C | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-3403G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792143 | |||||||
| chr8:39792286 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.571-3546C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792286 | |||||||
| chr8:39792288 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-3548C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792288 | |||||||
| chr8:39792520 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.571-3780C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792520 | |||||||
| chr8:39792528 | C | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3788G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792528 | |||||||
| chr8:39792709 | C | CA | 5 | a0001c0001t0001g0019 a0001c0001t0001g0245 a0001c0001t0001g0268 others(2): Show |
6 | HG02129.hp2 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-3970dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792709 | |||||||
| chr8:39792750 | T | C | 2 | a0003c0003t0001g0012 a0003c0003t0001g0171 |
3 | NA18998.hp2 NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.571-4010A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792750 | |||||||
| chr8:39792768 | G | A | 3 | a0001c0001t0001g0067 a0001c0007t0001g0066 a0001c0007t0001g0241 |
3 | NA18992.hp2 NA19068.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.571-4028C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792768 | |||||||
| chr8:39792837 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.571-4097A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39792837 | |||||||
| chr8:39793046 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-4306G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793046 | |||||||
| chr8:39793144 | T | G | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.571-4404A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793144 | |||||||
| chr8:39793212 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.571-4472C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793212 | |||||||
| chr8:39793229 | T | C | 2 | a0002c0002t0001g0303 a0002c0002t0001g0304 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-4489A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793229 | |||||||
| chr8:39793250 | C | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-4510G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793250 | |||||||
| chr8:39793313 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.571-4573C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793313 | |||||||
| chr8:39793322 | T | TAAGAAAT others(358): Show |
1 | a0001c0001t0001g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.571-4583_571-4582i others(367): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793322 | |||||||
| chr8:39793421 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-4681T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793421 | |||||||
| chr8:39793682 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.571-4942G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793682 | |||||||
| chr8:39793829 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | NA18959.hp2 NA19005.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-5089T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793829 | |||||||
| chr8:39793861 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-5121G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793861 | |||||||
| chr8:39793968 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0042 others(21): Show |
26 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-5228G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39793968 | |||||||
| chr8:39794031 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.571-5291T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794031 | |||||||
| chr8:39794283 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571-5543A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794283 | |||||||
| chr8:39794422 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-5682C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794422 | |||||||
| chr8:39794452 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0020 others(57): Show |
64 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.571-5712G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794452 | |||||||
| chr8:39794701 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571-5961G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794701 | |||||||
| chr8:39794740 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.571-6000G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794740 | |||||||
| chr8:39794883 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-6143A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39794883 | |||||||
| chr8:39795411 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.571-6671A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795411 | |||||||
| chr8:39795441 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.571-6701T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795441 | |||||||
| chr8:39795543 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-6803G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795543 | |||||||
| chr8:39795717 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6977A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795717 | |||||||
| chr8:39795718 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6978C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795718 | |||||||
| chr8:39795719 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6979A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795719 | |||||||
| chr8:39795721 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0219 |
2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.571-6981G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795721 | |||||||
| chr8:39795723 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6983A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795723 | |||||||
| chr8:39795726 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6986G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795726 | |||||||
| chr8:39795727 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6987G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795727 | |||||||
| chr8:39795729 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-6989A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795729 | |||||||
| chr8:39795836 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571-7096T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795836 | |||||||
| chr8:39795887 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.571-7147A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39795887 | |||||||
| chr8:39796064 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.571-7324A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796064 | |||||||
| chr8:39796081 | TA | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-7342delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796081 | |||||||
| chr8:39796099 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.571-7359G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796099 | |||||||
| chr8:39796254 | A | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-7514T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796254 | |||||||
| chr8:39796492 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571-7752G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796492 | |||||||
| chr8:39796671 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.571-7931C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796671 | |||||||
| chr8:39796679 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
265 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.571-7939G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796679 | |||||||
| chr8:39796787 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.571-8047A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796787 | |||||||
| chr8:39796811 | T | C | 12 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(9): Show |
12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-8071A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796811 | |||||||
| chr8:39796992 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.571-8252C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39796992 | |||||||
| chr8:39797008 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.571-8268G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797008 | |||||||
| chr8:39797029 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-8289G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797029 | |||||||
| chr8:39797071 | T | G | 5 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG01109.hp2 HG01255.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-8331A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797071 | |||||||
| chr8:39797087 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-8347T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797087 | |||||||
| chr8:39797153 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.571-8413C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797153 | |||||||
| chr8:39797330 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.571-8590C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797330 | |||||||
| chr8:39797422 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.571-8682G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797422 | |||||||
| chr8:39797523 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(78): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.571-8783G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797523 | |||||||
| chr8:39797638 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.571-8898G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797638 | |||||||
| chr8:39797749 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(78): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.571-9009A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797749 | |||||||
| chr8:39797884 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-9144A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797884 | |||||||
| chr8:39797950 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(3): Show |
9 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-9210C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39797950 | |||||||
| chr8:39798015 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-9275A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798015 | |||||||
| chr8:39798434 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.571-9694C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798434 | |||||||
| chr8:39798604 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-9864T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798604 | |||||||
| chr8:39798688 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0143 |
3 | NA18987.hp1 NA19007.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.571-9948T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798688 | |||||||
| chr8:39798853 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-10113C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798853 | |||||||
| chr8:39798889 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.571-10149G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39798889 | |||||||
| chr8:39799005 | AT | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.571-10266delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799005 | |||||||
| chr8:39799020 | T | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-10280A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799020 | |||||||
| chr8:39799176 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.570+10234C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799176 | |||||||
| chr8:39799630 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+9780C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799630 | |||||||
| chr8:39799707 | C | G | 1 | a0002c0002t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+9703G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799707 | |||||||
| chr8:39799719 | T | C | 5 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0152 others(2): Show |
5 | HG02148.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+9691A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799719 | |||||||
| chr8:39799780 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+9630G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799780 | |||||||
| chr8:39799936 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+9474C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39799936 | |||||||
| chr8:39800040 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.570+9370A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800040 | |||||||
| chr8:39800078 | TG | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+9331delC | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800078 | |||||||
| chr8:39800265 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0042 |
2 | HG02148.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.570+9145T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800265 | |||||||
| chr8:39800384 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.570+9026A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800384 | |||||||
| chr8:39800497 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.570+8913A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800497 | |||||||
| chr8:39800641 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+8769G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800641 | |||||||
| chr8:39800810 | C | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(89): Show |
102 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.570+8600G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800810 | |||||||
| chr8:39800823 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+8587C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800823 | |||||||
| chr8:39800824 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+8586T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39800824 | |||||||
| chr8:39801024 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.570+8386T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801024 | |||||||
| chr8:39801118 | T | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.570+8292A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801118 | |||||||
| chr8:39801585 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+7825C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801585 | |||||||
| chr8:39801653 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0042 others(21): Show |
26 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+7757C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801653 | |||||||
| chr8:39801773 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+7637C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39801773 | |||||||
| chr8:39802022 | G | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.570+7388C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802022 | |||||||
| chr8:39802112 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.570+7298G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802112 | |||||||
| chr8:39802175 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0231 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.570+7235A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802175 | |||||||
| chr8:39802182 | C | G | 2 | a0001c0001t0001g0228 a0001c0001t0001g0231 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.570+7228G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802182 | |||||||
| chr8:39802240 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0278 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.570+7170G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802240 | |||||||
| chr8:39802263 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+7147G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802263 | |||||||
| chr8:39802311 | G | A | 10 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+7099C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802311 | |||||||
| chr8:39802359 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.570+7051A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802359 | |||||||
| chr8:39802428 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+6982C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802428 | |||||||
| chr8:39802435 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+6975G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802435 | |||||||
| chr8:39802438 | C | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0276 |
2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.570+6972G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802438 | |||||||
| chr8:39802511 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.570+6899C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802511 | |||||||
| chr8:39802529 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
267 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.570+6881A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802529 | |||||||
| chr8:39802749 | T | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.570+6661A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802749 | |||||||
| chr8:39802964 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.570+6446C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39802964 | |||||||
| chr8:39803063 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0167 a0001c0001t0001g0250 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+6347T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803063 | |||||||
| chr8:39803076 | T | C | 1 | a0012c0013t0001g0037 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.570+6334A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803076 | |||||||
| chr8:39803109 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG01081.hp1 HG02486.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.570+6301C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803109 | |||||||
| chr8:39803160 | T | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG01496.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.570+6250A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803160 | |||||||
| chr8:39803227 | G | A | 1 | a0005c0009t0001g0009 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.570+6183C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803227 | |||||||
| chr8:39803409 | G | C | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+6001C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803409 | |||||||
| chr8:39803454 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+5956G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803454 | |||||||
| chr8:39803455 | G | T | 11 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(8): Show |
11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+5955C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803455 | |||||||
| chr8:39803505 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.570+5905G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803505 | |||||||
| chr8:39803554 | A | T | 17 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(14): Show |
17 | HG00733.hp2 HG01891.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.570+5856T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803554 | |||||||
| chr8:39803670 | G | A | 20 | a0001c0001t0001g0071 a0001c0001t0001g0169 a0001c0001t0001g0200 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+5740C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803670 | |||||||
| chr8:39803743 | T | C | 1 | a0001c0020t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.570+5667A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803743 | |||||||
| chr8:39803987 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.570+5423C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39803987 | |||||||
| chr8:39804002 | A | G | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0015t0001g0221 others(1): Show |
4 | HG01884.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+5408T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804002 | |||||||
| chr8:39804169 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0257 a0008c0010t0001g0023 others(1): Show |
4 | HG00621.hp2 NA18992.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+5241G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804169 | |||||||
| chr8:39804249 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.570+5161A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804249 | |||||||
| chr8:39804338 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.570+5072G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804338 | |||||||
| chr8:39804382 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(6): Show |
9 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+5028G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804382 | |||||||
| chr8:39804423 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.570+4987T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804423 | |||||||
| chr8:39804920 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.570+4490A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804920 | |||||||
| chr8:39804921 | G | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.570+4489C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39804921 | |||||||
| chr8:39805009 | T | C | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0015t0001g0221 others(1): Show |
4 | HG01884.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+4401A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805009 | |||||||
| chr8:39805420 | C | A | 1 | a0003c0003t0001g0171 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.570+3990G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805420 | |||||||
| chr8:39805439 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570+3971C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805439 | |||||||
| chr8:39805551 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.570+3859T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805551 | |||||||
| chr8:39805642 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+3768T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39805642 | |||||||
| chr8:39806045 | G | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570+3365C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806045 | |||||||
| chr8:39806139 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.570+3271A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806139 | |||||||
| chr8:39806585 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.570+2825C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806585 | |||||||
| chr8:39806678 | C | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | NA18949.hp2 NA19010.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2732G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806678 | |||||||
| chr8:39806683 | C | A | 1 | a0001c0001t0001g0266 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570+2727G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39806683 | |||||||
| chr8:39807077 | C | T | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+2333G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807077 | |||||||
| chr8:39807177 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+2233C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807177 | |||||||
| chr8:39807260 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.570+2150T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807260 | |||||||
| chr8:39807428 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.570+1982C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807428 | |||||||
| chr8:39807874 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0219 |
2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.570+1536T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807874 | |||||||
| chr8:39807947 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.570+1463A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39807947 | |||||||
| chr8:39808108 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.570+1302T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808108 | |||||||
| chr8:39808122 | T | A | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+1288A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808122 | |||||||
| chr8:39808189 | T | TAC | 45 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0063 others(42): Show |
48 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.570+1219_570+1220d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808189 | T | TACAC | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
162 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.570+1217_570+1220d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808189 | T | TACACAC | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0026 others(8): Show |
13 | HG01496.hp1 HG02148.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.570+1215_570+1220d others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808189 | TAC | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0290 a0001c0001t0001g0294 others(2): Show |
5 | HG02809.hp1 HG02886.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1219_570+1220d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808189 | TACAC | T | 6 | a0001c0001t0001g0176 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
6 | HG01167.hp1 HG02055.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+1217_570+1220d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808189 | TACACAC | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0002c0002t0001g0300 |
3 | HG02109.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.570+1215_570+1220d others(8): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808189 | TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0059 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.570+1199_570+1220d others(24): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808189 | |||||||
| chr8:39808467 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.570+943C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808467 | |||||||
| chr8:39808634 | T | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+776A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808634 | |||||||
| chr8:39808683 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.570+727G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808683 | |||||||
| chr8:39808731 | T | C | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+679A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808731 | |||||||
| chr8:39808847 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.570+563G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808847 | |||||||
| chr8:39808848 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.570+562C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808848 | |||||||
| chr8:39808903 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.570+507C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808903 | |||||||
| chr8:39808982 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.570+428G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39808982 | |||||||
| chr8:39809080 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(73): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.570+330T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809080 | |||||||
| chr8:39809110 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.570+300T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809110 | |||||||
| chr8:39809111 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+299C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809111 | |||||||
| chr8:39809133 | T | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570+277A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | 39809133 | |||||||
| chr8:39809879 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.514-413C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39809879 | |||||||
| chr8:39809913 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0259 a0001c0001t0001g0296 |
4 | NA18991.hp1 NA19058.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-447T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39809913 | |||||||
| chr8:39810040 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.514-574A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810040 | |||||||
| chr8:39810261 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-795T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810261 | |||||||
| chr8:39810500 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0170 others(7): Show |
11 | HG00423.hp2 HG00673.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-1034G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810500 | |||||||
| chr8:39810522 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.514-1056T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810522 | |||||||
| chr8:39810900 | C | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0001c0001t0001g0250 others(1): Show |
4 | HG02109.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1434G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39810900 | |||||||
| chr8:39811101 | G | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.514-1635C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811101 | |||||||
| chr8:39811151 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.514-1685A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811151 | |||||||
| chr8:39811641 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.514-2175C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811641 | |||||||
| chr8:39811693 | C | A | 11 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0001g0084 others(8): Show |
11 | HG00621.hp2 NA18949.hp2 NA18992.hp1 others(8): Show |
intron_variant | MODIFIER | c.514-2227G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811693 | |||||||
| chr8:39811729 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0045 others(33): Show |
38 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.514-2263C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811729 | |||||||
| chr8:39811862 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.514-2396A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811862 | |||||||
| chr8:39811884 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.514-2418G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811884 | |||||||
| chr8:39811940 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.514-2474T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811940 | |||||||
| chr8:39811966 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-2500A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811966 | |||||||
| chr8:39811988 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.514-2522C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39811988 | |||||||
| chr8:39812074 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-2608C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812074 | |||||||
| chr8:39812238 | AAGG | A | 6 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG01167.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-2775_514-2773d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812238 | |||||||
| chr8:39812316 | GGAAGAAT others(7): Show |
G | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.514-2864_514-2851d others(16): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812316 | |||||||
| chr8:39812345 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2879T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812345 | |||||||
| chr8:39812392 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.514-2926A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812392 | |||||||
| chr8:39812439 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0114 a0005c0009t0001g0009 |
4 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2973A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812439 | |||||||
| chr8:39812457 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | NA19002.hp2 NA19054.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.514-2991G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812457 | |||||||
| chr8:39812463 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.514-2997C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812463 | |||||||
| chr8:39812620 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.514-3154G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812620 | |||||||
| chr8:39812648 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.514-3182G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812648 | |||||||
| chr8:39812809 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(103): Show |
117 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.514-3343C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812809 | |||||||
| chr8:39812825 | AAC | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG00558.hp2 HG00597.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-3361_514-3360d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812825 | |||||||
| chr8:39812924 | C | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-3458G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812924 | |||||||
| chr8:39812981 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.514-3515G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812981 | |||||||
| chr8:39812988 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
5 | NA18954.hp2 NA18962.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-3522A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39812988 | |||||||
| chr8:39813081 | C | G | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.514-3615G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813081 | |||||||
| chr8:39813100 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.514-3634C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813100 | |||||||
| chr8:39813164 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.514-3698T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813164 | |||||||
| chr8:39813174 | C | T | 1 | a0002c0002t0001g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.514-3708G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813174 | |||||||
| chr8:39813315 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.514-3849C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813315 | |||||||
| chr8:39813700 | C | G | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.514-4234G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813700 | |||||||
| chr8:39813732 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.514-4266C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813732 | |||||||
| chr8:39813782 | C | T | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.514-4316G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813782 | |||||||
| chr8:39813832 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-4366C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813832 | |||||||
| chr8:39813903 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.514-4437T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39813903 | |||||||
| chr8:39814084 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.514-4618C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814084 | |||||||
| chr8:39814093 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0167 a0001c0001t0001g0176 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-4627G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814093 | |||||||
| chr8:39814119 | A | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(7): Show |
10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.514-4653T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814119 | |||||||
| chr8:39814146 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.514-4680G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814146 | |||||||
| chr8:39814407 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0071 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.514-4941T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814407 | |||||||
| chr8:39814467 | T | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0053 others(2): Show |
7 | NA18983.hp2 NA18987.hp1 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-5001A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814467 | |||||||
| chr8:39814927 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.514-5461T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39814927 | |||||||
| chr8:39815178 | G | A | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(7): Show |
10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.514-5712C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815178 | |||||||
| chr8:39815358 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.513+5644A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815358 | |||||||
| chr8:39815483 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(85): Show |
98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.513+5519C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815483 | |||||||
| chr8:39815610 | C | G | 2 | a0002c0002t0001g0303 a0002c0002t0001g0304 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513+5392G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815610 | |||||||
| chr8:39815743 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.513+5259T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815743 | |||||||
| chr8:39815769 | A | G | 3 | a0003c0003t0001g0012 a0003c0003t0001g0171 a0003c0003t0001g0184 |
4 | NA18954.hp1 NA18998.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+5233T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815769 | |||||||
| chr8:39815953 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.513+5049T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815953 | |||||||
| chr8:39815977 | T | A | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.513+5025A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39815977 | |||||||
| chr8:39816153 | C | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(7): Show |
10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+4849G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816153 | |||||||
| chr8:39816154 | G | A | 1 | a0009c0016t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.513+4848C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816154 | |||||||
| chr8:39816222 | G | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(70): Show |
83 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.513+4780C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816222 | |||||||
| chr8:39816261 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.513+4741G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816261 | |||||||
| chr8:39816304 | T | TA | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(7): Show |
10 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+4697dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816304 | |||||||
| chr8:39816367 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(119): Show |
131 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.513+4635A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816367 | |||||||
| chr8:39816541 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+4461C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816541 | |||||||
| chr8:39816599 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+4403G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816599 | |||||||
| chr8:39816736 | A | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.513+4266T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39816736 | |||||||
| chr8:39817001 | G | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(9): Show |
12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+4001C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817001 | |||||||
| chr8:39817169 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.513+3833C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817169 | |||||||
| chr8:39817181 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+3821T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817181 | |||||||
| chr8:39817350 | G | A | 1 | a0003c0003t0001g0171 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.513+3652C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817350 | |||||||
| chr8:39817393 | TAGA | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0167 a0001c0001t0001g0176 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.513+3606_513+3608d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817393 | |||||||
| chr8:39817466 | C | A | 2 | a0001c0015t0001g0221 a0009c0016t0001g0289 |
2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.513+3536G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817466 | |||||||
| chr8:39817479 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.513+3523C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817479 | |||||||
| chr8:39817584 | A | T | 1 | a0001c0001t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513+3418T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817584 | |||||||
| chr8:39817658 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+3344C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817658 | |||||||
| chr8:39817728 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
132 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.513+3274G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817728 | |||||||
| chr8:39817792 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.513+3210C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817792 | |||||||
| chr8:39817953 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513+3049G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39817953 | |||||||
| chr8:39818071 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.513+2931T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818071 | |||||||
| chr8:39818529 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18954.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.513+2473G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818529 | |||||||
| chr8:39818532 | T | G | 1 | a0001c0001t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+2470A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818532 | |||||||
| chr8:39818619 | G | C | 2 | a0002c0002t0001g0303 a0002c0002t0001g0304 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513+2383C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818619 | |||||||
| chr8:39818771 | T | C | 17 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(14): Show |
17 | HG00733.hp2 HG01891.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+2231A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818771 | |||||||
| chr8:39818772 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.513+2230C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818772 | |||||||
| chr8:39818909 | C | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(125): Show |
139 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+2093G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818909 | |||||||
| chr8:39818981 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.513+2021C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39818981 | |||||||
| chr8:39819106 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.513+1896C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819106 | |||||||
| chr8:39819376 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0177 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.513+1626T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819376 | |||||||
| chr8:39819865 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0003g0080 |
2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.513+1137A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819865 | |||||||
| chr8:39819911 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.513+1091A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39819911 | |||||||
| chr8:39820219 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(125): Show |
139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+783G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820219 | |||||||
| chr8:39820220 | A | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(125): Show |
139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.513+782T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820220 | |||||||
| chr8:39820238 | T | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(9): Show |
12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+764A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820238 | |||||||
| chr8:39820424 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.513+578T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820424 | |||||||
| chr8:39820428 | G | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0172 a0001c0001t0001g0202 others(5): Show |
9 | HG00408.hp2 HG00544.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.513+574C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820428 | |||||||
| chr8:39820627 | A | G | 1 | a0001c0020t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.513+375T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820627 | |||||||
| chr8:39820649 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.513+353G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820649 | |||||||
| chr8:39820810 | T | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+192A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820810 | |||||||
| chr8:39820848 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG02055.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+154T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820848 | |||||||
| chr8:39820993 | A | G | 3 | a0001c0001t0001g0027 a0007c0004t0001g0162 a0007c0004t0001g0163 |
3 | HG02572.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+9T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | 39820993 | |||||||
| chr8:39821204 | C | T | 40 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(37): Show |
40 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.345-34G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 5/20 | chr8 | 39821204 | |||||||
| chr8:39821286 | G | A | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.345-116C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 5/20 | chr8 | 39821286 | |||||||
| chr8:39821765 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.268-103T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821765 | |||||||
| chr8:39821805 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268-143C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821805 | |||||||
| chr8:39821971 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.268-309A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821971 | |||||||
| chr8:39821974 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0219 |
2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.268-312T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39821974 | |||||||
| chr8:39822086 | C | G | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-424G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822086 | |||||||
| chr8:39822281 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.268-619C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822281 | |||||||
| chr8:39822324 | T | C | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-662A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822324 | |||||||
| chr8:39822506 | T | TTGCATTG others(313): Show |
1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.268-845_268-844ins others(320): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(314): Show |
1 | a0001c0001t0001g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268-845_268-844ins others(321): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(321): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(328): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(322): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0159 |
3 | HG02723.hp1 HG03471.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(329): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(323): Show |
1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(330): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(323): Show |
2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02148.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(330): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(324): Show |
1 | a0001c0001t0001g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(331): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTG others(329): Show |
1 | a0001c0001t0001g0146 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(336): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTT others(320): Show |
1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268-845_268-844ins others(327): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822506 | T | TTGCATTT others(321): Show |
3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02109.hp1 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.268-845_268-844ins others(328): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822506 | |||||||
| chr8:39822569 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.268-907A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822569 | |||||||
| chr8:39822658 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.268-996C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822658 | |||||||
| chr8:39822712 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.268-1050T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822712 | |||||||
| chr8:39822715 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.268-1053T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822715 | |||||||
| chr8:39822752 | T | G | 1 | a0002c0002t0001g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.268-1090A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822752 | |||||||
| chr8:39822752 | T | TG | 19 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.268-1091_268-1090i others(3): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822752 | |||||||
| chr8:39822754 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-1092A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822754 | |||||||
| chr8:39822830 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.268-1168C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39822830 | |||||||
| chr8:39823013 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.268-1351G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823013 | |||||||
| chr8:39823013 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.268-1351G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823013 | |||||||
| chr8:39823044 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.268-1382C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823044 | |||||||
| chr8:39823139 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0279 |
2 | HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.268-1477T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823139 | |||||||
| chr8:39823212 | G | T | 2 | a0002c0002t0001g0303 a0002c0002t0001g0304 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.268-1550C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823212 | |||||||
| chr8:39823237 | G | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.268-1575C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823237 | |||||||
| chr8:39823482 | C | T | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.267+1337G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823482 | |||||||
| chr8:39823530 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0098 |
2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.267+1289A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823530 | |||||||
| chr8:39823547 | T | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.267+1272A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823547 | |||||||
| chr8:39823652 | G | A | 2 | a0008c0010t0001g0023 a0008c0011t0001g0022 |
2 | NA18992.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.267+1167C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39823652 | |||||||
| chr8:39824105 | G | A | 61 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(58): Show |
66 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.267+714C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824105 | |||||||
| chr8:39824203 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.267+616T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824203 | |||||||
| chr8:39824219 | G | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.267+600C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824219 | |||||||
| chr8:39824249 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.267+570G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824249 | |||||||
| chr8:39824274 | C | CA | 56 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(53): Show |
61 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.267+544dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824274 | |||||||
| chr8:39824274 | C | CAA | 17 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
18 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.267+543_267+544dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824274 | |||||||
| chr8:39824274 | CA | C | 28 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0081 others(25): Show |
28 | HG00733.hp2 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.267+544delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824274 | |||||||
| chr8:39824318 | C | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.267+501G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824318 | |||||||
| chr8:39824345 | TA | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG01109.hp2 HG01255.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+473delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824345 | |||||||
| chr8:39824352 | T | TA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(7): Show |
11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.267+466dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824352 | |||||||
| chr8:39824487 | C | A | 1 | a0001c0001t0001g0017 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.267+332G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824487 | |||||||
| chr8:39824676 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.267+143C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824676 | |||||||
| chr8:39824751 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.267+68C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 4/20 | chr8 | 39824751 | |||||||
| chr8:39824932 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0142 |
2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.189-35G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39824932 | |||||||
| chr8:39824994 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.189-97C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39824994 | |||||||
| chr8:39825325 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189-428T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39825325 | |||||||
| chr8:39825763 | G | T | 20 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.189-866C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39825763 | |||||||
| chr8:39826217 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.189-1320C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826217 | |||||||
| chr8:39826328 | A | T | 1 | a0001c0001t0001g0284 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189-1431T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826328 | |||||||
| chr8:39826383 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.189-1486G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826383 | |||||||
| chr8:39826444 | C | T | 1 | a0001c0015t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.189-1547G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826444 | |||||||
| chr8:39826478 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.189-1581G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826478 | |||||||
| chr8:39826506 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG00738.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.189-1609C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826506 | |||||||
| chr8:39826636 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(42): Show |
50 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.189-1739A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826636 | |||||||
| chr8:39826976 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.189-2079T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826976 | |||||||
| chr8:39826999 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-2102A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39826999 | |||||||
| chr8:39827037 | AAAC | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
9 | HG00140.hp1 HG00639.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-2143_189-2141d others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827037 | |||||||
| chr8:39827047 | GA | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-2151delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827047 | |||||||
| chr8:39827107 | A | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0292 |
2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.189-2210T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827107 | |||||||
| chr8:39827161 | A | T | 38 | a0001c0001t0001g0026 a0001c0001t0001g0146 a0001c0001t0001g0147 others(35): Show |
38 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.189-2264T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827161 | |||||||
| chr8:39827468 | C | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.189-2571G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827468 | |||||||
| chr8:39827849 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
54 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.189-2952G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827849 | |||||||
| chr8:39827912 | T | A | 1 | a0002c0002t0001g0302 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.189-3015A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827912 | |||||||
| chr8:39827940 | T | A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189-3043A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827940 | |||||||
| chr8:39827963 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.189-3066G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39827963 | |||||||
| chr8:39828075 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.189-3178G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828075 | |||||||
| chr8:39828317 | A | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.189-3420T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828317 | |||||||
| chr8:39828426 | A | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.189-3529T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828426 | |||||||
| chr8:39828519 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.189-3622A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828519 | |||||||
| chr8:39828664 | G | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(42): Show |
50 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.189-3767C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828664 | |||||||
| chr8:39828674 | C | G | 1 | a0001c0015t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.189-3777G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828674 | |||||||
| chr8:39828792 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.189-3895T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828792 | |||||||
| chr8:39828814 | A | G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(2): Show |
5 | HG00323.hp2 HG01243.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-3917T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39828814 | |||||||
| chr8:39829218 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.189-4321T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829218 | |||||||
| chr8:39829280 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.189-4383T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829280 | |||||||
| chr8:39829326 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0278 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.189-4429A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829326 | |||||||
| chr8:39829376 | C | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.189-4479G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829376 | |||||||
| chr8:39829414 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.189-4517A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829414 | |||||||
| chr8:39829466 | C | T | 21 | a0001c0001t0001g0026 a0001c0001t0001g0222 a0001c0001t0001g0223 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.188+4478G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829466 | |||||||
| chr8:39829505 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+4439T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829505 | |||||||
| chr8:39829594 | C | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.188+4350G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829594 | |||||||
| chr8:39829736 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.188+4208A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829736 | |||||||
| chr8:39829807 | C | T | 1 | a0001c0001t0001g0011 | 2 | NA18984.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.188+4137G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829807 | |||||||
| chr8:39829821 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+4123G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829821 | |||||||
| chr8:39829941 | T | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0008c0010t0001g0023 others(1): Show |
4 | HG00673.hp2 NA18968.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+4003A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829941 | |||||||
| chr8:39829973 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+3971G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39829973 | |||||||
| chr8:39830190 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.188+3754T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830190 | |||||||
| chr8:39830236 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.188+3708G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830236 | |||||||
| chr8:39830238 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.188+3706G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830238 | |||||||
| chr8:39830444 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.188+3500A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830444 | |||||||
| chr8:39830523 | T | C | 5 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
5 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3421A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830523 | |||||||
| chr8:39830782 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188+3162T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830782 | |||||||
| chr8:39830805 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.188+3139A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830805 | |||||||
| chr8:39830831 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.188+3113A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39830831 | |||||||
| chr8:39831193 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.188+2751T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831193 | |||||||
| chr8:39831204 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.188+2740G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831204 | |||||||
| chr8:39831251 | TCTAAA | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(79): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.188+2688_188+2692d others(7): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831251 | |||||||
| chr8:39831499 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG00735.hp2 HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.188+2445G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831499 | |||||||
| chr8:39831529 | A | G | 7 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+2415T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831529 | |||||||
| chr8:39831639 | T | C | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.188+2305A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831639 | |||||||
| chr8:39831747 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.188+2197C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831747 | |||||||
| chr8:39831806 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.188+2138C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831806 | |||||||
| chr8:39831971 | T | C | 7 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+1973A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39831971 | |||||||
| chr8:39832399 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.188+1545T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832399 | |||||||
| chr8:39832606 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1338A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832606 | |||||||
| chr8:39832610 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1334T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832610 | |||||||
| chr8:39832611 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1333G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832611 | |||||||
| chr8:39832612 | A | ATATTTGA others(13): Show |
1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+1331_188+1332i others(22): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832612 | |||||||
| chr8:39832726 | C | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.188+1218G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832726 | |||||||
| chr8:39832758 | G | T | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.188+1186C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832758 | |||||||
| chr8:39832834 | ATATG | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.188+1106_188+1109d others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832834 | |||||||
| chr8:39832866 | T | C | 1 | a0007c0004t0001g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188+1078A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39832866 | |||||||
| chr8:39833237 | G | T | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.188+707C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833237 | |||||||
| chr8:39833246 | A | T | 1 | a0002c0002t0001g0300 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.188+698T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833246 | |||||||
| chr8:39833420 | A | G | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00544.hp2 NA18942.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.188+524T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833420 | |||||||
| chr8:39833657 | A | T | 1 | a0001c0015t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.188+287T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833657 | |||||||
| chr8:39833694 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.188+250G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833694 | |||||||
| chr8:39833825 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.188+119C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833825 | |||||||
| chr8:39833842 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.188+102G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3/20 | chr8 | 39833842 | |||||||
| chr8:39834045 | G | T | 1 | a0001c0015t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133-46C>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834045 | |||||||
| chr8:39834240 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.133-241A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834240 | |||||||
| chr8:39834424 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.133-425A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834424 | |||||||
| chr8:39834445 | TG | T | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.133-447delC | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834445 | |||||||
| chr8:39834471 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.133-472T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834471 | |||||||
| chr8:39834508 | G | C | 1 | a0001c0015t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133-509C>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834508 | |||||||
| chr8:39834516 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.133-517A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834516 | |||||||
| chr8:39834591 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.133-592G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834591 | |||||||
| chr8:39834592 | G | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.133-593C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834592 | |||||||
| chr8:39834602 | C | T | 19 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.133-603G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834602 | |||||||
| chr8:39834635 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0218 |
3 | NA18990.hp1 NA18994.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.133-636C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834635 | |||||||
| chr8:39834666 | C | T | 2 | a0001c0001t0001g0071 a0006c0005t0001g0008 |
3 | HG01891.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.133-667G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834666 | |||||||
| chr8:39834713 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133-714G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834713 | |||||||
| chr8:39834732 | C | CA | 66 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(63): Show |
71 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.133-734dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834732 | C | CAA | 36 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0029 others(33): Show |
37 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.133-735_133-734dup others(2): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834732 | C | CAAAA | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0172 others(3): Show |
6 | HG00423.hp2 HG01074.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-737_133-734dup others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834732 | C | CAAAAA | 52 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
60 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.133-738_133-734dup others(5): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834732 | C | CAAAAAA | 13 | a0001c0001t0001g0003 a0001c0001t0001g0166 a0001c0001t0001g0208 others(10): Show |
15 | HG00544.hp1 HG00597.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-739_133-734dup others(6): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834732 | CA | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0049 others(7): Show |
10 | HG00735.hp1 HG01978.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.133-734delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834732 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133-743_133-734del others(10): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834732 | |||||||
| chr8:39834742 | A | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-743T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834742 | |||||||
| chr8:39834972 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
6 | NA18983.hp2 NA18987.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-973T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39834972 | |||||||
| chr8:39835254 | C | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0282 a0001c0001t0001g0283 others(9): Show |
12 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-1255G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835254 | |||||||
| chr8:39835412 | C | CG | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(68): Show |
77 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.133-1414dupC | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835412 | |||||||
| chr8:39835498 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133-1499G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835498 | |||||||
| chr8:39835509 | C | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(58): Show |
66 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.133-1510G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835509 | |||||||
| chr8:39835542 | G | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.133-1543C>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835542 | |||||||
| chr8:39835544 | T | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.133-1545A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835544 | |||||||
| chr8:39835681 | C | CA | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(97): Show |
112 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.132+1454dupT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835681 | |||||||
| chr8:39835681 | C | CAA | 20 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0222 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.132+1453_132+1454d others(4): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835681 | |||||||
| chr8:39835764 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.132+1372T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835764 | |||||||
| chr8:39835765 | T | C | 2 | a0002c0002t0001g0303 a0002c0002t0001g0304 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.132+1371A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39835765 | |||||||
| chr8:39836067 | A | G | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+1069T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836067 | |||||||
| chr8:39836204 | CATTTTTT | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0296 |
5 | NA19007.hp1 NA19058.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+925_132+931del others(7): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836204 | |||||||
| chr8:39836205 | A | AT | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+930dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836205 | |||||||
| chr8:39836218 | T | A | 16 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
16 | HG02109.hp1 HG02148.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+918A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836218 | |||||||
| chr8:39836228 | A | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.132+908T>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836228 | |||||||
| chr8:39836247 | A | G | 20 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.132+889T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836247 | |||||||
| chr8:39836257 | GT | G | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+878delA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836257 | |||||||
| chr8:39836301 | C | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.132+835G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836301 | |||||||
| chr8:39836491 | C | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.132+645G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836491 | |||||||
| chr8:39836538 | CA | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0222 a0001c0001t0001g0223 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+597delT | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836538 | |||||||
| chr8:39836696 | TAATCATT others(11): Show |
T | 1 | a0001c0006t0001g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.132+422_132+439del others(18): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836696 | |||||||
| chr8:39836707 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.132+429T>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836707 | |||||||
| chr8:39836855 | T | A | 2 | a0007c0004t0001g0162 a0007c0004t0001g0163 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.132+281A>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39836855 | |||||||
| chr8:39837091 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.132+45G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 2/20 | chr8 | 39837091 | |||||||
| chr8:39837248 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-36G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837248 | |||||||
| chr8:39837280 | T | C | 7 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-68A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837280 | |||||||
| chr8:39837334 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.56-122G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837334 | |||||||
| chr8:39837341 | C | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(71): Show |
84 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.56-129G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837341 | |||||||
| chr8:39837352 | T | C | 20 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-140A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837352 | |||||||
| chr8:39837381 | G | GT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(12): Show |
18 | HG00639.hp2 HG01515.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.56-170dupA | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837381 | |||||||
| chr8:39837382 | T | G | 5 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
5 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-170A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837382 | |||||||
| chr8:39837537 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.56-325G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837537 | |||||||
| chr8:39837547 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(7): Show |
11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.56-335G>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837547 | |||||||
| chr8:39837666 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.56-454A>G | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837666 | |||||||
| chr8:39837687 | A | T | 1 | a0001c0001t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.55+444T>A | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837687 | |||||||
| chr8:39837841 | C | A | 1 | a0001c0007t0001g0241 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.55+290G>T | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39837841 | |||||||
| chr8:39838016 | T | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(58): Show |
66 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.55+115A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39838016 | |||||||
| chr8:39838020 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.55+111A>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39838020 | |||||||
| chr8:39838097 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.55+34G>C | ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 1/20 | chr8 | 39838097 |