Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8754 |
| ensemblid | ENSG00000168615.13 |
| hgncid | 216 |
| symbol | ADAM9 |
| name | ADAM metallopeptidase domain 9 |
| refseq_nuc | NM_003816.3 |
| refseq_prot | NP_003807.1 |
| ensembl_nuc | ENST00000487273.7 |
| ensembl_prot | ENSP00000419446.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 38996973 |
| end | 39105261 |
| strand | + |
| ver | v1.2 |
| region | chr8:38996973-39105261 |
| region5000 | chr8:38991973-39110261 |
| regionname0 | ADAM9_chr8_38996973_39105261 |
| regionname5000 | ADAM9_chr8_38991973_39110261 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 819 | 313 | 71 | 59 | 129 | 10 | 42 | 101 | ADAM9_chr8_38991973_39110261 | ADAM9 | MGSGA others(814): Show |
chr8 | 38991973 | 39110261 |
| a0002 | 0/0 | 819 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | MGSGA others(814): Show |
chr8 | 38991973 | 39110261 |
| a0003 | 0/0 | 819 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAM9_chr8_38991973_39110261 | ADAM9 | MGSGA others(814): Show |
chr8 | 38991973 | 39110261 |
| a0004 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | MGSGA others(814): Show |
chr8 | 38991973 | 39110261 |
| a0005 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | MGSGA others(814): Show |
chr8 | 38991973 | 39110261 |
| a0006 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | MGSGA others(814): Show |
chr8 | 38991973 | 39110261 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2457 | 304 | 70 | 54 | 127 | 9 | 42 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0001c0003 | 0/0 | 2457 | 7 | 1 | 5 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0001c0006 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0001c0007 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0002c0002 | 0/0 | 2457 | 13 | 13 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0002c0010 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0003c0004 | 0/0 | 2457 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0004c0005 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0005c0008 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 | ||
| a0006c0009 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | ATGGG others(2452): Show |
chr8 | 38991973 | 39110261 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4112 | 301 | 68 | 54 | 127 | 9 | 42 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0001c0001t0002 | 1/0 | 4112 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0001c0001t0003 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0001c0001t0004 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0001c0003t0001 | 0/0 | 4112 | 7 | 1 | 5 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0001c0006t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0001c0007t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0002c0002t0002 | 0/0 | 4112 | 13 | 13 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0002c0010t0002 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0003c0004t0001 | 0/0 | 4112 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0004c0005t0001 | 0/0 | 4112 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0005c0008t0001 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| a0006c0009t0001 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | AGACT others(4107): Show |
chr8 | 38991973 | 39110261 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0002g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0001c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0002c0010t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0003c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0004c0005t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0005c0008t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| a0006c0009t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | GBR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0294 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0290 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0245 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02165 | hp1 | a0001 | c0007 | t0001 | g0268 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0187 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0197 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0332 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02717 | hp2 | a0005 | c0008 | t0001 | g0120 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0194 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0193 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0189 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0130 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18945 | hp1 | a0001 | c0006 | t0001 | g0256 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18963 | hp2 | a0003 | c0004 | t0001 | g0302 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0301 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19066 | hp1 | a0006 | c0009 | t0001 | g0163 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | YRI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20129 | hp1 | a0002 | c0010 | t0002 | g0198 | AFR | ASW | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ASW | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0295 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG01123 | hp2 | a0004 | c0005 | t0001 | g0292 | AMR | CLM | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0293 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | USA | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | LWK | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0110 | REF | REF | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0171 | REF | REF | ADAM9_chr8_38991973_39110261 | ADAM9 | chr8 | 38991973 | 39110261 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997149 | C | T | 1 | a0004 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.86C>T | p.Ala29Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/22 | 177/4112 | 86/2460 | 29/819 | chr8 | 38997149 | |||
| chr8:39021671 | C | T | 1 | a0002 | 14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
missense_variant | MODERATE | c.701C>T | p.Ala234Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/22 | 792/4112 | 701/2460 | 234/819 | chr8 | 39021671 | |||
| chr8:39026784 | G | T | 1 | a0006 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.1104G>T | p.Lys368Asn | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/22 | 1195/4112 | 1104/2460 | 368/819 | chr8 | 39026784 | |||
| chr8:39054572 | G | A | 1 | a0003 | 2 | NA18963.hp2 NA19064.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1394G>A | p.Arg465Gln | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/22 | 1485/4112 | 1394/2460 | 465/819 | chr8 | 39054572 | |||
| chr8:39090082 | T | G | 1 | a0005 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2104T>G | p.Phe702Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/22 | 2195/4112 | 2104/2460 | 702/819 | chr8 | 39090082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997141 | C | A | 2 | a0001c0003 a0004c0005 |
8 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(5): Show |
synonymous_variant | LOW | c.78C>A | p.Val26Val | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/22 | 169/4112 | 78/2460 | 26/819 | chr8 | 38997141 | |||
| chr8:39042033 | A | G | 1 | a0002c0002 | 13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.1218A>G | p.Pro406Pro | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/22 | 1309/4112 | 1218/2460 | 406/819 | chr8 | 39042033 | |||
| chr8:39042051 | T | C | 1 | a0001c0006 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.1236T>C | p.Tyr412Tyr | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/22 | 1327/4112 | 1236/2460 | 412/819 | chr8 | 39042051 | |||
| chr8:39077258 | G | A | 1 | a0001c0007 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1728G>A | p.Glu576Glu | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/22 | 1819/4112 | 1728/2460 | 576/819 | chr8 | 39077258 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997060 | C | T | 1 | a0001c0001t0004 | 1 | HG02647.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/22 | chr8 | 38997060 | |||||||
| chr8:39104031 | G | T | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(7): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 22/22 | 331 | chr8 | 39104031 | ||||||
| chr8:39104186 | A | G | 1 | a0001c0001t0003 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 22/22 | 486 | chr8 | 39104186 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38997399 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+239C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997399 | |||||||
| chr8:38997440 | C | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+280C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997440 | |||||||
| chr8:38997450 | C | T | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.97+290C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997450 | |||||||
| chr8:38997543 | G | T | 127 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(124): Show |
127 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.97+383G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997543 | |||||||
| chr8:38997651 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.97+491T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997651 | |||||||
| chr8:38997857 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97+697C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38997857 | |||||||
| chr8:38998026 | T | C | 1 | a0001c0003t0001g0206 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.97+866T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998026 | |||||||
| chr8:38998181 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.97+1021A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998181 | |||||||
| chr8:38998192 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.97+1032G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998192 | |||||||
| chr8:38998228 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(1): Show |
4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1068G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998228 | |||||||
| chr8:38998246 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.97+1086G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998246 | |||||||
| chr8:38998263 | G | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+1103G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998263 | |||||||
| chr8:38998328 | T | C | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.97+1168T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998328 | |||||||
| chr8:38998340 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.97+1180A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998340 | |||||||
| chr8:38998396 | AT | A | 105 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(102): Show |
105 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.97+1245delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38998396 | ||||||
| chr8:38998467 | C | G | 1 | a0001c0001t0001g0329 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.97+1307C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998467 | |||||||
| chr8:38998511 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97+1351T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998511 | |||||||
| chr8:38998778 | T | TGAAAGAA others(350): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.97+1633_97+1634ins others(357): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38998778 | ||||||
| chr8:38998817 | A | G | 138 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.97+1657A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998817 | |||||||
| chr8:38998928 | C | A | 1 | a0002c0002t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+1768C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38998928 | |||||||
| chr8:38998991 | TAAG | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0133 |
3 | HG02055.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.97+1834_97+1836del others(3): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38998991 | ||||||
| chr8:38999054 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.97+1894C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999054 | |||||||
| chr8:38999112 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA18953.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.97+1952C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999112 | |||||||
| chr8:38999146 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.97+1986G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999146 | |||||||
| chr8:38999249 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.97+2089T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999249 | |||||||
| chr8:38999328 | CT | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.97+2183delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 38999328 | ||||||
| chr8:38999340 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | NA18969.hp2 NA19001.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2180T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999340 | |||||||
| chr8:38999608 | C | T | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.97+2448C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 38999608 | |||||||
| chr8:39000088 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97+2928G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000088 | |||||||
| chr8:39000118 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97+2958G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000118 | |||||||
| chr8:39000235 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.97+3075G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000235 | |||||||
| chr8:39000289 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.97+3129A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000289 | |||||||
| chr8:39000313 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+3153G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000313 | |||||||
| chr8:39000354 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+3194G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000354 | |||||||
| chr8:39000390 | A | T | 84 | a0001c0001t0001g0207 a0001c0001t0001g0213 a0001c0001t0001g0214 others(81): Show |
84 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.97+3230A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000390 | |||||||
| chr8:39000482 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97+3322G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000482 | |||||||
| chr8:39000638 | T | C | 29 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0186 others(26): Show |
29 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.97+3478T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000638 | |||||||
| chr8:39000691 | TCCTGGGC others(13): Show |
T | 1 | a0001c0001t0001g0325 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.97+3533_97+3552del others(20): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39000691 | ||||||
| chr8:39000758 | C | T | 137 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.97+3598C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000758 | |||||||
| chr8:39000759 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.97+3599A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000759 | |||||||
| chr8:39000912 | A | T | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
137 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.97+3752A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000912 | |||||||
| chr8:39000965 | G | A | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
140 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.97+3805G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39000965 | |||||||
| chr8:39001417 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97+4257G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001417 | |||||||
| chr8:39001424 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+4264C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001424 | |||||||
| chr8:39001542 | TAAAC | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+4389_97+4392del others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39001542 | ||||||
| chr8:39001585 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4425G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001585 | |||||||
| chr8:39001849 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97+4689T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001849 | |||||||
| chr8:39001851 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.97+4691G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001851 | |||||||
| chr8:39001994 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.97+4834G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39001994 | |||||||
| chr8:39002008 | T | G | 12 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(9): Show |
12 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4848T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002008 | |||||||
| chr8:39002018 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+4858G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002018 | |||||||
| chr8:39002033 | T | TA | 33 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(30): Show |
33 | HG00280.hp2 HG01192.hp2 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+4893dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002033 | ||||||
| chr8:39002033 | T | TAA | 12 | a0001c0001t0001g0217 a0002c0002t0002g0130 a0002c0002t0002g0187 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+4892_97+4893dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002033 | ||||||
| chr8:39002033 | TA | T | 17 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
17 | HG00323.hp2 HG01255.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.97+4893delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002033 | ||||||
| chr8:39002034 | A | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97+4874A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002034 | |||||||
| chr8:39002291 | G | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5131G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002291 | |||||||
| chr8:39002312 | C | CT | 148 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.97+5176dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002312 | ||||||
| chr8:39002312 | C | CTT | 21 | a0001c0001t0001g0024 a0001c0001t0001g0124 a0001c0001t0001g0128 others(18): Show |
21 | HG00673.hp2 HG01952.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.97+5175_97+5176dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002312 | ||||||
| chr8:39002312 | CT | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(7): Show |
10 | HG02055.hp2 HG03130.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+5176delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39002312 | ||||||
| chr8:39002371 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+5211T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002371 | |||||||
| chr8:39002475 | C | T | 108 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(105): Show |
108 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.97+5315C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002475 | |||||||
| chr8:39002511 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.97+5351C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002511 | |||||||
| chr8:39002548 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.98-5338C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002548 | |||||||
| chr8:39002658 | C | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-5228C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002658 | |||||||
| chr8:39002728 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.98-5158C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002728 | |||||||
| chr8:39002768 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.98-5118C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002768 | |||||||
| chr8:39002805 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.98-5081A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002805 | |||||||
| chr8:39002869 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-5017C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39002869 | |||||||
| chr8:39003025 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-4861C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003025 | |||||||
| chr8:39003065 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.98-4821A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003065 | |||||||
| chr8:39003082 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98-4804G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003082 | |||||||
| chr8:39003225 | TG | T | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-4659delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39003225 | ||||||
| chr8:39003358 | C | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-4528C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003358 | |||||||
| chr8:39003480 | G | A | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98-4406G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003480 | |||||||
| chr8:39003485 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-4401T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003485 | |||||||
| chr8:39003485 | T | TA | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.98-4387dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39003485 | ||||||
| chr8:39003485 | T | TAA | 7 | a0001c0001t0001g0041 a0001c0001t0001g0088 a0001c0001t0001g0219 others(4): Show |
7 | HG00438.hp2 HG01928.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-4388_98-4387dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39003485 | ||||||
| chr8:39003568 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.98-4318G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003568 | |||||||
| chr8:39003739 | T | A | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.98-4147T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003739 | |||||||
| chr8:39003828 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | NA18962.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.98-4058C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003828 | |||||||
| chr8:39003888 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.98-3998C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003888 | |||||||
| chr8:39003896 | C | G | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-3990C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003896 | |||||||
| chr8:39003936 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-3950C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39003936 | |||||||
| chr8:39004030 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-3856A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004030 | |||||||
| chr8:39004071 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.98-3815A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004071 | |||||||
| chr8:39004285 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.98-3601C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004285 | |||||||
| chr8:39004303 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3583T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004303 | |||||||
| chr8:39004305 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3581C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004305 | |||||||
| chr8:39004307 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3579A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004307 | |||||||
| chr8:39004308 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3578G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004308 | |||||||
| chr8:39004310 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3576C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004310 | |||||||
| chr8:39004313 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3573A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004313 | |||||||
| chr8:39004314 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3572G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004314 | |||||||
| chr8:39004319 | T | G | 108 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(105): Show |
108 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.98-3567T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004319 | |||||||
| chr8:39004324 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-3562C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004324 | |||||||
| chr8:39004544 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.98-3342A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004544 | |||||||
| chr8:39004790 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-3096G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39004790 | |||||||
| chr8:39005210 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.98-2676G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39005210 | |||||||
| chr8:39005530 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.98-2356C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39005530 | |||||||
| chr8:39005576 | G | A | 137 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.98-2310G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39005576 | |||||||
| chr8:39006083 | C | T | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.98-1803C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006083 | |||||||
| chr8:39006160 | T | G | 1 | a0001c0003t0001g0258 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.98-1726T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006160 | |||||||
| chr8:39006401 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.98-1485A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006401 | |||||||
| chr8:39006512 | G | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-1374G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006512 | |||||||
| chr8:39006520 | T | C | 62 | a0001c0001t0001g0207 a0001c0001t0001g0214 a0001c0001t0001g0215 others(59): Show |
62 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.98-1366T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006520 | |||||||
| chr8:39006541 | T | TAAAAAGG others(307): Show |
1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.98-1328_98-1327ins others(314): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | ||||||
| chr8:39006541 | T | TAAAAAGG others(305): Show |
3 | a0001c0001t0001g0248 a0001c0001t0001g0300 a0001c0001t0001g0327 |
3 | HG01069.hp2 HG01169.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(312): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | ||||||
| chr8:39006541 | T | TAAAAAGG others(306): Show |
124 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(313): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | ||||||
| chr8:39006541 | T | TAAAAAGG others(307): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0220 others(1): Show |
4 | HG02630.hp2 HG03516.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(314): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | ||||||
| chr8:39006541 | T | TAAAAAGG others(308): Show |
1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.98-1328_98-1327ins others(315): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | ||||||
| chr8:39006541 | T | TAAAAAGG others(306): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | NA18962.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.98-1329_98-1328ins others(313): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006541 | ||||||
| chr8:39006543 | A | AAAAGGTA others(306): Show |
2 | a0003c0004t0001g0301 a0003c0004t0001g0302 |
2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.98-1328_98-1327ins others(313): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 39006543 | ||||||
| chr8:39006582 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.98-1304G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006582 | |||||||
| chr8:39006618 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.98-1268G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006618 | |||||||
| chr8:39006643 | A | G | 1 | a0003c0004t0001g0302 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.98-1243A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006643 | |||||||
| chr8:39006863 | G | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
137 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.98-1023G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006863 | |||||||
| chr8:39006997 | G | A | 137 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.98-889G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39006997 | |||||||
| chr8:39007165 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.98-721G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007165 | |||||||
| chr8:39007174 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.98-712C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007174 | |||||||
| chr8:39007175 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98-711A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007175 | |||||||
| chr8:39007312 | A | G | 22 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0072 others(19): Show |
22 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.98-574A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007312 | |||||||
| chr8:39007341 | C | T | 109 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(106): Show |
109 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.98-545C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007341 | |||||||
| chr8:39007695 | T | A | 1 | a0001c0001t0001g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-191T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007695 | |||||||
| chr8:39007733 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-153A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007733 | |||||||
| chr8:39007762 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-124A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | chr8 | 39007762 | |||||||
| chr8:39008008 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.195+25A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008008 | |||||||
| chr8:39008173 | C | CT | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
135 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.195+203dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39008173 | ||||||
| chr8:39008296 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.195+313G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008296 | |||||||
| chr8:39008366 | G | A | 137 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.195+383G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008366 | |||||||
| chr8:39008449 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.195+466C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008449 | |||||||
| chr8:39008645 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.195+662A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008645 | |||||||
| chr8:39008699 | C | T | 108 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(105): Show |
108 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.195+716C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008699 | |||||||
| chr8:39008714 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195+731A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008714 | |||||||
| chr8:39008829 | T | C | 2 | a0003c0004t0001g0301 a0003c0004t0001g0302 |
2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.195+846T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008829 | |||||||
| chr8:39008868 | A | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(17): Show |
20 | HG01496.hp1 HG02148.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.195+885A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39008868 | |||||||
| chr8:39009063 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.195+1080A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009063 | |||||||
| chr8:39009121 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.195+1138A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009121 | |||||||
| chr8:39009162 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.195+1179A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009162 | |||||||
| chr8:39009349 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.195+1366C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009349 | |||||||
| chr8:39009360 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.195+1377C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009360 | |||||||
| chr8:39009755 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0200 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.195+1772G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009755 | |||||||
| chr8:39009792 | G | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.195+1809G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009792 | |||||||
| chr8:39009895 | TG | T | 135 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.196-1751delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009895 | ||||||
| chr8:39009895 | TGG | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00280.hp1 HG02055.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.196-1752_196-1751d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009895 | ||||||
| chr8:39009895 | TGGG | T | 37 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(34): Show |
37 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.196-1753_196-1751d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009895 | ||||||
| chr8:39009898 | G | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.196-1760G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009898 | |||||||
| chr8:39009905 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.196-1753G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009905 | |||||||
| chr8:39009905 | G | GCA | 37 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(34): Show |
37 | HG00639.hp2 HG00673.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.196-1753_196-1752i others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009905 | |||||||
| chr8:39009907 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0088 others(1): Show |
4 | NA18972.hp1 NA18974.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1751G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009907 | |||||||
| chr8:39009908 | C | G | 50 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(47): Show |
50 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.196-1750C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009908 | |||||||
| chr8:39009911 | G | A | 50 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(47): Show |
50 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.196-1747G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009911 | |||||||
| chr8:39009911 | G | GGA | 3 | a0001c0001t0001g0017 a0001c0001t0001g0327 a0001c0003t0001g0290 |
3 | HG01081.hp1 HG02922.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.196-1726_196-1725d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009911 | ||||||
| chr8:39009930 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.196-1728G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009930 | |||||||
| chr8:39009932 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.196-1726G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009932 | |||||||
| chr8:39009932 | G | GAGACAAA others(1): Show |
210 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.196-1725_196-1724i others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009932 | ||||||
| chr8:39009943 | A | AAACAAC | 10 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(7): Show |
10 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-1706_196-1701d others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009943 | ||||||
| chr8:39009943 | A | C | 213 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.196-1715A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009943 | |||||||
| chr8:39009958 | A | C | 57 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(54): Show |
57 | HG00639.hp2 HG00673.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.196-1700A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009958 | |||||||
| chr8:39009962 | A | AAAAAC | 3 | a0001c0001t0001g0327 a0001c0001t0004g0332 a0001c0003t0001g0290 |
3 | HG01081.hp1 HG02647.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.196-1694_196-1693i others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009962 | ||||||
| chr8:39009964 | A | AAACAAAC | 6 | a0001c0001t0001g0068 a0001c0001t0001g0103 a0002c0002t0002g0194 others(3): Show |
6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-1694_196-1693i others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | |||||||
| chr8:39009964 | A | AAACAAAC others(1): Show |
33 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(30): Show |
33 | HG00639.hp2 HG01109.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.196-1694_196-1693i others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | |||||||
| chr8:39009964 | A | AAACAAAC others(2): Show |
14 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0033 others(11): Show |
14 | HG00673.hp1 HG01192.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-1694_196-1693i others(11): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | |||||||
| chr8:39009964 | A | AAACAAAC others(3): Show |
1 | a0001c0001t0001g0041 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.196-1694_196-1693i others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | |||||||
| chr8:39009964 | A | AC | 20 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0111 others(17): Show |
20 | HG00280.hp2 HG00621.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-1683dupC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009964 | ||||||
| chr8:39009964 | A | ACC | 18 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(15): Show |
18 | HG00735.hp1 HG00738.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-1684_196-1683d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009964 | ||||||
| chr8:39009964 | A | ACCC | 32 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(29): Show |
32 | HG00733.hp2 HG01069.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-1685_196-1683d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39009964 | ||||||
| chr8:39009964 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.196-1694A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009964 | |||||||
| chr8:39009965 | C | A | 3 | a0001c0001t0001g0327 a0001c0001t0004g0332 a0001c0003t0001g0290 |
3 | HG01081.hp1 HG02647.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.196-1693C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39009965 | |||||||
| chr8:39010016 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.196-1642A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010016 | |||||||
| chr8:39010431 | C | T | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.196-1227C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010431 | |||||||
| chr8:39010936 | T | C | 135 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.196-722T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010936 | |||||||
| chr8:39010942 | A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.196-716A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010942 | |||||||
| chr8:39010976 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.196-682C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010976 | |||||||
| chr8:39010984 | T | C | 87 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(84): Show |
87 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.196-674T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39010984 | |||||||
| chr8:39011007 | T | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196-651T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011007 | |||||||
| chr8:39011092 | C | CA | 18 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0138 others(15): Show |
18 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-549dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 39011092 | ||||||
| chr8:39011349 | A | C | 2 | a0002c0002t0002g0192 a0002c0002t0002g0193 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196-309A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011349 | |||||||
| chr8:39011391 | C | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-267C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011391 | |||||||
| chr8:39011444 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0024 |
3 | HG02257.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.196-214T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011444 | |||||||
| chr8:39011524 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.196-134C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011524 | |||||||
| chr8:39011588 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.196-70A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | chr8 | 39011588 | |||||||
| chr8:39012213 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.254+497G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012213 | |||||||
| chr8:39012231 | G | A | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.254+515G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012231 | |||||||
| chr8:39012314 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.254+598C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012314 | |||||||
| chr8:39012352 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.254+636T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012352 | |||||||
| chr8:39012737 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.254+1021A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012737 | |||||||
| chr8:39012794 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.254+1078C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012794 | |||||||
| chr8:39012875 | A | G | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.255-1090A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012875 | |||||||
| chr8:39012927 | C | T | 38 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(35): Show |
38 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.255-1038C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39012927 | |||||||
| chr8:39012940 | G | GATA | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.255-1014_255-1012d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 39012940 | ||||||
| chr8:39013000 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.255-965G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013000 | |||||||
| chr8:39013020 | A | G | 1 | a0001c0001t0001g0319 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.255-945A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013020 | |||||||
| chr8:39013081 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.255-884C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013081 | |||||||
| chr8:39013090 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.255-875C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013090 | |||||||
| chr8:39013178 | A | G | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.255-787A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013178 | |||||||
| chr8:39013383 | A | AT | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.255-576dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 39013383 | ||||||
| chr8:39013391 | G | C | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.255-574G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013391 | |||||||
| chr8:39013505 | CT | C | 15 | a0001c0001t0001g0048 a0001c0001t0001g0112 a0001c0001t0001g0126 others(12): Show |
15 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.255-447delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 39013505 | ||||||
| chr8:39013806 | T | G | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.255-159T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | chr8 | 39013806 | |||||||
| chr8:39014470 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.333+427G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014470 | |||||||
| chr8:39014528 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.333+485C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014528 | |||||||
| chr8:39014563 | T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+520T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014563 | |||||||
| chr8:39014667 | C | A | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.333+624C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014667 | |||||||
| chr8:39014824 | C | CTTTAG | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.333+782_333+786dup others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 39014824 | ||||||
| chr8:39014868 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.333+825A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39014868 | |||||||
| chr8:39015173 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.334-945A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015173 | |||||||
| chr8:39015199 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | HG00099.hp1 HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.334-919C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015199 | |||||||
| chr8:39015489 | T | A | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.334-629T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015489 | |||||||
| chr8:39015554 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.334-564A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015554 | |||||||
| chr8:39015690 | A | G | 57 | a0001c0001t0001g0207 a0001c0001t0001g0214 a0001c0001t0001g0215 others(54): Show |
57 | HG00099.hp1 HG00438.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.334-428A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4/21 | chr8 | 39015690 | |||||||
| chr8:39016282 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.410+88G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016282 | |||||||
| chr8:39016286 | C | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.410+92C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016286 | |||||||
| chr8:39016426 | A | C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.410+232A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016426 | |||||||
| chr8:39016708 | T | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-511T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016708 | |||||||
| chr8:39016875 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.411-344C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016875 | |||||||
| chr8:39016876 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.411-343G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016876 | |||||||
| chr8:39016925 | C | T | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.411-294C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39016925 | |||||||
| chr8:39017105 | A | G | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.411-114A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39017105 | |||||||
| chr8:39017179 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-40C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 5/21 | chr8 | 39017179 | |||||||
| chr8:39017589 | C | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.606+175C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39017589 | |||||||
| chr8:39017618 | C | T | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.606+204C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39017618 | |||||||
| chr8:39017931 | A | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.606+517A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39017931 | |||||||
| chr8:39018130 | G | A | 87 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(84): Show |
87 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.606+716G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39018130 | |||||||
| chr8:39018421 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.607-432A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39018421 | |||||||
| chr8:39018453 | C | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.607-400C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 6/21 | chr8 | 39018453 | |||||||
| chr8:39018947 | T | C | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.672+29T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39018947 | |||||||
| chr8:39018949 | C | T | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.672+31C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39018949 | |||||||
| chr8:39018957 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672+39G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39018957 | |||||||
| chr8:39019104 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.672+186A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019104 | |||||||
| chr8:39019317 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.672+399T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019317 | |||||||
| chr8:39019383 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.672+465C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019383 | |||||||
| chr8:39019475 | T | C | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+557T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019475 | |||||||
| chr8:39019513 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.672+595T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019513 | |||||||
| chr8:39019569 | G | A | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.672+651G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019569 | |||||||
| chr8:39019597 | A | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.672+679A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019597 | |||||||
| chr8:39019615 | A | T | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.672+697A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019615 | |||||||
| chr8:39019859 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672+941A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019859 | |||||||
| chr8:39019896 | C | T | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
138 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.672+978C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019896 | |||||||
| chr8:39019935 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.672+1017G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39019935 | |||||||
| chr8:39020067 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.672+1149C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020067 | |||||||
| chr8:39020154 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672+1236G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020154 | |||||||
| chr8:39020184 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.672+1266G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020184 | |||||||
| chr8:39020217 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01891.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.672+1299A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020217 | |||||||
| chr8:39020273 | A | G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.672+1355A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020273 | |||||||
| chr8:39020387 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673-1256T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020387 | |||||||
| chr8:39020399 | C | CT | 9 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | HG01257.hp1 HG01928.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-1242dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 39020399 | ||||||
| chr8:39020645 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0078 |
2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.673-998C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39020645 | |||||||
| chr8:39020892 | TA | T | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.673-738delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 39020892 | ||||||
| chr8:39021162 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.673-481C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021162 | |||||||
| chr8:39021225 | T | G | 1 | a0001c0001t0001g0260 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.673-418T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021225 | |||||||
| chr8:39021441 | G | A | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.673-202G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021441 | |||||||
| chr8:39021503 | C | T | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.673-140C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | chr8 | 39021503 | |||||||
| chr8:39022064 | T | TTG | 23 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0055 others(20): Show |
23 | HG01069.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.744+383_744+384dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022064 | ||||||
| chr8:39022064 | TTG | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(8): Show |
11 | HG02055.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+383_744+384del others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022064 | ||||||
| chr8:39022064 | TTGTG | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00621.hp1 HG00735.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.744+381_744+384del others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022064 | ||||||
| chr8:39022089 | TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.744+377_744+388del others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022089 | ||||||
| chr8:39022095 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.744+381T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022095 | |||||||
| chr8:39022097 | T | A | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0153 others(6): Show |
9 | HG02109.hp1 HG03927.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+383T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022097 | |||||||
| chr8:39022097 | T | TGTGTGAG others(1): Show |
12 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.744+384_744+385ins others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | 39022097 | ||||||
| chr8:39022099 | A | T | 2 | a0001c0001t0001g0209 a0002c0002t0002g0191 |
2 | HG02559.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.744+385A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022099 | |||||||
| chr8:39022101 | A | T | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.744+387A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022101 | |||||||
| chr8:39022239 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.744+525C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022239 | |||||||
| chr8:39022355 | A | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.744+641A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022355 | |||||||
| chr8:39022356 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.744+642C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022356 | |||||||
| chr8:39022882 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.745-274T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | chr8 | 39022882 | |||||||
| chr8:39023399 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.914+74A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023399 | |||||||
| chr8:39023740 | G | GT | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.914+438dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | ||||||
| chr8:39023740 | G | GTT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0014 others(22): Show |
25 | HG00621.hp1 HG01106.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.914+437_914+438dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | ||||||
| chr8:39023740 | G | GTTT | 6 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0109 others(3): Show |
6 | HG00735.hp1 HG02083.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.914+436_914+438dup others(3): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | ||||||
| chr8:39023740 | GTTTTTTT others(4): Show |
G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.914+428_914+438del others(11): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | ||||||
| chr8:39023740 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0230 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.914+425_914+438del others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39023740 | ||||||
| chr8:39023764 | G | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.914+439G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023764 | |||||||
| chr8:39023786 | G | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | NA18969.hp2 NA19001.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+461G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023786 | |||||||
| chr8:39023791 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.914+466G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023791 | |||||||
| chr8:39023871 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.914+546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023871 | |||||||
| chr8:39023946 | A | G | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.914+621A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39023946 | |||||||
| chr8:39024028 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.914+703G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024028 | |||||||
| chr8:39024051 | C | T | 2 | a0003c0004t0001g0301 a0003c0004t0001g0302 |
2 | NA18963.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.914+726C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024051 | |||||||
| chr8:39024052 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.914+727G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024052 | |||||||
| chr8:39024111 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0005c0008t0001g0120 |
3 | HG01884.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.914+786C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024111 | |||||||
| chr8:39024343 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1018G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024343 | |||||||
| chr8:39024548 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.914+1223A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024548 | |||||||
| chr8:39024646 | A | T | 7 | a0001c0003t0001g0206 a0001c0003t0001g0258 a0001c0003t0001g0290 others(4): Show |
7 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-1157A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024646 | |||||||
| chr8:39024756 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.915-1047A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024756 | |||||||
| chr8:39024798 | C | T | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.915-1005C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024798 | |||||||
| chr8:39024907 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.915-896G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39024907 | |||||||
| chr8:39025052 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.915-751G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025052 | |||||||
| chr8:39025092 | C | CT | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.915-701dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | 39025092 | ||||||
| chr8:39025108 | G | T | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
138 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.915-695G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025108 | |||||||
| chr8:39025149 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.915-654G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025149 | |||||||
| chr8:39025388 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.915-415C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025388 | |||||||
| chr8:39025444 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.915-359G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025444 | |||||||
| chr8:39025592 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.915-211C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025592 | |||||||
| chr8:39025655 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.915-148A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025655 | |||||||
| chr8:39025708 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.915-95G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 9/21 | chr8 | 39025708 | |||||||
| chr8:39025963 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.996+79C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39025963 | |||||||
| chr8:39026023 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.996+139T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026023 | |||||||
| chr8:39026134 | T | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.996+250T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026134 | |||||||
| chr8:39026158 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.996+274A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026158 | |||||||
| chr8:39026657 | T | C | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.997-20T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 10/21 | chr8 | 39026657 | |||||||
| chr8:39026823 | G | GTTCT | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+15_1130+18dup others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39026823 | ||||||
| chr8:39026946 | A | G | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1130+136A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39026946 | |||||||
| chr8:39026959 | C | CT | 17 | a0001c0001t0001g0124 a0001c0001t0001g0186 a0001c0001t0001g0204 others(14): Show |
17 | HG01070.hp2 HG01106.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+164dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39026959 | ||||||
| chr8:39026974 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1130+164T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39026974 | |||||||
| chr8:39027138 | A | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1130+328A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027138 | |||||||
| chr8:39027218 | C | T | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+408C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027218 | |||||||
| chr8:39027462 | A | T | 9 | a0001c0001t0001g0215 a0001c0001t0001g0257 a0001c0001t0001g0280 others(6): Show |
9 | HG01928.hp1 HG01952.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1130+652A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027462 | |||||||
| chr8:39027470 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1130+660A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027470 | |||||||
| chr8:39027782 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+972A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027782 | |||||||
| chr8:39027798 | C | A | 1 | a0001c0001t0001g0093 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1130+988C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027798 | |||||||
| chr8:39027909 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1130+1099A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39027909 | |||||||
| chr8:39028013 | A | G | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1130+1203A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028013 | |||||||
| chr8:39028115 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1130+1305T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028115 | |||||||
| chr8:39028186 | G | A | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+1376G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028186 | |||||||
| chr8:39028190 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1130+1380T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028190 | |||||||
| chr8:39028256 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+1446C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028256 | |||||||
| chr8:39028365 | TA | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1130+1565delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39028365 | ||||||
| chr8:39028382 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1130+1572A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028382 | |||||||
| chr8:39028475 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1130+1665C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028475 | |||||||
| chr8:39028554 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1130+1744G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39028554 | |||||||
| chr8:39029071 | A | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1130+2261A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029071 | |||||||
| chr8:39029131 | G | GT | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1130+2336dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39029131 | ||||||
| chr8:39029133 | T | TG | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0004g0332 |
3 | HG01168.hp2 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1130+2323_1130+232 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029133 | |||||||
| chr8:39029237 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1130+2427G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029237 | |||||||
| chr8:39029242 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0235 |
2 | HG02056.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1130+2432A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029242 | |||||||
| chr8:39029277 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 |
3 | HG02615.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1130+2467G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029277 | |||||||
| chr8:39029322 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1130+2512C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029322 | |||||||
| chr8:39029341 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1130+2531G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029341 | |||||||
| chr8:39029380 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+2570T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029380 | |||||||
| chr8:39029673 | G | A | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+2863G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029673 | |||||||
| chr8:39029747 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0182 |
3 | NA18966.hp2 NA18973.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1130+2937G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39029747 | |||||||
| chr8:39030239 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+3429G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39030239 | |||||||
| chr8:39030604 | G | A | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+3794G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39030604 | |||||||
| chr8:39030679 | CT | C | 17 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+3871delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39030679 | ||||||
| chr8:39030766 | G | A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130+3956G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39030766 | |||||||
| chr8:39031381 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02155.hp2 NA18943.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130+4571C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031381 | |||||||
| chr8:39031416 | A | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1130+4606A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031416 | |||||||
| chr8:39031425 | C | G | 1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1130+4615C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031425 | |||||||
| chr8:39031432 | T | C | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+4622T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031432 | |||||||
| chr8:39031460 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1130+4650G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031460 | |||||||
| chr8:39031534 | A | C | 1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1130+4724A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031534 | |||||||
| chr8:39031580 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1130+4770C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031580 | |||||||
| chr8:39031686 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1130+4876C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39031686 | |||||||
| chr8:39032008 | C | T | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+5198C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032008 | |||||||
| chr8:39032079 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+5269C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032079 | |||||||
| chr8:39032216 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+5406G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032216 | |||||||
| chr8:39032323 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1130+5513C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032323 | |||||||
| chr8:39032352 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+5542G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032352 | |||||||
| chr8:39032363 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1130+5553C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032363 | |||||||
| chr8:39032403 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1130+5593T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032403 | |||||||
| chr8:39032448 | A | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1130+5638A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032448 | |||||||
| chr8:39032643 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1130+5833C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032643 | |||||||
| chr8:39032670 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1130+5860A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032670 | |||||||
| chr8:39032790 | C | T | 136 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1130+5980C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032790 | |||||||
| chr8:39032791 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1130+5981G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032791 | |||||||
| chr8:39032859 | A | T | 7 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0079 others(4): Show |
7 | HG00621.hp1 HG02132.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.1130+6049A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39032859 | |||||||
| chr8:39033136 | A | G | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130+6326A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033136 | |||||||
| chr8:39033198 | T | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1130+6388T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033198 | |||||||
| chr8:39033510 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1130+6700A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033510 | |||||||
| chr8:39033802 | T | G | 1 | a0001c0001t0001g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1130+6992T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39033802 | |||||||
| chr8:39034073 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1130+7263T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034073 | |||||||
| chr8:39034415 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-7531A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034415 | |||||||
| chr8:39034554 | T | C | 2 | a0001c0001t0001g0082 a0005c0008t0001g0120 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1131-7392T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034554 | |||||||
| chr8:39034649 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1131-7297A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39034649 | |||||||
| chr8:39035054 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1131-6892A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035054 | |||||||
| chr8:39035084 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1131-6862T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035084 | |||||||
| chr8:39035275 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1131-6671C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035275 | |||||||
| chr8:39035376 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1131-6570T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035376 | |||||||
| chr8:39035394 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1131-6552T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035394 | |||||||
| chr8:39035402 | C | T | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1131-6544C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035402 | |||||||
| chr8:39035674 | G | C | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-6272G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035674 | |||||||
| chr8:39035772 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1131-6174G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035772 | |||||||
| chr8:39035803 | C | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
32 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1131-6143C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035803 | |||||||
| chr8:39035804 | G | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02723.hp1 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131-6142G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035804 | |||||||
| chr8:39035815 | TCAAAACA others(3): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-6110_1131-610 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39035815 | ||||||
| chr8:39035922 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-6024C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035922 | |||||||
| chr8:39035958 | T | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
140 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.1131-5988T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39035958 | |||||||
| chr8:39036296 | A | G | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1131-5650A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036296 | |||||||
| chr8:39036373 | TC | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1131-5571delC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39036373 | ||||||
| chr8:39036473 | A | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-5473A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036473 | |||||||
| chr8:39036548 | C | T | 131 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1131-5398C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036548 | |||||||
| chr8:39036729 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1131-5217A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036729 | |||||||
| chr8:39036765 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1131-5181A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036765 | |||||||
| chr8:39036815 | G | A | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1131-5131G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036815 | |||||||
| chr8:39036930 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1131-5016T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39036930 | |||||||
| chr8:39037033 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1131-4913A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037033 | |||||||
| chr8:39037050 | C | CT | 26 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0091 others(23): Show |
26 | HG01261.hp1 HG01361.hp1 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.1131-4872dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037050 | ||||||
| chr8:39037050 | CT | C | 77 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0025 others(74): Show |
77 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1131-4872delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037050 | ||||||
| chr8:39037050 | CTT | C | 124 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1131-4873_1131-487 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037050 | ||||||
| chr8:39037080 | G | T | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG01106.hp1 HG01952.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-4866G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037080 | |||||||
| chr8:39037082 | AG | A | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1131-4863delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037082 | |||||||
| chr8:39037112 | A | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1131-4834A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037112 | |||||||
| chr8:39037150 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1131-4796G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037150 | |||||||
| chr8:39037206 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1131-4740C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037206 | |||||||
| chr8:39037441 | A | AGT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(5): Show |
8 | HG00280.hp2 HG01256.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131-4488_1131-448 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037441 | ||||||
| chr8:39037441 | AGT | A | 15 | a0001c0001t0001g0298 a0002c0002t0002g0130 a0002c0002t0002g0187 others(12): Show |
15 | HG01109.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1131-4488_1131-448 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037441 | ||||||
| chr8:39037458 | G | GT | 95 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(92): Show |
95 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1131-4472dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037458 | ||||||
| chr8:39037458 | G | GTGT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(17): Show |
20 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1131-4487_1131-448 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037458 | ||||||
| chr8:39037458 | G | GTGTGT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(9): Show |
12 | HG00621.hp1 HG00735.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-4487_1131-448 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39037458 | ||||||
| chr8:39037458 | G | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0323 a0001c0001t0003g0133 |
3 | HG02055.hp2 NA19012.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1131-4488G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037458 | |||||||
| chr8:39037459 | T | TG | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0055 others(8): Show |
11 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1131-4487_1131-448 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037459 | |||||||
| chr8:39037509 | A | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1131-4437A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037509 | |||||||
| chr8:39037553 | G | A | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG00673.hp2 HG02135.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1131-4393G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037553 | |||||||
| chr8:39037787 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1131-4159A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037787 | |||||||
| chr8:39037861 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1131-4085T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39037861 | |||||||
| chr8:39038614 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1131-3332G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39038614 | |||||||
| chr8:39038865 | T | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1131-3081T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39038865 | |||||||
| chr8:39038960 | G | GT | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1131-2978dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39038960 | ||||||
| chr8:39039031 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1131-2915A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039031 | |||||||
| chr8:39039048 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1131-2898A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039048 | |||||||
| chr8:39039184 | A | G | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-2762A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039184 | |||||||
| chr8:39039202 | G | A | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1131-2744G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039202 | |||||||
| chr8:39039518 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1131-2428A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039518 | |||||||
| chr8:39039530 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1131-2416G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039530 | |||||||
| chr8:39039674 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1131-2272C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039674 | |||||||
| chr8:39039884 | G | A | 1 | a0002c0002t0002g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1131-2062G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039884 | |||||||
| chr8:39039951 | A | C | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(37): Show |
40 | HG00673.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.1131-1995A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039951 | |||||||
| chr8:39039976 | A | G | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1131-1970A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39039976 | |||||||
| chr8:39040004 | A | T | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1131-1942A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040004 | |||||||
| chr8:39040041 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1131-1905C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040041 | |||||||
| chr8:39040076 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1131-1870G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040076 | |||||||
| chr8:39040159 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1131-1787C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040159 | |||||||
| chr8:39040237 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1131-1709C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040237 | |||||||
| chr8:39040303 | C | T | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1131-1643C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040303 | |||||||
| chr8:39040525 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG03710.hp2 NA18747.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1131-1421C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040525 | |||||||
| chr8:39040685 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1131-1261T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040685 | |||||||
| chr8:39040766 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1131-1180C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040766 | |||||||
| chr8:39040769 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-1177A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040769 | |||||||
| chr8:39040856 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-1090T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39040856 | |||||||
| chr8:39041132 | A | T | 126 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0126 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1131-814A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041132 | |||||||
| chr8:39041229 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1131-717C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041229 | |||||||
| chr8:39041287 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1131-659G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041287 | |||||||
| chr8:39041288 | C | G | 135 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1131-658C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041288 | |||||||
| chr8:39041338 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1131-608C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041338 | |||||||
| chr8:39041369 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1131-577T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041369 | |||||||
| chr8:39041495 | TC | T | 135 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1131-449delC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 39041495 | ||||||
| chr8:39041798 | T | C | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-148T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041798 | |||||||
| chr8:39041897 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1131-49A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | 39041897 | |||||||
| chr8:39042133 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1302+16G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042133 | |||||||
| chr8:39042229 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+112A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042229 | |||||||
| chr8:39042253 | G | A | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1302+136G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042253 | |||||||
| chr8:39042367 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1302+250A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042367 | |||||||
| chr8:39042575 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1302+458A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39042575 | |||||||
| chr8:39043134 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1302+1017G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043134 | |||||||
| chr8:39043158 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0100 |
3 | NA18961.hp2 NA18985.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1302+1041T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043158 | |||||||
| chr8:39043221 | T | C | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1302+1104T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043221 | |||||||
| chr8:39043227 | T | C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1302+1110T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043227 | |||||||
| chr8:39043748 | A | T | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+1631A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043748 | |||||||
| chr8:39043818 | A | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 |
3 | HG02615.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1302+1701A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043818 | |||||||
| chr8:39043931 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1302+1814A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39043931 | |||||||
| chr8:39044032 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+1915A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044032 | |||||||
| chr8:39044219 | T | G | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+2102T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044219 | |||||||
| chr8:39044358 | T | C | 135 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1302+2241T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044358 | |||||||
| chr8:39044484 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+2367G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044484 | |||||||
| chr8:39044547 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1302+2430C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044547 | |||||||
| chr8:39044582 | TCAGCCCT others(20): Show |
T | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+2494_1302+252 others(31): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044582 | ||||||
| chr8:39044663 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0182 |
3 | NA18966.hp2 NA18973.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1302+2546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044663 | |||||||
| chr8:39044688 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1302+2571G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044688 | |||||||
| chr8:39044689 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+2572C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044689 | |||||||
| chr8:39044774 | C | T | 2 | a0001c0003t0001g0290 a0001c0003t0001g0294 |
2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1302+2657C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044774 | |||||||
| chr8:39044842 | T | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
48 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1302+2725T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044842 | |||||||
| chr8:39044886 | A | ATG | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1302+2770_1302+277 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044886 | ||||||
| chr8:39044910 | A | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0076 others(15): Show |
18 | HG00621.hp1 HG00639.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+2793A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044910 | |||||||
| chr8:39044913 | T | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0052 others(1): Show |
4 | HG01261.hp1 HG02135.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2796T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044913 | |||||||
| chr8:39044920 | A | ATATATAT others(59): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1302+2808_1302+280 others(70): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044920 | ||||||
| chr8:39044920 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1302+2803A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044920 | |||||||
| chr8:39044942 | C | A | 201 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1302+2825C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044942 | |||||||
| chr8:39044945 | T | G | 85 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(82): Show |
85 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1302+2828T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044945 | |||||||
| chr8:39044952 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1302+2835G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044952 | |||||||
| chr8:39044952 | GTA | G | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG00280.hp2 HG01256.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2839_1302+284 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044952 | ||||||
| chr8:39044956 | A | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0085 a0002c0002t0002g0130 others(13): Show |
16 | HG00621.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302+2839A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044956 | |||||||
| chr8:39044956 | ATG | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0257 a0001c0001t0001g0311 |
3 | HG01928.hp1 HG01952.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1302+2846_1302+284 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044956 | ||||||
| chr8:39044967 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0085 |
2 | HG00621.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1302+2850C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044967 | |||||||
| chr8:39044974 | C | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+2857C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044974 | |||||||
| chr8:39044977 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0089 |
3 | HG01070.hp1 HG01071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1302+2860T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044977 | |||||||
| chr8:39044979 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2862T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044979 | |||||||
| chr8:39044985 | TATATGTG others(77): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+2880_1302+296 others(88): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39044985 | ||||||
| chr8:39044988 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0085 a0001c0001t0001g0157 others(21): Show |
24 | HG00621.hp1 HG00621.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1302+2871A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044988 | |||||||
| chr8:39044999 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0209 a0001c0001t0001g0222 others(1): Show |
4 | HG00621.hp1 HG02647.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+2882C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39044999 | |||||||
| chr8:39045006 | C | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0222 |
2 | NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1302+2889C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045006 | |||||||
| chr8:39045006 | C | CTATGTAT others(25): Show |
1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1302+2927_1302+295 others(36): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045006 | ||||||
| chr8:39045010 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2893G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045010 | |||||||
| chr8:39045018 | A | ATG | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1302+2910_1302+291 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045018 | ||||||
| chr8:39045020 | G | A | 77 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(74): Show |
77 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1302+2903G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045020 | |||||||
| chr8:39045020 | GTGTGTGT others(89): Show |
G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0222 |
2 | NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1302+2912_1302+300 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045020 | ||||||
| chr8:39045022 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2905G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045022 | |||||||
| chr8:39045028 | GCA | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0308 |
3 | HG01891.hp1 HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1302+2912_1302+291 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045028 | |||||||
| chr8:39045031 | T | C | 112 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(109): Show |
112 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.1302+2914T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045031 | |||||||
| chr8:39045032 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0308 |
3 | HG01891.hp1 HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1302+2915A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045032 | |||||||
| chr8:39045038 | A | C | 111 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(108): Show |
111 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(108): Show |
intron_variant | MODIFIER | c.1302+2921A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045038 | |||||||
| chr8:39045041 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1302+2924T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045041 | |||||||
| chr8:39045042 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1302+2925G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045042 | |||||||
| chr8:39045043 | T | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
32 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1302+2926T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045043 | |||||||
| chr8:39045048 | GTATGTGT others(15): Show |
G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG01243.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1302+3001_1302+302 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045048 | ||||||
| chr8:39045048 | GTATGTGT others(59): Show |
G | 4 | a0001c0001t0001g0261 a0001c0001t0001g0306 a0001c0001t0001g0316 others(1): Show |
4 | NA18953.hp2 NA18972.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+2957_1302+302 others(70): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045048 | ||||||
| chr8:39045050 | A | ATG | 60 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(57): Show |
60 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.1302+2942_1302+294 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045050 | ||||||
| chr8:39045052 | G | A | 13 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0085 others(10): Show |
13 | HG00438.hp2 HG00621.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+2935G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045052 | |||||||
| chr8:39045052 | GTGTGTGT others(57): Show |
G | 54 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1302+2944_1302+300 others(68): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045052 | ||||||
| chr8:39045054 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1302+2937G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045054 | |||||||
| chr8:39045058 | GTGCATAC others(85): Show |
G | 12 | a0001c0001t0001g0032 a0001c0001t0001g0216 a0001c0001t0001g0260 others(9): Show |
12 | HG00099.hp2 HG00673.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302+2944_1302+303 others(96): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045058 | ||||||
| chr8:39045058 | GTGCATAC others(113): Show |
G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0287 |
2 | HG03492.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1302+2944_1302+306 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045058 | ||||||
| chr8:39045058 | GTGCATAC others(141): Show |
G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+2944_1302+309 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045058 | ||||||
| chr8:39045061 | CATACATA others(87): Show |
C | 1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1302+2957_1302+305 others(98): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045061 | ||||||
| chr8:39045063 | T | C | 73 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(70): Show |
73 | HG00438.hp2 HG00673.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1302+2946T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045063 | |||||||
| chr8:39045069 | C | CCTATGTA others(3): Show |
33 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(30): Show |
33 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+2952_1302+295 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045069 | |||||||
| chr8:39045069 | C | CCTATGTA others(35): Show |
3 | a0002c0002t0002g0191 a0002c0002t0002g0192 a0002c0002t0002g0193 |
3 | HG02559.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1302+2952_1302+295 others(46): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045069 | |||||||
| chr8:39045070 | A | ATATGTAT others(3): Show |
1 | a0001c0001t0001g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1302+2958_1302+295 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045070 | ||||||
| chr8:39045070 | A | C | 36 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(33): Show |
36 | HG00673.hp1 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+2953A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045070 | |||||||
| chr8:39045070 | A | G | 36 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(33): Show |
36 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+2953A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045070 | |||||||
| chr8:39045072 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+2955A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045072 | |||||||
| chr8:39045074 | G | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
88 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.1302+2957G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045074 | |||||||
| chr8:39045076 | G | A | 74 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
74 | HG00639.hp2 HG00673.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1302+2959G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045076 | |||||||
| chr8:39045078 | G | GTATATA | 17 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0074 others(14): Show |
17 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1302+2962_1302+296 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045078 | ||||||
| chr8:39045078 | G | GTATATAT others(27): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
18 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2962_1302+296 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045078 | ||||||
| chr8:39045078 | G | GTATATAT others(55): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0079 others(1): Show |
4 | HG02647.hp1 NA18964.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2962_1302+296 others(66): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045078 | ||||||
| chr8:39045079 | TGTGCATA others(5): Show |
T | 19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(16): Show |
19 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302+2963_1302+297 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045079 | |||||||
| chr8:39045079 | TGTGCATA others(27): Show |
T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1302+2963_1302+299 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045079 | |||||||
| chr8:39045080 | GTGCATAC others(5): Show |
G | 36 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(33): Show |
36 | HG00673.hp1 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+2965_1302+297 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045080 | ||||||
| chr8:39045080 | GTGCATAC others(27): Show |
G | 1 | a0001c0001t0001g0262 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1302+2965_1302+299 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045080 | ||||||
| chr8:39045081 | TGCATACA others(3): Show |
T | 16 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0048 others(13): Show |
16 | HG00639.hp2 HG00733.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+2965_1302+297 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045081 | |||||||
| chr8:39045081 | TGCATACA others(25): Show |
T | 21 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
21 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+2965_1302+299 others(36): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045081 | |||||||
| chr8:39045083 | C | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(36): Show |
39 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1302+2966C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045083 | |||||||
| chr8:39045085 | T | C | 12 | a0001c0001t0001g0036 a0002c0002t0002g0130 a0002c0002t0002g0187 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1302+2968T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045085 | |||||||
| chr8:39045091 | C | CCTATGTA others(3): Show |
11 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+2974_1302+297 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045091 | |||||||
| chr8:39045092 | A | C | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+2975A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045092 | |||||||
| chr8:39045092 | A | G | 11 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+2975A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045092 | |||||||
| chr8:39045094 | A | G | 16 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0048 others(13): Show |
16 | HG00639.hp2 HG00733.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+2977A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045094 | |||||||
| chr8:39045096 | G | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
56 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1302+2979G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045096 | |||||||
| chr8:39045098 | G | A | 23 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(20): Show |
23 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1302+2981G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045098 | |||||||
| chr8:39045098 | G | GTATA | 5 | a0001c0001t0001g0037 a0001c0001t0001g0073 a0001c0001t0001g0076 others(2): Show |
5 | HG00621.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+2982_1302+298 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045098 | ||||||
| chr8:39045100 | G | A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0073 a0001c0001t0001g0076 others(2): Show |
5 | HG00621.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+2983G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045100 | |||||||
| chr8:39045100 | G | GTATATA | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00323.hp1 HG00735.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1302+2984_1302+298 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045100 | ||||||
| chr8:39045101 | TGTGCATA others(5): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+2985_1302+299 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045101 | |||||||
| chr8:39045102 | G | A | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(15): Show |
18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2985G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045102 | |||||||
| chr8:39045103 | TGCATACA others(3): Show |
T | 23 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(20): Show |
23 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1302+2987_1302+299 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045103 | |||||||
| chr8:39045104 | G | A | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(15): Show |
18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2987G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045104 | |||||||
| chr8:39045105 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
42 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1302+2988C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045105 | |||||||
| chr8:39045105 | CATACATA others(99): Show |
C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0098 others(4): Show |
7 | HG00733.hp2 HG01993.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3001_1302+310 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045105 | ||||||
| chr8:39045107 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0239 a0002c0002t0002g0189 others(1): Show |
4 | HG01192.hp1 HG03017.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+2990T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045107 | |||||||
| chr8:39045113 | C | CCTATGTA others(3): Show |
3 | a0001c0001t0001g0239 a0002c0002t0002g0189 a0002c0010t0002g0198 |
3 | HG01192.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1302+2996_1302+299 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045113 | |||||||
| chr8:39045113 | C | T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(15): Show |
18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+2996C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045113 | |||||||
| chr8:39045114 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1302+2997A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045114 | |||||||
| chr8:39045114 | A | G | 3 | a0001c0001t0001g0239 a0002c0002t0002g0189 a0002c0010t0002g0198 |
3 | HG01192.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1302+2997A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045114 | |||||||
| chr8:39045116 | A | G | 62 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(59): Show |
62 | HG00438.hp2 HG00735.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.1302+2999A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045116 | |||||||
| chr8:39045118 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1302+3001G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045118 | |||||||
| chr8:39045118 | G | GTA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(15): Show |
18 | HG00735.hp2 HG02083.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+3002_1302+300 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045118 | ||||||
| chr8:39045118 | G | GTGTGTGC others(13): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | HG01106.hp2 HG01123.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3007_1302+300 others(24): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045118 | ||||||
| chr8:39045118 | GTGTGTGT others(41): Show |
G | 1 | a0001c0001t0001g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1302+3003_1302+305 others(52): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045118 | ||||||
| chr8:39045120 | G | A | 52 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(49): Show |
52 | HG00673.hp1 HG00735.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1302+3003G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045120 | |||||||
| chr8:39045120 | G | GTATA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302+3004_1302+300 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045120 | ||||||
| chr8:39045120 | G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0085 |
3 | HG00621.hp1 NA18964.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1302+3004_1302+300 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045120 | ||||||
| chr8:39045120 | G | GTGTATAT others(27): Show |
4 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0178 others(1): Show |
4 | HG00621.hp2 NA18945.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045120 | ||||||
| chr8:39045122 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
40 | HG00621.hp1 HG00735.hp2 HG02083.hp2 others(37): Show |
intron_variant | MODIFIER | c.1302+3005G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045122 | |||||||
| chr8:39045122 | G | GTATATA | 43 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(40): Show |
43 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | ||||||
| chr8:39045122 | G | GTATATAT others(27): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0182 |
2 | NA18522.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | ||||||
| chr8:39045122 | G | GTATATAT others(55): Show |
3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02723.hp1 HG02895.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1302+3006_1302+300 others(66): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | ||||||
| chr8:39045122 | G | GTGTGTAT others(21): Show |
1 | a0001c0001t0001g0183 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1302+3009_1302+301 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045122 | ||||||
| chr8:39045123 | TGTGC | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
30 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1302+3007_1302+301 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045123 | |||||||
| chr8:39045124 | GTGCATAC others(35): Show |
G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | NA18961.hp2 NA18965.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3009_1302+305 others(46): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045124 | ||||||
| chr8:39045124 | GTGCATAC others(63): Show |
G | 27 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3009_1302+307 others(74): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045124 | ||||||
| chr8:39045127 | C | CATACATA others(21): Show |
6 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0001c0001t0001g0145 others(3): Show |
6 | HG01106.hp2 HG02083.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3135_1302+316 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | ||||||
| chr8:39045127 | C | CATACATA others(49): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0164 |
3 | HG02165.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1302+3107_1302+316 others(60): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | ||||||
| chr8:39045127 | C | CATACATA others(77): Show |
1 | a0001c0001t0001g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1302+3079_1302+316 others(88): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | ||||||
| chr8:39045127 | C | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
89 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1302+3010C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045127 | |||||||
| chr8:39045127 | CATACATA others(21): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0201 |
2 | HG01346.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1302+3135_1302+316 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045127 | ||||||
| chr8:39045129 | T | C | 3 | a0001c0001t0001g0239 a0001c0001t0004g0332 a0002c0010t0002g0198 |
3 | HG01192.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1302+3012T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045129 | |||||||
| chr8:39045135 | C | CATATGTG others(1): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
19 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302+3022_1302+302 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045135 | ||||||
| chr8:39045135 | CAT | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0074 others(8): Show |
11 | HG00639.hp2 HG00735.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+3023_1302+302 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045135 | ||||||
| chr8:39045138 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0004g0332 |
2 | HG01192.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1302+3021A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045138 | |||||||
| chr8:39045140 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0004g0332 |
3 | HG02647.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+3023A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045140 | |||||||
| chr8:39045144 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1302+3027G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045144 | |||||||
| chr8:39045148 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1302+3031A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045148 | |||||||
| chr8:39045149 | TATGTGTA others(3): Show |
T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3035_1302+304 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045149 | ||||||
| chr8:39045150 | A | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0239 others(3): Show |
6 | HG00639.hp2 HG01192.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3033A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045150 | |||||||
| chr8:39045151 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1302+3034T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045151 | |||||||
| chr8:39045155 | T | C | 15 | a0001c0001t0001g0032 a0001c0001t0001g0168 a0001c0001t0001g0185 others(12): Show |
15 | HG00099.hp2 HG00323.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1302+3038T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045155 | |||||||
| chr8:39045157 | T | C | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0004g0332 |
3 | HG00639.hp2 HG01192.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1302+3040T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045157 | |||||||
| chr8:39045159 | C | CATACATA others(17): Show |
1 | a0001c0001t0001g0165 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1302+3050_1302+307 others(28): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045159 | ||||||
| chr8:39045160 | A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3043A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045160 | |||||||
| chr8:39045163 | C | CATATGTG others(1): Show |
10 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0074 others(7): Show |
10 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3050_1302+305 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045163 | ||||||
| chr8:39045163 | C | CATATGTG others(27): Show |
1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1302+3050_1302+305 others(38): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045163 | ||||||
| chr8:39045163 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3046C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045163 | |||||||
| chr8:39045163 | CAT | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(1): Show |
4 | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3051_1302+305 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045163 | ||||||
| chr8:39045165 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3048T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045165 | |||||||
| chr8:39045166 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1302+3049A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045166 | |||||||
| chr8:39045168 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0240 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3051A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045168 | |||||||
| chr8:39045170 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3053G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045170 | |||||||
| chr8:39045172 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(1): Show |
4 | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3055G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045172 | |||||||
| chr8:39045172 | GTA | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | NA18961.hp2 NA18965.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3061_1302+306 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045172 | ||||||
| chr8:39045175 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3058T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045175 | |||||||
| chr8:39045176 | A | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0045 others(10): Show |
13 | HG01192.hp1 HG01361.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3059A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045176 | |||||||
| chr8:39045178 | A | ACATATAG others(3): Show |
1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3061_1302+306 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045178 | |||||||
| chr8:39045178 | A | G | 16 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0045 others(13): Show |
16 | HG01192.hp1 HG01361.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3061A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045178 | |||||||
| chr8:39045183 | T | C | 9 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG03492.hp1 NA18961.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3066T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045183 | |||||||
| chr8:39045184 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0103 |
2 | HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3067A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045184 | |||||||
| chr8:39045185 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(3): Show |
6 | HG00639.hp2 HG01361.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3068T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045185 | |||||||
| chr8:39045187 | C | CCT | 4 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(1): Show |
4 | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3070_1302+307 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045187 | |||||||
| chr8:39045187 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3070C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045187 | |||||||
| chr8:39045188 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1302+3071A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045188 | |||||||
| chr8:39045189 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0103 a0001c0001t0004g0332 |
3 | HG02109.hp1 HG02647.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3072T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045189 | |||||||
| chr8:39045190 | A | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0103 |
2 | HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3073A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045190 | |||||||
| chr8:39045191 | C | CATATATG others(3): Show |
1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3088_1302+309 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045191 | ||||||
| chr8:39045191 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0103 a0001c0001t0001g0240 |
3 | HG00639.hp2 HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3074C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045191 | |||||||
| chr8:39045191 | CAT | C | 31 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(28): Show |
31 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1302+3079_1302+308 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045191 | ||||||
| chr8:39045192 | A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3075A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045192 | |||||||
| chr8:39045193 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1302+3076T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045193 | |||||||
| chr8:39045194 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(2): Show |
5 | HG00639.hp2 HG01361.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+3077A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045194 | |||||||
| chr8:39045194 | ATATG | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3079_1302+308 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045194 | ||||||
| chr8:39045195 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0103 |
2 | HG02109.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3078T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045195 | |||||||
| chr8:39045196 | A | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(4): Show |
7 | HG00639.hp2 HG01361.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3079A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045196 | |||||||
| chr8:39045200 | G | A | 31 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(28): Show |
31 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1302+3083G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045200 | |||||||
| chr8:39045200 | G | GTACACC | 3 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01361.hp1 HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3085_1302+308 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045200 | ||||||
| chr8:39045200 | GTA | G | 27 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3089_1302+309 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045200 | ||||||
| chr8:39045204 | A | G | 60 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(57): Show |
60 | HG00438.hp2 HG00673.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.1302+3087A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045204 | |||||||
| chr8:39045205 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01361.hp1 HG02135.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3088T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045205 | |||||||
| chr8:39045206 | A | G | 70 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(67): Show |
70 | HG00438.hp2 HG00673.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1302+3089A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045206 | |||||||
| chr8:39045211 | T | C | 34 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(31): Show |
34 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+3094T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045211 | |||||||
| chr8:39045212 | A | G | 12 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(9): Show |
12 | HG00639.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1302+3095A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045212 | |||||||
| chr8:39045213 | T | C | 36 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(33): Show |
36 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1302+3096T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045213 | |||||||
| chr8:39045215 | C | CCT | 33 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(30): Show |
33 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+3098_1302+309 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045215 | |||||||
| chr8:39045217 | T | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3100T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045217 | |||||||
| chr8:39045218 | A | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3101A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045218 | |||||||
| chr8:39045219 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3102C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045219 | |||||||
| chr8:39045220 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0004g0332 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+3103A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045220 | |||||||
| chr8:39045222 | A | G | 33 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(30): Show |
33 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1302+3105A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045222 | |||||||
| chr8:39045223 | T | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3106T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045223 | |||||||
| chr8:39045224 | A | AGGTG | 3 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01361.hp1 HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3107_1302+310 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045224 | |||||||
| chr8:39045224 | A | G | 35 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(32): Show |
35 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1302+3107A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045224 | |||||||
| chr8:39045225 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1302+3108T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045225 | |||||||
| chr8:39045228 | G | GTACACC | 27 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(24): Show |
27 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | ||||||
| chr8:39045228 | G | GTACCCC | 3 | a0001c0001t0001g0092 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | NA18953.hp1 NA18981.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | ||||||
| chr8:39045228 | GTATA | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0240 a0001c0001t0004g0332 |
3 | HG00639.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+3115_1302+311 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | ||||||
| chr8:39045228 | GTATATA | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045228 | ||||||
| chr8:39045230 | A | ACACACAC others(1): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01361.hp1 HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045230 | |||||||
| chr8:39045230 | A | ACACC | 3 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0068 |
3 | HG01074.hp1 HG03927.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1302+3113_1302+311 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045230 | |||||||
| chr8:39045233 | T | C | 33 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(30): Show |
33 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1302+3116T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045233 | |||||||
| chr8:39045234 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0240 a0001c0001t0004g0332 |
3 | HG00639.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+3117A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045234 | |||||||
| chr8:39045240 | A | G | 32 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(29): Show |
32 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3123A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045240 | |||||||
| chr8:39045241 | T | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(12): Show |
15 | HG00639.hp2 HG01074.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3124T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045241 | |||||||
| chr8:39045243 | C | CCT | 9 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3126_1302+312 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045243 | |||||||
| chr8:39045244 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1302+3127A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045244 | |||||||
| chr8:39045245 | T | C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0054 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+3128T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045245 | |||||||
| chr8:39045247 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1302+3130C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045247 | |||||||
| chr8:39045248 | A | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0054 others(3): Show |
6 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3131A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045248 | |||||||
| chr8:39045249 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02135.hp1 HG03831.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1302+3132T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045249 | |||||||
| chr8:39045250 | A | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3133A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045250 | |||||||
| chr8:39045250 | A | G | 9 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3133A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045250 | |||||||
| chr8:39045252 | A | AGGTG | 8 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0094 others(5): Show |
8 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3135_1302+313 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045252 | |||||||
| chr8:39045252 | A | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(10): Show |
13 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3135A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045252 | |||||||
| chr8:39045253 | T | C | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1302+3136T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045253 | |||||||
| chr8:39045253 | T | G | 22 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(19): Show |
22 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1302+3136T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045253 | |||||||
| chr8:39045254 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02135.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1302+3137G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045254 | |||||||
| chr8:39045254 | G | GTGTATAT others(17): Show |
1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3155_1302+315 others(28): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045254 | ||||||
| chr8:39045256 | G | A | 2 | a0001c0001t0001g0249 a0003c0004t0001g0302 |
2 | HG03688.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1302+3139G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045256 | |||||||
| chr8:39045256 | G | GTACACC | 9 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3141_1302+314 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045256 | ||||||
| chr8:39045256 | GTATA | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0240 |
3 | HG00639.hp2 HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1302+3143_1302+314 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045256 | ||||||
| chr8:39045256 | GTATATA | G | 21 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): Show |
21 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3141_1302+314 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045256 | ||||||
| chr8:39045258 | A | ACACACAC others(1): Show |
8 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0094 others(5): Show |
8 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3141_1302+314 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045258 | |||||||
| chr8:39045258 | A | G | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3141A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045258 | |||||||
| chr8:39045259 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0068 a0001c0001t0001g0089 others(1): Show |
4 | HG02135.hp1 HG03831.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3142T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045259 | |||||||
| chr8:39045260 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG02080.hp1 HG02135.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3143A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045260 | |||||||
| chr8:39045261 | T | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(9): Show |
12 | HG00639.hp2 HG01074.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1302+3144T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045261 | |||||||
| chr8:39045262 | A | ACACACAC others(35): Show |
1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1302+3145_1302+314 others(46): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045262 | |||||||
| chr8:39045262 | A | ACACACAC others(113): Show |
1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1302+3145_1302+314 others(124): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045262 | |||||||
| chr8:39045262 | A | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0043 others(10): Show |
13 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3145A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045262 | |||||||
| chr8:39045263 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0004g0332 |
2 | HG02647.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1302+3146T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045263 | |||||||
| chr8:39045263 | T | TGTGC | 8 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0094 others(5): Show |
8 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3149_1302+315 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045263 | ||||||
| chr8:39045268 | A | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0026 others(18): Show |
21 | HG00438.hp2 HG01256.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3151A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045268 | |||||||
| chr8:39045269 | T | C | 29 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(26): Show |
29 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1302+3152T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045269 | |||||||
| chr8:39045272 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1302+3155A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045272 | |||||||
| chr8:39045273 | T | C | 39 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(36): Show |
39 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1302+3156T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045273 | |||||||
| chr8:39045276 | A | C | 28 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(25): Show |
28 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1302+3159A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045276 | |||||||
| chr8:39045276 | ATATG | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3163_1302+316 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045276 | ||||||
| chr8:39045277 | T | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0092 others(7): Show |
10 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3160T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045277 | |||||||
| chr8:39045278 | A | ATATG | 13 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0168 others(10): Show |
13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3162_1302+316 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045278 | ||||||
| chr8:39045278 | A | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0092 others(7): Show |
10 | HG00438.hp2 HG01257.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3161A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045278 | |||||||
| chr8:39045278 | ATG | A | 20 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(17): Show |
20 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1302+3163_1302+316 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045278 | ||||||
| chr8:39045280 | G | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0054 others(15): Show |
18 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+3163G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045280 | |||||||
| chr8:39045280 | GTA | G | 10 | a0001c0001t0001g0082 a0001c0001t0001g0113 a0001c0001t0001g0114 others(7): Show |
10 | HG01884.hp2 HG02622.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3167_1302+316 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045280 | ||||||
| chr8:39045282 | A | G | 8 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0054 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+3165A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045282 | |||||||
| chr8:39045283 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1302+3166T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045283 | |||||||
| chr8:39045283 | T | TATGTGTG others(13): Show |
1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1302+3183_1302+318 others(24): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045283 | ||||||
| chr8:39045283 | T | TATGTGTG others(13): Show |
1 | a0006c0009t0001g0163 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1302+3215_1302+323 others(24): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045283 | ||||||
| chr8:39045284 | A | G | 38 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(35): Show |
38 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1302+3167A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045284 | |||||||
| chr8:39045285 | T | C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0054 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+3168T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045285 | |||||||
| chr8:39045285 | T | G | 9 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1302+3168T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045285 | |||||||
| chr8:39045286 | G | A | 13 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0168 others(10): Show |
13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3169G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045286 | |||||||
| chr8:39045287 | T | C | 30 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(27): Show |
30 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1302+3170T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045287 | |||||||
| chr8:39045292 | G | A | 14 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0134 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+3175G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045292 | |||||||
| chr8:39045293 | T | TACAC | 44 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0039 others(41): Show |
44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+3177_1302+318 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045293 | ||||||
| chr8:39045295 | C | CAT | 13 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0168 others(10): Show |
13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3179_1302+318 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045295 | ||||||
| chr8:39045297 | CCTATACA others(9): Show |
C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0117 |
2 | HG03239.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1302+3181_1302+319 others(20): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045297 | |||||||
| chr8:39045298 | C | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0001c0001t0001g0077 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+3181C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045298 | |||||||
| chr8:39045299 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+3182T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045299 | |||||||
| chr8:39045300 | A | ATG | 13 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0168 others(10): Show |
13 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1302+3184_1302+318 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045300 | ||||||
| chr8:39045301 | T | C | 125 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0001c0001t0001g0126 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1302+3184T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045301 | |||||||
| chr8:39045303 | C | T | 58 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(55): Show |
58 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1302+3186C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045303 | |||||||
| chr8:39045304 | A | G | 44 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0039 others(41): Show |
44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+3187A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045304 | |||||||
| chr8:39045305 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+3188T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045305 | |||||||
| chr8:39045307 | T | C | 44 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0039 others(41): Show |
44 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302+3190T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045307 | |||||||
| chr8:39045313 | T | TACAC | 14 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1302+3197_1302+320 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045313 | ||||||
| chr8:39045313 | T | TGTACAC | 31 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(28): Show |
31 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1302+3196_1302+319 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045313 | |||||||
| chr8:39045321 | T | C | 130 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1302+3204T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045321 | |||||||
| chr8:39045323 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3206C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045323 | |||||||
| chr8:39045323 | C | T | 47 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(44): Show |
47 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1302+3206C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045323 | |||||||
| chr8:39045324 | A | G | 48 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(45): Show |
48 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1302+3207A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045324 | |||||||
| chr8:39045325 | T | TGC | 16 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
16 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3209_1302+321 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045325 | ||||||
| chr8:39045327 | T | C | 32 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(29): Show |
32 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3210T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045327 | |||||||
| chr8:39045331 | T | TACATACA others(15): Show |
1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1302+3214_1302+321 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045331 | |||||||
| chr8:39045332 | G | A | 14 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0059 others(11): Show |
14 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.1302+3215G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045332 | |||||||
| chr8:39045333 | T | C | 13 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3216T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045333 | |||||||
| chr8:39045333 | T | TACAC | 10 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0039 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1302+3217_1302+322 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045333 | ||||||
| chr8:39045333 | T | TGTACAC | 21 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0045 others(18): Show |
21 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1302+3216_1302+321 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045333 | |||||||
| chr8:39045335 | C | T | 13 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3218C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045335 | |||||||
| chr8:39045337 | CCTAT | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3221_1302+322 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045337 | |||||||
| chr8:39045338 | C | A | 13 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3221C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045338 | |||||||
| chr8:39045341 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(3): Show |
6 | HG02056.hp1 HG02165.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302+3224T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045341 | |||||||
| chr8:39045342 | A | AGGTGCGT others(427): Show |
1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3225_1302+322 others(438): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045342 | |||||||
| chr8:39045342 | A | ATGTG | 32 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(29): Show |
32 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3225_1302+322 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045342 | |||||||
| chr8:39045343 | C | G | 13 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG00733.hp2 HG01169.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1302+3226C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045343 | |||||||
| chr8:39045343 | CATGTGTG others(1): Show |
C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3228_1302+323 others(12): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045343 | ||||||
| chr8:39045344 | A | G | 47 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(44): Show |
47 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.1302+3227A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045344 | |||||||
| chr8:39045352 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3235A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045352 | |||||||
| chr8:39045353 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3236C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045353 | |||||||
| chr8:39045354 | A | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3237A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045354 | |||||||
| chr8:39045355 | T | C | 42 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(39): Show |
42 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1302+3238T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045355 | |||||||
| chr8:39045357 | C | T | 15 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3240C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045357 | |||||||
| chr8:39045358 | A | ACC | 46 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(43): Show |
46 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1302+3241_1302+324 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045358 | |||||||
| chr8:39045358 | A | C | 2 | a0001c0001t0001g0168 a0001c0001t0004g0332 |
2 | HG02647.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1302+3241A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045358 | |||||||
| chr8:39045360 | A | G | 15 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302+3243A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045360 | |||||||
| chr8:39045362 | A | ATGTG | 32 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(29): Show |
32 | HG00438.hp2 HG00639.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302+3245_1302+324 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045362 | |||||||
| chr8:39045362 | A | G | 16 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
16 | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302+3245A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045362 | |||||||
| chr8:39045363 | G | C | 51 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(48): Show |
51 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.1302+3246G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045363 | |||||||
| chr8:39045363 | G | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0098 others(4): Show |
7 | HG00733.hp2 HG01993.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3246G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045363 | |||||||
| chr8:39045364 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1302+3247G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045364 | |||||||
| chr8:39045365 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1302+3248T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045365 | |||||||
| chr8:39045365 | T | TGC | 6 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0098 others(3): Show |
6 | HG00733.hp2 HG01993.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3249_1302+325 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045365 | ||||||
| chr8:39045367 | T | C | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3250T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045367 | |||||||
| chr8:39045370 | G | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0267 a0001c0001t0001g0300 others(1): Show |
4 | HG01169.hp1 HG04204.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3253G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045370 | |||||||
| chr8:39045372 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3255A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045372 | |||||||
| chr8:39045375 | T | C | 104 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(101): Show |
104 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.1302+3258T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045375 | |||||||
| chr8:39045375 | T | TACACGCA others(65): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1302+3262_1302+326 others(76): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045375 | ||||||
| chr8:39045375 | T | TACACGCA others(89): Show |
1 | a0001c0001t0001g0081 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1302+3262_1302+326 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045375 | ||||||
| chr8:39045376 | A | ACACG | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
30 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1302+3262_1302+326 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045376 | ||||||
| chr8:39045380 | C | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
30 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1302+3263C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045380 | |||||||
| chr8:39045384 | A | ACGTGTGT others(89): Show |
1 | a0002c0002t0002g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(115): Show |
1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(126): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(163): Show |
1 | a0002c0002t0002g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(174): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(63): Show |
3 | a0002c0002t0002g0188 a0002c0002t0002g0194 a0002c0002t0002g0195 |
3 | HG02258.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(74): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(89): Show |
1 | a0002c0002t0002g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(115): Show |
1 | a0002c0002t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(126): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(141): Show |
1 | a0002c0002t0002g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(152): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(93): Show |
1 | a0002c0002t0002g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(104): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ACGTGTGT others(141): Show |
1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(152): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTACGT others(73): Show |
1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(84): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTACGT others(149): Show |
2 | a0001c0001t0001g0267 a0001c0003t0001g0293 |
2 | HG06807.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(160): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTG | 58 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(55): Show |
58 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTGCGT others(881): Show |
1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(892): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTGCGT others(21): Show |
1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(32): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTGCGT others(23): Show |
3 | a0001c0001t0001g0131 a0002c0002t0002g0192 a0002c0002t0002g0193 |
3 | HG02965.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1302+3267_1302+326 others(34): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045384 | A | ATGTGCGT others(153): Show |
1 | a0001c0001t0001g0300 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1302+3267_1302+326 others(164): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045384 | |||||||
| chr8:39045385 | G | C | 78 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0036 others(75): Show |
78 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1302+3268G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045385 | |||||||
| chr8:39045385 | G | GGTGTGTC others(171): Show |
1 | a0001c0001t0001g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(119): Show |
1 | a0001c0001t0001g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(95): Show |
1 | a0001c0006t0001g0256 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(106): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(121): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0213 a0001c0003t0001g0294 |
3 | HG00738.hp1 HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(132): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(147): Show |
1 | a0001c0003t0001g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(158): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(67): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0208 a0001c0001t0001g0219 others(1): Show |
4 | HG02055.hp1 HG02738.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(78): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(93): Show |
16 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0209 others(13): Show |
16 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(104): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(171): Show |
1 | a0001c0001t0001g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(119): Show |
18 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
18 | HG00099.hp1 HG01255.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(145): Show |
15 | a0001c0001t0001g0186 a0001c0001t0001g0246 a0001c0001t0001g0247 others(12): Show |
15 | HG00639.hp1 HG01123.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(171): Show |
16 | a0001c0001t0001g0126 a0001c0001t0001g0207 a0001c0001t0001g0253 others(13): Show |
16 | HG00323.hp1 HG01168.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(197): Show |
8 | a0001c0001t0001g0127 a0001c0001t0001g0205 a0001c0001t0001g0255 others(5): Show |
8 | HG00735.hp2 HG02523.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(208): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(223): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0308 |
2 | HG01891.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(234): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(249): Show |
1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(260): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(275): Show |
1 | a0001c0001t0001g0216 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(286): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(145): Show |
1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(143): Show |
1 | a0001c0001t0001g0262 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(154): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(171): Show |
1 | a0001c0001t0001g0286 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(182): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(173): Show |
1 | a0001c0001t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(184): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(69): Show |
1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(80): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(95): Show |
1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(106): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(121): Show |
2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18954.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(132): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(145): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0282 |
2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(223): Show |
1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(234): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(71): Show |
1 | a0001c0001t0001g0271 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(82): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(97): Show |
3 | a0001c0001t0001g0226 a0001c0001t0001g0272 a0001c0001t0001g0291 |
3 | HG02083.hp2 NA18952.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(108): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(123): Show |
4 | a0001c0001t0001g0227 a0001c0001t0001g0234 a0001c0001t0001g0273 others(1): Show |
4 | NA18992.hp1 NA19009.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(134): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(149): Show |
1 | a0001c0001t0001g0328 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(160): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(175): Show |
1 | a0001c0001t0001g0287 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(186): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(121): Show |
7 | a0001c0001t0001g0236 a0001c0001t0001g0257 a0001c0001t0001g0311 others(4): Show |
7 | HG01928.hp1 HG01952.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(132): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(147): Show |
4 | a0001c0001t0001g0228 a0001c0001t0001g0250 a0001c0001t0001g0251 others(1): Show |
4 | HG01106.hp1 HG02622.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(158): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(173): Show |
2 | a0001c0001t0001g0229 a0001c0001t0001g0280 |
2 | HG01952.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1302+3274_1302+327 others(184): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(199): Show |
1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(210): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(251): Show |
1 | a0001c0001t0001g0278 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(262): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTC others(277): Show |
1 | a0001c0001t0001g0215 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(288): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTG others(45): Show |
1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1302+3292_1302+329 others(56): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | GGTGTGTG others(19): Show |
1 | a0002c0002t0002g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1302+3270_1302+329 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045385 | ||||||
| chr8:39045385 | G | T | 34 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
34 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+3268G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045385 | |||||||
| chr8:39045387 | T | TGC | 34 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
34 | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1302+3271_1302+327 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | ||||||
| chr8:39045387 | T | TGTGTGTA others(19): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0149 a0001c0001t0001g0184 |
3 | HG01361.hp2 HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1302+3322_1302+334 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | ||||||
| chr8:39045387 | T | TGTGTGTA others(45): Show |
1 | a0001c0001t0001g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1302+3296_1302+334 others(56): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | ||||||
| chr8:39045387 | TGTGTGTA others(19): Show |
T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0174 |
2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1302+3322_1302+334 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045387 | ||||||
| chr8:39045389 | T | TGTCTACA others(119): Show |
1 | a0001c0001t0001g0313 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | ||||||
| chr8:39045389 | T | TGTCTACA others(119): Show |
1 | a0001c0001t0001g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | ||||||
| chr8:39045389 | T | TGTCTACA others(145): Show |
1 | a0001c0001t0001g0314 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | ||||||
| chr8:39045389 | T | TGTCTACA others(199): Show |
1 | a0001c0001t0001g0277 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1302+3274_1302+327 others(210): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045389 | ||||||
| chr8:39045394 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3277A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045394 | |||||||
| chr8:39045395 | C | CACACACC others(39): Show |
23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
23 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1302+3295_1302+329 others(50): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045395 | ||||||
| chr8:39045395 | C | CACACACC others(63): Show |
5 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0080 others(2): Show |
5 | HG00621.hp1 HG02132.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302+3295_1302+329 others(74): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045395 | ||||||
| chr8:39045395 | C | CACACACC others(87): Show |
1 | a0001c0001t0001g0079 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1302+3295_1302+329 others(98): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045395 | ||||||
| chr8:39045398 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3281A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045398 | |||||||
| chr8:39045407 | T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3290T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045407 | |||||||
| chr8:39045407 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3290T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045407 | |||||||
| chr8:39045409 | TGC | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0100 others(1): Show |
4 | HG02572.hp1 NA18961.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3296_1302+329 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045409 | ||||||
| chr8:39045411 | C | CGTGTGTA others(15): Show |
1 | a0001c0001t0001g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1302+3295_1302+329 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045411 | ||||||
| chr8:39045412 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+3295G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045412 | |||||||
| chr8:39045413 | C | T | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1302+3296C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045413 | |||||||
| chr8:39045415 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1302+3298T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045415 | |||||||
| chr8:39045419 | TAC | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3309_1302+331 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045419 | ||||||
| chr8:39045420 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3303A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045420 | |||||||
| chr8:39045424 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3307A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045424 | |||||||
| chr8:39045433 | T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3316T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045433 | |||||||
| chr8:39045433 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3316T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045433 | |||||||
| chr8:39045439 | C | T | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+3322C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045439 | |||||||
| chr8:39045439 | CGTGTGTA others(19): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1302+3353_1302+337 others(30): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045439 | ||||||
| chr8:39045445 | TAC | T | 18 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
18 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1302+3335_1302+333 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045445 | ||||||
| chr8:39045446 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3329A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045446 | |||||||
| chr8:39045450 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3333A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045450 | |||||||
| chr8:39045454 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1302+3337C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045454 | |||||||
| chr8:39045459 | T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3342T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045459 | |||||||
| chr8:39045459 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3342T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045459 | |||||||
| chr8:39045464 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1302+3347G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045464 | |||||||
| chr8:39045471 | TAC | T | 31 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(28): Show |
31 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1302+3361_1302+336 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045471 | ||||||
| chr8:39045472 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1302+3355A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045472 | |||||||
| chr8:39045473 | C | CACACACC others(17): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0224 |
3 | HG02155.hp1 HG02602.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(28): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(169): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0112 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(180): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(271): Show |
1 | a0001c0001t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(282): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(197): Show |
1 | a0001c0001t0001g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(208): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(195): Show |
3 | a0001c0001t0001g0064 a0001c0001t0001g0100 a0001c0001t0001g0125 |
3 | NA18961.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(206): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(219): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0119 |
2 | HG01496.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(230): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(145): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0070 |
2 | HG02698.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(156): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(169): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01109.hp1 HG04115.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(180): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(193): Show |
1 | a0001c0001t0001g0101 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(204): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(119): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0106 |
2 | NA18982.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(130): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(143): Show |
7 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG02523.hp1 HG03017.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(154): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(167): Show |
1 | a0001c0001t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(178): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(93): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0092 |
3 | HG03927.hp1 NA18960.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(104): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(117): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0107 others(1): Show |
4 | HG02572.hp1 HG04199.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(128): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(141): Show |
3 | a0001c0001t0001g0067 a0001c0001t0001g0104 a0001c0001t0001g0223 |
3 | HG00673.hp1 NA18977.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(152): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(213): Show |
1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(224): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(67): Show |
1 | a0001c0001t0001g0026 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(78): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(91): Show |
1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(102): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(115): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0071 |
2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(126): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(139): Show |
1 | a0001c0001t0001g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(150): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(41): Show |
1 | a0001c0001t0001g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(52): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(65): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01256.hp1 HG01258.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1302+3378_1302+337 others(76): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(89): Show |
1 | a0001c0001t0001g0108 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(100): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACACC others(69): Show |
1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1302+3378_1302+337 others(80): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045473 | C | CACACCTA others(15): Show |
5 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0096 others(2): Show |
5 | HG00733.hp2 HG01928.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+3360_1302+336 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045473 | ||||||
| chr8:39045476 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1302+3359A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045476 | |||||||
| chr8:39045485 | T | C | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3368T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045485 | |||||||
| chr8:39045485 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3368T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045485 | |||||||
| chr8:39045496 | A | G | 6 | a0001c0001t0001g0056 a0001c0001t0001g0200 a0001c0001t0001g0215 others(3): Show |
6 | HG02055.hp2 HG02148.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+3379A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045496 | |||||||
| chr8:39045510 | G | A | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1302+3393G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045510 | |||||||
| chr8:39045540 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1302+3423A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045540 | |||||||
| chr8:39045540 | ATATATGT others(7): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1302+3439_1302+345 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045540 | ||||||
| chr8:39045556 | ATATGTGT others(7): Show |
A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302+3443_1302+345 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045556 | ||||||
| chr8:39045568 | G | GTATA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
27 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | ||||||
| chr8:39045568 | G | GTATATA | 4 | a0001c0001t0001g0037 a0001c0001t0001g0073 a0001c0001t0001g0075 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | ||||||
| chr8:39045568 | G | GTATATAT others(3): Show |
10 | a0002c0002t0002g0187 a0002c0002t0002g0188 a0002c0002t0002g0189 others(7): Show |
10 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | ||||||
| chr8:39045568 | G | GTATATAT others(5): Show |
2 | a0002c0002t0002g0130 a0002c0002t0002g0190 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1302+3452_1302+345 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | ||||||
| chr8:39045568 | G | GTATATAT others(7): Show |
1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+3452_1302+345 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | ||||||
| chr8:39045568 | GTGTA | G | 133 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1302+3453_1302+345 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045568 | ||||||
| chr8:39045570 | G | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
51 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1302+3453G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045570 | |||||||
| chr8:39045570 | GTA | G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1302+3470_1302+347 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39045570 | ||||||
| chr8:39045587 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1302+3470T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045587 | |||||||
| chr8:39045609 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1302+3492C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045609 | |||||||
| chr8:39045663 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1302+3546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045663 | |||||||
| chr8:39045707 | T | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+3590T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045707 | |||||||
| chr8:39045796 | T | A | 4 | a0002c0002t0002g0187 a0002c0002t0002g0189 a0002c0002t0002g0197 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+3679T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045796 | |||||||
| chr8:39045815 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1302+3698A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045815 | |||||||
| chr8:39045872 | G | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(325): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1302+3755G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045872 | |||||||
| chr8:39045927 | T | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+3810T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045927 | |||||||
| chr8:39045954 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1302+3837A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045954 | |||||||
| chr8:39045979 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1302+3862G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39045979 | |||||||
| chr8:39046435 | C | T | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+4318C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046435 | |||||||
| chr8:39046497 | T | G | 3 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0178 |
3 | HG00621.hp2 NA18945.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1302+4380T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046497 | |||||||
| chr8:39046510 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1302+4393C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046510 | |||||||
| chr8:39046685 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1302+4568C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046685 | |||||||
| chr8:39046775 | AT | A | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+4671delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39046775 | ||||||
| chr8:39046797 | G | T | 2 | a0002c0002t0002g0192 a0002c0002t0002g0193 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1302+4680G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39046797 | |||||||
| chr8:39047024 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1302+4907C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047024 | |||||||
| chr8:39047044 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1302+4927C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047044 | |||||||
| chr8:39047395 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+5278T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047395 | |||||||
| chr8:39047410 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1302+5293C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047410 | |||||||
| chr8:39047456 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1302+5339A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047456 | |||||||
| chr8:39047614 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1302+5497T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047614 | |||||||
| chr8:39047696 | A | C | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+5579A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047696 | |||||||
| chr8:39047825 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302+5708G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39047825 | |||||||
| chr8:39048065 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1302+5948C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048065 | |||||||
| chr8:39048298 | G | A | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1302+6181G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048298 | |||||||
| chr8:39048567 | C | G | 1 | a0001c0007t0001g0268 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1303-5914C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048567 | |||||||
| chr8:39048574 | T | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0156 |
2 | HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1303-5907T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048574 | |||||||
| chr8:39048623 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0327 |
3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1303-5858C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048623 | |||||||
| chr8:39048984 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1303-5497G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39048984 | |||||||
| chr8:39048998 | G | GT | 6 | a0001c0001t0001g0045 a0001c0001t0001g0125 a0001c0001t0001g0134 others(3): Show |
6 | HG01361.hp1 HG02074.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-5464dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39048998 | ||||||
| chr8:39048998 | GT | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1303-5464delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39048998 | ||||||
| chr8:39048998 | GTT | G | 15 | a0001c0001t0001g0136 a0002c0002t0002g0130 a0002c0002t0002g0187 others(12): Show |
15 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1303-5465_1303-546 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39048998 | ||||||
| chr8:39049651 | C | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0112 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1303-4830C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39049651 | |||||||
| chr8:39049696 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1303-4785C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39049696 | |||||||
| chr8:39049757 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0212 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1303-4724T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39049757 | |||||||
| chr8:39050008 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0112 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1303-4473A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050008 | |||||||
| chr8:39050144 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1303-4337G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050144 | |||||||
| chr8:39050350 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1303-4131T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050350 | |||||||
| chr8:39050393 | T | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1303-4088T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050393 | |||||||
| chr8:39050452 | C | CT | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1303-4016dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050452 | ||||||
| chr8:39050452 | CT | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
7 | HG00639.hp2 HG03704.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-4016delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050452 | ||||||
| chr8:39050500 | G | A | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1303-3981G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050500 | |||||||
| chr8:39050565 | T | G | 1 | a0001c0001t0001g0279 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1303-3916T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050565 | |||||||
| chr8:39050571 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1303-3910G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050571 | |||||||
| chr8:39050703 | A | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1303-3778A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050703 | |||||||
| chr8:39050751 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1303-3730T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050751 | |||||||
| chr8:39050830 | G | GT | 11 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0066 others(8): Show |
11 | HG00621.hp2 HG02683.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303-3626dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050830 | ||||||
| chr8:39050830 | GT | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1303-3626delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050830 | ||||||
| chr8:39050830 | GTT | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(5): Show |
8 | HG01168.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-3627_1303-362 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39050830 | ||||||
| chr8:39050863 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1303-3618A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39050863 | |||||||
| chr8:39051140 | C | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0073 a0001c0001t0001g0075 others(2): Show |
5 | HG02970.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-3341C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051140 | |||||||
| chr8:39051340 | T | G | 1 | a0001c0006t0001g0256 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1303-3141T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051340 | |||||||
| chr8:39051390 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1303-3091G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051390 | |||||||
| chr8:39051612 | C | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-2869C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051612 | |||||||
| chr8:39051637 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1303-2844G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051637 | |||||||
| chr8:39051742 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1303-2739T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39051742 | |||||||
| chr8:39052042 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1303-2439G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052042 | |||||||
| chr8:39052130 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1303-2351C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052130 | |||||||
| chr8:39052342 | A | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1303-2139A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052342 | |||||||
| chr8:39052530 | CTA | C | 7 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0001g0263 others(4): Show |
7 | HG02074.hp2 NA18944.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-1944_1303-194 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | 39052530 | ||||||
| chr8:39052542 | C | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-1939C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052542 | |||||||
| chr8:39052728 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1303-1753A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052728 | |||||||
| chr8:39052897 | A | G | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1303-1584A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39052897 | |||||||
| chr8:39053097 | G | A | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1303-1384G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053097 | |||||||
| chr8:39053114 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1303-1367T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053114 | |||||||
| chr8:39053225 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1303-1256A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053225 | |||||||
| chr8:39053327 | A | C | 1 | a0001c0001t0001g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1303-1154A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053327 | |||||||
| chr8:39053472 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1303-1009C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053472 | |||||||
| chr8:39053872 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1303-609T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39053872 | |||||||
| chr8:39054121 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01256.hp1 HG01258.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1303-360A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054121 | |||||||
| chr8:39054137 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1303-344C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054137 | |||||||
| chr8:39054291 | T | C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1303-190T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054291 | |||||||
| chr8:39054419 | T | G | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1303-62T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054419 | |||||||
| chr8:39054434 | C | A | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1303-47C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | 39054434 | |||||||
| chr8:39054602 | G | GA | 143 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1395+49dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 39054602 | ||||||
| chr8:39054602 | GA | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(33): Show |
36 | HG00621.hp1 HG01255.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1395+49delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 39054602 | ||||||
| chr8:39054602 | GAA | G | 16 | a0001c0001t0001g0072 a0001c0001t0001g0109 a0002c0002t0002g0130 others(13): Show |
16 | HG01257.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1395+48_1395+49del others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 39054602 | ||||||
| chr8:39054714 | G | A | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395+141G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054714 | |||||||
| chr8:39054736 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1395+163C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054736 | |||||||
| chr8:39054875 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1395+302T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054875 | |||||||
| chr8:39054947 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1395+374G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054947 | |||||||
| chr8:39054989 | A | C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1395+416A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39054989 | |||||||
| chr8:39055148 | C | T | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1396-429C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39055148 | |||||||
| chr8:39055287 | G | T | 287 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1396-290G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39055287 | |||||||
| chr8:39055323 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1396-254G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | chr8 | 39055323 | |||||||
| chr8:39055805 | G | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1591+33G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39055805 | |||||||
| chr8:39056037 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1591+265A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056037 | |||||||
| chr8:39056380 | GT | G | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+613delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39056380 | ||||||
| chr8:39056544 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1591+772C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056544 | |||||||
| chr8:39056555 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1591+783G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056555 | |||||||
| chr8:39056657 | T | G | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+885T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056657 | |||||||
| chr8:39056719 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1591+947A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056719 | |||||||
| chr8:39056898 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1591+1126A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39056898 | |||||||
| chr8:39057019 | CTATGTTT others(3): Show |
C | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1591+1260_1591+126 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057019 | ||||||
| chr8:39057061 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1591+1289C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057061 | |||||||
| chr8:39057084 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1591+1312A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057084 | |||||||
| chr8:39057344 | T | TAATATAT others(20): Show |
1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1591+1583_1591+160 others(31): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057344 | ||||||
| chr8:39057493 | TTG | T | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+1726_1591+172 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057493 | ||||||
| chr8:39057749 | A | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1591+1977A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057749 | |||||||
| chr8:39057874 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1591+2102C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057874 | |||||||
| chr8:39057891 | C | CTTTTTAG others(6): Show |
1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1591+2120_1591+212 others(17): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39057891 | ||||||
| chr8:39057924 | C | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1591+2152C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39057924 | |||||||
| chr8:39058085 | G | T | 132 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1591+2313G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39058085 | |||||||
| chr8:39058818 | C | T | 57 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0214 others(54): Show |
57 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1591+3046C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39058818 | |||||||
| chr8:39059082 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0053 others(2): Show |
5 | HG01074.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1591+3310A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059082 | |||||||
| chr8:39059182 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1591+3410G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059182 | |||||||
| chr8:39059217 | G | A | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1591+3445G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059217 | |||||||
| chr8:39059484 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1591+3712C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059484 | |||||||
| chr8:39059485 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1591+3713C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059485 | |||||||
| chr8:39059660 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1591+3888C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059660 | |||||||
| chr8:39059930 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1591+4158T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39059930 | |||||||
| chr8:39060141 | G | C | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1591+4369G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060141 | |||||||
| chr8:39060200 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1591+4428A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060200 | |||||||
| chr8:39060330 | G | A | 48 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(45): Show |
48 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1591+4558G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060330 | |||||||
| chr8:39060354 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1591+4582G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060354 | |||||||
| chr8:39060837 | G | T | 1 | a0002c0010t0002g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1591+5065G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39060837 | |||||||
| chr8:39061154 | T | C | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1591+5382T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061154 | |||||||
| chr8:39061182 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1591+5410G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061182 | |||||||
| chr8:39061190 | T | G | 1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1591+5418T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061190 | |||||||
| chr8:39061249 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1591+5477A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061249 | |||||||
| chr8:39061472 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1591+5700A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061472 | |||||||
| chr8:39061516 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1591+5744T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061516 | |||||||
| chr8:39061546 | C | A | 8 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
8 | HG02074.hp2 NA18944.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1591+5774C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061546 | |||||||
| chr8:39061888 | T | C | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.1591+6116T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39061888 | |||||||
| chr8:39062003 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1591+6231G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062003 | |||||||
| chr8:39062613 | A | G | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1591+6841A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062613 | |||||||
| chr8:39062870 | G | A | 132 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1591+7098G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062870 | |||||||
| chr8:39062994 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1591+7222C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39062994 | |||||||
| chr8:39063217 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1591+7445G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063217 | |||||||
| chr8:39063461 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1591+7689G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063461 | |||||||
| chr8:39063579 | A | G | 1 | a0002c0002t0002g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1592-7719A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063579 | |||||||
| chr8:39063686 | C | T | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1592-7612C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063686 | |||||||
| chr8:39063777 | A | G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1592-7521A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063777 | |||||||
| chr8:39063794 | C | G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1592-7504C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063794 | |||||||
| chr8:39063947 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1592-7351C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39063947 | |||||||
| chr8:39064026 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1592-7272C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064026 | |||||||
| chr8:39064081 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0030 |
2 | NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1592-7217T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064081 | |||||||
| chr8:39064082 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1592-7216C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064082 | |||||||
| chr8:39064216 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1592-7082G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064216 | |||||||
| chr8:39064339 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1592-6959T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064339 | |||||||
| chr8:39064463 | G | A | 20 | a0001c0001t0001g0216 a0001c0001t0001g0254 a0001c0001t0001g0261 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1592-6835G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064463 | |||||||
| chr8:39064505 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-6793T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064505 | |||||||
| chr8:39064514 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-6784T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064514 | |||||||
| chr8:39064595 | T | A | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1592-6703T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064595 | |||||||
| chr8:39064630 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0066 a0001c0001t0001g0105 others(1): Show |
4 | HG02698.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-6668C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064630 | |||||||
| chr8:39064702 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0078 |
2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1592-6596C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064702 | |||||||
| chr8:39064790 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1592-6508G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064790 | |||||||
| chr8:39064972 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1592-6326T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39064972 | |||||||
| chr8:39065012 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0170 |
2 | HG01106.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1592-6286C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065012 | |||||||
| chr8:39065202 | G | GT | 9 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0242 others(6): Show |
9 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1592-6087dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065202 | ||||||
| chr8:39065212 | G | GT | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
51 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(48): Show |
intron_variant | MODIFIER | c.1592-6074dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065212 | ||||||
| chr8:39065217 | T | C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1592-6081T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065217 | |||||||
| chr8:39065439 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1592-5859G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065439 | |||||||
| chr8:39065501 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1592-5797A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065501 | |||||||
| chr8:39065584 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1592-5714C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065584 | |||||||
| chr8:39065620 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0005c0008t0001g0120 |
3 | HG01884.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1592-5678A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065620 | |||||||
| chr8:39065647 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1592-5651G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065647 | |||||||
| chr8:39065659 | C | CA | 7 | a0001c0001t0001g0111 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG01192.hp2 HG02055.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1592-5616dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065659 | ||||||
| chr8:39065659 | CA | C | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
120 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1592-5616delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065659 | ||||||
| chr8:39065659 | CAA | C | 130 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1592-5617_1592-561 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39065659 | ||||||
| chr8:39065710 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0174 |
2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1592-5588C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065710 | |||||||
| chr8:39065800 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1592-5498G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065800 | |||||||
| chr8:39065908 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0107 |
2 | NA18944.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1592-5390C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065908 | |||||||
| chr8:39065934 | A | G | 39 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(36): Show |
39 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1592-5364A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39065934 | |||||||
| chr8:39066040 | C | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1592-5258C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066040 | |||||||
| chr8:39066042 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1592-5256G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066042 | |||||||
| chr8:39066067 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1592-5231C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066067 | |||||||
| chr8:39066115 | T | C | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1592-5183T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066115 | |||||||
| chr8:39066130 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0230 |
2 | HG01070.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1592-5168T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066130 | |||||||
| chr8:39066163 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1592-5135T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066163 | |||||||
| chr8:39066204 | A | G | 1 | a0005c0008t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1592-5094A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066204 | |||||||
| chr8:39066486 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0078 |
2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1592-4812G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066486 | |||||||
| chr8:39066560 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1592-4738A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066560 | |||||||
| chr8:39066703 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1592-4595C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066703 | |||||||
| chr8:39066742 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1592-4556G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066742 | |||||||
| chr8:39066773 | A | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-4525A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066773 | |||||||
| chr8:39066779 | G | T | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1592-4519G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066779 | |||||||
| chr8:39066800 | G | C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1592-4498G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066800 | |||||||
| chr8:39066877 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0327 |
3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1592-4421G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066877 | |||||||
| chr8:39066878 | A | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1592-4420A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066878 | |||||||
| chr8:39066993 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1592-4305A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39066993 | |||||||
| chr8:39067084 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1592-4214G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067084 | |||||||
| chr8:39067311 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0235 |
2 | HG02056.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1592-3987G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067311 | |||||||
| chr8:39067379 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1592-3919C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067379 | |||||||
| chr8:39067494 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1592-3804A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067494 | |||||||
| chr8:39067622 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1592-3676T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067622 | |||||||
| chr8:39067954 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1592-3344A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067954 | |||||||
| chr8:39067974 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1592-3324A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39067974 | |||||||
| chr8:39068027 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1592-3271G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068027 | |||||||
| chr8:39068057 | G | C | 1 | a0001c0001t0001g0325 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1592-3241G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068057 | |||||||
| chr8:39068153 | G | A | 3 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0277 |
3 | HG02155.hp2 NA18954.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1592-3145G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068153 | |||||||
| chr8:39068440 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1592-2858C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068440 | |||||||
| chr8:39068449 | T | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-2849T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068449 | |||||||
| chr8:39068508 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1592-2790C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068508 | |||||||
| chr8:39068633 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-2665C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068633 | |||||||
| chr8:39068675 | C | CA | 11 | a0001c0001t0001g0159 a0001c0001t0001g0165 a0001c0001t0001g0175 others(8): Show |
11 | HG01109.hp2 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1592-2584dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CA | C | 59 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0032 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1592-2584delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAA | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
50 | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-2585_1592-258 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAA | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(9): Show |
12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1592-2586_1592-258 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAA | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0124 others(5): Show |
8 | HG02132.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1592-2587_1592-258 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAA | C | 7 | a0002c0002t0002g0130 a0002c0002t0002g0191 a0002c0002t0002g0192 others(4): Show |
7 | HG02559.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1592-2588_1592-258 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0178 a0001c0001t0001g0249 |
3 | HG00621.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1592-2593_1592-258 others(14): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1592-2594_1592-258 others(15): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0141 |
2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1592-2595_1592-258 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(6): Show |
C | 13 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0060 others(10): Show |
13 | HG01192.hp1 HG01361.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1592-2596_1592-258 others(17): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(7): Show |
C | 75 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(72): Show |
75 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1592-2597_1592-258 others(18): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0266 others(1): Show |
4 | NA18944.hp1 NA18974.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1592-2598_1592-258 others(19): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0205 |
2 | HG02523.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1592-2599_1592-258 others(20): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(15): Show |
C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1592-2605_1592-258 others(26): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068675 | CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1592-2608_1592-258 others(29): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39068675 | ||||||
| chr8:39068749 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1592-2549A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39068749 | |||||||
| chr8:39069020 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-2278C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069020 | |||||||
| chr8:39069081 | G | C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1592-2217G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069081 | |||||||
| chr8:39069260 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-2038C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069260 | |||||||
| chr8:39069489 | A | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1592-1809A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069489 | |||||||
| chr8:39069507 | G | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1592-1791G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069507 | |||||||
| chr8:39069766 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1592-1532A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069766 | |||||||
| chr8:39069783 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-1515T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069783 | |||||||
| chr8:39069815 | A | G | 1 | a0002c0002t0002g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1592-1483A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069815 | |||||||
| chr8:39069853 | A | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0327 |
3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1592-1445A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069853 | |||||||
| chr8:39069904 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1592-1394A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069904 | |||||||
| chr8:39069950 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1592-1348C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39069950 | |||||||
| chr8:39069979 | TA | T | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1592-1295delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39069979 | ||||||
| chr8:39069979 | TAA | T | 95 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(92): Show |
95 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1592-1296_1592-129 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39069979 | ||||||
| chr8:39070152 | CA | C | 253 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1592-1125delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 39070152 | ||||||
| chr8:39070191 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-1107C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070191 | |||||||
| chr8:39070241 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1592-1057T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070241 | |||||||
| chr8:39070612 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1592-686G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070612 | |||||||
| chr8:39070713 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1592-585G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070713 | |||||||
| chr8:39070806 | A | T | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1592-492A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39070806 | |||||||
| chr8:39071067 | A | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-231A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071067 | |||||||
| chr8:39071132 | G | T | 21 | a0001c0001t0001g0213 a0001c0001t0001g0291 a0001c0001t0001g0296 others(18): Show |
21 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1592-166G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071132 | |||||||
| chr8:39071164 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(14): Show |
17 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1592-134A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071164 | |||||||
| chr8:39071216 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1592-82G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | chr8 | 39071216 | |||||||
| chr8:39071450 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1697+47C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071450 | |||||||
| chr8:39071465 | C | CT | 19 | a0001c0001t0001g0043 a0001c0001t0001g0090 a0001c0001t0001g0115 others(16): Show |
19 | HG01346.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1697+82dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39071465 | ||||||
| chr8:39071465 | C | CTT | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1697+81_1697+82dup others(2): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39071465 | ||||||
| chr8:39071465 | CT | C | 131 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1697+82delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39071465 | ||||||
| chr8:39071540 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1697+137C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071540 | |||||||
| chr8:39071569 | T | C | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1697+166T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071569 | |||||||
| chr8:39071619 | A | G | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1697+216A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071619 | |||||||
| chr8:39071624 | G | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1697+221G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071624 | |||||||
| chr8:39071754 | T | C | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1697+351T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071754 | |||||||
| chr8:39071764 | C | T | 2 | a0002c0002t0002g0187 a0002c0010t0002g0198 |
2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1697+361C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39071764 | |||||||
| chr8:39072128 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1697+725T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39072128 | |||||||
| chr8:39072619 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1697+1216G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39072619 | |||||||
| chr8:39072702 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1697+1299A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39072702 | |||||||
| chr8:39073221 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1697+1818G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073221 | |||||||
| chr8:39073672 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1697+2269C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073672 | |||||||
| chr8:39073738 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1697+2335T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073738 | |||||||
| chr8:39073808 | A | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1697+2405A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073808 | |||||||
| chr8:39073848 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0278 |
2 | NA18984.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1697+2445T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39073848 | |||||||
| chr8:39074011 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1697+2608C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074011 | |||||||
| chr8:39074073 | A | G | 5 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG00621.hp1 HG02132.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1697+2670A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074073 | |||||||
| chr8:39074229 | T | C | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1697+2826T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074229 | |||||||
| chr8:39074247 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1697+2844G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074247 | |||||||
| chr8:39074375 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1698-2853T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074375 | |||||||
| chr8:39074555 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0269 |
2 | NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1698-2673A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074555 | |||||||
| chr8:39074674 | C | A | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1698-2554C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39074674 | |||||||
| chr8:39074903 | C | CT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0103 others(10): Show |
13 | HG01255.hp2 HG01891.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1698-2303dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39074903 | ||||||
| chr8:39074903 | CT | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0143 a0001c0001t0001g0240 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-2303delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | 39074903 | ||||||
| chr8:39075078 | T | C | 90 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(87): Show |
90 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1698-2150T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075078 | |||||||
| chr8:39075107 | A | G | 1 | a0002c0002t0002g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1698-2121A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075107 | |||||||
| chr8:39075176 | G | A | 1 | a0001c0007t0001g0268 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1698-2052G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075176 | |||||||
| chr8:39075187 | G | T | 39 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(36): Show |
39 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1698-2041G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075187 | |||||||
| chr8:39075338 | C | G | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1698-1890C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075338 | |||||||
| chr8:39075450 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0103 |
2 | NA18943.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1698-1778T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075450 | |||||||
| chr8:39075622 | T | C | 4 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG02886.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1698-1606T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075622 | |||||||
| chr8:39075646 | G | C | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1698-1582G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075646 | |||||||
| chr8:39075686 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1698-1542G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075686 | |||||||
| chr8:39075748 | C | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1698-1480C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075748 | |||||||
| chr8:39075825 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1698-1403G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39075825 | |||||||
| chr8:39076452 | A | T | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1698-776A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076452 | |||||||
| chr8:39076538 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1698-690A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076538 | |||||||
| chr8:39076739 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1698-489T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076739 | |||||||
| chr8:39076814 | A | G | 132 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1698-414A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076814 | |||||||
| chr8:39076983 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1698-245G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39076983 | |||||||
| chr8:39077064 | C | T | 129 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1698-164C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39077064 | |||||||
| chr8:39077065 | G | A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698-163G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39077065 | |||||||
| chr8:39077218 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | NA18962.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1698-10C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | chr8 | 39077218 | |||||||
| chr8:39077590 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1881+179C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077590 | |||||||
| chr8:39077627 | A | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0162 others(5): Show |
8 | HG00621.hp2 HG02074.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1881+216A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077627 | |||||||
| chr8:39077702 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0174 |
2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1881+291T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077702 | |||||||
| chr8:39077705 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1881+294C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077705 | |||||||
| chr8:39077768 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1881+357A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077768 | |||||||
| chr8:39077778 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1881+367C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39077778 | |||||||
| chr8:39078175 | C | A | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1881+764C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078175 | |||||||
| chr8:39078308 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1881+897A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078308 | |||||||
| chr8:39078362 | C | CA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1881+968dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078362 | ||||||
| chr8:39078362 | C | CAAA | 117 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1881+966_1881+968d others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078362 | ||||||
| chr8:39078362 | CA | C | 8 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG00323.hp2 HG01070.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1881+968delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078362 | ||||||
| chr8:39078379 | A | AAAT | 8 | a0001c0001t0001g0216 a0001c0001t0001g0261 a0001c0001t0001g0306 others(5): Show |
8 | HG00673.hp2 HG02135.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.1881+968_1881+969i others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078379 | |||||||
| chr8:39078425 | TATCTA | T | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1881+1019_1881+102 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39078425 | ||||||
| chr8:39078507 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1881+1096C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078507 | |||||||
| chr8:39078654 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1881+1243G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078654 | |||||||
| chr8:39078768 | G | A | 133 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1881+1357G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39078768 | |||||||
| chr8:39079257 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1881+1846G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079257 | |||||||
| chr8:39079340 | C | CT | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1881+1929_1881+193 others(5): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079340 | |||||||
| chr8:39079379 | T | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1881+1968T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079379 | |||||||
| chr8:39079415 | T | TTCCATGT others(10): Show |
1 | a0001c0001t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1881+2012_1881+202 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39079415 | ||||||
| chr8:39079468 | T | C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1881+2057T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079468 | |||||||
| chr8:39079588 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1881+2177T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079588 | |||||||
| chr8:39079594 | A | AT | 81 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(78): Show |
81 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1881+2201dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39079594 | ||||||
| chr8:39079595 | T | A | 132 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1881+2184T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079595 | |||||||
| chr8:39079725 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1881+2314C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079725 | |||||||
| chr8:39079771 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1881+2360G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079771 | |||||||
| chr8:39079781 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1881+2370C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079781 | |||||||
| chr8:39079973 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1881+2562A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39079973 | |||||||
| chr8:39080097 | ATTAT | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0186 |
3 | HG03492.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1882-2537_1882-253 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080097 | ||||||
| chr8:39080185 | C | CA | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1882-2449dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080185 | ||||||
| chr8:39080190 | AAAT | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | NA18969.hp2 NA19001.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1882-2450_1882-244 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080190 | |||||||
| chr8:39080247 | G | T | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1882-2394G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080247 | |||||||
| chr8:39080412 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1882-2229T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080412 | |||||||
| chr8:39080424 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1882-2217A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080424 | |||||||
| chr8:39080548 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1882-2093G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080548 | |||||||
| chr8:39080561 | A | G | 90 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(87): Show |
90 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1882-2080A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080561 | |||||||
| chr8:39080587 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0056 |
3 | HG01993.hp2 HG03491.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1882-2054C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080587 | |||||||
| chr8:39080681 | T | C | 2 | a0001c0001t0003g0133 a0001c0001t0004g0332 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1882-1960T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080681 | |||||||
| chr8:39080724 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0054 |
2 | HG01074.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1882-1917C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080724 | |||||||
| chr8:39080725 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1882-1916G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080725 | |||||||
| chr8:39080846 | G | C | 273 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1882-1795G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080846 | |||||||
| chr8:39080853 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1788C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080853 | |||||||
| chr8:39080855 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1786A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080855 | |||||||
| chr8:39080857 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1784T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080857 | |||||||
| chr8:39080859 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1782G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080859 | |||||||
| chr8:39080860 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1781C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080860 | |||||||
| chr8:39080861 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1780T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080861 | |||||||
| chr8:39080863 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1778C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080863 | |||||||
| chr8:39080864 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1777G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080864 | |||||||
| chr8:39080869 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1772G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080869 | |||||||
| chr8:39080870 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1771G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080870 | |||||||
| chr8:39080873 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1768G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080873 | |||||||
| chr8:39080875 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1766T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080875 | |||||||
| chr8:39080876 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1765G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080876 | |||||||
| chr8:39080877 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1764G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080877 | |||||||
| chr8:39080879 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1762G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080879 | |||||||
| chr8:39080880 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1761G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080880 | |||||||
| chr8:39080882 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1759G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080882 | |||||||
| chr8:39080883 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1758G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080883 | |||||||
| chr8:39080884 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1757C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080884 | |||||||
| chr8:39080885 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1756C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080885 | |||||||
| chr8:39080889 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1752G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080889 | |||||||
| chr8:39080891 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1750T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080891 | |||||||
| chr8:39080892 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1749G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080892 | |||||||
| chr8:39080903 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1738T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080903 | |||||||
| chr8:39080905 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1736G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080905 | |||||||
| chr8:39080907 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1734A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080907 | |||||||
| chr8:39080908 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1733G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080908 | |||||||
| chr8:39080910 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1731A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080910 | |||||||
| chr8:39080911 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1730G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080911 | |||||||
| chr8:39080914 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1727T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080914 | |||||||
| chr8:39080915 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1726G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080915 | |||||||
| chr8:39080916 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1725T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080916 | |||||||
| chr8:39080917 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1724G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080917 | |||||||
| chr8:39080919 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1722G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080919 | |||||||
| chr8:39080921 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1720G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080921 | |||||||
| chr8:39080922 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1719G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080922 | |||||||
| chr8:39080926 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1715G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080926 | |||||||
| chr8:39080932 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1709C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080932 | |||||||
| chr8:39080933 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1708C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080933 | |||||||
| chr8:39080936 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1705C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080936 | |||||||
| chr8:39080937 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1704C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080937 | |||||||
| chr8:39080938 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1703C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080938 | |||||||
| chr8:39080944 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1697G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080944 | |||||||
| chr8:39080946 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1695G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080946 | |||||||
| chr8:39080948 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1693G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080948 | |||||||
| chr8:39080948 | G | GT | 158 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1882-1673dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080948 | ||||||
| chr8:39080948 | G | GTT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0083 others(6): Show |
9 | HG00733.hp1 HG01168.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1882-1674_1882-167 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 39080948 | ||||||
| chr8:39080950 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1691T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080950 | |||||||
| chr8:39080953 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1688T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080953 | |||||||
| chr8:39080954 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1687T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080954 | |||||||
| chr8:39080956 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1685T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080956 | |||||||
| chr8:39080957 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1684T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080957 | |||||||
| chr8:39080960 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1681T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080960 | |||||||
| chr8:39080961 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1680T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080961 | |||||||
| chr8:39080966 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1675T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080966 | |||||||
| chr8:39080967 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1674T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080967 | |||||||
| chr8:39080972 | GCAGGGTC others(4): Show |
G | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1882-1668_1882-165 others(15): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39080972 | |||||||
| chr8:39081009 | A | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1882-1632A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081009 | |||||||
| chr8:39081088 | C | G | 133 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1882-1553C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081088 | |||||||
| chr8:39081109 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
50 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1882-1532G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081109 | |||||||
| chr8:39081228 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1882-1413C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081228 | |||||||
| chr8:39081287 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1882-1354G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081287 | |||||||
| chr8:39081409 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1882-1232A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081409 | |||||||
| chr8:39081414 | A | G | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1882-1227A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081414 | |||||||
| chr8:39081813 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02622.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1882-828A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081813 | |||||||
| chr8:39081991 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1882-650G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39081991 | |||||||
| chr8:39082020 | G | A | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1882-621G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082020 | |||||||
| chr8:39082134 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1882-507A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082134 | |||||||
| chr8:39082214 | C | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1882-427C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082214 | |||||||
| chr8:39082570 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1882-71T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | chr8 | 39082570 | |||||||
| chr8:39082773 | GAAATCTC others(9): Show |
G | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1962+53_1962+68del others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082773 | |||||||
| chr8:39082811 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1962+90G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082811 | |||||||
| chr8:39082873 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0067 |
2 | HG00673.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1963-95A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082873 | |||||||
| chr8:39082948 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1963-20G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 17/21 | chr8 | 39082948 | |||||||
| chr8:39083096 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2068+23A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083096 | |||||||
| chr8:39083147 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2068+74C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083147 | |||||||
| chr8:39083168 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2068+95A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083168 | |||||||
| chr8:39083293 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+220A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083293 | |||||||
| chr8:39083302 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2068+229C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083302 | |||||||
| chr8:39083403 | G | A | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2068+330G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083403 | |||||||
| chr8:39083415 | A | G | 22 | a0001c0001t0001g0213 a0001c0001t0001g0291 a0001c0001t0001g0296 others(19): Show |
22 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2068+342A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083415 | |||||||
| chr8:39083630 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0278 |
2 | NA18984.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2068+557A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083630 | |||||||
| chr8:39083787 | CAG | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0078 others(1): Show |
4 | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+715_2068+716d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39083787 | |||||||
| chr8:39084128 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2068+1055C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084128 | |||||||
| chr8:39084220 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0214 a0001c0001t0001g0282 |
3 | HG00099.hp2 HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2068+1147A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084220 | |||||||
| chr8:39084285 | G | T | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2068+1212G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084285 | |||||||
| chr8:39084430 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2068+1357A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084430 | |||||||
| chr8:39084502 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2068+1429C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084502 | |||||||
| chr8:39084537 | T | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2068+1464T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084537 | |||||||
| chr8:39084583 | C | CT | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2068+1522dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39084583 | ||||||
| chr8:39084728 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
6 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068+1655C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084728 | |||||||
| chr8:39084803 | G | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0053 others(2): Show |
5 | HG01074.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2068+1730G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084803 | |||||||
| chr8:39084999 | A | G | 7 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0079 others(4): Show |
7 | HG00621.hp1 HG02132.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.2068+1926A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39084999 | |||||||
| chr8:39085220 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2068+2147C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085220 | |||||||
| chr8:39085433 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+2360T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085433 | |||||||
| chr8:39085597 | CA | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+2526delA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39085597 | ||||||
| chr8:39085600 | G | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+2527G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085600 | |||||||
| chr8:39085741 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0282 |
2 | HG00099.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2068+2668T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085741 | |||||||
| chr8:39085772 | T | C | 223 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2068+2699T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085772 | |||||||
| chr8:39085929 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2068+2856A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39085929 | |||||||
| chr8:39086048 | T | C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2068+2975T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086048 | |||||||
| chr8:39086163 | TG | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+3091delG | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086163 | |||||||
| chr8:39086214 | G | C | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2068+3141G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086214 | |||||||
| chr8:39086431 | G | A | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2068+3358G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086431 | |||||||
| chr8:39086493 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2068+3420A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086493 | |||||||
| chr8:39086852 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | NA19074.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.2069-3195A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39086852 | |||||||
| chr8:39087209 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2069-2838G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087209 | |||||||
| chr8:39087278 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2069-2769T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087278 | |||||||
| chr8:39087304 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2069-2743C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087304 | |||||||
| chr8:39087465 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069-2582G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087465 | |||||||
| chr8:39087831 | C | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-2216C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087831 | |||||||
| chr8:39087878 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2069-2169T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087878 | |||||||
| chr8:39087961 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-2086A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087961 | |||||||
| chr8:39087966 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2069-2081A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39087966 | |||||||
| chr8:39088144 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-1903G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088144 | |||||||
| chr8:39088150 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2069-1897A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088150 | |||||||
| chr8:39088181 | C | T | 12 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2069-1866C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088181 | |||||||
| chr8:39088239 | GATAA | G | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2069-1804_2069-180 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39088239 | ||||||
| chr8:39088270 | C | CT | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2069-1764dupT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39088270 | ||||||
| chr8:39088310 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2069-1737C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088310 | |||||||
| chr8:39088508 | C | T | 12 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2069-1539C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088508 | |||||||
| chr8:39088521 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2069-1526C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088521 | |||||||
| chr8:39088527 | G | GAT | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2069-1519_2069-151 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 39088527 | ||||||
| chr8:39088548 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2069-1499C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088548 | |||||||
| chr8:39088558 | G | A | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2069-1489G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088558 | |||||||
| chr8:39088688 | A | C | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2069-1359A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088688 | |||||||
| chr8:39088728 | G | A | 286 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2069-1319G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088728 | |||||||
| chr8:39088777 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2069-1270C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39088777 | |||||||
| chr8:39089021 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-1026G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089021 | |||||||
| chr8:39089086 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0024 |
3 | HG02257.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2069-961A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089086 | |||||||
| chr8:39089117 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2069-930C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089117 | |||||||
| chr8:39089172 | C | A | 1 | a0001c0001t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2069-875C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089172 | |||||||
| chr8:39089286 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2069-761A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089286 | |||||||
| chr8:39089309 | A | G | 92 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(89): Show |
92 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.2069-738A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089309 | |||||||
| chr8:39089399 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2069-648G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089399 | |||||||
| chr8:39089417 | G | A | 14 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(11): Show |
14 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2069-630G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089417 | |||||||
| chr8:39089720 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2069-327A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089720 | |||||||
| chr8:39089755 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(1): Show |
4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-292A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089755 | |||||||
| chr8:39089804 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2069-243C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089804 | |||||||
| chr8:39089963 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2069-84A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | 39089963 | |||||||
| chr8:39090308 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2210+120G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090308 | |||||||
| chr8:39090355 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2210+167A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090355 | |||||||
| chr8:39090503 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2210+315G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090503 | |||||||
| chr8:39090638 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2210+450G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090638 | |||||||
| chr8:39090639 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2210+451T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090639 | |||||||
| chr8:39090640 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2210+452T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090640 | |||||||
| chr8:39090725 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2211-534C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 19/21 | chr8 | 39090725 | |||||||
| chr8:39091514 | GC | G | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(37): Show |
40 | HG00673.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.2298+170delC | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39091514 | ||||||
| chr8:39091530 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0307 a0001c0001t0001g0317 |
3 | HG02698.hp2 NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2298+184C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39091530 | |||||||
| chr8:39091531 | G | A | 6 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2298+185G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39091531 | |||||||
| chr8:39091866 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2298+520C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39091866 | |||||||
| chr8:39092013 | C | T | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2298+667C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092013 | |||||||
| chr8:39092014 | T | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2298+668T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092014 | |||||||
| chr8:39092128 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2298+782G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092128 | |||||||
| chr8:39092166 | T | C | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2298+820T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092166 | |||||||
| chr8:39092195 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+849A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092195 | |||||||
| chr8:39092300 | AT | A | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2298+956delT | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092300 | ||||||
| chr8:39092324 | A | G | 1 | a0001c0001t0001g0323 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2298+978A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092324 | |||||||
| chr8:39092331 | T | TAC | 14 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0131 others(11): Show |
14 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2298+1009_2298+101 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | ||||||
| chr8:39092331 | T | TACAC | 87 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(84): Show |
87 | HG00438.hp2 HG00639.hp2 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.2298+1007_2298+101 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | ||||||
| chr8:39092331 | T | TACACAC | 16 | a0001c0001t0001g0067 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
16 | HG00673.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2298+1005_2298+101 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | ||||||
| chr8:39092331 | TAC | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2298+1009_2298+101 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39092331 | ||||||
| chr8:39092473 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2298+1127C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092473 | |||||||
| chr8:39092599 | T | C | 1 | a0001c0003t0001g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2298+1253T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092599 | |||||||
| chr8:39092725 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2298+1379G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092725 | |||||||
| chr8:39092859 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2298+1513A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092859 | |||||||
| chr8:39092937 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2298+1591G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39092937 | |||||||
| chr8:39093395 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2298+2049C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093395 | |||||||
| chr8:39093830 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2298+2484C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093830 | |||||||
| chr8:39093923 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2298+2577C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093923 | |||||||
| chr8:39093981 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2298+2635A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39093981 | |||||||
| chr8:39094047 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2298+2701C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094047 | |||||||
| chr8:39094186 | A | G | 14 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2298+2840A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094186 | |||||||
| chr8:39094256 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2298+2910G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094256 | |||||||
| chr8:39094260 | C | A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2298+2914C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094260 | |||||||
| chr8:39094670 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2298+3324G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094670 | |||||||
| chr8:39094849 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2298+3503A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094849 | |||||||
| chr8:39094892 | C | T | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2298+3546C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094892 | |||||||
| chr8:39094924 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.2298+3578A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39094924 | |||||||
| chr8:39095045 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2298+3699G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095045 | |||||||
| chr8:39095283 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2298+3937A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095283 | |||||||
| chr8:39095321 | C | A | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2298+3975C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095321 | |||||||
| chr8:39095406 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2298+4060T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095406 | |||||||
| chr8:39095476 | C | T | 21 | a0001c0001t0001g0213 a0001c0001t0001g0291 a0001c0001t0001g0296 others(18): Show |
21 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2298+4130C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095476 | |||||||
| chr8:39095850 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2298+4504C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095850 | |||||||
| chr8:39095855 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2298+4509C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39095855 | |||||||
| chr8:39096046 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2298+4700C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096046 | |||||||
| chr8:39096077 | T | TA | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2298+4738dupA | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39096077 | ||||||
| chr8:39096096 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2298+4750T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096096 | |||||||
| chr8:39096100 | TAATAGTT others(252): Show |
T | 28 | a0001c0001t0001g0124 a0001c0001t0001g0186 a0001c0001t0001g0205 others(25): Show |
28 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2298+4758_2298+501 others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39096100 | ||||||
| chr8:39096136 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2298+4790T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096136 | |||||||
| chr8:39096236 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(41): Show |
44 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2298+4890T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096236 | |||||||
| chr8:39096362 | T | A | 28 | a0001c0001t0001g0124 a0001c0001t0001g0186 a0001c0001t0001g0205 others(25): Show |
28 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2298+5016T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096362 | |||||||
| chr8:39096533 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2298+5187A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39096533 | |||||||
| chr8:39097228 | C | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2299-4635C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097228 | |||||||
| chr8:39097282 | G | C | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-4581G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097282 | |||||||
| chr8:39097292 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2299-4571T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097292 | |||||||
| chr8:39097392 | CGCCTCCC others(5): Show |
C | 89 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2299-4470_2299-445 others(16): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097392 | |||||||
| chr8:39097548 | C | T | 87 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(84): Show |
87 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.2299-4315C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097548 | |||||||
| chr8:39097552 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02148.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2299-4311C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097552 | |||||||
| chr8:39097560 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2299-4303C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097560 | |||||||
| chr8:39097633 | T | A | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-4230T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097633 | |||||||
| chr8:39097634 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2299-4229A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097634 | |||||||
| chr8:39097738 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2299-4125C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097738 | |||||||
| chr8:39097970 | G | C | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-3893G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39097970 | |||||||
| chr8:39098015 | C | CTTCAACT others(14): Show |
1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2299-3847_2299-382 others(25): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39098015 | ||||||
| chr8:39098049 | G | A | 130 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.2299-3814G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098049 | |||||||
| chr8:39098300 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-3563G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098300 | |||||||
| chr8:39098450 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2299-3413A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098450 | |||||||
| chr8:39098567 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2299-3296A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098567 | |||||||
| chr8:39098706 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2299-3157G>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098706 | |||||||
| chr8:39098940 | A | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2299-2923A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39098940 | |||||||
| chr8:39099087 | A | C | 133 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2299-2776A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099087 | |||||||
| chr8:39099191 | C | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2299-2672C>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099191 | |||||||
| chr8:39099234 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0327 |
3 | NA18987.hp1 NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2299-2629A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099234 | |||||||
| chr8:39099260 | A | G | 130 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.2299-2603A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099260 | |||||||
| chr8:39099325 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0003g0133 a0001c0001t0004g0332 |
3 | HG02055.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-2538G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099325 | |||||||
| chr8:39099460 | T | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0133 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2299-2403T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099460 | |||||||
| chr8:39099499 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2299-2364T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099499 | |||||||
| chr8:39099660 | A | C | 12 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(9): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2299-2203A>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099660 | |||||||
| chr8:39099668 | T | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2299-2195T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099668 | |||||||
| chr8:39099875 | GTT | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0028 others(11): Show |
14 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2299-1967_2299-196 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39099875 | ||||||
| chr8:39099875 | GTTT | G | 239 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2299-1968_2299-196 others(7): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39099875 | ||||||
| chr8:39099875 | GTTTT | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2299-1969_2299-196 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 39099875 | ||||||
| chr8:39099881 | T | G | 5 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG00621.hp1 HG02132.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-1982T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099881 | |||||||
| chr8:39099882 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2299-1981T>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099882 | |||||||
| chr8:39099951 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2299-1912C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39099951 | |||||||
| chr8:39100025 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0096 |
3 | HG01257.hp1 HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2299-1838G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100025 | |||||||
| chr8:39100081 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0066 a0001c0001t0001g0105 others(1): Show |
4 | HG02698.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2299-1782C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100081 | |||||||
| chr8:39100216 | G | A | 129 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.2299-1647G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100216 | |||||||
| chr8:39100257 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2299-1606A>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100257 | |||||||
| chr8:39100334 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2299-1529G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100334 | |||||||
| chr8:39100536 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2299-1327A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100536 | |||||||
| chr8:39100715 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2299-1148G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100715 | |||||||
| chr8:39100767 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-1096A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100767 | |||||||
| chr8:39100790 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2299-1073A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100790 | |||||||
| chr8:39100864 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2299-999A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39100864 | |||||||
| chr8:39101046 | A | G | 94 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(91): Show |
94 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.2299-817A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101046 | |||||||
| chr8:39101198 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.2299-665G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101198 | |||||||
| chr8:39101366 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2299-497T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101366 | |||||||
| chr8:39101678 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0182 |
3 | NA18966.hp2 NA18973.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2299-185C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101678 | |||||||
| chr8:39101847 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2299-16T>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | chr8 | 39101847 | |||||||
| chr8:39101979 | G | A | 93 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(90): Show |
93 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.2366+49G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39101979 | |||||||
| chr8:39102032 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2366+102T>C | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102032 | |||||||
| chr8:39102069 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2366+139G>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102069 | |||||||
| chr8:39102082 | C | T | 8 | a0001c0001t0001g0299 a0001c0003t0001g0206 a0001c0003t0001g0258 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.2366+152C>T | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102082 | |||||||
| chr8:39102551 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2366+621G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102551 | |||||||
| chr8:39102675 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2366+745G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102675 | |||||||
| chr8:39102698 | A | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG00280.hp2 HG01256.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2366+768A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102698 | |||||||
| chr8:39102787 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2367-820A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102787 | |||||||
| chr8:39102983 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2367-624A>G | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102983 | |||||||
| chr8:39102986 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2367-621C>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39102986 | |||||||
| chr8:39103225 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2367-382G>A | ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | chr8 | 39103225 | |||||||
| chr8:39103406 | ATT | A | 3 | a0002c0002t0002g0194 a0002c0002t0002g0195 a0002c0002t0002g0196 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2367-199_2367-198d others(4): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 39103406 |