Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8749 |
| ensemblid | ENSG00000168619.16 |
| hgncid | 196 |
| symbol | ADAM18 |
| name | ADAM metallopeptidase domain 18 |
| refseq_nuc | NM_014237.3 |
| refseq_prot | NP_055052.1 |
| ensembl_nuc | ENST00000265707.10 |
| ensembl_prot | ENSP00000265707.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 39584568 |
| end | 39730065 |
| strand | + |
| ver | v1.2 |
| region | chr8:39584568-39730065 |
| region5000 | chr8:39579568-39735065 |
| regionname0 | ADAM18_chr8_39584568_39730065 |
| regionname5000 | ADAM18_chr8_39579568_39735065 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 739 | 303 | 57 | 71 | 130 | 8 | 36 | 93 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0002 | 0/0 | 739 | 12 | 10 | 1 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0003 | 0/0 | 739 | 10 | 9 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0004 | 0/0 | 739 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0005 | 0/0 | 739 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0006 | 0/0 | 739 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0007 | 0/0 | 739 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0008 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0009 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0010 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0011 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0012 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0013 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| a0014 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | MFLLL others(734): Show |
chr8 | 39579568 | 39735065 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2217 | 148 | 18 | 32 | 84 | 4 | 10 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0002 | 0/1 | 2217 | 145 | 32 | 38 | 44 | 4 | 26 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0007 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0008 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0010 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0012 | 0/0 | 2217 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0014 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0001c0015 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0002c0003 | 0/0 | 2217 | 12 | 10 | 1 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0003c0004 | 0/0 | 2217 | 10 | 9 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0004c0005 | 0/0 | 2217 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0004c0019 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0004c0022 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0005c0011 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0005c0016 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0006c0006 | 0/0 | 2217 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0007c0009 | 0/0 | 2217 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0008c0023 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0009c0021 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0010c0013 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0011c0024 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0012c0018 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0013c0020 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 | ||
| a0014c0017 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | ATGTT others(2212): Show |
chr8 | 39579568 | 39735065 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2400 | 148 | 18 | 32 | 84 | 4 | 10 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0002t0001 | 0/1 | 2400 | 145 | 32 | 38 | 44 | 4 | 26 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0007t0001 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0008t0003 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0010t0001 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0012t0001 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0014t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0001c0015t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0002c0003t0001 | 0/0 | 2400 | 12 | 10 | 1 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0003c0004t0001 | 0/0 | 2400 | 7 | 6 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0003c0004t0002 | 0/0 | 2400 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0004c0005t0001 | 0/0 | 2400 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0004c0019t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0004c0022t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0005c0011t0001 | 0/0 | 2400 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0005c0016t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0006c0006t0001 | 0/0 | 2400 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0007c0009t0001 | 0/0 | 2400 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0008c0023t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0009c0021t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0010c0013t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0011c0024t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0012c0018t0001 | 0/0 | 2400 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0013c0020t0001 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| a0014c0017t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | AACGC others(2395): Show |
chr8 | 39579568 | 39735065 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0007t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0008t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0008t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0010t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0012t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0014t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0001c0015t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0003c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0005t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0019t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0004c0022t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0005c0011t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0005c0011t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0005c0016t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0006c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0006c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0006c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0007c0009t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0007c0009t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0008c0023t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0009c0021t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0010c0013t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0011c0024t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0012c0018t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0013c0020t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| a0014c0017t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0147 | EUR | GBR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | GBR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0156 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0308 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0085 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0023 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG00738 | hp2 | a0001 | c0015 | t0001 | g0031 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01167 | hp2 | a0008 | c0023 | t0001 | g0016 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01192 | hp2 | a0009 | c0021 | t0001 | g0226 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01884 | hp1 | a0010 | c0013 | t0001 | g0162 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02055 | hp1 | a0004 | c0022 | t0001 | g0194 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02055 | hp2 | a0001 | c0008 | t0003 | g0015 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CDX | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02257 | hp2 | a0003 | c0004 | t0002 | g0010 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02280 | hp2 | a0004 | c0005 | t0001 | g0288 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02572 | hp2 | a0004 | c0005 | t0001 | g0307 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0212 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02630 | hp1 | a0005 | c0011 | t0001 | g0190 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0020 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02717 | hp2 | a0006 | c0006 | t0001 | g0263 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0215 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02895 | hp2 | a0004 | c0019 | t0001 | g0080 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0181 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03041 | hp1 | a0001 | c0014 | t0001 | g0219 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03098 | hp1 | a0001 | c0008 | t0003 | g0014 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03098 | hp2 | a0004 | c0005 | t0001 | g0292 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03130 | hp1 | a0003 | c0004 | t0002 | g0009 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03139 | hp1 | a0003 | c0004 | t0002 | g0008 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0198 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0229 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03209 | hp1 | a0001 | c0010 | t0001 | g0035 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03209 | hp2 | a0005 | c0016 | t0001 | g0079 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03239 | hp2 | a0003 | c0004 | t0001 | g0245 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03516 | hp1 | a0011 | c0024 | t0001 | g0213 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03516 | hp2 | a0001 | c0010 | t0001 | g0043 | AFR | ESN | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03579 | hp1 | a0006 | c0006 | t0001 | g0264 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04199 | hp1 | a0012 | c0018 | t0001 | g0040 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | STU | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0216 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | CHB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18906 | hp1 | a0005 | c0011 | t0001 | g0247 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18961 | hp1 | a0013 | c0020 | t0001 | g0069 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18980 | hp1 | a0001 | c0012 | t0001 | g0007 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18986 | hp2 | a0001 | c0012 | t0001 | g0007 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19043 | hp1 | a0006 | c0006 | t0001 | g0262 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19043 | hp2 | a0014 | c0017 | t0001 | g0255 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19074 | hp1 | a0007 | c0009 | t0001 | g0155 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19077 | hp2 | a0007 | c0009 | t0001 | g0111 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0217 | AFR | YRI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20129 | hp1 | a0004 | c0005 | t0001 | g0314 | AFR | ASW | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ASW | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0258 | EUR | TSI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0340 | EUR | TSI | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | GIH | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | GIH | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA20300 | hp2 | a0004 | c0005 | t0001 | g0318 | AFR | USA | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA21309 | hp1 | a0003 | c0004 | t0001 | g0214 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | LWK | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0153 | REF | REF | ADAM18_chr8_39579568_39735065 | ADAM18 | chr8 | 39579568 | 39735065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39610551 | A | C | 1 | a0006 | 3 | HG02717.hp2 HG03579.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.367A>C | p.Ile123Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/20 | 422/2400 | 367/2220 | 123/739 | chr8 | 39610551 | |||
| chr8:39610609 | A | T | 2 | a0003 a0011 |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
missense_variant | MODERATE | c.425A>T | p.Gln142Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/20 | 480/2400 | 425/2220 | 142/739 | chr8 | 39610609 | |||
| chr8:39637309 | G | T | 2 | a0002 a0008 |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
missense_variant | MODERATE | c.634G>T | p.Val212Phe | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 8/20 | 689/2400 | 634/2220 | 212/739 | chr8 | 39637309 | |||
| chr8:39648379 | G | A | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1082G>A | p.Ser361Asn | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/20 | 1137/2400 | 1082/2220 | 361/739 | chr8 | 39648379 | |||
| chr8:39648410 | A | T | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1113A>T | p.Lys371Asn | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/20 | 1168/2400 | 1113/2220 | 371/739 | chr8 | 39648410 | |||
| chr8:39668113 | G | A | 1 | a0009 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1442G>A | p.Arg481His | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1497/2400 | 1442/2220 | 481/739 | chr8 | 39668113 | |||
| chr8:39668137 | A | G | 1 | a0013 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.1466A>G | p.Tyr489Cys | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1521/2400 | 1466/2220 | 489/739 | chr8 | 39668137 | |||
| chr8:39680074 | C | T | 1 | a0012 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1669C>T | p.His557Tyr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/20 | 1724/2400 | 1669/2220 | 557/739 | chr8 | 39680074 | |||
| chr8:39692661 | C | T | 1 | a0007 | 2 | NA19074.hp1 NA19077.hp2 |
missense_variant | MODERATE | c.1883C>T | p.Thr628Ile | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/20 | 1938/2400 | 1883/2220 | 628/739 | chr8 | 39692661 | |||
| chr8:39706848 | A | G | 3 | a0002 a0008 a0014 |
14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
missense_variant | MODERATE | c.1961A>G | p.Lys654Arg | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/20 | 2016/2400 | 1961/2220 | 654/739 | chr8 | 39706848 | |||
| chr8:39723859 | G | T | 1 | a0005 | 3 | HG02630.hp1 HG03209.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.2129G>T | p.Arg710Ile | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2184/2400 | 2129/2220 | 710/739 | chr8 | 39723859 | |||
| chr8:39723876 | T | A | 3 | a0004 a0008 a0011 |
9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.2146T>A | p.Ser716Thr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2201/2400 | 2146/2220 | 716/739 | chr8 | 39723876 | |||
| chr8:39723898 | A | G | 3 | a0004 a0008 a0011 |
9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.2168A>G | p.Glu723Gly | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2223/2400 | 2168/2220 | 723/739 | chr8 | 39723898 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39584664 | G | A | 1 | a0001c0007 | 2 | HG03139.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.42G>A | p.Leu14Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/20 | 97/2400 | 42/2220 | 14/739 | chr8 | 39584664 | |||
| chr8:39637555 | T | C | 3 | a0001c0008 a0002c0003 a0008c0023 |
15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
synonymous_variant | LOW | c.679T>C | p.Leu227Leu | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/20 | 734/2400 | 679/2220 | 227/739 | chr8 | 39637555 | |||
| chr8:39638510 | T | C | 18 | a0001c0002 a0001c0008 a0001c0010 others(15): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
synonymous_variant | LOW | c.873T>C | p.Thr291Thr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/20 | 928/2400 | 873/2220 | 291/739 | chr8 | 39638510 | |||
| chr8:39663842 | G | A | 1 | a0001c0014 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1278G>A | p.Lys426Lys | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/20 | 1333/2400 | 1278/2220 | 426/739 | chr8 | 39663842 | |||
| chr8:39668147 | C | T | 1 | a0004c0019 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1476C>T | p.Asn492Asn | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1531/2400 | 1476/2220 | 492/739 | chr8 | 39668147 | |||
| chr8:39668162 | T | C | 1 | a0001c0015 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1491T>C | p.Thr497Thr | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/20 | 1546/2400 | 1491/2220 | 497/739 | chr8 | 39668162 | |||
| chr8:39680097 | C | T | 5 | a0001c0010 a0002c0003 a0003c0004 others(2): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
synonymous_variant | LOW | c.1692C>T | p.Asp564Asp | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/20 | 1747/2400 | 1692/2220 | 564/739 | chr8 | 39680097 | |||
| chr8:39723770 | C | T | 1 | a0001c0012 | 2 | NA18980.hp1 NA18986.hp2 |
synonymous_variant | LOW | c.2040C>T | p.Gly680Gly | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2095/2400 | 2040/2220 | 680/739 | chr8 | 39723770 | |||
| chr8:39723854 | T | C | 1 | a0008c0023 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.2124T>C | p.Phe708Phe | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/20 | 2179/2400 | 2124/2220 | 708/739 | chr8 | 39723854 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39584586 | C | G | 1 | a0003c0004t0002 | 3 | HG02257.hp2 HG03130.hp1 HG03139.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/20 | chr8 | 39584586 | |||||||
| chr8:39584607 | G | C | 1 | a0001c0008t0003 | 2 | HG02055.hp2 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-16G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/20 | 16 | chr8 | 39584607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:39584773 | T | G | 287 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(284): Show |
294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.55+96T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | chr8 | 39584773 | |||||||
| chr8:39584985 | ACTC | A | 3 | a0003c0004t0002g0008 a0003c0004t0002g0009 a0003c0004t0002g0010 |
3 | HG02257.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.56-287_56-285delCT others(1): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr8 | 39584985 | ||||||
| chr8:39585065 | A | AT | 6 | a0001c0001t0001g0284 a0001c0002t0001g0283 a0001c0002t0001g0285 others(3): Show |
6 | HG00621.hp1 HG02280.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-202dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr8 | 39585065 | ||||||
| chr8:39585130 | T | C | 2 | a0001c0002t0001g0011 a0001c0002t0001g0012 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.56-146T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 1/19 | chr8 | 39585130 | |||||||
| chr8:39586117 | T | C | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.132+765T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586117 | |||||||
| chr8:39586131 | G | T | 17 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(14): Show |
17 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.132+779G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586131 | |||||||
| chr8:39586260 | C | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+908C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586260 | |||||||
| chr8:39586261 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.132+909A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586261 | |||||||
| chr8:39586513 | C | T | 7 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0260 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+1161C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586513 | |||||||
| chr8:39586535 | T | C | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.132+1183T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586535 | |||||||
| chr8:39586604 | G | A | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+1252G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586604 | |||||||
| chr8:39586605 | T | C | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+1253T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586605 | |||||||
| chr8:39586615 | T | G | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.132+1263T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586615 | |||||||
| chr8:39586641 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132+1289C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586641 | |||||||
| chr8:39586699 | C | G | 1 | a0001c0001t0001g0340 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.132+1347C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586699 | |||||||
| chr8:39586755 | A | ACTAT | 29 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0249 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.132+1448_132+1451d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | A | ACTATCTA others(1): Show |
4 | a0001c0001t0001g0254 a0001c0002t0001g0157 a0003c0004t0002g0010 others(1): Show |
4 | HG00738.hp1 HG02257.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1444_132+1451d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | A | ACTATCTA others(5): Show |
2 | a0001c0001t0001g0256 a0001c0001t0001g0339 |
2 | HG00597.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.132+1440_132+1451d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | ACTAT | A | 102 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(99): Show |
104 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.132+1448_132+1451d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | ACTATCTA others(1): Show |
A | 34 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(31): Show |
34 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.132+1444_132+1451d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | ACTATCTA others(5): Show |
A | 22 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(19): Show |
23 | HG01081.hp1 HG01167.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.132+1440_132+1451d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | ACTATCTA others(9): Show |
A | 5 | a0001c0001t0001g0161 a0001c0002t0001g0006 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+1436_132+1451d others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | ACTATCTA others(13): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.132+1432_132+1451d others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586755 | ACTATCTA others(17): Show |
A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+1428_132+1451d others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586755 | ||||||
| chr8:39586789 | T | TATC | 3 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0012c0018t0001g0040 |
3 | HG02698.hp2 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.132+1438_132+1440d others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586789 | ||||||
| chr8:39586792 | CTATCTAT others(3): Show |
C | 1 | a0001c0001t0001g0253 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.132+1452_132+1461d others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586792 | ||||||
| chr8:39586794 | ATC | A | 3 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0260 |
3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.132+1444_132+1445d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586794 | ||||||
| chr8:39586794 | ATCTATCT others(5): Show |
A | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+1444_132+1455d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586794 | ||||||
| chr8:39586796 | C | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1444C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586796 | |||||||
| chr8:39586798 | ATCTATAT others(1): Show |
A | 13 | a0001c0001t0001g0086 a0001c0002t0001g0003 a0001c0002t0001g0004 others(10): Show |
14 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+1448_132+1455d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586798 | ||||||
| chr8:39586800 | C | A | 3 | a0001c0002t0001g0261 a0006c0006t0001g0262 a0006c0006t0001g0264 |
3 | HG02300.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132+1448C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586800 | |||||||
| chr8:39586800 | CTA | C | 3 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0260 |
3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.132+1452_132+1453d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586800 | ||||||
| chr8:39586802 | A | ATC | 4 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0078 others(1): Show |
4 | HG01074.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+1451_132+1452i others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586802 | ||||||
| chr8:39586802 | A | C | 3 | a0001c0002t0001g0261 a0006c0006t0001g0262 a0006c0006t0001g0264 |
3 | HG02300.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132+1450A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586802 | |||||||
| chr8:39586802 | ATATC | A | 21 | a0001c0001t0001g0087 a0001c0002t0001g0004 a0001c0002t0001g0081 others(18): Show |
21 | HG00544.hp2 HG00609.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+1463_132+1466d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586802 | ||||||
| chr8:39586804 | A | C | 29 | a0001c0001t0001g0139 a0001c0002t0001g0011 a0001c0002t0001g0012 others(26): Show |
29 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.132+1452A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586804 | |||||||
| chr8:39586806 | C | A | 29 | a0001c0001t0001g0139 a0001c0002t0001g0011 a0001c0002t0001g0012 others(26): Show |
29 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.132+1454C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39586806 | |||||||
| chr8:39586806 | C | CTA | 5 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0077 others(2): Show |
5 | HG01074.hp2 HG01099.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1456_132+1457d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39586806 | ||||||
| chr8:39587387 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.132+2035C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587387 | |||||||
| chr8:39587594 | G | A | 1 | a0001c0002t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132+2242G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587594 | |||||||
| chr8:39587620 | T | C | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.132+2268T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587620 | |||||||
| chr8:39587721 | C | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+2369C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587721 | |||||||
| chr8:39587826 | A | G | 1 | a0001c0002t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.132+2474A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587826 | |||||||
| chr8:39587923 | T | G | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+2571T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39587923 | |||||||
| chr8:39588079 | A | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2727A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588079 | |||||||
| chr8:39588173 | C | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+2821C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588173 | |||||||
| chr8:39588231 | T | TTG | 109 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(106): Show |
110 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.132+2880_132+2881i others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39588231 | ||||||
| chr8:39588233 | T | G | 164 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(161): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.132+2881T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588233 | |||||||
| chr8:39588324 | T | G | 1 | a0001c0002t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132+2972T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588324 | |||||||
| chr8:39588352 | C | T | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3000C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588352 | |||||||
| chr8:39588618 | C | G | 1 | a0001c0012t0001g0007 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.132+3266C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588618 | |||||||
| chr8:39588634 | CT | C | 107 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(104): Show |
108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+3283delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588634 | |||||||
| chr8:39588747 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0284 |
2 | HG00621.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.132+3395G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588747 | |||||||
| chr8:39588837 | G | A | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.132+3485G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39588837 | |||||||
| chr8:39589047 | C | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3695C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589047 | |||||||
| chr8:39589071 | G | A | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+3719G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589071 | |||||||
| chr8:39589233 | C | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.132+3881C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589233 | |||||||
| chr8:39589444 | G | C | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+4092G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589444 | |||||||
| chr8:39589485 | T | C | 2 | a0001c0002t0001g0075 a0001c0002t0001g0121 |
2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.132+4133T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589485 | |||||||
| chr8:39589553 | C | T | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.132+4201C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589553 | |||||||
| chr8:39589653 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.132+4301T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589653 | |||||||
| chr8:39589698 | A | G | 8 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0116 others(5): Show |
8 | HG01993.hp2 HG02273.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.132+4346A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589698 | |||||||
| chr8:39589809 | A | G | 107 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(104): Show |
108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+4457A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589809 | |||||||
| chr8:39589913 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.132+4561G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589913 | |||||||
| chr8:39589967 | G | A | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.132+4615G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39589967 | |||||||
| chr8:39590203 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.132+4851A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590203 | |||||||
| chr8:39590351 | C | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+4999C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590351 | |||||||
| chr8:39590459 | T | C | 68 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(65): Show |
70 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.132+5107T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590459 | |||||||
| chr8:39590607 | A | T | 1 | a0001c0002t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.132+5255A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590607 | |||||||
| chr8:39590741 | T | C | 287 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(284): Show |
294 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.132+5389T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39590741 | |||||||
| chr8:39591064 | T | A | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+5712T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591064 | |||||||
| chr8:39591166 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0001g0329 |
2 | NA18952.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.132+5814C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591166 | |||||||
| chr8:39591302 | A | G | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(48): Show |
54 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.132+5950A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591302 | |||||||
| chr8:39591375 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+6023A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591375 | |||||||
| chr8:39591447 | C | T | 69 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(66): Show |
71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+6095C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591447 | |||||||
| chr8:39591502 | C | T | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.132+6150C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591502 | |||||||
| chr8:39591559 | G | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.132+6207G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591559 | |||||||
| chr8:39591581 | C | T | 7 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0260 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+6229C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591581 | |||||||
| chr8:39591668 | C | T | 69 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(66): Show |
71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+6316C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591668 | |||||||
| chr8:39591747 | A | C | 2 | a0001c0002t0001g0113 a0001c0002t0001g0156 |
2 | HG00280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.132+6395A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591747 | |||||||
| chr8:39591783 | A | G | 1 | a0001c0010t0001g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.132+6431A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39591783 | |||||||
| chr8:39592054 | A | T | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+6702A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592054 | |||||||
| chr8:39592117 | G | A | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.132+6765G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592117 | |||||||
| chr8:39592230 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+6878G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592230 | |||||||
| chr8:39592280 | T | G | 107 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(104): Show |
108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+6928T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592280 | |||||||
| chr8:39592381 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+7029C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592381 | |||||||
| chr8:39592561 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0104 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.132+7209C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592561 | |||||||
| chr8:39592671 | A | G | 1 | a0003c0004t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.132+7319A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592671 | |||||||
| chr8:39592765 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+7413C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592765 | |||||||
| chr8:39592862 | C | T | 3 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+7510C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592862 | |||||||
| chr8:39592996 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.132+7644C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39592996 | |||||||
| chr8:39593049 | A | G | 2 | a0001c0002t0001g0011 a0001c0002t0001g0012 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.132+7697A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593049 | |||||||
| chr8:39593219 | C | A | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0183 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+7867C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593219 | |||||||
| chr8:39593421 | T | C | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+8069T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593421 | |||||||
| chr8:39593514 | A | G | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132+8162A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593514 | |||||||
| chr8:39593664 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.132+8312T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593664 | |||||||
| chr8:39593666 | T | C | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 |
3 | NA18957.hp2 NA18966.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.132+8314T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593666 | |||||||
| chr8:39593876 | T | G | 1 | a0001c0002t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.132+8524T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39593876 | |||||||
| chr8:39594013 | T | C | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.132+8661T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594013 | |||||||
| chr8:39594035 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.132+8683G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594035 | |||||||
| chr8:39594069 | T | G | 69 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(66): Show |
71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+8717T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594069 | |||||||
| chr8:39594094 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01168.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.132+8742T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594094 | |||||||
| chr8:39594481 | G | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+9129G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594481 | |||||||
| chr8:39594618 | T | C | 1 | a0001c0002t0001g0287 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.132+9266T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594618 | |||||||
| chr8:39594706 | G | A | 4 | a0002c0003t0001g0024 a0002c0003t0001g0025 a0002c0003t0001g0026 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+9354G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594706 | |||||||
| chr8:39594793 | G | GT | 15 | a0001c0008t0003g0015 a0002c0003t0001g0017 a0002c0003t0001g0018 others(12): Show |
15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+9464dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39594793 | ||||||
| chr8:39594793 | GT | G | 235 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(232): Show |
242 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.132+9464delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39594793 | ||||||
| chr8:39594793 | GTT | G | 7 | a0001c0001t0001g0188 a0001c0001t0001g0244 a0001c0001t0001g0246 others(4): Show |
7 | HG00639.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+9463_132+9464d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39594793 | ||||||
| chr8:39594795 | T | G | 2 | a0001c0002t0001g0285 a0001c0002t0001g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+9443T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594795 | |||||||
| chr8:39594928 | C | T | 105 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(102): Show |
106 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.132+9576C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594928 | |||||||
| chr8:39594986 | A | G | 8 | a0001c0002t0001g0258 a0001c0002t0001g0259 a0001c0002t0001g0260 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+9634A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39594986 | |||||||
| chr8:39595058 | G | A | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+9706G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39595058 | |||||||
| chr8:39595331 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.132+9979G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39595331 | |||||||
| chr8:39595899 | T | A | 1 | a0001c0001t0001g0289 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.133-10408T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39595899 | |||||||
| chr8:39596003 | T | C | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-10304T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596003 | |||||||
| chr8:39596134 | C | T | 47 | a0001c0001t0001g0139 a0001c0002t0001g0003 a0001c0002t0001g0004 others(44): Show |
49 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.133-10173C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596134 | |||||||
| chr8:39596199 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.133-10108C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596199 | |||||||
| chr8:39596325 | T | C | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-9982T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596325 | |||||||
| chr8:39596575 | C | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-9732C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596575 | |||||||
| chr8:39596906 | T | A | 110 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(107): Show |
112 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.133-9401T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596906 | |||||||
| chr8:39596997 | C | T | 25 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(22): Show |
25 | HG00733.hp1 HG01167.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.133-9310C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39596997 | |||||||
| chr8:39597051 | A | T | 3 | a0003c0004t0001g0181 a0003c0004t0001g0215 a0003c0004t0001g0216 |
3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.133-9256A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597051 | |||||||
| chr8:39597058 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.133-9249T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597058 | |||||||
| chr8:39597158 | G | T | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-9149G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597158 | |||||||
| chr8:39597322 | T | C | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-8985T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597322 | |||||||
| chr8:39597403 | G | T | 1 | a0001c0001t0001g0240 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.133-8904G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597403 | |||||||
| chr8:39597407 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-8900A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597407 | |||||||
| chr8:39597607 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.133-8700G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597607 | |||||||
| chr8:39597697 | G | T | 5 | a0001c0001t0001g0267 a0001c0001t0001g0273 a0001c0001t0001g0274 others(2): Show |
5 | NA18950.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-8610G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597697 | |||||||
| chr8:39597703 | A | C | 1 | a0001c0002t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133-8604A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597703 | |||||||
| chr8:39597969 | T | C | 1 | a0005c0011t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.133-8338T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39597969 | |||||||
| chr8:39598147 | T | C | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-8160T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598147 | |||||||
| chr8:39598283 | T | A | 1 | a0001c0002t0001g0054 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.133-8024T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598283 | |||||||
| chr8:39598370 | G | A | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133-7937G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598370 | |||||||
| chr8:39598762 | C | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-7545C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598762 | |||||||
| chr8:39598767 | C | CA | 46 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0185 others(43): Show |
49 | HG00733.hp1 HG00738.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.133-7525dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39598767 | ||||||
| chr8:39598767 | CA | C | 26 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0209 others(23): Show |
26 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.133-7525delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39598767 | ||||||
| chr8:39598874 | C | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-7433C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39598874 | |||||||
| chr8:39599062 | C | T | 1 | a0001c0002t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.133-7245C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599062 | |||||||
| chr8:39599102 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.133-7205C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599102 | |||||||
| chr8:39599516 | G | A | 148 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(145): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.133-6791G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599516 | |||||||
| chr8:39599708 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA18944.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.133-6599C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599708 | |||||||
| chr8:39599872 | A | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-6435A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599872 | |||||||
| chr8:39599895 | C | A | 8 | a0003c0004t0001g0212 a0003c0004t0001g0214 a0003c0004t0001g0217 others(5): Show |
8 | HG02257.hp2 HG02622.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-6412C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599895 | |||||||
| chr8:39599949 | T | A | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.133-6358T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39599949 | |||||||
| chr8:39600113 | T | C | 2 | a0003c0004t0001g0212 a0003c0004t0001g0217 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-6194T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600113 | |||||||
| chr8:39600149 | T | G | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-6158T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600149 | |||||||
| chr8:39600167 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0316 a0001c0001t0001g0332 |
3 | HG00609.hp1 NA18948.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.133-6140G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600167 | |||||||
| chr8:39600232 | A | G | 284 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(281): Show |
291 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.133-6075A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600232 | |||||||
| chr8:39600405 | T | C | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-5902T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600405 | |||||||
| chr8:39600436 | A | G | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.133-5871A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600436 | |||||||
| chr8:39600811 | G | C | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.133-5496G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600811 | |||||||
| chr8:39600880 | C | T | 150 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(147): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.133-5427C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600880 | |||||||
| chr8:39600968 | C | A | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.133-5339C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600968 | |||||||
| chr8:39600987 | G | T | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133-5320G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39600987 | |||||||
| chr8:39601004 | G | A | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-5303G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601004 | |||||||
| chr8:39601088 | G | A | 5 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(2): Show |
5 | HG01109.hp2 HG01255.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-5219G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601088 | |||||||
| chr8:39601126 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.133-5181C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601126 | |||||||
| chr8:39601202 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-5105C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601202 | |||||||
| chr8:39601461 | T | G | 1 | a0001c0002t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.133-4846T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601461 | |||||||
| chr8:39601531 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.133-4776A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601531 | |||||||
| chr8:39601626 | T | C | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.133-4681T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601626 | |||||||
| chr8:39601653 | C | G | 2 | a0001c0002t0001g0112 a0001c0002t0001g0157 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.133-4654C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601653 | |||||||
| chr8:39601700 | C | A | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.133-4607C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601700 | |||||||
| chr8:39601786 | T | C | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-4521T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39601786 | |||||||
| chr8:39602079 | G | T | 1 | a0001c0002t0001g0073 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.133-4228G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602079 | |||||||
| chr8:39602329 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.133-3978G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602329 | |||||||
| chr8:39602543 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.133-3764C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602543 | |||||||
| chr8:39602560 | C | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.133-3747C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602560 | |||||||
| chr8:39602592 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.133-3715G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602592 | |||||||
| chr8:39602716 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.133-3591T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39602716 | |||||||
| chr8:39602749 | GCTTTTTT others(18): Show |
G | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-3553_133-3529d others(27): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39602749 | ||||||
| chr8:39603113 | G | A | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.133-3194G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603113 | |||||||
| chr8:39603140 | A | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-3167A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603140 | |||||||
| chr8:39603261 | A | G | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.133-3046A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603261 | |||||||
| chr8:39603312 | G | C | 1 | a0001c0002t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.133-2995G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603312 | |||||||
| chr8:39603602 | A | T | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-2705A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39603602 | |||||||
| chr8:39603852 | CTGTT | C | 10 | a0001c0002t0001g0075 a0001c0002t0001g0078 a0001c0002t0001g0090 others(7): Show |
10 | HG00544.hp2 HG01496.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-2453_133-2450d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr8 | 39603852 | ||||||
| chr8:39604047 | A | G | 1 | a0001c0002t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.133-2260A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604047 | |||||||
| chr8:39604088 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.133-2219C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604088 | |||||||
| chr8:39604250 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.133-2057T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604250 | |||||||
| chr8:39604255 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.133-2052C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604255 | |||||||
| chr8:39604256 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133-2051G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604256 | |||||||
| chr8:39604384 | A | T | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.133-1923A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604384 | |||||||
| chr8:39604403 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133-1904T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604403 | |||||||
| chr8:39604478 | G | A | 1 | a0001c0002t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.133-1829G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604478 | |||||||
| chr8:39604560 | G | A | 1 | a0001c0002t0001g0003 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.133-1747G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604560 | |||||||
| chr8:39604648 | C | T | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.133-1659C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604648 | |||||||
| chr8:39604708 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-1599G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604708 | |||||||
| chr8:39604735 | C | T | 1 | a0004c0005t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.133-1572C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39604735 | |||||||
| chr8:39605252 | T | G | 15 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(12): Show |
15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-1055T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605252 | |||||||
| chr8:39605466 | A | G | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-841A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605466 | |||||||
| chr8:39605524 | T | C | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-783T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605524 | |||||||
| chr8:39605544 | T | C | 315 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(312): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.133-763T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605544 | |||||||
| chr8:39605545 | G | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.133-762G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605545 | |||||||
| chr8:39605615 | G | T | 4 | a0001c0002t0001g0113 a0001c0002t0001g0151 a0001c0002t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01256.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-692G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605615 | |||||||
| chr8:39605619 | T | C | 3 | a0001c0002t0001g0093 a0001c0002t0001g0094 a0001c0002t0001g0095 |
3 | NA18965.hp2 NA18985.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.133-688T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605619 | |||||||
| chr8:39605677 | T | A | 10 | a0001c0001t0001g0195 a0001c0001t0001g0227 a0001c0001t0001g0248 others(7): Show |
11 | HG00323.hp2 HG00733.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-630T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605677 | |||||||
| chr8:39605683 | A | T | 1 | a0003c0004t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133-624A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605683 | |||||||
| chr8:39605747 | T | G | 15 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(12): Show |
15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-560T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605747 | |||||||
| chr8:39605809 | C | T | 6 | a0001c0001t0001g0139 a0001c0002t0001g0003 a0001c0002t0001g0102 others(3): Show |
7 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-498C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39605809 | |||||||
| chr8:39606095 | C | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.133-212C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39606095 | |||||||
| chr8:39606201 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.133-106G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39606201 | |||||||
| chr8:39606304 | T | C | 70 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(67): Show |
72 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.133-3T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 2/19 | chr8 | 39606304 | |||||||
| chr8:39606619 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(48): Show |
54 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.188+257C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39606619 | |||||||
| chr8:39606754 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.188+392G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39606754 | |||||||
| chr8:39607244 | T | G | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+882T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607244 | |||||||
| chr8:39607463 | C | T | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188+1101C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607463 | |||||||
| chr8:39607519 | G | A | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+1157G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607519 | |||||||
| chr8:39607530 | G | A | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.188+1168G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607530 | |||||||
| chr8:39607587 | T | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188+1225T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607587 | |||||||
| chr8:39607742 | A | AT | 105 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(102): Show |
106 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.189-1287dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39607742 | ||||||
| chr8:39607742 | AT | A | 12 | a0001c0001t0001g0334 a0001c0002t0001g0106 a0002c0003t0001g0013 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-1287delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39607742 | ||||||
| chr8:39607774 | G | A | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.189-1268G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607774 | |||||||
| chr8:39607813 | GT | G | 90 | a0001c0001t0001g0189 a0001c0002t0001g0001 a0001c0002t0001g0002 others(87): Show |
94 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.189-1218delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39607813 | ||||||
| chr8:39607824 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.189-1218T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607824 | |||||||
| chr8:39607939 | A | G | 1 | a0002c0003t0001g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-1103A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39607939 | |||||||
| chr8:39608095 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.189-947C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608095 | |||||||
| chr8:39608108 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189-934G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608108 | |||||||
| chr8:39608177 | A | ATATATC | 30 | a0001c0001t0001g0161 a0001c0001t0001g0189 a0001c0001t0001g0203 others(27): Show |
30 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.189-850_189-845dup others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr8 | 39608177 | ||||||
| chr8:39608187 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.189-855A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608187 | |||||||
| chr8:39608264 | A | G | 1 | a0001c0015t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.189-778A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608264 | |||||||
| chr8:39608417 | A | G | 2 | a0001c0001t0001g0174 a0004c0022t0001g0194 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.189-625A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608417 | |||||||
| chr8:39608511 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.189-531C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608511 | |||||||
| chr8:39608701 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189-341A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608701 | |||||||
| chr8:39608832 | T | A | 1 | a0001c0002t0001g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-210T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608832 | |||||||
| chr8:39608884 | T | C | 1 | a0001c0002t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189-158T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 3/19 | chr8 | 39608884 | |||||||
| chr8:39609275 | G | T | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.267+155G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609275 | |||||||
| chr8:39609432 | C | A | 1 | a0001c0001t0001g0320 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.268-53C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609432 | |||||||
| chr8:39609456 | T | C | 1 | a0001c0002t0001g0077 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.268-29T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609456 | |||||||
| chr8:39609475 | T | C | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | NA18960.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.268-10T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 4/19 | chr8 | 39609475 | |||||||
| chr8:39609576 | T | C | 8 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0259 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+15T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609576 | |||||||
| chr8:39609606 | A | T | 1 | a0001c0001t0001g0313 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.344+45A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609606 | |||||||
| chr8:39609805 | A | G | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.344+244A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609805 | |||||||
| chr8:39609846 | C | G | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+285C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609846 | |||||||
| chr8:39609921 | C | G | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.344+360C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39609921 | |||||||
| chr8:39610140 | G | A | 1 | a0001c0002t0001g0283 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.345-389G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610140 | |||||||
| chr8:39610173 | A | G | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-356A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610173 | |||||||
| chr8:39610187 | T | G | 3 | a0002c0003t0001g0024 a0002c0003t0001g0025 a0002c0003t0001g0027 |
3 | HG02965.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345-342T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610187 | |||||||
| chr8:39610377 | GC | G | 7 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-145delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr8 | 39610377 | ||||||
| chr8:39610452 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.345-77C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 5/19 | chr8 | 39610452 | |||||||
| chr8:39611054 | A | T | 2 | a0001c0002t0001g0287 a0004c0005t0001g0288 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.522+348A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611054 | |||||||
| chr8:39611076 | G | A | 3 | a0003c0004t0001g0181 a0003c0004t0001g0215 a0003c0004t0001g0216 |
3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.522+370G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611076 | |||||||
| chr8:39611315 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.522+609A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611315 | |||||||
| chr8:39611330 | G | T | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.522+624G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611330 | |||||||
| chr8:39611380 | T | A | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.522+674T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611380 | |||||||
| chr8:39611423 | G | GA | 279 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(276): Show |
286 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.522+727dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39611423 | ||||||
| chr8:39611443 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+737G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611443 | |||||||
| chr8:39611736 | A | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.522+1030A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611736 | |||||||
| chr8:39611745 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.522+1039C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611745 | |||||||
| chr8:39611909 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.522+1203A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611909 | |||||||
| chr8:39611948 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.522+1242T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39611948 | |||||||
| chr8:39612098 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.522+1392A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612098 | |||||||
| chr8:39612132 | G | GA | 16 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(13): Show |
16 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.522+1437dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39612132 | ||||||
| chr8:39612508 | C | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+1802C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612508 | |||||||
| chr8:39612617 | T | G | 143 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(140): Show |
148 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.522+1911T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612617 | |||||||
| chr8:39612698 | T | G | 1 | a0001c0002t0001g0129 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.522+1992T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612698 | |||||||
| chr8:39612908 | C | T | 2 | a0001c0001t0001g0174 a0004c0022t0001g0194 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.522+2202C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39612908 | |||||||
| chr8:39613099 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.522+2393C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613099 | |||||||
| chr8:39613148 | T | G | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.522+2442T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613148 | |||||||
| chr8:39613289 | A | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0273 a0001c0001t0001g0274 others(1): Show |
4 | NA18950.hp1 NA18962.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+2583A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613289 | |||||||
| chr8:39613316 | A | G | 1 | a0002c0003t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.522+2610A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613316 | |||||||
| chr8:39613349 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0316 |
2 | HG00609.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.522+2643A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613349 | |||||||
| chr8:39613489 | G | C | 40 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(37): Show |
40 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.522+2783G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613489 | |||||||
| chr8:39613748 | A | G | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.522+3042A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613748 | |||||||
| chr8:39613912 | A | G | 1 | a0001c0002t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.522+3206A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39613912 | |||||||
| chr8:39614137 | A | G | 2 | a0005c0011t0001g0190 a0005c0011t0001g0247 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.522+3431A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614137 | |||||||
| chr8:39614146 | C | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+3440C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614146 | |||||||
| chr8:39614290 | G | A | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.522+3584G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614290 | |||||||
| chr8:39614714 | C | T | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.522+4008C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614714 | |||||||
| chr8:39614896 | AG | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0196 a0001c0001t0001g0228 |
3 | HG00438.hp1 HG00621.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.522+4191delG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614896 | |||||||
| chr8:39614941 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.522+4235G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39614941 | |||||||
| chr8:39615101 | A | G | 1 | a0006c0006t0001g0263 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.522+4395A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615101 | |||||||
| chr8:39615112 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+4406A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615112 | |||||||
| chr8:39615226 | TA | T | 45 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0028 others(42): Show |
47 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.522+4533delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39615226 | ||||||
| chr8:39615236 | A | G | 1 | a0001c0002t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.522+4530A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615236 | |||||||
| chr8:39615247 | A | G | 5 | a0001c0002t0001g0257 a0001c0002t0001g0290 a0004c0005t0001g0292 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.522+4541A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615247 | |||||||
| chr8:39615426 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.522+4720A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615426 | |||||||
| chr8:39615531 | A | G | 69 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(66): Show |
71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.522+4825A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615531 | |||||||
| chr8:39615604 | T | C | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.522+4898T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615604 | |||||||
| chr8:39615635 | C | G | 15 | a0001c0001t0001g0169 a0001c0001t0001g0187 a0001c0001t0001g0206 others(12): Show |
15 | HG00323.hp2 HG02132.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.522+4929C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615635 | |||||||
| chr8:39615636 | T | C | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.522+4930T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615636 | |||||||
| chr8:39615697 | A | G | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.522+4991A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615697 | |||||||
| chr8:39615744 | A | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.522+5038A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615744 | |||||||
| chr8:39615778 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+5072A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615778 | |||||||
| chr8:39615902 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0163 a0001c0014t0001g0219 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+5196G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39615902 | |||||||
| chr8:39616084 | C | G | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.522+5378C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616084 | |||||||
| chr8:39616181 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.522+5475A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616181 | |||||||
| chr8:39616286 | T | C | 7 | a0001c0001t0001g0197 a0001c0001t0001g0218 a0001c0001t0001g0221 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+5580T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616286 | |||||||
| chr8:39616502 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.522+5796C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616502 | |||||||
| chr8:39616503 | G | A | 10 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0055 others(7): Show |
11 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.522+5797G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616503 | |||||||
| chr8:39616512 | C | A | 1 | a0001c0002t0001g0143 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.522+5806C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616512 | |||||||
| chr8:39616657 | G | A | 1 | a0001c0002t0001g0146 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.522+5951G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616657 | |||||||
| chr8:39616797 | G | A | 2 | a0001c0002t0001g0129 a0001c0002t0001g0130 |
2 | HG01943.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.522+6091G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616797 | |||||||
| chr8:39616860 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.522+6154A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39616860 | |||||||
| chr8:39617166 | A | G | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.522+6460A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617166 | |||||||
| chr8:39617229 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.522+6523A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617229 | |||||||
| chr8:39617460 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.522+6754C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617460 | |||||||
| chr8:39617536 | A | T | 1 | a0001c0002t0001g0138 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.522+6830A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617536 | |||||||
| chr8:39617573 | A | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0163 a0001c0014t0001g0219 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+6867A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617573 | |||||||
| chr8:39617586 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.522+6880C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617586 | |||||||
| chr8:39617784 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.522+7078C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39617784 | |||||||
| chr8:39618041 | G | C | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+7335G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618041 | |||||||
| chr8:39618202 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.522+7496C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618202 | |||||||
| chr8:39618234 | C | A | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.522+7528C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618234 | |||||||
| chr8:39618379 | A | T | 1 | a0005c0016t0001g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.522+7673A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618379 | |||||||
| chr8:39618466 | T | C | 1 | a0001c0002t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.522+7760T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618466 | |||||||
| chr8:39618504 | AAC | A | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+7802_522+7803d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39618504 | ||||||
| chr8:39618572 | G | A | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+7866G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618572 | |||||||
| chr8:39618690 | G | A | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+7984G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618690 | |||||||
| chr8:39618691 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.522+7985C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618691 | |||||||
| chr8:39618734 | G | A | 2 | a0001c0002t0001g0011 a0001c0002t0001g0012 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.522+8028G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618734 | |||||||
| chr8:39618750 | T | G | 1 | a0001c0002t0001g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.522+8044T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618750 | |||||||
| chr8:39618753 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.522+8047C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618753 | |||||||
| chr8:39618754 | G | A | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.522+8048G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618754 | |||||||
| chr8:39618840 | C | T | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+8134C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618840 | |||||||
| chr8:39618881 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.522+8175G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618881 | |||||||
| chr8:39618948 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.522+8242T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39618948 | |||||||
| chr8:39619280 | G | A | 8 | a0001c0002t0001g0077 a0001c0002t0001g0081 a0001c0002t0001g0082 others(5): Show |
8 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+8574G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619280 | |||||||
| chr8:39619355 | T | G | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+8649T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619355 | |||||||
| chr8:39619411 | T | A | 6 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+8705T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619411 | |||||||
| chr8:39619459 | T | C | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.522+8753T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619459 | |||||||
| chr8:39619573 | AC | A | 70 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(67): Show |
72 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.522+8868delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619573 | |||||||
| chr8:39619673 | G | A | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.522+8967G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39619673 | |||||||
| chr8:39620000 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.522+9294A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620000 | |||||||
| chr8:39620013 | C | T | 3 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0045 |
3 | HG01069.hp1 HG02738.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.522+9307C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620013 | |||||||
| chr8:39620019 | C | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+9313C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620019 | |||||||
| chr8:39620097 | A | G | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.523-9277A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620097 | |||||||
| chr8:39620102 | G | A | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-9272G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620102 | |||||||
| chr8:39620302 | T | C | 1 | a0004c0005t0001g0292 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.523-9072T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620302 | |||||||
| chr8:39620329 | A | C | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.523-9045A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620329 | |||||||
| chr8:39620341 | G | A | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.523-9033G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620341 | |||||||
| chr8:39620357 | C | CA | 8 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(5): Show |
8 | HG00438.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-9000dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620357 | ||||||
| chr8:39620357 | CAA | C | 10 | a0001c0008t0003g0015 a0003c0004t0001g0181 a0003c0004t0001g0214 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.523-9001_523-9000d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620357 | ||||||
| chr8:39620358 | A | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-9016A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620358 | |||||||
| chr8:39620366 | A | G | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.523-9008A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620366 | |||||||
| chr8:39620372 | A | C | 5 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(2): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-9002A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620372 | |||||||
| chr8:39620373 | A | C | 185 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(182): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.523-9001A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620373 | |||||||
| chr8:39620373 | AAC | A | 5 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(2): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-8999_523-8998d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620373 | ||||||
| chr8:39620374 | A | C | 147 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(144): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.523-9000A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620374 | |||||||
| chr8:39620374 | AC | A | 118 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(115): Show |
119 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.523-8999delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620374 | |||||||
| chr8:39620375 | C | A | 143 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(140): Show |
148 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.523-8999C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620375 | |||||||
| chr8:39620375 | C | CA | 6 | a0001c0002t0001g0044 a0001c0002t0001g0047 a0001c0002t0001g0065 others(3): Show |
6 | HG03491.hp1 HG03516.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-8990dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39620375 | ||||||
| chr8:39620380 | A | C | 3 | a0001c0002t0001g0091 a0001c0002t0001g0127 a0001c0002t0001g0128 |
3 | HG00544.hp2 NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.523-8994A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620380 | |||||||
| chr8:39620414 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.523-8960A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620414 | |||||||
| chr8:39620420 | A | C | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-8954A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620420 | |||||||
| chr8:39620422 | C | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.523-8952C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620422 | |||||||
| chr8:39620537 | C | A | 6 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.523-8837C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620537 | |||||||
| chr8:39620609 | A | C | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.523-8765A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620609 | |||||||
| chr8:39620702 | A | G | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.523-8672A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620702 | |||||||
| chr8:39620847 | A | G | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-8527A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39620847 | |||||||
| chr8:39621098 | T | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0302 |
2 | NA18969.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.523-8276T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621098 | |||||||
| chr8:39621265 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.523-8109C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621265 | |||||||
| chr8:39621309 | T | TCA | 74 | a0001c0001t0001g0139 a0001c0001t0001g0161 a0001c0001t0001g0169 others(71): Show |
74 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.523-8017_523-8016d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | T | TCACA | 21 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0179 others(18): Show |
22 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.523-8019_523-8016d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | T | TCACACA | 5 | a0001c0001t0001g0301 a0001c0001t0001g0333 a0001c0002t0001g0093 others(2): Show |
5 | HG02572.hp2 NA18957.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-8021_523-8016d others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | T | TCACACAC others(3): Show |
1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.523-8025_523-8016d others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCA | T | 42 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(39): Show |
42 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.523-8017_523-8016d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACA | T | 9 | a0001c0001t0001g0186 a0001c0001t0001g0210 a0001c0001t0001g0233 others(6): Show |
9 | HG00597.hp2 HG01257.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-8019_523-8016d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACACA | T | 19 | a0001c0002t0001g0067 a0001c0002t0001g0106 a0001c0002t0001g0108 others(16): Show |
19 | HG00733.hp1 HG01167.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.523-8021_523-8016d others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACACAC others(1): Show |
T | 40 | a0001c0001t0001g0175 a0001c0002t0001g0002 a0001c0002t0001g0005 others(37): Show |
42 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.523-8023_523-8016d others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACACAC others(3): Show |
T | 18 | a0001c0001t0001g0279 a0001c0002t0001g0001 a0001c0002t0001g0028 others(15): Show |
19 | HG02055.hp2 HG02257.hp1 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.523-8025_523-8016d others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACACAC others(5): Show |
T | 39 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(36): Show |
40 | HG00544.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.523-8027_523-8016d others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACACAC others(7): Show |
T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0276 |
3 | HG00597.hp1 NA18955.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.523-8029_523-8016d others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621309 | TCACACAC others(9): Show |
T | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.523-8031_523-8016d others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39621309 | ||||||
| chr8:39621495 | A | G | 1 | a0001c0002t0001g0095 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.523-7879A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621495 | |||||||
| chr8:39621530 | G | T | 1 | a0002c0003t0001g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.523-7844G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621530 | |||||||
| chr8:39621656 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.523-7718G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621656 | |||||||
| chr8:39621668 | A | G | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.523-7706A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39621668 | |||||||
| chr8:39622226 | T | C | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.523-7148T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622226 | |||||||
| chr8:39622295 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-7079A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622295 | |||||||
| chr8:39622370 | T | G | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-7004T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622370 | |||||||
| chr8:39622781 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.523-6593T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622781 | |||||||
| chr8:39622847 | T | C | 107 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(104): Show |
108 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.523-6527T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622847 | |||||||
| chr8:39622876 | A | G | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.523-6498A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39622876 | |||||||
| chr8:39623027 | C | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-6347C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623027 | |||||||
| chr8:39623190 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.523-6184T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623190 | |||||||
| chr8:39623298 | G | A | 3 | a0001c0002t0001g0076 a0001c0002t0001g0096 a0001c0002t0001g0132 |
3 | HG01074.hp2 HG01109.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.523-6076G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623298 | |||||||
| chr8:39623306 | A | G | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523-6068A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623306 | |||||||
| chr8:39623347 | T | G | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.523-6027T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623347 | |||||||
| chr8:39623507 | AT | A | 284 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(281): Show |
291 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.523-5853delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39623507 | ||||||
| chr8:39623617 | G | A | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.523-5757G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623617 | |||||||
| chr8:39623635 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.523-5739C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623635 | |||||||
| chr8:39623813 | G | C | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.523-5561G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623813 | |||||||
| chr8:39623916 | A | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0070 |
3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.523-5458A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39623916 | |||||||
| chr8:39624025 | T | C | 59 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0165 others(56): Show |
60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.523-5349T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39624025 | |||||||
| chr8:39624491 | A | G | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-4883A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39624491 | |||||||
| chr8:39625044 | T | C | 15 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(12): Show |
15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-4330T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625044 | |||||||
| chr8:39625083 | G | C | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.523-4291G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625083 | |||||||
| chr8:39625257 | G | A | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.523-4117G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625257 | |||||||
| chr8:39625400 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.523-3974T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625400 | |||||||
| chr8:39625560 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.523-3814C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625560 | |||||||
| chr8:39625591 | A | G | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.523-3783A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625591 | |||||||
| chr8:39625727 | T | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0066 |
2 | NA18747.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.523-3647T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625727 | |||||||
| chr8:39625745 | A | G | 7 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(4): Show |
7 | HG00733.hp1 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.523-3629A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625745 | |||||||
| chr8:39625782 | A | G | 2 | a0003c0004t0001g0212 a0003c0004t0001g0217 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.523-3592A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39625782 | |||||||
| chr8:39626160 | G | C | 149 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(146): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.523-3214G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626160 | |||||||
| chr8:39626252 | G | A | 106 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0164 others(103): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.523-3122G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626252 | |||||||
| chr8:39626529 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.523-2845G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626529 | |||||||
| chr8:39626562 | C | T | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.523-2812C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626562 | |||||||
| chr8:39626607 | A | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-2767A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626607 | |||||||
| chr8:39626818 | C | G | 1 | a0001c0002t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.523-2556C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626818 | |||||||
| chr8:39626974 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02080.hp2 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-2400C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39626974 | |||||||
| chr8:39627203 | G | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0180 |
2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.523-2171G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627203 | |||||||
| chr8:39627356 | A | G | 2 | a0001c0002t0001g0011 a0001c0002t0001g0012 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.523-2018A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627356 | |||||||
| chr8:39627377 | C | G | 3 | a0001c0002t0001g0054 a0001c0002t0001g0066 a0001c0002t0001g0073 |
3 | NA18747.hp2 NA18945.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.523-1997C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627377 | |||||||
| chr8:39627445 | G | T | 1 | a0001c0001t0001g0282 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.523-1929G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627445 | |||||||
| chr8:39627708 | T | C | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-1666T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627708 | |||||||
| chr8:39627759 | T | C | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-1615T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627759 | |||||||
| chr8:39627966 | T | C | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523-1408T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39627966 | |||||||
| chr8:39628250 | A | G | 3 | a0001c0001t0001g0308 a0001c0001t0001g0319 a0001c0001t0001g0340 |
3 | HG00280.hp2 HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.523-1124A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628250 | |||||||
| chr8:39628297 | T | C | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.523-1077T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628297 | |||||||
| chr8:39628309 | T | C | 2 | a0003c0004t0002g0009 a0003c0004t0002g0010 |
2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.523-1065T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628309 | |||||||
| chr8:39628416 | A | AATAG | 95 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0166 others(92): Show |
97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.523-918_523-915dup others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628416 | A | AATAGATA others(1): Show |
14 | a0001c0001t0001g0189 a0001c0001t0001g0253 a0001c0002t0001g0001 others(11): Show |
15 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-922_523-915dup others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628416 | A | AATAGATA others(5): Show |
1 | a0001c0002t0001g0056 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.523-926_523-915dup others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628416 | AATAG | A | 96 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(93): Show |
96 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.523-918_523-915del others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628416 | AATAGATA others(1): Show |
A | 20 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(17): Show |
20 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.523-922_523-915del others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628416 | AATAGATA others(5): Show |
A | 2 | a0001c0001t0001g0250 a0012c0018t0001g0040 |
2 | HG04199.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.523-926_523-915del others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628416 | AATAGATA others(9): Show |
A | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-930_523-915del others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr8 | 39628416 | ||||||
| chr8:39628554 | G | T | 1 | a0003c0004t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.523-820G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628554 | |||||||
| chr8:39628624 | T | A | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-750T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628624 | |||||||
| chr8:39628686 | T | C | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.523-688T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628686 | |||||||
| chr8:39628964 | G | T | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.523-410G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39628964 | |||||||
| chr8:39629183 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.523-191C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39629183 | |||||||
| chr8:39629332 | A | G | 1 | a0003c0004t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.523-42A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 6/19 | chr8 | 39629332 | |||||||
| chr8:39629503 | C | T | 252 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(249): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.588+64C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39629503 | |||||||
| chr8:39629869 | G | C | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.588+430G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39629869 | |||||||
| chr8:39629891 | G | T | 1 | a0001c0002t0001g0117 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.588+452G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39629891 | |||||||
| chr8:39630011 | A | G | 17 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(14): Show |
18 | HG00733.hp1 HG01167.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.588+572A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630011 | |||||||
| chr8:39630341 | G | A | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+902G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630341 | |||||||
| chr8:39630350 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.588+911C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630350 | |||||||
| chr8:39630439 | A | T | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.588+1000A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630439 | |||||||
| chr8:39630472 | T | C | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1033T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630472 | |||||||
| chr8:39630624 | C | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.588+1185C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630624 | |||||||
| chr8:39630740 | A | G | 1 | a0002c0003t0001g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+1301A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630740 | |||||||
| chr8:39630791 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.588+1352G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630791 | |||||||
| chr8:39630811 | G | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.588+1372G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630811 | |||||||
| chr8:39630833 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.588+1394G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39630833 | |||||||
| chr8:39631155 | C | A | 1 | a0001c0002t0001g0066 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.588+1716C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631155 | |||||||
| chr8:39631373 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.588+1934C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631373 | |||||||
| chr8:39631433 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.588+1994C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631433 | |||||||
| chr8:39631513 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.588+2074T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631513 | |||||||
| chr8:39631560 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+2121A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631560 | |||||||
| chr8:39631733 | A | G | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.588+2294A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631733 | |||||||
| chr8:39631734 | T | C | 2 | a0001c0002t0001g0259 a0001c0002t0001g0260 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.588+2295T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631734 | |||||||
| chr8:39631773 | A | G | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.588+2334A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631773 | |||||||
| chr8:39631817 | C | T | 3 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 |
3 | HG01257.hp2 HG01258.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.588+2378C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631817 | |||||||
| chr8:39631862 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.588+2423T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631862 | |||||||
| chr8:39631936 | T | C | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+2497T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631936 | |||||||
| chr8:39631992 | C | G | 1 | a0002c0003t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.588+2553C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39631992 | |||||||
| chr8:39632134 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.588+2695T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632134 | |||||||
| chr8:39632252 | C | T | 6 | a0001c0002t0001g0257 a0001c0002t0001g0290 a0004c0005t0001g0292 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+2813C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632252 | |||||||
| chr8:39632706 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.588+3267C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632706 | |||||||
| chr8:39632719 | AT | A | 11 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(8): Show |
11 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.588+3282delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39632719 | ||||||
| chr8:39632867 | C | G | 1 | a0001c0002t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.588+3428C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632867 | |||||||
| chr8:39632929 | T | A | 6 | a0001c0001t0001g0197 a0001c0001t0001g0218 a0001c0001t0001g0221 others(3): Show |
6 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+3490T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39632929 | |||||||
| chr8:39633149 | T | A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.588+3710T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633149 | |||||||
| chr8:39633193 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0240 |
2 | HG02027.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.588+3754A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633193 | |||||||
| chr8:39633282 | T | C | 1 | a0001c0002t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.588+3843T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633282 | |||||||
| chr8:39633434 | A | G | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(50): Show |
56 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.589-3830A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633434 | |||||||
| chr8:39633441 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.589-3823A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633441 | |||||||
| chr8:39633509 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-3755G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633509 | |||||||
| chr8:39633582 | G | A | 187 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(184): Show |
193 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.589-3682G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633582 | |||||||
| chr8:39633661 | A | G | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.589-3603A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39633661 | |||||||
| chr8:39633830 | TA | T | 7 | a0001c0002t0001g0012 a0001c0002t0001g0257 a0001c0002t0001g0290 others(4): Show |
7 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-3421delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39633830 | ||||||
| chr8:39634152 | G | T | 1 | a0004c0005t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.589-3112G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634152 | |||||||
| chr8:39634364 | G | T | 2 | a0001c0001t0001g0174 a0004c0022t0001g0194 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.589-2900G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634364 | |||||||
| chr8:39634463 | G | A | 38 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(35): Show |
38 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.589-2801G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634463 | |||||||
| chr8:39634548 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.589-2716G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634548 | |||||||
| chr8:39634567 | G | A | 4 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG00597.hp1 NA18954.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2697G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634567 | |||||||
| chr8:39634568 | C | T | 6 | a0001c0001t0001g0197 a0001c0001t0001g0218 a0001c0001t0001g0221 others(3): Show |
6 | HG02258.hp2 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2696C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634568 | |||||||
| chr8:39634722 | A | G | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-2542A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634722 | |||||||
| chr8:39634748 | A | C | 6 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2516A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39634748 | |||||||
| chr8:39635024 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.589-2240G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39635024 | |||||||
| chr8:39635443 | T | G | 1 | a0001c0002t0001g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.589-1821T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39635443 | |||||||
| chr8:39635870 | G | C | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-1394G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39635870 | |||||||
| chr8:39636001 | G | GT | 14 | a0001c0002t0001g0004 a0001c0002t0001g0028 a0001c0002t0001g0029 others(11): Show |
15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.589-1256dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39636001 | ||||||
| chr8:39636009 | G | GT | 22 | a0001c0001t0001g0086 a0001c0001t0001g0195 a0001c0001t0001g0224 others(19): Show |
22 | HG00621.hp2 HG00733.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.589-1242dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39636009 | ||||||
| chr8:39636009 | G | T | 15 | a0001c0002t0001g0004 a0001c0002t0001g0028 a0001c0002t0001g0029 others(12): Show |
16 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-1255G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636009 | |||||||
| chr8:39636040 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0275 |
2 | NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.589-1224A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636040 | |||||||
| chr8:39636042 | G | A | 183 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(180): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.589-1222G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636042 | |||||||
| chr8:39636081 | A | C | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.589-1183A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636081 | |||||||
| chr8:39636115 | C | T | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-1149C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636115 | |||||||
| chr8:39636193 | A | T | 2 | a0006c0006t0001g0262 a0006c0006t0001g0264 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.589-1071A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636193 | |||||||
| chr8:39636396 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-868T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636396 | |||||||
| chr8:39636523 | A | T | 1 | a0004c0005t0001g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.589-741A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636523 | |||||||
| chr8:39636628 | A | T | 159 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(156): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.589-636A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636628 | |||||||
| chr8:39636770 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.589-494C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636770 | |||||||
| chr8:39636793 | T | G | 15 | a0001c0008t0003g0014 a0001c0008t0003g0015 a0002c0003t0001g0013 others(12): Show |
15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-471T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636793 | |||||||
| chr8:39636899 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.589-365T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636899 | |||||||
| chr8:39636983 | A | T | 159 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(156): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.589-281A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39636983 | |||||||
| chr8:39637016 | ATT | A | 71 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(68): Show |
73 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.589-245_589-244del others(2): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637016 | ||||||
| chr8:39637017 | TTTTA | T | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(56): Show |
62 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(59): Show |
intron_variant | MODIFIER | c.589-245_589-242del others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | ||||||
| chr8:39637017 | TTTTATA | T | 26 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(23): Show |
26 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.589-245_589-240del others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | ||||||
| chr8:39637017 | TTTTATAT others(7): Show |
T | 1 | a0001c0002t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.589-245_589-232del others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | ||||||
| chr8:39637017 | TTTTATAT others(9): Show |
T | 4 | a0001c0002t0001g0257 a0004c0005t0001g0292 a0004c0005t0001g0307 others(1): Show |
4 | HG02572.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-245_589-230del others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | ||||||
| chr8:39637017 | TTTTATAT others(11): Show |
T | 1 | a0004c0005t0001g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.589-245_589-228del others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637017 | ||||||
| chr8:39637018 | TTTA | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0273 |
3 | NA18977.hp1 NA18977.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.589-244_589-242del others(3): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637018 | ||||||
| chr8:39637019 | T | A | 2 | a0001c0002t0001g0128 a0007c0009t0001g0155 |
2 | NA18975.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.589-245T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637019 | |||||||
| chr8:39637019 | TTA | T | 24 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0001t0001g0170 others(21): Show |
24 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.589-199_589-198del others(2): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATA | T | 38 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0174 others(35): Show |
38 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.589-201_589-198del others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATA | T | 29 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0159 others(26): Show |
30 | HG01074.hp1 HG01175.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.589-203_589-198del others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(1): Show |
T | 28 | a0001c0001t0001g0161 a0001c0001t0001g0182 a0001c0001t0001g0193 others(25): Show |
28 | HG00280.hp2 HG00544.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.589-205_589-198del others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(3): Show |
T | 7 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0001t0001g0228 others(4): Show |
7 | HG00621.hp2 HG00733.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-207_589-198del others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(5): Show |
T | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0209 others(6): Show |
9 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.589-209_589-198del others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(7): Show |
T | 6 | a0001c0001t0001g0220 a0001c0001t0001g0230 a0001c0001t0001g0243 others(3): Show |
7 | HG01884.hp2 HG02148.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-211_589-198del others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(9): Show |
T | 1 | a0001c0001t0001g0139 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.589-213_589-198del others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(13): Show |
T | 1 | a0002c0003t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.589-217_589-198del others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637019 | TTATATAT others(15): Show |
T | 3 | a0002c0003t0001g0024 a0002c0003t0001g0025 a0002c0003t0001g0027 |
3 | HG02965.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.589-219_589-198del others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr8 | 39637019 | ||||||
| chr8:39637029 | A | G | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-235A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637029 | |||||||
| chr8:39637031 | A | G | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-233A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637031 | |||||||
| chr8:39637033 | A | T | 1 | a0001c0002t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.589-231A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637033 | |||||||
| chr8:39637034 | T | C | 20 | a0001c0002t0001g0003 a0001c0002t0001g0081 a0001c0002t0001g0082 others(17): Show |
21 | HG00609.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.589-230T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637034 | |||||||
| chr8:39637035 | A | T | 3 | a0001c0002t0001g0006 a0001c0002t0001g0163 a0001c0014t0001g0219 |
4 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-229A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637035 | |||||||
| chr8:39637036 | T | C | 122 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(119): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.589-228T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637036 | |||||||
| chr8:39637038 | T | C | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(56): Show |
62 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(59): Show |
intron_variant | MODIFIER | c.589-226T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637038 | |||||||
| chr8:39637040 | T | C | 26 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(23): Show |
26 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.589-224T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637040 | |||||||
| chr8:39637042 | T | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589-222T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637042 | |||||||
| chr8:39637043 | A | G | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-221A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637043 | |||||||
| chr8:39637050 | T | C | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-214T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637050 | |||||||
| chr8:39637053 | A | G | 146 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(143): Show |
151 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.589-211A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637053 | |||||||
| chr8:39637055 | A | G | 158 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(155): Show |
163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.589-209A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637055 | |||||||
| chr8:39637067 | G | A | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-197G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637067 | |||||||
| chr8:39637196 | C | T | 1 | a0001c0002t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.589-68C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637196 | |||||||
| chr8:39637233 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.589-31A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 7/19 | chr8 | 39637233 | |||||||
| chr8:39637740 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.827+37A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39637740 | |||||||
| chr8:39637806 | G | A | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(181): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.827+103G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39637806 | |||||||
| chr8:39637959 | T | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.827+256T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39637959 | |||||||
| chr8:39638009 | G | T | 1 | a0001c0002t0001g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.827+306G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638009 | |||||||
| chr8:39638130 | G | A | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.828-335G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638130 | |||||||
| chr8:39638229 | T | A | 1 | a0001c0002t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.828-236T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638229 | |||||||
| chr8:39638267 | TA | T | 61 | a0001c0002t0001g0003 a0001c0002t0001g0041 a0001c0002t0001g0042 others(58): Show |
62 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.828-195delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr8 | 39638267 | ||||||
| chr8:39638291 | GATTTAGT | G | 17 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0055 others(14): Show |
18 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.828-155_828-149del others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr8 | 39638291 | ||||||
| chr8:39638375 | T | TAAAATTT others(236): Show |
6 | a0001c0002t0001g0257 a0001c0002t0001g0290 a0004c0005t0001g0292 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.828-77_828-76insGC others(241): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr8 | 39638375 | ||||||
| chr8:39638423 | T | A | 1 | a0002c0003t0001g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.828-42T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 9/19 | chr8 | 39638423 | |||||||
| chr8:39638683 | G | A | 159 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(156): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.909+137G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638683 | |||||||
| chr8:39638695 | A | G | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.909+149A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638695 | |||||||
| chr8:39638772 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.909+226C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638772 | |||||||
| chr8:39638786 | A | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.909+240A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638786 | |||||||
| chr8:39638796 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.909+250C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39638796 | |||||||
| chr8:39639135 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+589T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639135 | |||||||
| chr8:39639161 | G | T | 1 | a0002c0003t0001g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+615G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639161 | |||||||
| chr8:39639451 | C | T | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(181): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.909+905C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639451 | |||||||
| chr8:39639492 | C | T | 147 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(144): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.909+946C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639492 | |||||||
| chr8:39639557 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0070 |
3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1011T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639557 | |||||||
| chr8:39639567 | ATT | A | 2 | a0001c0002t0001g0002 a0001c0002t0001g0070 |
3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1023_909+1024d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39639567 | ||||||
| chr8:39639572 | G | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0070 |
3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1026G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639572 | |||||||
| chr8:39639573 | AC | A | 2 | a0001c0002t0001g0002 a0001c0002t0001g0070 |
3 | HG01168.hp1 HG01169.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.909+1028delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639573 | |||||||
| chr8:39639603 | A | C | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(181): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.909+1057A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639603 | |||||||
| chr8:39639618 | G | A | 1 | a0001c0002t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.909+1072G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639618 | |||||||
| chr8:39639790 | G | A | 1 | a0004c0005t0001g0292 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.909+1244G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639790 | |||||||
| chr8:39639844 | T | G | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.909+1298T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639844 | |||||||
| chr8:39639974 | G | T | 1 | a0001c0002t0001g0130 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.909+1428G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39639974 | |||||||
| chr8:39640119 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.909+1573C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640119 | |||||||
| chr8:39640303 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.909+1757A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640303 | |||||||
| chr8:39640441 | G | A | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(181): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.909+1895G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640441 | |||||||
| chr8:39640815 | A | AT | 147 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(144): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.909+2279dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39640815 | ||||||
| chr8:39640834 | T | A | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+2288T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640834 | |||||||
| chr8:39640851 | T | C | 5 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0116 others(2): Show |
5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+2305T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39640851 | |||||||
| chr8:39640867 | GT | G | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+2331delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39640867 | ||||||
| chr8:39641340 | C | G | 147 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(144): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.909+2794C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641340 | |||||||
| chr8:39641354 | G | A | 1 | a0002c0003t0001g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.909+2808G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641354 | |||||||
| chr8:39641470 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.909+2924C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641470 | |||||||
| chr8:39641475 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.909+2929C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641475 | |||||||
| chr8:39641557 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0236 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.909+3011C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641557 | |||||||
| chr8:39641678 | C | A | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.909+3132C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641678 | |||||||
| chr8:39641678 | C | T | 1 | a0005c0011t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.909+3132C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641678 | |||||||
| chr8:39641679 | G | T | 159 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(156): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.909+3133G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641679 | |||||||
| chr8:39641773 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.909+3227C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641773 | |||||||
| chr8:39641857 | A | G | 6 | a0001c0002t0001g0257 a0001c0002t0001g0290 a0004c0005t0001g0292 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+3311A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641857 | |||||||
| chr8:39641873 | A | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.909+3327A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39641873 | |||||||
| chr8:39642052 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0205 |
2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.910-3286A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642052 | |||||||
| chr8:39642212 | T | C | 7 | a0001c0001t0001g0295 a0001c0001t0001g0311 a0001c0001t0001g0320 others(4): Show |
7 | HG01106.hp1 HG01257.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-3126T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642212 | |||||||
| chr8:39642336 | G | T | 3 | a0001c0002t0001g0076 a0001c0002t0001g0096 a0001c0002t0001g0132 |
3 | HG01074.hp2 HG01109.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.910-3002G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642336 | |||||||
| chr8:39642390 | G | T | 15 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(12): Show |
15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.910-2948G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642390 | |||||||
| chr8:39642706 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.910-2632T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642706 | |||||||
| chr8:39642717 | T | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.910-2621T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642717 | |||||||
| chr8:39642762 | G | A | 1 | a0003c0004t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.910-2576G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642762 | |||||||
| chr8:39642830 | G | A | 147 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(144): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.910-2508G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642830 | |||||||
| chr8:39642987 | A | G | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(69): Show |
75 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.910-2351A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39642987 | |||||||
| chr8:39643077 | C | G | 1 | a0001c0002t0001g0130 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.910-2261C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643077 | |||||||
| chr8:39643142 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.910-2196G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643142 | |||||||
| chr8:39643329 | A | G | 1 | a0001c0002t0001g0158 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.910-2009A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643329 | |||||||
| chr8:39643397 | A | G | 3 | a0001c0002t0001g0076 a0001c0002t0001g0096 a0001c0002t0001g0132 |
3 | HG01074.hp2 HG01109.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.910-1941A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643397 | |||||||
| chr8:39643493 | G | T | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.910-1845G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643493 | |||||||
| chr8:39643523 | A | C | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-1815A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643523 | |||||||
| chr8:39643593 | A | T | 1 | a0002c0003t0001g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-1745A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643593 | |||||||
| chr8:39643673 | C | G | 3 | a0003c0004t0002g0008 a0003c0004t0002g0009 a0003c0004t0002g0010 |
3 | HG02257.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.910-1665C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643673 | |||||||
| chr8:39643787 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.910-1551C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39643787 | |||||||
| chr8:39644133 | G | C | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(181): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.910-1205G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644133 | |||||||
| chr8:39644163 | G | C | 6 | a0001c0002t0001g0257 a0001c0002t0001g0290 a0004c0005t0001g0292 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-1175G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644163 | |||||||
| chr8:39644213 | GATAA | G | 6 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-1120_910-1117d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr8 | 39644213 | ||||||
| chr8:39644319 | A | G | 183 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(180): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.910-1019A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644319 | |||||||
| chr8:39644476 | C | T | 1 | a0003c0004t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.910-862C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644476 | |||||||
| chr8:39644698 | C | T | 160 | a0001c0001t0001g0222 a0001c0002t0001g0001 a0001c0002t0001g0002 others(157): Show |
165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.910-640C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644698 | |||||||
| chr8:39644710 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.910-628G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39644710 | |||||||
| chr8:39645113 | G | A | 1 | a0001c0002t0001g0050 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.910-225G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39645113 | |||||||
| chr8:39645288 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.910-50A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39645288 | |||||||
| chr8:39645294 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-44A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 10/19 | chr8 | 39645294 | |||||||
| chr8:39645518 | T | C | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1046+44T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645518 | |||||||
| chr8:39645558 | C | T | 4 | a0002c0003t0001g0024 a0002c0003t0001g0025 a0002c0003t0001g0026 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+84C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645558 | |||||||
| chr8:39645560 | G | A | 178 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(175): Show |
184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1046+86G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645560 | |||||||
| chr8:39645592 | G | C | 15 | a0001c0008t0003g0014 a0001c0008t0003g0015 a0002c0003t0001g0013 others(12): Show |
15 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046+118G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645592 | |||||||
| chr8:39645642 | T | C | 6 | a0001c0002t0001g0257 a0001c0002t0001g0290 a0004c0005t0001g0292 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1046+168T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645642 | |||||||
| chr8:39645688 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1046+214A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645688 | |||||||
| chr8:39645759 | A | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+285A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645759 | |||||||
| chr8:39645932 | C | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+458C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645932 | |||||||
| chr8:39645984 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1046+510G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39645984 | |||||||
| chr8:39646095 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1046+621A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646095 | |||||||
| chr8:39646192 | A | T | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1046+718A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646192 | |||||||
| chr8:39646222 | T | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+748T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646222 | |||||||
| chr8:39646223 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+749A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646223 | |||||||
| chr8:39646267 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+793A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646267 | |||||||
| chr8:39646563 | G | A | 10 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0055 others(7): Show |
11 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+1089G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646563 | |||||||
| chr8:39646721 | C | T | 1 | a0001c0002t0001g0032 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1046+1247C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646721 | |||||||
| chr8:39646904 | A | AG | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+1435dupG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr8 | 39646904 | ||||||
| chr8:39646993 | G | T | 3 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 |
3 | HG01257.hp2 HG01258.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1047-1351G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39646993 | |||||||
| chr8:39647136 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-1208G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647136 | |||||||
| chr8:39647215 | A | T | 1 | a0001c0002t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1047-1129A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647215 | |||||||
| chr8:39647222 | G | A | 1 | a0001c0002t0001g0154 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1047-1122G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647222 | |||||||
| chr8:39647223 | G | T | 163 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(160): Show |
168 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047-1121G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647223 | |||||||
| chr8:39647234 | C | CA | 100 | a0001c0001t0001g0087 a0001c0001t0001g0186 a0001c0001t0001g0201 others(97): Show |
103 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1047-1093dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr8 | 39647234 | ||||||
| chr8:39647234 | C | CAA | 80 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(77): Show |
82 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1047-1094_1047-109 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr8 | 39647234 | ||||||
| chr8:39647320 | C | T | 1 | a0001c0002t0001g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047-1024C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647320 | |||||||
| chr8:39647436 | T | C | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047-908T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647436 | |||||||
| chr8:39647488 | A | G | 1 | a0004c0005t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1047-856A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647488 | |||||||
| chr8:39647584 | C | T | 2 | a0006c0006t0001g0262 a0006c0006t0001g0264 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1047-760C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647584 | |||||||
| chr8:39647656 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1047-688G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647656 | |||||||
| chr8:39647672 | G | A | 81 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(78): Show |
83 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1047-672G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647672 | |||||||
| chr8:39647775 | A | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG00609.hp1 HG02523.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-569A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647775 | |||||||
| chr8:39647794 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1047-550C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647794 | |||||||
| chr8:39647827 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0239 |
2 | NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1047-517A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647827 | |||||||
| chr8:39647863 | A | G | 190 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(187): Show |
196 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1047-481A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647863 | |||||||
| chr8:39647909 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0205 |
2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1047-435A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647909 | |||||||
| chr8:39647961 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1047-383G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647961 | |||||||
| chr8:39647998 | G | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-346G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39647998 | |||||||
| chr8:39648026 | G | A | 1 | a0004c0005t0001g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1047-318G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39648026 | |||||||
| chr8:39648183 | G | C | 41 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0036 others(38): Show |
43 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047-161G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39648183 | |||||||
| chr8:39648307 | C | A | 168 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(165): Show |
174 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1047-37C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 11/19 | chr8 | 39648307 | |||||||
| chr8:39648562 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1230+35T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39648562 | |||||||
| chr8:39648671 | T | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+144T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39648671 | |||||||
| chr8:39648694 | T | G | 16 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 others(13): Show |
16 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1230+167T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39648694 | |||||||
| chr8:39649247 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+720T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649247 | |||||||
| chr8:39649282 | T | A | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1230+755T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649282 | |||||||
| chr8:39649299 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1230+772G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649299 | |||||||
| chr8:39649346 | A | T | 12 | a0003c0004t0001g0181 a0003c0004t0001g0212 a0003c0004t0001g0214 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1230+819A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649346 | |||||||
| chr8:39649348 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+821G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649348 | |||||||
| chr8:39649350 | T | A | 190 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(187): Show |
196 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1230+823T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649350 | |||||||
| chr8:39649380 | G | GTA | 39 | a0001c0002t0001g0005 a0001c0002t0001g0036 a0001c0002t0001g0037 others(36): Show |
40 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.1230+867_1230+868d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649380 | ||||||
| chr8:39649380 | G | GTATA | 4 | a0001c0002t0001g0002 a0001c0002t0001g0070 a0001c0002t0001g0071 others(1): Show |
5 | HG01168.hp1 HG01169.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+865_1230+868d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649380 | ||||||
| chr8:39649380 | GTA | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+867_1230+868d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649380 | ||||||
| chr8:39649403 | A | T | 1 | a0001c0002t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1230+876A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649403 | |||||||
| chr8:39649526 | A | G | 1 | a0001c0002t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1230+999A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39649526 | |||||||
| chr8:39649822 | C | CT | 164 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(161): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1230+1297dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39649822 | ||||||
| chr8:39650006 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1230+1479A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650006 | |||||||
| chr8:39650170 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1230+1643C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650170 | |||||||
| chr8:39650246 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1230+1719T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650246 | |||||||
| chr8:39650350 | T | G | 168 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(165): Show |
174 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1230+1823T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650350 | |||||||
| chr8:39650506 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0206 a0001c0001t0001g0232 others(1): Show |
4 | HG02132.hp2 NA18612.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+1979A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650506 | |||||||
| chr8:39650732 | T | C | 1 | a0001c0002t0001g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1230+2205T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650732 | |||||||
| chr8:39650812 | C | G | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+2285C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650812 | |||||||
| chr8:39650840 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2313G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650840 | |||||||
| chr8:39650873 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2346C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650873 | |||||||
| chr8:39650966 | A | G | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+2439A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39650966 | |||||||
| chr8:39651243 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2716C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651243 | |||||||
| chr8:39651393 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+2866A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651393 | |||||||
| chr8:39651468 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1230+2941C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651468 | |||||||
| chr8:39651570 | A | G | 164 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(161): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1230+3043A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39651570 | |||||||
| chr8:39651574 | CTTAATCC others(13): Show |
C | 16 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 others(13): Show |
16 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1230+3050_1230+306 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651574 | ||||||
| chr8:39651607 | GT | G | 190 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(187): Show |
196 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1230+3084delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651607 | ||||||
| chr8:39651637 | GT | G | 164 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(161): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1230+3112delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651637 | ||||||
| chr8:39651923 | GC | G | 42 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0036 others(39): Show |
44 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.1230+3399delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651923 | ||||||
| chr8:39651972 | AG | A | 164 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(161): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1230+3447delG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39651972 | ||||||
| chr8:39652206 | A | G | 1 | a0001c0002t0001g0287 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1230+3679A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652206 | |||||||
| chr8:39652399 | G | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+3872G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652399 | |||||||
| chr8:39652571 | G | C | 14 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(11): Show |
14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1230+4044G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652571 | |||||||
| chr8:39652638 | C | T | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+4111C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652638 | |||||||
| chr8:39652643 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4116A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652643 | |||||||
| chr8:39652695 | C | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4168C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652695 | |||||||
| chr8:39652702 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4175C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652702 | |||||||
| chr8:39652840 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4313T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652840 | |||||||
| chr8:39652863 | A | G | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1230+4336A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652863 | |||||||
| chr8:39652984 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4457A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39652984 | |||||||
| chr8:39653160 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4633T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653160 | |||||||
| chr8:39653160 | T | TA | 5 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(2): Show |
5 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4634dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39653160 | ||||||
| chr8:39653192 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4665C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653192 | |||||||
| chr8:39653221 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4694C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653221 | |||||||
| chr8:39653289 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1230+4762G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653289 | |||||||
| chr8:39653296 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1230+4769T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653296 | |||||||
| chr8:39653312 | A | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4785A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653312 | |||||||
| chr8:39653397 | T | C | 190 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(187): Show |
196 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1230+4870T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653397 | |||||||
| chr8:39653404 | T | C | 1 | a0001c0002t0001g0090 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1230+4877T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653404 | |||||||
| chr8:39653457 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1230+4930A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653457 | |||||||
| chr8:39653471 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4944A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653471 | |||||||
| chr8:39653494 | A | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+4967A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653494 | |||||||
| chr8:39653554 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5027T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653554 | |||||||
| chr8:39653636 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5109A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653636 | |||||||
| chr8:39653723 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5196C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653723 | |||||||
| chr8:39653730 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | NA18985.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1230+5203G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653730 | |||||||
| chr8:39653824 | G | T | 70 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(67): Show |
71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1230+5297G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653824 | |||||||
| chr8:39653935 | T | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5408T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39653935 | |||||||
| chr8:39654021 | A | G | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5494A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654021 | |||||||
| chr8:39654040 | CTTCCACA others(53): Show |
C | 2 | a0001c0007t0001g0198 a0001c0007t0001g0229 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1230+5514_1230+557 others(64): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654040 | |||||||
| chr8:39654064 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5537T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654064 | |||||||
| chr8:39654092 | T | C | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1230+5565T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654092 | |||||||
| chr8:39654115 | A | G | 80 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(77): Show |
82 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1230+5588A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654115 | |||||||
| chr8:39654134 | CCACTGAC others(371): Show |
C | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+5610_1230+598 others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39654134 | ||||||
| chr8:39654152 | TC | T | 5 | a0001c0002t0001g0058 a0001c0002t0001g0064 a0001c0002t0001g0095 others(2): Show |
5 | HG01975.hp2 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+5627delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39654152 | ||||||
| chr8:39654153 | C | CT | 7 | a0001c0002t0001g0011 a0001c0002t0001g0037 a0001c0002t0001g0082 others(4): Show |
7 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+5626_1230+562 others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654153 | |||||||
| chr8:39654153 | C | CTTTTTTT | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+5626_1230+562 others(11): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654153 | |||||||
| chr8:39654154 | C | CT | 11 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0001g0184 others(8): Show |
11 | HG01071.hp2 HG01192.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1230+5647dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39654154 | ||||||
| chr8:39654154 | C | T | 175 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(172): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1230+5627C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654154 | |||||||
| chr8:39654200 | A | C | 31 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(28): Show |
32 | HG00733.hp1 HG01167.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1230+5673A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654200 | |||||||
| chr8:39654200 | A | T | 152 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1230+5673A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654200 | |||||||
| chr8:39654244 | G | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+5717G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654244 | |||||||
| chr8:39654261 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5734G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654261 | |||||||
| chr8:39654298 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1230+5771C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654298 | |||||||
| chr8:39654359 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1230+5832C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654359 | |||||||
| chr8:39654525 | G | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+5998G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654525 | |||||||
| chr8:39654664 | A | AG | 183 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(180): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1230+6137_1230+613 others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654664 | |||||||
| chr8:39654803 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+6276T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654803 | |||||||
| chr8:39654938 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1230+6411C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39654938 | |||||||
| chr8:39655027 | G | C | 13 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0003c0004t0001g0181 others(10): Show |
13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1230+6500G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655027 | |||||||
| chr8:39655238 | A | T | 192 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(189): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1230+6711A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655238 | |||||||
| chr8:39655260 | CCCAGTG | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+6737_1230+674 others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39655260 | ||||||
| chr8:39655573 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+7046A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655573 | |||||||
| chr8:39655729 | A | C | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+7202A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655729 | |||||||
| chr8:39655828 | C | CATAAAAA others(11): Show |
1 | a0011c0024t0001g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1230+7301_1230+730 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39655828 | |||||||
| chr8:39656066 | G | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+7539G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656066 | |||||||
| chr8:39656163 | A | G | 1 | a0001c0002t0001g0138 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1231-7632A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656163 | |||||||
| chr8:39656306 | A | G | 81 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(78): Show |
83 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1231-7489A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656306 | |||||||
| chr8:39656380 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1231-7415G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656380 | |||||||
| chr8:39656410 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1231-7385C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656410 | |||||||
| chr8:39656411 | G | A | 1 | a0011c0024t0001g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1231-7384G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656411 | |||||||
| chr8:39656432 | T | G | 5 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(2): Show |
6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-7363T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656432 | |||||||
| chr8:39656482 | T | C | 4 | a0001c0002t0001g0001 a0001c0002t0001g0055 a0001c0002t0001g0059 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-7313T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656482 | |||||||
| chr8:39656656 | A | T | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1231-7139A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656656 | |||||||
| chr8:39656657 | G | C | 5 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(2): Show |
6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-7138G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656657 | |||||||
| chr8:39656790 | T | A | 157 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(154): Show |
163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1231-7005T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656790 | |||||||
| chr8:39656837 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1231-6958T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656837 | |||||||
| chr8:39656844 | C | G | 70 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(67): Show |
71 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1231-6951C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39656844 | |||||||
| chr8:39657113 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1231-6682A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657113 | |||||||
| chr8:39657200 | A | G | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-6595A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657200 | |||||||
| chr8:39657318 | G | GT | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-6472dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39657318 | ||||||
| chr8:39657364 | T | G | 1 | a0002c0003t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1231-6431T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657364 | |||||||
| chr8:39657562 | C | T | 1 | a0001c0002t0001g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1231-6233C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657562 | |||||||
| chr8:39657808 | A | G | 5 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(2): Show |
6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-5987A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657808 | |||||||
| chr8:39657820 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1231-5975A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657820 | |||||||
| chr8:39657822 | A | C | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-5973A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657822 | |||||||
| chr8:39657916 | CAT | C | 4 | a0001c0001t0001g0203 a0001c0001t0001g0210 a0001c0001t0001g0238 others(1): Show |
4 | HG02074.hp2 NA18949.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-5878_1231-587 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39657916 | |||||||
| chr8:39658054 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1231-5741G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658054 | |||||||
| chr8:39658085 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1231-5710C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658085 | |||||||
| chr8:39658194 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1231-5601A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658194 | |||||||
| chr8:39658408 | A | T | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1231-5387A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658408 | |||||||
| chr8:39658650 | A | T | 1 | a0001c0002t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1231-5145A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658650 | |||||||
| chr8:39658808 | T | G | 4 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(1): Show |
4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-4987T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658808 | |||||||
| chr8:39658963 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-4832T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39658963 | |||||||
| chr8:39659206 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1231-4589T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659206 | |||||||
| chr8:39659406 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1231-4389T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659406 | |||||||
| chr8:39659410 | T | A | 2 | a0001c0002t0001g0285 a0001c0002t0001g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1231-4385T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659410 | |||||||
| chr8:39659557 | A | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-4238A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659557 | |||||||
| chr8:39659729 | A | T | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1231-4066A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659729 | |||||||
| chr8:39659875 | C | G | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1231-3920C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39659875 | |||||||
| chr8:39660053 | A | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0274 |
2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1231-3742A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39660053 | |||||||
| chr8:39660084 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-3711C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39660084 | |||||||
| chr8:39660322 | T | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-3473T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39660322 | |||||||
| chr8:39661117 | T | TA | 13 | a0001c0001t0001g0311 a0002c0003t0001g0013 a0002c0003t0001g0017 others(10): Show |
13 | HG00733.hp1 HG01106.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1231-2668dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661117 | ||||||
| chr8:39661122 | A | T | 1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1231-2673A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661122 | |||||||
| chr8:39661129 | C | A | 157 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(154): Show |
163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1231-2666C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661129 | |||||||
| chr8:39661144 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1231-2651T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661144 | |||||||
| chr8:39661154 | C | CT | 90 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(87): Show |
91 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1231-2623dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661154 | ||||||
| chr8:39661154 | C | CTT | 6 | a0001c0001t0001g0225 a0001c0001t0001g0233 a0001c0001t0001g0265 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2624_1231-262 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661154 | ||||||
| chr8:39661154 | CT | C | 72 | a0001c0001t0001g0174 a0001c0001t0001g0268 a0001c0002t0001g0001 others(69): Show |
76 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1231-2623delT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661154 | ||||||
| chr8:39661157 | T | C | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1231-2638T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661157 | |||||||
| chr8:39661158 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-2637T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661158 | |||||||
| chr8:39661207 | C | T | 1 | a0001c0002t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1231-2588C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661207 | |||||||
| chr8:39661222 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-2573G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661222 | |||||||
| chr8:39661298 | G | A | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-2497G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661298 | |||||||
| chr8:39661319 | A | AT | 74 | a0001c0001t0001g0087 a0001c0001t0001g0139 a0001c0001t0001g0161 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1231-2448dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | ||||||
| chr8:39661319 | A | ATT | 74 | a0001c0001t0001g0086 a0001c0001t0001g0159 a0001c0001t0001g0164 others(71): Show |
75 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1231-2449_1231-244 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | ||||||
| chr8:39661319 | A | ATTT | 19 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0001g0185 others(16): Show |
20 | HG00438.hp1 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-2450_1231-244 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | ||||||
| chr8:39661319 | ATTTTTTT others(4): Show |
A | 5 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(2): Show |
5 | HG01109.hp2 HG01255.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-2458_1231-244 others(15): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | ||||||
| chr8:39661319 | ATTTTTTT others(5): Show |
A | 142 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(139): Show |
147 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1231-2459_1231-244 others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | ||||||
| chr8:39661319 | ATTTTTTT others(6): Show |
A | 6 | a0001c0002t0001g0045 a0001c0002t0001g0113 a0001c0002t0001g0136 others(3): Show |
6 | HG01069.hp1 HG01070.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-2460_1231-244 others(17): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661319 | ||||||
| chr8:39661349 | T | G | 153 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(150): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1231-2446T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661349 | |||||||
| chr8:39661406 | C | T | 7 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-2389C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661406 | |||||||
| chr8:39661409 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1231-2386C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661409 | |||||||
| chr8:39661410 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-2385G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661410 | |||||||
| chr8:39661418 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1231-2377C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661418 | |||||||
| chr8:39661449 | C | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-2346C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661449 | |||||||
| chr8:39661536 | A | G | 13 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-2259A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39661536 | |||||||
| chr8:39661928 | T | TTA | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-1855_1231-185 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39661928 | ||||||
| chr8:39662110 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1231-1685T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662110 | |||||||
| chr8:39662337 | T | A | 225 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(222): Show |
231 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1231-1458T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662337 | |||||||
| chr8:39662400 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1231-1395G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662400 | |||||||
| chr8:39662563 | G | A | 1 | a0001c0002t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1231-1232G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662563 | |||||||
| chr8:39662608 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-1187T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662608 | |||||||
| chr8:39662757 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1231-1038T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662757 | |||||||
| chr8:39662781 | C | T | 19 | a0001c0002t0001g0077 a0001c0002t0001g0081 a0001c0002t0001g0082 others(16): Show |
19 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1231-1014C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662781 | |||||||
| chr8:39662800 | T | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-995T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662800 | |||||||
| chr8:39662903 | G | A | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-892G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662903 | |||||||
| chr8:39662905 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-890G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662905 | |||||||
| chr8:39662990 | G | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-805G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39662990 | |||||||
| chr8:39663001 | T | C | 1 | a0001c0002t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1231-794T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663001 | |||||||
| chr8:39663225 | T | C | 59 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1231-570T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663225 | |||||||
| chr8:39663235 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1231-560C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663235 | |||||||
| chr8:39663369 | A | G | 5 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(2): Show |
6 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-426A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663369 | |||||||
| chr8:39663377 | T | G | 1 | a0001c0002t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1231-418T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663377 | |||||||
| chr8:39663425 | C | CA | 141 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(138): Show |
146 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1231-354dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663425 | ||||||
| chr8:39663471 | C | T | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1231-324C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663471 | |||||||
| chr8:39663577 | T | C | 225 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(222): Show |
231 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1231-218T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663577 | |||||||
| chr8:39663598 | C | CA | 66 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0175 others(63): Show |
66 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1231-168dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | ||||||
| chr8:39663598 | C | CAA | 20 | a0001c0001t0001g0169 a0001c0001t0001g0199 a0001c0001t0001g0207 others(17): Show |
20 | HG02027.hp1 HG02074.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-169_1231-168d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | ||||||
| chr8:39663598 | CA | C | 55 | a0001c0001t0001g0204 a0001c0001t0001g0239 a0001c0001t0001g0275 others(52): Show |
58 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.1231-168delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | ||||||
| chr8:39663598 | CAA | C | 15 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(12): Show |
15 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1231-169_1231-168d others(4): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | ||||||
| chr8:39663598 | CAAAA | C | 5 | a0001c0001t0001g0197 a0001c0002t0001g0006 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-171_1231-168d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr8 | 39663598 | ||||||
| chr8:39663625 | A | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1231-170A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663625 | |||||||
| chr8:39663748 | T | C | 1 | a0004c0005t0001g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1231-47T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663748 | |||||||
| chr8:39663755 | T | C | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-40T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 12/19 | chr8 | 39663755 | |||||||
| chr8:39663900 | T | C | 225 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(222): Show |
231 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1326+10T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39663900 | |||||||
| chr8:39664028 | A | T | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1326+138A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664028 | |||||||
| chr8:39664324 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1326+434T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664324 | |||||||
| chr8:39664635 | G | A | 59 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1326+745G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664635 | |||||||
| chr8:39664665 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1326+775T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664665 | |||||||
| chr8:39664853 | A | G | 6 | a0001c0001t0001g0182 a0001c0001t0001g0192 a0001c0001t0001g0223 others(3): Show |
6 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326+963A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664853 | |||||||
| chr8:39664932 | G | T | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(77): Show |
84 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.1326+1042G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664932 | |||||||
| chr8:39664933 | T | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(77): Show |
84 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.1326+1043T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664933 | |||||||
| chr8:39664934 | TGAA | T | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(77): Show |
84 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.1326+1045_1326+104 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39664934 | |||||||
| chr8:39665094 | G | A | 225 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(222): Show |
231 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1326+1204G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665094 | |||||||
| chr8:39665115 | C | A | 1 | a0001c0001t0001g0333 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1326+1225C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665115 | |||||||
| chr8:39665456 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+1566A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665456 | |||||||
| chr8:39665549 | G | A | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326+1659G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665549 | |||||||
| chr8:39665773 | C | A | 1 | a0003c0004t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1326+1883C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665773 | |||||||
| chr8:39665803 | C | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+1913C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665803 | |||||||
| chr8:39665833 | T | A | 1 | a0001c0002t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1326+1943T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665833 | |||||||
| chr8:39665877 | TAAA | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+1989_1326+199 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr8 | 39665877 | ||||||
| chr8:39665882 | G | T | 1 | a0001c0002t0001g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1326+1992G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665882 | |||||||
| chr8:39665892 | A | T | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1326+2002A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665892 | |||||||
| chr8:39665900 | G | T | 59 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1326+2010G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665900 | |||||||
| chr8:39665961 | T | C | 1 | a0001c0010t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1327-2037T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39665961 | |||||||
| chr8:39666016 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1327-1982C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666016 | |||||||
| chr8:39666365 | G | A | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1327-1633G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666365 | |||||||
| chr8:39666482 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1327-1516A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666482 | |||||||
| chr8:39666512 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1327-1486G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666512 | |||||||
| chr8:39666652 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0276 |
2 | NA18955.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1327-1346G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666652 | |||||||
| chr8:39666781 | G | A | 6 | a0001c0002t0001g0089 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00609.hp2 NA18950.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1327-1217G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666781 | |||||||
| chr8:39666917 | T | G | 225 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(222): Show |
231 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1327-1081T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39666917 | |||||||
| chr8:39667128 | G | A | 59 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1327-870G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667128 | |||||||
| chr8:39667129 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0239 |
2 | NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1327-869C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667129 | |||||||
| chr8:39667295 | G | A | 5 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0083 others(2): Show |
5 | HG01109.hp2 HG01255.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-703G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667295 | |||||||
| chr8:39667401 | C | CA | 29 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0166 others(26): Show |
30 | HG00621.hp1 HG00733.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1327-578dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr8 | 39667401 | ||||||
| chr8:39667401 | CA | C | 12 | a0001c0001t0001g0193 a0001c0001t0001g0227 a0001c0001t0001g0236 others(9): Show |
12 | HG00323.hp2 HG01074.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1327-578delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr8 | 39667401 | ||||||
| chr8:39667427 | G | A | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327-571G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667427 | |||||||
| chr8:39667478 | T | C | 1 | a0001c0010t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1327-520T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667478 | |||||||
| chr8:39667478 | T | G | 1 | a0001c0002t0001g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1327-520T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667478 | |||||||
| chr8:39667543 | A | T | 1 | a0003c0004t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1327-455A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667543 | |||||||
| chr8:39667591 | A | G | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1327-407A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667591 | |||||||
| chr8:39667655 | C | T | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1327-343C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667655 | |||||||
| chr8:39667875 | T | C | 1 | a0004c0005t0001g0307 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1327-123T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 13/19 | chr8 | 39667875 | |||||||
| chr8:39668213 | C | T | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525+17C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668213 | |||||||
| chr8:39668225 | A | G | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1525+29A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668225 | |||||||
| chr8:39668231 | C | A | 192 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(189): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1525+35C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668231 | |||||||
| chr8:39668310 | A | C | 94 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(91): Show |
96 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.1525+114A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668310 | |||||||
| chr8:39668820 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1525+624T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39668820 | |||||||
| chr8:39669182 | G | A | 5 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0116 others(2): Show |
5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+986G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669182 | |||||||
| chr8:39669314 | A | T | 183 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(180): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1525+1118A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669314 | |||||||
| chr8:39669368 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0221 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1525+1172G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669368 | |||||||
| chr8:39669464 | C | G | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1525+1268C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669464 | |||||||
| chr8:39669474 | C | A | 2 | a0001c0002t0001g0076 a0001c0002t0001g0132 |
2 | HG01074.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1525+1278C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669474 | |||||||
| chr8:39669538 | T | C | 192 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(189): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1525+1342T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669538 | |||||||
| chr8:39669549 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1525+1353G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669549 | |||||||
| chr8:39669588 | G | T | 1 | a0001c0002t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1525+1392G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669588 | |||||||
| chr8:39669762 | C | A | 6 | a0001c0002t0001g0259 a0001c0002t0001g0260 a0001c0002t0001g0261 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+1566C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669762 | |||||||
| chr8:39669846 | T | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+1650T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669846 | |||||||
| chr8:39669885 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1525+1689A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39669885 | |||||||
| chr8:39670069 | T | C | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+1873T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670069 | |||||||
| chr8:39670132 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1525+1936C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670132 | |||||||
| chr8:39670205 | C | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | NA18944.hp2 NA19002.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+2009C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670205 | |||||||
| chr8:39670241 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1525+2045C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670241 | |||||||
| chr8:39670462 | A | G | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+2266A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670462 | |||||||
| chr8:39670495 | A | G | 1 | a0001c0012t0001g0007 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1525+2299A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670495 | |||||||
| chr8:39670693 | C | T | 13 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+2497C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39670693 | |||||||
| chr8:39671283 | A | G | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+3087A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671283 | |||||||
| chr8:39671750 | C | T | 1 | a0001c0002t0001g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1525+3554C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671750 | |||||||
| chr8:39671781 | A | C | 5 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0116 others(2): Show |
5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525+3585A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671781 | |||||||
| chr8:39671834 | A | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+3638A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671834 | |||||||
| chr8:39671886 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1525+3690G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671886 | |||||||
| chr8:39671931 | A | T | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525+3735A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671931 | |||||||
| chr8:39671977 | A | G | 95 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(92): Show |
98 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.1525+3781A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39671977 | |||||||
| chr8:39672081 | T | C | 152 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1525+3885T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672081 | |||||||
| chr8:39672101 | T | G | 152 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1525+3905T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672101 | |||||||
| chr8:39672432 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1525+4236G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672432 | |||||||
| chr8:39672485 | G | T | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525+4289G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672485 | |||||||
| chr8:39672583 | T | C | 7 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(4): Show |
7 | HG00733.hp1 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525+4387T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672583 | |||||||
| chr8:39672694 | T | C | 1 | a0001c0002t0001g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1525+4498T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672694 | |||||||
| chr8:39672726 | C | T | 1 | a0001c0002t0001g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1525+4530C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672726 | |||||||
| chr8:39672765 | A | C | 2 | a0001c0010t0001g0035 a0001c0010t0001g0043 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1525+4569A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672765 | |||||||
| chr8:39672891 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1526-4540G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39672891 | |||||||
| chr8:39673501 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0251 |
2 | NA18995.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1526-3930C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673501 | |||||||
| chr8:39673775 | C | T | 16 | a0001c0001t0001g0208 a0001c0001t0001g0266 a0001c0001t0001g0267 others(13): Show |
16 | HG00544.hp1 HG00597.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1526-3656C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673775 | |||||||
| chr8:39673928 | C | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1526-3503C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673928 | |||||||
| chr8:39673929 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1526-3502G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39673929 | |||||||
| chr8:39674032 | T | C | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1526-3399T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674032 | |||||||
| chr8:39674232 | T | C | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-3199T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674232 | |||||||
| chr8:39674256 | C | T | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1526-3175C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674256 | |||||||
| chr8:39674711 | T | A | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-2720T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674711 | |||||||
| chr8:39674712 | C | T | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-2719C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674712 | |||||||
| chr8:39674790 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1526-2641C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674790 | |||||||
| chr8:39674947 | T | G | 192 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(189): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1526-2484T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674947 | |||||||
| chr8:39674952 | C | A | 152 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1526-2479C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674952 | |||||||
| chr8:39674969 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1526-2462G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39674969 | |||||||
| chr8:39675009 | C | T | 1 | a0001c0008t0003g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1526-2422C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675009 | |||||||
| chr8:39675295 | A | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1526-2136A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675295 | |||||||
| chr8:39675420 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1526-2011T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675420 | |||||||
| chr8:39675437 | C | G | 5 | a0001c0002t0001g0113 a0001c0002t0001g0149 a0001c0002t0001g0151 others(2): Show |
5 | HG00280.hp1 HG01256.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1526-1994C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675437 | |||||||
| chr8:39675754 | T | C | 1 | a0004c0005t0001g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1526-1677T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675754 | |||||||
| chr8:39675782 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-1649A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675782 | |||||||
| chr8:39675852 | G | A | 1 | a0001c0002t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1526-1579G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39675852 | |||||||
| chr8:39676110 | C | T | 152 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1526-1321C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676110 | |||||||
| chr8:39676207 | G | A | 82 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(79): Show |
84 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1526-1224G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676207 | |||||||
| chr8:39676343 | C | T | 1 | a0004c0005t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1526-1088C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676343 | |||||||
| chr8:39676379 | G | A | 1 | a0004c0005t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1526-1052G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676379 | |||||||
| chr8:39676399 | C | T | 1 | a0013c0020t0001g0069 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1526-1032C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676399 | |||||||
| chr8:39676498 | G | T | 6 | a0001c0002t0001g0003 a0001c0002t0001g0102 a0001c0002t0001g0103 others(3): Show |
7 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1526-933G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676498 | |||||||
| chr8:39676583 | C | T | 1 | a0006c0006t0001g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1526-848C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676583 | |||||||
| chr8:39676610 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1526-821C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676610 | |||||||
| chr8:39676615 | C | T | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1526-816C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676615 | |||||||
| chr8:39676622 | C | T | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1526-809C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676622 | |||||||
| chr8:39676692 | C | T | 13 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0003c0004t0001g0181 others(10): Show |
13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1526-739C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676692 | |||||||
| chr8:39676767 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1526-664G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676767 | |||||||
| chr8:39676771 | A | G | 52 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(49): Show |
55 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1526-660A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676771 | |||||||
| chr8:39676918 | G | A | 8 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1526-513G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39676918 | |||||||
| chr8:39677141 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1526-290A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677141 | |||||||
| chr8:39677192 | A | G | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | NA18960.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1526-239A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677192 | |||||||
| chr8:39677200 | A | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-231A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677200 | |||||||
| chr8:39677239 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1526-192T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677239 | |||||||
| chr8:39677375 | C | G | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1526-56C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 14/19 | chr8 | 39677375 | |||||||
| chr8:39677543 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18965.hp2 | splice_region_variant&intron_variant | LOW | c.1631+7A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677543 | |||||||
| chr8:39677569 | T | G | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1631+33T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677569 | |||||||
| chr8:39677661 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1631+125A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677661 | |||||||
| chr8:39677709 | C | A | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1631+173C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677709 | |||||||
| chr8:39677762 | G | A | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631+226G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677762 | |||||||
| chr8:39677797 | T | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1631+261T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677797 | |||||||
| chr8:39677835 | G | A | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1631+299G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677835 | |||||||
| chr8:39677931 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1631+395T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39677931 | |||||||
| chr8:39678310 | T | C | 52 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(49): Show |
55 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1631+774T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678310 | |||||||
| chr8:39678467 | A | T | 33 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(30): Show |
33 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1631+931A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678467 | |||||||
| chr8:39678490 | A | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0287 |
3 | HG03041.hp2 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1631+954A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678490 | |||||||
| chr8:39678501 | A | C | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1631+965A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678501 | |||||||
| chr8:39678531 | C | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1631+995C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678531 | |||||||
| chr8:39678725 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1631+1189C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678725 | |||||||
| chr8:39678893 | G | C | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1632-1144G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39678893 | |||||||
| chr8:39679023 | G | C | 1 | a0001c0002t0001g0154 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1632-1014G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679023 | |||||||
| chr8:39679060 | G | T | 1 | a0006c0006t0001g0263 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1632-977G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679060 | |||||||
| chr8:39679209 | T | C | 1 | a0008c0023t0001g0016 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1632-828T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679209 | |||||||
| chr8:39679259 | T | C | 1 | a0001c0002t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1632-778T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679259 | |||||||
| chr8:39679765 | C | T | 153 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(150): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1632-272C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679765 | |||||||
| chr8:39679771 | A | C | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1632-266A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679771 | |||||||
| chr8:39679853 | T | A | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1632-184T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679853 | |||||||
| chr8:39679912 | C | T | 189 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(186): Show |
195 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1632-125C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 15/19 | chr8 | 39679912 | |||||||
| chr8:39680377 | C | G | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1821+151C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680377 | |||||||
| chr8:39680635 | A | T | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1821+409A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680635 | |||||||
| chr8:39680716 | C | T | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+490C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680716 | |||||||
| chr8:39680851 | C | CACTT | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+627_1821+630d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39680851 | ||||||
| chr8:39680882 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1821+656C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39680882 | |||||||
| chr8:39681220 | C | A | 13 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+994C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681220 | |||||||
| chr8:39681248 | G | T | 1 | a0001c0002t0001g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1821+1022G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681248 | |||||||
| chr8:39681281 | C | A | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1821+1055C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681281 | |||||||
| chr8:39681441 | G | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1821+1215G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681441 | |||||||
| chr8:39681552 | G | A | 1 | a0001c0002t0001g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1821+1326G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681552 | |||||||
| chr8:39681595 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1821+1369C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681595 | |||||||
| chr8:39681812 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1821+1586C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681812 | |||||||
| chr8:39681821 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1821+1595T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681821 | |||||||
| chr8:39681950 | A | G | 1 | a0004c0005t0001g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1821+1724A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39681950 | |||||||
| chr8:39682029 | G | C | 1 | a0001c0002t0001g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1821+1803G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682029 | |||||||
| chr8:39682191 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1821+1965C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682191 | |||||||
| chr8:39682268 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1821+2042C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682268 | |||||||
| chr8:39682269 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1821+2043G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682269 | |||||||
| chr8:39682370 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01168.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1821+2144G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682370 | |||||||
| chr8:39682397 | G | A | 69 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(66): Show |
72 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1821+2171G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682397 | |||||||
| chr8:39682430 | T | C | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+2204T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682430 | |||||||
| chr8:39682604 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1821+2378G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682604 | |||||||
| chr8:39682643 | C | A | 89 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(86): Show |
93 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1821+2417C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682643 | |||||||
| chr8:39682644 | C | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1821+2418C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39682644 | |||||||
| chr8:39683029 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1821+2803G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683029 | |||||||
| chr8:39683309 | G | A | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+3083G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683309 | |||||||
| chr8:39683396 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1821+3170C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683396 | |||||||
| chr8:39683932 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1821+3706T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39683932 | |||||||
| chr8:39684017 | C | T | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+3791C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684017 | |||||||
| chr8:39684058 | T | G | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1821+3832T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684058 | |||||||
| chr8:39684219 | T | C | 1 | a0001c0002t0001g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1821+3993T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684219 | |||||||
| chr8:39684249 | T | C | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+4023T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684249 | |||||||
| chr8:39684321 | G | A | 6 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(3): Show |
6 | HG01167.hp2 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+4095G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684321 | |||||||
| chr8:39684459 | C | T | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1821+4233C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684459 | |||||||
| chr8:39684497 | A | C | 1 | a0001c0002t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1821+4271A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684497 | |||||||
| chr8:39684572 | A | C | 1 | a0001c0002t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1821+4346A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684572 | |||||||
| chr8:39684883 | G | C | 1 | a0001c0002t0001g0004 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1821+4657G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684883 | |||||||
| chr8:39684978 | G | A | 1 | a0007c0009t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1821+4752G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39684978 | |||||||
| chr8:39685056 | T | C | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1821+4830T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685056 | |||||||
| chr8:39685155 | T | C | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821+4929T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685155 | |||||||
| chr8:39685318 | T | C | 315 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(312): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1821+5092T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685318 | |||||||
| chr8:39685474 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1821+5248G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685474 | |||||||
| chr8:39685506 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1821+5280C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685506 | |||||||
| chr8:39685545 | T | C | 5 | a0002c0003t0001g0022 a0002c0003t0001g0024 a0002c0003t0001g0025 others(2): Show |
5 | HG02074.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821+5319T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685545 | |||||||
| chr8:39685626 | G | A | 13 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(10): Show |
13 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821+5400G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685626 | |||||||
| chr8:39685939 | C | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(65): Show |
71 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1821+5713C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39685939 | |||||||
| chr8:39686006 | A | G | 1 | a0003c0004t0001g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1821+5780A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686006 | |||||||
| chr8:39686087 | C | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1821+5861C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686087 | |||||||
| chr8:39686116 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1821+5890G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686116 | |||||||
| chr8:39686164 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0196 |
2 | HG00438.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1821+5938C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686164 | |||||||
| chr8:39686242 | T | A | 13 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0003c0004t0001g0181 others(10): Show |
13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1821+6016T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686242 | |||||||
| chr8:39686307 | G | A | 1 | a0002c0003t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1821+6081G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686307 | |||||||
| chr8:39686316 | T | A | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1821+6090T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686316 | |||||||
| chr8:39686382 | G | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1821+6156G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686382 | |||||||
| chr8:39686446 | G | A | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1822-6154G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686446 | |||||||
| chr8:39686468 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0171 a0001c0001t0001g0180 others(1): Show |
4 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1822-6132A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686468 | |||||||
| chr8:39686580 | G | A | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1822-6020G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686580 | |||||||
| chr8:39686644 | C | A | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1822-5956C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686644 | |||||||
| chr8:39686662 | G | A | 1 | a0004c0019t0001g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1822-5938G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686662 | |||||||
| chr8:39686705 | G | A | 26 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0013 others(23): Show |
26 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1822-5895G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686705 | |||||||
| chr8:39686780 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1822-5820C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686780 | |||||||
| chr8:39686781 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1822-5819G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686781 | |||||||
| chr8:39686841 | T | A | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1822-5759T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39686841 | |||||||
| chr8:39687215 | A | G | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-5385A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687215 | |||||||
| chr8:39687569 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1822-5031G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687569 | |||||||
| chr8:39687597 | C | A | 1 | a0001c0001t0001g0289 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1822-5003C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687597 | |||||||
| chr8:39687599 | T | A | 1 | a0001c0002t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1822-5001T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687599 | |||||||
| chr8:39687646 | G | A | 152 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(149): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1822-4954G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687646 | |||||||
| chr8:39687714 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1822-4886A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687714 | |||||||
| chr8:39687716 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0240 |
2 | HG02027.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1822-4884G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687716 | |||||||
| chr8:39687841 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1822-4759G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687841 | |||||||
| chr8:39687908 | T | C | 29 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 others(26): Show |
29 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1822-4692T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39687908 | |||||||
| chr8:39688141 | A | G | 185 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(182): Show |
191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1822-4459A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688141 | |||||||
| chr8:39688186 | A | G | 14 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(11): Show |
14 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1822-4414A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688186 | |||||||
| chr8:39688317 | T | G | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1822-4283T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688317 | |||||||
| chr8:39688791 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1822-3809T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688791 | |||||||
| chr8:39688961 | C | T | 30 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 others(27): Show |
30 | HG00733.hp1 HG01167.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1822-3639C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688961 | |||||||
| chr8:39688993 | G | T | 1 | a0001c0002t0001g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1822-3607G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39688993 | |||||||
| chr8:39689283 | C | T | 6 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0001g0242 others(3): Show |
6 | HG01074.hp1 HG02148.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-3317C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689283 | |||||||
| chr8:39689284 | G | A | 53 | a0001c0001t0001g0202 a0001c0002t0001g0001 a0001c0002t0001g0002 others(50): Show |
56 | HG00099.hp1 HG00280.hp1 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.1822-3316G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689284 | |||||||
| chr8:39689469 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1822-3131G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689469 | |||||||
| chr8:39689692 | T | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1822-2908T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689692 | |||||||
| chr8:39689741 | G | A | 13 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1822-2859G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689741 | |||||||
| chr8:39689890 | C | T | 164 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(161): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1822-2710C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689890 | |||||||
| chr8:39689955 | C | T | 14 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(11): Show |
14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1822-2645C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689955 | |||||||
| chr8:39689973 | G | A | 100 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(97): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1822-2627G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39689973 | |||||||
| chr8:39690100 | G | T | 1 | a0001c0002t0001g0150 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1822-2500G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690100 | |||||||
| chr8:39690108 | G | A | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-2492G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690108 | |||||||
| chr8:39690123 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1822-2477C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690123 | |||||||
| chr8:39690258 | G | A | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-2342G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690258 | |||||||
| chr8:39690262 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1822-2338C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690262 | |||||||
| chr8:39690274 | G | T | 13 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1822-2326G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690274 | |||||||
| chr8:39690277 | C | A | 1 | a0001c0002t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1822-2323C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690277 | |||||||
| chr8:39690328 | G | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1822-2272G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690328 | |||||||
| chr8:39690414 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1822-2186G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690414 | |||||||
| chr8:39690460 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1822-2140G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690460 | |||||||
| chr8:39690528 | G | C | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1822-2072G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690528 | |||||||
| chr8:39690652 | C | T | 5 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0003c0004t0001g0181 others(2): Show |
5 | HG02723.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1822-1948C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690652 | |||||||
| chr8:39690839 | C | T | 145 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(142): Show |
146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1822-1761C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690839 | |||||||
| chr8:39690859 | C | T | 182 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(179): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.1822-1741C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690859 | |||||||
| chr8:39690867 | G | T | 2 | a0002c0003t0001g0013 a0014c0017t0001g0255 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1822-1733G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690867 | |||||||
| chr8:39690907 | A | G | 1 | a0001c0002t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1822-1693A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39690907 | |||||||
| chr8:39691128 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1822-1472G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691128 | |||||||
| chr8:39691340 | G | T | 175 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(172): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1822-1260G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691340 | |||||||
| chr8:39691567 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1822-1033A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691567 | |||||||
| chr8:39691734 | A | C | 2 | a0005c0011t0001g0190 a0005c0011t0001g0247 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1822-866A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39691734 | |||||||
| chr8:39691740 | TATC | T | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-857_1822-855d others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691740 | ||||||
| chr8:39691751 | CTTACTCA others(23): Show |
C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-847_1822-818d others(32): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691751 | ||||||
| chr8:39691884 | TA | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0001g0253 |
3 | HG02451.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822-713delA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691884 | ||||||
| chr8:39691909 | GAAGTAAT others(4): Show |
G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0001g0253 |
3 | HG02451.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822-687_1822-677d others(13): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691909 | ||||||
| chr8:39691996 | TAAAA | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-601_1822-598d others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr8 | 39691996 | ||||||
| chr8:39692000 | A | C | 1 | a0001c0002t0001g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1822-600A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692000 | |||||||
| chr8:39692260 | A | G | 2 | a0001c0002t0001g0057 a0001c0002t0001g0074 |
2 | NA18970.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1822-340A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692260 | |||||||
| chr8:39692295 | C | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | NA18960.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1822-305C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692295 | |||||||
| chr8:39692301 | G | A | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-299G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692301 | |||||||
| chr8:39692348 | A | G | 287 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(284): Show |
291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1822-252A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692348 | |||||||
| chr8:39692379 | T | A | 1 | a0001c0002t0001g0097 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1822-221T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 16/19 | chr8 | 39692379 | |||||||
| chr8:39692705 | G | T | 1 | a0001c0002t0001g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1902+25G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39692705 | |||||||
| chr8:39692737 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1902+57A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39692737 | |||||||
| chr8:39693178 | T | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0205 |
2 | NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1902+498T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693178 | |||||||
| chr8:39693210 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1902+530T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693210 | |||||||
| chr8:39693442 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1902+762T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693442 | |||||||
| chr8:39693446 | C | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0142 |
2 | HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1902+766C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693446 | |||||||
| chr8:39693524 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1902+844T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693524 | |||||||
| chr8:39693529 | C | T | 3 | a0001c0002t0001g0091 a0001c0002t0001g0127 a0001c0002t0001g0128 |
3 | HG00544.hp2 NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1902+849C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693529 | |||||||
| chr8:39693575 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+895A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693575 | |||||||
| chr8:39693632 | T | A | 144 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(141): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1902+952T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693632 | |||||||
| chr8:39693682 | A | C | 13 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0003c0004t0001g0181 others(10): Show |
13 | HG02257.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1902+1002A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693682 | |||||||
| chr8:39693700 | C | G | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1902+1020C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693700 | |||||||
| chr8:39693763 | A | C | 1 | a0001c0001t0001g0310 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1902+1083A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39693763 | |||||||
| chr8:39694113 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1902+1433T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694113 | |||||||
| chr8:39694487 | A | G | 162 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(159): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1902+1807A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694487 | |||||||
| chr8:39694854 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1902+2174C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694854 | |||||||
| chr8:39694855 | G | A | 7 | a0001c0001t0001g0295 a0001c0001t0001g0311 a0001c0001t0001g0320 others(4): Show |
7 | HG01106.hp1 HG01257.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1902+2175G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39694855 | |||||||
| chr8:39695013 | G | A | 1 | a0001c0002t0001g0283 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1902+2333G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695013 | |||||||
| chr8:39695086 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1902+2406T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695086 | |||||||
| chr8:39695333 | T | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1902+2653T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695333 | |||||||
| chr8:39695742 | T | C | 100 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(97): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+3062T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695742 | |||||||
| chr8:39695833 | C | T | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1902+3153C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39695833 | |||||||
| chr8:39696109 | T | C | 158 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(155): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1902+3429T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696109 | |||||||
| chr8:39696166 | C | A | 6 | a0001c0002t0001g0001 a0001c0002t0001g0053 a0001c0002t0001g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1902+3486C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696166 | |||||||
| chr8:39696169 | T | G | 29 | a0001c0001t0001g0170 a0001c0001t0001g0271 a0001c0001t0001g0289 others(26): Show |
29 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1902+3489T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696169 | |||||||
| chr8:39696248 | A | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+3568A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696248 | |||||||
| chr8:39696264 | A | G | 50 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(47): Show |
51 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1902+3584A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696264 | |||||||
| chr8:39696269 | T | A | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3589T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696269 | |||||||
| chr8:39696270 | ATATT | A | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3592_1902+359 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39696270 | ||||||
| chr8:39696277 | G | C | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3597G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696277 | |||||||
| chr8:39696278 | G | T | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3598G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696278 | |||||||
| chr8:39696280 | T | A | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3600T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696280 | |||||||
| chr8:39696284 | AATTCCTT others(29): Show |
A | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1902+3605_1902+364 others(40): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696284 | |||||||
| chr8:39696556 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1902+3876T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696556 | |||||||
| chr8:39696839 | G | T | 1 | a0014c0017t0001g0255 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1902+4159G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696839 | |||||||
| chr8:39696865 | T | C | 1 | a0001c0002t0001g0136 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1902+4185T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696865 | |||||||
| chr8:39696871 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1902+4191C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696871 | |||||||
| chr8:39696922 | T | A | 2 | a0001c0010t0001g0035 a0001c0010t0001g0043 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1902+4242T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39696922 | |||||||
| chr8:39697007 | G | A | 100 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(97): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+4327G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697007 | |||||||
| chr8:39697149 | A | G | 1 | a0003c0004t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1902+4469A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697149 | |||||||
| chr8:39697166 | C | T | 2 | a0001c0001t0001g0231 a0010c0013t0001g0162 |
2 | HG01884.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1902+4486C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697166 | |||||||
| chr8:39697167 | G | A | 1 | a0004c0005t0001g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1902+4487G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697167 | |||||||
| chr8:39697217 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1902+4537A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697217 | |||||||
| chr8:39697293 | G | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1902+4613G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697293 | |||||||
| chr8:39697532 | C | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0108 a0001c0002t0001g0109 |
3 | NA18971.hp2 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1902+4852C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697532 | |||||||
| chr8:39697617 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1902+4937C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697617 | |||||||
| chr8:39697904 | A | G | 1 | a0001c0002t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1902+5224A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39697904 | |||||||
| chr8:39698004 | C | A | 1 | a0001c0002t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1902+5324C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698004 | |||||||
| chr8:39698139 | G | A | 100 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(97): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+5459G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698139 | |||||||
| chr8:39698189 | C | T | 287 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(284): Show |
291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1902+5509C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698189 | |||||||
| chr8:39698230 | T | A | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1902+5550T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698230 | |||||||
| chr8:39698277 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0180 |
2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1902+5597T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698277 | |||||||
| chr8:39698290 | T | A | 100 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(97): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1902+5610T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698290 | |||||||
| chr8:39698347 | C | G | 1 | a0001c0002t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1902+5667C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698347 | |||||||
| chr8:39698365 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1902+5685G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698365 | |||||||
| chr8:39698472 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1902+5792A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698472 | |||||||
| chr8:39698563 | G | A | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1902+5883G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698563 | |||||||
| chr8:39698737 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1902+6057G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698737 | |||||||
| chr8:39698845 | T | G | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1902+6165T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698845 | |||||||
| chr8:39698867 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1902+6187C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39698867 | |||||||
| chr8:39699047 | A | G | 1 | a0013c0020t0001g0069 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1902+6367A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699047 | |||||||
| chr8:39699144 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1902+6464G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699144 | |||||||
| chr8:39699196 | A | G | 1 | a0003c0004t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1902+6516A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699196 | |||||||
| chr8:39699346 | G | T | 4 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(1): Show |
4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1902+6666G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699346 | |||||||
| chr8:39699454 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1902+6774G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699454 | |||||||
| chr8:39699532 | A | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0239 a0001c0001t0001g0278 |
3 | NA18612.hp2 NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1902+6852A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39699532 | |||||||
| chr8:39700126 | C | T | 100 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(97): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1903-6664C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700126 | |||||||
| chr8:39700202 | G | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6588G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700202 | |||||||
| chr8:39700272 | T | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6518T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700272 | |||||||
| chr8:39700350 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1903-6440T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700350 | |||||||
| chr8:39700446 | C | T | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6344C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700446 | |||||||
| chr8:39700449 | A | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6341A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700449 | |||||||
| chr8:39700459 | G | GA | 12 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(9): Show |
12 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1903-6325dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39700459 | ||||||
| chr8:39700470 | C | T | 1 | a0011c0024t0001g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1903-6320C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700470 | |||||||
| chr8:39700504 | G | A | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-6286G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700504 | |||||||
| chr8:39700581 | C | A | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1903-6209C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700581 | |||||||
| chr8:39700886 | G | A | 1 | a0002c0003t0001g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1903-5904G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700886 | |||||||
| chr8:39700887 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-5903G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39700887 | |||||||
| chr8:39701034 | C | T | 40 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(37): Show |
40 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1903-5756C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701034 | |||||||
| chr8:39701117 | C | CA | 71 | a0001c0001t0001g0087 a0001c0001t0001g0139 a0001c0001t0001g0161 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1903-5641dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAA | 31 | a0001c0001t0001g0086 a0001c0001t0001g0200 a0001c0001t0001g0201 others(28): Show |
31 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1903-5642_1903-564 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAA | 29 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(26): Show |
30 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1903-5643_1903-564 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAA | 39 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0001g0173 others(36): Show |
41 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1903-5644_1903-564 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAA | 33 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0171 others(30): Show |
33 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1903-5645_1903-564 others(9): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAA | 8 | a0001c0001t0001g0159 a0001c0001t0001g0169 a0001c0002t0001g0094 others(5): Show |
8 | HG01943.hp2 HG02148.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.1903-5646_1903-564 others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(3): Show |
2 | a0001c0002t0001g0118 a0001c0002t0001g0259 |
2 | HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1903-5650_1903-564 others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0001g0045 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1903-5653_1903-564 others(17): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0032 a0001c0002t0001g0048 |
2 | HG02004.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1903-5654_1903-564 others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(8): Show |
10 | a0001c0002t0001g0028 a0001c0002t0001g0033 a0001c0002t0001g0034 others(7): Show |
10 | HG01081.hp1 HG01952.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1903-5655_1903-564 others(19): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(9): Show |
3 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0038 |
3 | HG00642.hp2 HG01099.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1903-5656_1903-564 others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(11): Show |
3 | a0001c0002t0001g0011 a0001c0002t0001g0077 a0005c0011t0001g0190 |
3 | HG01099.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1903-5658_1903-564 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(12): Show |
7 | a0001c0002t0001g0012 a0001c0002t0001g0085 a0001c0002t0001g0115 others(4): Show |
7 | HG00323.hp1 HG01993.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903-5659_1903-564 others(23): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(13): Show |
3 | a0001c0002t0001g0114 a0001c0002t0001g0116 a0001c0002t0001g0261 |
3 | HG02300.hp1 NA18954.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1903-5660_1903-564 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(14): Show |
5 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0117 others(2): Show |
5 | HG01109.hp2 HG01255.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-5661_1903-564 others(25): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1903-5666_1903-564 others(30): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | C | CAAAAAAA others(32): Show |
1 | a0005c0011t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1903-5641_1903-564 others(43): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | CAAAAAAA others(1): Show |
C | 5 | a0001c0002t0001g0006 a0001c0002t0001g0104 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903-5648_1903-564 others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1903-5650_1903-564 others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0001g0158 a0010c0013t0001g0162 |
2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1903-5651_1903-564 others(15): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701117 | CAAAAAAA others(6): Show |
C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-5653_1903-564 others(17): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39701117 | ||||||
| chr8:39701143 | A | AG | 7 | a0002c0003t0001g0013 a0002c0003t0001g0018 a0002c0003t0001g0019 others(4): Show |
7 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-5647_1903-564 others(5): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701143 | |||||||
| chr8:39701143 | A | G | 7 | a0002c0003t0001g0017 a0002c0003t0001g0022 a0002c0003t0001g0023 others(4): Show |
7 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903-5647A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701143 | |||||||
| chr8:39701263 | C | G | 6 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1903-5527C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701263 | |||||||
| chr8:39701356 | C | T | 14 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0165 others(11): Show |
15 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1903-5434C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701356 | |||||||
| chr8:39701374 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1903-5416G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701374 | |||||||
| chr8:39701505 | G | T | 1 | a0001c0002t0001g0261 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1903-5285G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701505 | |||||||
| chr8:39701620 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1903-5170C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701620 | |||||||
| chr8:39701871 | G | A | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1903-4919G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701871 | |||||||
| chr8:39701910 | C | T | 4 | a0001c0001t0001g0210 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG02074.hp2 NA18949.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903-4880C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39701910 | |||||||
| chr8:39702130 | C | G | 2 | a0007c0009t0001g0111 a0007c0009t0001g0155 |
2 | NA19074.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1903-4660C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702130 | |||||||
| chr8:39702173 | C | T | 14 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0165 others(11): Show |
15 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1903-4617C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702173 | |||||||
| chr8:39702216 | G | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1903-4574G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702216 | |||||||
| chr8:39702337 | G | T | 1 | a0001c0001t0001g0322 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1903-4453G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702337 | |||||||
| chr8:39702345 | T | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1903-4445T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702345 | |||||||
| chr8:39702448 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-4342C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702448 | |||||||
| chr8:39702557 | C | T | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903-4233C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702557 | |||||||
| chr8:39702605 | T | C | 5 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0116 others(2): Show |
5 | NA18948.hp2 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-4185T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702605 | |||||||
| chr8:39702664 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-4126G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702664 | |||||||
| chr8:39702746 | C | T | 112 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(109): Show |
115 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.1903-4044C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702746 | |||||||
| chr8:39702780 | G | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0333 |
2 | NA18957.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1903-4010G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39702780 | |||||||
| chr8:39703110 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1903-3680C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703110 | |||||||
| chr8:39703273 | T | C | 1 | a0003c0004t0001g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1903-3517T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703273 | |||||||
| chr8:39703430 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1903-3360C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703430 | |||||||
| chr8:39703552 | T | A | 3 | a0001c0002t0001g0257 a0001c0008t0003g0014 a0001c0008t0003g0015 |
3 | HG02055.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1903-3238T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703552 | |||||||
| chr8:39703556 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1903-3234G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703556 | |||||||
| chr8:39703593 | G | A | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1903-3197G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703593 | |||||||
| chr8:39703914 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1903-2876A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39703914 | |||||||
| chr8:39704077 | A | G | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1903-2713A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704077 | |||||||
| chr8:39704119 | T | C | 1 | a0001c0002t0001g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1903-2671T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704119 | |||||||
| chr8:39704326 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-2464G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704326 | |||||||
| chr8:39704360 | A | G | 6 | a0001c0002t0001g0089 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00609.hp2 NA18950.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903-2430A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704360 | |||||||
| chr8:39704387 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1903-2403T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704387 | |||||||
| chr8:39704528 | C | T | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1903-2262C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704528 | |||||||
| chr8:39704537 | T | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 |
3 | HG00639.hp2 HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1903-2253T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704537 | |||||||
| chr8:39704975 | T | A | 175 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(172): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1903-1815T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39704975 | |||||||
| chr8:39705071 | T | C | 101 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(98): Show |
103 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1903-1719T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705071 | |||||||
| chr8:39705185 | A | C | 4 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(1): Show |
4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903-1605A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705185 | |||||||
| chr8:39705247 | T | A | 1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1903-1543T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705247 | |||||||
| chr8:39705271 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1903-1519C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705271 | |||||||
| chr8:39705506 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1903-1284C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705506 | |||||||
| chr8:39705653 | C | T | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1903-1137C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705653 | |||||||
| chr8:39705778 | G | A | 158 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(155): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1903-1012G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39705778 | |||||||
| chr8:39706319 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1903-471A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39706319 | |||||||
| chr8:39706632 | C | T | 287 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(284): Show |
291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1903-158C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | chr8 | 39706632 | |||||||
| chr8:39706714 | ATATCAGA others(13): Show |
A | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1903-59_1903-40del others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr8 | 39706714 | ||||||
| chr8:39706905 | G | T | 1 | a0001c0001t0001g0312 | 1 | HG02080.hp1 | splice_donor_variant&intron_variant | HIGH | c.2017+1G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39706905 | |||||||
| chr8:39706996 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2017+92A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39706996 | |||||||
| chr8:39707036 | A | G | 2 | a0001c0010t0001g0035 a0001c0010t0001g0043 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2017+132A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707036 | |||||||
| chr8:39707072 | T | C | 1 | a0001c0002t0001g0128 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2017+168T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707072 | |||||||
| chr8:39707222 | T | C | 83 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(80): Show |
85 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2017+318T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707222 | |||||||
| chr8:39707568 | C | G | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2017+664C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707568 | |||||||
| chr8:39707769 | A | G | 1 | a0001c0002t0001g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2017+865A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707769 | |||||||
| chr8:39707929 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2017+1025A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707929 | |||||||
| chr8:39707964 | G | C | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+1060G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39707964 | |||||||
| chr8:39708008 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2017+1104C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708008 | |||||||
| chr8:39708029 | C | A | 1 | a0001c0001t0001g0308 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2017+1125C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708029 | |||||||
| chr8:39708069 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2017+1165G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708069 | |||||||
| chr8:39708217 | G | A | 1 | a0001c0002t0001g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2017+1313G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708217 | |||||||
| chr8:39708312 | A | G | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+1408A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708312 | |||||||
| chr8:39708354 | T | G | 3 | a0003c0004t0001g0181 a0003c0004t0001g0215 a0003c0004t0001g0216 |
3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2017+1450T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708354 | |||||||
| chr8:39708377 | T | G | 2 | a0001c0010t0001g0035 a0001c0010t0001g0043 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2017+1473T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708377 | |||||||
| chr8:39708661 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2017+1757G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708661 | |||||||
| chr8:39708671 | C | A | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+1767C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708671 | |||||||
| chr8:39708701 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2017+1797G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708701 | |||||||
| chr8:39708749 | G | T | 1 | a0001c0002t0001g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2017+1845G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708749 | |||||||
| chr8:39708901 | C | G | 297 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(294): Show |
302 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.2017+1997C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708901 | |||||||
| chr8:39708916 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2017+2012G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39708916 | |||||||
| chr8:39709068 | T | C | 183 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(180): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2017+2164T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709068 | |||||||
| chr8:39709106 | TG | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0322 a0001c0001t0001g0335 others(3): Show |
6 | HG00438.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+2204delG | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39709106 | ||||||
| chr8:39709120 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2017+2216A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709120 | |||||||
| chr8:39709135 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2017+2231G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709135 | |||||||
| chr8:39709205 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2017+2301C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709205 | |||||||
| chr8:39709524 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0196 a0001c0001t0001g0228 |
3 | HG00438.hp1 HG00621.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2017+2620G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709524 | |||||||
| chr8:39709641 | G | A | 286 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(283): Show |
290 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.2017+2737G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709641 | |||||||
| chr8:39709748 | T | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+2844T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709748 | |||||||
| chr8:39709814 | T | C | 87 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(84): Show |
88 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2017+2910T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709814 | |||||||
| chr8:39709838 | A | G | 3 | a0006c0006t0001g0262 a0006c0006t0001g0263 a0006c0006t0001g0264 |
3 | HG02717.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2017+2934A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39709838 | |||||||
| chr8:39710113 | G | A | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+3209G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710113 | |||||||
| chr8:39710189 | G | C | 1 | a0003c0004t0001g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2017+3285G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710189 | |||||||
| chr8:39710214 | G | A | 1 | a0001c0012t0001g0007 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2017+3310G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710214 | |||||||
| chr8:39710262 | G | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+3358G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710262 | |||||||
| chr8:39710270 | C | T | 1 | a0001c0002t0001g0101 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2017+3366C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710270 | |||||||
| chr8:39710299 | A | C | 14 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(11): Show |
14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017+3395A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710299 | |||||||
| chr8:39710503 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+3599T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710503 | |||||||
| chr8:39710808 | T | C | 1 | a0001c0002t0001g0004 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2017+3904T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710808 | |||||||
| chr8:39710863 | A | G | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2017+3959A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39710863 | |||||||
| chr8:39711677 | T | A | 4 | a0001c0002t0001g0049 a0001c0002t0001g0104 a0001c0002t0001g0285 others(1): Show |
4 | HG02145.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+4773T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711677 | |||||||
| chr8:39711925 | C | T | 1 | a0001c0002t0001g0094 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2017+5021C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711925 | |||||||
| chr8:39711958 | C | T | 14 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(11): Show |
14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017+5054C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711958 | |||||||
| chr8:39711959 | G | A | 1 | a0003c0004t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2017+5055G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39711959 | |||||||
| chr8:39712003 | T | G | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2017+5099T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712003 | |||||||
| chr8:39712008 | A | C | 1 | a0001c0002t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2017+5104A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712008 | |||||||
| chr8:39712032 | G | GC | 159 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(156): Show |
160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.2017+5137dupC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39712032 | ||||||
| chr8:39712147 | C | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+5243C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712147 | |||||||
| chr8:39712158 | A | C | 1 | a0001c0002t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2017+5254A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712158 | |||||||
| chr8:39712252 | C | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2017+5348C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712252 | |||||||
| chr8:39712382 | CAAGAT | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+5482_2017+548 others(9): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39712382 | ||||||
| chr8:39712431 | A | G | 1 | a0001c0001t0001g0322 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2017+5527A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712431 | |||||||
| chr8:39712715 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2017+5811A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712715 | |||||||
| chr8:39712737 | G | A | 1 | a0003c0004t0001g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2017+5833G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712737 | |||||||
| chr8:39712750 | G | T | 288 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(285): Show |
292 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.2017+5846G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712750 | |||||||
| chr8:39712823 | A | G | 175 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(172): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2017+5919A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712823 | |||||||
| chr8:39712912 | G | C | 101 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(98): Show |
103 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.2017+6008G>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39712912 | |||||||
| chr8:39713012 | A | G | 1 | a0002c0003t0001g0023 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2017+6108A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713012 | |||||||
| chr8:39713360 | C | T | 175 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(172): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2017+6456C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713360 | |||||||
| chr8:39713567 | C | A | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2017+6663C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713567 | |||||||
| chr8:39713682 | A | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG00609.hp1 HG02523.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017+6778A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713682 | |||||||
| chr8:39713766 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2017+6862G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713766 | |||||||
| chr8:39713767 | C | CA | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017+6865dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39713767 | ||||||
| chr8:39713767 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2017+6863C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713767 | |||||||
| chr8:39713774 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2017+6870T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713774 | |||||||
| chr8:39713819 | A | C | 1 | a0003c0004t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2017+6915A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713819 | |||||||
| chr8:39713841 | G | A | 14 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(11): Show |
14 | HG00733.hp1 HG01167.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017+6937G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713841 | |||||||
| chr8:39713860 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+6956A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39713860 | |||||||
| chr8:39714076 | G | A | 77 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(74): Show |
79 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.2017+7172G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714076 | |||||||
| chr8:39714090 | C | T | 175 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(172): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2017+7186C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714090 | |||||||
| chr8:39714219 | C | T | 3 | a0001c0002t0001g0104 a0001c0002t0001g0285 a0001c0002t0001g0286 |
3 | HG02145.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2017+7315C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714219 | |||||||
| chr8:39714370 | A | G | 183 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(180): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2017+7466A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714370 | |||||||
| chr8:39714475 | A | G | 3 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0287 |
3 | HG03041.hp2 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2017+7571A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714475 | |||||||
| chr8:39714710 | A | T | 1 | a0004c0005t0001g0307 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2017+7806A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714710 | |||||||
| chr8:39714930 | G | A | 145 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(142): Show |
146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2017+8026G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39714930 | |||||||
| chr8:39715230 | T | C | 289 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(286): Show |
293 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2017+8326T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715230 | |||||||
| chr8:39715357 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2018-8391C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715357 | |||||||
| chr8:39715358 | G | A | 8 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2018-8390G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715358 | |||||||
| chr8:39715389 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2018-8359T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715389 | |||||||
| chr8:39715474 | G | GA | 174 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(171): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2018-8264dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39715474 | ||||||
| chr8:39715549 | C | A | 173 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(170): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.2018-8199C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715549 | |||||||
| chr8:39715579 | A | G | 1 | a0001c0002t0001g0097 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2018-8169A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715579 | |||||||
| chr8:39715716 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2018-8032C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715716 | |||||||
| chr8:39715887 | C | T | 7 | a0001c0001t0001g0296 a0001c0001t0001g0299 a0001c0001t0001g0301 others(4): Show |
7 | HG00609.hp1 HG02523.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018-7861C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715887 | |||||||
| chr8:39715904 | G | A | 5 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-7844G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715904 | |||||||
| chr8:39715955 | C | T | 2 | a0004c0005t0001g0318 a0004c0019t0001g0080 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2018-7793C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715955 | |||||||
| chr8:39715956 | G | A | 145 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(142): Show |
146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2018-7792G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39715956 | |||||||
| chr8:39716006 | C | G | 161 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(158): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2018-7742C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716006 | |||||||
| chr8:39716086 | C | T | 1 | a0001c0002t0001g0145 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2018-7662C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716086 | |||||||
| chr8:39716105 | G | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0239 a0001c0001t0001g0278 |
3 | NA18612.hp2 NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2018-7643G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716105 | |||||||
| chr8:39716161 | TTTTG | T | 175 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(172): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2018-7575_2018-757 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39716161 | ||||||
| chr8:39716270 | T | C | 1 | a0001c0002t0001g0004 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2018-7478T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716270 | |||||||
| chr8:39716302 | C | A | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2018-7446C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716302 | |||||||
| chr8:39716377 | C | T | 8 | a0003c0004t0001g0212 a0003c0004t0001g0214 a0003c0004t0001g0217 others(5): Show |
8 | HG01192.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2018-7371C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716377 | |||||||
| chr8:39716535 | A | T | 289 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(286): Show |
293 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2018-7213A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716535 | |||||||
| chr8:39716541 | C | G | 173 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(170): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.2018-7207C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716541 | |||||||
| chr8:39716662 | C | A | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2018-7086C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716662 | |||||||
| chr8:39716848 | T | A | 1 | a0001c0001t0001g0301 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2018-6900T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716848 | |||||||
| chr8:39716989 | G | A | 3 | a0003c0004t0001g0181 a0003c0004t0001g0215 a0003c0004t0001g0216 |
3 | HG02723.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2018-6759G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716989 | |||||||
| chr8:39716997 | A | G | 3 | a0001c0002t0001g0104 a0001c0002t0001g0285 a0001c0002t0001g0286 |
3 | HG02145.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2018-6751A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39716997 | |||||||
| chr8:39717125 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2018-6623G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717125 | |||||||
| chr8:39717203 | A | G | 1 | a0009c0021t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2018-6545A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717203 | |||||||
| chr8:39717299 | T | TTTAG | 285 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(282): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.2018-6446_2018-644 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39717299 | ||||||
| chr8:39717401 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2018-6347T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717401 | |||||||
| chr8:39717419 | C | G | 1 | a0001c0002t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2018-6329C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717419 | |||||||
| chr8:39717514 | C | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0246 |
3 | HG01243.hp2 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2018-6234C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717514 | |||||||
| chr8:39717609 | A | C | 7 | a0001c0002t0001g0290 a0004c0005t0001g0288 a0004c0005t0001g0292 others(4): Show |
7 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2018-6139A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717609 | |||||||
| chr8:39717674 | A | G | 1 | a0002c0003t0001g0013 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2018-6074A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717674 | |||||||
| chr8:39717720 | A | G | 6 | a0001c0002t0001g0118 a0001c0002t0001g0259 a0001c0002t0001g0260 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-6028A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717720 | |||||||
| chr8:39717805 | G | A | 272 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(269): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.2018-5943G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717805 | |||||||
| chr8:39717825 | A | C | 15 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0020 others(12): Show |
15 | HG01192.hp2 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2018-5923A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39717825 | |||||||
| chr8:39718042 | A | T | 1 | a0001c0002t0001g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2018-5706A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718042 | |||||||
| chr8:39718079 | A | C | 1 | a0005c0011t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2018-5669A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718079 | |||||||
| chr8:39718137 | C | G | 3 | a0001c0002t0001g0104 a0001c0002t0001g0285 a0001c0002t0001g0286 |
3 | HG02145.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2018-5611C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718137 | |||||||
| chr8:39718196 | C | G | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2018-5552C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718196 | |||||||
| chr8:39718334 | G | A | 290 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(287): Show |
294 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2018-5414G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718334 | |||||||
| chr8:39718529 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2018-5219A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39718529 | |||||||
| chr8:39718761 | A | AAAATACT others(13): Show |
89 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(86): Show |
91 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2018-4985_2018-496 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39718761 | ||||||
| chr8:39718761 | A | AATTT | 3 | a0001c0001t0001g0203 a0001c0001t0001g0302 a0002c0003t0001g0018 |
3 | HG02886.hp1 NA18969.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2018-4986_2018-498 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39718761 | ||||||
| chr8:39719070 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2018-4678C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719070 | |||||||
| chr8:39719324 | T | C | 9 | a0004c0005t0001g0288 a0004c0005t0001g0292 a0004c0005t0001g0307 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2018-4424T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719324 | |||||||
| chr8:39719351 | G | T | 172 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0171 others(169): Show |
176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2018-4397G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719351 | |||||||
| chr8:39719408 | C | T | 4 | a0001c0002t0001g0036 a0001c0002t0001g0050 a0001c0002t0001g0051 others(1): Show |
4 | NA18955.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-4340C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719408 | |||||||
| chr8:39719443 | C | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2018-4305C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719443 | |||||||
| chr8:39719533 | C | A | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2018-4215C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719533 | |||||||
| chr8:39719561 | A | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-4187A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719561 | |||||||
| chr8:39719784 | A | G | 316 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(313): Show |
322 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.2018-3964A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719784 | |||||||
| chr8:39719920 | A | G | 1 | a0001c0002t0001g0004 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2018-3828A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39719920 | |||||||
| chr8:39720070 | AGAT | A | 97 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(94): Show |
100 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2018-3673_2018-367 others(7): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39720070 | ||||||
| chr8:39720296 | G | A | 1 | a0003c0004t0001g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2018-3452G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720296 | |||||||
| chr8:39720323 | G | A | 9 | a0004c0005t0001g0288 a0004c0005t0001g0292 a0004c0005t0001g0307 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2018-3425G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720323 | |||||||
| chr8:39720395 | G | A | 2 | a0001c0008t0003g0014 a0001c0008t0003g0015 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2018-3353G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720395 | |||||||
| chr8:39720444 | T | G | 172 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0171 others(169): Show |
176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2018-3304T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720444 | |||||||
| chr8:39720660 | G | A | 93 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(90): Show |
95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2018-3088G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720660 | |||||||
| chr8:39720780 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2018-2968G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720780 | |||||||
| chr8:39720844 | A | C | 143 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(140): Show |
145 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.2018-2904A>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720844 | |||||||
| chr8:39720855 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2018-2893T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39720855 | |||||||
| chr8:39721000 | C | A | 1 | a0001c0012t0001g0007 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2018-2748C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721000 | |||||||
| chr8:39721062 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2018-2686G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721062 | |||||||
| chr8:39721241 | G | GT | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-2506dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39721241 | ||||||
| chr8:39721272 | A | T | 4 | a0001c0002t0001g0036 a0001c0002t0001g0050 a0001c0002t0001g0051 others(1): Show |
4 | NA18955.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-2476A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721272 | |||||||
| chr8:39721293 | A | G | 4 | a0001c0010t0001g0035 a0001c0010t0001g0043 a0002c0003t0001g0021 others(1): Show |
4 | HG02109.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-2455A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721293 | |||||||
| chr8:39721312 | G | A | 218 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(215): Show |
221 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.2018-2436G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721312 | |||||||
| chr8:39721558 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2018-2190C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721558 | |||||||
| chr8:39721657 | G | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | NA18957.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2018-2091G>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721657 | |||||||
| chr8:39721660 | A | G | 5 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(2): Show |
5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-2088A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721660 | |||||||
| chr8:39721670 | T | C | 1 | a0001c0002t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2018-2078T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721670 | |||||||
| chr8:39721723 | G | A | 152 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(149): Show |
154 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.2018-2025G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39721723 | |||||||
| chr8:39722098 | G | A | 109 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(106): Show |
110 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2018-1650G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722098 | |||||||
| chr8:39722190 | C | CGT | 6 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG01261.hp2 HG02602.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.2018-1531_2018-153 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722190 | ||||||
| chr8:39722190 | C | CGTGT | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0186 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1533_2018-153 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722190 | ||||||
| chr8:39722207 | GTGTGTGT others(5): Show |
G | 3 | a0004c0005t0001g0314 a0004c0022t0001g0194 a0011c0024t0001g0213 |
3 | HG02055.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2018-1539_2018-152 others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722207 | ||||||
| chr8:39722207 | GTGTGTGT others(9): Show |
G | 1 | a0004c0005t0001g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2018-1539_2018-152 others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722207 | ||||||
| chr8:39722209 | G | A | 1 | a0004c0005t0001g0307 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018-1539G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722209 | |||||||
| chr8:39722211 | G | A | 1 | a0004c0005t0001g0307 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018-1537G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722211 | |||||||
| chr8:39722212 | T | C | 1 | a0004c0005t0001g0307 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2018-1536T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722212 | |||||||
| chr8:39722213 | G | A | 3 | a0004c0005t0001g0288 a0004c0005t0001g0307 a0004c0019t0001g0080 |
3 | HG02280.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2018-1535G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722213 | |||||||
| chr8:39722213 | GTGTGTAT others(11): Show |
G | 1 | a0001c0002t0001g0006 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2018-1533_2018-151 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722213 | ||||||
| chr8:39722213 | GTGTGTAT others(13): Show |
G | 3 | a0001c0002t0001g0004 a0001c0002t0001g0163 a0001c0014t0001g0219 |
4 | HG02258.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-1533_2018-151 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722213 | ||||||
| chr8:39722213 | GTGTGTAT others(15): Show |
G | 6 | a0001c0002t0001g0160 a0002c0003t0001g0017 a0002c0003t0001g0018 others(3): Show |
6 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-1533_2018-151 others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722213 | ||||||
| chr8:39722215 | G | A | 5 | a0004c0005t0001g0288 a0004c0005t0001g0292 a0004c0005t0001g0307 others(2): Show |
5 | HG01167.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1533G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722215 | |||||||
| chr8:39722215 | GTGTATAT others(11): Show |
G | 1 | a0001c0002t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2018-1531_2018-151 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722215 | ||||||
| chr8:39722215 | GTGTATAT others(15): Show |
G | 5 | a0001c0002t0001g0118 a0001c0002t0001g0259 a0001c0002t0001g0260 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1531_2018-151 others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722215 | ||||||
| chr8:39722216 | T | C | 2 | a0004c0005t0001g0288 a0004c0019t0001g0080 |
2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2018-1532T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722216 | |||||||
| chr8:39722217 | G | A | 6 | a0001c0002t0001g0072 a0004c0005t0001g0288 a0004c0005t0001g0292 others(3): Show |
6 | HG01167.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-1531G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722217 | |||||||
| chr8:39722217 | G | GTA | 2 | a0001c0002t0001g0005 a0001c0002t0001g0108 |
3 | HG03490.hp1 HG03492.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2018-1487_2018-148 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTA | G | 18 | a0001c0001t0001g0139 a0001c0001t0001g0169 a0001c0001t0001g0184 others(15): Show |
18 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2018-1487_2018-148 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATA | G | 25 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0174 others(22): Show |
25 | HG00609.hp1 HG00673.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.2018-1489_2018-148 others(8): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATA | G | 25 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0199 others(22): Show |
26 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2018-1491_2018-148 others(10): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(1): Show |
G | 14 | a0001c0001t0001g0159 a0001c0001t0001g0187 a0001c0001t0001g0236 others(11): Show |
14 | HG00280.hp2 HG01168.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.2018-1493_2018-148 others(12): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(3): Show |
G | 15 | a0001c0001t0001g0189 a0001c0001t0001g0193 a0001c0001t0001g0220 others(12): Show |
15 | HG00544.hp1 HG01192.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2018-1495_2018-148 others(14): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(5): Show |
G | 33 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0171 others(30): Show |
33 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.2018-1497_2018-148 others(16): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(7): Show |
G | 11 | a0001c0001t0001g0207 a0001c0001t0001g0340 a0001c0002t0001g0058 others(8): Show |
11 | HG02109.hp2 HG02615.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2018-1499_2018-148 others(18): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(9): Show |
G | 21 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(18): Show |
23 | HG00621.hp1 HG01884.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-1501_2018-148 others(20): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(11): Show |
G | 5 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0008t0003g0014 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2018-1503_2018-148 others(22): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(13): Show |
G | 13 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0032 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.2018-1505_2018-148 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(15): Show |
G | 5 | a0001c0001t0001g0319 a0001c0002t0001g0028 a0001c0002t0001g0082 others(2): Show |
5 | HG01106.hp2 HG01109.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1507_2018-148 others(26): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722217 | GTATATAT others(17): Show |
G | 82 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(79): Show |
83 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2018-1509_2018-148 others(28): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722217 | ||||||
| chr8:39722218 | T | C | 2 | a0004c0005t0001g0292 a0008c0023t0001g0016 |
2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2018-1530T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722218 | |||||||
| chr8:39722219 | A | G | 26 | a0001c0001t0001g0175 a0001c0001t0001g0183 a0001c0001t0001g0185 others(23): Show |
26 | HG00438.hp1 HG01074.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.2018-1529A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722219 | |||||||
| chr8:39722221 | A | G | 35 | a0001c0001t0001g0139 a0001c0001t0001g0169 a0001c0001t0001g0175 others(32): Show |
35 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018-1527A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722221 | |||||||
| chr8:39722223 | A | G | 40 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0169 others(37): Show |
40 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2018-1525A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722223 | |||||||
| chr8:39722224 | T | C | 3 | a0004c0005t0001g0314 a0004c0022t0001g0194 a0011c0024t0001g0213 |
3 | HG02055.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2018-1524T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722224 | |||||||
| chr8:39722225 | A | G | 51 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0167 others(48): Show |
52 | HG00609.hp1 HG00673.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.2018-1523A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722225 | |||||||
| chr8:39722227 | A | G | 43 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0170 others(40): Show |
44 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.2018-1521A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722227 | |||||||
| chr8:39722228 | T | C | 1 | a0004c0005t0001g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2018-1520T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722228 | |||||||
| chr8:39722229 | A | G | 38 | a0001c0001t0001g0159 a0001c0001t0001g0170 a0001c0001t0001g0174 others(35): Show |
39 | HG00280.hp2 HG00544.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.2018-1519A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722229 | |||||||
| chr8:39722231 | A | G | 50 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0166 others(47): Show |
50 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2018-1517A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722231 | |||||||
| chr8:39722233 | A | G | 45 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0171 others(42): Show |
45 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2018-1515A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722233 | |||||||
| chr8:39722235 | A | G | 32 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(29): Show |
34 | HG00621.hp1 HG01884.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.2018-1513A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722235 | |||||||
| chr8:39722237 | A | G | 25 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(22): Show |
27 | HG00621.hp1 HG02040.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2018-1511A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722237 | |||||||
| chr8:39722239 | A | G | 36 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(33): Show |
37 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2018-1509A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722239 | |||||||
| chr8:39722241 | A | G | 34 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(31): Show |
35 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018-1507A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722241 | |||||||
| chr8:39722243 | A | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0328 a0001c0002t0001g0028 others(1): Show |
4 | HG02165.hp2 HG02602.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-1505A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722243 | |||||||
| chr8:39722315 | T | TTA | 34 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(31): Show |
35 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018-1423_2018-142 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39722315 | ||||||
| chr8:39722402 | C | T | 1 | a0003c0004t0001g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2018-1346C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722402 | |||||||
| chr8:39722566 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2018-1182A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722566 | |||||||
| chr8:39722627 | C | A | 1 | a0002c0003t0001g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2018-1121C>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722627 | |||||||
| chr8:39722666 | T | C | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2018-1082T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722666 | |||||||
| chr8:39722692 | A | G | 1 | a0001c0012t0001g0007 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2018-1056A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722692 | |||||||
| chr8:39722752 | G | A | 1 | a0001c0002t0001g0261 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2018-996G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722752 | |||||||
| chr8:39722841 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2018-907C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39722841 | |||||||
| chr8:39723002 | G | GA | 315 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(312): Show |
321 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.2018-744dupA | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr8 | 39723002 | ||||||
| chr8:39723085 | A | G | 1 | a0003c0004t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2018-663A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723085 | |||||||
| chr8:39723143 | A | G | 59 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0171 others(56): Show |
60 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2018-605A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723143 | |||||||
| chr8:39723179 | AC | A | 107 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(104): Show |
108 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2018-568delC | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723179 | |||||||
| chr8:39723284 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2018-464C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723284 | |||||||
| chr8:39723485 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-263T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 18/19 | chr8 | 39723485 | |||||||
| chr8:39723993 | T | C | 5 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(2): Show |
5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2177+86T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39723993 | |||||||
| chr8:39724210 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2177+303A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724210 | |||||||
| chr8:39724258 | C | G | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2177+351C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724258 | |||||||
| chr8:39724258 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2177+351C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724258 | |||||||
| chr8:39724335 | G | A | 5 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(2): Show |
5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2177+428G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724335 | |||||||
| chr8:39724415 | T | C | 1 | a0001c0002t0001g0045 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2177+508T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724415 | |||||||
| chr8:39724645 | A | G | 2 | a0001c0001t0001g0334 a0004c0005t0001g0307 |
2 | HG01943.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2177+738A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724645 | |||||||
| chr8:39724676 | T | C | 315 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(312): Show |
321 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.2177+769T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724676 | |||||||
| chr8:39724700 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2177+793G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724700 | |||||||
| chr8:39724847 | A | G | 93 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(90): Show |
95 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2177+940A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724847 | |||||||
| chr8:39724950 | A | AT | 314 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(311): Show |
320 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.2177+1049dupT | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39724950 | ||||||
| chr8:39724957 | A | T | 1 | a0001c0002t0001g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2177+1050A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39724957 | |||||||
| chr8:39725177 | C | T | 6 | a0001c0002t0001g0047 a0001c0002t0001g0104 a0001c0002t0001g0285 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2177+1270C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725177 | |||||||
| chr8:39725202 | C | T | 58 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(55): Show |
59 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.2177+1295C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725202 | |||||||
| chr8:39725325 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2177+1418T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725325 | |||||||
| chr8:39725344 | G | A | 1 | a0003c0004t0002g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2177+1437G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725344 | |||||||
| chr8:39725352 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2177+1445A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725352 | |||||||
| chr8:39725479 | C | T | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2177+1572C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725479 | |||||||
| chr8:39725520 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2177+1613C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725520 | |||||||
| chr8:39725532 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2177+1625C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725532 | |||||||
| chr8:39725563 | T | A | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2177+1656T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725563 | |||||||
| chr8:39725654 | T | A | 3 | a0001c0002t0001g0003 a0001c0002t0001g0122 a0001c0002t0001g0140 |
4 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177+1747T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725654 | |||||||
| chr8:39725691 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2177+1784T>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39725691 | |||||||
| chr8:39726073 | C | T | 4 | a0002c0003t0001g0024 a0002c0003t0001g0025 a0002c0003t0001g0026 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177+2166C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726073 | |||||||
| chr8:39726100 | G | A | 2 | a0001c0002t0001g0072 a0001c0002t0001g0150 |
2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2177+2193G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726100 | |||||||
| chr8:39726187 | G | A | 144 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(141): Show |
146 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2177+2280G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726187 | |||||||
| chr8:39726257 | T | TAC | 142 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(139): Show |
144 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.2177+2368_2177+236 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39726257 | ||||||
| chr8:39726257 | TAC | T | 11 | a0004c0005t0001g0288 a0004c0005t0001g0292 a0004c0005t0001g0307 others(8): Show |
11 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2177+2368_2177+236 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39726257 | ||||||
| chr8:39726278 | TTG | T | 9 | a0001c0002t0001g0001 a0001c0002t0001g0055 a0001c0002t0001g0058 others(6): Show |
10 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2177+2387_2177+238 others(6): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr8 | 39726278 | ||||||
| chr8:39726296 | A | G | 11 | a0001c0002t0001g0077 a0001c0002t0001g0081 a0001c0002t0001g0082 others(8): Show |
11 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2177+2389A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726296 | |||||||
| chr8:39726348 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2177+2441A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726348 | |||||||
| chr8:39726359 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0284 |
2 | HG00621.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2177+2452G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726359 | |||||||
| chr8:39726374 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2177+2467G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726374 | |||||||
| chr8:39726472 | A | G | 9 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2177+2565A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726472 | |||||||
| chr8:39726477 | G | A | 111 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(108): Show |
112 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2177+2570G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726477 | |||||||
| chr8:39726498 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0275 |
2 | NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2177+2591A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726498 | |||||||
| chr8:39726551 | T | C | 9 | a0004c0005t0001g0288 a0004c0005t0001g0292 a0004c0005t0001g0307 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2177+2644T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726551 | |||||||
| chr8:39726586 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2177+2679G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726586 | |||||||
| chr8:39726649 | C | G | 70 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(67): Show |
71 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2177+2742C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39726649 | |||||||
| chr8:39727044 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2178-2854A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727044 | |||||||
| chr8:39727251 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2178-2647G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727251 | |||||||
| chr8:39727289 | C | G | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-2609C>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727289 | |||||||
| chr8:39727310 | C | T | 1 | a0001c0002t0001g0052 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2178-2588C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727310 | |||||||
| chr8:39727335 | C | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178-2563C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727335 | |||||||
| chr8:39727657 | ACTTAACT others(13): Show |
A | 1 | a0005c0016t0001g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2178-2240_2178-222 others(24): Show |
ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727657 | |||||||
| chr8:39727765 | A | G | 5 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(2): Show |
5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2178-2133A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39727765 | |||||||
| chr8:39728024 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2178-1874T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728024 | |||||||
| chr8:39728050 | A | G | 218 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0139 others(215): Show |
221 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.2178-1848A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728050 | |||||||
| chr8:39728123 | A | T | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178-1775A>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728123 | |||||||
| chr8:39728227 | T | C | 9 | a0004c0005t0001g0288 a0004c0005t0001g0292 a0004c0005t0001g0307 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2178-1671T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728227 | |||||||
| chr8:39728561 | T | C | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-1337T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728561 | |||||||
| chr8:39728728 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2178-1170G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728728 | |||||||
| chr8:39728825 | A | G | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-1073A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728825 | |||||||
| chr8:39728839 | G | A | 8 | a0001c0001t0001g0182 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00738.hp1 HG01081.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2178-1059G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728839 | |||||||
| chr8:39728913 | A | G | 1 | a0010c0013t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2178-985A>G | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728913 | |||||||
| chr8:39728977 | C | T | 14 | a0001c0001t0001g0252 a0001c0002t0001g0028 a0001c0002t0001g0029 others(11): Show |
14 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2178-921C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728977 | |||||||
| chr8:39728993 | G | A | 5 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0019 others(2): Show |
5 | HG00733.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2178-905G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39728993 | |||||||
| chr8:39729042 | T | A | 5 | a0001c0002t0001g0006 a0001c0002t0001g0058 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2178-856T>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729042 | |||||||
| chr8:39729062 | C | T | 1 | a0001c0002t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2178-836C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729062 | |||||||
| chr8:39729083 | C | T | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-815C>T | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729083 | |||||||
| chr8:39729213 | T | C | 4 | a0001c0002t0001g0006 a0001c0002t0001g0160 a0001c0002t0001g0163 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2178-685T>C | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729213 | |||||||
| chr8:39729254 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2178-644G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729254 | |||||||
| chr8:39729520 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0301 |
2 | NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2178-378G>A | ADAM18 | ENSG00000168619.16 | transcript | ENST00000265707.10 | protein_coding | 19/19 | chr8 | 39729520 |