Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 157855 |
| ensemblid | ENSG00000215262.8 |
| hgncid | 18867 |
| symbol | KCNU1 |
| name | potassium calcium-activated channel subfamily U member 1 |
| refseq_nuc | NM_001031836.3 |
| refseq_prot | NP_001027006.2 |
| ensembl_nuc | ENST00000399881.8 |
| ensembl_prot | ENSP00000382770.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 36784374 |
| end | 36936125 |
| strand | + |
| ver | v1.2 |
| region | chr8:36784374-36936125 |
| region5000 | chr8:36779374-36941125 |
| regionname0 | KCNU1_chr8_36784374_36936125 |
| regionname5000 | KCNU1_chr8_36779374_36941125 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1149 | 130 | 28 | 24 | 58 | 6 | 13 | 41 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| a0002 | 1/0 | 1149 | 95 | 23 | 17 | 46 | 3 | 5 | 35 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| a0003 | 0/0 | 1149 | 65 | 18 | 9 | 30 | 2 | 6 | 22 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| a0004 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| a0005 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| a0006 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| a0007 | 0/0 | 1149 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | MFQTK others(1144): Show |
chr8 | 36779374 | 36941125 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 3447 | 83 | 22 | 22 | 24 | 6 | 8 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0001c0004 | 0/0 | 3447 | 38 | 0 | 1 | 34 | 0 | 3 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0001c0006 | 0/0 | 3447 | 5 | 5 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0001c0009 | 0/0 | 3447 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0001c0014 | 0/0 | 3447 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0001c0017 | 0/0 | 3447 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0001c0018 | 0/0 | 3447 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0002c0001 | 1/0 | 3447 | 89 | 19 | 16 | 45 | 3 | 5 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0002c0007 | 0/0 | 3447 | 3 | 3 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0002c0011 | 0/0 | 3447 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0002c0016 | 0/0 | 3447 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0002c0019 | 0/0 | 3447 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0003c0003 | 0/0 | 3447 | 55 | 17 | 8 | 22 | 2 | 6 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0003c0005 | 0/0 | 3447 | 9 | 1 | 0 | 8 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0003c0012 | 0/0 | 3447 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0004c0015 | 0/0 | 3447 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0005c0013 | 0/0 | 3447 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0006c0008 | 0/0 | 3447 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 | ||
| a0007c0010 | 0/0 | 3447 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | ATGTT others(3442): Show |
chr8 | 36779374 | 36941125 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 3692 | 83 | 22 | 22 | 24 | 6 | 8 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0004t0001 | 0/0 | 3692 | 37 | 0 | 1 | 33 | 0 | 3 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0004t0002 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0006t0001 | 0/0 | 3692 | 5 | 5 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0009t0001 | 0/0 | 3692 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0014t0001 | 0/0 | 3692 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0017t0001 | 0/0 | 3692 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0001c0018t0001 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0002c0001t0001 | 1/0 | 3692 | 89 | 19 | 16 | 45 | 3 | 5 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0002c0007t0001 | 0/0 | 3692 | 3 | 3 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0002c0011t0001 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0002c0016t0001 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0002c0019t0001 | 0/0 | 3692 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0003c0003t0001 | 0/0 | 3692 | 55 | 17 | 8 | 22 | 2 | 6 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0003c0005t0001 | 0/0 | 3692 | 9 | 1 | 0 | 8 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0003c0012t0001 | 0/0 | 3692 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0004c0015t0001 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0005c0013t0001 | 0/0 | 3692 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0006c0008t0001 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| a0007c0010t0001 | 0/0 | 3692 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | AAATG others(3687): Show |
chr8 | 36779374 | 36941125 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0006t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0009t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0014t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0017t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0001c0018t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0007t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0011t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0016t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0002c0019t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0003c0012t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0004c0015t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0005c0013t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0006c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| a0007c0010t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0076 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0249 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0097 | EUR | GBR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0139 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0215 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0199 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0142 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0115 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00621 | hp1 | a0003 | c0005 | t0001 | g0209 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00621 | hp2 | a0004 | c0015 | t0001 | g0248 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | CHS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0036 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0121 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0119 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0146 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0029 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0025 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0043 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01109 | hp2 | a0001 | c0009 | t0001 | g0168 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0079 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0083 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0178 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01255 | hp2 | a0003 | c0012 | t0001 | g0098 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0038 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0161 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0111 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0081 | AMR | CLM | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0013 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0257 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0056 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0012 | EUR | IBS | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01891 | hp2 | a0002 | c0001 | t0001 | g0021 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0110 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0082 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0149 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0104 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0037 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02015 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0212 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0189 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0148 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0200 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0231 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0040 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02148 | hp1 | a0002 | c0019 | t0001 | g0151 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02165 | hp1 | a0005 | c0013 | t0001 | g0120 | EAS | CDX | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | CDX | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02258 | hp1 | a0003 | c0005 | t0001 | g0222 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0071 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0080 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0150 | AMR | PEL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0210 | EAS | KHV | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0286 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02615 | hp2 | a0002 | c0007 | t0001 | g0046 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0099 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02647 | hp1 | a0001 | c0018 | t0001 | g0179 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0024 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02683 | hp1 | a0001 | c0014 | t0001 | g0232 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0064 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02717 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02717 | hp2 | a0006 | c0008 | t0001 | g0278 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0106 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02738 | hp2 | a0001 | c0017 | t0001 | g0216 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0085 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02818 | hp2 | a0001 | c0006 | t0001 | g0279 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02886 | hp1 | a0001 | c0006 | t0001 | g0170 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0068 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02922 | hp2 | a0002 | c0007 | t0001 | g0152 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0032 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0169 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0180 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0066 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0033 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0100 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03195 | hp1 | a0002 | c0011 | t0001 | g0072 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0078 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0102 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0087 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0283 | AFR | ESN | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0220 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0133 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0124 | SAS | PJL | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0218 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0224 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0065 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0135 | SAS | BEB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0144 | SAS | STU | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0181 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | CHB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0258 | EAS | CHB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0184 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0041 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18943 | hp1 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18945 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18953 | hp2 | a0003 | c0005 | t0001 | g0213 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0206 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0214 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18963 | hp2 | a0003 | c0005 | t0001 | g0198 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18965 | hp2 | a0001 | c0004 | t0002 | g0225 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18970 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0230 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0201 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18980 | hp1 | a0003 | c0005 | t0001 | g0196 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18982 | hp2 | a0003 | c0005 | t0001 | g0219 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0207 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0059 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18988 | hp2 | a0003 | c0005 | t0001 | g0195 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0060 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0129 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0141 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19030 | hp1 | a0001 | c0006 | t0001 | g0177 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0070 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0182 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19054 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19054 | hp2 | a0001 | c0004 | t0001 | g0160 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0208 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0191 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19077 | hp1 | a0003 | c0005 | t0001 | g0188 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0057 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19083 | hp2 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19084 | hp1 | a0001 | c0004 | t0001 | g0190 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19084 | hp2 | a0003 | c0005 | t0001 | g0221 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19087 | hp1 | a0002 | c0016 | t0001 | g0223 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0202 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0044 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA19240 | hp2 | a0002 | c0007 | t0001 | g0069 | AFR | YRI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20805 | hp1 | a0007 | c0010 | t0001 | g0022 | EUR | TSI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0263 | EUR | TSI | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0039 | SAS | GIH | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | GIH | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0185 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0052 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0284 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0183 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | ACB | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0101 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0088 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | USA | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | LWK | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0273 | REF | REF | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0055 | REF | REF | KCNU1_chr8_36779374_36941125 | KCNU1 | chr8 | 36779374 | 36941125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36840520 | C | A | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1576C>A | p.Leu526Met | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/27 | 1613/3692 | 1576/3450 | 526/1149 | chr8 | 36840520 | |||
| chr8:36840575 | G | T | 1 | a0004 | 1 | HG00621.hp2 | missense_variant&splice_region_variant | MODERATE | c.1631G>T | p.Arg544Leu | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/27 | 1668/3692 | 1631/3450 | 544/1149 | chr8 | 36840575 | |||
| chr8:36909403 | C | G | 1 | a0005 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2199C>G | p.Asn733Lys | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/27 | 2236/3692 | 2199/3450 | 733/1149 | chr8 | 36909403 | |||
| chr8:36909506 | T | C | 3 | a0001 a0005 a0006 |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
missense_variant | MODERATE | c.2302T>C | p.Trp768Arg | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/27 | 2339/3692 | 2302/3450 | 768/1149 | chr8 | 36909506 | |||
| chr8:36930961 | A | G | 1 | a0003 | 65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
missense_variant | MODERATE | c.2747A>G | p.Asn916Ser | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/27 | 2784/3692 | 2747/3450 | 916/1149 | chr8 | 36930961 | |||
| chr8:36935751 | C | T | 1 | a0007 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.3281C>T | p.Pro1094Leu | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 27/27 | 3318/3692 | 3281/3450 | 1094/1149 | chr8 | 36935751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36787356 | C | T | 1 | a0002c0019 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.246C>T | p.His82His | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/27 | 283/3692 | 246/3450 | 82/1149 | chr8 | 36787356 | |||
| chr8:36817716 | C | T | 1 | a0001c0018 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1062C>T | p.Arg354Arg | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/27 | 1099/3692 | 1062/3450 | 354/1149 | chr8 | 36817716 | |||
| chr8:36836876 | C | T | 4 | a0001c0004 a0001c0017 a0002c0016 others(1): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
synonymous_variant | LOW | c.1449C>T | p.Ile483Ile | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/27 | 1486/3692 | 1449/3450 | 483/1149 | chr8 | 36836876 | |||
| chr8:36864483 | A | G | 2 | a0001c0014 a0001c0017 |
2 | HG02683.hp1 HG02738.hp2 |
synonymous_variant | LOW | c.1971A>G | p.Val657Val | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/27 | 2008/3692 | 1971/3450 | 657/1149 | chr8 | 36864483 | |||
| chr8:36905708 | G | A | 1 | a0001c0009 | 1 | HG01109.hp2 | splice_region_variant&synonymous_variant | LOW | c.2010G>A | p.Arg670Arg | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/27 | 2047/3692 | 2010/3450 | 670/1149 | chr8 | 36905708 | |||
| chr8:36922620 | G | C | 2 | a0001c0006 a0001c0018 |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.2727G>C | p.Leu909Leu | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/27 | 2764/3692 | 2727/3450 | 909/1149 | chr8 | 36922620 | |||
| chr8:36931139 | C | T | 1 | a0002c0007 | 3 | HG02615.hp2 HG02922.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2925C>T | p.Asp975Asp | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/27 | 2962/3692 | 2925/3450 | 975/1149 | chr8 | 36931139 | |||
| chr8:36932931 | C | G | 1 | a0002c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2943C>G | p.Thr981Thr | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/27 | 2980/3692 | 2943/3450 | 981/1149 | chr8 | 36932931 | |||
| chr8:36935659 | A | G | 1 | a0003c0012 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.3189A>G | p.Ser1063Ser | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 27/27 | 3226/3692 | 3189/3450 | 1063/1149 | chr8 | 36935659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36936016 | C | T | 1 | a0001c0004t0002 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 27/27 | 96 | chr8 | 36936016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:36784779 | C | G | 6 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+174C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784779 | |||||||
| chr8:36784830 | A | G | 1 | a0003c0003t0001g0283 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.195+225A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784830 | |||||||
| chr8:36784918 | C | G | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.195+313C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784918 | |||||||
| chr8:36784954 | A | G | 137 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(134): Show |
140 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.195+349A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784954 | |||||||
| chr8:36784982 | A | G | 6 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+377A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784982 | |||||||
| chr8:36784988 | A | G | 137 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(134): Show |
140 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.195+383A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36784988 | |||||||
| chr8:36785067 | G | A | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.195+462G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785067 | |||||||
| chr8:36785107 | A | G | 1 | a0003c0003t0001g0153 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.195+502A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785107 | |||||||
| chr8:36785470 | C | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.195+865C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785470 | |||||||
| chr8:36785607 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.195+1002T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36785607 | |||||||
| chr8:36786001 | T | A | 1 | a0002c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.196-1305T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786001 | |||||||
| chr8:36786112 | C | CA | 11 | a0001c0002t0001g0162 a0001c0002t0001g0163 a0001c0002t0001g0164 others(8): Show |
11 | HG01358.hp2 HG02027.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-1179dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 36786112 | ||||||
| chr8:36786217 | A | T | 1 | a0002c0007t0001g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.196-1089A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786217 | |||||||
| chr8:36786311 | T | C | 2 | a0001c0002t0001g0165 a0001c0002t0001g0166 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.196-995T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786311 | |||||||
| chr8:36786386 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196-920T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786386 | |||||||
| chr8:36786616 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196-690A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786616 | |||||||
| chr8:36786756 | C | T | 3 | a0002c0001t0001g0149 a0002c0001t0001g0150 a0002c0019t0001g0151 |
3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.196-550C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36786756 | |||||||
| chr8:36787142 | C | T | 1 | a0001c0006t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196-164C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36787142 | |||||||
| chr8:36787199 | G | A | 1 | a0001c0004t0001g0167 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.196-107G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 1/26 | chr8 | 36787199 | |||||||
| chr8:36787462 | T | G | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.315+37T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787462 | |||||||
| chr8:36787688 | TATG | T | 30 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(27): Show |
30 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.315+266_315+268del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36787688 | ||||||
| chr8:36787700 | T | C | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.315+275T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787700 | |||||||
| chr8:36787740 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.315+315C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787740 | |||||||
| chr8:36787841 | A | G | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.315+416A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787841 | |||||||
| chr8:36787856 | C | CTAAT | 138 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(135): Show |
141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+434_315+437dup others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36787856 | ||||||
| chr8:36787958 | A | G | 57 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.315+533A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36787958 | |||||||
| chr8:36788024 | T | C | 47 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0158 others(44): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.315+599T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788024 | |||||||
| chr8:36788028 | T | C | 4 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0003c0003t0001g0230 others(1): Show |
4 | HG00438.hp2 HG02132.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+603T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788028 | |||||||
| chr8:36788544 | T | C | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.315+1119T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788544 | |||||||
| chr8:36788674 | A | C | 3 | a0002c0001t0001g0149 a0002c0001t0001g0150 a0002c0019t0001g0151 |
3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.315+1249A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788674 | |||||||
| chr8:36788699 | C | T | 138 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(135): Show |
141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+1274C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788699 | |||||||
| chr8:36788761 | T | C | 59 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(56): Show |
60 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.315+1336T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36788761 | |||||||
| chr8:36789135 | C | T | 1 | a0003c0003t0001g0146 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.315+1710C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789135 | |||||||
| chr8:36789196 | T | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.315+1771T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789196 | |||||||
| chr8:36789271 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.315+1846G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789271 | |||||||
| chr8:36789362 | T | TA | 9 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315+1948dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36789362 | ||||||
| chr8:36789792 | T | C | 61 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.315+2367T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789792 | |||||||
| chr8:36789810 | A | G | 1 | a0001c0002t0001g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.315+2385A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789810 | |||||||
| chr8:36789924 | G | A | 2 | a0002c0001t0001g0010 a0003c0003t0001g0011 |
2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.315+2499G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36789924 | |||||||
| chr8:36790001 | C | A | 27 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(24): Show |
27 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.315+2576C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790001 | |||||||
| chr8:36790427 | C | T | 1 | a0002c0001t0001g0145 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.315+3002C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790427 | |||||||
| chr8:36790511 | A | G | 61 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.315+3086A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790511 | |||||||
| chr8:36790664 | A | G | 27 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(24): Show |
27 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.315+3239A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790664 | |||||||
| chr8:36790801 | T | A | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.315+3376T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790801 | |||||||
| chr8:36790872 | C | A | 2 | a0002c0001t0001g0012 a0002c0001t0001g0013 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.315+3447C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790872 | |||||||
| chr8:36790874 | A | G | 1 | a0003c0003t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.315+3449A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36790874 | |||||||
| chr8:36790998 | GA | G | 137 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(134): Show |
140 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.315+3586delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36790998 | ||||||
| chr8:36791036 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.315+3611G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791036 | |||||||
| chr8:36791352 | G | A | 1 | a0002c0001t0001g0009 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.315+3927G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791352 | |||||||
| chr8:36791526 | C | A | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+4101C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791526 | |||||||
| chr8:36791527 | T | G | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+4102T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791527 | |||||||
| chr8:36791569 | TAGATAAA others(17): Show |
T | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315+4146_315+4169d others(26): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36791569 | ||||||
| chr8:36791603 | T | G | 138 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(135): Show |
141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+4178T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791603 | |||||||
| chr8:36791666 | G | A | 5 | a0001c0002t0001g0018 a0002c0001t0001g0016 a0002c0001t0001g0019 others(2): Show |
5 | NA18948.hp2 NA18953.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+4241G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791666 | |||||||
| chr8:36791978 | G | A | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.315+4553G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36791978 | |||||||
| chr8:36792030 | A | G | 1 | a0003c0003t0001g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.315+4605A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792030 | |||||||
| chr8:36792225 | T | A | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.315+4800T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792225 | |||||||
| chr8:36792601 | C | T | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.315+5176C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792601 | |||||||
| chr8:36792881 | G | T | 61 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.315+5456G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36792881 | |||||||
| chr8:36793093 | C | T | 57 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.315+5668C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793093 | |||||||
| chr8:36793100 | A | T | 3 | a0001c0002t0001g0274 a0001c0002t0001g0275 a0001c0002t0001g0276 |
3 | HG01167.hp2 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.315+5675A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793100 | |||||||
| chr8:36793215 | G | A | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.315+5790G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793215 | |||||||
| chr8:36793217 | G | A | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.315+5792G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793217 | |||||||
| chr8:36793338 | G | C | 1 | a0007c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.315+5913G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793338 | |||||||
| chr8:36793457 | C | T | 19 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0285 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.315+6032C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793457 | |||||||
| chr8:36793718 | AGTTGTCC others(10): Show |
A | 3 | a0001c0006t0001g0177 a0001c0018t0001g0179 a0002c0001t0001g0178 |
3 | HG01243.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.315+6297_315+6313d others(19): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36793718 | ||||||
| chr8:36793725 | C | T | 87 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(84): Show |
88 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.315+6300C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793725 | |||||||
| chr8:36793883 | G | A | 2 | a0002c0001t0001g0024 a0003c0003t0001g0023 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.315+6458G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793883 | |||||||
| chr8:36793920 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.315+6495G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793920 | |||||||
| chr8:36793957 | G | A | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.315+6532G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793957 | |||||||
| chr8:36793979 | G | T | 46 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0002c0001t0001g0009 others(43): Show |
46 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.315+6554G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36793979 | |||||||
| chr8:36794040 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.315+6615C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794040 | |||||||
| chr8:36794055 | C | CA | 41 | a0001c0002t0001g0108 a0001c0004t0001g0002 a0001c0004t0001g0158 others(38): Show |
43 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.315+6652dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | ||||||
| chr8:36794055 | CA | C | 25 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0285 others(22): Show |
25 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+6652delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | ||||||
| chr8:36794055 | CAA | C | 60 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0156 others(57): Show |
61 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.315+6651_315+6652d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | ||||||
| chr8:36794055 | CAAA | C | 8 | a0001c0002t0001g0155 a0001c0002t0001g0171 a0001c0002t0001g0172 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.315+6650_315+6652d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36794055 | ||||||
| chr8:36794270 | G | T | 3 | a0003c0003t0001g0096 a0003c0003t0001g0097 a0003c0012t0001g0098 |
3 | HG00140.hp2 HG00639.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.315+6845G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794270 | |||||||
| chr8:36794409 | A | C | 88 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.315+6984A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794409 | |||||||
| chr8:36794513 | C | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+7088C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794513 | |||||||
| chr8:36794955 | C | A | 138 | a0001c0002t0001g0003 a0001c0002t0001g0143 a0001c0002t0001g0154 others(135): Show |
141 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+7530C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36794955 | |||||||
| chr8:36795224 | C | T | 5 | a0001c0002t0001g0018 a0002c0001t0001g0016 a0002c0001t0001g0019 others(2): Show |
5 | NA18948.hp2 NA18953.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+7799C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795224 | |||||||
| chr8:36795455 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.315+8030C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795455 | |||||||
| chr8:36795550 | A | T | 86 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(83): Show |
87 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.315+8125A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795550 | |||||||
| chr8:36795676 | T | C | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315+8251T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795676 | |||||||
| chr8:36795818 | G | A | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-8209G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795818 | |||||||
| chr8:36795914 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.316-8113A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795914 | |||||||
| chr8:36795940 | G | C | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.316-8087G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36795940 | |||||||
| chr8:36796049 | T | A | 3 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 |
3 | HG02055.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-7978T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796049 | |||||||
| chr8:36796086 | G | T | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7941G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796086 | |||||||
| chr8:36796105 | C | A | 89 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(86): Show |
90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-7922C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796105 | |||||||
| chr8:36796131 | T | C | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7896T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796131 | |||||||
| chr8:36796132 | C | T | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7895C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796132 | |||||||
| chr8:36796133 | T | C | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.316-7894T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796133 | |||||||
| chr8:36796271 | T | C | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.316-7756T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796271 | |||||||
| chr8:36796285 | C | T | 2 | a0001c0002t0001g0282 a0002c0001t0001g0142 |
2 | HG00597.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.316-7742C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796285 | |||||||
| chr8:36796316 | G | C | 88 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.316-7711G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796316 | |||||||
| chr8:36796337 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-7690C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796337 | |||||||
| chr8:36796384 | A | G | 1 | a0001c0002t0001g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.316-7643A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796384 | |||||||
| chr8:36796407 | C | T | 86 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(83): Show |
87 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.316-7620C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796407 | |||||||
| chr8:36796533 | T | C | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-7494T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796533 | |||||||
| chr8:36796859 | G | T | 1 | a0003c0003t0001g0103 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.316-7168G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36796859 | |||||||
| chr8:36797250 | T | C | 19 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0285 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.316-6777T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797250 | |||||||
| chr8:36797293 | T | A | 1 | a0002c0001t0001g0234 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.316-6734T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797293 | |||||||
| chr8:36797304 | CT | C | 49 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0158 others(46): Show |
51 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.316-6713delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36797304 | ||||||
| chr8:36797491 | G | T | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-6536G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797491 | |||||||
| chr8:36797535 | C | T | 1 | a0002c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.316-6492C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797535 | |||||||
| chr8:36797634 | CT | C | 63 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(60): Show |
64 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.316-6380delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36797634 | ||||||
| chr8:36797737 | C | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-6290C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797737 | |||||||
| chr8:36797866 | T | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.316-6161T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36797866 | |||||||
| chr8:36798015 | T | C | 59 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(56): Show |
60 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.316-6012T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798015 | |||||||
| chr8:36798089 | C | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.316-5938C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798089 | |||||||
| chr8:36798201 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-5826G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798201 | |||||||
| chr8:36798251 | T | C | 8 | a0001c0002t0001g0186 a0002c0001t0001g0182 a0002c0001t0001g0183 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-5776T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798251 | |||||||
| chr8:36798406 | T | G | 57 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.316-5621T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798406 | |||||||
| chr8:36798650 | C | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-5377C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798650 | |||||||
| chr8:36798698 | A | T | 39 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0167 others(36): Show |
41 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.316-5329A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36798698 | |||||||
| chr8:36799100 | C | G | 1 | a0001c0002t0001g0270 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316-4927C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799100 | |||||||
| chr8:36799147 | C | A | 1 | a0002c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.316-4880C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799147 | |||||||
| chr8:36799258 | A | G | 90 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(87): Show |
91 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.316-4769A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799258 | |||||||
| chr8:36799484 | C | T | 88 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.316-4543C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799484 | |||||||
| chr8:36799510 | G | C | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.316-4517G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799510 | |||||||
| chr8:36799684 | G | A | 1 | a0001c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.316-4343G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799684 | |||||||
| chr8:36799700 | A | AT | 64 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(61): Show |
65 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.316-4314dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36799700 | ||||||
| chr8:36799700 | A | ATT | 25 | a0001c0002t0001g0164 a0001c0002t0001g0186 a0001c0002t0001g0187 others(22): Show |
25 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.316-4315_316-4314d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36799700 | ||||||
| chr8:36799793 | G | A | 8 | a0001c0002t0001g0186 a0002c0001t0001g0182 a0002c0001t0001g0183 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-4234G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799793 | |||||||
| chr8:36799860 | T | C | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-4167T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36799860 | |||||||
| chr8:36800005 | C | T | 59 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(56): Show |
60 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.316-4022C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800005 | |||||||
| chr8:36800310 | G | C | 89 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(86): Show |
90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-3717G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800310 | |||||||
| chr8:36800554 | G | A | 1 | a0002c0001t0001g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.316-3473G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800554 | |||||||
| chr8:36800636 | A | C | 1 | a0002c0001t0001g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.316-3391A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800636 | |||||||
| chr8:36800872 | G | A | 58 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(55): Show |
59 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.316-3155G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800872 | |||||||
| chr8:36800872 | G | T | 1 | a0001c0002t0001g0270 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316-3155G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800872 | |||||||
| chr8:36800918 | A | G | 1 | a0002c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.316-3109A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800918 | |||||||
| chr8:36800934 | G | T | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-3093G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36800934 | |||||||
| chr8:36801137 | C | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.316-2890C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801137 | |||||||
| chr8:36801396 | C | T | 54 | a0001c0002t0001g0018 a0001c0002t0001g0073 a0002c0001t0001g0004 others(51): Show |
56 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.316-2631C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801396 | |||||||
| chr8:36801431 | CT | C | 89 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(86): Show |
90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-2586delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36801431 | ||||||
| chr8:36801433 | T | C | 1 | a0002c0001t0001g0031 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.316-2594T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801433 | |||||||
| chr8:36801483 | T | G | 86 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(83): Show |
87 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.316-2544T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801483 | |||||||
| chr8:36801491 | G | A | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.316-2536G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801491 | |||||||
| chr8:36801510 | T | C | 6 | a0003c0003t0001g0006 a0003c0003t0001g0026 a0003c0003t0001g0032 others(3): Show |
6 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-2517T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801510 | |||||||
| chr8:36801641 | A | G | 1 | a0002c0001t0001g0138 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.316-2386A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801641 | |||||||
| chr8:36801868 | A | G | 139 | a0001c0002t0001g0003 a0001c0002t0001g0143 a0001c0002t0001g0154 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.316-2159A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36801868 | |||||||
| chr8:36802048 | G | T | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-1979G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802048 | |||||||
| chr8:36802076 | T | A | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.316-1951T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802076 | |||||||
| chr8:36802087 | G | C | 139 | a0001c0002t0001g0003 a0001c0002t0001g0143 a0001c0002t0001g0154 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.316-1940G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802087 | |||||||
| chr8:36802090 | A | C | 1 | a0001c0002t0001g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.316-1937A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802090 | |||||||
| chr8:36802108 | C | CA | 52 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0158 others(49): Show |
54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.316-1895dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | ||||||
| chr8:36802108 | CA | C | 12 | a0001c0002t0001g0172 a0001c0002t0001g0173 a0001c0002t0001g0174 others(9): Show |
14 | HG00609.hp1 HG02055.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-1895delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | ||||||
| chr8:36802108 | CAA | C | 9 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0238 others(6): Show |
9 | HG01934.hp2 HG02257.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-1896_316-1895d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | ||||||
| chr8:36802108 | CAAA | C | 70 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(67): Show |
71 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.316-1897_316-1895d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | ||||||
| chr8:36802108 | CAAAAAAA others(6): Show |
C | 4 | a0003c0003t0001g0096 a0003c0003t0001g0097 a0003c0003t0001g0146 others(1): Show |
4 | HG00140.hp2 HG00639.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-1907_316-1895d others(15): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36802108 | ||||||
| chr8:36802166 | A | G | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-1861A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802166 | |||||||
| chr8:36802167 | C | A | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-1860C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802167 | |||||||
| chr8:36802395 | G | A | 139 | a0001c0002t0001g0003 a0001c0002t0001g0143 a0001c0002t0001g0154 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.316-1632G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802395 | |||||||
| chr8:36802564 | T | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.316-1463T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802564 | |||||||
| chr8:36802580 | A | C | 1 | a0003c0003t0001g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.316-1447A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802580 | |||||||
| chr8:36802654 | G | A | 3 | a0002c0001t0001g0066 a0002c0001t0001g0068 a0003c0003t0001g0067 |
3 | HG02559.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.316-1373G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802654 | |||||||
| chr8:36802664 | G | C | 1 | a0001c0002t0001g0241 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.316-1363G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802664 | |||||||
| chr8:36802669 | G | A | 139 | a0001c0002t0001g0003 a0001c0002t0001g0143 a0001c0002t0001g0154 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.316-1358G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802669 | |||||||
| chr8:36802675 | G | T | 4 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-1352G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802675 | |||||||
| chr8:36802771 | T | A | 139 | a0001c0002t0001g0003 a0001c0002t0001g0143 a0001c0002t0001g0154 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.316-1256T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802771 | |||||||
| chr8:36802804 | A | C | 18 | a0001c0002t0001g0186 a0001c0002t0001g0285 a0001c0002t0001g0287 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-1223A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802804 | |||||||
| chr8:36802952 | G | A | 1 | a0002c0001t0001g0178 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.316-1075G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36802952 | |||||||
| chr8:36803306 | T | C | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.316-721T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803306 | |||||||
| chr8:36803439 | C | T | 88 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.316-588C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803439 | |||||||
| chr8:36803486 | T | TA | 18 | a0001c0002t0001g0186 a0001c0002t0001g0285 a0001c0002t0001g0287 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-533dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 36803486 | ||||||
| chr8:36803500 | T | G | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.316-527T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803500 | |||||||
| chr8:36803754 | A | T | 4 | a0002c0001t0001g0102 a0003c0003t0001g0099 a0003c0003t0001g0100 others(1): Show |
4 | HG02630.hp1 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-273A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803754 | |||||||
| chr8:36803826 | T | C | 7 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0242 others(4): Show |
7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-201T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803826 | |||||||
| chr8:36803930 | G | A | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.316-97G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 2/26 | chr8 | 36803930 | |||||||
| chr8:36804168 | A | C | 69 | a0001c0002t0001g0003 a0001c0002t0001g0108 a0001c0002t0001g0154 others(66): Show |
70 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.377+80A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804168 | |||||||
| chr8:36804191 | A | G | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.377+103A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804191 | |||||||
| chr8:36804236 | T | C | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.377+148T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804236 | |||||||
| chr8:36804453 | C | T | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377+365C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804453 | |||||||
| chr8:36804662 | T | C | 1 | a0001c0002t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.378-533T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804662 | |||||||
| chr8:36804696 | G | A | 4 | a0002c0001t0001g0070 a0002c0001t0001g0071 a0002c0007t0001g0069 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-499G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804696 | |||||||
| chr8:36804869 | T | A | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.378-326T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804869 | |||||||
| chr8:36804897 | T | C | 139 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0143 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.378-298T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804897 | |||||||
| chr8:36804946 | C | G | 1 | a0003c0003t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.378-249C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804946 | |||||||
| chr8:36804994 | G | T | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.378-201G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36804994 | |||||||
| chr8:36805162 | G | T | 91 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(88): Show |
92 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.378-33G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 3/26 | chr8 | 36805162 | |||||||
| chr8:36805629 | G | A | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.468+344G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805629 | |||||||
| chr8:36805661 | A | C | 1 | a0001c0002t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.468+376A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805661 | |||||||
| chr8:36805703 | T | C | 1 | a0002c0001t0001g0038 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.468+418T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805703 | |||||||
| chr8:36805997 | C | T | 1 | a0002c0001t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.469-272C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36805997 | |||||||
| chr8:36806000 | C | T | 48 | a0001c0002t0001g0018 a0002c0001t0001g0004 a0002c0001t0001g0016 others(45): Show |
50 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.469-269C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36806000 | |||||||
| chr8:36806089 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-180C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36806089 | |||||||
| chr8:36806118 | G | A | 24 | a0001c0002t0001g0061 a0002c0001t0001g0010 a0002c0001t0001g0021 others(21): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-151G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 4/26 | chr8 | 36806118 | |||||||
| chr8:36806553 | A | C | 88 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.580+173A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36806553 | |||||||
| chr8:36806695 | A | G | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.580+315A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36806695 | |||||||
| chr8:36806760 | T | G | 139 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0143 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.580+380T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36806760 | |||||||
| chr8:36807195 | A | C | 65 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(62): Show |
66 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.581-180A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36807195 | |||||||
| chr8:36807312 | C | T | 1 | a0002c0001t0001g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.581-63C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36807312 | |||||||
| chr8:36807316 | G | A | 6 | a0001c0002t0001g0014 a0001c0002t0001g0047 a0001c0002t0001g0048 others(3): Show |
6 | HG00099.hp2 HG01074.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.581-59G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 5/26 | chr8 | 36807316 | |||||||
| chr8:36807506 | T | C | 2 | a0002c0001t0001g0104 a0002c0001t0001g0110 |
2 | HG01928.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.656+56T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807506 | |||||||
| chr8:36807729 | C | CA | 50 | a0001c0002t0001g0143 a0001c0002t0001g0187 a0001c0004t0001g0002 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.656+295dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 36807729 | ||||||
| chr8:36807737 | A | C | 1 | a0003c0003t0001g0153 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.656+287A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807737 | |||||||
| chr8:36807791 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.656+341A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807791 | |||||||
| chr8:36807813 | T | TA | 88 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.656+373dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 36807813 | ||||||
| chr8:36807902 | T | C | 88 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.656+452T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36807902 | |||||||
| chr8:36808344 | A | C | 139 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0143 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.657-374A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36808344 | |||||||
| chr8:36808583 | C | T | 2 | a0002c0001t0001g0010 a0003c0003t0001g0011 |
2 | HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.657-135C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36808583 | |||||||
| chr8:36808665 | G | A | 89 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(86): Show |
90 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.657-53G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 6/26 | chr8 | 36808665 | |||||||
| chr8:36808800 | A | G | 17 | a0001c0002t0001g0186 a0001c0002t0001g0285 a0001c0002t0001g0287 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.732+7A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36808800 | |||||||
| chr8:36808811 | A | G | 3 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0087 |
3 | HG02683.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.732+18A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36808811 | |||||||
| chr8:36808883 | T | C | 2 | a0002c0001t0001g0012 a0002c0001t0001g0013 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.732+90T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36808883 | |||||||
| chr8:36809220 | C | T | 3 | a0003c0003t0001g0096 a0003c0003t0001g0097 a0003c0012t0001g0098 |
3 | HG00140.hp2 HG00639.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.732+427C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809220 | |||||||
| chr8:36809369 | G | A | 88 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.732+576G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809369 | |||||||
| chr8:36809511 | C | G | 137 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0143 others(134): Show |
140 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.732+718C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809511 | |||||||
| chr8:36809725 | G | C | 1 | a0002c0001t0001g0112 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.732+932G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809725 | |||||||
| chr8:36809814 | A | C | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.732+1021A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809814 | |||||||
| chr8:36809859 | T | C | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.732+1066T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809859 | |||||||
| chr8:36809926 | G | A | 2 | a0002c0001t0001g0113 a0002c0001t0001g0114 |
2 | HG02071.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.732+1133G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36809926 | |||||||
| chr8:36810029 | G | T | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.732+1236G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810029 | |||||||
| chr8:36810193 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.732+1400A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810193 | |||||||
| chr8:36810250 | C | CA | 143 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0143 others(140): Show |
146 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.732+1471dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36810250 | ||||||
| chr8:36810501 | A | G | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.732+1708A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810501 | |||||||
| chr8:36810768 | A | C | 88 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.732+1975A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810768 | |||||||
| chr8:36810975 | G | A | 1 | a0003c0003t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.732+2182G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36810975 | |||||||
| chr8:36811328 | T | G | 9 | a0001c0002t0001g0061 a0002c0001t0001g0030 a0002c0001t0001g0036 others(6): Show |
9 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+2535T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811328 | |||||||
| chr8:36811431 | C | G | 2 | a0002c0001t0001g0102 a0003c0003t0001g0101 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.732+2638C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811431 | |||||||
| chr8:36811448 | A | G | 1 | a0002c0007t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.732+2655A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811448 | |||||||
| chr8:36811813 | A | C | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.733-2394A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811813 | |||||||
| chr8:36811829 | G | A | 1 | a0002c0001t0001g0038 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.733-2378G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811829 | |||||||
| chr8:36811865 | G | A | 47 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(44): Show |
49 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.733-2342G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36811865 | |||||||
| chr8:36812032 | C | G | 17 | a0001c0002t0001g0186 a0001c0002t0001g0285 a0001c0002t0001g0287 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.733-2175C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812032 | |||||||
| chr8:36812074 | C | A | 1 | a0002c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733-2133C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812074 | |||||||
| chr8:36812177 | C | G | 17 | a0001c0002t0001g0186 a0001c0002t0001g0285 a0001c0002t0001g0287 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.733-2030C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812177 | |||||||
| chr8:36812308 | A | G | 58 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(55): Show |
59 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.733-1899A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812308 | |||||||
| chr8:36812378 | C | CA | 26 | a0001c0002t0001g0186 a0001c0002t0001g0282 a0001c0002t0001g0285 others(23): Show |
26 | HG00735.hp2 HG01358.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.733-1810dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36812378 | ||||||
| chr8:36812378 | C | CAA | 49 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(46): Show |
51 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.733-1811_733-1810d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36812378 | ||||||
| chr8:36812378 | CA | C | 73 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(70): Show |
74 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.733-1810delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 36812378 | ||||||
| chr8:36812933 | A | C | 58 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(55): Show |
59 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.733-1274A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36812933 | |||||||
| chr8:36813012 | G | A | 1 | a0001c0004t0001g0190 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.733-1195G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813012 | |||||||
| chr8:36813273 | T | C | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.733-934T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813273 | |||||||
| chr8:36813430 | A | T | 1 | a0001c0002t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.733-777A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813430 | |||||||
| chr8:36813503 | A | G | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733-704A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813503 | |||||||
| chr8:36813664 | G | T | 1 | a0002c0001t0001g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.733-543G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813664 | |||||||
| chr8:36813670 | T | TA | 75 | a0001c0002t0001g0003 a0001c0002t0001g0154 a0001c0002t0001g0155 others(72): Show |
76 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.733-537_733-536ins others(1): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813670 | |||||||
| chr8:36813670 | T | TAA | 12 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.733-537_733-536ins others(2): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813670 | |||||||
| chr8:36813671 | T | A | 88 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0154 others(85): Show |
89 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.733-536T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813671 | |||||||
| chr8:36813855 | C | T | 23 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(20): Show |
23 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.733-352C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813855 | |||||||
| chr8:36813865 | G | GA | 139 | a0001c0002t0001g0003 a0001c0002t0001g0073 a0001c0002t0001g0143 others(136): Show |
142 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.733-342_733-341ins others(1): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813865 | |||||||
| chr8:36813932 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.733-275T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813932 | |||||||
| chr8:36813992 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.733-215G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36813992 | |||||||
| chr8:36814066 | A | T | 1 | a0001c0006t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733-141A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36814066 | |||||||
| chr8:36814082 | T | G | 1 | a0001c0002t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.733-125T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 7/26 | chr8 | 36814082 | |||||||
| chr8:36814483 | A | G | 7 | a0002c0001t0001g0178 a0003c0003t0001g0006 a0003c0003t0001g0026 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+106A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814483 | |||||||
| chr8:36814664 | T | A | 1 | a0003c0003t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.903+287T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814664 | |||||||
| chr8:36814671 | A | G | 2 | a0003c0003t0001g0045 a0003c0003t0001g0062 |
2 | HG02027.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.903+294A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814671 | |||||||
| chr8:36814945 | G | A | 1 | a0002c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.903+568G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36814945 | |||||||
| chr8:36815007 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.904-589T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815007 | |||||||
| chr8:36815075 | A | C | 1 | a0001c0004t0001g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.904-521A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815075 | |||||||
| chr8:36815213 | C | A | 3 | a0002c0001t0001g0044 a0002c0007t0001g0046 a0002c0007t0001g0152 |
3 | HG02615.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-383C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815213 | |||||||
| chr8:36815563 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.904-33G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 8/26 | chr8 | 36815563 | |||||||
| chr8:36815701 | T | A | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.995+14T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815701 | |||||||
| chr8:36815761 | A | G | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.995+74A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815761 | |||||||
| chr8:36815795 | A | G | 1 | a0002c0001t0001g0060 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.995+108A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815795 | |||||||
| chr8:36815842 | A | T | 1 | a0003c0003t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.995+155A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36815842 | |||||||
| chr8:36816101 | A | ATAAT | 141 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.995+416_995+419dup others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36816101 | ||||||
| chr8:36816101 | A | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.995+414A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816101 | |||||||
| chr8:36816234 | T | A | 141 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.995+547T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816234 | |||||||
| chr8:36816246 | T | C | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.995+559T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816246 | |||||||
| chr8:36816255 | A | G | 91 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.995+568A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816255 | |||||||
| chr8:36816262 | A | G | 91 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.995+575A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816262 | |||||||
| chr8:36816315 | G | A | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.995+628G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816315 | |||||||
| chr8:36816452 | C | T | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.995+765C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816452 | |||||||
| chr8:36816528 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.995+841G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816528 | |||||||
| chr8:36816644 | AC | A | 91 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.995+958delC | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816644 | |||||||
| chr8:36816649 | A | T | 91 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.995+962A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36816649 | |||||||
| chr8:36816944 | AAAC | A | 90 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.996-685_996-683del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36816944 | ||||||
| chr8:36817116 | T | A | 2 | a0001c0004t0001g0191 a0001c0004t0001g0214 |
2 | NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.996-534T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817116 | |||||||
| chr8:36817128 | G | A | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.996-522G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817128 | |||||||
| chr8:36817131 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.996-519G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817131 | |||||||
| chr8:36817195 | A | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.996-455A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817195 | |||||||
| chr8:36817274 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.996-376C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817274 | |||||||
| chr8:36817289 | C | T | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.996-361C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817289 | |||||||
| chr8:36817359 | C | T | 1 | a0001c0004t0001g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.996-291C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817359 | |||||||
| chr8:36817376 | T | G | 267 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0047 others(264): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.996-274T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817376 | |||||||
| chr8:36817385 | G | A | 2 | a0002c0001t0001g0027 a0002c0001t0001g0052 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.996-265G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817385 | |||||||
| chr8:36817499 | C | CA | 13 | a0002c0001t0001g0027 a0002c0001t0001g0039 a0002c0001t0001g0052 others(10): Show |
13 | HG00673.hp2 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.996-125dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | ||||||
| chr8:36817499 | C | CAAAAAA | 26 | a0001c0002t0001g0156 a0001c0004t0001g0002 a0001c0004t0001g0008 others(23): Show |
28 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.996-130_996-125dup others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | ||||||
| chr8:36817499 | C | CAAAAAAA | 15 | a0001c0002t0001g0186 a0001c0002t0001g0282 a0001c0004t0001g0159 others(12): Show |
15 | HG00544.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.996-131_996-125dup others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | ||||||
| chr8:36817499 | CA | C | 51 | a0001c0002t0001g0018 a0001c0002t0001g0051 a0001c0002t0001g0108 others(48): Show |
51 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.996-125delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | ||||||
| chr8:36817499 | CAAA | C | 24 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0247 others(21): Show |
24 | HG01891.hp1 HG01934.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.996-127_996-125del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | ||||||
| chr8:36817499 | CAAAA | C | 63 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.996-128_996-125del others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 36817499 | ||||||
| chr8:36817541 | T | C | 1 | a0005c0013t0001g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.996-109T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817541 | |||||||
| chr8:36817579 | T | C | 50 | a0001c0002t0001g0143 a0001c0002t0001g0186 a0001c0002t0001g0282 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.996-71T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817579 | |||||||
| chr8:36817632 | C | T | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.996-18C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 9/26 | chr8 | 36817632 | |||||||
| chr8:36817909 | C | A | 1 | a0002c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1106+149C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36817909 | |||||||
| chr8:36817997 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1106+237G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36817997 | |||||||
| chr8:36818268 | C | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1106+508C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818268 | |||||||
| chr8:36818320 | T | A | 1 | a0001c0004t0001g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1106+560T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818320 | |||||||
| chr8:36818367 | CT | C | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+610delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36818367 | ||||||
| chr8:36818427 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1106+667A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818427 | |||||||
| chr8:36818447 | C | T | 1 | a0002c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1106+687C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818447 | |||||||
| chr8:36818644 | C | T | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1106+884C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818644 | |||||||
| chr8:36818689 | T | G | 3 | a0002c0001t0001g0024 a0002c0001t0001g0088 a0003c0003t0001g0023 |
3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1106+929T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818689 | |||||||
| chr8:36818856 | A | G | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1106+1096A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36818856 | |||||||
| chr8:36819964 | T | C | 2 | a0002c0001t0001g0040 a0002c0001t0001g0041 |
2 | HG02132.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1106+2204T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36819964 | |||||||
| chr8:36820064 | A | G | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1106+2304A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820064 | |||||||
| chr8:36820116 | T | C | 141 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1106+2356T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820116 | |||||||
| chr8:36820361 | G | A | 9 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106+2601G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820361 | |||||||
| chr8:36820484 | C | T | 9 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106+2724C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820484 | |||||||
| chr8:36820573 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1106+2813C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820573 | |||||||
| chr8:36820614 | G | GA | 7 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106+2867dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36820614 | ||||||
| chr8:36820614 | GA | G | 50 | a0001c0002t0001g0268 a0001c0004t0001g0002 a0001c0004t0001g0008 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106+2867delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36820614 | ||||||
| chr8:36820816 | G | A | 2 | a0003c0003t0001g0074 a0003c0003t0001g0075 |
2 | NA18952.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1106+3056G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36820816 | |||||||
| chr8:36821103 | T | G | 2 | a0002c0001t0001g0039 a0007c0010t0001g0022 |
2 | NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1106+3343T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821103 | |||||||
| chr8:36821186 | A | G | 4 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+3426A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821186 | |||||||
| chr8:36821322 | G | A | 3 | a0002c0001t0001g0029 a0002c0001t0001g0031 a0002c0001t0001g0037 |
3 | HG01074.hp2 HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1106+3562G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821322 | |||||||
| chr8:36821347 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1106+3587G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821347 | |||||||
| chr8:36821834 | C | CTT | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1106+4075_1106+407 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36821834 | ||||||
| chr8:36821917 | C | T | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+4157C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821917 | |||||||
| chr8:36821926 | G | A | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1106+4166G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36821926 | |||||||
| chr8:36822178 | T | C | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1106+4418T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822178 | |||||||
| chr8:36822233 | T | TGTATGTA others(26): Show |
4 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0003c0003t0001g0230 others(1): Show |
4 | HG00438.hp2 HG02132.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106+4482_1106+451 others(37): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36822233 | ||||||
| chr8:36822263 | A | G | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1106+4503A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822263 | |||||||
| chr8:36822295 | T | C | 142 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(139): Show |
145 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1106+4535T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822295 | |||||||
| chr8:36822840 | C | A | 1 | a0002c0001t0001g0107 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1106+5080C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36822840 | |||||||
| chr8:36823046 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1106+5286G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823046 | |||||||
| chr8:36823211 | C | T | 3 | a0002c0001t0001g0058 a0002c0001t0001g0059 a0002c0001t0001g0060 |
3 | NA18984.hp2 NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1106+5451C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823211 | |||||||
| chr8:36823223 | A | G | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+5463A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823223 | |||||||
| chr8:36823353 | T | G | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106+5593T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823353 | |||||||
| chr8:36823463 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1106+5703T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823463 | |||||||
| chr8:36823835 | C | A | 1 | a0001c0002t0001g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1106+6075C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823835 | |||||||
| chr8:36823836 | C | CT | 42 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(39): Show |
44 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1106+6094dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36823836 | ||||||
| chr8:36823836 | C | CTT | 8 | a0001c0004t0001g0158 a0001c0004t0001g0159 a0001c0004t0001g0160 others(5): Show |
8 | HG01358.hp2 HG02258.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106+6093_1106+609 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36823836 | ||||||
| chr8:36823836 | CT | C | 93 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(90): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1106+6094delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36823836 | ||||||
| chr8:36823838 | T | C | 1 | a0001c0002t0001g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1106+6078T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823838 | |||||||
| chr8:36823922 | C | T | 1 | a0003c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1106+6162C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36823922 | |||||||
| chr8:36824000 | A | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1106+6240A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824000 | |||||||
| chr8:36824084 | G | A | 1 | a0001c0004t0001g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1106+6324G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824084 | |||||||
| chr8:36824247 | G | A | 1 | a0002c0001t0001g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1106+6487G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824247 | |||||||
| chr8:36824363 | G | A | 3 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0003c0003t0001g0181 |
3 | HG02965.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1106+6603G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824363 | |||||||
| chr8:36824528 | G | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106+6768G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824528 | |||||||
| chr8:36824665 | A | G | 2 | a0002c0001t0001g0131 a0002c0001t0001g0132 |
2 | NA18945.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1106+6905A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824665 | |||||||
| chr8:36824716 | C | G | 50 | a0001c0002t0001g0143 a0001c0002t0001g0186 a0001c0002t0001g0282 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106+6956C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824716 | |||||||
| chr8:36824739 | T | A | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1106+6979T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824739 | |||||||
| chr8:36824819 | T | C | 2 | a0002c0001t0001g0102 a0003c0003t0001g0101 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1106+7059T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824819 | |||||||
| chr8:36824941 | T | C | 1 | a0002c0001t0001g0031 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1106+7181T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824941 | |||||||
| chr8:36824966 | G | A | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1106+7206G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824966 | |||||||
| chr8:36824979 | T | C | 1 | a0002c0001t0001g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1106+7219T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36824979 | |||||||
| chr8:36825031 | G | T | 2 | a0001c0002t0001g0014 a0002c0001t0001g0028 |
2 | HG01074.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1106+7271G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825031 | |||||||
| chr8:36825035 | G | A | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1106+7275G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825035 | |||||||
| chr8:36825071 | C | G | 2 | a0001c0002t0001g0237 a0001c0002t0001g0265 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1106+7311C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825071 | |||||||
| chr8:36825153 | A | C | 1 | a0001c0002t0001g0268 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1106+7393A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825153 | |||||||
| chr8:36825504 | C | T | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106+7744C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825504 | |||||||
| chr8:36825516 | A | ATTG | 50 | a0001c0002t0001g0143 a0001c0002t0001g0186 a0001c0002t0001g0282 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1106+7758_1106+775 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36825516 | ||||||
| chr8:36825559 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1106+7799A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825559 | |||||||
| chr8:36825692 | A | G | 3 | a0003c0003t0001g0077 a0003c0003t0001g0081 a0003c0003t0001g0082 |
3 | HG01496.hp2 HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1107-7862A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825692 | |||||||
| chr8:36825960 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-7594T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36825960 | |||||||
| chr8:36826262 | C | T | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1107-7292C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826262 | |||||||
| chr8:36826266 | G | C | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1107-7288G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826266 | |||||||
| chr8:36826271 | C | G | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1107-7283C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826271 | |||||||
| chr8:36826272 | T | C | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1107-7282T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826272 | |||||||
| chr8:36826473 | G | C | 1 | a0003c0003t0001g0089 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1107-7081G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826473 | |||||||
| chr8:36826501 | C | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1107-7053C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826501 | |||||||
| chr8:36826718 | T | A | 4 | a0002c0001t0001g0029 a0002c0001t0001g0031 a0002c0001t0001g0037 others(1): Show |
4 | HG01074.hp2 HG01258.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107-6836T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826718 | |||||||
| chr8:36826719 | A | T | 1 | a0007c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1107-6835A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826719 | |||||||
| chr8:36826727 | T | G | 1 | a0001c0002t0001g0122 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1107-6827T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826727 | |||||||
| chr8:36826934 | G | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-6620G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826934 | |||||||
| chr8:36826975 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-6579C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36826975 | |||||||
| chr8:36827152 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1107-6402G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827152 | |||||||
| chr8:36827274 | T | C | 1 | a0002c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1107-6280T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827274 | |||||||
| chr8:36827531 | T | C | 39 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0167 others(36): Show |
41 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1107-6023T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827531 | |||||||
| chr8:36827838 | A | T | 50 | a0001c0002t0001g0143 a0001c0002t0001g0186 a0001c0002t0001g0282 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1107-5716A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827838 | |||||||
| chr8:36827843 | A | T | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1107-5711A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827843 | |||||||
| chr8:36827983 | A | C | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1107-5571A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36827983 | |||||||
| chr8:36828566 | G | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-4988G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828566 | |||||||
| chr8:36828618 | T | C | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1107-4936T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828618 | |||||||
| chr8:36828636 | C | T | 1 | a0003c0003t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1107-4918C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828636 | |||||||
| chr8:36828780 | G | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-4774G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828780 | |||||||
| chr8:36828825 | G | T | 45 | a0001c0002t0001g0051 a0001c0002t0001g0108 a0001c0002t0001g0122 others(42): Show |
45 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1107-4729G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828825 | |||||||
| chr8:36828858 | T | C | 1 | a0004c0015t0001g0248 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1107-4696T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36828858 | |||||||
| chr8:36829146 | G | A | 50 | a0001c0002t0001g0143 a0001c0002t0001g0186 a0001c0002t0001g0282 others(47): Show |
52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1107-4408G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829146 | |||||||
| chr8:36829348 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-4206T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829348 | |||||||
| chr8:36829397 | T | C | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107-4157T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829397 | |||||||
| chr8:36829405 | G | A | 1 | a0001c0017t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1107-4149G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829405 | |||||||
| chr8:36829486 | A | G | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1107-4068A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829486 | |||||||
| chr8:36829499 | T | A | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1107-4055T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829499 | |||||||
| chr8:36829572 | A | AT | 49 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(46): Show |
51 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1107-3973dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 36829572 | ||||||
| chr8:36829738 | T | C | 1 | a0002c0001t0001g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1107-3816T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829738 | |||||||
| chr8:36829775 | G | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1107-3779G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829775 | |||||||
| chr8:36829800 | T | A | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1107-3754T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829800 | |||||||
| chr8:36829890 | T | C | 2 | a0001c0002t0001g0237 a0001c0002t0001g0265 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1107-3664T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829890 | |||||||
| chr8:36829962 | A | G | 45 | a0001c0002t0001g0051 a0001c0002t0001g0108 a0001c0002t0001g0122 others(42): Show |
45 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1107-3592A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36829962 | |||||||
| chr8:36830142 | T | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-3412T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830142 | |||||||
| chr8:36830443 | C | A | 1 | a0002c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1107-3111C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830443 | |||||||
| chr8:36830443 | C | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1107-3111C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830443 | |||||||
| chr8:36830444 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-3110G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830444 | |||||||
| chr8:36830496 | C | T | 3 | a0003c0003t0001g0077 a0003c0003t0001g0081 a0003c0003t0001g0082 |
3 | HG01496.hp2 HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1107-3058C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830496 | |||||||
| chr8:36830529 | T | C | 3 | a0002c0001t0001g0024 a0002c0001t0001g0088 a0003c0003t0001g0023 |
3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1107-3025T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830529 | |||||||
| chr8:36830601 | G | T | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1107-2953G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830601 | |||||||
| chr8:36830631 | G | A | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1107-2923G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830631 | |||||||
| chr8:36830755 | T | A | 1 | a0002c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1107-2799T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830755 | |||||||
| chr8:36830755 | T | G | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1107-2799T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830755 | |||||||
| chr8:36830891 | G | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-2663G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36830891 | |||||||
| chr8:36831028 | G | A | 1 | a0001c0017t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1107-2526G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831028 | |||||||
| chr8:36831056 | A | G | 62 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1107-2498A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831056 | |||||||
| chr8:36831207 | C | T | 6 | a0003c0003t0001g0006 a0003c0003t0001g0026 a0003c0003t0001g0032 others(3): Show |
6 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107-2347C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831207 | |||||||
| chr8:36831297 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-2257T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831297 | |||||||
| chr8:36831306 | T | C | 1 | a0001c0002t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1107-2248T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831306 | |||||||
| chr8:36831329 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
2 | HG03704.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1107-2225G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831329 | |||||||
| chr8:36831350 | G | C | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1107-2204G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831350 | |||||||
| chr8:36831513 | T | C | 1 | a0003c0005t0001g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1107-2041T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831513 | |||||||
| chr8:36831520 | C | T | 1 | a0001c0002t0001g0263 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1107-2034C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831520 | |||||||
| chr8:36831585 | T | C | 1 | a0003c0003t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1107-1969T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831585 | |||||||
| chr8:36831586 | G | A | 1 | a0003c0003t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1107-1968G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831586 | |||||||
| chr8:36831663 | T | A | 1 | a0001c0002t0001g0241 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1107-1891T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831663 | |||||||
| chr8:36831683 | T | C | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1107-1871T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831683 | |||||||
| chr8:36831734 | C | A | 1 | a0001c0002t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1107-1820C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831734 | |||||||
| chr8:36831875 | G | A | 1 | a0001c0004t0001g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1107-1679G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831875 | |||||||
| chr8:36831917 | G | A | 145 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(142): Show |
148 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1107-1637G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831917 | |||||||
| chr8:36831973 | A | C | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1107-1581A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36831973 | |||||||
| chr8:36832036 | G | A | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1107-1518G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832036 | |||||||
| chr8:36832311 | C | T | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1107-1243C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832311 | |||||||
| chr8:36832805 | C | T | 127 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1107-749C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832805 | |||||||
| chr8:36832868 | A | G | 37 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0167 others(34): Show |
39 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1107-686A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832868 | |||||||
| chr8:36832878 | G | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1107-676G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832878 | |||||||
| chr8:36832896 | G | T | 1 | a0003c0003t0001g0146 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1107-658G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36832896 | |||||||
| chr8:36833082 | C | G | 1 | a0002c0001t0001g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1107-472C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833082 | |||||||
| chr8:36833131 | T | G | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107-423T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833131 | |||||||
| chr8:36833314 | A | T | 2 | a0002c0001t0001g0024 a0003c0003t0001g0023 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1107-240A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833314 | |||||||
| chr8:36833403 | A | G | 1 | a0003c0003t0001g0017 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1107-151A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 10/26 | chr8 | 36833403 | |||||||
| chr8:36833671 | C | T | 143 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1212+12C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36833671 | |||||||
| chr8:36833873 | A | G | 3 | a0001c0004t0001g0158 a0001c0004t0001g0159 a0001c0004t0001g0160 |
3 | NA18944.hp1 NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1212+214A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36833873 | |||||||
| chr8:36833965 | C | A | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1212+306C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36833965 | |||||||
| chr8:36834041 | A | G | 1 | a0007c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1212+382A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834041 | |||||||
| chr8:36834082 | A | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1212+423A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834082 | |||||||
| chr8:36834123 | C | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212+464C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834123 | |||||||
| chr8:36834293 | C | G | 2 | a0001c0002t0001g0237 a0001c0002t0001g0265 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1213-493C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834293 | |||||||
| chr8:36834548 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1213-238T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834548 | |||||||
| chr8:36834601 | C | T | 3 | a0002c0001t0001g0131 a0002c0001t0001g0132 a0002c0001t0001g0140 |
3 | NA18945.hp2 NA19001.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1213-185C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 11/26 | chr8 | 36834601 | |||||||
| chr8:36834898 | G | T | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1295+30G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36834898 | |||||||
| chr8:36834997 | G | A | 2 | a0001c0002t0001g0165 a0001c0002t0001g0166 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1295+129G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36834997 | |||||||
| chr8:36835121 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1295+253C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835121 | |||||||
| chr8:36835205 | T | C | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1295+337T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835205 | |||||||
| chr8:36835274 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1295+406G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835274 | |||||||
| chr8:36835282 | A | T | 5 | a0002c0001t0001g0070 a0002c0001t0001g0071 a0002c0001t0001g0080 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295+414A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835282 | |||||||
| chr8:36835348 | C | CTTTTCT | 47 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(44): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1295+484_1295+485i others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr8 | 36835348 | ||||||
| chr8:36835576 | G | C | 6 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1295+708G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835576 | |||||||
| chr8:36835631 | C | T | 4 | a0001c0002t0001g0236 a0001c0002t0001g0262 a0001c0002t0001g0267 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296-665C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835631 | |||||||
| chr8:36835664 | A | T | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1296-632A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835664 | |||||||
| chr8:36835706 | T | A | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1296-590T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835706 | |||||||
| chr8:36835954 | C | A | 1 | a0002c0007t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1296-342C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835954 | |||||||
| chr8:36835976 | T | A | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1296-320T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 12/26 | chr8 | 36835976 | |||||||
| chr8:36836440 | G | T | 1 | a0002c0001t0001g0178 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1365+75G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 13/26 | chr8 | 36836440 | |||||||
| chr8:36836660 | C | A | 1 | a0001c0004t0001g0224 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1366-133C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 13/26 | chr8 | 36836660 | |||||||
| chr8:36836962 | C | A | 52 | a0001c0002t0001g0143 a0001c0002t0001g0156 a0001c0002t0001g0157 others(49): Show |
54 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1518+17C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36836962 | |||||||
| chr8:36837433 | C | A | 2 | a0001c0002t0001g0014 a0002c0001t0001g0028 |
2 | HG01074.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1518+488C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837433 | |||||||
| chr8:36837466 | C | T | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+521C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837466 | |||||||
| chr8:36837563 | G | A | 8 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+618G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837563 | |||||||
| chr8:36837590 | T | G | 1 | a0001c0002t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1518+645T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837590 | |||||||
| chr8:36837639 | C | T | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1518+694C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837639 | |||||||
| chr8:36837852 | A | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1518+907A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837852 | |||||||
| chr8:36837867 | A | G | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1518+922A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837867 | |||||||
| chr8:36837900 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1518+955G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837900 | |||||||
| chr8:36837905 | TTCCTC | T | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1518+962_1518+966d others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr8 | 36837905 | ||||||
| chr8:36837931 | C | T | 1 | a0003c0003t0001g0103 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1518+986C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36837931 | |||||||
| chr8:36838116 | G | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1518+1171G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838116 | |||||||
| chr8:36838180 | G | A | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518+1235G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838180 | |||||||
| chr8:36838218 | G | A | 1 | a0002c0001t0001g0123 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1518+1273G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838218 | |||||||
| chr8:36838304 | T | C | 4 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518+1359T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838304 | |||||||
| chr8:36838325 | A | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1518+1380A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838325 | |||||||
| chr8:36838538 | T | C | 1 | a0001c0002t0001g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1518+1593T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838538 | |||||||
| chr8:36838636 | G | T | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1518+1691G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838636 | |||||||
| chr8:36838675 | C | T | 6 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518+1730C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36838675 | |||||||
| chr8:36839058 | T | G | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1519-1405T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839058 | |||||||
| chr8:36839101 | C | G | 2 | a0001c0002t0001g0260 a0001c0002t0001g0261 |
2 | HG02523.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1519-1362C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839101 | |||||||
| chr8:36839125 | C | T | 2 | a0002c0001t0001g0024 a0003c0003t0001g0023 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1519-1338C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839125 | |||||||
| chr8:36839135 | A | G | 1 | a0001c0002t0001g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1519-1328A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839135 | |||||||
| chr8:36839353 | C | A | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1519-1110C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839353 | |||||||
| chr8:36839473 | G | A | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1519-990G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839473 | |||||||
| chr8:36839639 | C | T | 1 | a0003c0003t0001g0096 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1519-824C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839639 | |||||||
| chr8:36839761 | G | T | 50 | a0001c0002t0001g0018 a0002c0001t0001g0004 a0002c0001t0001g0016 others(47): Show |
52 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1519-702G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839761 | |||||||
| chr8:36839788 | A | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1519-675A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839788 | |||||||
| chr8:36839885 | G | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1519-578G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36839885 | |||||||
| chr8:36840266 | T | C | 3 | a0001c0002t0001g0274 a0001c0002t0001g0275 a0001c0002t0001g0276 |
3 | HG01167.hp2 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1519-197T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 14/26 | chr8 | 36840266 | |||||||
| chr8:36840652 | A | G | 1 | a0002c0016t0001g0223 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1631+77A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840652 | |||||||
| chr8:36840671 | A | C | 1 | a0001c0004t0001g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1631+96A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840671 | |||||||
| chr8:36840687 | G | A | 4 | a0002c0001t0001g0104 a0002c0001t0001g0110 a0002c0001t0001g0133 others(1): Show |
4 | HG01928.hp1 HG01981.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631+112G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840687 | |||||||
| chr8:36840915 | C | T | 1 | a0002c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1632-17C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 15/26 | chr8 | 36840915 | |||||||
| chr8:36841034 | G | GT | 68 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1703+53dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841034 | ||||||
| chr8:36841034 | G | T | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1703+31G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841034 | |||||||
| chr8:36841034 | GT | G | 20 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(17): Show |
20 | HG01081.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1703+53delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841034 | ||||||
| chr8:36841053 | TTTTC | T | 43 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0158 others(40): Show |
45 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1703+51_1703+54del others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841053 | |||||||
| chr8:36841055 | TTC | T | 9 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0171 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1703+53_1703+54del others(2): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841055 | |||||||
| chr8:36841057 | C | T | 1 | a0001c0004t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1703+54C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841057 | |||||||
| chr8:36841236 | C | T | 47 | a0001c0004t0001g0002 a0001c0004t0001g0008 a0001c0004t0001g0158 others(44): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1703+233C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841236 | |||||||
| chr8:36841467 | G | A | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1703+464G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841467 | |||||||
| chr8:36841785 | T | C | 4 | a0002c0001t0001g0070 a0002c0001t0001g0071 a0002c0007t0001g0069 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1703+782T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841785 | |||||||
| chr8:36841910 | A | C | 16 | a0001c0002t0001g0122 a0002c0001t0001g0015 a0002c0001t0001g0107 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.1703+907A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36841910 | |||||||
| chr8:36841978 | T | TA | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1703+985dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841978 | ||||||
| chr8:36841978 | TA | T | 10 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1703+985delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36841978 | ||||||
| chr8:36842045 | G | C | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1703+1042G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842045 | |||||||
| chr8:36842207 | A | G | 7 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1703+1204A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842207 | |||||||
| chr8:36842369 | A | T | 10 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0171 others(7): Show |
10 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1703+1366A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842369 | |||||||
| chr8:36842430 | C | G | 2 | a0001c0004t0001g0190 a0001c0004t0001g0197 |
2 | NA18963.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1703+1427C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842430 | |||||||
| chr8:36842637 | C | T | 3 | a0002c0001t0001g0066 a0002c0001t0001g0068 a0003c0003t0001g0067 |
3 | HG02559.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1703+1634C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842637 | |||||||
| chr8:36842688 | G | C | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1703+1685G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36842688 | |||||||
| chr8:36843112 | G | A | 1 | a0002c0001t0001g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1703+2109G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843112 | |||||||
| chr8:36843278 | G | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1703+2275G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843278 | |||||||
| chr8:36843356 | T | C | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1704-2224T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843356 | |||||||
| chr8:36843360 | C | A | 1 | a0001c0002t0001g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1704-2220C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843360 | |||||||
| chr8:36843387 | C | A | 58 | a0001c0002t0001g0143 a0001c0002t0001g0156 a0001c0002t0001g0157 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1704-2193C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843387 | |||||||
| chr8:36843562 | T | C | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1704-2018T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843562 | |||||||
| chr8:36843638 | T | A | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1704-1942T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843638 | |||||||
| chr8:36843818 | C | T | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1704-1762C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36843818 | |||||||
| chr8:36844067 | C | A | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1704-1513C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844067 | |||||||
| chr8:36844080 | A | T | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1704-1500A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844080 | |||||||
| chr8:36844087 | T | C | 126 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(123): Show |
129 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1704-1493T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844087 | |||||||
| chr8:36844268 | T | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1704-1312T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844268 | |||||||
| chr8:36844374 | C | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1704-1206C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844374 | |||||||
| chr8:36844376 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1704-1204G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844376 | |||||||
| chr8:36844390 | C | CA | 14 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0171 others(11): Show |
14 | HG02055.hp1 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1704-1180dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36844390 | ||||||
| chr8:36844394 | A | AC | 48 | a0001c0002t0001g0143 a0001c0004t0001g0002 a0001c0004t0001g0008 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1704-1186_1704-118 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844394 | |||||||
| chr8:36844396 | A | AT | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1704-1184_1704-118 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844396 | |||||||
| chr8:36844402 | G | T | 1 | a0002c0001t0001g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1704-1178G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844402 | |||||||
| chr8:36844521 | A | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1704-1059A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36844521 | |||||||
| chr8:36845038 | C | T | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1704-542C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845038 | |||||||
| chr8:36845092 | G | A | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1704-488G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845092 | |||||||
| chr8:36845093 | C | G | 67 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1704-487C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845093 | |||||||
| chr8:36845401 | TCAAA | T | 7 | a0001c0004t0001g0158 a0001c0004t0001g0159 a0001c0004t0001g0160 others(4): Show |
7 | HG01358.hp2 HG02258.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1704-174_1704-171d others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 36845401 | ||||||
| chr8:36845505 | T | G | 16 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1704-75T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 16/26 | chr8 | 36845505 | |||||||
| chr8:36846137 | A | T | 9 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891+238A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846137 | |||||||
| chr8:36846169 | G | A | 5 | a0001c0004t0001g0002 a0001c0004t0001g0199 a0001c0004t0001g0201 others(2): Show |
7 | HG00558.hp2 HG00597.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1891+270G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846169 | |||||||
| chr8:36846326 | C | G | 4 | a0001c0002t0001g0187 a0001c0002t0001g0280 a0001c0002t0001g0281 others(1): Show |
4 | HG01109.hp2 HG02257.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891+427C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846326 | |||||||
| chr8:36846405 | T | G | 2 | a0002c0001t0001g0104 a0002c0001t0001g0110 |
2 | HG01928.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1891+506T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846405 | |||||||
| chr8:36846524 | T | C | 282 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(279): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1891+625T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846524 | |||||||
| chr8:36846532 | G | A | 1 | a0003c0003t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1891+633G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846532 | |||||||
| chr8:36846671 | G | A | 7 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891+772G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846671 | |||||||
| chr8:36846764 | G | A | 1 | a0001c0004t0001g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1891+865G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846764 | |||||||
| chr8:36846788 | G | GA | 16 | a0001c0002t0001g0051 a0001c0002t0001g0257 a0001c0006t0001g0177 others(13): Show |
16 | HG01496.hp2 HG01515.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1891+907dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36846788 | ||||||
| chr8:36846788 | G | GAA | 111 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(108): Show |
114 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1891+906_1891+907d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36846788 | ||||||
| chr8:36846788 | G | GAAA | 8 | a0001c0002t0001g0172 a0001c0002t0001g0186 a0001c0002t0001g0282 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1891+905_1891+907d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36846788 | ||||||
| chr8:36846811 | G | A | 3 | a0002c0001t0001g0102 a0003c0003t0001g0100 a0003c0003t0001g0101 |
3 | HG03139.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1891+912G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846811 | |||||||
| chr8:36846877 | A | T | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1891+978A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846877 | |||||||
| chr8:36846927 | G | A | 4 | a0001c0002t0001g0108 a0002c0001t0001g0093 a0002c0001t0001g0134 others(1): Show |
4 | NA18612.hp1 NA18969.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891+1028G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36846927 | |||||||
| chr8:36847299 | A | G | 1 | a0002c0001t0001g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1891+1400A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847299 | |||||||
| chr8:36847355 | T | G | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1891+1456T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847355 | |||||||
| chr8:36847379 | C | A | 1 | a0001c0002t0001g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1891+1480C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847379 | |||||||
| chr8:36847776 | C | T | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1891+1877C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847776 | |||||||
| chr8:36847791 | A | G | 1 | a0001c0002t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1891+1892A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847791 | |||||||
| chr8:36847881 | T | A | 1 | a0003c0003t0001g0081 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1891+1982T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36847881 | |||||||
| chr8:36848165 | C | A | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1891+2266C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848165 | |||||||
| chr8:36848173 | T | A | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1891+2274T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848173 | |||||||
| chr8:36848254 | G | A | 7 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891+2355G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848254 | |||||||
| chr8:36848817 | A | C | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1891+2918A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36848817 | |||||||
| chr8:36849040 | T | C | 1 | a0001c0002t0001g0263 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1891+3141T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849040 | |||||||
| chr8:36849132 | A | G | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1891+3233A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849132 | |||||||
| chr8:36849182 | A | T | 134 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(131): Show |
137 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1891+3283A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849182 | |||||||
| chr8:36849265 | T | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1891+3366T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849265 | |||||||
| chr8:36849418 | G | A | 10 | a0002c0001t0001g0102 a0003c0003t0001g0006 a0003c0003t0001g0026 others(7): Show |
10 | HG02280.hp2 HG02630.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1891+3519G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849418 | |||||||
| chr8:36849698 | A | G | 1 | a0001c0004t0001g0215 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1891+3799A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849698 | |||||||
| chr8:36849791 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1891+3892G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849791 | |||||||
| chr8:36849905 | A | G | 1 | a0001c0002t0001g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1891+4006A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849905 | |||||||
| chr8:36849925 | C | T | 3 | a0002c0001t0001g0024 a0002c0001t0001g0088 a0003c0003t0001g0023 |
3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1891+4026C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36849925 | |||||||
| chr8:36850123 | A | G | 2 | a0002c0001t0001g0027 a0002c0001t0001g0052 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1891+4224A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850123 | |||||||
| chr8:36850133 | A | T | 1 | a0001c0004t0001g0201 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1891+4234A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850133 | |||||||
| chr8:36850159 | G | T | 48 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(45): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1891+4260G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850159 | |||||||
| chr8:36850403 | C | T | 135 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1891+4504C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850403 | |||||||
| chr8:36850455 | C | CT | 121 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1891+4570dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36850455 | ||||||
| chr8:36850536 | A | G | 1 | a0002c0001t0001g0178 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1891+4637A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850536 | |||||||
| chr8:36850590 | G | T | 2 | a0001c0002t0001g0275 a0001c0002t0001g0276 |
2 | HG01167.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1891+4691G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850590 | |||||||
| chr8:36850672 | T | G | 135 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1891+4773T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850672 | |||||||
| chr8:36850737 | A | G | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1891+4838A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36850737 | |||||||
| chr8:36851368 | T | TTCCCTTC others(4): Show |
1 | a0002c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1891+5472_1891+548 others(15): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851368 | ||||||
| chr8:36851373 | T | TTC | 27 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0054 others(24): Show |
27 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1891+5486_1891+548 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | ||||||
| chr8:36851373 | T | TTCTC | 20 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0172 others(17): Show |
20 | HG00673.hp1 HG01243.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.1891+5484_1891+548 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | ||||||
| chr8:36851373 | T | TTCTCTC | 34 | a0001c0002t0001g0051 a0001c0002t0001g0061 a0001c0002t0001g0073 others(31): Show |
36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1891+5482_1891+548 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | ||||||
| chr8:36851373 | T | TTCTCTCT others(1): Show |
12 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0163 others(9): Show |
13 | HG01169.hp1 HG01358.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1891+5480_1891+548 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | ||||||
| chr8:36851373 | T | TTCTCTCT others(3): Show |
6 | a0001c0002t0001g0235 a0001c0002t0001g0262 a0001c0002t0001g0263 others(3): Show |
6 | HG01433.hp2 HG02080.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891+5478_1891+548 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | ||||||
| chr8:36851373 | T | TTCTCTCT others(5): Show |
1 | a0001c0002t0001g0272 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1891+5476_1891+548 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851373 | ||||||
| chr8:36851381 | CTCTCTA | C | 3 | a0001c0002t0001g0014 a0001c0002t0001g0174 a0001c0002t0001g0176 |
3 | HG01074.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1891+5488_1891+549 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851381 | ||||||
| chr8:36851385 | CTA | C | 4 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0228 others(1): Show |
4 | HG01109.hp2 HG02165.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891+5488_1891+548 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851385 | ||||||
| chr8:36851387 | A | ATC | 8 | a0001c0002t0001g0143 a0002c0001t0001g0027 a0002c0001t0001g0052 others(5): Show |
8 | HG02004.hp1 HG02109.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1891+5512_1891+551 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851387 | ||||||
| chr8:36851387 | A | ATCTC | 8 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1891+5510_1891+551 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36851387 | ||||||
| chr8:36851387 | A | C | 113 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0049 others(110): Show |
116 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1891+5488A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851387 | |||||||
| chr8:36851387 | A | G | 4 | a0002c0001t0001g0093 a0002c0001t0001g0134 a0002c0001t0001g0135 others(1): Show |
4 | HG04184.hp2 NA18969.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1891+5488A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851387 | |||||||
| chr8:36851469 | A | G | 2 | a0001c0002t0001g0164 a0001c0002t0001g0256 |
2 | NA19086.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1891+5570A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851469 | |||||||
| chr8:36851493 | G | C | 133 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(130): Show |
136 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1891+5594G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851493 | |||||||
| chr8:36851587 | G | A | 1 | a0003c0005t0001g0213 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1891+5688G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851587 | |||||||
| chr8:36851656 | T | C | 121 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1891+5757T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36851656 | |||||||
| chr8:36852112 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1891+6213G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852112 | |||||||
| chr8:36852423 | A | G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1891+6524A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852423 | |||||||
| chr8:36852492 | G | A | 1 | a0002c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1891+6593G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852492 | |||||||
| chr8:36852623 | A | G | 65 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1891+6724A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852623 | |||||||
| chr8:36852700 | T | C | 2 | a0002c0001t0001g0012 a0002c0001t0001g0013 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1891+6801T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852700 | |||||||
| chr8:36852849 | T | A | 1 | a0002c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1891+6950T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36852849 | |||||||
| chr8:36853112 | G | A | 1 | a0007c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1891+7213G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853112 | |||||||
| chr8:36853516 | A | G | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1891+7617A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853516 | |||||||
| chr8:36853714 | C | A | 1 | a0002c0001t0001g0118 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1891+7815C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853714 | |||||||
| chr8:36853865 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1891+7966C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36853865 | |||||||
| chr8:36854025 | C | T | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1891+8126C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854025 | |||||||
| chr8:36854114 | G | A | 121 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1891+8215G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854114 | |||||||
| chr8:36854139 | T | A | 1 | a0001c0002t0001g0270 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1891+8240T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854139 | |||||||
| chr8:36854139 | T | G | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1891+8240T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854139 | |||||||
| chr8:36854289 | T | C | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1891+8390T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854289 | |||||||
| chr8:36854377 | G | A | 2 | a0002c0001t0001g0234 a0004c0015t0001g0248 |
2 | HG00621.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1891+8478G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854377 | |||||||
| chr8:36854390 | G | T | 1 | a0002c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1891+8491G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854390 | |||||||
| chr8:36854472 | C | CT | 130 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(127): Show |
133 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1891+8587dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36854472 | ||||||
| chr8:36854501 | G | C | 1 | a0001c0002t0001g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1891+8602G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854501 | |||||||
| chr8:36854922 | C | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1891+9023C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36854922 | |||||||
| chr8:36855024 | C | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1891+9125C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855024 | |||||||
| chr8:36855344 | C | T | 3 | a0002c0001t0001g0104 a0002c0001t0001g0110 a0002c0001t0001g0133 |
3 | HG01928.hp1 HG01981.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1892-9060C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855344 | |||||||
| chr8:36855421 | G | A | 1 | a0003c0003t0001g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1892-8983G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855421 | |||||||
| chr8:36855563 | T | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-8841T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855563 | |||||||
| chr8:36855629 | G | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-8775G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855629 | |||||||
| chr8:36855646 | G | C | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1892-8758G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855646 | |||||||
| chr8:36855652 | G | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0218 |
2 | HG02015.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1892-8752G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855652 | |||||||
| chr8:36855739 | C | T | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1892-8665C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855739 | |||||||
| chr8:36855740 | G | A | 1 | a0002c0001t0001g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1892-8664G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855740 | |||||||
| chr8:36855841 | T | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-8563T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36855841 | |||||||
| chr8:36856073 | A | C | 7 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0242 others(4): Show |
7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892-8331A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856073 | |||||||
| chr8:36856159 | T | G | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1892-8245T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856159 | |||||||
| chr8:36856467 | T | G | 1 | a0002c0001t0001g0131 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1892-7937T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856467 | |||||||
| chr8:36856595 | AT | A | 132 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(129): Show |
135 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1892-7805delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36856595 | ||||||
| chr8:36856751 | C | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-7653C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856751 | |||||||
| chr8:36856801 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-7603C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856801 | |||||||
| chr8:36856947 | G | A | 7 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-7457G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856947 | |||||||
| chr8:36856991 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-7413C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36856991 | |||||||
| chr8:36857307 | C | G | 1 | a0002c0001t0001g0109 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1892-7097C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857307 | |||||||
| chr8:36857398 | G | C | 1 | a0002c0001t0001g0178 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1892-7006G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857398 | |||||||
| chr8:36857632 | G | GT | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1892-6765dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36857632 | ||||||
| chr8:36857722 | T | C | 1 | a0001c0002t0001g0266 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1892-6682T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857722 | |||||||
| chr8:36857775 | A | AGCTGGGA others(128): Show |
1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-6601_1892-660 others(139): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36857775 | ||||||
| chr8:36857804 | T | C | 132 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(129): Show |
135 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1892-6600T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857804 | |||||||
| chr8:36857939 | C | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1892-6465C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36857939 | |||||||
| chr8:36858176 | C | CA | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.1892-6205dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36858176 | ||||||
| chr8:36858176 | C | CAA | 51 | a0001c0002t0001g0061 a0001c0002t0001g0122 a0001c0002t0001g0143 others(48): Show |
51 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1892-6206_1892-620 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36858176 | ||||||
| chr8:36858176 | C | CAAA | 7 | a0001c0002t0001g0280 a0001c0006t0001g0177 a0001c0006t0001g0279 others(4): Show |
7 | HG00438.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-6207_1892-620 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36858176 | ||||||
| chr8:36858205 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-6199C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858205 | |||||||
| chr8:36858240 | A | C | 135 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1892-6164A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858240 | |||||||
| chr8:36858295 | A | T | 119 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(116): Show |
122 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1892-6109A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858295 | |||||||
| chr8:36858673 | C | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-5731C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858673 | |||||||
| chr8:36858853 | A | G | 1 | a0002c0001t0001g0109 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1892-5551A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858853 | |||||||
| chr8:36858889 | C | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-5515C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36858889 | |||||||
| chr8:36859078 | C | A | 2 | a0003c0003t0001g0079 a0003c0003t0001g0083 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1892-5326C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859078 | |||||||
| chr8:36859345 | T | A | 121 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1892-5059T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859345 | |||||||
| chr8:36859441 | C | T | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1892-4963C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859441 | |||||||
| chr8:36859449 | T | C | 6 | a0003c0003t0001g0001 a0003c0003t0001g0089 a0003c0003t0001g0090 others(3): Show |
8 | HG00609.hp1 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-4955T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859449 | |||||||
| chr8:36859451 | C | T | 1 | a0001c0002t0001g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1892-4953C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859451 | |||||||
| chr8:36859454 | A | T | 1 | a0001c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1892-4950A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859454 | |||||||
| chr8:36859484 | C | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1892-4920C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859484 | |||||||
| chr8:36859553 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1892-4851C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859553 | |||||||
| chr8:36859614 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1892-4790G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859614 | |||||||
| chr8:36859767 | T | C | 7 | a0002c0001t0001g0182 a0002c0001t0001g0183 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1892-4637T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859767 | |||||||
| chr8:36859821 | C | T | 3 | a0001c0002t0001g0014 a0001c0002t0001g0174 a0001c0002t0001g0175 |
3 | HG01074.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1892-4583C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859821 | |||||||
| chr8:36859888 | A | G | 4 | a0002c0001t0001g0093 a0002c0001t0001g0134 a0002c0001t0001g0135 others(1): Show |
4 | HG04184.hp2 NA18969.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1892-4516A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36859888 | |||||||
| chr8:36860081 | A | AT | 132 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(129): Show |
135 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1892-4315dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36860081 | ||||||
| chr8:36860108 | C | G | 2 | a0002c0001t0001g0027 a0002c0001t0001g0052 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1892-4296C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860108 | |||||||
| chr8:36860306 | T | C | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1892-4098T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860306 | |||||||
| chr8:36860429 | T | A | 1 | a0001c0002t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1892-3975T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860429 | |||||||
| chr8:36860481 | A | G | 7 | a0003c0003t0001g0001 a0003c0003t0001g0084 a0003c0003t0001g0089 others(4): Show |
9 | HG00609.hp1 HG01168.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.1892-3923A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860481 | |||||||
| chr8:36860485 | G | A | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1892-3919G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860485 | |||||||
| chr8:36860598 | G | A | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-3806G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860598 | |||||||
| chr8:36860655 | A | C | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1892-3749A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860655 | |||||||
| chr8:36860659 | C | T | 8 | a0002c0001t0001g0112 a0002c0001t0001g0118 a0002c0001t0001g0129 others(5): Show |
8 | HG00544.hp1 HG00558.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.1892-3745C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860659 | |||||||
| chr8:36860911 | C | CT | 6 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(3): Show |
6 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1892-3479dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 36860911 | ||||||
| chr8:36860974 | A | G | 1 | a0002c0001t0001g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1892-3430A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36860974 | |||||||
| chr8:36861035 | T | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-3369T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861035 | |||||||
| chr8:36861101 | C | A | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1892-3303C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861101 | |||||||
| chr8:36861102 | T | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1892-3302T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861102 | |||||||
| chr8:36861179 | T | C | 9 | a0002c0001t0001g0016 a0002c0001t0001g0019 a0002c0001t0001g0020 others(6): Show |
9 | HG01258.hp2 HG02004.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1892-3225T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861179 | |||||||
| chr8:36861235 | G | A | 124 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0047 others(121): Show |
127 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1892-3169G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861235 | |||||||
| chr8:36861484 | A | G | 125 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1892-2920A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861484 | |||||||
| chr8:36861509 | G | A | 1 | a0003c0005t0001g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1892-2895G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861509 | |||||||
| chr8:36861669 | A | G | 1 | a0003c0003t0001g0258 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1892-2735A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861669 | |||||||
| chr8:36861704 | G | A | 11 | a0001c0002t0001g0073 a0001c0002t0001g0162 a0001c0002t0001g0163 others(8): Show |
11 | HG02027.hp1 HG02071.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1892-2700G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36861704 | |||||||
| chr8:36862141 | G | A | 1 | a0001c0002t0001g0266 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1892-2263G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36862141 | |||||||
| chr8:36862915 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1892-1489G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36862915 | |||||||
| chr8:36863044 | T | G | 1 | a0001c0004t0001g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1892-1360T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863044 | |||||||
| chr8:36863093 | A | G | 1 | a0002c0001t0001g0052 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1892-1311A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863093 | |||||||
| chr8:36863233 | A | G | 6 | a0003c0003t0001g0001 a0003c0003t0001g0089 a0003c0003t0001g0090 others(3): Show |
8 | HG00609.hp1 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-1171A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863233 | |||||||
| chr8:36863683 | T | G | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-721T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863683 | |||||||
| chr8:36863773 | T | C | 2 | a0002c0016t0001g0223 a0003c0005t0001g0221 |
2 | NA19084.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1892-631T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863773 | |||||||
| chr8:36863931 | C | T | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1892-473C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36863931 | |||||||
| chr8:36864194 | A | G | 1 | a0001c0004t0001g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1892-210A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 18/26 | chr8 | 36864194 | |||||||
| chr8:36864529 | C | T | 1 | a0002c0001t0001g0106 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.2009+8C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36864529 | |||||||
| chr8:36864649 | A | G | 1 | a0001c0002t0001g0242 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2009+128A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36864649 | |||||||
| chr8:36864753 | T | C | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2009+232T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36864753 | |||||||
| chr8:36865013 | G | T | 1 | a0002c0001t0001g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2009+492G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865013 | |||||||
| chr8:36865024 | G | A | 118 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2009+503G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865024 | |||||||
| chr8:36865365 | A | G | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2009+844A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865365 | |||||||
| chr8:36865558 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+1037G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36865558 | |||||||
| chr8:36865610 | TA | T | 11 | a0001c0002t0001g0252 a0001c0006t0001g0177 a0001c0006t0001g0279 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2009+1105delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865610 | ||||||
| chr8:36865610 | TAA | T | 118 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2009+1104_2009+110 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865610 | ||||||
| chr8:36865773 | C | CA | 10 | a0001c0002t0001g0143 a0001c0002t0001g0289 a0001c0006t0001g0177 others(7): Show |
10 | HG01081.hp1 HG01109.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009+1277dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | ||||||
| chr8:36865773 | CA | C | 9 | a0001c0002t0001g0282 a0001c0006t0001g0286 a0002c0001t0001g0009 others(6): Show |
9 | HG00639.hp1 HG02004.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009+1277delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | ||||||
| chr8:36865773 | CAAAAA | C | 107 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(104): Show |
110 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2009+1273_2009+127 others(9): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | ||||||
| chr8:36865773 | CAAAAAA | C | 6 | a0001c0002t0001g0238 a0001c0002t0001g0241 a0001c0002t0001g0246 others(3): Show |
6 | HG01515.hp2 HG01978.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+1272_2009+127 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36865773 | ||||||
| chr8:36866114 | C | CTTA | 4 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+1599_2009+160 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36866114 | ||||||
| chr8:36866142 | G | A | 1 | a0003c0003t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2009+1621G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866142 | |||||||
| chr8:36866346 | A | G | 3 | a0002c0001t0001g0044 a0002c0007t0001g0046 a0002c0007t0001g0152 |
3 | HG02615.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2009+1825A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866346 | |||||||
| chr8:36866425 | C | T | 1 | a0001c0002t0001g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2009+1904C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866425 | |||||||
| chr8:36866652 | T | C | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2009+2131T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866652 | |||||||
| chr8:36866678 | A | G | 4 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+2157A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866678 | |||||||
| chr8:36866709 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2009+2188T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866709 | |||||||
| chr8:36866801 | G | A | 125 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2009+2280G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36866801 | |||||||
| chr8:36867011 | G | A | 2 | a0002c0001t0001g0027 a0002c0001t0001g0052 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2009+2490G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867011 | |||||||
| chr8:36867136 | T | C | 3 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0003c0003t0001g0230 |
3 | HG00438.hp2 HG02165.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2009+2615T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867136 | |||||||
| chr8:36867154 | A | C | 1 | a0003c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2009+2633A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867154 | |||||||
| chr8:36867239 | G | T | 6 | a0002c0001t0001g0016 a0002c0001t0001g0019 a0002c0001t0001g0020 others(3): Show |
6 | HG01258.hp2 HG02004.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+2718G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867239 | |||||||
| chr8:36867286 | C | G | 1 | a0002c0001t0001g0114 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2009+2765C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867286 | |||||||
| chr8:36867307 | T | C | 44 | a0002c0001t0001g0009 a0002c0001t0001g0012 a0002c0001t0001g0013 others(41): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2009+2786T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867307 | |||||||
| chr8:36867507 | T | C | 2 | a0001c0006t0001g0177 a0001c0018t0001g0179 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+2986T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867507 | |||||||
| chr8:36867613 | A | C | 125 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2009+3092A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867613 | |||||||
| chr8:36867645 | G | T | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2009+3124G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867645 | |||||||
| chr8:36867722 | A | G | 4 | a0001c0002t0001g0238 a0001c0002t0001g0251 a0001c0002t0001g0252 others(1): Show |
4 | HG00639.hp2 HG01978.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+3201A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36867722 | |||||||
| chr8:36868118 | G | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+3597G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868118 | |||||||
| chr8:36868296 | C | A | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2009+3775C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868296 | |||||||
| chr8:36868445 | T | C | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2009+3924T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868445 | |||||||
| chr8:36868635 | A | G | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2009+4114A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868635 | |||||||
| chr8:36868756 | A | T | 1 | a0001c0004t0001g0192 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2009+4235A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868756 | |||||||
| chr8:36868803 | C | T | 3 | a0001c0002t0001g0247 a0001c0002t0001g0262 a0001c0002t0001g0272 |
3 | HG01255.hp1 HG01433.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2009+4282C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36868803 | |||||||
| chr8:36869249 | G | A | 1 | a0001c0002t0001g0250 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2009+4728G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869249 | |||||||
| chr8:36869605 | T | G | 4 | a0003c0003t0001g0006 a0003c0003t0001g0026 a0003c0003t0001g0032 others(1): Show |
4 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+5084T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869605 | |||||||
| chr8:36869643 | A | G | 1 | a0001c0018t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2009+5122A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869643 | |||||||
| chr8:36869855 | G | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+5334G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36869855 | |||||||
| chr8:36870011 | A | C | 125 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2009+5490A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870011 | |||||||
| chr8:36870038 | C | A | 5 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+5517C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870038 | |||||||
| chr8:36870045 | G | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+5524G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870045 | |||||||
| chr8:36870090 | C | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+5569C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870090 | |||||||
| chr8:36870330 | C | T | 125 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2009+5809C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870330 | |||||||
| chr8:36870342 | G | A | 1 | a0001c0004t0001g0212 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2009+5821G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870342 | |||||||
| chr8:36870376 | C | G | 3 | a0002c0001t0001g0044 a0002c0007t0001g0046 a0002c0007t0001g0152 |
3 | HG02615.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2009+5855C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870376 | |||||||
| chr8:36870576 | G | T | 7 | a0003c0005t0001g0188 a0003c0005t0001g0195 a0003c0005t0001g0196 others(4): Show |
7 | HG00621.hp1 NA18953.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009+6055G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870576 | |||||||
| chr8:36870738 | G | A | 1 | a0002c0001t0001g0052 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2009+6217G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870738 | |||||||
| chr8:36870996 | G | A | 1 | a0003c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2009+6475G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36870996 | |||||||
| chr8:36871038 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2009+6517G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871038 | |||||||
| chr8:36871081 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2009+6560T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871081 | |||||||
| chr8:36871126 | A | C | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2009+6605A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871126 | |||||||
| chr8:36871390 | C | CAT | 111 | a0001c0002t0001g0014 a0001c0002t0001g0018 a0001c0002t0001g0047 others(108): Show |
113 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2009+6885_2009+688 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871390 | ||||||
| chr8:36871390 | C | CATAT | 3 | a0001c0002t0001g0176 a0001c0002t0001g0280 a0001c0002t0001g0281 |
3 | HG02257.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2009+6883_2009+688 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871390 | ||||||
| chr8:36871406 | T | TAC | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+6887_2009+688 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871406 | ||||||
| chr8:36871408 | C | T | 5 | a0001c0002t0001g0003 a0001c0002t0001g0164 a0001c0002t0001g0256 others(2): Show |
6 | HG01167.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2009+6887C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871408 | |||||||
| chr8:36871410 | T | TACATAG | 5 | a0001c0002t0001g0003 a0001c0002t0001g0164 a0001c0002t0001g0256 others(2): Show |
6 | HG01167.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2009+6890_2009+689 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871410 | ||||||
| chr8:36871410 | T | TAG | 59 | a0001c0002t0001g0018 a0001c0002t0001g0047 a0001c0002t0001g0048 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.2009+6904_2009+690 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36871410 | ||||||
| chr8:36871580 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2009+7059G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871580 | |||||||
| chr8:36871771 | C | T | 1 | a0001c0002t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2009+7250C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871771 | |||||||
| chr8:36871929 | C | G | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+7408C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36871929 | |||||||
| chr8:36872076 | T | C | 118 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2009+7555T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872076 | |||||||
| chr8:36872198 | A | G | 118 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2009+7677A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872198 | |||||||
| chr8:36872205 | C | A | 1 | a0002c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2009+7684C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872205 | |||||||
| chr8:36872291 | G | A | 44 | a0002c0001t0001g0009 a0002c0001t0001g0012 a0002c0001t0001g0013 others(41): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2009+7770G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872291 | |||||||
| chr8:36872338 | T | C | 8 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0242 others(5): Show |
8 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009+7817T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872338 | |||||||
| chr8:36872422 | C | T | 16 | a0002c0001t0001g0015 a0002c0001t0001g0107 a0002c0001t0001g0109 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.2009+7901C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872422 | |||||||
| chr8:36872496 | T | C | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+7975T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872496 | |||||||
| chr8:36872512 | A | G | 1 | a0003c0003t0001g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2009+7991A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36872512 | |||||||
| chr8:36873066 | C | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0288 a0001c0006t0001g0286 |
3 | HG01891.hp1 HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2009+8545C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873066 | |||||||
| chr8:36873098 | C | A | 169 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(166): Show |
172 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.2009+8577C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873098 | |||||||
| chr8:36873109 | A | G | 5 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+8588A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873109 | |||||||
| chr8:36873274 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2009+8753C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873274 | |||||||
| chr8:36873339 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2009+8818C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873339 | |||||||
| chr8:36873373 | A | G | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2009+8852A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873373 | |||||||
| chr8:36873486 | T | C | 1 | a0003c0003t0001g0087 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2009+8965T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873486 | |||||||
| chr8:36873561 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2009+9040A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873561 | |||||||
| chr8:36873600 | A | G | 1 | a0002c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2009+9079A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873600 | |||||||
| chr8:36873721 | G | A | 3 | a0002c0016t0001g0223 a0003c0005t0001g0221 a0003c0005t0001g0222 |
3 | HG02258.hp1 NA19084.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2009+9200G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873721 | |||||||
| chr8:36873807 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2009+9286A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36873807 | |||||||
| chr8:36874108 | C | G | 1 | a0003c0003t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2009+9587C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874108 | |||||||
| chr8:36874224 | G | A | 2 | a0002c0001t0001g0111 a0002c0001t0001g0121 |
2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2009+9703G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874224 | |||||||
| chr8:36874337 | C | A | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2009+9816C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874337 | |||||||
| chr8:36874378 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+9857C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874378 | |||||||
| chr8:36874571 | T | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+10050T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874571 | |||||||
| chr8:36874684 | A | T | 1 | a0002c0001t0001g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2009+10163A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874684 | |||||||
| chr8:36874724 | T | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+10203T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36874724 | |||||||
| chr8:36875013 | C | A | 1 | a0001c0002t0001g0073 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2009+10492C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875013 | |||||||
| chr8:36875040 | A | C | 1 | a0002c0001t0001g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2009+10519A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875040 | |||||||
| chr8:36875482 | A | G | 1 | a0002c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2009+10961A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875482 | |||||||
| chr8:36875637 | A | G | 1 | a0003c0003t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2009+11116A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875637 | |||||||
| chr8:36875911 | T | C | 3 | a0001c0002t0001g0241 a0001c0002t0001g0253 a0001c0002t0001g0268 |
3 | NA18942.hp1 NA18948.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2009+11390T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875911 | |||||||
| chr8:36875930 | G | A | 2 | a0003c0005t0001g0188 a0003c0005t0001g0196 |
2 | NA18980.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2009+11409G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36875930 | |||||||
| chr8:36876178 | C | T | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2009+11657C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876178 | |||||||
| chr8:36876185 | C | T | 1 | a0003c0003t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2009+11664C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876185 | |||||||
| chr8:36876202 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2009+11681T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876202 | |||||||
| chr8:36876341 | C | A | 3 | a0003c0003t0001g0006 a0003c0003t0001g0032 a0003c0003t0001g0033 |
3 | HG02280.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2009+11820C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876341 | |||||||
| chr8:36876630 | G | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+12109G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876630 | |||||||
| chr8:36876845 | T | C | 1 | a0003c0003t0001g0074 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2009+12324T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876845 | |||||||
| chr8:36876848 | G | A | 4 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+12327G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36876848 | |||||||
| chr8:36877036 | CTT | C | 3 | a0001c0002t0001g0280 a0001c0002t0001g0281 a0001c0009t0001g0168 |
3 | HG01109.hp2 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2009+12518_2009+12 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36877036 | ||||||
| chr8:36877089 | C | T | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2009+12568C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877089 | |||||||
| chr8:36877101 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2009+12580T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877101 | |||||||
| chr8:36877145 | A | G | 1 | a0003c0005t0001g0195 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2009+12624A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877145 | |||||||
| chr8:36877305 | G | GT | 6 | a0001c0002t0001g0061 a0001c0002t0001g0186 a0001c0002t0001g0282 others(3): Show |
6 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+12798dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36877305 | ||||||
| chr8:36877337 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2009+12816T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877337 | |||||||
| chr8:36877347 | G | T | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+12826G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877347 | |||||||
| chr8:36877410 | C | G | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2009+12889C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877410 | |||||||
| chr8:36877448 | G | A | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2009+12927G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877448 | |||||||
| chr8:36877719 | T | C | 125 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2009+13198T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877719 | |||||||
| chr8:36877845 | C | T | 1 | a0001c0002t0001g0261 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2009+13324C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36877845 | |||||||
| chr8:36878096 | T | C | 45 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(42): Show |
47 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2009+13575T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878096 | |||||||
| chr8:36878128 | A | G | 1 | a0001c0006t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2009+13607A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878128 | |||||||
| chr8:36878420 | C | G | 1 | a0003c0003t0001g0033 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2009+13899C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878420 | |||||||
| chr8:36878436 | A | C | 1 | a0003c0003t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2009+13915A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878436 | |||||||
| chr8:36878484 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2009+13963C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878484 | |||||||
| chr8:36878583 | G | A | 4 | a0002c0001t0001g0016 a0002c0001t0001g0019 a0002c0001t0001g0020 others(1): Show |
4 | NA18948.hp2 NA18953.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+14062G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878583 | |||||||
| chr8:36878716 | T | C | 2 | a0001c0004t0001g0189 a0001c0004t0001g0217 |
2 | HG02074.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2009+14195T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878716 | |||||||
| chr8:36878892 | C | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+14371C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36878892 | |||||||
| chr8:36879138 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+14617C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879138 | |||||||
| chr8:36879191 | A | ATG | 16 | a0001c0002t0001g0143 a0002c0001t0001g0039 a0002c0001t0001g0042 others(13): Show |
16 | HG00621.hp1 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2009+14690_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879191 | ||||||
| chr8:36879191 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2009+14670A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879191 | |||||||
| chr8:36879203 | G | A | 2 | a0003c0003t0001g0011 a0003c0003t0001g0101 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2009+14682G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879203 | |||||||
| chr8:36879207 | G | GTATATAT others(5): Show |
1 | a0001c0002t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2009+14687_2009+14 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879207 | ||||||
| chr8:36879209 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2009+14688G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879209 | |||||||
| chr8:36879209 | G | GTATATA | 3 | a0001c0002t0001g0247 a0001c0004t0001g0208 a0001c0006t0001g0170 |
3 | HG02886.hp1 HG04228.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | G | GTATATAT others(1): Show |
10 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(7): Show |
10 | HG01255.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | G | GTATATAT others(3): Show |
25 | a0001c0002t0001g0047 a0001c0002t0001g0049 a0001c0002t0001g0164 others(22): Show |
25 | HG00099.hp2 HG01167.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | G | GTATATAT others(5): Show |
22 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0154 others(19): Show |
23 | HG00735.hp1 HG01081.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | G | GTATATAT others(7): Show |
28 | a0001c0002t0001g0050 a0001c0002t0001g0061 a0001c0002t0001g0108 others(25): Show |
30 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(20): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | G | GTATATAT others(9): Show |
9 | a0001c0002t0001g0051 a0001c0002t0001g0054 a0001c0002t0001g0243 others(6): Show |
9 | HG01099.hp2 HG01243.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(22): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | G | GTATATAT others(11): Show |
4 | a0001c0002t0001g0014 a0001c0002t0001g0249 a0001c0004t0001g0201 others(1): Show |
4 | HG00140.hp1 HG01074.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14689_2009+14 others(24): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879209 | GTGTATAT others(3): Show |
G | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+14690_2009+14 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879209 | ||||||
| chr8:36879211 | G | A | 107 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(104): Show |
110 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2009+14690G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879211 | |||||||
| chr8:36879211 | G | GTA | 76 | a0002c0001t0001g0009 a0002c0001t0001g0015 a0002c0001t0001g0016 others(73): Show |
76 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2009+14717_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATA | 21 | a0002c0001t0001g0004 a0002c0001t0001g0012 a0002c0001t0001g0013 others(18): Show |
21 | HG00558.hp1 HG00738.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.2009+14715_2009+14 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATATA | 8 | a0002c0001t0001g0070 a0002c0001t0001g0071 a0002c0001t0001g0125 others(5): Show |
8 | HG02015.hp2 HG02258.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009+14713_2009+14 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATATAT others(1): Show |
3 | a0001c0002t0001g0073 a0002c0001t0001g0178 a0003c0003t0001g0153 |
3 | HG01243.hp1 HG02083.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2009+14711_2009+14 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATATAT others(3): Show |
2 | a0001c0002t0001g0238 a0002c0001t0001g0080 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2009+14709_2009+14 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATATAT others(5): Show |
4 | a0001c0002t0001g0048 a0001c0002t0001g0162 a0001c0002t0001g0163 others(1): Show |
4 | HG01109.hp2 HG02027.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14707_2009+14 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATATAT others(7): Show |
4 | a0001c0002t0001g0187 a0001c0002t0001g0242 a0001c0002t0001g0254 others(1): Show |
4 | HG01981.hp2 HG02257.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14705_2009+14 others(20): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTATATAT others(9): Show |
1 | a0001c0002t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2009+14703_2009+14 others(22): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | G | GTGTA | 4 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0003c0003t0001g0100 others(1): Show |
4 | HG02965.hp2 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+14691_2009+14 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879211 | GTA | G | 12 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2009+14717_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879211 | ||||||
| chr8:36879213 | A | G | 1 | a0003c0005t0001g0213 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2009+14692A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879213 | |||||||
| chr8:36879215 | A | G | 4 | a0001c0002t0001g0285 a0001c0002t0001g0288 a0001c0002t0001g0289 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009+14694A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879215 | |||||||
| chr8:36879238 | T | C | 5 | a0001c0002t0001g0143 a0001c0002t0001g0186 a0001c0002t0001g0282 others(2): Show |
5 | HG02055.hp1 HG02683.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+14717T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879238 | |||||||
| chr8:36879238 | T | TAC | 3 | a0002c0001t0001g0147 a0002c0001t0001g0148 a0003c0003t0001g0065 |
3 | HG02056.hp1 HG02129.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2009+14725_2009+14 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36879238 | ||||||
| chr8:36879326 | A | T | 5 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009+14805A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879326 | |||||||
| chr8:36879823 | C | G | 3 | a0002c0001t0001g0149 a0002c0001t0001g0150 a0002c0019t0001g0151 |
3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2009+15302C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879823 | |||||||
| chr8:36879974 | G | A | 1 | a0001c0004t0001g0224 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2009+15453G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36879974 | |||||||
| chr8:36880450 | A | T | 2 | a0001c0002t0001g0239 a0001c0002t0001g0255 |
2 | NA18980.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.2009+15929A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880450 | |||||||
| chr8:36880458 | C | T | 3 | a0002c0001t0001g0058 a0002c0001t0001g0059 a0002c0001t0001g0060 |
3 | NA18984.hp2 NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2009+15937C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880458 | |||||||
| chr8:36880485 | G | A | 1 | a0003c0003t0001g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2009+15964G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880485 | |||||||
| chr8:36880493 | G | A | 5 | a0002c0001t0001g0070 a0002c0001t0001g0071 a0002c0001t0001g0080 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2009+15972G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880493 | |||||||
| chr8:36880688 | C | T | 44 | a0002c0001t0001g0009 a0002c0001t0001g0012 a0002c0001t0001g0013 others(41): Show |
44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2009+16167C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880688 | |||||||
| chr8:36880784 | C | T | 3 | a0003c0003t0001g0006 a0003c0003t0001g0032 a0003c0003t0001g0033 |
3 | HG02280.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2009+16263C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36880784 | |||||||
| chr8:36881033 | C | G | 1 | a0001c0004t0001g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2009+16512C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881033 | |||||||
| chr8:36881135 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2009+16614G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881135 | |||||||
| chr8:36881246 | G | A | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2009+16725G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881246 | |||||||
| chr8:36881361 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2009+16840T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881361 | |||||||
| chr8:36881408 | G | A | 1 | a0003c0003t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2009+16887G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881408 | |||||||
| chr8:36881504 | C | T | 1 | a0003c0003t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2009+16983C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881504 | |||||||
| chr8:36881668 | T | C | 1 | a0001c0002t0001g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2009+17147T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881668 | |||||||
| chr8:36881768 | C | G | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2009+17247C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881768 | |||||||
| chr8:36881796 | T | TCA | 26 | a0001c0002t0001g0186 a0001c0002t0001g0282 a0002c0001t0001g0037 others(23): Show |
28 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.2009+17322_2009+17 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | T | TCACA | 14 | a0003c0003t0001g0005 a0003c0003t0001g0045 a0003c0003t0001g0064 others(11): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2009+17320_2009+17 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | T | TCACACA | 7 | a0003c0003t0001g0062 a0003c0003t0001g0081 a0003c0003t0001g0082 others(4): Show |
7 | HG00140.hp2 HG00639.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.2009+17318_2009+17 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | TCA | T | 22 | a0001c0002t0001g0143 a0002c0001t0001g0016 a0002c0001t0001g0019 others(19): Show |
22 | HG00621.hp2 HG01516.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2009+17322_2009+17 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | TCACA | T | 72 | a0001c0002t0001g0047 a0001c0002t0001g0287 a0001c0002t0001g0288 others(69): Show |
72 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2009+17320_2009+17 others(10): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | TCACACA | T | 18 | a0001c0002t0001g0122 a0001c0002t0001g0187 a0001c0002t0001g0251 others(15): Show |
18 | HG00544.hp2 HG00673.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.2009+17318_2009+17 others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | TCACACAC others(1): Show |
T | 44 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(41): Show |
46 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2009+17316_2009+17 others(14): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | TCACACAC others(3): Show |
T | 70 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(67): Show |
71 | HG00140.hp1 HG00438.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2009+17314_2009+17 others(16): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881796 | TCACACAC others(5): Show |
T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0253 |
2 | NA18948.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2009+17312_2009+17 others(18): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36881796 | ||||||
| chr8:36881932 | C | A | 1 | a0001c0002t0001g0266 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2009+17411C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36881932 | |||||||
| chr8:36882027 | G | T | 4 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+17506G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882027 | |||||||
| chr8:36882086 | A | T | 3 | a0001c0006t0001g0177 a0001c0006t0001g0279 a0001c0018t0001g0179 |
3 | HG02647.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2009+17565A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882086 | |||||||
| chr8:36882500 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+17979G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882500 | |||||||
| chr8:36882687 | G | A | 1 | a0001c0002t0001g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2009+18166G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882687 | |||||||
| chr8:36882771 | T | C | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2009+18250T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36882771 | |||||||
| chr8:36883278 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2009+18757G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36883278 | |||||||
| chr8:36883469 | G | T | 1 | a0001c0004t0001g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2009+18948G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36883469 | |||||||
| chr8:36883544 | A | T | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2009+19023A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36883544 | |||||||
| chr8:36884041 | C | T | 124 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(121): Show |
127 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2009+19520C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884041 | |||||||
| chr8:36884104 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2009+19583G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884104 | |||||||
| chr8:36884188 | AG | A | 55 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0156 others(52): Show |
57 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2009+19669delG | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36884188 | ||||||
| chr8:36884361 | G | C | 1 | a0003c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2009+19840G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884361 | |||||||
| chr8:36884402 | G | A | 1 | a0002c0001t0001g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2009+19881G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884402 | |||||||
| chr8:36884411 | G | A | 2 | a0001c0002t0001g0186 a0001c0002t0001g0282 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2009+19890G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884411 | |||||||
| chr8:36884463 | C | T | 2 | a0001c0004t0001g0190 a0001c0004t0001g0197 |
2 | NA18963.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2009+19942C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884463 | |||||||
| chr8:36884464 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2009+19943G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884464 | |||||||
| chr8:36884472 | A | G | 1 | a0001c0002t0001g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2009+19951A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884472 | |||||||
| chr8:36884697 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2009+20176C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884697 | |||||||
| chr8:36884765 | A | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2009+20244A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884765 | |||||||
| chr8:36884771 | A | T | 4 | a0001c0002t0001g0143 a0001c0006t0001g0177 a0001c0006t0001g0279 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2009+20250A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884771 | |||||||
| chr8:36884773 | C | A | 1 | a0001c0002t0001g0252 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2009+20252C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884773 | |||||||
| chr8:36884777 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2009+20256A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36884777 | |||||||
| chr8:36885014 | C | T | 1 | a0001c0004t0001g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2009+20493C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885014 | |||||||
| chr8:36885197 | A | G | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2010-20511A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885197 | |||||||
| chr8:36885242 | A | G | 1 | a0003c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2010-20466A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885242 | |||||||
| chr8:36885272 | T | A | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2010-20436T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885272 | |||||||
| chr8:36885305 | A | G | 1 | a0003c0003t0001g0103 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2010-20403A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885305 | |||||||
| chr8:36885336 | C | G | 1 | a0001c0002t0001g0228 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2010-20372C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885336 | |||||||
| chr8:36885587 | G | A | 11 | a0001c0002t0001g0073 a0001c0002t0001g0162 a0001c0002t0001g0163 others(8): Show |
11 | HG02027.hp1 HG02071.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010-20121G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885587 | |||||||
| chr8:36885640 | A | G | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2010-20068A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885640 | |||||||
| chr8:36885702 | A | G | 47 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(44): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2010-20006A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36885702 | |||||||
| chr8:36886011 | C | A | 2 | a0001c0004t0001g0161 a0001c0004t0001g0220 |
2 | HG01358.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2010-19697C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886011 | |||||||
| chr8:36886015 | G | A | 2 | a0001c0004t0001g0161 a0001c0004t0001g0220 |
2 | HG01358.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2010-19693G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886015 | |||||||
| chr8:36886135 | G | C | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-19573G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886135 | |||||||
| chr8:36886377 | T | C | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2010-19331T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886377 | |||||||
| chr8:36886499 | A | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-19209A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886499 | |||||||
| chr8:36886509 | G | T | 1 | a0002c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2010-19199G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886509 | |||||||
| chr8:36886555 | G | A | 1 | a0003c0003t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2010-19153G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886555 | |||||||
| chr8:36886615 | T | G | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2010-19093T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886615 | |||||||
| chr8:36886684 | T | A | 1 | a0002c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2010-19024T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886684 | |||||||
| chr8:36886962 | G | A | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2010-18746G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886962 | |||||||
| chr8:36886981 | T | G | 1 | a0003c0005t0001g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2010-18727T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36886981 | |||||||
| chr8:36887159 | T | C | 1 | a0002c0001t0001g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2010-18549T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887159 | |||||||
| chr8:36887232 | C | T | 3 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0282 |
3 | HG02055.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2010-18476C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887232 | |||||||
| chr8:36887413 | G | A | 1 | a0001c0009t0001g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2010-18295G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887413 | |||||||
| chr8:36887415 | A | G | 1 | a0003c0003t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2010-18293A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887415 | |||||||
| chr8:36887442 | G | GT | 62 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(59): Show |
63 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2010-18257dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36887442 | ||||||
| chr8:36887452 | G | GT | 57 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(54): Show |
59 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.2010-18239dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36887452 | ||||||
| chr8:36887452 | G | GTT | 12 | a0001c0002t0001g0281 a0001c0004t0001g0158 a0001c0004t0001g0190 others(9): Show |
12 | HG00544.hp2 HG01168.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.2010-18240_2010-18 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36887452 | ||||||
| chr8:36887452 | G | T | 13 | a0001c0002t0001g0049 a0001c0002t0001g0073 a0001c0002t0001g0162 others(10): Show |
13 | HG00099.hp2 HG01243.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.2010-18256G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887452 | |||||||
| chr8:36887453 | T | G | 6 | a0001c0002t0001g0049 a0001c0006t0001g0169 a0001c0006t0001g0170 others(3): Show |
6 | HG00099.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-18255T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887453 | |||||||
| chr8:36887459 | T | G | 16 | a0003c0003t0001g0007 a0003c0003t0001g0064 a0003c0003t0001g0065 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.2010-18249T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887459 | |||||||
| chr8:36887548 | G | C | 2 | a0003c0003t0001g0180 a0003c0003t0001g0181 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2010-18160G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887548 | |||||||
| chr8:36887567 | C | T | 2 | a0001c0006t0001g0177 a0001c0018t0001g0179 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2010-18141C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887567 | |||||||
| chr8:36887568 | G | A | 5 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-18140G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887568 | |||||||
| chr8:36887618 | A | T | 7 | a0001c0002t0001g0143 a0001c0006t0001g0169 a0001c0006t0001g0170 others(4): Show |
7 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010-18090A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887618 | |||||||
| chr8:36887709 | T | C | 46 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(43): Show |
48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2010-17999T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887709 | |||||||
| chr8:36887960 | G | A | 46 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(43): Show |
48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2010-17748G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36887960 | |||||||
| chr8:36888146 | G | A | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-17562G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888146 | |||||||
| chr8:36888221 | A | G | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-17487A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888221 | |||||||
| chr8:36888304 | G | T | 1 | a0002c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2010-17404G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888304 | |||||||
| chr8:36888339 | A | G | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2010-17369A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888339 | |||||||
| chr8:36888417 | C | T | 1 | a0002c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2010-17291C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888417 | |||||||
| chr8:36888504 | G | A | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-17204G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888504 | |||||||
| chr8:36888559 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2010-17149G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36888559 | |||||||
| chr8:36889022 | G | A | 1 | a0003c0005t0001g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2010-16686G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889022 | |||||||
| chr8:36889122 | A | G | 1 | a0002c0001t0001g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2010-16586A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889122 | |||||||
| chr8:36889243 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2010-16465G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889243 | |||||||
| chr8:36889319 | G | T | 1 | a0002c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2010-16389G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889319 | |||||||
| chr8:36889404 | T | G | 2 | a0002c0001t0001g0012 a0002c0001t0001g0013 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2010-16304T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889404 | |||||||
| chr8:36889419 | C | A | 7 | a0001c0002t0001g0143 a0001c0006t0001g0169 a0001c0006t0001g0170 others(4): Show |
7 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010-16289C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889419 | |||||||
| chr8:36889430 | T | A | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-16278T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889430 | |||||||
| chr8:36889464 | C | T | 1 | a0002c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2010-16244C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889464 | |||||||
| chr8:36889902 | C | G | 2 | a0001c0006t0001g0177 a0001c0018t0001g0179 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2010-15806C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36889902 | |||||||
| chr8:36890183 | G | A | 3 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 |
3 | HG02055.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2010-15525G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890183 | |||||||
| chr8:36890231 | A | G | 2 | a0002c0001t0001g0012 a0002c0001t0001g0013 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2010-15477A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890231 | |||||||
| chr8:36890551 | A | G | 1 | a0001c0002t0001g0238 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2010-15157A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890551 | |||||||
| chr8:36890686 | A | G | 4 | a0002c0001t0001g0053 a0002c0001t0001g0058 a0002c0001t0001g0059 others(1): Show |
4 | HG00673.hp2 NA18984.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.2010-15022A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890686 | |||||||
| chr8:36890970 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2010-14738T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36890970 | |||||||
| chr8:36891021 | T | C | 10 | a0003c0003t0001g0006 a0003c0003t0001g0011 a0003c0003t0001g0026 others(7): Show |
10 | HG02280.hp2 HG02630.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-14687T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891021 | |||||||
| chr8:36891177 | C | A | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-14531C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891177 | |||||||
| chr8:36891395 | C | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-14313C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891395 | |||||||
| chr8:36891412 | A | C | 2 | a0003c0003t0001g0023 a0003c0003t0001g0067 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2010-14296A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891412 | |||||||
| chr8:36891499 | G | C | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2010-14209G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891499 | |||||||
| chr8:36891688 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2010-14020G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891688 | |||||||
| chr8:36891772 | A | G | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-13936A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36891772 | |||||||
| chr8:36892036 | A | G | 7 | a0001c0002t0001g0143 a0001c0006t0001g0169 a0001c0006t0001g0170 others(4): Show |
7 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010-13672A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892036 | |||||||
| chr8:36892236 | C | A | 1 | a0002c0001t0001g0123 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2010-13472C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892236 | |||||||
| chr8:36892336 | A | T | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2010-13372A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892336 | |||||||
| chr8:36892449 | A | G | 1 | a0002c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2010-13259A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892449 | |||||||
| chr8:36892492 | C | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2010-13216C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892492 | |||||||
| chr8:36892596 | C | G | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-13112C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892596 | |||||||
| chr8:36892631 | C | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-13077C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36892631 | |||||||
| chr8:36893070 | T | C | 5 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-12638T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893070 | |||||||
| chr8:36893118 | T | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-12590T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893118 | |||||||
| chr8:36893143 | T | TTG | 8 | a0001c0002t0001g0229 a0001c0002t0001g0280 a0001c0002t0001g0281 others(5): Show |
8 | HG00438.hp2 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-12565_2010-12 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893143 | |||||||
| chr8:36893144 | G | GT | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.2010-12554dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36893144 | ||||||
| chr8:36893144 | G | T | 8 | a0001c0002t0001g0229 a0001c0002t0001g0280 a0001c0002t0001g0281 others(5): Show |
8 | HG00438.hp2 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-12564G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893144 | |||||||
| chr8:36893262 | C | G | 3 | a0003c0003t0001g0011 a0003c0003t0001g0100 a0003c0003t0001g0101 |
3 | HG03139.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2010-12446C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893262 | |||||||
| chr8:36893266 | A | T | 1 | a0003c0003t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2010-12442A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893266 | |||||||
| chr8:36893327 | C | CT | 10 | a0001c0002t0001g0162 a0001c0002t0001g0163 a0001c0002t0001g0176 others(7): Show |
10 | HG02027.hp1 HG02071.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-12369dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36893327 | ||||||
| chr8:36893327 | CT | C | 11 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0049 others(8): Show |
11 | HG00099.hp2 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010-12369delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36893327 | ||||||
| chr8:36893341 | C | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0089 a0003c0003t0001g0090 others(3): Show |
8 | HG00609.hp1 NA18946.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-12367C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893341 | |||||||
| chr8:36893342 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2010-12366G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893342 | |||||||
| chr8:36893396 | A | G | 3 | a0002c0001t0001g0004 a0002c0001t0001g0068 a0002c0001t0001g0183 |
3 | HG02559.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2010-12312A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893396 | |||||||
| chr8:36893885 | T | G | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-11823T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36893885 | |||||||
| chr8:36894048 | C | T | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-11660C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894048 | |||||||
| chr8:36894348 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-11360T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894348 | |||||||
| chr8:36894445 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-11263T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894445 | |||||||
| chr8:36894478 | T | G | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-11230T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894478 | |||||||
| chr8:36894480 | G | A | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-11228G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894480 | |||||||
| chr8:36894814 | A | G | 6 | a0003c0003t0001g0007 a0003c0003t0001g0076 a0003c0003t0001g0078 others(3): Show |
6 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-10894A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36894814 | |||||||
| chr8:36895001 | A | T | 1 | a0001c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2010-10707A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895001 | |||||||
| chr8:36895039 | A | G | 1 | a0002c0001t0001g0037 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2010-10669A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895039 | |||||||
| chr8:36895046 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-10662T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895046 | |||||||
| chr8:36895089 | AT | A | 4 | a0003c0003t0001g0001 a0003c0003t0001g0090 a0003c0003t0001g0136 others(1): Show |
6 | NA18946.hp1 NA18969.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-10607delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36895089 | ||||||
| chr8:36895223 | C | T | 1 | a0002c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2010-10485C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895223 | |||||||
| chr8:36895325 | C | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-10383C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895325 | |||||||
| chr8:36895457 | C | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-10251C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895457 | |||||||
| chr8:36895673 | T | G | 1 | a0002c0001t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2010-10035T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36895673 | |||||||
| chr8:36896034 | T | C | 1 | a0001c0002t0001g0261 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2010-9674T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896034 | |||||||
| chr8:36896111 | A | AT | 114 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(111): Show |
117 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.2010-9590dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36896111 | ||||||
| chr8:36896342 | C | T | 1 | a0001c0018t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2010-9366C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896342 | |||||||
| chr8:36896580 | G | A | 1 | a0002c0001t0001g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2010-9128G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896580 | |||||||
| chr8:36896586 | C | T | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-9122C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896586 | |||||||
| chr8:36896595 | A | G | 1 | a0001c0004t0001g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2010-9113A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896595 | |||||||
| chr8:36896612 | T | G | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-9096T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896612 | |||||||
| chr8:36896623 | A | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-9085A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896623 | |||||||
| chr8:36896636 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2010-9072G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896636 | |||||||
| chr8:36896646 | A | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2010-9062A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896646 | |||||||
| chr8:36896667 | G | C | 3 | a0001c0004t0001g0226 a0001c0004t0001g0227 a0001c0004t0002g0225 |
3 | NA18943.hp1 NA18965.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2010-9041G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896667 | |||||||
| chr8:36896813 | A | T | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2010-8895A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36896813 | |||||||
| chr8:36897256 | C | T | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-8452C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36897256 | |||||||
| chr8:36897331 | CTT | C | 5 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-8372_2010-837 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36897331 | ||||||
| chr8:36897454 | G | C | 1 | a0001c0002t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2010-8254G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36897454 | |||||||
| chr8:36897887 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-7821T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36897887 | |||||||
| chr8:36898201 | C | T | 1 | a0002c0001t0001g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2010-7507C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898201 | |||||||
| chr8:36898241 | C | T | 6 | a0003c0003t0001g0007 a0003c0003t0001g0076 a0003c0003t0001g0078 others(3): Show |
6 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010-7467C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898241 | |||||||
| chr8:36898270 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-7438T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898270 | |||||||
| chr8:36898315 | C | CAT | 12 | a0001c0002t0001g0143 a0001c0002t0001g0285 a0001c0002t0001g0287 others(9): Show |
12 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2010-7393_2010-739 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898315 | |||||||
| chr8:36898578 | GA | G | 8 | a0001c0002t0001g0143 a0001c0004t0001g0193 a0001c0006t0001g0169 others(5): Show |
8 | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2010-7120delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36898578 | ||||||
| chr8:36898980 | A | G | 8 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0242 others(5): Show |
8 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-6728A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36898980 | |||||||
| chr8:36899288 | G | A | 1 | a0003c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2010-6420G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36899288 | |||||||
| chr8:36899288 | GA | G | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-6410delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36899288 | ||||||
| chr8:36899328 | A | T | 3 | a0002c0001t0001g0004 a0002c0001t0001g0068 a0002c0001t0001g0183 |
3 | HG02559.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2010-6380A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36899328 | |||||||
| chr8:36899427 | AAC | A | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-6277_2010-627 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36899427 | ||||||
| chr8:36899543 | T | C | 21 | a0002c0001t0001g0009 a0002c0001t0001g0015 a0002c0001t0001g0093 others(18): Show |
21 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.2010-6165T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36899543 | |||||||
| chr8:36900159 | GAC | G | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-5545_2010-554 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36900159 | ||||||
| chr8:36900227 | G | A | 1 | a0001c0004t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2010-5481G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900227 | |||||||
| chr8:36900275 | G | A | 3 | a0001c0002t0001g0236 a0001c0002t0001g0257 a0001c0002t0001g0267 |
3 | HG01168.hp2 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2010-5433G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900275 | |||||||
| chr8:36900421 | AG | A | 111 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(108): Show |
114 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2010-5286delG | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900421 | |||||||
| chr8:36900456 | G | A | 1 | a0003c0003t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2010-5252G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900456 | |||||||
| chr8:36900666 | A | G | 1 | a0001c0002t0001g0263 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2010-5042A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900666 | |||||||
| chr8:36900927 | G | T | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2010-4781G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900927 | |||||||
| chr8:36900928 | C | T | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2010-4780C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36900928 | |||||||
| chr8:36901081 | G | A | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-4627G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901081 | |||||||
| chr8:36901196 | A | C | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-4512A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901196 | |||||||
| chr8:36901240 | C | G | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2010-4468C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901240 | |||||||
| chr8:36901266 | T | C | 1 | a0002c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2010-4442T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901266 | |||||||
| chr8:36901428 | C | T | 46 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0007 others(43): Show |
48 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2010-4280C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901428 | |||||||
| chr8:36901596 | C | T | 3 | a0001c0004t0001g0158 a0001c0004t0001g0159 a0001c0004t0001g0160 |
3 | NA18944.hp1 NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2010-4112C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901596 | |||||||
| chr8:36901808 | C | T | 1 | a0001c0004t0001g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2010-3900C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36901808 | |||||||
| chr8:36902025 | T | C | 1 | a0002c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2010-3683T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902025 | |||||||
| chr8:36902044 | A | G | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2010-3664A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902044 | |||||||
| chr8:36902068 | C | T | 2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2010-3640C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902068 | |||||||
| chr8:36902280 | T | C | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2010-3428T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902280 | |||||||
| chr8:36902337 | G | A | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2010-3371G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902337 | |||||||
| chr8:36902385 | C | A | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-3323C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902385 | |||||||
| chr8:36902442 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2010-3266G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902442 | |||||||
| chr8:36902523 | G | A | 1 | a0003c0005t0001g0195 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2010-3185G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902523 | |||||||
| chr8:36902540 | A | C | 1 | a0002c0001t0001g0010 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2010-3168A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902540 | |||||||
| chr8:36902861 | G | T | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-2847G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902861 | |||||||
| chr8:36902882 | T | G | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-2826T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902882 | |||||||
| chr8:36902892 | A | G | 8 | a0002c0001t0001g0105 a0002c0001t0001g0113 a0002c0001t0001g0114 others(5): Show |
8 | HG00597.hp2 HG00609.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2010-2816A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36902892 | |||||||
| chr8:36903352 | C | A | 2 | a0001c0006t0001g0169 a0001c0006t0001g0170 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2010-2356C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903352 | |||||||
| chr8:36903399 | A | G | 1 | a0002c0001t0001g0123 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2010-2309A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903399 | |||||||
| chr8:36903466 | C | T | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-2242C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903466 | |||||||
| chr8:36903632 | T | A | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-2076T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903632 | |||||||
| chr8:36903667 | G | T | 1 | a0001c0004t0001g0167 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2010-2041G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903667 | |||||||
| chr8:36903802 | TGGAAGGG others(8): Show |
T | 1 | a0001c0002t0001g0256 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2010-1904_2010-189 others(19): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36903802 | ||||||
| chr8:36903814 | C | A | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2010-1894C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36903814 | |||||||
| chr8:36904094 | C | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-1614C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904094 | |||||||
| chr8:36904288 | C | G | 2 | a0001c0002t0001g0260 a0001c0002t0001g0261 |
2 | HG02523.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2010-1420C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904288 | |||||||
| chr8:36904318 | G | C | 1 | a0003c0003t0001g0081 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2010-1390G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904318 | |||||||
| chr8:36904344 | C | G | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-1364C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904344 | |||||||
| chr8:36904555 | G | A | 3 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0282 |
3 | HG02055.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2010-1153G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904555 | |||||||
| chr8:36904571 | C | T | 5 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010-1137C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904571 | |||||||
| chr8:36904584 | G | A | 1 | a0002c0001t0001g0015 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2010-1124G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904584 | |||||||
| chr8:36904614 | A | G | 1 | a0002c0001t0001g0016 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2010-1094A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904614 | |||||||
| chr8:36904620 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-1088T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904620 | |||||||
| chr8:36904736 | G | C | 1 | a0002c0011t0001g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2010-972G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904736 | |||||||
| chr8:36904761 | T | C | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2010-947T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904761 | |||||||
| chr8:36904799 | C | G | 2 | a0003c0003t0001g0017 a0003c0005t0001g0221 |
2 | NA19084.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2010-909C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904799 | |||||||
| chr8:36904891 | T | C | 116 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2010-817T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904891 | |||||||
| chr8:36904954 | C | T | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2010-754C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904954 | |||||||
| chr8:36904987 | G | T | 1 | a0003c0003t0001g0153 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2010-721G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36904987 | |||||||
| chr8:36905015 | C | G | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2010-693C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905015 | |||||||
| chr8:36905073 | A | G | 1 | a0001c0004t0001g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2010-635A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905073 | |||||||
| chr8:36905091 | G | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2010-617G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905091 | |||||||
| chr8:36905190 | A | G | 1 | a0002c0001t0001g0119 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2010-518A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905190 | |||||||
| chr8:36905460 | C | CA | 239 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2010-233dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36905460 | ||||||
| chr8:36905460 | C | CAA | 10 | a0001c0002t0001g0249 a0001c0004t0001g0192 a0002c0001t0001g0031 others(7): Show |
10 | HG00140.hp1 HG01258.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.2010-234_2010-233d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr8 | 36905460 | ||||||
| chr8:36905561 | T | G | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2010-147T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905561 | |||||||
| chr8:36905693 | A | G | 1 | a0003c0003t0001g0283 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2010-15A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 19/26 | chr8 | 36905693 | |||||||
| chr8:36906181 | C | CT | 28 | a0001c0002t0001g0285 a0002c0001t0001g0025 a0002c0001t0001g0027 others(25): Show |
28 | HG00673.hp2 HG00735.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2106+391dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36906181 | ||||||
| chr8:36906181 | C | CTT | 243 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2106+390_2106+391d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36906181 | ||||||
| chr8:36906181 | C | CTTT | 6 | a0001c0002t0001g0073 a0001c0002t0001g0162 a0001c0002t0001g0163 others(3): Show |
6 | HG00544.hp1 HG01517.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+389_2106+391d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36906181 | ||||||
| chr8:36906248 | T | C | 1 | a0001c0006t0001g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2106+444T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906248 | |||||||
| chr8:36906312 | A | G | 5 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+508A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906312 | |||||||
| chr8:36906452 | T | G | 1 | a0002c0001t0001g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2106+648T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906452 | |||||||
| chr8:36906571 | C | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+767C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906571 | |||||||
| chr8:36906600 | T | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2106+796T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906600 | |||||||
| chr8:36906872 | C | T | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2106+1068C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906872 | |||||||
| chr8:36906996 | T | C | 4 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+1192T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36906996 | |||||||
| chr8:36907417 | A | G | 58 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0143 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2106+1613A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907417 | |||||||
| chr8:36907564 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2107-1747A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907564 | |||||||
| chr8:36907626 | G | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2107-1685G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907626 | |||||||
| chr8:36907982 | G | T | 1 | a0001c0002t0001g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2107-1329G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36907982 | |||||||
| chr8:36908032 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2107-1279G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908032 | |||||||
| chr8:36908073 | C | A | 3 | a0001c0002t0001g0171 a0001c0002t0001g0172 a0001c0002t0001g0173 |
3 | HG02055.hp2 HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2107-1238C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908073 | |||||||
| chr8:36908131 | T | A | 1 | a0001c0002t0001g0256 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2107-1180T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908131 | |||||||
| chr8:36908178 | A | C | 1 | a0001c0002t0001g0256 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2107-1133A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908178 | |||||||
| chr8:36908265 | A | G | 6 | a0003c0003t0001g0007 a0003c0003t0001g0076 a0003c0003t0001g0078 others(3): Show |
6 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107-1046A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908265 | |||||||
| chr8:36908273 | T | C | 1 | a0003c0003t0001g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2107-1038T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908273 | |||||||
| chr8:36908558 | A | G | 1 | a0001c0014t0001g0232 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2107-753A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908558 | |||||||
| chr8:36908569 | A | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2107-742A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908569 | |||||||
| chr8:36908755 | A | G | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-556A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908755 | |||||||
| chr8:36908756 | T | C | 2 | a0003c0003t0001g0079 a0003c0003t0001g0083 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2107-555T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908756 | |||||||
| chr8:36908799 | T | TA | 5 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-507dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 36908799 | ||||||
| chr8:36908834 | T | C | 1 | a0002c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2107-477T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36908834 | |||||||
| chr8:36909152 | A | T | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2107-159A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36909152 | |||||||
| chr8:36909178 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2107-133A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36909178 | |||||||
| chr8:36909260 | A | T | 2 | a0001c0002t0001g0235 a0001c0002t0001g0271 |
2 | NA18966.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2107-51A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 20/26 | chr8 | 36909260 | |||||||
| chr8:36909545 | A | T | 1 | a0001c0002t0001g0256 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2331+10A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909545 | |||||||
| chr8:36909567 | A | G | 59 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0047 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2331+32A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909567 | |||||||
| chr8:36909627 | C | G | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2331+92C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909627 | |||||||
| chr8:36909707 | T | A | 1 | a0001c0002t0001g0256 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2331+172T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909707 | |||||||
| chr8:36909734 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2331+199G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909734 | |||||||
| chr8:36909901 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2331+366T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36909901 | |||||||
| chr8:36910169 | C | T | 3 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0087 |
3 | HG02683.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2331+634C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910169 | |||||||
| chr8:36910345 | G | A | 3 | a0001c0006t0001g0177 a0001c0006t0001g0286 a0001c0018t0001g0179 |
3 | HG02615.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2332-585G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910345 | |||||||
| chr8:36910618 | G | C | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2332-312G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910618 | |||||||
| chr8:36910643 | C | T | 1 | a0007c0010t0001g0022 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2332-287C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910643 | |||||||
| chr8:36910717 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2332-213G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910717 | |||||||
| chr8:36910734 | G | T | 128 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2332-196G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910734 | |||||||
| chr8:36910896 | G | A | 7 | a0003c0003t0001g0023 a0003c0003t0001g0067 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2332-34G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 21/26 | chr8 | 36910896 | |||||||
| chr8:36911156 | G | A | 1 | a0002c0001t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2521+37G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911156 | |||||||
| chr8:36911425 | C | T | 1 | a0002c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2521+306C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911425 | |||||||
| chr8:36911469 | G | C | 3 | a0001c0002t0001g0236 a0001c0002t0001g0257 a0001c0002t0001g0267 |
3 | HG01168.hp2 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2521+350G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911469 | |||||||
| chr8:36911540 | T | G | 1 | a0001c0006t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2521+421T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911540 | |||||||
| chr8:36911541 | G | C | 4 | a0001c0002t0001g0018 a0001c0002t0001g0239 a0001c0002t0001g0240 others(1): Show |
4 | NA18978.hp2 NA18980.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+422G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911541 | |||||||
| chr8:36911564 | C | G | 1 | a0003c0003t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2521+445C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36911564 | |||||||
| chr8:36912192 | G | A | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2521+1073G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912192 | |||||||
| chr8:36912228 | G | A | 1 | a0002c0001t0001g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2521+1109G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912228 | |||||||
| chr8:36912359 | A | G | 7 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0242 others(4): Show |
7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2521+1240A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912359 | |||||||
| chr8:36912371 | T | C | 67 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2521+1252T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912371 | |||||||
| chr8:36912501 | C | T | 46 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(43): Show |
48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2521+1382C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912501 | |||||||
| chr8:36912682 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+1563G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912682 | |||||||
| chr8:36912697 | C | T | 1 | a0002c0001t0001g0058 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2521+1578C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912697 | |||||||
| chr8:36912700 | G | A | 67 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2521+1581G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912700 | |||||||
| chr8:36912738 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+1619G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912738 | |||||||
| chr8:36912836 | C | T | 1 | a0003c0003t0001g0081 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2521+1717C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912836 | |||||||
| chr8:36912840 | C | T | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2521+1721C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912840 | |||||||
| chr8:36912860 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2521+1741C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912860 | |||||||
| chr8:36912861 | G | A | 2 | a0002c0001t0001g0031 a0002c0001t0001g0037 |
2 | HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2521+1742G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36912861 | |||||||
| chr8:36912953 | C | CA | 34 | a0001c0002t0001g0287 a0001c0002t0001g0288 a0001c0004t0001g0212 others(31): Show |
34 | HG00438.hp1 HG00544.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.2521+1860dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36912953 | ||||||
| chr8:36912953 | CA | C | 138 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2521+1860delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36912953 | ||||||
| chr8:36913072 | G | T | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2521+1953G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913072 | |||||||
| chr8:36913114 | C | T | 1 | a0003c0003t0001g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2521+1995C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913114 | |||||||
| chr8:36913134 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2521+2015G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913134 | |||||||
| chr8:36913175 | G | T | 46 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(43): Show |
48 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2521+2056G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913175 | |||||||
| chr8:36913185 | C | T | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2521+2066C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913185 | |||||||
| chr8:36913465 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+2346G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913465 | |||||||
| chr8:36913509 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2521+2390C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913509 | |||||||
| chr8:36913599 | C | T | 6 | a0002c0001t0001g0024 a0002c0001t0001g0031 a0002c0001t0001g0037 others(3): Show |
6 | HG01258.hp2 HG02004.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2521+2480C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913599 | |||||||
| chr8:36913600 | A | AT | 13 | a0002c0001t0001g0009 a0002c0001t0001g0021 a0002c0001t0001g0104 others(10): Show |
13 | HG00438.hp1 HG01891.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2521+2500dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36913600 | ||||||
| chr8:36913600 | AT | A | 76 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2521+2500delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36913600 | ||||||
| chr8:36913847 | T | C | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2521+2728T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913847 | |||||||
| chr8:36913853 | G | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2521+2734G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913853 | |||||||
| chr8:36913891 | A | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2521+2772A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36913891 | |||||||
| chr8:36914153 | A | G | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2521+3034A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914153 | |||||||
| chr8:36914261 | G | C | 67 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2521+3142G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914261 | |||||||
| chr8:36914446 | A | G | 5 | a0003c0003t0001g0006 a0003c0003t0001g0026 a0003c0003t0001g0032 others(2): Show |
5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2521+3327A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914446 | |||||||
| chr8:36914452 | C | T | 2 | a0002c0001t0001g0010 a0002c0001t0001g0102 |
2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2521+3333C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914452 | |||||||
| chr8:36914589 | A | G | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2521+3470A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914589 | |||||||
| chr8:36914605 | T | G | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2521+3486T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914605 | |||||||
| chr8:36914694 | G | A | 1 | a0002c0001t0001g0114 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2521+3575G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914694 | |||||||
| chr8:36914751 | G | A | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2521+3632G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914751 | |||||||
| chr8:36914840 | C | A | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2521+3721C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914840 | |||||||
| chr8:36914940 | C | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+3821C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914940 | |||||||
| chr8:36914960 | G | A | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2521+3841G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36914960 | |||||||
| chr8:36915013 | A | C | 1 | a0002c0001t0001g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2522-3810A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915013 | |||||||
| chr8:36915043 | G | A | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2522-3780G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915043 | |||||||
| chr8:36915050 | G | A | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-3773G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915050 | |||||||
| chr8:36915082 | T | C | 7 | a0003c0005t0001g0188 a0003c0005t0001g0195 a0003c0005t0001g0196 others(4): Show |
7 | HG00621.hp1 NA18953.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2522-3741T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915082 | |||||||
| chr8:36915561 | T | C | 3 | a0001c0002t0001g0236 a0001c0002t0001g0257 a0001c0002t0001g0267 |
3 | HG01168.hp2 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2522-3262T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915561 | |||||||
| chr8:36915748 | C | A | 1 | a0002c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2522-3075C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915748 | |||||||
| chr8:36915919 | T | C | 1 | a0001c0002t0001g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2522-2904T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915919 | |||||||
| chr8:36915971 | G | A | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-2852G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36915971 | |||||||
| chr8:36916353 | AGAAG | A | 4 | a0001c0002t0001g0238 a0001c0002t0001g0251 a0001c0002t0001g0252 others(1): Show |
4 | HG00639.hp2 HG01978.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522-2453_2522-245 others(8): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36916353 | ||||||
| chr8:36916703 | G | A | 1 | a0003c0003t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2522-2120G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916703 | |||||||
| chr8:36916860 | A | G | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522-1963A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916860 | |||||||
| chr8:36916957 | G | C | 1 | a0001c0002t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2522-1866G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916957 | |||||||
| chr8:36916969 | C | T | 1 | a0001c0002t0001g0018 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2522-1854C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36916969 | |||||||
| chr8:36917017 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2522-1806C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917017 | |||||||
| chr8:36917156 | A | C | 41 | a0002c0001t0001g0009 a0002c0001t0001g0012 a0002c0001t0001g0013 others(38): Show |
41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2522-1667A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917156 | |||||||
| chr8:36917354 | C | CT | 60 | a0002c0001t0001g0137 a0003c0003t0001g0001 a0003c0003t0001g0005 others(57): Show |
62 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2522-1456dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36917354 | ||||||
| chr8:36917354 | CT | C | 14 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(11): Show |
14 | HG01891.hp1 HG02132.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.2522-1456delT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36917354 | ||||||
| chr8:36917356 | T | C | 15 | a0002c0001t0001g0015 a0002c0001t0001g0107 a0002c0001t0001g0109 others(12): Show |
15 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.2522-1467T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917356 | |||||||
| chr8:36917357 | T | C | 1 | a0002c0001t0001g0140 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2522-1466T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917357 | |||||||
| chr8:36917517 | A | AT | 186 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2522-1294dupT | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 36917517 | ||||||
| chr8:36917566 | G | T | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2522-1257G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917566 | |||||||
| chr8:36917840 | A | G | 41 | a0002c0001t0001g0009 a0002c0001t0001g0012 a0002c0001t0001g0013 others(38): Show |
41 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2522-983A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917840 | |||||||
| chr8:36917957 | G | A | 7 | a0003c0003t0001g0023 a0003c0003t0001g0067 a0003c0003t0001g0180 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2522-866G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36917957 | |||||||
| chr8:36918102 | T | C | 1 | a0003c0003t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2522-721T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918102 | |||||||
| chr8:36918209 | C | G | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2522-614C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918209 | |||||||
| chr8:36918591 | C | G | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-232C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918591 | |||||||
| chr8:36918664 | A | G | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2522-159A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918664 | |||||||
| chr8:36918718 | A | C | 2 | a0001c0002t0001g0262 a0001c0002t0001g0272 |
2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2522-105A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918718 | |||||||
| chr8:36918749 | T | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2522-74T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918749 | |||||||
| chr8:36918756 | T | G | 8 | a0001c0002t0001g0143 a0001c0006t0001g0169 a0001c0006t0001g0170 others(5): Show |
8 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2522-67T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918756 | |||||||
| chr8:36918815 | C | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2522-8C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 22/26 | chr8 | 36918815 | |||||||
| chr8:36919296 | G | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2596+399G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919296 | |||||||
| chr8:36919332 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2596+435G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919332 | |||||||
| chr8:36919379 | C | G | 1 | a0002c0001t0001g0109 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2596+482C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919379 | |||||||
| chr8:36919428 | C | CA | 30 | a0001c0002t0001g0018 a0001c0002t0001g0143 a0001c0002t0001g0239 others(27): Show |
30 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.2596+549dupA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | ||||||
| chr8:36919428 | C | CAA | 50 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0001g0048 others(47): Show |
51 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.2596+548_2596+549d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | ||||||
| chr8:36919428 | C | CAAA | 55 | a0001c0002t0001g0014 a0001c0002t0001g0051 a0001c0002t0001g0054 others(52): Show |
57 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2596+547_2596+549d others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | ||||||
| chr8:36919428 | C | CAAAA | 7 | a0001c0004t0001g0190 a0001c0004t0001g0194 a0001c0004t0001g0217 others(4): Show |
7 | HG02080.hp1 HG02738.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.2596+546_2596+549d others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | ||||||
| chr8:36919428 | CA | C | 67 | a0002c0001t0001g0004 a0002c0001t0001g0044 a0002c0001t0001g0053 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2596+549delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36919428 | ||||||
| chr8:36919605 | C | T | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2596+708C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919605 | |||||||
| chr8:36919960 | C | T | 1 | a0002c0001t0001g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2596+1063C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36919960 | |||||||
| chr8:36920091 | A | G | 1 | a0002c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2596+1194A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920091 | |||||||
| chr8:36920498 | T | C | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2596+1601T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920498 | |||||||
| chr8:36920548 | CTTG | C | 71 | a0001c0002t0001g0143 a0001c0006t0001g0169 a0001c0006t0001g0170 others(68): Show |
73 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2596+1656_2596+165 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36920548 | ||||||
| chr8:36920730 | G | A | 1 | a0002c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2597-1760G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920730 | |||||||
| chr8:36920801 | G | A | 71 | a0001c0002t0001g0143 a0001c0006t0001g0169 a0001c0006t0001g0170 others(68): Show |
73 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2597-1689G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920801 | |||||||
| chr8:36920889 | A | G | 5 | a0003c0003t0001g0006 a0003c0003t0001g0026 a0003c0003t0001g0032 others(2): Show |
5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2597-1601A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920889 | |||||||
| chr8:36920914 | C | A | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2597-1576C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36920914 | |||||||
| chr8:36921060 | C | T | 8 | a0001c0002t0001g0122 a0001c0004t0001g0167 a0001c0004t0001g0191 others(5): Show |
8 | HG00673.hp1 HG02080.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.2597-1430C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921060 | |||||||
| chr8:36921142 | A | G | 1 | a0002c0001t0001g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2597-1348A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921142 | |||||||
| chr8:36921261 | C | T | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2597-1229C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921261 | |||||||
| chr8:36921395 | T | A | 117 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(114): Show |
120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2597-1095T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921395 | |||||||
| chr8:36921485 | C | G | 1 | a0001c0004t0001g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2597-1005C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921485 | |||||||
| chr8:36921596 | T | C | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2597-894T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921596 | |||||||
| chr8:36921647 | C | T | 1 | a0002c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2597-843C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921647 | |||||||
| chr8:36921659 | GA | G | 245 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(242): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.2597-810delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36921659 | ||||||
| chr8:36921659 | GAA | G | 17 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0257 others(14): Show |
17 | HG00099.hp1 HG00735.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.2597-811_2597-810d others(4): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36921659 | ||||||
| chr8:36921659 | GAAAAAAA others(3): Show |
G | 1 | a0003c0003t0001g0005 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2597-819_2597-810d others(12): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36921659 | ||||||
| chr8:36921808 | G | A | 1 | a0002c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2597-682G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36921808 | |||||||
| chr8:36922172 | C | T | 1 | a0001c0002t0001g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2597-318C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36922172 | |||||||
| chr8:36922284 | A | G | 1 | a0002c0001t0001g0129 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2597-206A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36922284 | |||||||
| chr8:36922330 | GA | G | 76 | a0001c0002t0001g0143 a0001c0002t0001g0262 a0001c0002t0001g0285 others(73): Show |
78 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2597-150delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36922330 | ||||||
| chr8:36922421 | G | T | 40 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0004t0001g0002 others(37): Show |
42 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2597-69G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | chr8 | 36922421 | |||||||
| chr8:36922432 | ACTT | A | 6 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2597-54_2597-52del others(3): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr8 | 36922432 | ||||||
| chr8:36922691 | A | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2736+62A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36922691 | |||||||
| chr8:36922768 | C | T | 1 | a0001c0004t0001g0200 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2736+139C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36922768 | |||||||
| chr8:36923142 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2736+513T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923142 | |||||||
| chr8:36923228 | A | G | 1 | a0002c0016t0001g0223 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2736+599A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923228 | |||||||
| chr8:36923408 | A | G | 1 | a0002c0001t0001g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2736+779A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923408 | |||||||
| chr8:36923527 | G | C | 1 | a0002c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2736+898G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923527 | |||||||
| chr8:36923844 | G | A | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2736+1215G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923844 | |||||||
| chr8:36923979 | T | C | 1 | a0002c0001t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2736+1350T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923979 | |||||||
| chr8:36923986 | G | A | 120 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2736+1357G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36923986 | |||||||
| chr8:36924017 | G | T | 1 | a0001c0002t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2736+1388G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924017 | |||||||
| chr8:36924031 | A | G | 1 | a0001c0002t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2736+1402A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924031 | |||||||
| chr8:36924655 | G | T | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2736+2026G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924655 | |||||||
| chr8:36924896 | T | C | 6 | a0002c0001t0001g0024 a0002c0001t0001g0031 a0002c0001t0001g0037 others(3): Show |
6 | HG01258.hp2 HG02004.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2736+2267T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36924896 | |||||||
| chr8:36925114 | T | A | 1 | a0006c0008t0001g0278 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2736+2485T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925114 | |||||||
| chr8:36925259 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2736+2630C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925259 | |||||||
| chr8:36925354 | G | A | 6 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2736+2725G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925354 | |||||||
| chr8:36925675 | C | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2736+3046C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36925675 | |||||||
| chr8:36926009 | A | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2736+3380A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926009 | |||||||
| chr8:36926291 | C | A | 2 | a0001c0002t0001g0237 a0001c0002t0001g0265 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2736+3662C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926291 | |||||||
| chr8:36926297 | G | C | 1 | a0001c0002t0001g0253 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2736+3668G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926297 | |||||||
| chr8:36926501 | A | T | 1 | a0002c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2736+3872A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926501 | |||||||
| chr8:36926622 | C | T | 44 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0171 others(41): Show |
46 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2736+3993C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926622 | |||||||
| chr8:36926825 | C | T | 1 | a0002c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2737-4126C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926825 | |||||||
| chr8:36926840 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2737-4111T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926840 | |||||||
| chr8:36926878 | G | A | 1 | a0002c0016t0001g0223 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2737-4073G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926878 | |||||||
| chr8:36926890 | G | A | 1 | a0003c0003t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2737-4061G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926890 | |||||||
| chr8:36926891 | G | A | 1 | a0002c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2737-4060G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36926891 | |||||||
| chr8:36927002 | C | T | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-3949C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927002 | |||||||
| chr8:36927338 | T | C | 3 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0282 |
3 | HG02055.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2737-3613T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927338 | |||||||
| chr8:36927350 | T | C | 1 | a0001c0002t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2737-3601T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927350 | |||||||
| chr8:36927457 | A | T | 1 | a0002c0001t0001g0019 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2737-3494A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927457 | |||||||
| chr8:36927545 | G | T | 1 | a0003c0003t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2737-3406G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927545 | |||||||
| chr8:36927792 | A | T | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-3159A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927792 | |||||||
| chr8:36927857 | G | T | 1 | a0001c0004t0001g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2737-3094G>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927857 | |||||||
| chr8:36927942 | G | C | 1 | a0001c0002t0001g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2737-3009G>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927942 | |||||||
| chr8:36927966 | C | T | 1 | a0001c0017t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2737-2985C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927966 | |||||||
| chr8:36927986 | A | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2737-2965A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36927986 | |||||||
| chr8:36928097 | C | T | 1 | a0002c0001t0001g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2737-2854C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928097 | |||||||
| chr8:36928647 | G | A | 2 | a0001c0002t0001g0275 a0001c0002t0001g0276 |
2 | HG01167.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2737-2304G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928647 | |||||||
| chr8:36928649 | C | G | 2 | a0002c0001t0001g0027 a0002c0001t0001g0052 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2737-2302C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928649 | |||||||
| chr8:36928716 | C | T | 286 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(283): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2737-2235C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928716 | |||||||
| chr8:36928760 | C | G | 286 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(283): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2737-2191C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928760 | |||||||
| chr8:36928861 | C | A | 65 | a0001c0002t0001g0003 a0001c0002t0001g0018 a0001c0002t0001g0047 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.2737-2090C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928861 | |||||||
| chr8:36928878 | C | T | 191 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2737-2073C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928878 | |||||||
| chr8:36928884 | C | G | 1 | a0002c0001t0001g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2737-2067C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928884 | |||||||
| chr8:36928942 | T | C | 2 | a0003c0003t0001g0096 a0003c0003t0001g0097 |
2 | HG00140.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.2737-2009T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36928942 | |||||||
| chr8:36929260 | T | C | 4 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(1): Show |
4 | HG01891.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2737-1691T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929260 | |||||||
| chr8:36929303 | G | A | 1 | a0003c0003t0001g0258 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2737-1648G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929303 | |||||||
| chr8:36929387 | CA | C | 17 | a0001c0002t0001g0285 a0001c0002t0001g0287 a0001c0002t0001g0288 others(14): Show |
17 | HG01515.hp1 HG01516.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2737-1544delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36929387 | ||||||
| chr8:36929387 | CAA | C | 63 | a0001c0002t0001g0051 a0001c0004t0001g0226 a0001c0004t0001g0227 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2737-1545_2737-154 others(6): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36929387 | ||||||
| chr8:36929387 | CAAA | C | 119 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(116): Show |
122 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2737-1546_2737-154 others(7): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36929387 | ||||||
| chr8:36929429 | A | AC | 42 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0156 others(39): Show |
44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2737-1522_2737-152 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929429 | |||||||
| chr8:36929435 | A | AG | 72 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2737-1516_2737-151 others(5): Show |
KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929435 | |||||||
| chr8:36929435 | A | C | 2 | a0003c0003t0001g0086 a0003c0003t0001g0117 |
2 | NA18962.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2737-1516A>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929435 | |||||||
| chr8:36929435 | A | G | 42 | a0001c0002t0001g0108 a0001c0002t0001g0122 a0001c0002t0001g0156 others(39): Show |
44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2737-1516A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929435 | |||||||
| chr8:36929635 | T | C | 2 | a0001c0002t0001g0014 a0001c0002t0001g0174 |
2 | HG01074.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2737-1316T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929635 | |||||||
| chr8:36929772 | A | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2737-1179A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36929772 | |||||||
| chr8:36930219 | T | TG | 5 | a0003c0005t0001g0188 a0003c0005t0001g0195 a0003c0005t0001g0196 others(2): Show |
5 | HG00621.hp1 NA18980.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2737-731dupG | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr8 | 36930219 | ||||||
| chr8:36930382 | T | A | 1 | a0001c0002t0001g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2737-569T>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930382 | |||||||
| chr8:36930473 | A | T | 1 | a0001c0004t0001g0215 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2737-478A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930473 | |||||||
| chr8:36930498 | C | T | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2737-453C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930498 | |||||||
| chr8:36930866 | C | T | 3 | a0003c0003t0001g0017 a0003c0005t0001g0221 a0003c0005t0001g0222 |
3 | HG02258.hp1 NA19084.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2737-85C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930866 | |||||||
| chr8:36930873 | A | T | 1 | a0003c0003t0001g0146 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2737-78A>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930873 | |||||||
| chr8:36930887 | T | G | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-64T>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930887 | |||||||
| chr8:36930889 | C | A | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-62C>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930889 | |||||||
| chr8:36930891 | C | T | 2 | a0001c0002t0001g0143 a0006c0008t0001g0278 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2737-60C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930891 | |||||||
| chr8:36930938 | C | G | 2 | a0002c0001t0001g0147 a0002c0001t0001g0148 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2737-13C>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 24/26 | chr8 | 36930938 | |||||||
| chr8:36931175 | T | C | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2931+30T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931175 | |||||||
| chr8:36931418 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2931+273A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931418 | |||||||
| chr8:36931798 | T | C | 1 | a0003c0003t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2931+653T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931798 | |||||||
| chr8:36931805 | T | C | 1 | a0002c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2931+660T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36931805 | |||||||
| chr8:36932073 | A | G | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2932-847A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932073 | |||||||
| chr8:36932108 | G | A | 6 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932-812G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932108 | |||||||
| chr8:36932215 | C | T | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2932-705C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932215 | |||||||
| chr8:36932518 | G | A | 6 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2932-402G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932518 | |||||||
| chr8:36932665 | CA | C | 10 | a0002c0001t0001g0030 a0002c0001t0001g0036 a0002c0001t0001g0039 others(7): Show |
10 | HG00621.hp2 HG00735.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2932-254delA | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932665 | |||||||
| chr8:36932821 | G | A | 63 | a0003c0003t0001g0001 a0003c0003t0001g0005 a0003c0003t0001g0006 others(60): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2932-99G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932821 | |||||||
| chr8:36932914 | C | T | 1 | a0003c0003t0001g0230 | 1 | NA18972.hp2 | splice_region_variant&intron_variant | LOW | c.2932-6C>T | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 25/26 | chr8 | 36932914 | |||||||
| chr8:36933202 | G | A | 1 | a0003c0003t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3044+170G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933202 | |||||||
| chr8:36933252 | G | A | 6 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0177 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3044+220G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933252 | |||||||
| chr8:36933617 | A | G | 3 | a0002c0007t0001g0046 a0002c0007t0001g0069 a0002c0007t0001g0152 |
3 | HG02615.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3044+585A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933617 | |||||||
| chr8:36933699 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3044+667G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36933699 | |||||||
| chr8:36934446 | T | C | 1 | a0001c0002t0001g0280 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3045-1069T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934446 | |||||||
| chr8:36934525 | G | A | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.3045-990G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934525 | |||||||
| chr8:36934614 | T | C | 16 | a0002c0001t0001g0015 a0002c0001t0001g0107 a0002c0001t0001g0109 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.3045-901T>C | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934614 | |||||||
| chr8:36934745 | A | G | 1 | a0002c0001t0001g0066 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3045-770A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934745 | |||||||
| chr8:36934903 | G | A | 195 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0018 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.3045-612G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36934903 | |||||||
| chr8:36935098 | G | A | 2 | a0002c0001t0001g0010 a0002c0001t0001g0102 |
2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3045-417G>A | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36935098 | |||||||
| chr8:36935173 | A | G | 6 | a0001c0002t0001g0143 a0001c0002t0001g0285 a0001c0002t0001g0287 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3045-342A>G | KCNU1 | ENSG00000215262.8 | transcript | ENST00000399881.8 | protein_coding | 26/26 | chr8 | 36935173 |