Item | Value |
---|---|
geneid | 7443 |
ensemblid | ENSG00000100749.9 |
hgncid | 12718 |
symbol | VRK1 |
name | VRK serine/threonine kinase 1 |
refseq_nuc | NM_003384.3 |
refseq_prot | NP_003375.1 |
ensembl_nuc | ENST00000216639.8 |
ensembl_prot | ENSP00000216639.3 |
mane_status | MANE Select |
chr | chr14 |
start | 96797382 |
end | 96881609 |
strand | + |
ver | v1.2 |
region | chr14:96797382-96881609 |
region5000 | chr14:96792382-96886609 |
regionname0 | VRK1_chr14_96797382_96881609 |
regionname5000 | VRK1_chr14_96792382_96886609 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 396 | 277 | 88 | 60 | 77 | 10 | 40 | 68 | VRK1_chr14_96792382_96886609 | VRK1 | MPRVK others(391): Show |
chr14 | 96792382 | 96886609 |
a0002 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | MPRVK others(369): Show |
chr14 | 96792382 | 96886609 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1188 | 106 | 15 | 28 | 43 | 5 | 15 | VRK1_chr14_96792382_96886609 | VRK1 | ATGCC others(1183): Show |
chr14 | 96792382 | 96886609 | ||
a0001c0002 | 1/0 | 1188 | 101 | 54 | 12 | 18 | 2 | 14 | VRK1_chr14_96792382_96886609 | VRK1 | ATGCC others(1183): Show |
chr14 | 96792382 | 96886609 | ||
a0001c0003 | 0/1 | 1188 | 70 | 19 | 20 | 16 | 3 | 11 | VRK1_chr14_96792382_96886609 | VRK1 | ATGCC others(1183): Show |
chr14 | 96792382 | 96886609 | ||
a0002c0004 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | ATGCC others(1183): Show |
chr14 | 96792382 | 96886609 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1663 | 105 | 14 | 28 | 43 | 5 | 15 | VRK1_chr14_96792382_96886609 | VRK1 | GTTAC others(1658): Show |
chr14 | 96792382 | 96886609 |
a0001c0001t0002 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | GTTAC others(1658): Show |
chr14 | 96792382 | 96886609 |
a0001c0002t0001 | 1/0 | 1663 | 100 | 53 | 12 | 18 | 2 | 14 | VRK1_chr14_96792382_96886609 | VRK1 | GTTAC others(1658): Show |
chr14 | 96792382 | 96886609 |
a0001c0002t0003 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | GTTAC others(1658): Show |
chr14 | 96792382 | 96886609 |
a0001c0003t0001 | 0/1 | 1663 | 70 | 19 | 20 | 16 | 3 | 11 | VRK1_chr14_96792382_96886609 | VRK1 | GTTAC others(1658): Show |
chr14 | 96792382 | 96886609 |
a0002c0004t0001 | 0/0 | 1663 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | GTTAC others(1658): Show |
chr14 | 96792382 | 96886609 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | GBR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0026 | EUR | GBR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00438 | hp2 | a0002 | c0004 | t0001 | g0184 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | CHS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0052 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0062 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0050 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0045 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | CLM | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0055 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0016 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0053 | EUR | IBS | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | KHV | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0244 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0051 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0044 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0060 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0095 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0072 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0054 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0059 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0092 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0047 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0080 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0049 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0046 | SAS | STU | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0240 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18945 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0237 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | LWK | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19055 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | YRI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ASW | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | TSI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | MSL | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | USA | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0074 | REF | REF | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0195 | REF | REF | VRK1_chr14_96792382_96886609 | VRK1 | chr14 | 96792382 | 96886609 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96876085 | G | A | 1 | a0002 | 1 | HG00438.hp2 | stop_gained | HIGH | c.1124G>A | p.Trp375* | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/13 | 1195/1663 | 1124/1191 | 375/396 | chr14 | 96876085 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96833516 | A | G | 1 | a0001c0003 | 69 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
synonymous_variant | LOW | c.45A>G | p.Ala15Ala | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/13 | 116/1663 | 45/1191 | 15/396 | chr14 | 96833516 | |||
chr14:96855352 | C | T | 2 | a0001c0001 a0002c0004 |
107 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
synonymous_variant | LOW | c.705C>T | p.Gly235Gly | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/13 | 776/1663 | 705/1191 | 235/396 | chr14 | 96855352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96881263 | C | G | 1 | a0001c0002t0003 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 13/13 | 55 | chr14 | 96881263 | ||||||
chr14:96881388 | C | T | 1 | a0001c0001t0002 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 13/13 | 180 | chr14 | 96881388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96797538 | C | T | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+91C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797538 | |||||||
chr14:96797592 | T | C | 133 | a0001c0001t0001g0039 a0001c0002t0001g0008 a0001c0002t0001g0017 others(130): Show |
152 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-6+145T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797592 | |||||||
chr14:96797716 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+269C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797716 | |||||||
chr14:96797737 | C | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+290C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797737 | |||||||
chr14:96797775 | G | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+328G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797775 | |||||||
chr14:96797813 | G | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+366G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797813 | |||||||
chr14:96797937 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0138 |
4 | HG01891.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+490G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96797937 | |||||||
chr14:96798045 | A | G | 20 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(17): Show |
23 | HG01069.hp1 HG01071.hp2 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.-6+598A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798045 | |||||||
chr14:96798241 | C | T | 16 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+794C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798241 | |||||||
chr14:96798247 | C | G | 31 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(28): Show |
35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+800C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798247 | |||||||
chr14:96798495 | A | G | 11 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0126 others(8): Show |
13 | NA18943.hp2 NA18960.hp2 NA18962.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6+1048A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798495 | |||||||
chr14:96798530 | G | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+1083G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798530 | |||||||
chr14:96798594 | G | A | 2 | a0001c0003t0001g0037 a0001c0003t0001g0038 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-6+1147G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798594 | |||||||
chr14:96798835 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+1388C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798835 | |||||||
chr14:96798884 | C | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+1437C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798884 | |||||||
chr14:96798958 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-6+1511T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798958 | |||||||
chr14:96798970 | G | A | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+1523G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96798970 | |||||||
chr14:96799026 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-6+1579A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96799026 | |||||||
chr14:96799326 | C | CT | 26 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(23): Show |
29 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-6+1889dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96799326 | ||||||
chr14:96799576 | A | G | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-6+2129A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96799576 | |||||||
chr14:96799792 | G | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+2345G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96799792 | |||||||
chr14:96799947 | C | CT | 5 | a0001c0001t0001g0234 a0001c0003t0001g0092 a0001c0003t0001g0093 others(2): Show |
5 | HG02738.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2517dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96799947 | ||||||
chr14:96799947 | CT | C | 13 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
14 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6+2517delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96799947 | ||||||
chr14:96800015 | C | A | 125 | a0001c0002t0001g0008 a0001c0002t0001g0018 a0001c0002t0001g0019 others(122): Show |
143 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-6+2568C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800015 | |||||||
chr14:96800174 | A | G | 1 | a0001c0002t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-6+2727A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800174 | |||||||
chr14:96800720 | A | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+3273A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800720 | |||||||
chr14:96800790 | G | A | 6 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+3343G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800790 | |||||||
chr14:96800813 | T | C | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+3366T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800813 | |||||||
chr14:96800844 | G | T | 1 | a0001c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-6+3397G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96800844 | |||||||
chr14:96801252 | A | T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0082 |
3 | HG01069.hp2 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-6+3805A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801252 | |||||||
chr14:96801358 | G | A | 1 | a0001c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-6+3911G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801358 | |||||||
chr14:96801850 | G | A | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+4403G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801850 | |||||||
chr14:96801923 | A | G | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+4476A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96801923 | |||||||
chr14:96802209 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18966.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-6+4762C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802209 | |||||||
chr14:96802210 | G | A | 59 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(56): Show |
65 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.-6+4763G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802210 | |||||||
chr14:96802221 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+4774C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802221 | |||||||
chr14:96802287 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-6+4840C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802287 | |||||||
chr14:96802318 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+4871A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802318 | |||||||
chr14:96802321 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-6+4874C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802321 | |||||||
chr14:96802394 | A | G | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+4947A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802394 | |||||||
chr14:96802403 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-6+4956C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802403 | |||||||
chr14:96802565 | C | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+5118C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802565 | |||||||
chr14:96802635 | G | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+5188G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802635 | |||||||
chr14:96802796 | T | C | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+5349T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802796 | |||||||
chr14:96802860 | C | A | 64 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(61): Show |
76 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-6+5413C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802860 | |||||||
chr14:96802965 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-6+5518A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96802965 | |||||||
chr14:96803030 | C | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
72 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6+5583C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803030 | |||||||
chr14:96803168 | A | AT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0192 a0001c0001t0001g0227 others(6): Show |
11 | HG01952.hp1 HG02258.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+5741dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96803168 | ||||||
chr14:96803168 | AT | A | 32 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0002t0001g0018 others(29): Show |
36 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6+5741delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96803168 | ||||||
chr14:96803186 | T | C | 58 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(55): Show |
70 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-6+5739T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803186 | |||||||
chr14:96803187 | T | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0041 |
3 | HG00642.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6+5740T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803187 | |||||||
chr14:96803228 | A | G | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+5781A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803228 | |||||||
chr14:96803257 | C | T | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-6+5810C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803257 | |||||||
chr14:96803305 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+5858G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803305 | |||||||
chr14:96803315 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-6+5868C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803315 | |||||||
chr14:96803388 | C | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+5941C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803388 | |||||||
chr14:96803740 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+6293A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96803740 | |||||||
chr14:96804502 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
266 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.-6+7055A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804502 | |||||||
chr14:96804555 | T | C | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+7108T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804555 | |||||||
chr14:96804660 | A | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-6+7213A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804660 | |||||||
chr14:96804892 | A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6+7445A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804892 | |||||||
chr14:96804919 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+7472T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804919 | |||||||
chr14:96804954 | A | C | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+7507A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96804954 | |||||||
chr14:96805141 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-6+7694T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805141 | |||||||
chr14:96805404 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+7957A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805404 | |||||||
chr14:96805422 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-6+7975C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805422 | |||||||
chr14:96805477 | A | G | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+8030A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805477 | |||||||
chr14:96805651 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+8204C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805651 | |||||||
chr14:96805984 | C | CT | 4 | a0001c0002t0001g0117 a0001c0003t0001g0015 a0001c0003t0001g0093 others(1): Show |
5 | HG02970.hp1 HG02976.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8554dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96805984 | ||||||
chr14:96805984 | CT | C | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0002t0001g0118 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+8554delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96805984 | ||||||
chr14:96805984 | CTTTTTTT | C | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8548_-6+8554del others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96805984 | ||||||
chr14:96805990 | T | C | 3 | a0001c0002t0001g0135 a0001c0002t0001g0136 a0001c0002t0001g0137 |
3 | HG02965.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+8543T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96805990 | |||||||
chr14:96806045 | T | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
76 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-6+8598T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806045 | |||||||
chr14:96806067 | C | T | 1 | a0001c0003t0001g0080 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-6+8620C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806067 | |||||||
chr14:96806216 | C | T | 6 | a0001c0002t0001g0018 a0001c0002t0001g0096 a0001c0002t0001g0097 others(3): Show |
7 | HG01074.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+8769C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806216 | |||||||
chr14:96806227 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+8780G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806227 | |||||||
chr14:96806292 | C | T | 3 | a0001c0002t0001g0120 a0001c0002t0001g0124 a0001c0002t0001g0125 |
3 | NA18944.hp1 NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-6+8845C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806292 | |||||||
chr14:96806294 | T | G | 1 | a0001c0003t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6+8847T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806294 | |||||||
chr14:96806441 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-6+8994T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806441 | |||||||
chr14:96806622 | C | T | 56 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0020 others(53): Show |
61 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6+9175C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806622 | |||||||
chr14:96806660 | A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6+9213A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806660 | |||||||
chr14:96806740 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-6+9293A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806740 | |||||||
chr14:96806834 | T | C | 1 | a0001c0003t0001g0015 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-6+9387T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96806834 | |||||||
chr14:96807104 | T | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0193 a0001c0001t0001g0206 others(11): Show |
15 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6+9657T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807104 | |||||||
chr14:96807115 | C | T | 6 | a0001c0001t0001g0193 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG01192.hp1 HG01346.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+9668C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807115 | |||||||
chr14:96807165 | G | T | 1 | a0001c0003t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-6+9718G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807165 | |||||||
chr14:96807264 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6+9817C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807264 | |||||||
chr14:96807633 | A | G | 6 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+10186A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807633 | |||||||
chr14:96807669 | A | G | 4 | a0001c0003t0001g0075 a0001c0003t0001g0076 a0001c0003t0001g0077 others(1): Show |
4 | HG02080.hp2 NA18964.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+10222A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807669 | |||||||
chr14:96807955 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-6+10508G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96807955 | |||||||
chr14:96808002 | C | CCTCTCTC others(21): Show |
2 | a0001c0002t0001g0104 a0001c0002t0001g0105 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(30): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(3): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0140 |
4 | HG01261.hp2 HG01496.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(5): Show |
28 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(25): Show |
32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(7): Show |
1 | a0001c0002t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-6+10562_-6+10563i others(16): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(9): Show |
4 | a0001c0002t0001g0109 a0001c0003t0001g0081 a0001c0003t0001g0093 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(18): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(39): Show |
2 | a0001c0002t0001g0116 a0001c0002t0001g0137 |
2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(48): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(29): Show |
2 | a0001c0002t0001g0089 a0001c0002t0001g0090 |
2 | HG02602.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(38): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(35): Show |
5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(44): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CCTCTCTC others(13): Show |
30 | a0001c0002t0001g0040 a0001c0002t0001g0106 a0001c0003t0001g0002 others(27): Show |
37 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(22): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808002 | ||||||
chr14:96808002 | C | CGTCTCTC others(1): Show |
6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | |||||||
chr14:96808002 | C | CGTCTCTC others(35): Show |
2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(44): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | |||||||
chr14:96808002 | C | CGTCTCTC others(3): Show |
3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | |||||||
chr14:96808002 | C | CGTCTCTC others(5): Show |
4 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0003t0001g0092 others(1): Show |
4 | HG02630.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10555_-6+10556i others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | |||||||
chr14:96808002 | C | T | 2 | a0001c0002t0001g0034 a0001c0002t0001g0035 |
2 | NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-6+10555C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808002 | |||||||
chr14:96808003 | C | CTCTCTCC others(27): Show |
2 | a0001c0002t0001g0017 a0001c0002t0001g0088 |
3 | HG02572.hp1 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(36): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808003 | ||||||
chr14:96808003 | C | CTCTCTCC others(13): Show |
2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(22): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808003 | ||||||
chr14:96808003 | C | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10556C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808003 | |||||||
chr14:96808005 | C | CTCTCCGT others(35): Show |
8 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(5): Show |
9 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(44): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808005 | ||||||
chr14:96808007 | C | CTCCGTCT others(23): Show |
3 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0091 |
3 | HG03098.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(32): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808007 | ||||||
chr14:96808009 | C | CCG | 24 | a0001c0003t0001g0001 a0001c0003t0001g0010 a0001c0003t0001g0011 others(21): Show |
29 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-6+10562_-6+10563i others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808009 | |||||||
chr14:96808012 | TCC | T | 7 | a0001c0002t0001g0008 a0001c0002t0001g0027 a0001c0002t0001g0028 others(4): Show |
8 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10567_-6+10568d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808012 | ||||||
chr14:96808014 | C | T | 88 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0002t0001g0017 others(85): Show |
101 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.-6+10567C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808014 | |||||||
chr14:96808017 | C | CTCTCTCT others(19): Show |
22 | a0001c0003t0001g0001 a0001c0003t0001g0010 a0001c0003t0001g0011 others(19): Show |
27 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-6+10571_-6+10572i others(28): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | C | CTCTCTCT others(21): Show |
1 | a0001c0003t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-6+10571_-6+10572i others(30): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | C | CTCTCTCT others(23): Show |
1 | a0001c0003t0001g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-6+10571_-6+10572i others(32): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | C | CTG | 9 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0107 others(6): Show |
9 | HG01099.hp2 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10607_-6+10608d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | C | CTGTG | 7 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0083 others(4): Show |
7 | HG02486.hp2 HG03098.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+10605_-6+10608d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | C | CTGTGTG | 24 | a0001c0002t0001g0036 a0001c0002t0001g0084 a0001c0003t0001g0009 others(21): Show |
29 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-6+10603_-6+10608d others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | C | CTGTGTGT others(3): Show |
1 | a0001c0002t0001g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-6+10599_-6+10608d others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | CTGTGTG | C | 4 | a0001c0001t0001g0141 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG01099.hp1 HG03491.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10603_-6+10608d others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | CTGTGTGT others(1): Show |
C | 26 | a0001c0001t0001g0025 a0001c0001t0001g0142 a0001c0001t0001g0189 others(23): Show |
27 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6+10601_-6+10608d others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | CTGTGTGT others(3): Show |
C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
72 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-6+10599_-6+10608d others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808017 | CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA18982.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-6+10597_-6+10608d others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808017 | ||||||
chr14:96808018 | T | C | 24 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(21): Show |
25 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6+10571T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808018 | |||||||
chr14:96808019 | G | C | 71 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0002t0001g0008 others(68): Show |
80 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-6+10572G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808019 | |||||||
chr14:96808020 | T | C | 2 | a0001c0002t0001g0040 a0001c0002t0001g0123 |
2 | HG00733.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-6+10573T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808020 | |||||||
chr14:96808021 | G | C | 71 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0002t0001g0008 others(68): Show |
80 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-6+10574G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808021 | |||||||
chr14:96808022 | T | C | 28 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(25): Show |
32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-6+10575T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808022 | |||||||
chr14:96808023 | G | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0002t0001g0008 others(44): Show |
55 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-6+10576G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808023 | |||||||
chr14:96808024 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0140 |
4 | HG01261.hp2 HG01496.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+10577T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808024 | |||||||
chr14:96808025 | G | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0002t0001g0008 others(42): Show |
53 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.-6+10578G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808025 | |||||||
chr14:96808027 | G | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0140 a0001c0002t0001g0008 others(14): Show |
21 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6+10580G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808027 | |||||||
chr14:96808028 | T | C | 1 | a0001c0002t0001g0026 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6+10581T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808028 | |||||||
chr14:96808029 | G | C | 15 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0026 others(12): Show |
17 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+10582G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808029 | |||||||
chr14:96808030 | T | C | 7 | a0001c0002t0001g0008 a0001c0002t0001g0027 a0001c0002t0001g0028 others(4): Show |
8 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10583T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808030 | |||||||
chr14:96808031 | G | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+10584G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808031 | |||||||
chr14:96808033 | G | C | 7 | a0001c0002t0001g0008 a0001c0002t0001g0027 a0001c0002t0001g0028 others(4): Show |
8 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+10586G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808033 | |||||||
chr14:96808054 | T | C | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+10607T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808054 | |||||||
chr14:96808057 | A | G | 31 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(28): Show |
35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+10610A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808057 | |||||||
chr14:96808091 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6+10644G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808091 | |||||||
chr14:96808117 | G | A | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+10670G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808117 | |||||||
chr14:96808264 | T | C | 12 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(9): Show |
12 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+10817T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808264 | |||||||
chr14:96808415 | G | A | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-6+10968G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808415 | |||||||
chr14:96808433 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
266 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.-6+10986G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808433 | |||||||
chr14:96808658 | C | CT | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0002t0001g0244 others(2): Show |
5 | HG00738.hp1 HG01261.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+11228dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808658 | ||||||
chr14:96808658 | CTTTTT | C | 38 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(35): Show |
43 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-6+11224_-6+11228d others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96808658 | ||||||
chr14:96808910 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+11463C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808910 | |||||||
chr14:96808919 | A | G | 129 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(126): Show |
147 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.-6+11472A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96808919 | |||||||
chr14:96809012 | G | A | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+11565G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809012 | |||||||
chr14:96809230 | C | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+11783C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809230 | |||||||
chr14:96809384 | C | G | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+11937C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809384 | |||||||
chr14:96809548 | A | AGCTT | 114 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(111): Show |
131 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-6+12118_-6+12121d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96809548 | ||||||
chr14:96809569 | T | G | 29 | a0001c0001t0001g0202 a0001c0002t0001g0019 a0001c0002t0001g0026 others(26): Show |
30 | HG00140.hp2 HG01109.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.-6+12122T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809569 | |||||||
chr14:96809570 | C | CT | 11 | a0001c0001t0001g0186 a0001c0001t0001g0225 a0001c0002t0001g0008 others(8): Show |
12 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+12141dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96809570 | ||||||
chr14:96809571 | T | TTTC | 7 | a0001c0002t0001g0086 a0001c0002t0001g0242 a0001c0002t0001g0243 others(4): Show |
7 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+12126_-6+12127i others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96809571 | ||||||
chr14:96809668 | G | A | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6+12221G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809668 | |||||||
chr14:96809950 | A | C | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+12503A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96809950 | |||||||
chr14:96810330 | A | G | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+12883A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810330 | |||||||
chr14:96810352 | C | T | 2 | a0001c0001t0001g0185 a0001c0003t0001g0011 |
3 | HG01256.hp1 HG01258.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-6+12905C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810352 | |||||||
chr14:96810668 | C | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
80 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-6+13221C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810668 | |||||||
chr14:96810683 | A | C | 16 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+13236A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810683 | |||||||
chr14:96810704 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-6+13257G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810704 | |||||||
chr14:96810786 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+13339T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810786 | |||||||
chr14:96810837 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-6+13390T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810837 | |||||||
chr14:96810858 | T | C | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-6+13411T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810858 | |||||||
chr14:96810894 | T | C | 2 | a0001c0002t0001g0006 a0001c0002t0001g0194 |
4 | HG01891.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+13447T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96810894 | |||||||
chr14:96810933 | A | AT | 34 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(31): Show |
38 | HG01071.hp2 HG01074.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.-6+13497dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96810933 | ||||||
chr14:96810933 | AT | A | 61 | a0001c0002t0001g0040 a0001c0002t0001g0083 a0001c0002t0001g0084 others(58): Show |
73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-6+13497delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96810933 | ||||||
chr14:96810960 | T | TG | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+13515dupG | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96810960 | ||||||
chr14:96811032 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-6+13585C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811032 | |||||||
chr14:96811086 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+13639C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811086 | |||||||
chr14:96811105 | A | G | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+13658A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811105 | |||||||
chr14:96811188 | C | T | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-6+13741C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811188 | |||||||
chr14:96811284 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02818.hp1 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-6+13837T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811284 | |||||||
chr14:96811348 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+13901G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811348 | |||||||
chr14:96811410 | A | G | 1 | a0001c0003t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-6+13963A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811410 | |||||||
chr14:96811485 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+14038A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811485 | |||||||
chr14:96811537 | G | A | 60 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(57): Show |
72 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-6+14090G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811537 | |||||||
chr14:96811585 | A | C | 31 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(28): Show |
35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6+14138A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811585 | |||||||
chr14:96811628 | G | C | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+14181G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811628 | |||||||
chr14:96811685 | T | G | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-6+14238T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811685 | |||||||
chr14:96811755 | A | C | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-6+14308A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811755 | |||||||
chr14:96811773 | C | CT | 134 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(131): Show |
153 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.-6+14337dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96811773 | ||||||
chr14:96811915 | A | G | 1 | a0001c0002t0003g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-6+14468A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811915 | |||||||
chr14:96811993 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-6+14546G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96811993 | |||||||
chr14:96812315 | C | T | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-6+14868C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812315 | |||||||
chr14:96812381 | G | T | 1 | a0001c0002t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+14934G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812381 | |||||||
chr14:96812808 | T | C | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+15361T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812808 | |||||||
chr14:96812811 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-6+15364A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812811 | |||||||
chr14:96812834 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+15387C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812834 | |||||||
chr14:96812883 | T | C | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-6+15436T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812883 | |||||||
chr14:96812957 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+15510G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96812957 | |||||||
chr14:96813120 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-6+15673C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813120 | |||||||
chr14:96813590 | C | T | 1 | a0001c0003t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-6+16143C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813590 | |||||||
chr14:96813703 | A | G | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6+16256A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813703 | |||||||
chr14:96813784 | A | G | 12 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(9): Show |
13 | HG02145.hp2 HG02572.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6+16337A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813784 | |||||||
chr14:96813857 | T | G | 1 | a0001c0002t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6+16410T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813857 | |||||||
chr14:96813880 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-6+16433G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96813880 | |||||||
chr14:96814003 | A | G | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+16556A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814003 | |||||||
chr14:96814037 | G | A | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+16590G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814037 | |||||||
chr14:96814288 | G | GATCA | 2 | a0001c0003t0001g0009 a0001c0003t0001g0041 |
3 | HG00642.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6+16841_-6+16842i others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814288 | |||||||
chr14:96814291 | T | C | 2 | a0001c0003t0001g0009 a0001c0003t0001g0041 |
3 | HG00642.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6+16844T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814291 | |||||||
chr14:96814341 | A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6+16894A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814341 | |||||||
chr14:96814647 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+17200G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814647 | |||||||
chr14:96814681 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-6+17234C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814681 | |||||||
chr14:96814908 | C | T | 100 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(97): Show |
116 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6+17461C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814908 | |||||||
chr14:96814919 | A | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+17472A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96814919 | |||||||
chr14:96815009 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+17562G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815009 | |||||||
chr14:96815410 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6+17963G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815410 | |||||||
chr14:96815474 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-17993C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815474 | |||||||
chr14:96815823 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-5-17644G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815823 | |||||||
chr14:96815965 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-5-17502G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96815965 | |||||||
chr14:96816015 | A | T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0082 |
3 | HG01069.hp2 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-5-17452A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816015 | |||||||
chr14:96816098 | T | C | 36 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(33): Show |
40 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-5-17369T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816098 | |||||||
chr14:96816175 | C | T | 2 | a0001c0002t0001g0115 a0001c0002t0001g0117 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-5-17292C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816175 | |||||||
chr14:96816209 | G | A | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-17258G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816209 | |||||||
chr14:96816230 | G | A | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-17237G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816230 | |||||||
chr14:96816436 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5-17031C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816436 | |||||||
chr14:96816765 | TGAC | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-16701_-5-16699d others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96816765 | |||||||
chr14:96817158 | C | T | 137 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(134): Show |
156 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-5-16309C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817158 | |||||||
chr14:96817186 | G | T | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-16281G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817186 | |||||||
chr14:96817276 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
76 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-5-16191T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817276 | |||||||
chr14:96817349 | T | C | 137 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(134): Show |
156 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-5-16118T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817349 | |||||||
chr14:96817612 | T | C | 6 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(3): Show |
7 | HG02055.hp2 HG02109.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-15855T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817612 | |||||||
chr14:96817708 | A | T | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5-15759A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817708 | |||||||
chr14:96817744 | C | A | 1 | a0001c0002t0001g0028 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-15723C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817744 | |||||||
chr14:96817883 | A | T | 1 | a0001c0002t0001g0022 | 2 | NA18991.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-5-15584A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817883 | |||||||
chr14:96817898 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-5-15569G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96817898 | |||||||
chr14:96818064 | T | TGGATCCT others(300): Show |
1 | a0001c0002t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5-15100_-5-15099i others(309): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96818064 | ||||||
chr14:96818169 | G | GCTTGTGT others(300): Show |
2 | a0001c0002t0001g0083 a0001c0002t0001g0085 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-15100_-5-15099i others(309): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96818169 | ||||||
chr14:96818416 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-5-15051A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818416 | |||||||
chr14:96818903 | G | T | 1 | a0001c0003t0001g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5-14564G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818903 | |||||||
chr14:96818956 | A | G | 6 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-14511A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818956 | |||||||
chr14:96818981 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5-14486C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818981 | |||||||
chr14:96818988 | G | A | 1 | a0001c0003t0001g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-5-14479G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96818988 | |||||||
chr14:96819094 | T | A | 2 | a0001c0003t0001g0093 a0001c0003t0001g0094 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-5-14373T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819094 | |||||||
chr14:96819147 | A | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-14320A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819147 | |||||||
chr14:96819284 | C | G | 1 | a0001c0002t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-5-14183C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819284 | |||||||
chr14:96819333 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5-14134A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819333 | |||||||
chr14:96819429 | C | T | 1 | a0001c0002t0001g0035 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-5-14038C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819429 | |||||||
chr14:96819542 | G | A | 2 | a0001c0001t0001g0152 a0001c0002t0001g0128 |
2 | HG01978.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-5-13925G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819542 | |||||||
chr14:96819768 | A | G | 137 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(134): Show |
156 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-5-13699A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819768 | |||||||
chr14:96819807 | C | T | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-13660C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819807 | |||||||
chr14:96819914 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-5-13553C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96819914 | |||||||
chr14:96820152 | C | CT | 131 | a0001c0002t0001g0008 a0001c0002t0001g0018 a0001c0002t0001g0019 others(128): Show |
149 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.-5-13312dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96820152 | ||||||
chr14:96820167 | G | A | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-13300G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820167 | |||||||
chr14:96820273 | T | C | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-13194T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820273 | |||||||
chr14:96820393 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5-13074A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820393 | |||||||
chr14:96820443 | C | T | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-13024C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820443 | |||||||
chr14:96820536 | T | G | 6 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(3): Show |
7 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-12931T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820536 | |||||||
chr14:96820570 | G | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-12897G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820570 | |||||||
chr14:96820653 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-5-12814G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820653 | |||||||
chr14:96820685 | T | C | 15 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-12782T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820685 | |||||||
chr14:96820705 | C | T | 1 | a0001c0003t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-5-12762C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820705 | |||||||
chr14:96820773 | A | G | 6 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-12694A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820773 | |||||||
chr14:96820803 | T | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-12664T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820803 | |||||||
chr14:96820910 | A | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0088 |
3 | HG02572.hp1 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-5-12557A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96820910 | |||||||
chr14:96821176 | T | G | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-12291T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821176 | |||||||
chr14:96821237 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-12230G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821237 | |||||||
chr14:96821315 | C | T | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-12152C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821315 | |||||||
chr14:96821387 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-5-12080C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821387 | |||||||
chr14:96821413 | G | A | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-5-12054G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821413 | |||||||
chr14:96821422 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-5-12045C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821422 | |||||||
chr14:96821437 | T | TA | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-12022dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96821437 | ||||||
chr14:96821448 | A | G | 1 | a0001c0002t0001g0019 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-5-12019A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821448 | |||||||
chr14:96821500 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-5-11967T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821500 | |||||||
chr14:96821551 | T | C | 1 | a0001c0003t0001g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-5-11916T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821551 | |||||||
chr14:96821633 | G | A | 132 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(129): Show |
151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-5-11834G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821633 | |||||||
chr14:96821655 | A | G | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5-11812A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821655 | |||||||
chr14:96821674 | G | A | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-11793G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821674 | |||||||
chr14:96821899 | C | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-5-11568C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96821899 | |||||||
chr14:96821969 | C | CT | 75 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0213 others(72): Show |
88 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-5-11483dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96821969 | ||||||
chr14:96821969 | CT | C | 13 | a0001c0001t0001g0154 a0001c0002t0001g0006 a0001c0002t0001g0019 others(10): Show |
16 | HG01071.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-11483delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96821969 | ||||||
chr14:96822080 | C | CT | 6 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(3): Show |
7 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-11374dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96822080 | ||||||
chr14:96822080 | CT | C | 68 | a0001c0002t0001g0008 a0001c0002t0001g0019 a0001c0002t0001g0026 others(65): Show |
82 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-5-11374delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96822080 | ||||||
chr14:96822397 | C | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-11070C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822397 | |||||||
chr14:96822402 | A | AGTT | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-11063_-5-11061d others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96822402 | ||||||
chr14:96822466 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-5-11001G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822466 | |||||||
chr14:96822686 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-5-10781C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822686 | |||||||
chr14:96822756 | A | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-10711A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96822756 | |||||||
chr14:96823377 | C | T | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-10090C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823377 | |||||||
chr14:96823455 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-5-10012T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823455 | |||||||
chr14:96823670 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-5-9797G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823670 | |||||||
chr14:96823739 | C | T | 26 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-9728C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823739 | |||||||
chr14:96823789 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-9678G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823789 | |||||||
chr14:96823953 | T | C | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-5-9514T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823953 | |||||||
chr14:96823992 | G | A | 47 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0020 others(44): Show |
52 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-5-9475G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96823992 | |||||||
chr14:96824208 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-9259A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824208 | |||||||
chr14:96824289 | A | G | 1 | a0001c0002t0001g0132 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-5-9178A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824289 | |||||||
chr14:96824306 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5-9161G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824306 | |||||||
chr14:96824329 | A | G | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-9138A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824329 | |||||||
chr14:96824462 | A | G | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-9005A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824462 | |||||||
chr14:96824574 | C | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-8893C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824574 | |||||||
chr14:96824575 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-8892G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824575 | |||||||
chr14:96824662 | T | A | 1 | a0001c0002t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-5-8805T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824662 | |||||||
chr14:96824665 | A | AT | 9 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(6): Show |
10 | HG00558.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5-8784dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96824665 | ||||||
chr14:96824665 | AT | A | 35 | a0001c0001t0001g0156 a0001c0001t0001g0224 a0001c0002t0001g0018 others(32): Show |
39 | HG00140.hp1 HG00733.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-5-8784delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96824665 | ||||||
chr14:96824693 | G | A | 6 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
6 | HG03942.hp2 NA18944.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-8774G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824693 | |||||||
chr14:96824725 | C | T | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-8742C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824725 | |||||||
chr14:96824727 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-5-8740C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824727 | |||||||
chr14:96824763 | C | T | 3 | a0001c0002t0001g0008 a0001c0002t0001g0031 a0001c0002t0001g0032 |
4 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-8704C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824763 | |||||||
chr14:96824938 | C | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-8529C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96824938 | |||||||
chr14:96825458 | C | G | 15 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(12): Show |
16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-8009C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825458 | |||||||
chr14:96825512 | T | C | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-7955T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825512 | |||||||
chr14:96825695 | A | G | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-7772A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825695 | |||||||
chr14:96825752 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0232 |
2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-5-7715T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825752 | |||||||
chr14:96825780 | C | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-7687C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825780 | |||||||
chr14:96825800 | A | G | 15 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(12): Show |
16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-7667A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825800 | |||||||
chr14:96825860 | T | A | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-7607T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825860 | |||||||
chr14:96825905 | T | G | 60 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(57): Show |
72 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5-7562T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96825905 | |||||||
chr14:96825994 | G | GT | 20 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0016 others(17): Show |
23 | HG00438.hp1 HG00558.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-7472dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96825994 | ||||||
chr14:96826060 | T | C | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-7407T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826060 | |||||||
chr14:96826182 | C | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-7285C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826182 | |||||||
chr14:96826276 | G | T | 3 | a0001c0002t0001g0018 a0001c0002t0001g0096 a0001c0002t0001g0097 |
4 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-7191G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826276 | |||||||
chr14:96826284 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-7183A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826284 | |||||||
chr14:96826636 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
79 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.-5-6831C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826636 | |||||||
chr14:96826637 | G | A | 132 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(129): Show |
151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-5-6830G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826637 | |||||||
chr14:96826673 | G | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-6794G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826673 | |||||||
chr14:96826855 | C | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-6612C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826855 | |||||||
chr14:96826877 | T | C | 61 | a0001c0002t0001g0040 a0001c0002t0001g0083 a0001c0002t0001g0084 others(58): Show |
73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5-6590T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96826877 | |||||||
chr14:96827139 | T | TTC | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-5-6326_-5-6325dup others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96827139 | ||||||
chr14:96827257 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.-5-6210A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827257 | |||||||
chr14:96827376 | A | G | 132 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(129): Show |
151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-5-6091A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827376 | |||||||
chr14:96827396 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-6071G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827396 | |||||||
chr14:96827404 | G | T | 3 | a0001c0002t0001g0111 a0001c0002t0001g0112 a0001c0002t0001g0113 |
3 | HG02055.hp2 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-5-6063G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827404 | |||||||
chr14:96827426 | G | C | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-5-6041G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827426 | |||||||
chr14:96827505 | G | A | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-5962G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827505 | |||||||
chr14:96827566 | C | T | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-5-5901C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827566 | |||||||
chr14:96827622 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5-5845C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827622 | |||||||
chr14:96827669 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-5-5798C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827669 | |||||||
chr14:96827675 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-5-5792C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827675 | |||||||
chr14:96827682 | A | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-5785A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827682 | |||||||
chr14:96827818 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-5-5649G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827818 | |||||||
chr14:96827860 | A | G | 57 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(54): Show |
69 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-5-5607A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827860 | |||||||
chr14:96827946 | T | C | 76 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(73): Show |
89 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-5-5521T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827946 | |||||||
chr14:96827963 | C | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-5504C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96827963 | |||||||
chr14:96828017 | G | C | 1 | a0001c0003t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-5-5450G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828017 | |||||||
chr14:96828130 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-5-5337C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828130 | |||||||
chr14:96828155 | CTGT | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
109 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-5-5306_-5-5304del others(3): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96828155 | ||||||
chr14:96828164 | G | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-5303G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828164 | |||||||
chr14:96828383 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-5-5084T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828383 | |||||||
chr14:96828424 | T | G | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-5043T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828424 | |||||||
chr14:96828468 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-5-4999T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828468 | |||||||
chr14:96828568 | A | G | 1 | a0001c0002t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-5-4899A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828568 | |||||||
chr14:96828598 | A | G | 75 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(72): Show |
88 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-5-4869A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828598 | |||||||
chr14:96828653 | TA | T | 26 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5-4807delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96828653 | ||||||
chr14:96828702 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-5-4765G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828702 | |||||||
chr14:96828796 | G | A | 15 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-4671G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828796 | |||||||
chr14:96828823 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5-4644C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96828823 | |||||||
chr14:96829206 | A | AT | 14 | a0001c0001t0001g0202 a0001c0002t0001g0135 a0001c0002t0001g0136 others(11): Show |
14 | HG01109.hp1 HG02145.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5-4244dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96829206 | ||||||
chr14:96829206 | AT | A | 15 | a0001c0001t0001g0141 a0001c0001t0001g0220 a0001c0002t0001g0033 others(12): Show |
15 | HG01074.hp2 HG01981.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5-4244delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96829206 | ||||||
chr14:96829277 | A | G | 1 | a0001c0002t0001g0028 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-4190A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829277 | |||||||
chr14:96829282 | T | C | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-4185T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829282 | |||||||
chr14:96829294 | G | T | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-4173G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829294 | |||||||
chr14:96829444 | A | G | 1 | a0001c0002t0001g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-5-4023A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829444 | |||||||
chr14:96829469 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-5-3998G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829469 | |||||||
chr14:96829544 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0232 |
2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-5-3923A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829544 | |||||||
chr14:96829734 | C | T | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-3733C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829734 | |||||||
chr14:96829957 | T | A | 1 | a0001c0003t0001g0070 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-5-3510T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96829957 | |||||||
chr14:96830059 | CT | C | 58 | a0001c0001t0001g0160 a0001c0003t0001g0001 a0001c0003t0001g0002 others(55): Show |
70 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-5-3407delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830059 | |||||||
chr14:96830177 | G | C | 1 | a0001c0002t0001g0129 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-5-3290G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830177 | |||||||
chr14:96830394 | C | T | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-3073C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830394 | |||||||
chr14:96830416 | G | A | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-3051G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830416 | |||||||
chr14:96830451 | C | G | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-3016C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830451 | |||||||
chr14:96830615 | A | G | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-2852A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830615 | |||||||
chr14:96830761 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0188 a0001c0001t0001g0190 |
3 | HG02027.hp1 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-5-2706G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96830761 | |||||||
chr14:96831008 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-2459C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831008 | |||||||
chr14:96831213 | G | A | 2 | a0001c0003t0001g0047 a0001c0003t0001g0072 |
2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-5-2254G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831213 | |||||||
chr14:96831261 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-5-2206G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831261 | |||||||
chr14:96831329 | T | C | 1 | a0001c0003t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-5-2138T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831329 | |||||||
chr14:96831433 | T | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-2034T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831433 | |||||||
chr14:96831464 | T | C | 1 | a0001c0003t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-5-2003T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831464 | |||||||
chr14:96831488 | C | T | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 |
3 | HG03942.hp2 NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-5-1979C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831488 | |||||||
chr14:96831816 | G | A | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-1651G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96831816 | |||||||
chr14:96832032 | CTT | C | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-1432_-5-1431del others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96832032 | ||||||
chr14:96832060 | T | G | 1 | a0001c0002t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-5-1407T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832060 | |||||||
chr14:96832121 | TA | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
274 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.-5-1341delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 96832121 | ||||||
chr14:96832158 | G | C | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-1309G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832158 | |||||||
chr14:96832199 | G | C | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-1268G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832199 | |||||||
chr14:96832315 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-5-1152A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832315 | |||||||
chr14:96832351 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-5-1116C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832351 | |||||||
chr14:96832353 | A | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-1114A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832353 | |||||||
chr14:96832588 | G | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-879G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832588 | |||||||
chr14:96832715 | A | G | 1 | a0001c0002t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-5-752A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832715 | |||||||
chr14:96832773 | C | CTTGCCCA others(6): Show |
3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-694_-5-693insTT others(11): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832773 | |||||||
chr14:96832774 | A | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-693A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832774 | |||||||
chr14:96832775 | C | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-5-692C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96832775 | |||||||
chr14:96833067 | T | C | 1 | a0001c0003t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-5-400T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96833067 | |||||||
chr14:96833080 | C | T | 53 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(50): Show |
65 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5-387C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96833080 | |||||||
chr14:96833254 | G | A | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-213G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 1/12 | chr14 | 96833254 | |||||||
chr14:96833692 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160+61G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833692 | |||||||
chr14:96833705 | T | G | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+74T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833705 | |||||||
chr14:96833861 | G | C | 1 | a0001c0003t0001g0013 | 2 | NA18945.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.160+230G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833861 | |||||||
chr14:96833928 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+297G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96833928 | |||||||
chr14:96834016 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+385G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834016 | |||||||
chr14:96834149 | C | A | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.160+518C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834149 | |||||||
chr14:96834195 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+564T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834195 | |||||||
chr14:96834386 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.160+755C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834386 | |||||||
chr14:96834404 | C | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+773C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834404 | |||||||
chr14:96834506 | A | T | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+875A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834506 | |||||||
chr14:96834511 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0231 |
2 | NA18962.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.160+880T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834511 | |||||||
chr14:96834530 | C | T | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.160+899C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834530 | |||||||
chr14:96834669 | A | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+1038A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834669 | |||||||
chr14:96834782 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160+1151A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834782 | |||||||
chr14:96834903 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160+1272A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834903 | |||||||
chr14:96834910 | C | G | 28 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(25): Show |
32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.160+1279C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834910 | |||||||
chr14:96834993 | G | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.160+1362G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96834993 | |||||||
chr14:96835147 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+1516G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835147 | |||||||
chr14:96835187 | A | G | 1 | a0001c0003t0001g0062 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.160+1556A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835187 | |||||||
chr14:96835497 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.160+1866C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835497 | |||||||
chr14:96835743 | A | G | 3 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0003t0001g0041 |
3 | HG00642.hp2 HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.161-2019A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835743 | |||||||
chr14:96835889 | A | G | 1 | a0001c0002t0001g0194 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-1873A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835889 | |||||||
chr14:96835937 | C | T | 2 | a0001c0003t0001g0093 a0001c0003t0001g0094 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.161-1825C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835937 | |||||||
chr14:96835938 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161-1824G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96835938 | |||||||
chr14:96836127 | A | T | 17 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(14): Show |
18 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.161-1635A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96836127 | |||||||
chr14:96836518 | C | CT | 5 | a0001c0001t0001g0024 a0001c0001t0001g0152 a0001c0001t0001g0207 others(2): Show |
6 | HG01168.hp2 HG01978.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-1222dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | ||||||
chr14:96836518 | CT | C | 89 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0002t0001g0008 others(86): Show |
104 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.161-1222delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | ||||||
chr14:96836518 | CTT | C | 17 | a0001c0002t0001g0018 a0001c0002t0001g0040 a0001c0002t0001g0083 others(14): Show |
18 | HG00733.hp1 HG01074.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.161-1223_161-1222d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | ||||||
chr14:96836518 | CTTTTT | C | 16 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(13): Show |
19 | HG01069.hp1 HG01071.hp2 HG03017.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-1226_161-1222d others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr14 | 96836518 | ||||||
chr14:96836717 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-1045G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96836717 | |||||||
chr14:96836778 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.161-984G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96836778 | |||||||
chr14:96837243 | C | T | 1 | a0001c0003t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-519C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837243 | |||||||
chr14:96837268 | G | A | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-494G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837268 | |||||||
chr14:96837451 | T | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01168.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.161-311T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837451 | |||||||
chr14:96837479 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-283C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837479 | |||||||
chr14:96837542 | A | G | 54 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(51): Show |
66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-220A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837542 | |||||||
chr14:96837617 | A | G | 61 | a0001c0002t0001g0040 a0001c0002t0001g0083 a0001c0002t0001g0084 others(58): Show |
73 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.161-145A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837617 | |||||||
chr14:96837688 | A | T | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-74A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837688 | |||||||
chr14:96837741 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.161-21A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 2/12 | chr14 | 96837741 | |||||||
chr14:96837836 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.216+19A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96837836 | |||||||
chr14:96838116 | T | C | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.216+299T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838116 | |||||||
chr14:96838223 | G | GTTTA | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+408_216+409ins others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96838223 | ||||||
chr14:96838358 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.216+541C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838358 | |||||||
chr14:96838571 | T | TA | 56 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(53): Show |
68 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.216+754_216+755ins others(1): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838571 | |||||||
chr14:96838664 | C | T | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+847C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838664 | |||||||
chr14:96838743 | A | C | 1 | a0001c0002t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.216+926A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838743 | |||||||
chr14:96838770 | C | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
274 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.216+953C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838770 | |||||||
chr14:96838799 | C | T | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+982C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838799 | |||||||
chr14:96838856 | C | G | 1 | a0001c0002t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.216+1039C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838856 | |||||||
chr14:96838874 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.216+1057A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96838874 | |||||||
chr14:96838916 | CATAG | C | 56 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(53): Show |
68 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.216+1103_216+1106d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96838916 | ||||||
chr14:96839062 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.216+1245T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839062 | |||||||
chr14:96839084 | G | GT | 21 | a0001c0001t0001g0138 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00735.hp1 HG01361.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.216+1286dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96839084 | ||||||
chr14:96839084 | G | GTT | 36 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(33): Show |
40 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.216+1285_216+1286d others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96839084 | ||||||
chr14:96839084 | G | GTTT | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+1284_216+1286d others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96839084 | ||||||
chr14:96839295 | A | T | 1 | a0001c0003t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.216+1478A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839295 | |||||||
chr14:96839318 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.216+1501G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839318 | |||||||
chr14:96839376 | CT | C | 56 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(53): Show |
68 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.216+1560delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839376 | |||||||
chr14:96839464 | ATAATATA others(2): Show |
A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.216+1648_216+1656d others(11): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839464 | |||||||
chr14:96839548 | G | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1731G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839548 | |||||||
chr14:96839558 | G | A | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+1741G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839558 | |||||||
chr14:96839571 | T | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.216+1754T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839571 | |||||||
chr14:96839589 | T | A | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.216+1772T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839589 | |||||||
chr14:96839679 | C | G | 1 | a0001c0002t0001g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.216+1862C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839679 | |||||||
chr14:96839923 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.216+2106C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96839923 | |||||||
chr14:96840049 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.216+2232T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840049 | |||||||
chr14:96840147 | C | A | 1 | a0001c0003t0001g0050 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.216+2330C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840147 | |||||||
chr14:96840252 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.216+2435G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840252 | |||||||
chr14:96840372 | G | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.216+2555G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840372 | |||||||
chr14:96840464 | T | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2647T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840464 | |||||||
chr14:96840469 | T | C | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2652T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840469 | |||||||
chr14:96840552 | A | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.216+2735A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840552 | |||||||
chr14:96840573 | T | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.216+2756T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840573 | |||||||
chr14:96840601 | A | G | 54 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(51): Show |
66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.216+2784A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840601 | |||||||
chr14:96840681 | A | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+2864A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840681 | |||||||
chr14:96840801 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.216+2984A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840801 | |||||||
chr14:96840834 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.216+3017C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840834 | |||||||
chr14:96840858 | C | CT | 37 | a0001c0001t0001g0025 a0001c0001t0001g0141 a0001c0001t0001g0159 others(34): Show |
39 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.216+3056dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96840858 | ||||||
chr14:96840858 | CT | C | 43 | a0001c0001t0001g0146 a0001c0002t0001g0018 a0001c0002t0001g0020 others(40): Show |
47 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.216+3056delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96840858 | ||||||
chr14:96840875 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+3058A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840875 | |||||||
chr14:96840887 | A | G | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.216+3070A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96840887 | |||||||
chr14:96841006 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0216 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.216+3189C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841006 | |||||||
chr14:96841016 | C | T | 2 | a0001c0003t0001g0093 a0001c0003t0001g0094 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.216+3199C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841016 | |||||||
chr14:96841151 | C | T | 2 | a0001c0003t0001g0060 a0001c0003t0001g0080 |
2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.216+3334C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841151 | |||||||
chr14:96841749 | C | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+3932C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841749 | |||||||
chr14:96841834 | C | CA | 33 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(30): Show |
37 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.216+4031dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96841834 | ||||||
chr14:96841934 | C | T | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+4117C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841934 | |||||||
chr14:96841957 | A | G | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.217-4138A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841957 | |||||||
chr14:96841965 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.217-4130C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841965 | |||||||
chr14:96841995 | A | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.217-4100A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96841995 | |||||||
chr14:96842209 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0175 |
2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.217-3886A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842209 | |||||||
chr14:96842343 | A | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-3752A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842343 | |||||||
chr14:96842490 | G | C | 1 | a0001c0002t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.217-3605G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842490 | |||||||
chr14:96842632 | G | C | 1 | a0001c0001t0001g0163 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.217-3463G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96842632 | |||||||
chr14:96843011 | C | T | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-3084C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843011 | |||||||
chr14:96843089 | A | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.217-3006A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843089 | |||||||
chr14:96843150 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.217-2945C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843150 | |||||||
chr14:96843242 | A | G | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-2853A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843242 | |||||||
chr14:96843417 | T | C | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-2678T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96843417 | |||||||
chr14:96844091 | T | C | 15 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.217-2004T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844091 | |||||||
chr14:96844298 | A | G | 7 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0001g0173 others(4): Show |
7 | HG00639.hp2 HG01257.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-1797A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844298 | |||||||
chr14:96844560 | G | T | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-1535G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844560 | |||||||
chr14:96844592 | A | C | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.217-1503A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844592 | |||||||
chr14:96844763 | A | G | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-1332A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844763 | |||||||
chr14:96844826 | C | T | 6 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
6 | HG03942.hp2 NA18944.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-1269C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844826 | |||||||
chr14:96844876 | T | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-1219T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844876 | |||||||
chr14:96844877 | A | G | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG02886.hp1 HG03017.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-1218A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844877 | |||||||
chr14:96844917 | G | T | 16 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.217-1178G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844917 | |||||||
chr14:96844984 | C | T | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-1111C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844984 | |||||||
chr14:96844990 | A | G | 1 | a0001c0003t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.217-1105A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96844990 | |||||||
chr14:96845211 | C | CT | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
114 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.217-877dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96845211 | ||||||
chr14:96845211 | C | CTT | 133 | a0001c0001t0001g0222 a0001c0002t0001g0008 a0001c0002t0001g0017 others(130): Show |
152 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.217-878_217-877dup others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 96845211 | ||||||
chr14:96845356 | A | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0116 |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-739A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845356 | |||||||
chr14:96845523 | A | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-572A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845523 | |||||||
chr14:96845557 | G | A | 6 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 others(3): Show |
6 | HG03942.hp2 NA18944.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-538G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845557 | |||||||
chr14:96845563 | T | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-532T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845563 | |||||||
chr14:96845630 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.217-465C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845630 | |||||||
chr14:96845812 | T | C | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.217-283T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845812 | |||||||
chr14:96845851 | T | C | 60 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(57): Show |
72 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.217-244T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 3/12 | chr14 | 96845851 | |||||||
chr14:96846209 | G | GT | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+51dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 96846209 | ||||||
chr14:96846257 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.286+93C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846257 | |||||||
chr14:96846276 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.286+112T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846276 | |||||||
chr14:96846305 | G | A | 139 | a0001c0001t0001g0222 a0001c0002t0001g0008 a0001c0002t0001g0017 others(136): Show |
158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.286+141G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846305 | |||||||
chr14:96846628 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+464G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846628 | |||||||
chr14:96846642 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0138 a0001c0001t0001g0172 |
5 | HG01891.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+478A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846642 | |||||||
chr14:96846643 | G | GGATA | 32 | a0001c0001t0001g0222 a0001c0002t0001g0018 a0001c0002t0001g0020 others(29): Show |
36 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.286+481_286+484dup others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 96846643 | ||||||
chr14:96846714 | GA | G | 17 | a0001c0001t0001g0208 a0001c0002t0001g0019 a0001c0002t0001g0104 others(14): Show |
18 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.287-531delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 96846714 | ||||||
chr14:96846727 | G | A | 1 | a0001c0003t0001g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.287-530G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846727 | |||||||
chr14:96846733 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.287-524A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846733 | |||||||
chr14:96846821 | A | G | 10 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(7): Show |
11 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-436A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846821 | |||||||
chr14:96846837 | A | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.287-420A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846837 | |||||||
chr14:96846841 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.287-416A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846841 | |||||||
chr14:96846914 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.287-343G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96846914 | |||||||
chr14:96847065 | G | T | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.287-192G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96847065 | |||||||
chr14:96847071 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.287-186T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96847071 | |||||||
chr14:96847103 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.287-154C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 4/12 | chr14 | 96847103 | |||||||
chr14:96847433 | T | TA | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.374+90dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 96847433 | ||||||
chr14:96847548 | T | C | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.374+204T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847548 | |||||||
chr14:96847614 | A | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.374+270A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847614 | |||||||
chr14:96847647 | T | TC | 26 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.374+305dupC | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 96847647 | ||||||
chr14:96847833 | T | C | 21 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(18): Show |
22 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.374+489T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847833 | |||||||
chr14:96847836 | A | G | 54 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(51): Show |
66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.374+492A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96847836 | |||||||
chr14:96848168 | T | G | 26 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.374+824T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848168 | |||||||
chr14:96848264 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.374+920A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848264 | |||||||
chr14:96848267 | G | A | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.374+923G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848267 | |||||||
chr14:96848442 | C | T | 13 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(10): Show |
13 | HG02630.hp1 HG02886.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.374+1098C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848442 | |||||||
chr14:96848456 | C | T | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02630.hp1 HG03942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.374+1112C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848456 | |||||||
chr14:96848627 | T | C | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.374+1283T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848627 | |||||||
chr14:96848894 | T | C | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.374+1550T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848894 | |||||||
chr14:96848906 | A | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.374+1562A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96848906 | |||||||
chr14:96849023 | G | A | 60 | a0001c0002t0001g0040 a0001c0002t0001g0083 a0001c0002t0001g0084 others(57): Show |
72 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.374+1679G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849023 | |||||||
chr14:96849086 | C | T | 26 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
30 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.374+1742C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849086 | |||||||
chr14:96849183 | G | A | 1 | a0001c0003t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.374+1839G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849183 | |||||||
chr14:96849199 | C | T | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.374+1855C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849199 | |||||||
chr14:96849448 | T | TA | 16 | a0001c0002t0001g0019 a0001c0002t0001g0105 a0001c0002t0001g0106 others(13): Show |
17 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.374+2116dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 96849448 | ||||||
chr14:96849573 | T | C | 21 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(18): Show |
22 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.374+2229T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849573 | |||||||
chr14:96849691 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0156 a0001c0001t0001g0171 others(1): Show |
5 | NA18944.hp2 NA18977.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+2347C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849691 | |||||||
chr14:96849765 | G | T | 138 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(135): Show |
157 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.374+2421G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849765 | |||||||
chr14:96849864 | C | A | 1 | a0001c0002t0001g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.374+2520C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849864 | |||||||
chr14:96849995 | G | A | 2 | a0001c0002t0001g0099 a0001c0002t0001g0100 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.374+2651G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96849995 | |||||||
chr14:96850044 | C | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.374+2700C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850044 | |||||||
chr14:96850210 | T | C | 9 | a0001c0002t0001g0019 a0001c0002t0001g0110 a0001c0002t0001g0111 others(6): Show |
10 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.375-2621T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850210 | |||||||
chr14:96850242 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.375-2589A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850242 | |||||||
chr14:96850251 | A | G | 17 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(14): Show |
18 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-2580A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850251 | |||||||
chr14:96850490 | G | A | 3 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 |
3 | HG02145.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.375-2341G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850490 | |||||||
chr14:96850609 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.375-2222A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850609 | |||||||
chr14:96850736 | A | G | 1 | a0001c0003t0001g0070 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.375-2095A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850736 | |||||||
chr14:96850966 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.375-1865C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850966 | |||||||
chr14:96850980 | A | G | 2 | a0001c0003t0001g0037 a0001c0003t0001g0038 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.375-1851A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96850980 | |||||||
chr14:96851001 | G | A | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.375-1830G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851001 | |||||||
chr14:96851062 | A | G | 1 | a0001c0002t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375-1769A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851062 | |||||||
chr14:96851261 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.375-1570C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851261 | |||||||
chr14:96851295 | C | T | 3 | a0001c0001t0001g0222 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.375-1536C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851295 | |||||||
chr14:96851390 | C | T | 8 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0159 others(5): Show |
8 | HG02027.hp2 HG02056.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.375-1441C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851390 | |||||||
chr14:96851548 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.375-1283C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851548 | |||||||
chr14:96851586 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
108 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.375-1245A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851586 | |||||||
chr14:96851615 | T | C | 17 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(14): Show |
18 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-1216T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851615 | |||||||
chr14:96851816 | T | C | 1 | a0001c0003t0001g0012 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.375-1015T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851816 | |||||||
chr14:96851876 | A | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.375-955A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96851876 | |||||||
chr14:96852421 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.375-410T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852421 | |||||||
chr14:96852809 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.375-22G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852809 | |||||||
chr14:96852817 | A | G | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.375-14A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852817 | |||||||
chr14:96852823 | G | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0216 |
2 | HG02683.hp1 HG02698.hp1 |
splice_region_variant&intron_variant | LOW | c.375-8G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 5/12 | chr14 | 96852823 | |||||||
chr14:96852992 | AG | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+55delG | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr14 | 96852992 | ||||||
chr14:96853174 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.576+8T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96853174 | |||||||
chr14:96853303 | T | C | 1 | a0001c0003t0001g0080 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.576+137T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96853303 | |||||||
chr14:96853649 | A | AT | 13 | a0001c0002t0001g0017 a0001c0002t0001g0040 a0001c0002t0001g0086 others(10): Show |
14 | HG00733.hp1 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.576+493dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 96853649 | ||||||
chr14:96853756 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.576+590G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96853756 | |||||||
chr14:96854020 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.576+854C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854020 | |||||||
chr14:96854062 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.576+896G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854062 | |||||||
chr14:96854086 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.576+920T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854086 | |||||||
chr14:96854184 | T | C | 1 | a0001c0003t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.576+1018T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854184 | |||||||
chr14:96854208 | A | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0217 |
3 | HG01192.hp1 HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.577-1016A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854208 | |||||||
chr14:96854249 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.577-975A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854249 | |||||||
chr14:96854278 | T | C | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-946T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854278 | |||||||
chr14:96854364 | T | C | 11 | a0001c0003t0001g0001 a0001c0003t0001g0010 a0001c0003t0001g0011 others(8): Show |
15 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.577-860T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854364 | |||||||
chr14:96854796 | A | G | 5 | a0001c0003t0001g0002 a0001c0003t0001g0042 a0001c0003t0001g0061 others(2): Show |
7 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-428A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854796 | |||||||
chr14:96854801 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.577-423C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854801 | |||||||
chr14:96854923 | C | T | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.577-301C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96854923 | |||||||
chr14:96854953 | TATAAC | T | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.577-267_577-263del others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 96854953 | ||||||
chr14:96855037 | A | T | 2 | a0001c0003t0001g0002 a0001c0003t0001g0061 |
4 | HG02145.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-187A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 7/12 | chr14 | 96855037 | |||||||
chr14:96855431 | G | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+75G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855431 | |||||||
chr14:96855432 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+76C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855432 | |||||||
chr14:96855499 | G | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.709+143G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855499 | |||||||
chr14:96855799 | G | A | 25 | a0001c0001t0001g0025 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
26 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-331G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855799 | |||||||
chr14:96855821 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.710-309A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96855821 | |||||||
chr14:96856117 | C | T | 1 | a0001c0002t0003g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.710-13C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 8/12 | chr14 | 96856117 | |||||||
chr14:96856749 | A | T | 15 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+163A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856749 | |||||||
chr14:96856773 | C | T | 1 | a0001c0003t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.889+187C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856773 | |||||||
chr14:96856847 | G | T | 54 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(51): Show |
66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.889+261G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856847 | |||||||
chr14:96856892 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+306C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856892 | |||||||
chr14:96856893 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(3): Show |
7 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+307G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856893 | |||||||
chr14:96856897 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.889+311G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856897 | |||||||
chr14:96856935 | A | T | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.889+349A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96856935 | |||||||
chr14:96856969 | G | GAAAA | 15 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+389_889+392dup others(4): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 96856969 | ||||||
chr14:96857193 | T | C | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.889+607T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857193 | |||||||
chr14:96857337 | CTTGGAAG others(22): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.889+752_889+780del others(29): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857337 | |||||||
chr14:96857338 | T | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
106 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.889+752T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857338 | |||||||
chr14:96857917 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.889+1331A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857917 | |||||||
chr14:96857952 | A | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.889+1366A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857952 | |||||||
chr14:96857975 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0181 |
2 | HG00735.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.889+1389A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96857975 | |||||||
chr14:96858011 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.889+1425C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858011 | |||||||
chr14:96858063 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0181 |
2 | HG00735.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.889+1477G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858063 | |||||||
chr14:96858240 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
78 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.889+1654C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858240 | |||||||
chr14:96858273 | T | G | 1 | a0001c0003t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.889+1687T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858273 | |||||||
chr14:96858384 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.889+1798G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858384 | |||||||
chr14:96858674 | T | C | 31 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(28): Show |
35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.890-1883T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858674 | |||||||
chr14:96858779 | A | G | 2 | a0001c0002t0001g0099 a0001c0002t0001g0100 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.890-1778A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858779 | |||||||
chr14:96858922 | C | A | 1 | a0001c0002t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.890-1635C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96858922 | |||||||
chr14:96859074 | G | T | 1 | a0001c0002t0001g0108 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.890-1483G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859074 | |||||||
chr14:96859264 | GTAGT | G | 25 | a0001c0001t0001g0025 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
26 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.890-1291_890-1288d others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 96859264 | ||||||
chr14:96859325 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.890-1232G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859325 | |||||||
chr14:96859379 | G | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.890-1178G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859379 | |||||||
chr14:96859398 | A | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.890-1159A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859398 | |||||||
chr14:96859586 | T | G | 1 | a0001c0003t0001g0015 | 2 | NA18941.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.890-971T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859586 | |||||||
chr14:96859773 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.890-784C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859773 | |||||||
chr14:96859829 | C | T | 28 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(25): Show |
32 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.890-728C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859829 | |||||||
chr14:96859897 | C | CAAGTCTG others(3): Show |
1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.890-659_890-650dup others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 96859897 | ||||||
chr14:96859931 | A | G | 64 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(61): Show |
77 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.890-626A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96859931 | |||||||
chr14:96860029 | C | A | 68 | a0001c0002t0001g0008 a0001c0002t0001g0018 a0001c0002t0001g0019 others(65): Show |
74 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.890-528C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860029 | |||||||
chr14:96860055 | T | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0158 a0001c0001t0001g0173 others(4): Show |
7 | HG00639.hp2 HG01257.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.890-502T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860055 | |||||||
chr14:96860391 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | NA18940.hp1 NA18952.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.890-166A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 10/12 | chr14 | 96860391 | |||||||
chr14:96860761 | T | TTG | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1068+27_1068+28dup others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96860761 | ||||||
chr14:96860798 | AAG | A | 3 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0001g0100 |
3 | HG02717.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1068+65_1068+66del others(2): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96860798 | ||||||
chr14:96860842 | A | G | 1 | a0001c0002t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1068+107A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96860842 | |||||||
chr14:96860845 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+110G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96860845 | |||||||
chr14:96860942 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1068+207A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96860942 | |||||||
chr14:96861034 | C | T | 2 | a0001c0003t0001g0054 a0001c0003t0001g0059 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1068+299C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861034 | |||||||
chr14:96861114 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1068+379G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861114 | |||||||
chr14:96861360 | A | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+625A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861360 | |||||||
chr14:96861483 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1068+748A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861483 | |||||||
chr14:96861650 | A | G | 2 | a0001c0003t0001g0002 a0001c0003t0001g0061 |
4 | HG02145.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068+915A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861650 | |||||||
chr14:96861707 | C | T | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1068+972C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861707 | |||||||
chr14:96861752 | T | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+1017T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861752 | |||||||
chr14:96861814 | A | G | 7 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(4): Show |
7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+1079A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96861814 | |||||||
chr14:96861828 | CTG | C | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1068+1095_1068+109 others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96861828 | ||||||
chr14:96862076 | C | T | 2 | a0001c0003t0001g0093 a0001c0003t0001g0094 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1068+1341C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862076 | |||||||
chr14:96862145 | A | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+1410A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862145 | |||||||
chr14:96862152 | A | C | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+1417A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862152 | |||||||
chr14:96862328 | A | G | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+1593A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862328 | |||||||
chr14:96862396 | T | C | 2 | a0001c0002t0001g0104 a0001c0002t0001g0105 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1068+1661T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862396 | |||||||
chr14:96862510 | G | GC | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+1776dupC | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96862510 | ||||||
chr14:96862511 | C | CT | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
195 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.1068+1789dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96862511 | ||||||
chr14:96862796 | C | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1068+2061C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862796 | |||||||
chr14:96862889 | A | G | 10 | a0001c0003t0001g0014 a0001c0003t0001g0043 a0001c0003t0001g0057 others(7): Show |
11 | HG00558.hp2 HG02080.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1068+2154A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862889 | |||||||
chr14:96862919 | G | A | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1068+2184G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862919 | |||||||
chr14:96862979 | T | A | 2 | a0001c0003t0001g0093 a0001c0003t0001g0094 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1068+2244T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96862979 | |||||||
chr14:96863222 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1068+2487G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863222 | |||||||
chr14:96863336 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1068+2601A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863336 | |||||||
chr14:96863387 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1068+2652C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863387 | |||||||
chr14:96863635 | T | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+2900T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863635 | |||||||
chr14:96863750 | A | G | 1 | a0001c0003t0001g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1068+3015A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863750 | |||||||
chr14:96863812 | A | T | 1 | a0001c0002t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1068+3077A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863812 | |||||||
chr14:96863813 | T | C | 126 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(123): Show |
145 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.1068+3078T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863813 | |||||||
chr14:96863843 | A | G | 1 | a0001c0002t0001g0027 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1068+3108A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863843 | |||||||
chr14:96863917 | T | G | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1068+3182T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863917 | |||||||
chr14:96863933 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1068+3198C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863933 | |||||||
chr14:96863960 | A | G | 1 | a0001c0003t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1068+3225A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96863960 | |||||||
chr14:96864005 | A | T | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+3270A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864005 | |||||||
chr14:96864061 | A | G | 53 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(50): Show |
65 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1068+3326A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864061 | |||||||
chr14:96864121 | T | C | 7 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(4): Show |
7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+3386T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864121 | |||||||
chr14:96864197 | A | C | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+3462A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864197 | |||||||
chr14:96864261 | AG | A | 30 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(27): Show |
34 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1068+3527delG | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864261 | |||||||
chr14:96864379 | T | G | 1 | a0001c0002t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1068+3644T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864379 | |||||||
chr14:96864399 | T | C | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1068+3664T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864399 | |||||||
chr14:96864438 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1068+3703C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864438 | |||||||
chr14:96864500 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1068+3765C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864500 | |||||||
chr14:96864509 | T | C | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1068+3774T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864509 | |||||||
chr14:96864523 | A | G | 1 | a0001c0003t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1068+3788A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864523 | |||||||
chr14:96864780 | A | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1068+4045A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864780 | |||||||
chr14:96864792 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1068+4057G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864792 | |||||||
chr14:96864921 | T | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
72 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1068+4186T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96864921 | |||||||
chr14:96864921 | T | TA | 58 | a0001c0002t0001g0017 a0001c0002t0001g0088 a0001c0003t0001g0001 others(55): Show |
71 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1068+4198dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96864921 | ||||||
chr14:96865046 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1068+4311A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865046 | |||||||
chr14:96865160 | G | GA | 16 | a0001c0001t0001g0160 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068+4427dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96865160 | ||||||
chr14:96865281 | T | C | 16 | a0001c0001t0001g0160 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068+4546T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865281 | |||||||
chr14:96865328 | G | C | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1068+4593G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865328 | |||||||
chr14:96865570 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0088 a0001c0003t0001g0009 others(1): Show |
6 | HG00642.hp2 HG02572.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+4835T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865570 | |||||||
chr14:96865624 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0232 |
2 | NA18966.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1068+4889T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865624 | |||||||
chr14:96865683 | C | T | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1068+4948C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865683 | |||||||
chr14:96865742 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1068+5007A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865742 | |||||||
chr14:96865760 | T | TA | 42 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(39): Show |
46 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1068+5025_1068+502 others(5): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865760 | |||||||
chr14:96865761 | G | A | 87 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0019 others(84): Show |
102 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1068+5026G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865761 | |||||||
chr14:96865761 | G | GT | 7 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(4): Show |
7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+5038dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96865761 | ||||||
chr14:96865761 | G | T | 43 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(40): Show |
47 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1068+5026G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96865761 | |||||||
chr14:96866061 | A | T | 55 | a0001c0002t0001g0017 a0001c0002t0001g0088 a0001c0003t0001g0001 others(52): Show |
68 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1068+5326A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866061 | |||||||
chr14:96866140 | T | C | 12 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(9): Show |
13 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1068+5405T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866140 | |||||||
chr14:96866337 | G | A | 6 | a0001c0002t0001g0018 a0001c0002t0001g0096 a0001c0002t0001g0097 others(3): Show |
7 | HG01074.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068+5602G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866337 | |||||||
chr14:96866361 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1068+5626C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866361 | |||||||
chr14:96866434 | A | G | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1068+5699A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866434 | |||||||
chr14:96866535 | A | G | 2 | a0001c0002t0001g0099 a0001c0002t0001g0100 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1068+5800A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866535 | |||||||
chr14:96866559 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1068+5824G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866559 | |||||||
chr14:96866657 | C | G | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG01884.hp1 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1068+5922C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96866657 | |||||||
chr14:96867020 | A | C | 142 | a0001c0001t0001g0160 a0001c0001t0001g0203 a0001c0001t0001g0204 others(139): Show |
161 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(158): Show |
intron_variant | MODIFIER | c.1068+6285A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867020 | |||||||
chr14:96867123 | A | T | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+6388A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867123 | |||||||
chr14:96867225 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1068+6490A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867225 | |||||||
chr14:96867456 | A | AGT | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
71 | HG00438.hp1 HG00639.hp2 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.1068+6756_1068+675 others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | A | AGTGT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0165 a0001c0001t0001g0166 others(5): Show |
8 | HG00735.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+6754_1068+675 others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGT | A | 8 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0002t0001g0006 others(5): Show |
11 | HG00558.hp1 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1068+6756_1068+675 others(6): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGTGT | A | 74 | a0001c0001t0001g0193 a0001c0001t0001g0213 a0001c0001t0001g0214 others(71): Show |
86 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1068+6754_1068+675 others(8): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGTGTGT | A | 27 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(24): Show |
32 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1068+6752_1068+675 others(10): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGTGTGTG others(1): Show |
A | 8 | a0001c0002t0001g0027 a0001c0002t0001g0031 a0001c0002t0001g0032 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1068+6750_1068+675 others(12): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGTGTGTG others(3): Show |
A | 16 | a0001c0002t0001g0017 a0001c0002t0001g0083 a0001c0002t0001g0084 others(13): Show |
17 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068+6748_1068+675 others(14): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGTGTGTG others(5): Show |
A | 7 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(4): Show |
7 | HG02602.hp1 HG02630.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068+6746_1068+675 others(16): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867456 | AGTGTGTG others(9): Show |
A | 3 | a0001c0003t0001g0081 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG02970.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1068+6742_1068+675 others(20): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96867456 | ||||||
chr14:96867646 | C | T | 2 | a0001c0002t0001g0237 a0001c0002t0003g0240 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1068+6911C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867646 | |||||||
chr14:96867739 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1068+7004G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867739 | |||||||
chr14:96867865 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1068+7130A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867865 | |||||||
chr14:96867892 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1068+7157T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867892 | |||||||
chr14:96867973 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1068+7238G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96867973 | |||||||
chr14:96868026 | G | C | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+7291G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868026 | |||||||
chr14:96868107 | A | G | 52 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0009 others(49): Show |
64 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1068+7372A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868107 | |||||||
chr14:96868402 | A | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-7628A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868402 | |||||||
chr14:96868405 | A | G | 137 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(134): Show |
156 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.1069-7625A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868405 | |||||||
chr14:96868470 | A | C | 2 | a0001c0002t0001g0083 a0001c0002t0001g0085 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1069-7560A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868470 | |||||||
chr14:96868499 | A | C | 16 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1069-7531A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868499 | |||||||
chr14:96868779 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
79 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1069-7251G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868779 | |||||||
chr14:96868801 | C | CT | 6 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0183 others(3): Show |
6 | HG00738.hp2 HG02738.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-7211dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96868801 | ||||||
chr14:96868801 | CT | C | 114 | a0001c0002t0001g0006 a0001c0002t0001g0018 a0001c0002t0001g0019 others(111): Show |
133 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(130): Show |
intron_variant | MODIFIER | c.1069-7211delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96868801 | ||||||
chr14:96868808 | T | A | 1 | a0001c0002t0001g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1069-7222T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868808 | |||||||
chr14:96868882 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1069-7148A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868882 | |||||||
chr14:96868889 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1069-7141G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868889 | |||||||
chr14:96868968 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
266 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.1069-7062C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96868968 | |||||||
chr14:96869200 | T | C | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1069-6830T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869200 | |||||||
chr14:96869222 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1069-6808C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869222 | |||||||
chr14:96869277 | A | C | 7 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(4): Show |
7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069-6753A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869277 | |||||||
chr14:96869354 | T | C | 3 | a0001c0003t0001g0076 a0001c0003t0001g0077 a0001c0003t0001g0078 |
3 | HG02080.hp2 NA18964.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1069-6676T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869354 | |||||||
chr14:96869631 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1069-6399G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869631 | |||||||
chr14:96869691 | C | T | 131 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(128): Show |
150 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1069-6339C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869691 | |||||||
chr14:96869720 | A | G | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-6310A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869720 | |||||||
chr14:96869720 | A | T | 7 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(4): Show |
7 | HG02698.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069-6310A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869720 | |||||||
chr14:96869880 | A | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-6150A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869880 | |||||||
chr14:96869963 | T | C | 2 | a0001c0003t0001g0093 a0001c0003t0001g0094 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1069-6067T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869963 | |||||||
chr14:96869969 | T | G | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1069-6061T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96869969 | |||||||
chr14:96870122 | G | A | 20 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(17): Show |
23 | HG01069.hp1 HG01071.hp2 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.1069-5908G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870122 | |||||||
chr14:96870134 | T | A | 2 | a0001c0003t0001g0012 a0001c0003t0001g0066 |
3 | HG02717.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1069-5896T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870134 | |||||||
chr14:96870198 | T | C | 131 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(128): Show |
150 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1069-5832T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870198 | |||||||
chr14:96870273 | T | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-5757T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870273 | |||||||
chr14:96870415 | G | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
81 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1069-5615G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870415 | |||||||
chr14:96870554 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-5476C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870554 | |||||||
chr14:96870635 | A | G | 1 | a0001c0002t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1069-5395A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96870635 | |||||||
chr14:96871020 | GT | G | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-5003delT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96871020 | ||||||
chr14:96871021 | T | C | 1 | a0001c0003t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1069-5009T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871021 | |||||||
chr14:96871358 | A | G | 6 | a0001c0003t0001g0010 a0001c0003t0001g0050 a0001c0003t0001g0051 others(3): Show |
7 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069-4672A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871358 | |||||||
chr14:96871387 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1069-4643A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871387 | |||||||
chr14:96871408 | TA | T | 58 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(55): Show |
70 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1069-4621delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871408 | |||||||
chr14:96871659 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0169 |
2 | NA18946.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1069-4371T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871659 | |||||||
chr14:96871843 | C | T | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-4187C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96871843 | |||||||
chr14:96872003 | G | C | 4 | a0001c0002t0001g0238 a0001c0002t0001g0239 a0001c0002t0001g0241 others(1): Show |
4 | HG02698.hp2 HG03017.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-4027G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872003 | |||||||
chr14:96872053 | C | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-3977C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872053 | |||||||
chr14:96872106 | C | G | 1 | a0001c0002t0001g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1069-3924C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872106 | |||||||
chr14:96872149 | T | G | 1 | a0001c0001t0001g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1069-3881T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872149 | |||||||
chr14:96872194 | C | A | 1 | a0001c0002t0001g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1069-3836C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872194 | |||||||
chr14:96872415 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0232 |
2 | NA18966.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1069-3615T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872415 | |||||||
chr14:96872440 | G | A | 137 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(134): Show |
156 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.1069-3590G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872440 | |||||||
chr14:96872479 | A | G | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-3551A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872479 | |||||||
chr14:96872488 | A | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
108 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1069-3542A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872488 | |||||||
chr14:96872587 | C | T | 2 | a0001c0001t0001g0193 a0001c0003t0001g0069 |
2 | HG00438.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1069-3443C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872587 | |||||||
chr14:96872588 | G | A | 1 | a0001c0003t0001g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1069-3442G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872588 | |||||||
chr14:96872623 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0121 a0001c0002t0001g0122 |
4 | HG03017.hp1 HG03239.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-3407A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872623 | |||||||
chr14:96872724 | A | G | 10 | a0001c0003t0001g0014 a0001c0003t0001g0043 a0001c0003t0001g0057 others(7): Show |
11 | HG00558.hp2 HG02080.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069-3306A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872724 | |||||||
chr14:96872850 | T | A | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-3180T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872850 | |||||||
chr14:96872851 | T | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
266 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.1069-3179T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872851 | |||||||
chr14:96872995 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1069-3035A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96872995 | |||||||
chr14:96873086 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1069-2944C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873086 | |||||||
chr14:96873199 | T | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0206 a0001c0001t0001g0209 others(2): Show |
6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-2831T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873199 | |||||||
chr14:96873220 | G | T | 5 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0089 others(2): Show |
5 | HG02602.hp1 HG03098.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-2810G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873220 | |||||||
chr14:96873275 | C | T | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-2755C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873275 | |||||||
chr14:96873681 | T | C | 1 | a0001c0003t0001g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1069-2349T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873681 | |||||||
chr14:96873691 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0226 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1069-2339G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96873691 | |||||||
chr14:96874090 | A | G | 16 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1069-1940A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96874090 | |||||||
chr14:96874670 | G | T | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-1360G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96874670 | |||||||
chr14:96875020 | C | T | 3 | a0001c0003t0001g0046 a0001c0003t0001g0053 a0001c0003t0001g0055 |
3 | HG01515.hp1 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1069-1010C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875020 | |||||||
chr14:96875100 | T | G | 56 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(53): Show |
62 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.1069-930T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875100 | |||||||
chr14:96875111 | CTACAGAA others(2): Show |
C | 5 | a0001c0001t0001g0160 a0001c0002t0001g0033 a0001c0002t0001g0034 others(2): Show |
5 | HG02630.hp1 HG03942.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-916_1069-908d others(11): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr14 | 96875111 | ||||||
chr14:96875169 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1069-861G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875169 | |||||||
chr14:96875220 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1069-810G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875220 | |||||||
chr14:96875226 | T | G | 1 | a0001c0001t0001g0171 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1069-804T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875226 | |||||||
chr14:96875306 | C | T | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-724C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875306 | |||||||
chr14:96875479 | A | T | 1 | a0002c0004t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1069-551A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875479 | |||||||
chr14:96875491 | A | T | 139 | a0001c0001t0001g0160 a0001c0002t0001g0008 a0001c0002t0001g0017 others(136): Show |
158 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1069-539A>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875491 | |||||||
chr14:96875541 | T | C | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG02622.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1069-489T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875541 | |||||||
chr14:96875546 | T | G | 5 | a0001c0003t0001g0010 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
6 | HG00639.hp1 HG00735.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-484T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875546 | |||||||
chr14:96875619 | C | T | 1 | a0001c0003t0001g0068 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1069-411C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875619 | |||||||
chr14:96875743 | T | G | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-287T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875743 | |||||||
chr14:96875793 | TA | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
104 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1069-236delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875793 | |||||||
chr14:96875919 | C | T | 3 | a0001c0003t0001g0046 a0001c0003t0001g0053 a0001c0003t0001g0055 |
3 | HG01515.hp1 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1069-111C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 11/12 | chr14 | 96875919 | |||||||
chr14:96876163 | C | G | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+43C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876163 | |||||||
chr14:96876258 | G | A | 5 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0089 others(2): Show |
5 | HG02602.hp1 HG03098.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+138G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876258 | |||||||
chr14:96876390 | G | A | 1 | a0001c0003t0001g0010 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1159+270G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876390 | |||||||
chr14:96876411 | T | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+291T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876411 | |||||||
chr14:96876560 | A | G | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1159+440A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876560 | |||||||
chr14:96876694 | G | A | 3 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0001g0100 |
3 | HG02717.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1159+574G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876694 | |||||||
chr14:96876776 | C | CA | 8 | a0001c0001t0001g0146 a0001c0001t0001g0182 a0001c0001t0001g0183 others(5): Show |
8 | HG00558.hp1 HG02027.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1159+671dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96876776 | ||||||
chr14:96876776 | CA | C | 130 | a0001c0001t0001g0160 a0001c0001t0001g0193 a0001c0001t0001g0213 others(127): Show |
149 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.1159+671delA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96876776 | ||||||
chr14:96876789 | A | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG00140.hp1 HG01175.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1159+669A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876789 | |||||||
chr14:96876794 | C | A | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1159+674C>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876794 | |||||||
chr14:96876986 | T | A | 1 | a0001c0001t0001g0171 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1159+866T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876986 | |||||||
chr14:96876986 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
117 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1159+866T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96876986 | |||||||
chr14:96877067 | C | CT | 7 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0176 others(4): Show |
7 | HG00438.hp2 HG01515.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1159+960dupT | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96877067 | ||||||
chr14:96877634 | T | A | 1 | a0001c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1159+1514T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96877634 | |||||||
chr14:96877729 | C | G | 29 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(26): Show |
33 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1159+1609C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96877729 | |||||||
chr14:96877807 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1159+1687A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96877807 | |||||||
chr14:96878120 | C | T | 31 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(28): Show |
35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1159+2000C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878120 | |||||||
chr14:96878493 | G | A | 4 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02630.hp1 HG03942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159+2373G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878493 | |||||||
chr14:96878675 | G | T | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-2502G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878675 | |||||||
chr14:96878859 | A | G | 1 | a0001c0003t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1160-2318A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878859 | |||||||
chr14:96878921 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1160-2256C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878921 | |||||||
chr14:96878932 | T | C | 1 | a0001c0003t0001g0011 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1160-2245T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96878932 | |||||||
chr14:96879236 | T | TAAG | 135 | a0001c0001t0001g0160 a0001c0001t0001g0203 a0001c0001t0001g0204 others(132): Show |
154 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.1160-1940_1160-193 others(7): Show |
VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96879236 | ||||||
chr14:96879244 | T | G | 11 | a0001c0002t0001g0019 a0001c0002t0001g0109 a0001c0002t0001g0110 others(8): Show |
12 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160-1933T>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879244 | |||||||
chr14:96879369 | C | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1160-1808C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879369 | |||||||
chr14:96879469 | G | A | 131 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0018 others(128): Show |
150 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1160-1708G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879469 | |||||||
chr14:96879472 | A | G | 16 | a0001c0002t0001g0019 a0001c0002t0001g0104 a0001c0002t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1160-1705A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879472 | |||||||
chr14:96879493 | T | C | 1 | a0001c0002t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1160-1684T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879493 | |||||||
chr14:96879535 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-1642G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879535 | |||||||
chr14:96879651 | G | A | 2 | a0001c0002t0001g0006 a0001c0002t0001g0194 |
4 | HG01891.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1526G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879651 | |||||||
chr14:96879758 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1160-1419A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879758 | |||||||
chr14:96879877 | A | G | 2 | a0001c0003t0001g0002 a0001c0003t0001g0061 |
4 | HG02145.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1300A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879877 | |||||||
chr14:96879882 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1160-1295C>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879882 | |||||||
chr14:96879926 | C | CA | 21 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(18): Show |
22 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1160-1240dupA | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr14 | 96879926 | ||||||
chr14:96879957 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1160-1220A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96879957 | |||||||
chr14:96880036 | A | C | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1160-1141A>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880036 | |||||||
chr14:96880074 | G | A | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | HG01074.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1160-1103G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880074 | |||||||
chr14:96880101 | G | A | 6 | a0001c0002t0001g0040 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG00733.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-1076G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880101 | |||||||
chr14:96880211 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1160-966A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880211 | |||||||
chr14:96880283 | G | A | 7 | a0001c0002t0001g0017 a0001c0002t0001g0086 a0001c0002t0001g0087 others(4): Show |
8 | HG02572.hp1 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-894G>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880283 | |||||||
chr14:96880296 | A | G | 37 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(34): Show |
41 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1160-881A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880296 | |||||||
chr14:96880625 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1160-552C>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880625 | |||||||
chr14:96880633 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1160-544A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880633 | |||||||
chr14:96880676 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1160-501G>T | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880676 | |||||||
chr14:96880719 | G | C | 25 | a0001c0001t0001g0025 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
26 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1160-458G>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880719 | |||||||
chr14:96880720 | T | C | 5 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-457T>C | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880720 | |||||||
chr14:96880760 | T | A | 8 | a0001c0002t0001g0008 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1160-417T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880760 | |||||||
chr14:96880769 | A | G | 4 | a0001c0001t0001g0160 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | NA18940.hp1 NA18952.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-408A>G | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880769 | |||||||
chr14:96880794 | T | A | 58 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(55): Show |
70 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1160-383T>A | VRK1 | ENSG00000100749.9 | transcript | ENST00000216639.8 | protein_coding | 12/12 | chr14 | 96880794 |