Item | Value |
---|---|
geneid | 23433 |
ensemblid | ENSG00000119729.12 |
hgncid | 17736 |
symbol | RHOQ |
name | ras homolog family member Q |
refseq_nuc | NM_012249.4 |
refseq_prot | NP_036381.2 |
ensembl_nuc | ENST00000238738.9 |
ensembl_prot | ENSP00000238738.4 |
mane_status | MANE Select |
chr | chr2 |
start | 46542490 |
end | 46584688 |
strand | + |
ver | v1.2 |
region | chr2:46542490-46584688 |
region5000 | chr2:46537490-46589688 |
regionname0 | RHOQ_chr2_46542490_46584688 |
regionname5000 | RHOQ_chr2_46537490_46589688 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 205 | 328 | 98 | 76 | 108 | 12 | 32 | 81 | RHOQ_chr2_46537490_46589688 | RHOQ | MAHGP others(200): Show |
chr2 | 46537490 | 46589688 |
a0002 | 0/0 | 205 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | RHOQ_chr2_46537490_46589688 | RHOQ | MAHGP others(200): Show |
chr2 | 46537490 | 46589688 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 615 | 318 | 98 | 68 | 107 | 11 | 32 | RHOQ_chr2_46537490_46589688 | RHOQ | ATGGC others(610): Show |
chr2 | 46537490 | 46589688 | ||
a0001c0002 | 0/0 | 615 | 9 | 0 | 8 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | ATGGC others(610): Show |
chr2 | 46537490 | 46589688 | ||
a0001c0004 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | ATGGC others(610): Show |
chr2 | 46537490 | 46589688 | ||
a0002c0003 | 0/0 | 615 | 4 | 0 | 0 | 4 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | ATGGC others(610): Show |
chr2 | 46537490 | 46589688 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4780 | 101 | 15 | 27 | 50 | 3 | 5 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0002 | 1/0 | 4780 | 54 | 16 | 9 | 18 | 2 | 8 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0003 | 0/0 | 4780 | 60 | 30 | 5 | 14 | 3 | 8 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0004 | 0/0 | 4778 | 42 | 1 | 19 | 13 | 2 | 7 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4773): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0005 | 0/0 | 4780 | 11 | 11 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0006 | 0/0 | 4778 | 9 | 1 | 2 | 6 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4773): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0007 | 0/0 | 4780 | 8 | 7 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0008 | 0/0 | 4780 | 5 | 4 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0009 | 0/0 | 4780 | 4 | 3 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0010 | 0/0 | 4780 | 4 | 0 | 0 | 4 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0011 | 0/0 | 4780 | 3 | 3 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0012 | 0/0 | 4780 | 3 | 3 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0013 | 0/0 | 4780 | 2 | 0 | 0 | 0 | 0 | 2 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0014 | 0/0 | 4780 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0015 | 0/0 | 4780 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0016 | 0/0 | 4780 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0017 | 0/0 | 4780 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0019 | 0/0 | 4780 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0020 | 0/0 | 4780 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0021 | 0/0 | 4780 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0022 | 0/0 | 4780 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0023 | 0/0 | 4780 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0024 | 0/0 | 4780 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0025 | 0/0 | 4778 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4773): Show |
chr2 | 46537490 | 46589688 |
a0001c0001t0026 | 0/0 | 4780 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0002t0002 | 0/0 | 4780 | 9 | 0 | 8 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0001c0004t0018 | 0/0 | 4780 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
a0002c0003t0001 | 0/0 | 4780 | 4 | 0 | 0 | 4 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | CTCCT others(4775): Show |
chr2 | 46537490 | 46589688 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0009g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0010g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0010g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0013g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0015g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0016g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0017g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0019g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0021g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0022g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0023g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0024g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0025g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0001t0026g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0001c0004t0018g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0002c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0097 | EUR | GBR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0102 | EUR | GBR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0051 | EUR | FIN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0142 | EUR | FIN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00597 | hp1 | a0001 | c0001 | t0010 | g0292 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00642 | hp1 | a0001 | c0001 | t0026 | g0062 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01070 | hp2 | a0001 | c0001 | t0019 | g0315 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01081 | hp2 | a0001 | c0001 | t0009 | g0300 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0205 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0072 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01257 | hp1 | a0001 | c0001 | t0017 | g0172 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0023 | EUR | IBS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0130 | EUR | IBS | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0184 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02055 | hp2 | a0001 | c0001 | t0024 | g0018 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02071 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0027 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CDX | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02293 | hp1 | a0001 | c0001 | t0025 | g0061 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0118 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0117 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02818 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0271 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0150 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0105 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02976 | hp1 | a0001 | c0001 | t0022 | g0024 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0162 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0204 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0013 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03490 | hp1 | a0001 | c0001 | t0021 | g0278 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0110 | SAS | STU | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | STU | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | BEB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | BEB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03942 | hp1 | a0001 | c0001 | t0013 | g0096 | SAS | BEB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | STU | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG04115 | hp2 | a0001 | c0001 | t0013 | g0107 | SAS | STU | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG04228 | hp1 | a0001 | c0001 | t0015 | g0084 | SAS | STU | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | STU | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | YRI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | CHB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0112 | AFR | YRI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18942 | hp2 | a0001 | c0001 | t0010 | g0282 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18953 | hp1 | a0001 | c0001 | t0010 | g0280 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18956 | hp2 | a0001 | c0001 | t0023 | g0283 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0269 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0263 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18965 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18983 | hp1 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0248 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18987 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18999 | hp1 | a0001 | c0001 | t0010 | g0281 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | LWK | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | LWK | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | LWK | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | LWK | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19068 | hp2 | a0001 | c0004 | t0018 | g0279 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19087 | hp1 | a0001 | c0001 | t0016 | g0194 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | YRI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | YRI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ASW | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ASW | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | TSI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0032 | EUR | TSI | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0090 | SAS | GIH | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | GIH | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0306 | AMR | CLM | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0301 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | MSL | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | USA | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | USA | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | USA | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | LWK | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0308 | REF | REF | RHOQ_chr2_46537490_46589688 | RHOQ | chr2 | 46537490 | 46589688 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46543771 | G | A | 1 | a0002 | 4 | NA18612.hp1 NA18957.hp1 NA18962.hp1 others(1): Show |
missense_variant | MODERATE | c.160G>A | p.Gly54Ser | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/5 | 717/4780 | 160/618 | 54/205 | chr2 | 46543771 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46543109 | C | T | 1 | a0001c0004 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.63C>T | p.Gly21Gly | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 620/4780 | 63/618 | 21/205 | chr2 | 46543109 | |||
chr2:46581029 | C | T | 1 | a0001c0002 | 9 | HG00741.hp2 HG01074.hp1 HG01074.hp2 others(6): Show |
synonymous_variant | LOW | c.564C>T | p.His188His | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1121/4780 | 564/618 | 188/205 | chr2 | 46581029 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46542797 | G | A | 1 | a0001c0001t0014 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-250G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 250 | chr2 | 46542797 | ||||||
chr2:46542807 | G | A | 9 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(6): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
5_prime_UTR_variant | MODIFIER | c.-240G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 240 | chr2 | 46542807 | ||||||
chr2:46542927 | G | T | 1 | a0001c0001t0026 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 120 | chr2 | 46542927 | ||||||
chr2:46542973 | G | T | 1 | a0001c0004t0018 | 1 | NA19068.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 74 | chr2 | 46542973 | ||||||
chr2:46542988 | G | A | 1 | a0001c0001t0015 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 59 | chr2 | 46542988 | ||||||
chr2:46542990 | C | T | 1 | a0001c0001t0025 | 1 | HG02293.hp1 | 5_prime_UTR_variant | MODIFIER | c.-57C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 57 | chr2 | 46542990 | ||||||
chr2:46543016 | G | A | 1 | a0001c0001t0009 | 4 | HG01081.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-31G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/5 | 31 | chr2 | 46543016 | ||||||
chr2:46581104 | GGA | G | 3 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0025 |
52 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*22_*23delGA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 22 | chr2 | 46581104 | ||||||
chr2:46581164 | A | G | 1 | a0001c0001t0024 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 81 | chr2 | 46581164 | ||||||
chr2:46581428 | T | G | 1 | a0001c0001t0019 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*345T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 345 | chr2 | 46581428 | ||||||
chr2:46581447 | C | G | 1 | a0001c0001t0017 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 364 | chr2 | 46581447 | ||||||
chr2:46581663 | A | G | 3 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0015 |
14 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 580 | chr2 | 46581663 | ||||||
chr2:46581907 | C | T | 3 | a0001c0001t0010 a0001c0001t0023 a0001c0004t0018 |
6 | HG00597.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*824C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 824 | chr2 | 46581907 | ||||||
chr2:46582102 | T | C | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(2): Show |
77 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1019T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1019 | chr2 | 46582102 | ||||||
chr2:46582232 | G | A | 3 | a0001c0001t0010 a0001c0001t0023 a0001c0004t0018 |
6 | HG00597.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1149G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1149 | chr2 | 46582232 | ||||||
chr2:46582263 | A | T | 1 | a0001c0001t0022 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1180A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1180 | chr2 | 46582263 | ||||||
chr2:46582418 | T | C | 1 | a0001c0001t0020 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1335 | chr2 | 46582418 | ||||||
chr2:46582482 | T | C | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(5): Show |
81 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1399T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1399 | chr2 | 46582482 | ||||||
chr2:46582833 | C | G | 1 | a0001c0001t0023 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1750C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1750 | chr2 | 46582833 | ||||||
chr2:46582845 | T | G | 1 | a0001c0001t0021 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1762T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 1762 | chr2 | 46582845 | ||||||
chr2:46583765 | G | C | 1 | a0001c0001t0011 | 3 | HG02886.hp1 HG03041.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2682G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 5/5 | 2682 | chr2 | 46583765 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46543507 | G | A | 1 | a0001c0001t0011g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.143-247G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/4 | chr2 | 46543507 | |||||||
chr2:46543547 | G | T | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143-207G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/4 | chr2 | 46543547 | |||||||
chr2:46543617 | A | AG | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0002g0016 others(6): Show |
9 | HG00621.hp2 HG01106.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-132dupG | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | 46543617 | ||||||
chr2:46543720 | G | A | 1 | a0001c0002t0002g0023 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.143-34G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 1/4 | chr2 | 46543720 | |||||||
chr2:46543981 | A | G | 1 | a0001c0001t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.201+169A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46543981 | |||||||
chr2:46543995 | G | C | 294 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(291): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.201+183G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46543995 | |||||||
chr2:46544062 | G | A | 3 | a0001c0001t0011g0013 a0001c0001t0011g0025 a0001c0001t0022g0024 |
3 | HG02886.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.201+250G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46544062 | |||||||
chr2:46544244 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.201+432G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46544244 | |||||||
chr2:46544297 | G | A | 1 | a0001c0001t0004g0026 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.201+485G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46544297 | |||||||
chr2:46544634 | C | T | 1 | a0001c0001t0003g0293 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.201+822C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46544634 | |||||||
chr2:46544813 | G | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 |
3 | HG02145.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+1001G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46544813 | |||||||
chr2:46545017 | G | T | 1 | a0001c0001t0010g0292 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.201+1205G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545017 | |||||||
chr2:46545144 | T | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 |
3 | HG02145.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+1332T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545144 | |||||||
chr2:46545167 | T | C | 55 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0043 others(52): Show |
58 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.201+1355T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545167 | |||||||
chr2:46545497 | C | G | 8 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+1685C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545497 | |||||||
chr2:46545507 | A | C | 293 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(290): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.201+1695A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545507 | |||||||
chr2:46545854 | C | A | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2042C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545854 | |||||||
chr2:46545856 | C | A | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2044C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545856 | |||||||
chr2:46545857 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2045C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545857 | |||||||
chr2:46545858 | A | G | 7 | a0001c0001t0003g0078 a0001c0001t0010g0280 a0001c0001t0010g0281 others(4): Show |
7 | HG00597.hp1 HG03490.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+2046A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545858 | |||||||
chr2:46545859 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2047C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545859 | |||||||
chr2:46545863 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2051C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545863 | |||||||
chr2:46545865 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2053A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545865 | |||||||
chr2:46545867 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2055A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545867 | |||||||
chr2:46545868 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2056C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545868 | |||||||
chr2:46545869 | C | A | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2057C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545869 | |||||||
chr2:46545871 | G | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2059G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545871 | |||||||
chr2:46545874 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2062C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545874 | |||||||
chr2:46545877 | T | A | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2065T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545877 | |||||||
chr2:46545878 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2066C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545878 | |||||||
chr2:46545879 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2067C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545879 | |||||||
chr2:46545880 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2068A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545880 | |||||||
chr2:46545883 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2071T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545883 | |||||||
chr2:46545886 | G | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2074G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545886 | |||||||
chr2:46545887 | G | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG02056.hp1 HG02129.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+2075G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545887 | |||||||
chr2:46545895 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2083T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545895 | |||||||
chr2:46545897 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2085C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545897 | |||||||
chr2:46545898 | T | A | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2086T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545898 | |||||||
chr2:46545899 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2087C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545899 | |||||||
chr2:46545900 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2088T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545900 | |||||||
chr2:46545903 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2091T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545903 | |||||||
chr2:46545904 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2092T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545904 | |||||||
chr2:46545905 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2093A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545905 | |||||||
chr2:46545907 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2095T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545907 | |||||||
chr2:46545909 | G | T | 1 | a0001c0001t0021g0278 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.201+2097G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545909 | |||||||
chr2:46545910 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2098A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545910 | |||||||
chr2:46545915 | C | G | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2103C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545915 | |||||||
chr2:46545927 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.201+2115A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46545927 | |||||||
chr2:46546221 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.201+2409A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546221 | |||||||
chr2:46546231 | G | C | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | NA18979.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.201+2419G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546231 | |||||||
chr2:46546376 | T | C | 101 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(98): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.201+2564T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546376 | |||||||
chr2:46546416 | T | TTA | 3 | a0001c0001t0001g0164 a0001c0001t0002g0296 a0001c0001t0006g0006 |
4 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+2618_201+2619d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546416 | ||||||
chr2:46546430 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.201+2618A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546430 | |||||||
chr2:46546449 | T | C | 1 | a0001c0002t0002g0023 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.201+2637T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546449 | |||||||
chr2:46546451 | C | CATATATA others(29): Show |
1 | a0001c0001t0002g0297 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.201+2663_201+2664i others(38): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | C | CATATATA others(23): Show |
2 | a0001c0001t0002g0295 a0001c0001t0002g0317 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.201+2659_201+2660i others(32): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(19): Show |
C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0089 a0001c0001t0003g0078 others(4): Show |
8 | HG00741.hp2 HG02886.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+2662_201+2687d others(28): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(21): Show |
C | 6 | a0001c0001t0003g0091 a0001c0001t0003g0092 a0001c0001t0003g0093 others(3): Show |
6 | HG01106.hp2 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+2662_201+2689d others(30): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(23): Show |
C | 14 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0002g0016 others(11): Show |
15 | HG00140.hp1 HG01074.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+2662_201+2691d others(32): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(25): Show |
C | 27 | a0001c0001t0001g0168 a0001c0001t0002g0017 a0001c0001t0002g0038 others(24): Show |
27 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.201+2662_201+2693d others(34): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(27): Show |
C | 14 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(11): Show |
15 | HG01255.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+2662_201+2695d others(36): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(29): Show |
C | 26 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(23): Show |
26 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.201+2662_201+2697d others(38): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546451 | CATATATA others(31): Show |
C | 9 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(6): Show |
9 | HG01346.hp1 HG01515.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+2664_201+2701d others(40): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546451 | ||||||
chr2:46546452 | ATATATAT others(17): Show |
A | 11 | a0001c0001t0002g0133 a0001c0001t0002g0144 a0001c0001t0002g0145 others(8): Show |
12 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+2662_201+2685d others(26): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546452 | ||||||
chr2:46546453 | TATATATA others(59): Show |
T | 1 | a0001c0001t0004g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.201+2655_201+2720d others(68): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546453 | ||||||
chr2:46546459 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.201+2647T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546459 | |||||||
chr2:46546459 | TATATATA others(53): Show |
T | 1 | a0001c0001t0001g0242 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.201+2661_201+2720d others(62): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546459 | ||||||
chr2:46546461 | TATATATA others(51): Show |
T | 1 | a0001c0001t0024g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.201+2662_201+2719d others(60): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546461 | ||||||
chr2:46546462 | ATATATAT others(7): Show |
A | 5 | a0001c0001t0002g0146 a0001c0001t0002g0182 a0001c0001t0003g0005 others(2): Show |
5 | HG01516.hp2 HG02698.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+2662_201+2675d others(16): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546462 | ||||||
chr2:46546463 | TATATATA others(49): Show |
T | 1 | a0001c0001t0008g0142 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.201+2662_201+2717d others(58): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546463 | ||||||
chr2:46546464 | ATATATAT others(5): Show |
A | 4 | a0001c0001t0002g0067 a0001c0001t0002g0132 a0001c0001t0003g0005 others(1): Show |
4 | HG01516.hp1 HG02451.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+2662_201+2673d others(14): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546464 | ||||||
chr2:46546466 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0004g0073 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.201+2662_201+2671d others(12): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546466 | ||||||
chr2:46546468 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.201+2656A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546468 | |||||||
chr2:46546468 | ATATATGT others(37): Show |
A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
29 | HG00408.hp1 HG00558.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.201+2662_201+2705d others(46): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546468 | ||||||
chr2:46546469 | TATATGTG others(43): Show |
T | 17 | a0001c0001t0001g0230 a0001c0001t0002g0074 a0001c0001t0002g0320 others(14): Show |
17 | HG02027.hp2 HG02965.hp2 HG03453.hp2 others(14): Show |
intron_variant | MODIFIER | c.201+2662_201+2711d others(52): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546469 | ||||||
chr2:46546470 | ATATGTGT others(35): Show |
A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0001c0001t0001g0216 others(17): Show |
20 | HG00558.hp1 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.201+2662_201+2703d others(44): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546470 | ||||||
chr2:46546471 | TATGTGTA others(41): Show |
T | 38 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(35): Show |
39 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.201+2662_201+2709d others(50): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546471 | ||||||
chr2:46546472 | ATGTG | A | 8 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0291 others(5): Show |
8 | HG00621.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+2662_201+2665d others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546472 | ||||||
chr2:46546472 | ATGTGTAT others(33): Show |
A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
18 | HG00544.hp2 HG00621.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.201+2662_201+2701d others(42): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546472 | ||||||
chr2:46546473 | TGTGTATA others(39): Show |
T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0197 others(27): Show |
31 | HG00323.hp1 HG00597.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.201+2662_201+2707d others(48): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546473 | |||||||
chr2:46546474 | G | A | 10 | a0001c0001t0002g0075 a0001c0001t0002g0286 a0001c0001t0002g0295 others(7): Show |
10 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+2662G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546474 | |||||||
chr2:46546474 | GTGTA | G | 4 | a0001c0001t0002g0298 a0001c0001t0002g0311 a0001c0001t0008g0029 others(1): Show |
4 | HG01433.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+2664_201+2667d others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546474 | ||||||
chr2:46546476 | G | A | 16 | a0001c0001t0002g0075 a0001c0001t0002g0286 a0001c0001t0002g0294 others(13): Show |
16 | HG00735.hp2 HG01070.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+2664G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546476 | |||||||
chr2:46546478 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0314 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.201+2691_201+2692i others(28): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546478 | ||||||
chr2:46546478 | A | C | 2 | a0001c0001t0008g0027 a0001c0001t0008g0028 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2666A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546478 | |||||||
chr2:46546479 | T | C | 2 | a0001c0001t0008g0027 a0001c0001t0008g0028 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2667T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546479 | |||||||
chr2:46546480 | A | G | 3 | a0001c0001t0002g0305 a0001c0001t0008g0027 a0001c0001t0008g0028 |
3 | HG01192.hp1 HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2668A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546480 | |||||||
chr2:46546482 | A | C | 1 | a0001c0001t0008g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.201+2670A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546482 | |||||||
chr2:46546483 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.201+2671T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546483 | |||||||
chr2:46546484 | A | G | 1 | a0001c0001t0008g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.201+2672A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546484 | |||||||
chr2:46546485 | T | C | 2 | a0001c0001t0008g0027 a0001c0001t0008g0028 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2673T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546485 | |||||||
chr2:46546487 | T | C | 2 | a0001c0001t0008g0027 a0001c0001t0008g0028 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2675T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546487 | |||||||
chr2:46546489 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.201+2677T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546489 | |||||||
chr2:46546491 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.201+2679T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546491 | |||||||
chr2:46546493 | T | C | 2 | a0001c0001t0008g0027 a0001c0001t0008g0028 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2681T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546493 | |||||||
chr2:46546497 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.201+2685T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546497 | |||||||
chr2:46546506 | ATATATGT others(18): Show |
A | 1 | a0001c0001t0003g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201+2695_201+2719d others(27): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546506 | |||||||
chr2:46546507 | TATATGTA others(5): Show |
T | 2 | a0001c0001t0008g0027 a0001c0001t0008g0028 |
2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+2700_201+2711d others(14): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546507 | ||||||
chr2:46546507 | TATATGTA others(19): Show |
T | 2 | a0001c0001t0003g0155 a0001c0001t0003g0290 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.201+2697_201+2722d others(28): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546507 | ||||||
chr2:46546509 | TATGTATA others(17): Show |
T | 2 | a0001c0001t0002g0286 a0001c0001t0003g0289 |
2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.201+2699_201+2722d others(26): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46546509 | ||||||
chr2:46546511 | T | C | 1 | a0001c0001t0019g0315 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.201+2699T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546511 | |||||||
chr2:46546511 | TGTATATA others(1): Show |
T | 11 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0132 others(8): Show |
12 | HG00639.hp1 HG01516.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+2700_201+2707d others(10): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546511 | |||||||
chr2:46546511 | TGTATATA others(15): Show |
T | 5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0291 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+2700_201+2721d others(24): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546511 | |||||||
chr2:46546512 | G | A | 115 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(112): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.201+2700G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546512 | |||||||
chr2:46546519 | C | T | 208 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(205): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.201+2707C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546519 | |||||||
chr2:46546531 | T | C | 8 | a0001c0001t0002g0089 a0001c0001t0002g0145 a0001c0001t0002g0147 others(5): Show |
8 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+2719T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546531 | |||||||
chr2:46546533 | C | T | 14 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 others(11): Show |
14 | HG00597.hp1 HG01175.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.201+2721C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546533 | |||||||
chr2:46546782 | T | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0128 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.201+2970T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546782 | |||||||
chr2:46546854 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.201+3042C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546854 | |||||||
chr2:46546944 | G | T | 1 | a0001c0001t0002g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.201+3132G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46546944 | |||||||
chr2:46547340 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.201+3528A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46547340 | |||||||
chr2:46547387 | T | C | 1 | a0001c0001t0003g0129 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.201+3575T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46547387 | |||||||
chr2:46547460 | A | G | 131 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.201+3648A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46547460 | |||||||
chr2:46547764 | C | T | 2 | a0001c0002t0002g0122 a0001c0002t0002g0123 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.201+3952C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46547764 | |||||||
chr2:46547824 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.201+4012T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46547824 | |||||||
chr2:46547920 | T | C | 62 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0038 others(59): Show |
65 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.201+4108T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46547920 | |||||||
chr2:46548085 | GA | G | 5 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0008g0027 others(2): Show |
5 | HG02145.hp2 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+4275delA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46548085 | ||||||
chr2:46548157 | G | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0130 |
2 | HG01516.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.201+4345G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548157 | |||||||
chr2:46548245 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.201+4433A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548245 | |||||||
chr2:46548405 | G | C | 3 | a0001c0001t0004g0015 a0001c0001t0004g0033 a0001c0001t0004g0065 |
3 | HG01168.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.201+4593G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548405 | |||||||
chr2:46548442 | A | G | 3 | a0001c0001t0011g0013 a0001c0001t0011g0025 a0001c0001t0022g0024 |
3 | HG02886.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.201+4630A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548442 | |||||||
chr2:46548600 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.201+4788C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548600 | |||||||
chr2:46548618 | G | A | 3 | a0001c0001t0011g0013 a0001c0001t0011g0025 a0001c0001t0022g0024 |
3 | HG02886.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.201+4806G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548618 | |||||||
chr2:46548722 | G | A | 4 | a0001c0001t0003g0099 a0001c0001t0003g0100 a0001c0001t0003g0115 others(1): Show |
4 | HG02896.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+4910G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46548722 | |||||||
chr2:46549011 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.201+5199G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549011 | |||||||
chr2:46549163 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.201+5351C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549163 | |||||||
chr2:46549240 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.201+5428C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549240 | |||||||
chr2:46549404 | T | G | 290 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(287): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.201+5592T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549404 | |||||||
chr2:46549445 | C | T | 87 | a0001c0001t0002g0017 a0001c0001t0002g0089 a0001c0001t0002g0103 others(84): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.201+5633C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549445 | |||||||
chr2:46549457 | C | T | 5 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0008g0027 others(2): Show |
5 | HG02145.hp2 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+5645C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549457 | |||||||
chr2:46549472 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.201+5660G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549472 | |||||||
chr2:46549590 | A | G | 1 | a0001c0001t0024g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.201+5778A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549590 | |||||||
chr2:46549814 | G | T | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.201+6002G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46549814 | |||||||
chr2:46550030 | G | A | 10 | a0001c0001t0003g0129 a0001c0001t0003g0134 a0001c0001t0003g0135 others(7): Show |
10 | HG02027.hp2 NA18941.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+6218G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550030 | |||||||
chr2:46550055 | C | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0133 |
3 | HG02257.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.201+6243C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550055 | |||||||
chr2:46550065 | T | TA | 4 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(1): Show |
5 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+6256dupA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46550065 | ||||||
chr2:46550069 | T | A | 62 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0038 others(59): Show |
65 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.201+6257T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550069 | |||||||
chr2:46550239 | T | TA | 7 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.201+6442dupA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46550239 | ||||||
chr2:46550239 | TA | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(7): Show |
10 | HG01070.hp2 HG01099.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+6442delA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46550239 | ||||||
chr2:46550279 | G | C | 2 | a0001c0001t0001g0164 a0001c0001t0006g0006 |
3 | HG01123.hp1 HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.201+6467G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550279 | |||||||
chr2:46550323 | G | C | 68 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(65): Show |
72 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.201+6511G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550323 | |||||||
chr2:46550480 | T | G | 227 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.201+6668T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550480 | |||||||
chr2:46550491 | C | T | 2 | a0001c0001t0002g0004 a0001c0001t0002g0133 |
3 | HG02257.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.201+6679C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550491 | |||||||
chr2:46550507 | A | G | 53 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0043 others(50): Show |
56 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.201+6695A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550507 | |||||||
chr2:46550554 | C | T | 128 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
132 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.201+6742C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550554 | |||||||
chr2:46550633 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.201+6821T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550633 | |||||||
chr2:46550654 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG00741.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.201+6842G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550654 | |||||||
chr2:46550662 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.201+6850G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550662 | |||||||
chr2:46550803 | C | T | 291 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.201+6991C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550803 | |||||||
chr2:46550845 | A | G | 1 | a0001c0001t0008g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.201+7033A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550845 | |||||||
chr2:46550973 | G | C | 1 | a0001c0001t0002g0296 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.201+7161G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46550973 | |||||||
chr2:46551066 | C | G | 292 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(289): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.201+7254C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551066 | |||||||
chr2:46551129 | C | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(76): Show |
81 | HG00140.hp1 HG00597.hp1 HG01099.hp2 others(78): Show |
intron_variant | MODIFIER | c.201+7317C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551129 | |||||||
chr2:46551229 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.201+7417G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551229 | |||||||
chr2:46551268 | T | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02056.hp1 HG02129.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+7456T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551268 | |||||||
chr2:46551469 | G | A | 2 | a0001c0001t0003g0155 a0001c0001t0005g0083 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.201+7657G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551469 | |||||||
chr2:46551700 | A | G | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.201+7888A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551700 | |||||||
chr2:46551776 | G | A | 1 | a0001c0001t0004g0031 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.201+7964G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551776 | |||||||
chr2:46551844 | T | G | 1 | a0001c0001t0003g0318 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.201+8032T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551844 | |||||||
chr2:46551845 | A | AC | 3 | a0001c0001t0003g0116 a0001c0004t0018g0279 a0002c0003t0001g0269 |
3 | HG01255.hp1 NA18957.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.201+8035dupC | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46551845 | ||||||
chr2:46551899 | T | G | 4 | a0001c0001t0002g0049 a0001c0001t0009g0012 a0001c0001t0009g0300 others(1): Show |
5 | HG01081.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+8087T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551899 | |||||||
chr2:46551912 | A | G | 152 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(149): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.201+8100A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551912 | |||||||
chr2:46551948 | G | A | 1 | a0001c0001t0006g0189 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.201+8136G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551948 | |||||||
chr2:46551994 | T | G | 1 | a0001c0001t0003g0156 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.201+8182T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46551994 | |||||||
chr2:46552167 | A | G | 1 | a0002c0003t0001g0263 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.201+8355A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552167 | |||||||
chr2:46552228 | T | G | 4 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(1): Show |
4 | HG00323.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+8416T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552228 | |||||||
chr2:46552252 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.201+8440A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552252 | |||||||
chr2:46552352 | C | G | 1 | a0001c0001t0004g0031 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.201+8540C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552352 | |||||||
chr2:46552426 | G | A | 152 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(149): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.201+8614G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552426 | |||||||
chr2:46552792 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.201+8980A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552792 | |||||||
chr2:46552852 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.201+9040G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552852 | |||||||
chr2:46552875 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.201+9063C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46552875 | |||||||
chr2:46553261 | G | A | 1 | a0001c0001t0004g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.201+9449G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46553261 | |||||||
chr2:46553380 | G | A | 1 | a0001c0001t0004g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.201+9568G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46553380 | |||||||
chr2:46553433 | G | C | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.201+9621G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46553433 | |||||||
chr2:46553664 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.201+9852C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46553664 | |||||||
chr2:46553721 | A | G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG03041.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.201+9909A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46553721 | |||||||
chr2:46553729 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+9917G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46553729 | |||||||
chr2:46553754 | A | AT | 221 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(218): Show |
230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.201+9946dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46553754 | ||||||
chr2:46554121 | G | GT | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG02056.hp1 HG02129.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.201+10321dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46554121 | ||||||
chr2:46554121 | GT | G | 145 | a0001c0001t0002g0016 a0001c0001t0002g0034 a0001c0001t0002g0038 others(142): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.201+10321delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46554121 | ||||||
chr2:46554121 | GTT | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+10320_201+1032 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46554121 | ||||||
chr2:46554193 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.201+10381T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554193 | |||||||
chr2:46554206 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.201+10394A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554206 | |||||||
chr2:46554243 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.201+10431A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554243 | |||||||
chr2:46554382 | C | T | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.201+10570C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554382 | |||||||
chr2:46554428 | A | G | 5 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(2): Show |
5 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+10616A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554428 | |||||||
chr2:46554441 | C | G | 69 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(66): Show |
74 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.201+10629C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554441 | |||||||
chr2:46554487 | G | C | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+10675G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554487 | |||||||
chr2:46554638 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201+10826G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554638 | |||||||
chr2:46554759 | G | C | 151 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(148): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.201+10947G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554759 | |||||||
chr2:46554789 | C | CT | 75 | a0001c0001t0002g0074 a0001c0001t0002g0154 a0001c0001t0002g0286 others(72): Show |
76 | HG00140.hp1 HG00597.hp1 HG01099.hp2 others(73): Show |
intron_variant | MODIFIER | c.201+10992dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46554789 | ||||||
chr2:46554789 | CT | C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG01496.hp1 HG01993.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+10992delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46554789 | ||||||
chr2:46554809 | T | G | 83 | a0001c0001t0002g0074 a0001c0001t0002g0154 a0001c0001t0002g0284 others(80): Show |
84 | HG00140.hp1 HG00597.hp1 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.201+10997T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554809 | |||||||
chr2:46554851 | A | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+11039A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554851 | |||||||
chr2:46554954 | T | C | 1 | a0001c0001t0021g0278 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.201+11142T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554954 | |||||||
chr2:46554991 | T | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+11179T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46554991 | |||||||
chr2:46555031 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.201+11219C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555031 | |||||||
chr2:46555050 | G | A | 49 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0043 others(46): Show |
52 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.201+11238G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555050 | |||||||
chr2:46555406 | C | G | 2 | a0001c0001t0012g0105 a0001c0001t0012g0112 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.201+11594C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555406 | |||||||
chr2:46555698 | A | C | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.201+11886A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555698 | |||||||
chr2:46555844 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.201+12032G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555844 | |||||||
chr2:46555936 | G | C | 1 | a0001c0001t0005g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.201+12124G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555936 | |||||||
chr2:46555944 | A | G | 1 | a0001c0001t0004g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.201+12132A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555944 | |||||||
chr2:46555945 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.201+12133A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46555945 | |||||||
chr2:46556037 | C | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+12225C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556037 | |||||||
chr2:46556487 | AT | A | 149 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(146): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.201+12688delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46556487 | ||||||
chr2:46556487 | ATT | A | 7 | a0001c0001t0003g0318 a0001c0001t0010g0280 a0001c0001t0010g0281 others(4): Show |
7 | HG00597.hp1 HG02630.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+12687_201+1268 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46556487 | ||||||
chr2:46556578 | C | A | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.201+12766C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556578 | |||||||
chr2:46556646 | A | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+12834A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556646 | |||||||
chr2:46556662 | C | T | 3 | a0001c0001t0011g0013 a0001c0001t0011g0025 a0001c0001t0022g0024 |
3 | HG02886.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.201+12850C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556662 | |||||||
chr2:46556742 | G | A | 76 | a0001c0001t0002g0154 a0001c0001t0002g0284 a0001c0001t0002g0285 others(73): Show |
77 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(74): Show |
intron_variant | MODIFIER | c.201+12930G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556742 | |||||||
chr2:46556751 | A | G | 56 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0043 others(53): Show |
60 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.201+12939A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556751 | |||||||
chr2:46556847 | C | T | 1 | a0002c0003t0001g0181 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.201+13035C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556847 | |||||||
chr2:46556967 | A | G | 1 | a0001c0001t0003g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.201+13155A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46556967 | |||||||
chr2:46557037 | A | G | 6 | a0001c0001t0001g0169 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG00408.hp2 HG02071.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+13225A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557037 | |||||||
chr2:46557092 | A | C | 50 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0043 others(47): Show |
53 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.201+13280A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557092 | |||||||
chr2:46557224 | C | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | NA18944.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.201+13412C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557224 | |||||||
chr2:46557243 | C | T | 1 | a0001c0001t0006g0177 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.201+13431C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557243 | |||||||
chr2:46557314 | T | C | 1 | a0001c0001t0006g0189 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.201+13502T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557314 | |||||||
chr2:46557326 | A | G | 2 | a0001c0001t0003g0110 a0001c0001t0003g0111 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.201+13514A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557326 | |||||||
chr2:46557402 | A | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG00544.hp2 HG00558.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+13590A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557402 | |||||||
chr2:46557504 | G | A | 8 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 others(5): Show |
8 | HG01175.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+13692G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557504 | |||||||
chr2:46557921 | G | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(77): Show |
82 | HG00140.hp1 HG01099.hp2 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.201+14109G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46557921 | |||||||
chr2:46558173 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.201+14361G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558173 | |||||||
chr2:46558316 | G | T | 3 | a0001c0001t0003g0090 a0001c0001t0003g0110 a0001c0001t0003g0111 |
3 | HG03688.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.201+14504G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558316 | |||||||
chr2:46558352 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.201+14540A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558352 | |||||||
chr2:46558445 | T | C | 11 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(8): Show |
11 | HG00323.hp2 HG00597.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+14633T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558445 | |||||||
chr2:46558500 | G | A | 4 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 others(1): Show |
4 | HG00323.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+14688G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558500 | |||||||
chr2:46558522 | T | C | 1 | a0001c0002t0002g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.201+14710T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558522 | |||||||
chr2:46558671 | CAA | C | 3 | a0001c0001t0001g0218 a0001c0001t0001g0273 a0001c0001t0001g0276 |
3 | HG01256.hp2 HG01258.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.201+14861_201+1486 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46558671 | ||||||
chr2:46558705 | G | C | 8 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+14893G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558705 | |||||||
chr2:46558735 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | NA18982.hp1 NA18990.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.201+14923A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46558735 | |||||||
chr2:46559247 | C | T | 1 | a0001c0001t0004g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.201+15435C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559247 | |||||||
chr2:46559333 | T | G | 1 | a0001c0001t0004g0050 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.201+15521T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559333 | |||||||
chr2:46559345 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.201+15533T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559345 | |||||||
chr2:46559352 | G | A | 152 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(149): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.201+15540G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559352 | |||||||
chr2:46559396 | C | T | 1 | a0001c0001t0005g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.201+15584C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559396 | |||||||
chr2:46559459 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.201+15647G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559459 | |||||||
chr2:46559572 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.201+15760G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559572 | |||||||
chr2:46559657 | G | A | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+15845G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559657 | |||||||
chr2:46559696 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.201+15884A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559696 | |||||||
chr2:46559843 | C | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+16031C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559843 | |||||||
chr2:46559848 | C | T | 8 | a0001c0001t0002g0182 a0001c0001t0010g0280 a0001c0001t0010g0281 others(5): Show |
8 | HG00597.hp1 HG02818.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+16036C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559848 | |||||||
chr2:46559936 | G | A | 3 | a0001c0001t0008g0027 a0001c0001t0008g0028 a0001c0001t0008g0029 |
3 | HG02145.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.201+16124G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46559936 | |||||||
chr2:46560039 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.202-16048G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560039 | |||||||
chr2:46560160 | TCTG | T | 8 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-15923_202-1592 others(7): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46560160 | ||||||
chr2:46560201 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.202-15886G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560201 | |||||||
chr2:46560205 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.202-15882C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560205 | |||||||
chr2:46560538 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.202-15549C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560538 | |||||||
chr2:46560667 | C | T | 1 | a0001c0001t0004g0036 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.202-15420C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560667 | |||||||
chr2:46560759 | C | A | 1 | a0001c0001t0021g0278 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202-15328C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560759 | |||||||
chr2:46560857 | TG | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-15227delG | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46560857 | ||||||
chr2:46560878 | G | A | 3 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0067 |
3 | NA18942.hp1 NA19054.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.202-15209G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46560878 | |||||||
chr2:46561001 | A | AAC | 17 | a0001c0001t0001g0170 a0001c0001t0001g0190 a0001c0001t0001g0213 others(14): Show |
17 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.202-15046_202-1504 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561001 | A | AACAC | 5 | a0001c0001t0001g0216 a0001c0001t0010g0280 a0001c0001t0010g0282 others(2): Show |
5 | NA18942.hp2 NA18953.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-15048_202-1504 others(8): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561001 | AAC | A | 22 | a0001c0001t0001g0009 a0001c0001t0001g0079 a0001c0001t0001g0168 others(19): Show |
23 | HG00544.hp1 HG01081.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-15046_202-1504 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561001 | AACAC | A | 7 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 others(4): Show |
7 | HG01175.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-15048_202-1504 others(8): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561001 | AACACAC | A | 130 | a0001c0001t0001g0193 a0001c0001t0002g0004 a0001c0001t0002g0016 others(127): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.202-15050_202-1504 others(10): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561001 | AACACACA others(1): Show |
A | 4 | a0001c0001t0002g0182 a0001c0001t0003g0155 a0001c0001t0005g0083 others(1): Show |
4 | HG02055.hp2 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-15052_202-1504 others(12): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561001 | AACACACA others(3): Show |
A | 1 | a0001c0001t0004g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.202-15054_202-1504 others(14): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561001 | ||||||
chr2:46561039 | C | T | 3 | a0001c0002t0002g0094 a0001c0002t0002g0095 a0001c0002t0002g0149 |
3 | HG01074.hp2 HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.202-15048C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561039 | |||||||
chr2:46561041 | C | A | 1 | a0001c0001t0001g0229 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.202-15046C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561041 | |||||||
chr2:46561058 | C | G | 1 | a0001c0001t0008g0142 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.202-15029C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561058 | |||||||
chr2:46561102 | A | ATG | 11 | a0001c0001t0001g0164 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
12 | HG00323.hp1 HG00735.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-14976_202-1497 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561102 | ||||||
chr2:46561122 | A | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0177 others(1): Show |
4 | HG02071.hp2 NA18965.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-14965A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561122 | |||||||
chr2:46561128 | C | CTG | 8 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0005g0083 others(5): Show |
8 | HG00323.hp2 HG02145.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-14947_202-1494 others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561128 | ||||||
chr2:46561250 | G | GA | 151 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0034 others(148): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.202-14835dupA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561250 | ||||||
chr2:46561344 | C | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0213 a0001c0001t0001g0216 |
3 | NA19003.hp1 NA19057.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.202-14743C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561344 | |||||||
chr2:46561393 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.202-14694A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561393 | |||||||
chr2:46561493 | G | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-14594G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561493 | |||||||
chr2:46561656 | AT | A | 5 | a0001c0001t0003g0099 a0001c0001t0003g0100 a0001c0001t0003g0115 others(2): Show |
5 | HG02896.hp2 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-14429delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46561656 | ||||||
chr2:46561758 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.202-14329A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561758 | |||||||
chr2:46561910 | C | G | 2 | a0001c0001t0001g0193 a0001c0001t0002g0103 |
2 | HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.202-14177C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561910 | |||||||
chr2:46561915 | G | C | 1 | a0001c0001t0005g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202-14172G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46561915 | |||||||
chr2:46562271 | C | T | 2 | a0001c0001t0003g0290 a0001c0001t0004g0063 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.202-13816C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46562271 | |||||||
chr2:46562375 | A | G | 127 | a0001c0001t0002g0004 a0001c0001t0002g0043 a0001c0001t0002g0047 others(124): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.202-13712A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46562375 | |||||||
chr2:46562667 | G | A | 2 | a0001c0001t0004g0032 a0001c0001t0004g0039 |
2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.202-13420G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46562667 | |||||||
chr2:46562761 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0247 |
2 | HG00621.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.202-13326A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46562761 | |||||||
chr2:46562853 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0003g0098 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-13234C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46562853 | |||||||
chr2:46562989 | G | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG00544.hp2 HG00558.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-13098G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46562989 | |||||||
chr2:46563414 | G | C | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.202-12673G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563414 | |||||||
chr2:46563463 | C | T | 8 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0242 others(5): Show |
8 | HG00642.hp1 HG01928.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-12624C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563463 | |||||||
chr2:46563464 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-12623G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563464 | |||||||
chr2:46563478 | C | T | 1 | a0001c0001t0004g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.202-12609C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563478 | |||||||
chr2:46563479 | G | A | 2 | a0001c0001t0008g0027 a0001c0001t0008g0029 |
2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.202-12608G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563479 | |||||||
chr2:46563614 | A | T | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-12473A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563614 | |||||||
chr2:46563796 | T | A | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-12291T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563796 | |||||||
chr2:46563823 | T | A | 1 | a0001c0001t0024g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.202-12264T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563823 | |||||||
chr2:46563837 | G | A | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-12250G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563837 | |||||||
chr2:46563858 | G | T | 46 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(43): Show |
49 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.202-12229G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563858 | |||||||
chr2:46563888 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.202-12199G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46563888 | |||||||
chr2:46564029 | A | T | 1 | a0001c0001t0001g0222 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.202-12058A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564029 | |||||||
chr2:46564047 | A | G | 3 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0020g0118 |
3 | HG02572.hp1 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-12040A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564047 | |||||||
chr2:46564260 | G | A | 1 | a0001c0001t0008g0142 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.202-11827G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564260 | |||||||
chr2:46564488 | G | C | 70 | a0001c0001t0002g0154 a0001c0001t0003g0005 a0001c0001t0003g0078 others(67): Show |
72 | HG00140.hp1 HG01099.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.202-11599G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564488 | |||||||
chr2:46564525 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.202-11562T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564525 | |||||||
chr2:46564585 | G | C | 1 | a0001c0001t0003g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.202-11502G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564585 | |||||||
chr2:46564616 | C | T | 10 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0005g0083 others(7): Show |
10 | HG00597.hp1 HG03130.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-11471C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564616 | |||||||
chr2:46564710 | G | A | 45 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(42): Show |
48 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.202-11377G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564710 | |||||||
chr2:46564957 | A | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-11130A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564957 | |||||||
chr2:46564974 | A | C | 1 | a0001c0001t0021g0278 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202-11113A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46564974 | |||||||
chr2:46565023 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.202-11064G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565023 | |||||||
chr2:46565169 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0006g0006 |
3 | HG01123.hp1 HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.202-10918C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565169 | |||||||
chr2:46565222 | A | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0101 others(77): Show |
83 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.202-10865A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565222 | |||||||
chr2:46565464 | G | C | 1 | a0001c0001t0002g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-10623G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565464 | |||||||
chr2:46565494 | T | A | 6 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(3): Show |
6 | HG00597.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-10593T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565494 | |||||||
chr2:46565703 | G | C | 1 | a0001c0002t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-10384G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565703 | |||||||
chr2:46565721 | T | C | 1 | a0001c0001t0021g0278 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202-10366T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46565721 | |||||||
chr2:46566136 | C | T | 1 | a0001c0001t0003g0318 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.202-9951C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566136 | |||||||
chr2:46566145 | A | G | 1 | a0001c0001t0007g0007 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.202-9942A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566145 | |||||||
chr2:46566162 | G | C | 73 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(70): Show |
75 | HG00140.hp1 HG01099.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.202-9925G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566162 | |||||||
chr2:46566335 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0005g0083 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-9752G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566335 | |||||||
chr2:46566441 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.202-9646T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566441 | |||||||
chr2:46566791 | T | C | 1 | a0001c0001t0004g0306 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.202-9296T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566791 | |||||||
chr2:46566804 | G | A | 60 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(57): Show |
62 | HG00140.hp1 HG01099.hp2 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.202-9283G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566804 | |||||||
chr2:46566934 | A | G | 10 | a0001c0001t0007g0007 a0001c0001t0007g0204 a0001c0001t0007g0205 others(7): Show |
11 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-9153A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46566934 | |||||||
chr2:46567339 | A | G | 1 | a0001c0001t0003g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.202-8748A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567339 | |||||||
chr2:46567367 | C | G | 4 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0289 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-8720C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567367 | |||||||
chr2:46567503 | C | T | 2 | a0001c0001t0002g0298 a0001c0001t0002g0316 |
2 | HG01071.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.202-8584C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567503 | |||||||
chr2:46567793 | A | G | 63 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(60): Show |
65 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.202-8294A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567793 | |||||||
chr2:46567799 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.202-8288A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567799 | |||||||
chr2:46567854 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0197 others(10): Show |
14 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.202-8233C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567854 | |||||||
chr2:46567864 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.202-8223C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567864 | |||||||
chr2:46567962 | T | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0273 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.202-8125T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46567962 | |||||||
chr2:46568048 | GA | G | 3 | a0001c0001t0002g0016 a0001c0001t0003g0098 a0001c0001t0005g0083 |
3 | HG03130.hp2 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.202-8038delA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568048 | |||||||
chr2:46568251 | T | G | 14 | a0001c0001t0001g0164 a0001c0001t0001g0193 a0001c0001t0001g0208 others(11): Show |
15 | HG00323.hp1 HG00735.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.202-7836T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568251 | |||||||
chr2:46568263 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.202-7824G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568263 | |||||||
chr2:46568603 | G | C | 1 | a0001c0001t0002g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.202-7484G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568603 | |||||||
chr2:46568649 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.202-7438A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568649 | |||||||
chr2:46568716 | C | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-7371C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568716 | |||||||
chr2:46568810 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202-7277C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568810 | |||||||
chr2:46568832 | C | T | 1 | a0001c0001t0024g0018 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.202-7255C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568832 | |||||||
chr2:46568936 | A | G | 10 | a0001c0001t0007g0007 a0001c0001t0007g0204 a0001c0001t0007g0205 others(7): Show |
11 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-7151A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46568936 | |||||||
chr2:46569704 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.202-6383T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46569704 | |||||||
chr2:46569714 | A | G | 1 | a0001c0001t0003g0318 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.202-6373A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46569714 | |||||||
chr2:46569841 | G | T | 1 | a0001c0001t0003g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.202-6246G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46569841 | |||||||
chr2:46569872 | C | G | 4 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(1): Show |
5 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-6215C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46569872 | |||||||
chr2:46569906 | C | A | 1 | a0001c0001t0003g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.202-6181C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46569906 | |||||||
chr2:46569936 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0203 |
2 | HG02080.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.202-6151G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46569936 | |||||||
chr2:46570171 | T | G | 7 | a0001c0001t0003g0087 a0001c0001t0003g0106 a0001c0001t0003g0116 others(4): Show |
7 | HG01255.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-5916T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570171 | |||||||
chr2:46570216 | G | A | 19 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0178 others(16): Show |
19 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.202-5871G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570216 | |||||||
chr2:46570447 | TA | T | 6 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0253 others(3): Show |
6 | HG01515.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-5627delA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46570447 | ||||||
chr2:46570550 | C | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-5537C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570550 | |||||||
chr2:46570578 | C | T | 1 | a0001c0001t0022g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202-5509C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570578 | |||||||
chr2:46570659 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0020g0118 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.202-5428A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570659 | |||||||
chr2:46570687 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.202-5400G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570687 | |||||||
chr2:46570704 | C | G | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-5383C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570704 | |||||||
chr2:46570866 | C | A | 1 | a0001c0001t0004g0039 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.202-5221C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570866 | |||||||
chr2:46570866 | C | G | 136 | a0001c0001t0002g0004 a0001c0001t0002g0043 a0001c0001t0002g0047 others(133): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.202-5221C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46570866 | |||||||
chr2:46571019 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.202-5068G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571019 | |||||||
chr2:46571230 | C | T | 1 | a0001c0001t0022g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202-4857C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571230 | |||||||
chr2:46571259 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.202-4828T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571259 | |||||||
chr2:46571321 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.202-4766G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571321 | |||||||
chr2:46571424 | A | G | 26 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(23): Show |
26 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-4663A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571424 | |||||||
chr2:46571429 | A | G | 19 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(16): Show |
19 | HG00323.hp2 HG01109.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.202-4658A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571429 | |||||||
chr2:46571793 | G | A | 6 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(3): Show |
6 | HG00597.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-4294G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571793 | |||||||
chr2:46571824 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.202-4263T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571824 | |||||||
chr2:46571870 | T | C | 18 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
18 | HG00323.hp2 HG01109.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-4217T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571870 | |||||||
chr2:46571981 | G | A | 8 | a0001c0001t0003g0099 a0001c0001t0003g0115 a0001c0001t0003g0131 others(5): Show |
8 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-4106G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46571981 | |||||||
chr2:46572057 | G | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(23): Show |
26 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-4030G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572057 | |||||||
chr2:46572100 | A | AGT | 37 | a0001c0001t0002g0064 a0001c0001t0004g0001 a0001c0001t0004g0002 others(34): Show |
41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.202-3980_202-3979d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572100 | ||||||
chr2:46572107 | G | GT | 35 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0176 others(32): Show |
35 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.202-3953dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572107 | G | GTGT | 12 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0004g0031 others(9): Show |
12 | HG01928.hp2 HG01934.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-3979_202-3978i others(5): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572107 | G | GTTT | 24 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(21): Show |
27 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-3955_202-3953d others(5): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572107 | G | GTTTT | 35 | a0001c0001t0003g0078 a0001c0001t0003g0090 a0001c0001t0003g0092 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.202-3956_202-3953d others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572107 | G | GTTTTT | 19 | a0001c0001t0003g0005 a0001c0001t0003g0086 a0001c0001t0003g0100 others(16): Show |
20 | HG01192.hp2 HG01255.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.202-3957_202-3953d others(7): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572107 | G | GTTTTTT | 10 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0003g0087 others(7): Show |
10 | HG00323.hp2 HG02056.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-3958_202-3953d others(8): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572107 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0007g0205 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.202-3962_202-3953d others(12): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46572107 | ||||||
chr2:46572119 | T | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0177 others(1): Show |
4 | HG02071.hp2 NA18965.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-3968T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572119 | |||||||
chr2:46572121 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.202-3966T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572121 | |||||||
chr2:46572168 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.202-3919T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572168 | |||||||
chr2:46572204 | C | G | 163 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(160): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.202-3883C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572204 | |||||||
chr2:46572346 | C | T | 23 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(20): Show |
23 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-3741C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572346 | |||||||
chr2:46572581 | T | C | 1 | a0001c0001t0008g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.202-3506T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572581 | |||||||
chr2:46572614 | G | C | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-3473G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572614 | |||||||
chr2:46572713 | G | T | 162 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(159): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.202-3374G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572713 | |||||||
chr2:46572914 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.202-3173C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572914 | |||||||
chr2:46572927 | G | A | 1 | a0001c0001t0004g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.202-3160G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46572927 | |||||||
chr2:46573011 | C | T | 132 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(129): Show |
139 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.202-3076C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573011 | |||||||
chr2:46573065 | AT | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(208): Show |
221 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.202-3006delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46573065 | ||||||
chr2:46573065 | ATT | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(23): Show |
26 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-3007_202-3006d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46573065 | ||||||
chr2:46573112 | G | A | 1 | a0001c0001t0022g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202-2975G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573112 | |||||||
chr2:46573151 | C | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-2936C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573151 | |||||||
chr2:46573188 | C | T | 1 | a0001c0002t0002g0023 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.202-2899C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573188 | |||||||
chr2:46573276 | C | G | 73 | a0001c0001t0003g0005 a0001c0001t0003g0078 a0001c0001t0003g0085 others(70): Show |
74 | HG00140.hp1 HG01099.hp2 HG01109.hp1 others(71): Show |
intron_variant | MODIFIER | c.202-2811C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573276 | |||||||
chr2:46573558 | T | C | 19 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(16): Show |
19 | HG00323.hp2 HG01109.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.202-2529T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573558 | |||||||
chr2:46573817 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.202-2270T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573817 | |||||||
chr2:46573990 | A | C | 1 | a0001c0001t0002g0147 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.202-2097A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46573990 | |||||||
chr2:46574209 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0020g0118 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.202-1878A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46574209 | |||||||
chr2:46574235 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.202-1852G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46574235 | |||||||
chr2:46574264 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.202-1823C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46574264 | |||||||
chr2:46574336 | CT | C | 97 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(94): Show |
99 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.202-1737delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46574336 | ||||||
chr2:46575084 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.202-1003C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575084 | |||||||
chr2:46575194 | G | T | 6 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(3): Show |
6 | HG00597.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-893G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575194 | |||||||
chr2:46575245 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.202-842T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575245 | |||||||
chr2:46575313 | C | G | 1 | a0001c0001t0022g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202-774C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575313 | |||||||
chr2:46575370 | G | T | 5 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0001g0174 others(2): Show |
5 | HG00544.hp1 HG01952.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-717G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575370 | |||||||
chr2:46575399 | T | TCA | 59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0019 others(56): Show |
63 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.202-645_202-644dup others(2): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | T | TCACA | 43 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0001c0001t0001g0238 others(40): Show |
44 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-647_202-644dup others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | T | TCACACA | 3 | a0001c0001t0001g0180 a0001c0001t0002g0067 a0001c0001t0004g0030 |
3 | NA18942.hp1 NA18966.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.202-649_202-644dup others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | TCA | T | 55 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0178 others(52): Show |
56 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.202-645_202-644del others(2): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | TCACA | T | 46 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0164 others(43): Show |
48 | HG00408.hp1 HG00741.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.202-647_202-644del others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | TCACACA | T | 50 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0002g0004 others(47): Show |
52 | HG00140.hp1 HG00280.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.202-649_202-644del others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | TCACACAC others(1): Show |
T | 14 | a0001c0001t0002g0101 a0001c0001t0002g0132 a0001c0001t0003g0087 others(11): Show |
14 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.202-651_202-644del others(8): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575399 | TCACACAC others(3): Show |
T | 5 | a0001c0001t0005g0173 a0001c0001t0005g0199 a0001c0001t0005g0200 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-653_202-644del others(10): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 46575399 | ||||||
chr2:46575506 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.202-581G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575506 | |||||||
chr2:46575541 | G | T | 4 | a0001c0001t0002g0074 a0001c0001t0009g0012 a0001c0001t0009g0300 others(1): Show |
5 | HG01081.hp2 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-546G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575541 | |||||||
chr2:46575793 | C | T | 1 | a0001c0001t0008g0142 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.202-294C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575793 | |||||||
chr2:46575795 | A | T | 131 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(128): Show |
137 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.202-292A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46575795 | |||||||
chr2:46576067 | G | A | 1 | a0001c0001t0020g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.202-20G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 2/4 | chr2 | 46576067 | |||||||
chr2:46576372 | G | A | 1 | a0001c0001t0004g0031 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.366+121G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 3/4 | chr2 | 46576372 | |||||||
chr2:46576479 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.367-82G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 3/4 | chr2 | 46576479 | |||||||
chr2:46576869 | A | C | 4 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+213A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46576869 | |||||||
chr2:46576873 | C | G | 19 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(16): Show |
20 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.462+217C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46576873 | |||||||
chr2:46576981 | A | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0002g0004 others(6): Show |
10 | HG00280.hp2 HG01981.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.462+325A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46576981 | |||||||
chr2:46577067 | G | C | 18 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
19 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.462+411G>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577067 | |||||||
chr2:46577151 | G | T | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+495G>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577151 | |||||||
chr2:46577263 | A | C | 7 | a0001c0001t0003g0098 a0001c0001t0003g0104 a0001c0001t0003g0287 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+607A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577263 | |||||||
chr2:46577362 | T | C | 1 | a0001c0001t0002g0313 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.462+706T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577362 | |||||||
chr2:46577396 | C | CT | 19 | a0001c0001t0001g0019 a0001c0001t0002g0004 a0001c0001t0002g0101 others(16): Show |
20 | HG00597.hp1 HG02027.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.462+761dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46577396 | ||||||
chr2:46577396 | C | CTT | 20 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(17): Show |
21 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.462+760_462+761dup others(2): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46577396 | ||||||
chr2:46577396 | CT | C | 7 | a0001c0001t0001g0166 a0001c0001t0001g0193 a0001c0001t0001g0208 others(4): Show |
7 | HG00323.hp1 HG01169.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.462+761delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46577396 | ||||||
chr2:46577430 | C | T | 1 | a0001c0001t0001g0010 | 2 | NA18941.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.462+774C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577430 | |||||||
chr2:46577461 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02056.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.462+805G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577461 | |||||||
chr2:46577477 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0020g0118 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.462+821G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577477 | |||||||
chr2:46577492 | C | T | 50 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(47): Show |
54 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.462+836C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577492 | |||||||
chr2:46577507 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(2): Show |
5 | HG00735.hp1 HG01257.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+851C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577507 | |||||||
chr2:46577556 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.462+900C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577556 | |||||||
chr2:46577565 | A | AT | 47 | a0001c0001t0001g0020 a0001c0001t0001g0081 a0001c0001t0001g0164 others(44): Show |
48 | HG00621.hp2 HG00735.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.462+933dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46577565 | ||||||
chr2:46577565 | AT | A | 20 | a0001c0001t0001g0171 a0001c0001t0002g0004 a0001c0001t0002g0076 others(17): Show |
21 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.462+933delT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46577565 | ||||||
chr2:46577663 | C | T | 1 | a0001c0001t0008g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.462+1007C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577663 | |||||||
chr2:46577989 | T | C | 1 | a0001c0001t0003g0159 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.462+1333T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46577989 | |||||||
chr2:46578030 | A | G | 13 | a0001c0001t0003g0087 a0001c0001t0003g0100 a0001c0001t0003g0106 others(10): Show |
13 | HG01255.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.462+1374A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578030 | |||||||
chr2:46578068 | A | T | 25 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(22): Show |
26 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.462+1412A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578068 | |||||||
chr2:46578089 | C | T | 11 | a0001c0001t0001g0164 a0001c0001t0001g0193 a0001c0001t0001g0208 others(8): Show |
11 | HG00323.hp1 HG00735.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.462+1433C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578089 | |||||||
chr2:46578221 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.462+1565C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578221 | |||||||
chr2:46578234 | A | G | 69 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(66): Show |
71 | HG00140.hp1 HG01099.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.462+1578A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578234 | |||||||
chr2:46578286 | T | C | 14 | a0001c0001t0001g0164 a0001c0001t0001g0193 a0001c0001t0001g0208 others(11): Show |
14 | HG00323.hp1 HG00735.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.462+1630T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578286 | |||||||
chr2:46578529 | C | T | 1 | a0001c0001t0004g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.462+1873C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578529 | |||||||
chr2:46578569 | C | CA | 17 | a0001c0001t0001g0214 a0001c0001t0001g0242 a0001c0001t0002g0077 others(14): Show |
17 | HG00597.hp2 HG00735.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.462+1950dupA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAA | 9 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0261 others(6): Show |
9 | HG00621.hp1 HG01175.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.462+1949_462+1950d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(1): Show |
13 | a0001c0001t0002g0297 a0001c0001t0004g0002 a0001c0001t0004g0030 others(10): Show |
14 | HG00280.hp1 HG01168.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.462+1943_462+1950d others(10): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(2): Show |
16 | a0001c0001t0004g0001 a0001c0001t0004g0015 a0001c0001t0004g0026 others(13): Show |
17 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.462+1942_462+1950d others(11): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0002g0043 a0001c0001t0002g0064 a0001c0001t0004g0003 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.462+1941_462+1950d others(12): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0004g0053 a0001c0001t0004g0059 a0001c0002t0002g0040 others(1): Show |
4 | HG01074.hp1 HG01074.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1940_462+1950d others(13): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0004g0031 a0001c0001t0006g0006 a0001c0001t0006g0189 others(1): Show |
5 | HG01099.hp1 HG01123.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+1939_462+1950d others(14): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0004g0052 a0001c0001t0004g0068 a0001c0001t0006g0022 others(1): Show |
4 | HG02155.hp1 HG02273.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1938_462+1950d others(15): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0004g0042 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.462+1937_462+1950d others(16): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0047 a0001c0001t0004g0014 |
2 | HG01106.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.462+1936_462+1950d others(17): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CA | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0019 others(38): Show |
42 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.462+1950delA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAA | C | 56 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0164 others(53): Show |
59 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.462+1949_462+1950d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAA | C | 11 | a0001c0001t0001g0197 a0001c0001t0001g0217 a0001c0001t0001g0225 others(8): Show |
11 | HG01993.hp2 HG02280.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.462+1948_462+1950d others(5): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAA | C | 17 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0003g0085 others(14): Show |
17 | HG01109.hp1 HG01891.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.462+1947_462+1950d others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAAA | C | 52 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0320 others(49): Show |
54 | HG00140.hp1 HG01099.hp2 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.462+1946_462+1950d others(7): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAAAA | C | 6 | a0001c0001t0003g0078 a0001c0001t0003g0293 a0001c0001t0007g0198 others(3): Show |
6 | HG02145.hp2 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+1945_462+1950d others(8): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAAAAA | C | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
13 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.462+1944_462+1950d others(9): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0248 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.462+1939_462+1950d others(14): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0003g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.462+1934_462+1950d others(19): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578569 | CAAAAAAA others(17): Show |
C | 1 | a0001c0001t0003g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.462+1927_462+1950d others(26): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578569 | ||||||
chr2:46578709 | T | C | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+2053T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578709 | |||||||
chr2:46578765 | G | A | 25 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(22): Show |
26 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.462+2109G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578765 | |||||||
chr2:46578769 | A | G | 53 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(50): Show |
57 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.462+2113A>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578769 | |||||||
chr2:46578895 | CGT | C | 139 | a0001c0001t0002g0004 a0001c0001t0002g0043 a0001c0001t0002g0047 others(136): Show |
146 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.463-2020_463-2019d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578895 | ||||||
chr2:46578895 | CGTGT | C | 7 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(4): Show |
7 | HG00597.hp1 HG03490.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.463-2022_463-2019d others(6): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46578895 | ||||||
chr2:46578947 | T | C | 57 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0002g0064 others(54): Show |
62 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.463-1981T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46578947 | |||||||
chr2:46579025 | G | A | 1 | a0001c0001t0012g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.463-1903G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579025 | |||||||
chr2:46579181 | C | T | 2 | a0001c0001t0002g0320 a0001c0001t0003g0138 |
2 | NA18957.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.463-1747C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579181 | |||||||
chr2:46579249 | A | T | 5 | a0001c0001t0002g0004 a0001c0001t0002g0101 a0001c0001t0002g0132 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.463-1679A>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579249 | |||||||
chr2:46579371 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0317 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.463-1557G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579371 | |||||||
chr2:46579422 | T | C | 1 | a0001c0001t0015g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.463-1506T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579422 | |||||||
chr2:46579471 | T | A | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.463-1457T>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579471 | |||||||
chr2:46579534 | G | A | 4 | a0001c0001t0002g0066 a0001c0001t0002g0295 a0001c0001t0002g0317 others(1): Show |
4 | HG00639.hp2 HG01070.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.463-1394G>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579534 | |||||||
chr2:46579799 | C | T | 1 | a0001c0001t0003g0137 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.463-1129C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579799 | |||||||
chr2:46579843 | C | CA | 64 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
66 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.463-1071dupA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46579843 | ||||||
chr2:46579843 | C | CAA | 68 | a0001c0001t0003g0005 a0001c0001t0003g0078 a0001c0001t0003g0085 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.463-1072_463-1071d others(4): Show |
RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46579843 | ||||||
chr2:46579843 | CA | C | 35 | a0001c0001t0002g0043 a0001c0001t0003g0135 a0001c0001t0003g0139 others(32): Show |
35 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.463-1071delA | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46579843 | ||||||
chr2:46579912 | C | T | 16 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(13): Show |
17 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.463-1016C>T | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46579912 | |||||||
chr2:46580470 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.463-458A>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46580470 | |||||||
chr2:46580502 | C | G | 1 | a0001c0001t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.463-426C>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46580502 | |||||||
chr2:46580645 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.463-283T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46580645 | |||||||
chr2:46580651 | T | G | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.463-277T>G | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46580651 | |||||||
chr2:46580852 | T | C | 93 | a0001c0001t0002g0182 a0001c0001t0003g0005 a0001c0001t0003g0078 others(90): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.463-76T>C | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46580852 | |||||||
chr2:46580908 | A | AT | 6 | a0001c0001t0010g0280 a0001c0001t0010g0281 a0001c0001t0010g0282 others(3): Show |
6 | HG00597.hp1 NA18942.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.463-12dupT | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 46580908 | ||||||
chr2:46580917 | C | A | 1 | a0001c0001t0020g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.463-11C>A | RHOQ | ENSG00000119729.12 | transcript | ENST00000238738.9 | protein_coding | 4/4 | chr2 | 46580917 |