Item | Value |
---|---|
geneid | 2909 |
ensemblid | ENSG00000160007.20 |
hgncid | 4591 |
symbol | ARHGAP35 |
name | Rho GTPase activating protein 35 |
refseq_nuc | NM_004491.5 |
refseq_prot | NP_004482.4 |
ensembl_nuc | ENST00000672722.1 |
ensembl_prot | ENSP00000500409.1 |
mane_status | MANE Select |
chr | chr19 |
start | 46860997 |
end | 47005077 |
strand | + |
ver | v1.2 |
region | chr19:46860997-47005077 |
region5000 | chr19:46855997-47010077 |
regionname0 | ARHGAP35_chr19_46860997_47005077 |
regionname5000 | ARHGAP35_chr19_46855997_47010077 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1499 | 292 | 87 | 49 | 116 | 10 | 28 | 84 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | MMMAR others(1494): Show |
chr19 | 46855997 | 47010077 |
a0002 | 0/0 | 1499 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | MMMAR others(1494): Show |
chr19 | 46855997 | 47010077 |
a0003 | 0/0 | 1499 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | MMMAR others(1494): Show |
chr19 | 46855997 | 47010077 |
a0004 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | MMMAR others(1494): Show |
chr19 | 46855997 | 47010077 |
a0005 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | MMMAR others(1494): Show |
chr19 | 46855997 | 47010077 |
a0006 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | MMMAR others(1494): Show |
chr19 | 46855997 | 47010077 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4497 | 271 | 70 | 46 | 116 | 10 | 27 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0002 | 0/0 | 4497 | 14 | 12 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0003 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0005 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0006 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0007 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0009 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0001c0011 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0002c0004 | 0/0 | 4497 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0003c0013 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0004c0012 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0005c0010 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 | ||
a0006c0008 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | ATGAT others(4492): Show |
chr19 | 46855997 | 47010077 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9290 | 108 | 20 | 21 | 51 | 6 | 9 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0002 | 0/0 | 9290 | 41 | 14 | 11 | 12 | 2 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0003 | 0/0 | 9286 | 27 | 2 | 0 | 21 | 0 | 4 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0004 | 0/0 | 9291 | 17 | 0 | 6 | 7 | 2 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9286): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0006 | 0/0 | 9290 | 5 | 0 | 3 | 0 | 0 | 2 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0007 | 0/0 | 9290 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0008 | 0/0 | 9283 | 5 | 0 | 0 | 4 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9278): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0009 | 0/0 | 9291 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9286): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0010 | 0/0 | 9293 | 4 | 0 | 2 | 1 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9288): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0011 | 0/0 | 9290 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0012 | 0/0 | 9290 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0013 | 0/0 | 9285 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9280): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0014 | 0/0 | 9290 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0015 | 0/0 | 9290 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0016 | 0/0 | 9294 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9289): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0017 | 0/0 | 9295 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9290): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0018 | 0/0 | 9289 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9284): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0019 | 0/0 | 9294 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9289): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0020 | 0/0 | 9290 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0021 | 0/0 | 9292 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9287): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0022 | 0/0 | 9290 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0023 | 0/0 | 9290 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0024 | 0/0 | 9294 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9289): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0025 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0026 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0027 | 0/0 | 9286 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0028 | 0/0 | 9295 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9290): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0029 | 0/0 | 9293 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9288): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0030 | 0/0 | 9291 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9286): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0031 | 0/1 | 9293 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9288): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0033 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0034 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0035 | 0/0 | 9286 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0036 | 0/0 | 9294 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9289): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0037 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0038 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0039 | 0/0 | 9280 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9275): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0040 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0041 | 0/0 | 9290 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0042 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0043 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0044 | 0/0 | 9300 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9295): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0045 | 0/0 | 9292 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9287): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0046 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0048 | 0/0 | 9283 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9278): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0049 | 0/0 | 9287 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9282): Show |
chr19 | 46855997 | 47010077 |
a0001c0001t0050 | 0/0 | 9283 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9278): Show |
chr19 | 46855997 | 47010077 |
a0001c0002t0001 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0002t0005 | 0/0 | 9290 | 11 | 9 | 2 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0002t0032 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0001c0002t0047 | 0/0 | 9292 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9287): Show |
chr19 | 46855997 | 47010077 |
a0001c0003t0001 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0003t0003 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0001c0005t0005 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0006t0005 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0007t0011 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0009t0006 | 0/0 | 9290 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0001c0011t0001 | 0/0 | 9290 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0002c0004t0002 | 0/0 | 9290 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0003c0013t0003 | 0/0 | 9286 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0004c0012t0007 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
a0005c0010t0003 | 0/0 | 9286 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9281): Show |
chr19 | 46855997 | 47010077 |
a0006c0008t0011 | 0/0 | 9290 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | GCCCC others(9285): Show |
chr19 | 46855997 | 47010077 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0010g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0012g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0015g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0015g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0016g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0016g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0017g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0017g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0019g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0020g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0020g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0021g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0021g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0022g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0022g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0023g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0023g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0024g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0025g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0028g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0029g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0030g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0031g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0033g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0034g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0035g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0036g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0037g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0038g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0039g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0040g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0041g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0042g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0043g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0044g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0045g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0046g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0048g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0049g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0001t0050g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0032g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0002t0047g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0005t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0006t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0007t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0009t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0001c0011t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0002c0004t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0002c0004t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0003c0013t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0004c0012t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0005c0010t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
a0006c0008t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | FIN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00408 | hp2 | a0001 | c0001 | t0012 | g0226 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00558 | hp2 | a0001 | c0001 | t0022 | g0187 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0250 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00597 | hp2 | a0001 | c0001 | t0022 | g0288 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00642 | hp1 | a0001 | c0002 | t0005 | g0207 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00642 | hp2 | a0001 | c0009 | t0006 | g0228 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01070 | hp1 | a0001 | c0001 | t0016 | g0024 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01071 | hp2 | a0001 | c0001 | t0016 | g0219 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01099 | hp1 | a0001 | c0001 | t0017 | g0109 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0260 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0217 | AMR | PUR | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0102 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01256 | hp1 | a0001 | c0001 | t0010 | g0097 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0035 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01433 | hp2 | a0003 | c0013 | t0003 | g0244 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0259 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0119 | EUR | IBS | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0056 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01891 | hp2 | a0001 | c0001 | t0014 | g0093 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0052 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02015 | hp2 | a0002 | c0004 | t0002 | g0003 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02027 | hp1 | a0002 | c0004 | t0002 | g0008 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02027 | hp2 | a0001 | c0001 | t0009 | g0111 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02055 | hp2 | a0001 | c0002 | t0005 | g0213 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02071 | hp2 | a0001 | c0001 | t0041 | g0043 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02080 | hp1 | a0001 | c0001 | t0050 | g0090 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02135 | hp2 | a0001 | c0001 | t0017 | g0254 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02145 | hp1 | a0001 | c0001 | t0024 | g0025 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | CDX | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02257 | hp2 | a0001 | c0001 | t0025 | g0277 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02258 | hp1 | a0001 | c0001 | t0023 | g0221 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02258 | hp2 | a0001 | c0002 | t0005 | g0298 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02280 | hp2 | a0001 | c0006 | t0005 | g0296 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | KHV | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02572 | hp2 | a0001 | c0001 | t0040 | g0053 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02622 | hp1 | a0001 | c0001 | t0020 | g0032 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02630 | hp2 | a0001 | c0001 | t0013 | g0069 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02647 | hp1 | a0004 | c0012 | t0007 | g0261 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02647 | hp2 | a0001 | c0001 | t0045 | g0229 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02809 | hp1 | a0001 | c0003 | t0003 | g0234 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02886 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0212 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02922 | hp1 | a0001 | c0002 | t0005 | g0209 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02922 | hp2 | a0001 | c0001 | t0014 | g0089 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02965 | hp2 | a0005 | c0010 | t0003 | g0027 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0297 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0210 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03098 | hp1 | a0001 | c0002 | t0047 | g0127 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03098 | hp2 | a0001 | c0001 | t0018 | g0258 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03130 | hp1 | a0001 | c0001 | t0023 | g0034 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03130 | hp2 | a0001 | c0001 | t0019 | g0039 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03139 | hp1 | a0001 | c0001 | t0013 | g0247 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03195 | hp1 | a0006 | c0008 | t0011 | g0037 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03195 | hp2 | a0001 | c0002 | t0032 | g0211 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0248 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03225 | hp1 | a0001 | c0001 | t0042 | g0018 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03225 | hp2 | a0001 | c0001 | t0038 | g0028 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03239 | hp2 | a0001 | c0001 | t0030 | g0105 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03486 | hp1 | a0001 | c0001 | t0021 | g0067 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03486 | hp2 | a0001 | c0001 | t0034 | g0252 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03516 | hp1 | a0001 | c0002 | t0005 | g0215 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0055 | AFR | ESN | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0214 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03669 | hp2 | a0001 | c0001 | t0037 | g0243 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03688 | hp1 | a0001 | c0001 | t0008 | g0246 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03688 | hp2 | a0001 | c0011 | t0001 | g0274 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03710 | hp2 | a0001 | c0001 | t0046 | g0066 | SAS | PJL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0122 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04204 | hp1 | a0001 | c0001 | t0043 | g0225 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0230 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04228 | hp1 | a0001 | c0001 | t0028 | g0104 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18522 | hp1 | a0001 | c0005 | t0005 | g0208 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18522 | hp2 | a0001 | c0001 | t0014 | g0094 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0216 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18906 | hp2 | a0001 | c0001 | t0015 | g0040 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18942 | hp1 | a0001 | c0001 | t0049 | g0092 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18950 | hp1 | a0001 | c0001 | t0021 | g0062 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18953 | hp2 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18961 | hp2 | a0001 | c0001 | t0009 | g0114 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18968 | hp1 | a0001 | c0001 | t0009 | g0112 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18970 | hp1 | a0001 | c0001 | t0039 | g0063 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18971 | hp1 | a0001 | c0001 | t0012 | g0047 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18971 | hp2 | a0001 | c0001 | t0029 | g0113 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18994 | hp1 | a0001 | c0001 | t0012 | g0049 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19009 | hp2 | a0001 | c0001 | t0008 | g0088 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19012 | hp1 | a0001 | c0001 | t0009 | g0255 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19030 | hp1 | a0001 | c0001 | t0044 | g0251 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19030 | hp2 | a0001 | c0001 | t0015 | g0227 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19060 | hp1 | a0001 | c0001 | t0027 | g0232 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19062 | hp1 | a0001 | c0001 | t0035 | g0078 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19064 | hp1 | a0001 | c0001 | t0048 | g0129 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19064 | hp2 | a0001 | c0001 | t0008 | g0249 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19066 | hp2 | a0001 | c0001 | t0010 | g0125 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | YRI | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ASW | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20905 | hp1 | a0001 | c0001 | t0033 | g0144 | SAS | GIH | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0023 | SAS | GIH | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02109 | hp1 | a0001 | c0001 | t0018 | g0115 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
HG06807 | hp2 | a0001 | c0001 | t0036 | g0026 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20300 | hp1 | a0001 | c0007 | t0011 | g0038 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA20300 | hp2 | a0001 | c0001 | t0026 | g0041 | AFR | USA | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
NA21309 | hp2 | a0001 | c0001 | t0020 | g0220 | AFR | LWK | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
homoSapiens | chm13v2 | a0001 | c0001 | t0031 | g0103 | REF | REF | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0145 | REF | REF | ARHGAP35_chr19_46855997_47010077 | ARHGAP35 | chr19 | 46855997 | 47010077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46920929 | A | G | 1 | a0003 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2254A>G | p.Ser752Gly | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2655/9290 | 2254/4500 | 752/1499 | chr19 | 46920929 | |||
chr19:46921181 | T | G | 1 | a0002 | 2 | HG02015.hp2 HG02027.hp1 |
missense_variant | MODERATE | c.2506T>G | p.Ser836Ala | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2907/9290 | 2506/4500 | 836/1499 | chr19 | 46921181 | |||
chr19:46921224 | G | A | 1 | a0006 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.2549G>A | p.Arg850Gln | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2950/9290 | 2549/4500 | 850/1499 | chr19 | 46921224 | |||
chr19:46921636 | A | C | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2961A>C | p.Glu987Asp | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 3362/9290 | 2961/4500 | 987/1499 | chr19 | 46921636 | |||
chr19:47000641 | A | G | 1 | a0005 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.4453A>G | p.Met1485Val | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 4854/9290 | 4453/4500 | 1485/1499 | chr19 | 47000641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46919983 | T | C | 1 | a0001c0003 | 2 | HG02809.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1308T>C | p.Phe436Phe | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 1709/9290 | 1308/4500 | 436/1499 | chr19 | 46919983 | |||
chr19:46920418 | G | A | 3 | a0001c0002 a0001c0005 a0001c0006 |
16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
synonymous_variant | LOW | c.1743G>A | p.Pro581Pro | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2144/9290 | 1743/4500 | 581/1499 | chr19 | 46920418 | |||
chr19:46920790 | G | A | 1 | a0001c0007 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.2115G>A | p.Lys705Lys | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 2516/9290 | 2115/4500 | 705/1499 | chr19 | 46920790 | |||
chr19:46921642 | C | T | 1 | a0001c0006 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2967C>T | p.Ile989Ile | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 3368/9290 | 2967/4500 | 989/1499 | chr19 | 46921642 | |||
chr19:46921675 | A | G | 1 | a0001c0005 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.3000A>G | p.Thr1000Thr | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 3401/9290 | 3000/4500 | 1000/1499 | chr19 | 46921675 | |||
chr19:46922296 | C | T | 1 | a0001c0011 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.3621C>T | p.Tyr1207Tyr | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/7 | 4022/9290 | 3621/4500 | 1207/1499 | chr19 | 46922296 | |||
chr19:47000604 | G | A | 1 | a0001c0009 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.4416G>A | p.Ser1472Ser | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 4817/9290 | 4416/4500 | 1472/1499 | chr19 | 47000604 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46861077 | GGCCCCCC | G | 5 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0048 others(2): Show |
12 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-317_-311delCCCCGC others(1): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/7 | 57589 | INFO_REALIGN_3_PRIME | chr19 | 46861077 | |||||
chr19:46861082 | C | CCCGCCGC others(5): Show |
1 | a0001c0001t0001 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-306_-295dupGAGCCG others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/7 | 57572 | INFO_REALIGN_3_PRIME | chr19 | 46861082 | |||||
chr19:47000723 | C | G | 1 | a0001c0002t0047 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 35 | chr19 | 47000723 | ||||||
chr19:47001002 | G | A | 1 | a0001c0001t0024 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 314 | chr19 | 47001002 | ||||||
chr19:47001032 | C | A | 1 | a0001c0001t0025 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 344 | chr19 | 47001032 | ||||||
chr19:47001033 | G | A | 1 | a0001c0001t0026 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*345G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 345 | chr19 | 47001033 | ||||||
chr19:47001240 | C | T | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 552 | chr19 | 47001240 | ||||||
chr19:47001638 | G | A | 1 | a0001c0001t0015 | 2 | NA18906.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 950 | chr19 | 47001638 | ||||||
chr19:47001794 | C | T | 1 | a0001c0001t0023 | 2 | HG02258.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1106C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1106 | chr19 | 47001794 | ||||||
chr19:47001886 | A | G | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1198A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1198 | chr19 | 47001886 | ||||||
chr19:47001910 | G | A | 1 | a0001c0001t0027 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1222 | chr19 | 47001910 | ||||||
chr19:47001977 | G | A | 1 | a0001c0001t0016 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1289 | chr19 | 47001977 | ||||||
chr19:47002012 | C | G | 1 | a0001c0001t0022 | 2 | HG00558.hp2 HG00597.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1324C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1324 | chr19 | 47002012 | ||||||
chr19:47002290 | C | T | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1602C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 1602 | chr19 | 47002290 | ||||||
chr19:47002707 | TG | T | 8 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0010 others(5): Show |
32 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2021delG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2021 | INFO_REALIGN_3_PRIME | chr19 | 47002707 | |||||
chr19:47002720 | T | C | 1 | a0001c0001t0028 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2032 | chr19 | 47002720 | ||||||
chr19:47002869 | C | A | 5 | a0001c0001t0023 a0001c0002t0005 a0001c0002t0032 others(2): Show |
16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2181C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2181 | chr19 | 47002869 | ||||||
chr19:47003095 | A | G | 19 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(16): Show |
60 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2407A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2407 | chr19 | 47003095 | ||||||
chr19:47003106 | C | T | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(13): Show |
69 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2418C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2418 | chr19 | 47003106 | ||||||
chr19:47003166 | C | T | 1 | a0001c0001t0013 | 4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2478C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2478 | chr19 | 47003166 | ||||||
chr19:47003177 | G | A | 1 | a0001c0001t0030 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2489G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2489 | chr19 | 47003177 | ||||||
chr19:47003234 | C | T | 5 | a0001c0001t0023 a0001c0002t0005 a0001c0002t0032 others(2): Show |
16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2546C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2546 | chr19 | 47003234 | ||||||
chr19:47003329 | A | G | 1 | a0001c0001t0043 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2641A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2641 | chr19 | 47003329 | ||||||
chr19:47003410 | C | T | 1 | a0001c0001t0042 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2722 | chr19 | 47003410 | ||||||
chr19:47003416 | C | T | 1 | a0001c0001t0020 | 2 | HG02622.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2728C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2728 | chr19 | 47003416 | ||||||
chr19:47003497 | C | T | 1 | a0001c0001t0045 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2809C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2809 | chr19 | 47003497 | ||||||
chr19:47003512 | C | T | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 others(13): Show |
49 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2824C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2824 | chr19 | 47003512 | ||||||
chr19:47003520 | G | A | 1 | a0001c0001t0033 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2832G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2832 | chr19 | 47003520 | ||||||
chr19:47003567 | G | T | 1 | a0001c0001t0015 | 2 | NA18906.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2879G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2879 | chr19 | 47003567 | ||||||
chr19:47003584 | C | T | 2 | a0001c0001t0007 a0004c0012t0007 |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2896C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2896 | chr19 | 47003584 | ||||||
chr19:47003594 | G | A | 1 | a0001c0001t0034 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2906G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 2906 | chr19 | 47003594 | ||||||
chr19:47003913 | G | GAC | 7 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0013 others(4): Show |
30 | HG00639.hp2 HG00735.hp2 HG01167.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3228_*3229dupAC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | |||||
chr19:47003913 | G | GACAC | 7 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0019 others(4): Show |
12 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3226_*3229dupACAC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | |||||
chr19:47003913 | G | GACACAC | 2 | a0001c0001t0017 a0001c0001t0028 |
3 | HG01099.hp1 HG02135.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3229_*3230insACAC others(2): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | |||||
chr19:47003913 | G | GACACACA others(3): Show |
1 | a0001c0001t0044 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3229_*3230insACAC others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | |||||
chr19:47003913 | GACACGCA others(3): Show |
G | 1 | a0001c0001t0039 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3230_*3239delGCAC others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003913 | |||||
chr19:47003914 | ACACG | A | 8 | a0001c0001t0003 a0001c0001t0027 a0001c0001t0035 others(5): Show |
34 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3230_*3233delGCAC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003914 | |||||
chr19:47003916 | ACG | A | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(20): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3230_*3231delGC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | 47003916 | |||||
chr19:47003918 | G | A | 27 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(24): Show |
70 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*3230G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | chr19 | 47003918 | ||||||
chr19:47003918 | G | GCA | 4 | a0001c0001t0001 a0001c0001t0033 a0001c0001t0048 others(1): Show |
40 | HG00438.hp1 HG01069.hp2 HG01261.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3261_*3262dupCA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3263 | INFO_REALIGN_3_PRIME | chr19 | 47003918 | |||||
chr19:47003918 | G | GCACA | 1 | a0001c0001t0001 | 5 | HG00099.hp1 HG01099.hp2 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3259_*3262dupCACA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3263 | INFO_REALIGN_3_PRIME | chr19 | 47003918 | |||||
chr19:47004134 | G | A | 1 | a0001c0001t0037 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3446G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3446 | chr19 | 47004134 | ||||||
chr19:47004177 | C | T | 21 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(18): Show |
77 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3489C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3489 | chr19 | 47004177 | ||||||
chr19:47004207 | G | A | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3519G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3519 | chr19 | 47004207 | ||||||
chr19:47004211 | G | A | 21 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(18): Show |
74 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3523G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3523 | chr19 | 47004211 | ||||||
chr19:47004268 | G | A | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3580G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3580 | chr19 | 47004268 | ||||||
chr19:47004288 | T | C | 1 | a0001c0001t0035 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3600T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3600 | chr19 | 47004288 | ||||||
chr19:47004299 | C | T | 1 | a0001c0001t0050 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3611C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3611 | chr19 | 47004299 | ||||||
chr19:47004324 | C | T | 1 | a0001c0001t0044 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3636C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3636 | chr19 | 47004324 | ||||||
chr19:47004347 | G | A | 2 | a0001c0001t0006 a0001c0009t0006 |
6 | HG00642.hp2 HG01257.hp1 HG01928.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3659G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3659 | chr19 | 47004347 | ||||||
chr19:47004423 | G | T | 4 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0049 others(1): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3735G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3735 | chr19 | 47004423 | ||||||
chr19:47004574 | A | G | 1 | a0001c0001t0050 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3886A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3886 | chr19 | 47004574 | ||||||
chr19:47004852 | A | T | 1 | a0001c0001t0024 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4164A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 4164 | chr19 | 47004852 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46861296 | C | A | 10 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(7): Show |
10 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-189+87C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861296 | |||||||
chr19:46861343 | G | C | 11 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(8): Show |
11 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-189+134G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861343 | |||||||
chr19:46861343 | G | GC | 82 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(79): Show |
82 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-189+144dupC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46861343 | ||||||
chr19:46861503 | T | G | 1 | a0001c0001t0003g0022 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-189+294T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861503 | |||||||
chr19:46861553 | T | C | 1 | a0001c0001t0006g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-189+344T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861553 | |||||||
chr19:46861865 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-189+656C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861865 | |||||||
chr19:46861885 | G | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+676G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861885 | |||||||
chr19:46861927 | CT | C | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-189+720delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46861927 | ||||||
chr19:46861936 | C | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+727C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861936 | |||||||
chr19:46861936 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-189+727C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46861936 | |||||||
chr19:46862040 | G | A | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189+831G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46862040 | |||||||
chr19:46862908 | ATTACGAT others(6): Show |
A | 1 | a0001c0001t0001g0264 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-189+1703_-189+171 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46862908 | ||||||
chr19:46863144 | C | T | 54 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(51): Show |
54 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-189+1935C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863144 | |||||||
chr19:46863186 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0294 |
2 | NA18951.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-189+1977A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863186 | |||||||
chr19:46863697 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-189+2488A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863697 | |||||||
chr19:46863732 | C | G | 16 | a0001c0001t0001g0295 a0001c0002t0005g0207 a0001c0002t0005g0209 others(13): Show |
16 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-189+2523C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863732 | |||||||
chr19:46863768 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0279 |
2 | HG02056.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-189+2559G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863768 | |||||||
chr19:46863828 | C | T | 34 | a0001c0001t0001g0118 a0001c0001t0002g0108 a0001c0001t0004g0102 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-189+2619C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863828 | |||||||
chr19:46863858 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-189+2649A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863858 | |||||||
chr19:46863903 | C | T | 7 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0099 others(4): Show |
7 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+2694C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863903 | |||||||
chr19:46863916 | A | G | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-189+2707A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46863916 | |||||||
chr19:46864194 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-189+2985T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864194 | |||||||
chr19:46864248 | T | TG | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+3041dupG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46864248 | ||||||
chr19:46864306 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-189+3097G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864306 | |||||||
chr19:46864433 | A | G | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+3224A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864433 | |||||||
chr19:46864459 | G | C | 2 | a0001c0001t0011g0029 a0001c0001t0038g0028 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-189+3250G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864459 | |||||||
chr19:46864590 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189+3381A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864590 | |||||||
chr19:46864763 | C | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+3554C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864763 | |||||||
chr19:46864920 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-189+3711T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864920 | |||||||
chr19:46864973 | A | T | 1 | a0001c0001t0036g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-189+3764A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46864973 | |||||||
chr19:46865044 | A | G | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-189+3835A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865044 | |||||||
chr19:46865094 | A | G | 1 | a0001c0001t0004g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-189+3885A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865094 | |||||||
chr19:46865139 | G | T | 1 | a0001c0001t0003g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-189+3930G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865139 | |||||||
chr19:46865398 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-189+4189C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865398 | |||||||
chr19:46865808 | C | A | 1 | a0001c0001t0013g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-189+4599C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865808 | |||||||
chr19:46865878 | T | A | 1 | a0001c0001t0002g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-189+4669T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865878 | |||||||
chr19:46865963 | C | T | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-189+4754C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46865963 | |||||||
chr19:46866123 | G | A | 3 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0027g0232 |
3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-189+4914G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866123 | |||||||
chr19:46866332 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-189+5123C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866332 | |||||||
chr19:46866496 | G | C | 35 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-189+5287G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866496 | |||||||
chr19:46866577 | G | A | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+5368G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866577 | |||||||
chr19:46866672 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-189+5463C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866672 | |||||||
chr19:46866792 | A | G | 3 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0027g0232 |
3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-189+5583A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866792 | |||||||
chr19:46866993 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+5784G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46866993 | |||||||
chr19:46867046 | A | G | 1 | a0001c0001t0014g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-189+5837A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867046 | |||||||
chr19:46867384 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG01433.hp1 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+6175G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867384 | |||||||
chr19:46867482 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-189+6273T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867482 | |||||||
chr19:46867500 | A | G | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+6291A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867500 | |||||||
chr19:46867545 | G | A | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+6336G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867545 | |||||||
chr19:46867557 | C | T | 1 | a0001c0002t0005g0298 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-189+6348C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867557 | |||||||
chr19:46867699 | G | C | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+6490G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867699 | |||||||
chr19:46867758 | T | G | 9 | a0001c0001t0002g0108 a0001c0001t0004g0102 a0001c0001t0004g0106 others(6): Show |
9 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189+6549T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867758 | |||||||
chr19:46867761 | G | T | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-189+6552G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867761 | |||||||
chr19:46867779 | T | G | 16 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(13): Show |
16 | HG00597.hp1 HG01891.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.-189+6570T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867779 | |||||||
chr19:46867867 | T | A | 1 | a0001c0001t0004g0102 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-189+6658T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867867 | |||||||
chr19:46867903 | A | G | 1 | a0001c0001t0006g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-189+6694A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46867903 | |||||||
chr19:46868157 | C | G | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+6948C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868157 | |||||||
chr19:46868359 | G | A | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-189+7150G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868359 | |||||||
chr19:46868372 | CAATT | C | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+7166_-189+716 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868372 | ||||||
chr19:46868477 | A | G | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-189+7268A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868477 | |||||||
chr19:46868587 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+7378C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868587 | |||||||
chr19:46868857 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-189+7648C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46868857 | |||||||
chr19:46868893 | A | AT | 115 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0152 others(112): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-189+7713dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | ||||||
chr19:46868893 | A | ATT | 40 | a0001c0001t0001g0156 a0001c0001t0001g0293 a0001c0001t0001g0294 others(37): Show |
40 | HG00408.hp2 HG00642.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-189+7712_-189+771 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | ||||||
chr19:46868893 | A | ATTT | 12 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(9): Show |
12 | HG00438.hp1 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-189+7711_-189+771 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | ||||||
chr19:46868893 | AT | A | 35 | a0001c0001t0001g0077 a0001c0001t0001g0265 a0001c0001t0001g0281 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.-189+7713delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | ||||||
chr19:46868893 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-189+7703_-189+771 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46868893 | ||||||
chr19:46869095 | T | A | 268 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(265): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-189+7886T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869095 | |||||||
chr19:46869182 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-189+7973C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869182 | |||||||
chr19:46869476 | T | TTG | 83 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0134 others(80): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.-189+8299_-189+830 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | T | TTGTG | 30 | a0001c0001t0001g0141 a0001c0001t0001g0155 a0001c0001t0001g0191 others(27): Show |
30 | HG00597.hp1 HG00639.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-189+8297_-189+830 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | T | TTGTGTG | 10 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0020 others(7): Show |
10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+8295_-189+830 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0002g0019 a0001c0001t0042g0018 |
2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-189+8291_-189+830 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | TTG | T | 18 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0160 others(15): Show |
18 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-189+8299_-189+830 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | TTGTG | T | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0009g0111 others(5): Show |
8 | HG01255.hp2 HG01496.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189+8297_-189+830 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(5): Show |
8 | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-189+8291_-189+830 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869476 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-189+8289_-189+830 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869476 | ||||||
chr19:46869734 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0265 |
2 | NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-189+8525G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869734 | |||||||
chr19:46869803 | G | C | 31 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(28): Show |
31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-189+8594G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869803 | |||||||
chr19:46869943 | C | CT | 6 | a0001c0001t0001g0276 a0001c0001t0002g0050 a0001c0001t0002g0064 others(3): Show |
6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+8755dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869943 | ||||||
chr19:46869943 | CT | C | 110 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0171 others(107): Show |
110 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.-189+8755delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869943 | ||||||
chr19:46869943 | CTT | C | 35 | a0001c0001t0001g0077 a0001c0001t0002g0001 a0001c0001t0003g0022 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-189+8754_-189+875 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46869943 | ||||||
chr19:46869972 | A | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+8763A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869972 | |||||||
chr19:46869985 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-189+8776C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46869985 | |||||||
chr19:46870091 | C | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-189+8882C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870091 | |||||||
chr19:46870139 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-189+8930C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870139 | |||||||
chr19:46870281 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+9072G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870281 | |||||||
chr19:46870350 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+9141C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870350 | |||||||
chr19:46870605 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-189+9396T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870605 | |||||||
chr19:46870846 | A | T | 1 | a0001c0001t0001g0292 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-189+9637A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870846 | |||||||
chr19:46870891 | T | G | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-189+9682T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870891 | |||||||
chr19:46870988 | A | T | 1 | a0001c0001t0001g0264 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-189+9779A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46870988 | |||||||
chr19:46871306 | A | G | 2 | a0001c0001t0022g0187 a0001c0001t0022g0288 |
2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.-189+10097A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871306 | |||||||
chr19:46871321 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+10112C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871321 | |||||||
chr19:46871355 | T | G | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+10146T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871355 | |||||||
chr19:46871588 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+10379C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871588 | |||||||
chr19:46871623 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0041g0043 |
2 | HG02071.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-189+10414G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871623 | |||||||
chr19:46871645 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+10436C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871645 | |||||||
chr19:46871754 | G | A | 1 | a0001c0001t0033g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-189+10545G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871754 | |||||||
chr19:46871776 | C | T | 7 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+10567C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871776 | |||||||
chr19:46871793 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-189+10584A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871793 | |||||||
chr19:46871904 | C | T | 3 | a0001c0001t0013g0087 a0001c0001t0013g0247 a0001c0001t0013g0248 |
3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-189+10695C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46871904 | |||||||
chr19:46872015 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-189+10806G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872015 | |||||||
chr19:46872113 | C | T | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+10904C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872113 | |||||||
chr19:46872251 | A | G | 1 | a0001c0001t0037g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-189+11042A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872251 | |||||||
chr19:46872705 | T | C | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-189+11496T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872705 | |||||||
chr19:46872707 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-189+11498C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872707 | |||||||
chr19:46872844 | A | G | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-189+11635A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872844 | |||||||
chr19:46872859 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-189+11650C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872859 | |||||||
chr19:46872866 | G | A | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-189+11657G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872866 | |||||||
chr19:46872875 | C | T | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+11666C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872875 | |||||||
chr19:46872880 | C | CA | 160 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(157): Show |
160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-189+11686dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46872880 | ||||||
chr19:46872905 | A | C | 1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-189+11696A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872905 | |||||||
chr19:46872994 | C | G | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-189+11785C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46872994 | |||||||
chr19:46873129 | C | T | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-189+11920C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873129 | |||||||
chr19:46873198 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-189+11989C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873198 | |||||||
chr19:46873410 | T | C | 1 | a0001c0001t0012g0226 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-189+12201T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873410 | |||||||
chr19:46873636 | C | CA | 116 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0152 others(113): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-189+12441dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46873636 | ||||||
chr19:46873835 | G | A | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+12626G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873835 | |||||||
chr19:46873844 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-189+12635G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873844 | |||||||
chr19:46873911 | G | C | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+12702G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46873911 | |||||||
chr19:46873983 | GGTGATCT others(1055): Show |
G | 1 | a0001c0001t0004g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-189+12788_-189+13 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46873983 | ||||||
chr19:46874069 | T | C | 1 | a0001c0001t0026g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-189+12860T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874069 | |||||||
chr19:46874162 | C | G | 33 | a0001c0001t0001g0118 a0001c0001t0002g0108 a0001c0001t0004g0102 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-189+12953C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874162 | |||||||
chr19:46874501 | C | CT | 116 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0137 others(113): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-189+13312dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874501 | ||||||
chr19:46874501 | C | CTT | 11 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(8): Show |
11 | HG02015.hp2 HG02027.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+13311_-189+13 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874501 | ||||||
chr19:46874501 | CT | C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0155 a0001c0001t0001g0159 others(3): Show |
6 | HG02145.hp1 HG02293.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+13312delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874501 | ||||||
chr19:46874507 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-189+13298T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874507 | |||||||
chr19:46874574 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0022g0187 a0001c0001t0022g0288 |
3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-189+13365G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874574 | |||||||
chr19:46874620 | TCAGCCTC others(17): Show |
T | 1 | a0001c0002t0005g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-189+13415_-189+13 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874620 | ||||||
chr19:46874661 | T | C | 270 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(267): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-189+13452T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874661 | |||||||
chr19:46874719 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-189+13510G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874719 | |||||||
chr19:46874810 | C | CT | 11 | a0001c0001t0001g0137 a0001c0001t0001g0188 a0001c0001t0001g0198 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+13620dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874810 | ||||||
chr19:46874810 | CT | C | 167 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(164): Show |
167 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-189+13620delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46874810 | ||||||
chr19:46874835 | G | A | 1 | a0006c0008t0011g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-189+13626G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46874835 | |||||||
chr19:46875056 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-189+13847C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875056 | |||||||
chr19:46875187 | G | A | 1 | a0001c0001t0004g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-189+13978G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875187 | |||||||
chr19:46875212 | T | C | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+14003T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875212 | |||||||
chr19:46875343 | G | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18942.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-189+14134G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875343 | |||||||
chr19:46875430 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-189+14221T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875430 | |||||||
chr19:46875600 | G | A | 34 | a0001c0001t0001g0118 a0001c0001t0002g0108 a0001c0001t0004g0102 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-189+14391G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875600 | |||||||
chr19:46875650 | AT | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+14446delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46875650 | ||||||
chr19:46875715 | A | C | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+14506A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875715 | |||||||
chr19:46875757 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+14548G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875757 | |||||||
chr19:46875768 | G | A | 185 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(182): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.-189+14559G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46875768 | |||||||
chr19:46876044 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+14835C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876044 | |||||||
chr19:46876088 | G | A | 1 | a0001c0002t0005g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-189+14879G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876088 | |||||||
chr19:46876126 | G | T | 2 | a0001c0001t0002g0054 a0001c0001t0040g0053 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-189+14917G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876126 | |||||||
chr19:46876193 | AT | A | 6 | a0001c0001t0001g0160 a0001c0001t0001g0192 a0001c0001t0004g0257 others(3): Show |
6 | HG02258.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+14996delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46876193 | ||||||
chr19:46876623 | G | A | 1 | a0001c0001t0018g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-189+15414G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876623 | |||||||
chr19:46876866 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-189+15657T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46876866 | |||||||
chr19:46877248 | C | CA | 11 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0001c0001t0001g0175 others(8): Show |
11 | HG00733.hp2 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+16061dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877248 | ||||||
chr19:46877248 | CA | C | 79 | a0001c0001t0001g0068 a0001c0001t0002g0001 a0001c0001t0002g0002 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-189+16061delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877248 | ||||||
chr19:46877248 | CAA | C | 80 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0002g0015 others(77): Show |
80 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-189+16060_-189+16 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877248 | ||||||
chr19:46877284 | T | C | 1 | a0001c0001t0013g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-189+16075T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877284 | |||||||
chr19:46877288 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-189+16079C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877288 | |||||||
chr19:46877305 | G | C | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+16096G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877305 | |||||||
chr19:46877388 | C | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+16179C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877388 | |||||||
chr19:46877569 | AAATAAC | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+16366_-189+16 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46877569 | ||||||
chr19:46877571 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-189+16362A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877571 | |||||||
chr19:46877665 | C | T | 1 | a0001c0007t0011g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-189+16456C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877665 | |||||||
chr19:46877916 | C | G | 4 | a0001c0001t0014g0089 a0001c0001t0014g0093 a0001c0001t0014g0094 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189+16707C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46877916 | |||||||
chr19:46878004 | G | A | 1 | a0001c0001t0048g0129 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-189+16795G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878004 | |||||||
chr19:46878084 | T | G | 12 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG00733.hp2 HG00738.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-189+16875T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878084 | |||||||
chr19:46878376 | G | A | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+17167G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878376 | |||||||
chr19:46878410 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-189+17201G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878410 | |||||||
chr19:46878583 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-189+17374T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878583 | |||||||
chr19:46878640 | G | T | 12 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG00733.hp2 HG00738.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-189+17431G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878640 | |||||||
chr19:46878876 | A | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+17667A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878876 | |||||||
chr19:46878960 | T | C | 1 | a0001c0001t0017g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-189+17751T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46878960 | |||||||
chr19:46879044 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-189+17835T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879044 | |||||||
chr19:46879168 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-189+17959C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879168 | |||||||
chr19:46879236 | T | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
7 | HG01433.hp1 HG01928.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+18027T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879236 | |||||||
chr19:46879271 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-189+18062A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879271 | |||||||
chr19:46879333 | A | T | 31 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(28): Show |
31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-189+18124A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879333 | |||||||
chr19:46879352 | G | C | 1 | a0004c0012t0007g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-189+18143G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879352 | |||||||
chr19:46879534 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-189+18325C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879534 | |||||||
chr19:46879587 | A | AAAAT | 3 | a0001c0001t0003g0086 a0001c0002t0032g0211 a0001c0002t0047g0127 |
3 | HG02071.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-189+18406_-189+18 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(1): Show |
6 | a0001c0001t0001g0295 a0001c0001t0009g0111 a0001c0001t0009g0112 others(3): Show |
6 | HG02027.hp2 HG02074.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+18402_-189+18 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(5): Show |
7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0289 others(4): Show |
7 | HG00621.hp2 HG00735.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189+18398_-189+18 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(9): Show |
67 | a0001c0001t0001g0118 a0001c0001t0001g0131 a0001c0001t0001g0132 others(64): Show |
67 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-189+18394_-189+18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(86): Show |
3 | a0001c0001t0001g0068 a0001c0001t0002g0012 a0001c0001t0002g0014 |
3 | HG03041.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(99): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(90): Show |
3 | a0001c0001t0002g0044 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG02895.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(103): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(94): Show |
39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(36): Show |
39 | HG00408.hp2 HG00733.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(107): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(98): Show |
22 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0009 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(111): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(102): Show |
3 | a0001c0001t0002g0061 a0001c0001t0006g0222 a0001c0001t0015g0227 |
3 | HG02004.hp2 HG04115.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-189+18397_-189+18 others(115): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(13): Show |
37 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(34): Show |
37 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-189+18390_-189+18 others(26): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(17): Show |
17 | a0001c0001t0001g0130 a0001c0001t0001g0165 a0001c0001t0001g0173 others(14): Show |
17 | HG00597.hp2 HG00735.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-189+18386_-189+18 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879587 | A | AAAATAAA others(21): Show |
1 | a0001c0001t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-189+18382_-189+18 others(34): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879587 | ||||||
chr19:46879615 | T | TAAATAAA others(17): Show |
1 | a0001c0001t0001g0285 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-189+18409_-189+18 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879615 | ||||||
chr19:46879619 | A | T | 4 | a0001c0001t0001g0068 a0001c0001t0002g0014 a0001c0001t0002g0231 others(1): Show |
4 | HG03041.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189+18410A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879619 | |||||||
chr19:46879708 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-189+18499C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879708 | |||||||
chr19:46879780 | G | A | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG01069.hp2 HG01261.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-189+18571G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879780 | |||||||
chr19:46879784 | C | CA | 49 | a0001c0001t0001g0077 a0001c0001t0001g0190 a0001c0001t0001g0196 others(46): Show |
49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-189+18593dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879784 | ||||||
chr19:46879784 | C | CAA | 6 | a0001c0001t0003g0095 a0001c0001t0003g0235 a0001c0001t0003g0236 others(3): Show |
6 | HG00621.hp1 HG02738.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+18592_-189+18 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879784 | ||||||
chr19:46879784 | CA | C | 22 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(19): Show |
22 | HG00438.hp1 HG02129.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+18593delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879784 | ||||||
chr19:46879833 | C | T | 7 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0099 others(4): Show |
7 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+18624C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46879833 | |||||||
chr19:46879944 | GGCATGGT others(339): Show |
G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+18746_-189+19 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46879944 | ||||||
chr19:46880000 | T | G | 1 | a0001c0001t0036g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-189+18791T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880000 | |||||||
chr19:46880163 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189+18954T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880163 | |||||||
chr19:46880215 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-189+19006C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880215 | |||||||
chr19:46880250 | T | C | 1 | a0001c0001t0002g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-189+19041T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880250 | |||||||
chr19:46880548 | CTT | C | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+19341_-189+19 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46880548 | ||||||
chr19:46880690 | T | G | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+19481T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880690 | |||||||
chr19:46880786 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-189+19577C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46880786 | |||||||
chr19:46880947 | C | CT | 34 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0138 others(31): Show |
34 | HG00642.hp1 HG01099.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-189+19757dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46880947 | ||||||
chr19:46881069 | C | T | 1 | a0001c0001t0020g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-189+19860C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881069 | |||||||
chr19:46881168 | C | T | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+19959C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881168 | |||||||
chr19:46881242 | A | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(53): Show |
56 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-189+20033A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881242 | |||||||
chr19:46881265 | T | C | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-189+20056T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881265 | |||||||
chr19:46881541 | C | T | 1 | a0001c0001t0003g0022 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-189+20332C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881541 | |||||||
chr19:46881638 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-189+20429A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881638 | |||||||
chr19:46881886 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0294 |
2 | NA18951.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-189+20677T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46881886 | |||||||
chr19:46882026 | G | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(2): Show |
5 | HG02015.hp2 HG02027.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+20817G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882026 | |||||||
chr19:46882064 | A | G | 1 | a0001c0001t0004g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-189+20855A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882064 | |||||||
chr19:46882178 | G | C | 1 | a0001c0001t0014g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-189+20969G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882178 | |||||||
chr19:46882254 | C | T | 1 | a0001c0001t0020g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-189+21045C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882254 | |||||||
chr19:46882447 | T | C | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-189+21238T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882447 | |||||||
chr19:46882669 | C | T | 2 | a0001c0001t0002g0098 a0001c0001t0010g0097 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-189+21460C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46882669 | |||||||
chr19:46883125 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+21916C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883125 | |||||||
chr19:46883158 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+21949G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883158 | |||||||
chr19:46883261 | A | AT | 69 | a0001c0001t0001g0068 a0001c0001t0001g0295 a0001c0001t0002g0001 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-189+22067dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46883261 | ||||||
chr19:46883274 | T | G | 10 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(7): Show |
10 | HG02015.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+22065T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883274 | |||||||
chr19:46883442 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-189+22233G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883442 | |||||||
chr19:46883512 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-189+22303A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883512 | |||||||
chr19:46883568 | C | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-189+22359C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883568 | |||||||
chr19:46883607 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-189+22398G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883607 | |||||||
chr19:46883740 | C | T | 1 | a0004c0012t0007g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-189+22531C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883740 | |||||||
chr19:46883766 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-189+22557G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883766 | |||||||
chr19:46883844 | C | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-189+22635C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46883844 | |||||||
chr19:46884003 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+22794C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884003 | |||||||
chr19:46884110 | G | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-189+22901G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884110 | |||||||
chr19:46884116 | A | T | 13 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(10): Show |
13 | HG00639.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-189+22907A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884116 | |||||||
chr19:46884210 | C | T | 1 | a0003c0013t0003g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-189+23001C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884210 | |||||||
chr19:46884250 | A | G | 7 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+23041A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884250 | |||||||
chr19:46884408 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-189+23199A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884408 | |||||||
chr19:46884493 | C | CT | 20 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0295 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-189+23307dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46884493 | ||||||
chr19:46884493 | CT | C | 11 | a0001c0001t0001g0130 a0001c0001t0004g0102 a0001c0001t0007g0059 others(8): Show |
11 | HG00408.hp2 HG01255.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-189+23307delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46884493 | ||||||
chr19:46884516 | T | C | 13 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(10): Show |
13 | HG00642.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-189+23307T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884516 | |||||||
chr19:46884585 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-189+23376C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884585 | |||||||
chr19:46884641 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+23432C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884641 | |||||||
chr19:46884657 | G | T | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-189+23448G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884657 | |||||||
chr19:46884733 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-189+23524C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46884733 | |||||||
chr19:46885024 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+23815T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885024 | |||||||
chr19:46885049 | G | A | 266 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(263): Show |
266 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-189+23840G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885049 | |||||||
chr19:46885053 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-189+23844G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885053 | |||||||
chr19:46885481 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-189+24272A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885481 | |||||||
chr19:46885576 | C | T | 5 | a0001c0001t0003g0022 a0001c0001t0003g0074 a0001c0001t0003g0079 others(2): Show |
5 | HG02015.hp1 HG02523.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+24367C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885576 | |||||||
chr19:46885786 | A | G | 5 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0249 others(2): Show |
5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+24577A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885786 | |||||||
chr19:46885799 | T | A | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-189+24590T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885799 | |||||||
chr19:46885941 | T | G | 1 | a0001c0001t0039g0063 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-189+24732T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46885941 | |||||||
chr19:46886056 | C | T | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-189+24847C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886056 | |||||||
chr19:46886113 | A | G | 29 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(26): Show |
29 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-189+24904A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886113 | |||||||
chr19:46886365 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+25156A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886365 | |||||||
chr19:46886381 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+25172G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886381 | |||||||
chr19:46886493 | T | G | 1 | a0001c0001t0004g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-189+25284T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886493 | |||||||
chr19:46886529 | C | T | 1 | a0001c0001t0004g0121 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-189+25320C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886529 | |||||||
chr19:46886602 | T | C | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-189+25393T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886602 | |||||||
chr19:46886620 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-189+25411G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886620 | |||||||
chr19:46886781 | CTTA | C | 82 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(79): Show |
82 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-189+25573_-189+25 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886781 | |||||||
chr19:46886784 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-189+25575A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886784 | |||||||
chr19:46886903 | T | G | 1 | a0001c0001t0036g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-189+25694T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46886903 | |||||||
chr19:46887171 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-189+25962T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887171 | |||||||
chr19:46887416 | C | T | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-189+26207C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887416 | |||||||
chr19:46887509 | C | T | 2 | a0001c0001t0003g0072 a0001c0001t0003g0240 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-189+26300C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887509 | |||||||
chr19:46887640 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-189+26431C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887640 | |||||||
chr19:46887758 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-189+26549C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46887758 | |||||||
chr19:46888038 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-189+26829G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888038 | |||||||
chr19:46888058 | T | C | 34 | a0001c0001t0001g0118 a0001c0001t0002g0108 a0001c0001t0004g0102 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-189+26849T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888058 | |||||||
chr19:46888096 | C | T | 2 | a0001c0001t0004g0262 a0001c0001t0010g0125 |
2 | NA18972.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-189+26887C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888096 | |||||||
chr19:46888101 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-189+26892G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888101 | |||||||
chr19:46888195 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0002g0098 a0001c0001t0010g0097 |
3 | HG01256.hp1 HG01258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-189+26986G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888195 | |||||||
chr19:46888234 | A | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | NA18612.hp1 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-189+27025A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888234 | |||||||
chr19:46888241 | C | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | NA18612.hp1 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-189+27032C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888241 | |||||||
chr19:46888261 | A | AAT | 14 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0178 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+27108_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | A | AATAT | 12 | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0001g0295 others(9): Show |
12 | HG01257.hp1 HG01261.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.-189+27106_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | A | AATATAT | 6 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0096 others(3): Show |
6 | HG01192.hp2 HG01496.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+27104_-189+27 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | A | AATATATA others(3): Show |
2 | a0001c0001t0002g0098 a0001c0001t0010g0097 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-189+27100_-189+27 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AAT | A | 25 | a0001c0001t0001g0068 a0001c0001t0001g0157 a0001c0001t0001g0159 others(22): Show |
25 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-189+27108_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATAT | A | 39 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(36): Show |
39 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-189+27106_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATAT | A | 33 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(30): Show |
33 | HG00140.hp2 HG00621.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-189+27104_-189+27 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(1): Show |
A | 21 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0155 others(18): Show |
21 | HG00408.hp2 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-189+27102_-189+27 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(3): Show |
A | 16 | a0001c0001t0001g0186 a0001c0001t0001g0267 a0001c0001t0002g0021 others(13): Show |
16 | HG00597.hp1 HG00738.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-189+27100_-189+27 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(5): Show |
A | 13 | a0001c0001t0001g0130 a0001c0001t0001g0142 a0001c0001t0001g0199 others(10): Show |
13 | HG00280.hp1 HG00733.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-189+27098_-189+27 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(7): Show |
A | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0185 others(4): Show |
7 | HG01255.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-189+27096_-189+27 others(20): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(9): Show |
A | 5 | a0001c0001t0003g0079 a0001c0001t0003g0082 a0001c0001t0003g0233 others(2): Show |
5 | HG01433.hp2 HG02155.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189+27094_-189+27 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(11): Show |
A | 10 | a0001c0001t0001g0169 a0001c0001t0001g0278 a0001c0001t0003g0022 others(7): Show |
10 | HG01891.hp2 HG02015.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+27092_-189+27 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(13): Show |
A | 9 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0080 others(6): Show |
9 | HG00438.hp2 HG02071.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189+27090_-189+27 others(26): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(15): Show |
A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0194 a0001c0001t0003g0072 others(7): Show |
10 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.-189+27088_-189+27 others(28): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(17): Show |
A | 6 | a0001c0001t0002g0054 a0001c0001t0003g0070 a0001c0001t0003g0071 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.-189+27086_-189+27 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(19): Show |
A | 7 | a0001c0001t0029g0113 a0001c0001t0034g0252 a0001c0002t0005g0207 others(4): Show |
7 | HG00642.hp1 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189+27084_-189+27 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(21): Show |
A | 12 | a0001c0001t0002g0019 a0001c0001t0004g0102 a0001c0001t0020g0032 others(9): Show |
12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-189+27082_-189+27 others(34): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(23): Show |
A | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp1 HG02280.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189+27080_-189+27 others(36): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(25): Show |
A | 1 | a0001c0001t0004g0123 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-189+27078_-189+27 others(38): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(27): Show |
A | 2 | a0001c0001t0025g0277 a0001c0002t0047g0127 |
2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-189+27076_-189+27 others(40): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(29): Show |
A | 2 | a0001c0002t0001g0033 a0001c0011t0001g0274 |
2 | HG02886.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-189+27074_-189+27 others(42): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888261 | AATATATA others(33): Show |
A | 1 | a0001c0001t0018g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-189+27070_-189+27 others(46): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888261 | ||||||
chr19:46888315 | T | A | 1 | a0001c0001t0023g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-189+27106T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888315 | |||||||
chr19:46888317 | T | A | 2 | a0001c0001t0001g0283 a0001c0001t0014g0094 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-189+27108T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888317 | |||||||
chr19:46888333 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-189+27124T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888333 | |||||||
chr19:46888333 | T | TAC | 24 | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0001g0143 others(21): Show |
24 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-189+27155_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | ||||||
chr19:46888333 | T | TACAC | 15 | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0002t0005g0207 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-189+27153_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | ||||||
chr19:46888333 | T | TACACAC | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 others(1): Show |
4 | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-189+27151_-189+27 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | ||||||
chr19:46888333 | TAC | T | 102 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-189+27155_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | ||||||
chr19:46888333 | TACAC | T | 22 | a0001c0001t0001g0077 a0001c0001t0003g0074 a0001c0001t0003g0075 others(19): Show |
22 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+27153_-189+27 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | ||||||
chr19:46888333 | TACACACA others(3): Show |
T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189+27147_-189+27 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888333 | ||||||
chr19:46888365 | C | CA | 3 | a0001c0001t0001g0154 a0001c0001t0001g0203 a0001c0001t0001g0290 |
3 | HG01099.hp2 NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-189+27156_-189+27 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888365 | |||||||
chr19:46888540 | A | ATT | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | NA18612.hp1 NA18950.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-189+27334_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888540 | ||||||
chr19:46888746 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-189+27537C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888746 | |||||||
chr19:46888829 | T | C | 31 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(28): Show |
31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-189+27620T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888829 | |||||||
chr19:46888837 | C | CA | 49 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0143 others(46): Show |
49 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-189+27650dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | ||||||
chr19:46888837 | C | CAA | 7 | a0001c0001t0001g0273 a0001c0001t0003g0081 a0001c0001t0003g0095 others(4): Show |
7 | HG00621.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-189+27649_-189+27 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | ||||||
chr19:46888837 | CA | C | 22 | a0001c0001t0001g0134 a0001c0001t0001g0141 a0001c0001t0001g0142 others(19): Show |
22 | HG01069.hp2 HG01261.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-189+27650delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | ||||||
chr19:46888837 | CAAAAAAA | C | 6 | a0001c0001t0002g0054 a0001c0001t0011g0029 a0001c0001t0015g0040 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+27644_-189+27 others(13): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | ||||||
chr19:46888837 | CAAAAAAA others(2): Show |
C | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+27642_-189+27 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46888837 | ||||||
chr19:46888891 | A | G | 1 | a0001c0001t0004g0120 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-189+27682A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888891 | |||||||
chr19:46888957 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-189+27748G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46888957 | |||||||
chr19:46889045 | A | G | 199 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(196): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.-189+27836A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889045 | |||||||
chr19:46889068 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-189+27859C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889068 | |||||||
chr19:46889328 | G | A | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-189+28119G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889328 | |||||||
chr19:46889487 | T | A | 164 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(161): Show |
164 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-189+28278T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889487 | |||||||
chr19:46889534 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-189+28325C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46889534 | |||||||
chr19:46889750 | C | CA | 151 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0285 others(148): Show |
151 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-189+28562dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46889750 | ||||||
chr19:46889750 | C | CAA | 6 | a0001c0001t0003g0095 a0001c0001t0004g0262 a0001c0001t0015g0227 others(3): Show |
6 | HG02622.hp1 HG02738.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-189+28561_-189+28 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46889750 | ||||||
chr19:46890087 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-188-28401A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890087 | |||||||
chr19:46890267 | T | G | 1 | a0001c0001t0002g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-188-28221T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890267 | |||||||
chr19:46890535 | T | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-188-27953T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890535 | |||||||
chr19:46890752 | G | T | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-188-27736G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46890752 | |||||||
chr19:46891274 | T | G | 1 | a0001c0001t0020g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-188-27214T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891274 | |||||||
chr19:46891421 | G | GT | 10 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0002g0015 others(7): Show |
10 | HG01255.hp1 HG02258.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-188-27055dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46891421 | ||||||
chr19:46891431 | T | G | 54 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(51): Show |
54 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-188-27057T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891431 | |||||||
chr19:46891434 | G | T | 2 | a0001c0001t0002g0061 a0001c0001t0015g0227 |
2 | HG04115.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-188-27054G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891434 | |||||||
chr19:46891459 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-188-27029G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891459 | |||||||
chr19:46891508 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-188-26980C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891508 | |||||||
chr19:46891586 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-188-26902C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891586 | |||||||
chr19:46891635 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-188-26853C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891635 | |||||||
chr19:46891638 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0265 a0001c0001t0001g0268 |
3 | HG02135.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-188-26850G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891638 | |||||||
chr19:46891749 | T | C | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG01433.hp1 HG01928.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-26739T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891749 | |||||||
chr19:46891790 | A | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-26698A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891790 | |||||||
chr19:46891968 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-188-26520C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46891968 | |||||||
chr19:46892026 | A | C | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-188-26462A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892026 | |||||||
chr19:46892101 | C | T | 1 | a0001c0001t0021g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-188-26387C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892101 | |||||||
chr19:46892123 | T | TA | 49 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0137 others(46): Show |
49 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-188-26341dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892123 | ||||||
chr19:46892123 | TA | T | 7 | a0001c0001t0001g0143 a0001c0001t0001g0265 a0001c0001t0003g0030 others(4): Show |
7 | HG00099.hp1 HG02071.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-26341delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892123 | ||||||
chr19:46892124 | A | G | 1 | a0001c0001t0003g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-188-26364A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892124 | |||||||
chr19:46892140 | A | G | 3 | a0001c0001t0002g0050 a0001c0001t0002g0064 a0001c0001t0002g0224 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-188-26348A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892140 | |||||||
chr19:46892148 | G | A | 3 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0036g0026 |
3 | HG01070.hp1 HG01071.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-188-26340G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892148 | |||||||
chr19:46892156 | A | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-188-26332A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892156 | |||||||
chr19:46892282 | G | A | 32 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(29): Show |
32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-188-26206G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892282 | |||||||
chr19:46892302 | C | CA | 10 | a0001c0001t0002g0045 a0001c0001t0009g0255 a0001c0001t0011g0029 others(7): Show |
10 | HG01261.hp1 HG02145.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-188-26172dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892302 | ||||||
chr19:46892334 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-188-26154G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892334 | |||||||
chr19:46892366 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-188-26122T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892366 | |||||||
chr19:46892420 | A | G | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-188-26068A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892420 | |||||||
chr19:46892468 | C | CA | 53 | a0001c0001t0001g0077 a0001c0001t0001g0167 a0001c0001t0001g0168 others(50): Show |
53 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-188-25999dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892468 | ||||||
chr19:46892468 | CA | C | 6 | a0001c0001t0001g0149 a0001c0001t0001g0286 a0001c0001t0002g0096 others(3): Show |
6 | HG01257.hp2 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-188-25999delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892468 | ||||||
chr19:46892621 | A | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-25867A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892621 | |||||||
chr19:46892646 | C | CT | 7 | a0001c0001t0001g0188 a0001c0001t0001g0266 a0001c0001t0001g0270 others(4): Show |
7 | HG01192.hp1 HG01261.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-188-25825dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892646 | ||||||
chr19:46892646 | CT | C | 119 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0183 others(116): Show |
119 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-188-25825delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46892646 | ||||||
chr19:46892663 | T | C | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-25825T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892663 | |||||||
chr19:46892702 | T | C | 1 | a0001c0001t0050g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-188-25786T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892702 | |||||||
chr19:46892776 | G | A | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-188-25712G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892776 | |||||||
chr19:46892940 | T | C | 5 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0249 others(2): Show |
5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-25548T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46892940 | |||||||
chr19:46893615 | C | A | 1 | a0001c0002t0005g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-188-24873C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893615 | |||||||
chr19:46893780 | T | C | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-24708T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893780 | |||||||
chr19:46893886 | C | CT | 30 | a0001c0001t0001g0118 a0001c0001t0001g0265 a0001c0001t0001g0272 others(27): Show |
30 | HG00735.hp2 HG01070.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-188-24583dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46893886 | ||||||
chr19:46893886 | CT | C | 26 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0148 others(23): Show |
26 | HG00408.hp1 HG01070.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.-188-24583delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46893886 | ||||||
chr19:46893915 | A | G | 187 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(184): Show |
187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-188-24573A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893915 | |||||||
chr19:46893932 | T | C | 35 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-188-24556T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46893932 | |||||||
chr19:46894216 | C | T | 1 | a0001c0001t0042g0018 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-188-24272C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894216 | |||||||
chr19:46894238 | C | T | 25 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0045 others(22): Show |
25 | HG00408.hp2 HG00642.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-188-24250C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894238 | |||||||
chr19:46894332 | T | G | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-24156T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894332 | |||||||
chr19:46894445 | G | GT | 24 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0158 others(21): Show |
24 | HG00621.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-188-24024dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46894445 | ||||||
chr19:46894445 | GT | G | 140 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(137): Show |
140 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-188-24024delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46894445 | ||||||
chr19:46894448 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-188-24040T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894448 | |||||||
chr19:46894454 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-188-24034T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894454 | |||||||
chr19:46894465 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-188-24023G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894465 | |||||||
chr19:46894476 | C | T | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-188-24012C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894476 | |||||||
chr19:46894509 | G | A | 1 | a0001c0001t0043g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-188-23979G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894509 | |||||||
chr19:46894677 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-188-23811C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894677 | |||||||
chr19:46894967 | C | A | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-188-23521C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46894967 | |||||||
chr19:46895103 | A | G | 1 | a0006c0008t0011g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-188-23385A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895103 | |||||||
chr19:46895165 | C | CT | 10 | a0001c0001t0001g0158 a0001c0001t0002g0046 a0001c0001t0002g0051 others(7): Show |
10 | HG02738.hp1 HG03130.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-188-23307dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46895165 | ||||||
chr19:46895257 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-188-23231G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895257 | |||||||
chr19:46895288 | C | T | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-23200C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895288 | |||||||
chr19:46895416 | C | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-188-23072C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895416 | |||||||
chr19:46895542 | T | C | 1 | a0001c0001t0009g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-188-22946T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895542 | |||||||
chr19:46895619 | A | G | 1 | a0001c0009t0006g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-188-22869A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895619 | |||||||
chr19:46895794 | C | T | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-188-22694C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895794 | |||||||
chr19:46895878 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-22610G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46895878 | |||||||
chr19:46896014 | A | G | 46 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-188-22474A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896014 | |||||||
chr19:46896102 | C | CA | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-22377dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46896102 | ||||||
chr19:46896132 | A | G | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-188-22356A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896132 | |||||||
chr19:46896202 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-188-22286C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896202 | |||||||
chr19:46896288 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-188-22200G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896288 | |||||||
chr19:46896298 | G | A | 13 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(10): Show |
13 | HG00597.hp1 HG02080.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-188-22190G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896298 | |||||||
chr19:46896503 | C | G | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-21985C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896503 | |||||||
chr19:46896526 | A | G | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-21962A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896526 | |||||||
chr19:46896734 | A | T | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
15 | HG01069.hp2 HG01261.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-188-21754A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896734 | |||||||
chr19:46896810 | A | G | 35 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-188-21678A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896810 | |||||||
chr19:46896955 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-21533G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46896955 | |||||||
chr19:46897060 | A | AT | 36 | a0001c0001t0001g0147 a0001c0001t0001g0191 a0001c0001t0001g0193 others(33): Show |
36 | HG00408.hp2 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-188-21409dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897060 | ||||||
chr19:46897060 | AT | A | 51 | a0001c0001t0001g0077 a0001c0001t0001g0265 a0001c0001t0003g0022 others(48): Show |
51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-188-21409delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897060 | ||||||
chr19:46897089 | A | G | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-188-21399A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897089 | |||||||
chr19:46897145 | C | T | 1 | a0004c0012t0007g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-188-21343C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897145 | |||||||
chr19:46897189 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-188-21299G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897189 | |||||||
chr19:46897407 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-188-21081T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897407 | |||||||
chr19:46897447 | C | CT | 41 | a0001c0001t0001g0077 a0001c0001t0001g0161 a0001c0001t0003g0022 others(38): Show |
41 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-188-21026dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897447 | ||||||
chr19:46897447 | CT | C | 7 | a0001c0001t0001g0197 a0001c0001t0001g0286 a0001c0001t0002g0015 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-188-21026delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897447 | ||||||
chr19:46897462 | T | C | 1 | a0001c0001t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-188-21026T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897462 | |||||||
chr19:46897681 | G | A | 1 | a0001c0009t0006g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-188-20807G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46897681 | |||||||
chr19:46897695 | C | CA | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0190 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-188-20778dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46897695 | ||||||
chr19:46898098 | C | T | 7 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0099 others(4): Show |
7 | HG00099.hp2 HG00280.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-20390C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898098 | |||||||
chr19:46898206 | C | T | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-20282C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898206 | |||||||
chr19:46898214 | C | G | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-188-20274C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898214 | |||||||
chr19:46898240 | C | CA | 12 | a0001c0001t0001g0282 a0001c0001t0002g0065 a0001c0001t0006g0052 others(9): Show |
12 | HG01243.hp2 HG01928.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-188-20233dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898240 | ||||||
chr19:46898249 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-188-20239A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898249 | |||||||
chr19:46898256 | C | A | 7 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-20232C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898256 | |||||||
chr19:46898452 | G | A | 8 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(5): Show |
8 | HG02615.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-188-20036G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898452 | |||||||
chr19:46898552 | T | C | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-188-19936T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898552 | |||||||
chr19:46898744 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-188-19744G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46898744 | |||||||
chr19:46898775 | A | AGCT | 52 | a0001c0001t0001g0077 a0001c0001t0001g0200 a0001c0001t0002g0001 others(49): Show |
52 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-188-19678_-188-19 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | ||||||
chr19:46898775 | A | AGCTGCT | 4 | a0001c0001t0001g0173 a0001c0001t0002g0012 a0001c0001t0003g0233 others(1): Show |
4 | HG02004.hp1 HG02155.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-188-19681_-188-19 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | ||||||
chr19:46898775 | AGCTGCT | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0289 |
3 | HG00621.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-188-19681_-188-19 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | ||||||
chr19:46898775 | AGCTGCTG others(11): Show |
A | 1 | a0001c0001t0001g0283 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-188-19693_-188-19 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46898775 | ||||||
chr19:46899017 | T | A | 3 | a0001c0001t0007g0057 a0001c0001t0007g0058 a0001c0001t0007g0059 |
3 | HG02622.hp2 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-188-19471T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899017 | |||||||
chr19:46899106 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-188-19382G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899106 | |||||||
chr19:46899132 | T | C | 1 | a0001c0001t0002g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-188-19356T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899132 | |||||||
chr19:46899247 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-188-19241C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899247 | |||||||
chr19:46899277 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-188-19211A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899277 | |||||||
chr19:46899329 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 |
3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-188-19159T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899329 | |||||||
chr19:46899432 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-188-19056C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899432 | |||||||
chr19:46899517 | A | C | 32 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(29): Show |
32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-188-18971A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899517 | |||||||
chr19:46899628 | AGGT | A | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-18859_-188-18 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899628 | |||||||
chr19:46899646 | G | C | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-18842G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899646 | |||||||
chr19:46899648 | C | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-188-18840C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899648 | |||||||
chr19:46899698 | C | CA | 53 | a0001c0001t0001g0077 a0001c0001t0001g0203 a0001c0001t0001g0264 others(50): Show |
53 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-188-18781dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46899698 | ||||||
chr19:46899726 | C | T | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-188-18762C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46899726 | |||||||
chr19:46900097 | T | C | 1 | a0001c0001t0004g0117 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-188-18391T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900097 | |||||||
chr19:46900222 | G | GT | 65 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0158 others(62): Show |
65 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-188-18249dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900222 | ||||||
chr19:46900222 | G | GTT | 27 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-188-18250_-188-18 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900222 | ||||||
chr19:46900222 | G | GTTT | 6 | a0001c0001t0002g0065 a0001c0001t0012g0049 a0001c0001t0012g0226 others(3): Show |
6 | HG00408.hp2 HG00642.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-188-18251_-188-18 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900222 | ||||||
chr19:46900239 | T | G | 1 | a0001c0001t0018g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-188-18249T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900239 | |||||||
chr19:46900290 | C | T | 164 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(161): Show |
164 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-188-18198C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900290 | |||||||
chr19:46900441 | G | A | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-18047G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900441 | |||||||
chr19:46900483 | A | G | 3 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0027g0232 |
3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-188-18005A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900483 | |||||||
chr19:46900581 | A | G | 1 | a0001c0001t0039g0063 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-188-17907A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900581 | |||||||
chr19:46900597 | T | C | 187 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(184): Show |
187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-188-17891T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900597 | |||||||
chr19:46900598 | G | A | 2 | a0001c0001t0003g0237 a0001c0001t0003g0241 |
2 | HG00408.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-188-17890G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900598 | |||||||
chr19:46900768 | G | GA | 187 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(184): Show |
187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-188-17710dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46900768 | ||||||
chr19:46900831 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-188-17657G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46900831 | |||||||
chr19:46901299 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-188-17189T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901299 | |||||||
chr19:46901754 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-188-16734G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901754 | |||||||
chr19:46901777 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-188-16711T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901777 | |||||||
chr19:46901919 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-188-16569C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901919 | |||||||
chr19:46901922 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-188-16566G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46901922 | |||||||
chr19:46902681 | T | G | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-15807T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902681 | |||||||
chr19:46902725 | T | A | 2 | a0001c0001t0003g0072 a0001c0001t0003g0240 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-188-15763T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902725 | |||||||
chr19:46902749 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-188-15739A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902749 | |||||||
chr19:46902829 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-15659C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902829 | |||||||
chr19:46902891 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-188-15597T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46902891 | |||||||
chr19:46903193 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-188-15295T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903193 | |||||||
chr19:46903368 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-188-15120C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903368 | |||||||
chr19:46903429 | G | A | 1 | a0001c0011t0001g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-188-15059G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903429 | |||||||
chr19:46903479 | G | A | 1 | a0001c0007t0011g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-188-15009G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903479 | |||||||
chr19:46903585 | G | C | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-14903G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903585 | |||||||
chr19:46903674 | A | G | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-14814A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903674 | |||||||
chr19:46903685 | G | A | 7 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-14803G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903685 | |||||||
chr19:46903791 | T | C | 1 | a0001c0001t0009g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-188-14697T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903791 | |||||||
chr19:46903899 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-14589G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903899 | |||||||
chr19:46903950 | G | C | 3 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0036g0026 |
3 | HG01070.hp1 HG01071.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-188-14538G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46903950 | |||||||
chr19:46904159 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-188-14329C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904159 | |||||||
chr19:46904239 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-188-14249C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904239 | |||||||
chr19:46904445 | G | A | 1 | a0001c0001t0011g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-188-14043G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904445 | |||||||
chr19:46904499 | G | A | 14 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0161 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-188-13989G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904499 | |||||||
chr19:46904815 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-188-13673G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904815 | |||||||
chr19:46904850 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0253 |
2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-188-13638G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904850 | |||||||
chr19:46904910 | C | T | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-188-13578C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904910 | |||||||
chr19:46904938 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-188-13550G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904938 | |||||||
chr19:46904947 | G | A | 1 | a0001c0001t0024g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-188-13541G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46904947 | |||||||
chr19:46905251 | G | C | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-188-13237G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905251 | |||||||
chr19:46905253 | C | T | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-188-13235C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905253 | |||||||
chr19:46905270 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0270 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-188-13218A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905270 | |||||||
chr19:46905288 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-188-13200G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905288 | |||||||
chr19:46905372 | CT | C | 8 | a0001c0001t0001g0133 a0001c0001t0001g0160 a0001c0001t0001g0179 others(5): Show |
8 | HG00735.hp1 HG01099.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-188-13097delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905372 | ||||||
chr19:46905391 | T | A | 115 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0002g0031 others(112): Show |
115 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-188-13097T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905391 | |||||||
chr19:46905391 | T | TA | 71 | a0001c0001t0001g0068 a0001c0001t0002g0001 a0001c0001t0002g0002 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-188-13095dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905391 | ||||||
chr19:46905435 | G | T | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-188-13053G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905435 | |||||||
chr19:46905475 | A | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-13013A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905475 | |||||||
chr19:46905504 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-188-12984T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905504 | |||||||
chr19:46905537 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-188-12951A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905537 | |||||||
chr19:46905555 | A | AC | 48 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0141 others(45): Show |
48 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-188-12921dupC | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905555 | ||||||
chr19:46905555 | A | ACC | 13 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0193 others(10): Show |
13 | HG00621.hp2 HG02055.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-188-12922_-188-12 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46905555 | ||||||
chr19:46905557 | C | CG | 10 | a0001c0001t0002g0009 a0001c0001t0004g0263 a0001c0001t0006g0052 others(7): Show |
10 | HG00639.hp2 HG00642.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-188-12931_-188-12 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905557 | |||||||
chr19:46905558 | C | G | 104 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(101): Show |
104 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.-188-12930C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905558 | |||||||
chr19:46905562 | C | CG | 32 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(29): Show |
32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-188-12926_-188-12 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905562 | |||||||
chr19:46905563 | C | G | 2 | a0001c0001t0016g0024 a0001c0001t0016g0219 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-188-12925C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905563 | |||||||
chr19:46905565 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-188-12923C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905565 | |||||||
chr19:46905566 | C | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0021 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-188-12922C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905566 | |||||||
chr19:46905612 | C | A | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-188-12876C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905612 | |||||||
chr19:46905740 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-188-12748C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905740 | |||||||
chr19:46905805 | G | C | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-12683G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905805 | |||||||
chr19:46905830 | G | A | 31 | a0001c0001t0001g0118 a0001c0001t0002g0108 a0001c0001t0004g0102 others(28): Show |
31 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-188-12658G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46905830 | |||||||
chr19:46906032 | A | G | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-12456A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906032 | |||||||
chr19:46906367 | A | T | 3 | a0001c0001t0001g0205 a0001c0001t0022g0187 a0001c0001t0022g0288 |
3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-188-12121A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906367 | |||||||
chr19:46906491 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-11997C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906491 | |||||||
chr19:46906518 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-188-11970A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906518 | |||||||
chr19:46906549 | C | T | 2 | a0001c0001t0004g0256 a0001c0001t0043g0225 |
2 | HG04204.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-188-11939C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906549 | |||||||
chr19:46906851 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-188-11637G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906851 | |||||||
chr19:46906870 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-188-11618C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906870 | |||||||
chr19:46906887 | G | A | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-11601G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906887 | |||||||
chr19:46906932 | T | A | 2 | a0001c0001t0011g0029 a0001c0001t0038g0028 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-188-11556T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906932 | |||||||
chr19:46906950 | G | A | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-188-11538G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46906950 | |||||||
chr19:46907091 | A | G | 3 | a0001c0001t0013g0087 a0001c0001t0013g0247 a0001c0001t0013g0248 |
3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-188-11397A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46907091 | |||||||
chr19:46907478 | T | TTTTG | 117 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0190 others(114): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-188-10986_-188-10 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46907478 | ||||||
chr19:46907767 | G | A | 5 | a0001c0001t0003g0022 a0001c0001t0003g0074 a0001c0001t0003g0079 others(2): Show |
5 | HG02015.hp1 HG02523.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-10721G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46907767 | |||||||
chr19:46908080 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-10408T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908080 | |||||||
chr19:46908173 | T | G | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-10315T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908173 | |||||||
chr19:46908189 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0270 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-188-10299T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908189 | |||||||
chr19:46908482 | TTTG | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-9997_-188-999 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46908482 | ||||||
chr19:46908793 | C | T | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-9695C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908793 | |||||||
chr19:46908967 | T | C | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-188-9521T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46908967 | |||||||
chr19:46909054 | CTT | C | 22 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0023g0034 others(19): Show |
22 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-188-9432_-188-943 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46909054 | ||||||
chr19:46909079 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-9409C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909079 | |||||||
chr19:46909149 | A | T | 1 | a0001c0001t0028g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-188-9339A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909149 | |||||||
chr19:46909164 | G | A | 1 | a0001c0001t0033g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-188-9324G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909164 | |||||||
chr19:46909346 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0264 |
2 | NA18968.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-188-9142C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909346 | |||||||
chr19:46909365 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-188-9123C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909365 | |||||||
chr19:46909416 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-188-9072T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909416 | |||||||
chr19:46909468 | A | G | 1 | a0001c0001t0021g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-188-9020A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909468 | |||||||
chr19:46909487 | C | G | 1 | a0001c0001t0003g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-188-9001C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909487 | |||||||
chr19:46909495 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-188-8993G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909495 | |||||||
chr19:46909659 | C | T | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-188-8829C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909659 | |||||||
chr19:46909727 | T | G | 2 | a0001c0001t0003g0072 a0001c0001t0003g0240 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-188-8761T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46909727 | |||||||
chr19:46910017 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-8471C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910017 | |||||||
chr19:46910030 | T | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-188-8458T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910030 | |||||||
chr19:46910456 | G | A | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-188-8032G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910456 | |||||||
chr19:46910467 | T | C | 1 | a0001c0001t0003g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-188-8021T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910467 | |||||||
chr19:46910685 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-7803G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910685 | |||||||
chr19:46910752 | G | A | 2 | a0001c0001t0022g0187 a0001c0001t0022g0288 |
2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.-188-7736G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910752 | |||||||
chr19:46910918 | C | G | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-7570C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46910918 | |||||||
chr19:46911059 | G | A | 1 | a0001c0007t0011g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-188-7429G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911059 | |||||||
chr19:46911327 | C | A | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-7161C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911327 | |||||||
chr19:46911567 | G | A | 1 | a0001c0002t0005g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-188-6921G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911567 | |||||||
chr19:46911729 | G | A | 252 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(249): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-188-6759G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911729 | |||||||
chr19:46911767 | C | G | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-188-6721C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46911767 | |||||||
chr19:46912065 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-188-6423C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912065 | |||||||
chr19:46912179 | G | T | 1 | a0001c0009t0006g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-188-6309G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912179 | |||||||
chr19:46912514 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-188-5974C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912514 | |||||||
chr19:46912608 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA19004.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-188-5880G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912608 | |||||||
chr19:46912659 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-188-5829T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912659 | |||||||
chr19:46912721 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-188-5767A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912721 | |||||||
chr19:46912722 | T | A | 49 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(46): Show |
49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-188-5766T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912722 | |||||||
chr19:46912983 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-188-5505C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46912983 | |||||||
chr19:46913126 | T | C | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-188-5362T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913126 | |||||||
chr19:46913177 | G | T | 4 | a0001c0001t0003g0072 a0001c0001t0003g0240 a0001c0001t0003g0242 others(1): Show |
4 | HG00558.hp1 NA18978.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-188-5311G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913177 | |||||||
chr19:46913232 | C | T | 1 | a0001c0001t0014g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-188-5256C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913232 | |||||||
chr19:46913353 | C | T | 33 | a0001c0001t0001g0118 a0001c0001t0002g0108 a0001c0001t0004g0102 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-188-5135C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46913353 | |||||||
chr19:46914023 | AATGT | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0016 a0001c0001t0002g0017 others(2): Show |
5 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-188-4462_-188-445 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46914023 | ||||||
chr19:46914110 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-188-4378G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914110 | |||||||
chr19:46914444 | C | A | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-188-4044C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914444 | |||||||
chr19:46914446 | A | AAAT | 12 | a0001c0001t0004g0117 a0001c0001t0008g0088 a0001c0001t0008g0091 others(9): Show |
12 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-188-4024_-188-402 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46914446 | ||||||
chr19:46914446 | AAAT | A | 5 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(2): Show |
5 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-188-4024_-188-402 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46914446 | ||||||
chr19:46914701 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-188-3787T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914701 | |||||||
chr19:46914894 | C | T | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-188-3594C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46914894 | |||||||
chr19:46915338 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-3150G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915338 | |||||||
chr19:46915455 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0019 |
2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-188-3033A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915455 | |||||||
chr19:46915499 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-188-2989C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915499 | |||||||
chr19:46915791 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 |
3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-188-2697G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915791 | |||||||
chr19:46915929 | C | CT | 22 | a0001c0001t0001g0077 a0001c0001t0001g0132 a0001c0001t0001g0133 others(19): Show |
22 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-188-2535dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46915929 | ||||||
chr19:46915929 | C | CTT | 7 | a0001c0001t0003g0080 a0001c0001t0008g0088 a0001c0001t0008g0091 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-188-2536_-188-253 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46915929 | ||||||
chr19:46915929 | CT | C | 10 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0169 others(7): Show |
10 | HG00733.hp1 HG00733.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-188-2535delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46915929 | ||||||
chr19:46915993 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-188-2495T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46915993 | |||||||
chr19:46916380 | A | G | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-188-2108A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46916380 | |||||||
chr19:46916382 | T | TCTGTCCC others(311): Show |
1 | a0001c0001t0049g0092 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-188-2091_-188-209 others(322): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | ||||||
chr19:46916382 | T | TCTGTCCC others(312): Show |
14 | a0001c0001t0003g0030 a0001c0001t0008g0088 a0001c0001t0008g0091 others(11): Show |
14 | HG00597.hp1 HG01891.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-188-2091_-188-209 others(323): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | ||||||
chr19:46916382 | T | TCTGTCCC others(313): Show |
30 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(27): Show |
30 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.-188-2091_-188-209 others(324): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | ||||||
chr19:46916382 | T | TCTGTCCC others(314): Show |
5 | a0001c0001t0003g0081 a0001c0001t0003g0085 a0001c0001t0003g0245 others(2): Show |
5 | HG02523.hp2 HG02630.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-188-2091_-188-209 others(325): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916382 | ||||||
chr19:46916646 | A | ATT | 48 | a0001c0001t0003g0022 a0001c0001t0003g0070 a0001c0001t0003g0071 others(45): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-188-1834_-188-183 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916646 | ||||||
chr19:46916727 | A | AT | 49 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(46): Show |
49 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-188-1750dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916727 | ||||||
chr19:46916727 | AT | A | 116 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0170 others(113): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-188-1750delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 46916727 | ||||||
chr19:46917033 | C | A | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-188-1455C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917033 | |||||||
chr19:46917623 | A | C | 1 | a0001c0001t0002g0001 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-188-865A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917623 | |||||||
chr19:46917721 | T | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-188-767T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917721 | |||||||
chr19:46917806 | C | G | 1 | a0001c0001t0033g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-188-682C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917806 | |||||||
chr19:46917956 | C | T | 1 | a0001c0001t0017g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-188-532C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917956 | |||||||
chr19:46917994 | G | A | 31 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(28): Show |
31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-188-494G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46917994 | |||||||
chr19:46918066 | G | T | 271 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(268): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.-188-422G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46918066 | |||||||
chr19:46918349 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-188-139C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | 46918349 | |||||||
chr19:46922450 | T | TA | 11 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0276 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.3681+104dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46922450 | ||||||
chr19:46922488 | A | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+132A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46922488 | |||||||
chr19:46922752 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3681+396C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46922752 | |||||||
chr19:46923010 | A | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+654A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923010 | |||||||
chr19:46923011 | T | C | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+655T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923011 | |||||||
chr19:46923012 | G | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+656G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923012 | |||||||
chr19:46923013 | G | C | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3681+657G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923013 | |||||||
chr19:46923102 | C | CT | 64 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0162 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.3681+766dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923102 | ||||||
chr19:46923102 | C | CTT | 14 | a0001c0001t0007g0059 a0001c0002t0005g0207 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3681+765_3681+766d others(4): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923102 | ||||||
chr19:46923102 | CT | C | 7 | a0001c0001t0001g0077 a0001c0001t0001g0134 a0001c0001t0001g0171 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3681+766delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923102 | ||||||
chr19:46923104 | T | C | 1 | a0001c0001t0008g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3681+748T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923104 | |||||||
chr19:46923161 | G | A | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3681+805G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923161 | |||||||
chr19:46923316 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3681+960G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923316 | |||||||
chr19:46923443 | T | C | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3681+1087T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923443 | |||||||
chr19:46923523 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3681+1167G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923523 | |||||||
chr19:46923627 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+1271A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923627 | |||||||
chr19:46923672 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3681+1316A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923672 | |||||||
chr19:46923748 | A | G | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3681+1392A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923748 | |||||||
chr19:46923920 | C | CA | 47 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(44): Show |
47 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.3681+1576dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46923920 | ||||||
chr19:46923953 | G | A | 185 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(182): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3681+1597G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923953 | |||||||
chr19:46923997 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3681+1641G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46923997 | |||||||
chr19:46924101 | C | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+1745C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924101 | |||||||
chr19:46924294 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+1938C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924294 | |||||||
chr19:46924302 | G | A | 1 | a0006c0008t0011g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3681+1946G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924302 | |||||||
chr19:46924306 | G | A | 1 | a0001c0001t0003g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3681+1950G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924306 | |||||||
chr19:46924493 | C | A | 1 | a0003c0013t0003g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3681+2137C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924493 | |||||||
chr19:46924649 | G | A | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3681+2293G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46924649 | |||||||
chr19:46925074 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3681+2718C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925074 | |||||||
chr19:46925246 | G | A | 1 | a0001c0006t0005g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3681+2890G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925246 | |||||||
chr19:46925580 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0266 |
2 | HG01069.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.3681+3224A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925580 | |||||||
chr19:46925682 | G | A | 1 | a0001c0001t0040g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3681+3326G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925682 | |||||||
chr19:46925711 | T | C | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3681+3355T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46925711 | |||||||
chr19:46926021 | G | A | 3 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0049g0092 |
3 | NA18942.hp1 NA18947.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3681+3665G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926021 | |||||||
chr19:46926260 | A | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+3904A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926260 | |||||||
chr19:46926351 | G | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3681+3995G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926351 | |||||||
chr19:46926541 | G | C | 113 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(110): Show |
113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3681+4185G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46926541 | |||||||
chr19:46926629 | T | TA | 19 | a0001c0001t0003g0030 a0001c0001t0008g0088 a0001c0001t0008g0091 others(16): Show |
19 | HG00597.hp1 HG01891.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.3681+4284dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46926629 | ||||||
chr19:46927201 | A | G | 1 | a0001c0001t0004g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3681+4845A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46927201 | |||||||
chr19:46927367 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3681+5011G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46927367 | |||||||
chr19:46927982 | C | A | 1 | a0001c0001t0002g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3681+5626C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46927982 | |||||||
chr19:46928044 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+5688T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928044 | |||||||
chr19:46928173 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3681+5817G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928173 | |||||||
chr19:46928572 | C | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | NA18953.hp1 NA18960.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.3681+6216C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928572 | |||||||
chr19:46928575 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3681+6219C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928575 | |||||||
chr19:46928594 | G | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+6238G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928594 | |||||||
chr19:46928616 | T | G | 14 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0161 others(11): Show |
14 | HG00733.hp2 HG00738.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3681+6260T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928616 | |||||||
chr19:46928660 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3681+6304G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928660 | |||||||
chr19:46928927 | C | CT | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3681+6572dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46928927 | ||||||
chr19:46928929 | C | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3681+6573C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928929 | |||||||
chr19:46928967 | T | C | 1 | a0001c0001t0045g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3681+6611T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46928967 | |||||||
chr19:46929101 | G | A | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3681+6745G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929101 | |||||||
chr19:46929427 | A | G | 5 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0249 others(2): Show |
5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.3681+7071A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929427 | |||||||
chr19:46929454 | T | C | 3 | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0001t0025g0277 |
3 | HG02257.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3681+7098T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929454 | |||||||
chr19:46929499 | G | A | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3681+7143G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929499 | |||||||
chr19:46929591 | C | CT | 39 | a0001c0001t0001g0147 a0001c0001t0001g0171 a0001c0001t0001g0175 others(36): Show |
39 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3681+7261dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929591 | ||||||
chr19:46929591 | C | CTT | 27 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(24): Show |
27 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3681+7260_3681+726 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929591 | ||||||
chr19:46929591 | CT | C | 42 | a0001c0001t0001g0118 a0001c0001t0001g0134 a0001c0001t0001g0149 others(39): Show |
42 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.3681+7261delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929591 | ||||||
chr19:46929658 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3681+7302A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929658 | |||||||
chr19:46929790 | G | A | 1 | a0001c0001t0003g0079 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3681+7434G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929790 | |||||||
chr19:46929843 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-7421G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929843 | |||||||
chr19:46929897 | A | G | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3682-7367A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929897 | |||||||
chr19:46929914 | C | CA | 52 | a0001c0001t0001g0077 a0001c0001t0002g0231 a0001c0001t0003g0022 others(49): Show |
52 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3682-7335dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46929914 | ||||||
chr19:46929939 | T | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-7325T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46929939 | |||||||
chr19:46930021 | C | T | 1 | a0001c0001t0002g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3682-7243C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930021 | |||||||
chr19:46930065 | T | C | 1 | a0001c0001t0014g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3682-7199T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930065 | |||||||
chr19:46930126 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3682-7138G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930126 | |||||||
chr19:46930177 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-7087G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930177 | |||||||
chr19:46930249 | G | T | 11 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
11 | HG01069.hp2 HG01261.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3682-7015G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930249 | |||||||
chr19:46930526 | T | C | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3682-6738T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930526 | |||||||
chr19:46930855 | G | A | 1 | a0001c0001t0018g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3682-6409G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930855 | |||||||
chr19:46930956 | C | T | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-6308C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930956 | |||||||
chr19:46930999 | C | T | 3 | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0001t0025g0277 |
3 | HG02257.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3682-6265C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46930999 | |||||||
chr19:46931220 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0003g0075 a0001c0001t0003g0076 others(6): Show |
9 | HG00438.hp2 HG02071.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.3682-6044A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931220 | |||||||
chr19:46931542 | C | A | 3 | a0001c0001t0001g0118 a0001c0001t0010g0122 a0001c0001t0010g0260 |
3 | HG01070.hp2 HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3682-5722C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931542 | |||||||
chr19:46931576 | A | C | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3682-5688A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931576 | |||||||
chr19:46931896 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3682-5368G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46931896 | |||||||
chr19:46932405 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3682-4859T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932405 | |||||||
chr19:46932488 | G | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3682-4776G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932488 | |||||||
chr19:46932676 | C | T | 5 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(2): Show |
5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-4588C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932676 | |||||||
chr19:46932931 | G | A | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3682-4333G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932931 | |||||||
chr19:46932998 | G | A | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3682-4266G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46932998 | |||||||
chr19:46933137 | C | CT | 156 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0152 others(153): Show |
156 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.3682-4105dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46933137 | ||||||
chr19:46933137 | C | CTT | 30 | a0001c0001t0001g0077 a0001c0001t0001g0190 a0001c0001t0003g0080 others(27): Show |
30 | HG00642.hp1 HG01346.hp1 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.3682-4106_3682-410 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46933137 | ||||||
chr19:46933137 | C | CTTT | 7 | a0001c0001t0003g0233 a0001c0001t0011g0029 a0001c0001t0025g0277 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-4107_3682-410 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46933137 | ||||||
chr19:46933211 | T | C | 1 | a0001c0001t0045g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3682-4053T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46933211 | |||||||
chr19:46933350 | C | T | 11 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(8): Show |
11 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3682-3914C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46933350 | |||||||
chr19:46934044 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3682-3220G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934044 | |||||||
chr19:46934197 | A | C | 30 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(27): Show |
30 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3682-3067A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934197 | |||||||
chr19:46934280 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3682-2984A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934280 | |||||||
chr19:46934374 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3682-2890C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934374 | |||||||
chr19:46934409 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3682-2855C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934409 | |||||||
chr19:46934454 | A | G | 71 | a0001c0001t0001g0068 a0001c0001t0001g0177 a0001c0001t0002g0001 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.3682-2810A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934454 | |||||||
chr19:46934529 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3682-2735G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934529 | |||||||
chr19:46934551 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3682-2713G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934551 | |||||||
chr19:46934694 | G | T | 1 | a0001c0001t0006g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3682-2570G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934694 | |||||||
chr19:46934699 | G | T | 185 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(182): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3682-2565G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934699 | |||||||
chr19:46934791 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3682-2473T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934791 | |||||||
chr19:46934805 | G | A | 1 | a0001c0001t0017g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3682-2459G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934805 | |||||||
chr19:46934818 | C | T | 2 | a0001c0001t0003g0072 a0001c0001t0003g0240 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3682-2446C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934818 | |||||||
chr19:46934886 | T | C | 1 | a0003c0013t0003g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3682-2378T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934886 | |||||||
chr19:46934912 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3682-2352A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934912 | |||||||
chr19:46934971 | C | G | 8 | a0001c0001t0004g0117 a0001c0001t0004g0120 a0001c0001t0004g0121 others(5): Show |
8 | NA18972.hp1 NA18973.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.3682-2293C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46934971 | |||||||
chr19:46935068 | G | A | 1 | a0001c0001t0026g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3682-2196G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46935068 | |||||||
chr19:46935070 | T | A | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3682-2194T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46935070 | |||||||
chr19:46935315 | T | G | 5 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-1949T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46935315 | |||||||
chr19:46936089 | G | T | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3682-1175G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936089 | |||||||
chr19:46936310 | T | TTGCTGCT others(11): Show |
1 | a0001c0001t0003g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3682-949_3682-932d others(20): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936310 | ||||||
chr19:46936611 | G | A | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3682-653G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936611 | |||||||
chr19:46936845 | C | CT | 13 | a0001c0001t0001g0146 a0001c0001t0001g0266 a0001c0001t0001g0275 others(10): Show |
13 | HG00738.hp1 HG01071.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3682-401dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936845 | ||||||
chr19:46936845 | C | CTT | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3682-402_3682-401d others(4): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936845 | ||||||
chr19:46936900 | C | T | 4 | a0001c0001t0014g0089 a0001c0001t0014g0093 a0001c0001t0014g0094 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3682-364C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936900 | |||||||
chr19:46936901 | GCAATCTC others(9): Show |
G | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3682-355_3682-340d others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 46936901 | ||||||
chr19:46936934 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3682-330G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936934 | |||||||
chr19:46936957 | A | G | 1 | a0001c0001t0003g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3682-307A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46936957 | |||||||
chr19:46937039 | C | T | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-225C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46937039 | |||||||
chr19:46937227 | C | G | 7 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-37C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | chr19 | 46937227 | |||||||
chr19:46937939 | T | C | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+531T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46937939 | |||||||
chr19:46938226 | G | C | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3826+818G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938226 | |||||||
chr19:46938322 | G | A | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3826+914G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938322 | |||||||
chr19:46938342 | A | ATTTTAT | 3 | a0001c0001t0001g0169 a0001c0001t0001g0278 a0001c0001t0002g0253 |
3 | HG00733.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3826+957_3826+962d others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46938342 | ||||||
chr19:46938417 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+1009G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938417 | |||||||
chr19:46938466 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3826+1058G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938466 | |||||||
chr19:46938498 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3826+1090G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938498 | |||||||
chr19:46938530 | T | C | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3826+1122T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938530 | |||||||
chr19:46938589 | G | C | 114 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.3826+1181G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938589 | |||||||
chr19:46938935 | A | G | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+1527A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938935 | |||||||
chr19:46938947 | G | T | 50 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(47): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3826+1539G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46938947 | |||||||
chr19:46939027 | GAA | G | 16 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(13): Show |
16 | HG01069.hp2 HG01261.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.3826+1621_3826+162 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939027 | ||||||
chr19:46939178 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3826+1770T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939178 | |||||||
chr19:46939255 | G | A | 1 | a0001c0001t0043g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3826+1847G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939255 | |||||||
chr19:46939264 | C | T | 1 | a0001c0001t0002g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3826+1856C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939264 | |||||||
chr19:46939354 | G | T | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3826+1946G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939354 | |||||||
chr19:46939372 | C | CATTT | 32 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(29): Show |
32 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3826+2004_3826+200 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | ||||||
chr19:46939372 | CATTT | C | 52 | a0001c0001t0001g0077 a0001c0001t0001g0148 a0001c0001t0001g0149 others(49): Show |
52 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3826+2004_3826+200 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | ||||||
chr19:46939372 | CATTTATT others(1): Show |
C | 126 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0160 others(123): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.3826+2000_3826+200 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | ||||||
chr19:46939372 | CATTTATT others(5): Show |
C | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+1996_3826+200 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | ||||||
chr19:46939372 | CATTTATT others(9): Show |
C | 4 | a0001c0001t0002g0054 a0001c0001t0015g0040 a0001c0001t0015g0227 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3826+1992_3826+200 others(20): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46939372 | ||||||
chr19:46939624 | G | C | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+2216G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939624 | |||||||
chr19:46939651 | A | G | 188 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(185): Show |
188 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3826+2243A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939651 | |||||||
chr19:46939780 | A | G | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+2372A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939780 | |||||||
chr19:46939919 | A | AC | 32 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(29): Show |
32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.3826+2511_3826+251 others(5): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46939919 | |||||||
chr19:46940009 | A | G | 32 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(29): Show |
32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.3826+2601A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940009 | |||||||
chr19:46940063 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3826+2655C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940063 | |||||||
chr19:46940181 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3826+2773G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940181 | |||||||
chr19:46940252 | G | A | 1 | a0001c0002t0005g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3826+2844G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940252 | |||||||
chr19:46940359 | CA | C | 182 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(179): Show |
182 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.3826+2970delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940359 | ||||||
chr19:46940396 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18612.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3826+2988C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940396 | |||||||
chr19:46940477 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+3069G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940477 | |||||||
chr19:46940550 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3826+3142A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940550 | |||||||
chr19:46940604 | C | CTT | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+3211_3826+321 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940604 | ||||||
chr19:46940604 | CT | C | 22 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0155 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3826+3212delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940604 | ||||||
chr19:46940712 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3826+3304C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940712 | |||||||
chr19:46940750 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3826+3342C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940750 | |||||||
chr19:46940750 | C | T | 1 | a0001c0001t0026g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3826+3342C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940750 | |||||||
chr19:46940788 | G | A | 2 | a0001c0001t0002g0098 a0001c0001t0002g0108 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3826+3380G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940788 | |||||||
chr19:46940795 | A | G | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+3387A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46940795 | |||||||
chr19:46940982 | C | CTTCCCGG others(16): Show |
3 | a0001c0001t0001g0118 a0001c0001t0010g0122 a0001c0001t0010g0260 |
3 | HG01070.hp2 HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3826+3575_3826+357 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46940982 | ||||||
chr19:46941004 | G | A | 5 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0249 others(2): Show |
5 | HG00597.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+3596G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941004 | |||||||
chr19:46941152 | C | T | 1 | a0001c0001t0012g0047 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3826+3744C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941152 | |||||||
chr19:46941206 | C | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+3798C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941206 | |||||||
chr19:46941399 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3826+3991C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941399 | |||||||
chr19:46941519 | T | C | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3826+4111T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941519 | |||||||
chr19:46941606 | C | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3826+4198C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941606 | |||||||
chr19:46941634 | G | A | 51 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(48): Show |
51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.3826+4226G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941634 | |||||||
chr19:46941657 | G | A | 5 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+4249G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941657 | |||||||
chr19:46941721 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+4313G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46941721 | |||||||
chr19:46941819 | CA | C | 165 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(162): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.3826+4414delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941819 | ||||||
chr19:46941876 | T | TA | 59 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0001g0282 others(56): Show |
59 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.3826+4492dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | ||||||
chr19:46941876 | T | TAA | 75 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0159 others(72): Show |
75 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.3826+4491_3826+449 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | ||||||
chr19:46941876 | T | TAAA | 29 | a0001c0001t0001g0190 a0001c0001t0002g0013 a0001c0001t0002g0016 others(26): Show |
29 | HG00738.hp1 HG01071.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.3826+4490_3826+449 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | ||||||
chr19:46941876 | TA | T | 9 | a0001c0001t0001g0140 a0001c0001t0001g0146 a0001c0001t0001g0156 others(6): Show |
9 | HG02258.hp2 HG02683.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3826+4492delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46941876 | ||||||
chr19:46942214 | C | G | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+4806C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942214 | |||||||
chr19:46942251 | C | A | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3826+4843C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942251 | |||||||
chr19:46942569 | G | A | 4 | a0001c0002t0005g0210 a0001c0002t0005g0212 a0001c0002t0005g0215 others(1): Show |
4 | HG02895.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+5161G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942569 | |||||||
chr19:46942599 | T | A | 36 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3826+5191T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942599 | |||||||
chr19:46942616 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+5208G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942616 | |||||||
chr19:46942718 | A | G | 22 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0023g0034 others(19): Show |
22 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.3826+5310A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942718 | |||||||
chr19:46942757 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3826+5349A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942757 | |||||||
chr19:46942815 | C | CA | 83 | a0001c0001t0001g0077 a0001c0001t0001g0146 a0001c0001t0001g0168 others(80): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.3826+5408dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46942815 | ||||||
chr19:46942815 | C | CAA | 7 | a0001c0001t0003g0072 a0001c0001t0003g0095 a0001c0001t0003g0236 others(4): Show |
7 | HG00558.hp1 HG02738.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3826+5408_3826+540 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46942815 | ||||||
chr19:46942816 | AG | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0281 a0001c0001t0016g0024 |
3 | HG01070.hp1 HG02155.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.3826+5409delG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942816 | |||||||
chr19:46942817 | G | A | 293 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3826+5409G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46942817 | |||||||
chr19:46943010 | A | G | 1 | a0001c0001t0018g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3826+5602A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943010 | |||||||
chr19:46943039 | AT | A | 33 | a0001c0001t0002g0020 a0001c0001t0002g0042 a0001c0001t0002g0044 others(30): Show |
33 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.3826+5647delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46943039 | ||||||
chr19:46943285 | C | T | 1 | a0001c0001t0030g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3826+5877C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943285 | |||||||
chr19:46943305 | A | G | 189 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(186): Show |
189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3826+5897A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943305 | |||||||
chr19:46943399 | T | C | 5 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+5991T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943399 | |||||||
chr19:46943434 | A | G | 112 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0190 others(109): Show |
112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3826+6026A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943434 | |||||||
chr19:46943901 | T | C | 180 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(177): Show |
180 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.3826+6493T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943901 | |||||||
chr19:46943995 | A | G | 1 | a0001c0001t0017g0109 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3826+6587A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46943995 | |||||||
chr19:46944100 | G | A | 1 | a0001c0001t0015g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3826+6692G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944100 | |||||||
chr19:46944277 | C | T | 1 | a0001c0001t0029g0113 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3826+6869C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944277 | |||||||
chr19:46944311 | A | G | 7 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.3826+6903A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944311 | |||||||
chr19:46944398 | C | A | 1 | a0001c0001t0003g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3826+6990C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944398 | |||||||
chr19:46944399 | T | C | 2 | a0001c0001t0003g0071 a0001c0001t0027g0232 |
2 | NA18969.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3826+6991T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944399 | |||||||
chr19:46944448 | G | A | 1 | a0001c0001t0045g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3826+7040G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944448 | |||||||
chr19:46944451 | C | A | 1 | a0001c0001t0023g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3826+7043C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944451 | |||||||
chr19:46944529 | T | C | 1 | a0006c0008t0011g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3826+7121T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944529 | |||||||
chr19:46944829 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3826+7421C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46944829 | |||||||
chr19:46945158 | AAGGAGGC others(18): Show |
A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA19004.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3826+7777_3826+780 others(29): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46945158 | ||||||
chr19:46945512 | G | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+8104G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945512 | |||||||
chr19:46945770 | C | G | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+8362C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945770 | |||||||
chr19:46945885 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3826+8477C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945885 | |||||||
chr19:46945965 | G | A | 3 | a0001c0001t0006g0035 a0001c0001t0006g0052 a0001c0001t0006g0222 |
3 | HG01257.hp1 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.3826+8557G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46945965 | |||||||
chr19:46946016 | C | T | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+8608C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946016 | |||||||
chr19:46946090 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3826+8682C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946090 | |||||||
chr19:46946442 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+9034A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946442 | |||||||
chr19:46946585 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+9177C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946585 | |||||||
chr19:46946741 | T | TTG | 5 | a0001c0001t0001g0130 a0001c0001t0001g0285 a0001c0001t0001g0289 others(2): Show |
5 | HG00621.hp2 HG01928.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.3826+9353_3826+935 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46946741 | ||||||
chr19:46946819 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3826+9411G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946819 | |||||||
chr19:46946920 | A | G | 1 | a0001c0001t0002g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3826+9512A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946920 | |||||||
chr19:46946985 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3826+9577A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46946985 | |||||||
chr19:46947501 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3826+10093A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947501 | |||||||
chr19:46947537 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3826+10129C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947537 | |||||||
chr19:46947576 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3826+10168C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947576 | |||||||
chr19:46947674 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+10266G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947674 | |||||||
chr19:46947721 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3826+10313C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46947721 | |||||||
chr19:46948105 | G | C | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3826+10697G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948105 | |||||||
chr19:46948396 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0040g0053 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3826+10988A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948396 | |||||||
chr19:46948681 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3826+11273G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948681 | |||||||
chr19:46948807 | G | C | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+11399G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948807 | |||||||
chr19:46948885 | C | T | 1 | a0001c0001t0014g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3826+11477C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46948885 | |||||||
chr19:46949181 | T | C | 1 | a0001c0002t0005g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3826+11773T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949181 | |||||||
chr19:46949552 | G | T | 1 | a0001c0001t0043g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3826+12144G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949552 | |||||||
chr19:46949676 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0287 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.3826+12268C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949676 | |||||||
chr19:46949679 | A | T | 1 | a0001c0001t0035g0078 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3826+12271A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949679 | |||||||
chr19:46949764 | A | T | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3826+12356A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46949764 | |||||||
chr19:46950524 | C | T | 1 | a0001c0001t0045g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3826+13116C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950524 | |||||||
chr19:46950689 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3826+13281G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950689 | |||||||
chr19:46950694 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3826+13286G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950694 | |||||||
chr19:46950847 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3826+13439G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950847 | |||||||
chr19:46950974 | T | C | 15 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(12): Show |
15 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3826+13566T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46950974 | |||||||
chr19:46951114 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+13706G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951114 | |||||||
chr19:46951185 | T | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+13777T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951185 | |||||||
chr19:46951450 | C | CT | 33 | a0001c0001t0001g0118 a0001c0001t0001g0133 a0001c0001t0001g0192 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.3826+14051dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46951450 | ||||||
chr19:46951557 | A | G | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3826+14149A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951557 | |||||||
chr19:46951562 | T | C | 7 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3826+14154T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951562 | |||||||
chr19:46951612 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3826+14204G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951612 | |||||||
chr19:46951615 | G | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3826+14207G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951615 | |||||||
chr19:46951648 | T | C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0020 a0001c0001t0042g0018 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3826+14240T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951648 | |||||||
chr19:46951724 | T | G | 1 | a0003c0013t0003g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3826+14316T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951724 | |||||||
chr19:46951808 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0199 |
2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3826+14400G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46951808 | |||||||
chr19:46952058 | A | G | 64 | a0001c0001t0001g0068 a0001c0001t0002g0001 a0001c0001t0002g0002 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.3826+14650A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952058 | |||||||
chr19:46952277 | CATTT | C | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3826+14873_3826+14 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46952277 | ||||||
chr19:46952286 | C | T | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3826+14878C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952286 | |||||||
chr19:46952298 | T | C | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+14890T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952298 | |||||||
chr19:46952445 | T | A | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3826+15037T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952445 | |||||||
chr19:46952480 | T | C | 1 | a0001c0001t0002g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3826+15072T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952480 | |||||||
chr19:46952599 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | NA18993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3826+15191T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952599 | |||||||
chr19:46952628 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3826+15220A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952628 | |||||||
chr19:46952639 | A | T | 36 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3826+15231A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952639 | |||||||
chr19:46952700 | G | A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0007 |
2 | NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.3826+15292G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952700 | |||||||
chr19:46952874 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3826+15466C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952874 | |||||||
chr19:46952877 | C | T | 1 | a0001c0002t0005g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3826+15469C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46952877 | |||||||
chr19:46953193 | G | C | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+15785G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953193 | |||||||
chr19:46953329 | G | T | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3826+15921G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953329 | |||||||
chr19:46953333 | G | C | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+15925G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953333 | |||||||
chr19:46953676 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+16268G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953676 | |||||||
chr19:46953816 | T | C | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0289 |
3 | HG00621.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3826+16408T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953816 | |||||||
chr19:46953904 | T | C | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3826+16496T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953904 | |||||||
chr19:46953905 | G | A | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3826+16497G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46953905 | |||||||
chr19:46954003 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3826+16595G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954003 | |||||||
chr19:46954156 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3826+16748G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954156 | |||||||
chr19:46954408 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3826+17000T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954408 | |||||||
chr19:46954494 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3826+17086G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954494 | |||||||
chr19:46954829 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3826+17421T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954829 | |||||||
chr19:46954965 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+17557A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46954965 | |||||||
chr19:46955265 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3826+17857A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46955265 | |||||||
chr19:46955470 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3826+18062C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46955470 | |||||||
chr19:46956144 | G | A | 81 | a0001c0001t0001g0068 a0001c0001t0001g0190 a0001c0001t0002g0001 others(78): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.3826+18736G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956144 | |||||||
chr19:46956219 | A | T | 45 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0172 others(42): Show |
45 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3826+18811A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956219 | |||||||
chr19:46956233 | A | G | 189 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(186): Show |
189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3826+18825A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956233 | |||||||
chr19:46956238 | A | G | 1 | a0001c0001t0040g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3826+18830A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956238 | |||||||
chr19:46956493 | C | G | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+19085C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956493 | |||||||
chr19:46956704 | G | T | 1 | a0001c0001t0004g0123 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3826+19296G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956704 | |||||||
chr19:46956756 | G | T | 1 | a0001c0001t0017g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3826+19348G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956756 | |||||||
chr19:46956956 | C | CCTT | 9 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(6): Show |
9 | HG00597.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3826+19548_3826+19 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956956 | |||||||
chr19:46956956 | C | CT | 132 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0130 others(129): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.3826+19569dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46956956 | ||||||
chr19:46956956 | C | CTT | 50 | a0001c0001t0001g0180 a0001c0001t0002g0009 a0001c0001t0002g0051 others(47): Show |
50 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.3826+19568_3826+19 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46956956 | ||||||
chr19:46956999 | G | A | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+19591G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46956999 | |||||||
chr19:46957051 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3826+19643T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957051 | |||||||
chr19:46957109 | A | C | 189 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(186): Show |
189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3826+19701A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957109 | |||||||
chr19:46957118 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3826+19710C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957118 | |||||||
chr19:46957587 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3826+20179C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957587 | |||||||
chr19:46957603 | C | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3826+20195C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957603 | |||||||
chr19:46957631 | A | T | 1 | a0001c0001t0029g0113 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3826+20223A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957631 | |||||||
chr19:46957686 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3826+20278T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957686 | |||||||
chr19:46957752 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3826+20344A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957752 | |||||||
chr19:46957783 | C | G | 2 | a0001c0001t0003g0072 a0001c0001t0003g0240 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3826+20375C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957783 | |||||||
chr19:46957963 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0019 |
2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3826+20555G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957963 | |||||||
chr19:46957967 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3826+20559G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957967 | |||||||
chr19:46957999 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3826+20591G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46957999 | |||||||
chr19:46958110 | A | G | 269 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(266): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.3826+20702A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958110 | |||||||
chr19:46958211 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3826+20803G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958211 | |||||||
chr19:46958253 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3826+20845G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958253 | |||||||
chr19:46958256 | C | T | 2 | a0001c0001t0015g0040 a0001c0001t0015g0227 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3826+20848C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958256 | |||||||
chr19:46958384 | C | CA | 6 | a0001c0001t0001g0199 a0001c0001t0002g0050 a0001c0001t0002g0064 others(3): Show |
6 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.3826+20993dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46958384 | ||||||
chr19:46958575 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3826+21167G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46958575 | |||||||
chr19:46959030 | G | GTTGT | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+21624_3826+21 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46959030 | ||||||
chr19:46959090 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3826+21682T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959090 | |||||||
chr19:46959107 | T | C | 187 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(184): Show |
187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3826+21699T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959107 | |||||||
chr19:46959125 | C | G | 3 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0027g0232 |
3 | NA18969.hp1 NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3826+21717C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959125 | |||||||
chr19:46959307 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3826+21899G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959307 | |||||||
chr19:46959478 | C | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+22070C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959478 | |||||||
chr19:46959504 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0060 |
2 | NA18964.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3826+22096A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959504 | |||||||
chr19:46959556 | C | T | 1 | a0001c0001t0002g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3826+22148C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959556 | |||||||
chr19:46959559 | C | G | 1 | a0001c0001t0021g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3826+22151C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959559 | |||||||
chr19:46959646 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3826+22238C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959646 | |||||||
chr19:46959665 | G | T | 1 | a0001c0007t0011g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3826+22257G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959665 | |||||||
chr19:46959674 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3826+22266A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959674 | |||||||
chr19:46959942 | A | T | 63 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(60): Show |
63 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.3826+22534A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959942 | |||||||
chr19:46959943 | T | A | 92 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0204 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.3826+22535T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959943 | |||||||
chr19:46959964 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0003g0233 |
2 | HG02155.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.3826+22556G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46959964 | |||||||
chr19:46960110 | C | CA | 13 | a0001c0001t0001g0205 a0001c0001t0001g0275 a0001c0001t0003g0082 others(10): Show |
13 | HG00558.hp2 HG00597.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.3826+22719dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46960110 | ||||||
chr19:46960166 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3826+22758G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960166 | |||||||
chr19:46960226 | A | G | 9 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(6): Show |
9 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3826+22818A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960226 | |||||||
chr19:46960327 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3826+22919G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960327 | |||||||
chr19:46960372 | C | T | 36 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3826+22964C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960372 | |||||||
chr19:46960392 | G | A | 12 | a0001c0001t0001g0130 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG00733.hp2 HG00738.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3826+22984G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960392 | |||||||
chr19:46960515 | A | G | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+23107A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960515 | |||||||
chr19:46960881 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3826+23473G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960881 | |||||||
chr19:46960893 | C | CT | 11 | a0001c0001t0001g0077 a0001c0001t0001g0180 a0001c0001t0001g0282 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3826+23501dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46960893 | ||||||
chr19:46960919 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3826+23511A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960919 | |||||||
chr19:46960996 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3826+23588G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46960996 | |||||||
chr19:46961137 | C | T | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+23729C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961137 | |||||||
chr19:46961163 | G | C | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3826+23755G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961163 | |||||||
chr19:46961224 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3826+23816C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961224 | |||||||
chr19:46961274 | T | C | 5 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(2): Show |
5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3826+23866T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961274 | |||||||
chr19:46961544 | G | A | 1 | a0001c0001t0014g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3826+24136G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961544 | |||||||
chr19:46961588 | T | C | 1 | a0001c0002t0005g0297 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3826+24180T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961588 | |||||||
chr19:46961879 | G | A | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3826+24471G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46961879 | |||||||
chr19:46961966 | GAGAA | G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3826+24562_3826+24 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46961966 | ||||||
chr19:46962081 | G | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3826+24673G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962081 | |||||||
chr19:46962109 | T | C | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3826+24701T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962109 | |||||||
chr19:46962153 | A | C | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3826+24745A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962153 | |||||||
chr19:46962196 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3826+24788G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962196 | |||||||
chr19:46962330 | C | A | 2 | a0001c0001t0014g0093 a0001c0001t0014g0094 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3826+24922C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962330 | |||||||
chr19:46962336 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3826+24928C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962336 | |||||||
chr19:46962742 | T | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-25247T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962742 | |||||||
chr19:46962851 | T | C | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3827-25138T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962851 | |||||||
chr19:46962857 | G | A | 2 | a0001c0001t0015g0040 a0001c0001t0015g0227 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3827-25132G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962857 | |||||||
chr19:46962884 | C | T | 1 | a0001c0001t0020g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3827-25105C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962884 | |||||||
chr19:46962960 | G | A | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3827-25029G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46962960 | |||||||
chr19:46963226 | T | C | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-24763T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963226 | |||||||
chr19:46963344 | G | A | 11 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(8): Show |
11 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3827-24645G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963344 | |||||||
chr19:46963370 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3827-24619T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963370 | |||||||
chr19:46963581 | C | G | 118 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0204 others(115): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.3827-24408C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963581 | |||||||
chr19:46963625 | T | A | 1 | a0001c0001t0004g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3827-24364T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963625 | |||||||
chr19:46963626 | A | T | 1 | a0001c0001t0004g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3827-24363A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963626 | |||||||
chr19:46963663 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3827-24326C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963663 | |||||||
chr19:46963699 | C | T | 1 | a0001c0001t0015g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3827-24290C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963699 | |||||||
chr19:46963744 | G | A | 36 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0003g0022 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3827-24245G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963744 | |||||||
chr19:46963752 | C | T | 1 | a0001c0001t0026g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3827-24237C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46963752 | |||||||
chr19:46964069 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0019 |
2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3827-23920T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964069 | |||||||
chr19:46964301 | A | G | 5 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(2): Show |
5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-23688A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964301 | |||||||
chr19:46964362 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-23627G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964362 | |||||||
chr19:46964372 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3827-23617A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964372 | |||||||
chr19:46964380 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-23609G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964380 | |||||||
chr19:46964743 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 |
3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3827-23246G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964743 | |||||||
chr19:46964984 | G | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0021 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3827-23005G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46964984 | |||||||
chr19:46965075 | G | A | 1 | a0001c0001t0013g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3827-22914G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965075 | |||||||
chr19:46965087 | C | T | 1 | a0006c0008t0011g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3827-22902C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965087 | |||||||
chr19:46965168 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0040g0053 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.3827-22821C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965168 | |||||||
chr19:46965212 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-22777C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965212 | |||||||
chr19:46965466 | T | TTTTG | 52 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(49): Show |
52 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.3827-22491_3827-22 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46965466 | ||||||
chr19:46965466 | T | TTTTGTTT others(1): Show |
10 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(7): Show |
10 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3827-22495_3827-22 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46965466 | ||||||
chr19:46965466 | TTTTG | T | 114 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0204 others(111): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3827-22491_3827-22 others(10): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46965466 | ||||||
chr19:46965575 | C | T | 1 | a0001c0002t0005g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3827-22414C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965575 | |||||||
chr19:46965715 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-22274G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965715 | |||||||
chr19:46965791 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-22198A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965791 | |||||||
chr19:46965905 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0195 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3827-22084G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46965905 | |||||||
chr19:46966082 | G | T | 1 | a0001c0001t0004g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3827-21907G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966082 | |||||||
chr19:46966319 | C | T | 3 | a0001c0001t0020g0032 a0001c0001t0020g0220 a0001c0001t0034g0252 |
3 | HG02622.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3827-21670C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966319 | |||||||
chr19:46966513 | T | C | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-21476T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966513 | |||||||
chr19:46966849 | A | T | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-21140A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966849 | |||||||
chr19:46966850 | G | C | 1 | a0001c0001t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3827-21139G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966850 | |||||||
chr19:46966874 | C | T | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-21115C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966874 | |||||||
chr19:46966986 | G | A | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-21003G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46966986 | |||||||
chr19:46967071 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0002g0231 a0001c0001t0021g0067 |
3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3827-20918C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967071 | |||||||
chr19:46967097 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0051 |
2 | HG02717.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3827-20892C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967097 | |||||||
chr19:46967213 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3827-20776G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967213 | |||||||
chr19:46967279 | C | T | 184 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(181): Show |
184 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3827-20710C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967279 | |||||||
chr19:46967370 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3827-20619G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967370 | |||||||
chr19:46967402 | A | G | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3827-20587A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967402 | |||||||
chr19:46967493 | T | A | 50 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(47): Show |
50 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.3827-20496T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967493 | |||||||
chr19:46967605 | T | C | 145 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0002g0001 others(142): Show |
145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.3827-20384T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967605 | |||||||
chr19:46967764 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-20225G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967764 | |||||||
chr19:46967815 | G | C | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-20174G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967815 | |||||||
chr19:46967821 | C | G | 1 | a0001c0001t0004g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3827-20168C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967821 | |||||||
chr19:46967918 | C | T | 1 | a0001c0001t0041g0043 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3827-20071C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967918 | |||||||
chr19:46967953 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0294 |
2 | NA18951.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3827-20036G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46967953 | |||||||
chr19:46968419 | T | C | 1 | a0001c0007t0011g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3827-19570T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968419 | |||||||
chr19:46968457 | A | G | 1 | a0001c0001t0036g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3827-19532A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968457 | |||||||
chr19:46968639 | C | T | 1 | a0001c0003t0003g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3827-19350C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968639 | |||||||
chr19:46968808 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3827-19181C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46968808 | |||||||
chr19:46969042 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3827-18947G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969042 | |||||||
chr19:46969336 | T | C | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-18653T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969336 | |||||||
chr19:46969393 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3827-18596A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969393 | |||||||
chr19:46969609 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3827-18380C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969609 | |||||||
chr19:46969728 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-18261G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969728 | |||||||
chr19:46969821 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3827-18168T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969821 | |||||||
chr19:46969919 | C | T | 1 | a0001c0001t0043g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3827-18070C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46969919 | |||||||
chr19:46970057 | T | A | 4 | a0001c0001t0002g0054 a0001c0001t0015g0040 a0001c0001t0015g0227 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3827-17932T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970057 | |||||||
chr19:46970142 | A | G | 2 | a0001c0001t0020g0032 a0001c0001t0020g0220 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3827-17847A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970142 | |||||||
chr19:46970316 | C | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-17673C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970316 | |||||||
chr19:46970387 | C | A | 3 | a0001c0001t0001g0118 a0001c0001t0010g0122 a0001c0001t0010g0260 |
3 | HG01070.hp2 HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3827-17602C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970387 | |||||||
chr19:46970409 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3827-17580G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970409 | |||||||
chr19:46970485 | T | C | 189 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(186): Show |
189 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3827-17504T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970485 | |||||||
chr19:46970596 | C | T | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-17393C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970596 | |||||||
chr19:46970794 | G | A | 33 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.3827-17195G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970794 | |||||||
chr19:46970921 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-17068G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46970921 | |||||||
chr19:46971380 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-16609C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46971380 | |||||||
chr19:46971477 | T | G | 3 | a0001c0001t0001g0170 a0001c0001t0002g0042 a0001c0001t0041g0043 |
3 | HG02071.hp2 NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.3827-16512T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46971477 | |||||||
chr19:46971949 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0286 |
3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3827-16040C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46971949 | |||||||
chr19:46972095 | C | T | 80 | a0001c0001t0001g0146 a0001c0001t0002g0001 a0001c0001t0002g0002 others(77): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3827-15894C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972095 | |||||||
chr19:46972117 | C | T | 35 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(32): Show |
35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.3827-15872C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972117 | |||||||
chr19:46972179 | T | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-15810T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972179 | |||||||
chr19:46972537 | C | A | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3827-15452C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972537 | |||||||
chr19:46972875 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3827-15114C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972875 | |||||||
chr19:46972974 | C | A | 1 | a0001c0001t0014g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3827-15015C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46972974 | |||||||
chr19:46973021 | A | AT | 186 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3827-14960dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46973021 | ||||||
chr19:46973103 | C | T | 1 | a0001c0007t0011g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3827-14886C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973103 | |||||||
chr19:46973266 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3827-14723G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973266 | |||||||
chr19:46973391 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-14598T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973391 | |||||||
chr19:46973485 | C | G | 1 | a0001c0001t0002g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3827-14504C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973485 | |||||||
chr19:46973509 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3827-14480G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973509 | |||||||
chr19:46973564 | G | A | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-14425G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973564 | |||||||
chr19:46973646 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-14343G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973646 | |||||||
chr19:46973711 | G | A | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3827-14278G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973711 | |||||||
chr19:46973754 | G | A | 1 | a0003c0013t0003g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3827-14235G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973754 | |||||||
chr19:46973784 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-14205G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973784 | |||||||
chr19:46973903 | G | T | 1 | a0001c0001t0040g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3827-14086G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46973903 | |||||||
chr19:46973995 | CA | C | 36 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0030 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3827-13983delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46973995 | ||||||
chr19:46974486 | A | G | 7 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-13503A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46974486 | |||||||
chr19:46974687 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3827-13302T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46974687 | |||||||
chr19:46974895 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3827-13094G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46974895 | |||||||
chr19:46975072 | A | G | 3 | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0002t0001g0033 |
3 | HG02258.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12917A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975072 | |||||||
chr19:46975122 | G | A | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3827-12867G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975122 | |||||||
chr19:46975171 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-12818G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975171 | |||||||
chr19:46975193 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3827-12796C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975193 | |||||||
chr19:46975275 | A | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12714A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975275 | |||||||
chr19:46975297 | A | G | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12692A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975297 | |||||||
chr19:46975304 | C | G | 1 | a0001c0001t0014g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3827-12685C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975304 | |||||||
chr19:46975410 | G | A | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-12579G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975410 | |||||||
chr19:46975527 | T | C | 186 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3827-12462T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975527 | |||||||
chr19:46975631 | C | CAGA | 65 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(62): Show |
65 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3827-12356_3827-12 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46975631 | ||||||
chr19:46975970 | T | G | 36 | a0001c0001t0001g0077 a0001c0001t0001g0130 a0001c0001t0003g0022 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.3827-12019T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46975970 | |||||||
chr19:46976210 | C | CT | 100 | a0001c0001t0001g0068 a0001c0001t0001g0130 a0001c0001t0001g0142 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3827-11759dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46976210 | ||||||
chr19:46976210 | CT | C | 13 | a0001c0001t0002g0050 a0001c0001t0002g0064 a0001c0001t0002g0224 others(10): Show |
13 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3827-11759delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46976210 | ||||||
chr19:46976210 | CTT | C | 30 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(27): Show |
30 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.3827-11760_3827-11 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46976210 | ||||||
chr19:46976325 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-11664A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976325 | |||||||
chr19:46976591 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3827-11398C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976591 | |||||||
chr19:46976619 | G | A | 3 | a0001c0001t0013g0087 a0001c0001t0013g0247 a0001c0001t0013g0248 |
3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3827-11370G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976619 | |||||||
chr19:46976679 | G | A | 1 | a0001c0001t0004g0117 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3827-11310G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976679 | |||||||
chr19:46976779 | G | C | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3827-11210G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46976779 | |||||||
chr19:46977065 | C | T | 1 | a0001c0001t0004g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3827-10924C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977065 | |||||||
chr19:46977417 | A | G | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-10572A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977417 | |||||||
chr19:46977603 | C | T | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-10386C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977603 | |||||||
chr19:46977617 | G | T | 1 | a0001c0001t0024g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3827-10372G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46977617 | |||||||
chr19:46978084 | G | A | 1 | a0001c0001t0018g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3827-9905G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978084 | |||||||
chr19:46978425 | G | A | 25 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0045 others(22): Show |
25 | HG00408.hp2 HG00642.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.3827-9564G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978425 | |||||||
chr19:46978474 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3827-9515T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978474 | |||||||
chr19:46978607 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3827-9382T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978607 | |||||||
chr19:46978607 | TGTG | T | 49 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0172 others(46): Show |
49 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.3827-9378_3827-937 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978607 | ||||||
chr19:46978686 | G | GATGTGTG others(11): Show |
185 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(182): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3827-9287_3827-928 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978686 | ||||||
chr19:46978687 | A | ATGTGTGT others(70): Show |
1 | a0001c0001t0002g0128 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3827-9287_3827-928 others(81): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978687 | ||||||
chr19:46978717 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-9272G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978717 | |||||||
chr19:46978796 | GTGGGATG others(56): Show |
G | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-9189_3827-912 others(67): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978796 | ||||||
chr19:46978893 | GGGGGTGT others(7): Show |
G | 1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3827-9083_3827-907 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46978893 | ||||||
chr19:46978939 | G | A | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3827-9050G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978939 | |||||||
chr19:46978968 | A | G | 295 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0118 others(292): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.3827-9021A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978968 | |||||||
chr19:46978969 | A | C | 1 | a0001c0001t0002g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-9020A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46978969 | |||||||
chr19:46979003 | G | A | 1 | a0001c0001t0018g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3827-8986G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979003 | |||||||
chr19:46979034 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3827-8955G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979034 | |||||||
chr19:46979054 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3827-8935A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979054 | |||||||
chr19:46979062 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-8927G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979062 | |||||||
chr19:46979147 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-8842G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979147 | |||||||
chr19:46979321 | C | T | 1 | a0001c0001t0002g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-8668C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979321 | |||||||
chr19:46979322 | T | C | 1 | a0001c0001t0002g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-8667T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979322 | |||||||
chr19:46979323 | C | T | 1 | a0001c0001t0002g0002 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3827-8666C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979323 | |||||||
chr19:46979334 | C | T | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-8655C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979334 | |||||||
chr19:46979345 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0218 |
2 | HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3827-8644T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979345 | |||||||
chr19:46979493 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3827-8496T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979493 | |||||||
chr19:46979779 | T | C | 5 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-8210T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979779 | |||||||
chr19:46979805 | A | G | 3 | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0002t0001g0033 |
3 | HG02258.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3827-8184A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979805 | |||||||
chr19:46979848 | A | G | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-8141A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46979848 | |||||||
chr19:46980043 | G | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0265 |
2 | NA18612.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.3827-7946G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980043 | |||||||
chr19:46980046 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3827-7943G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980046 | |||||||
chr19:46980049 | G | A | 3 | a0001c0001t0002g0231 a0001c0001t0021g0067 a0001c0001t0024g0025 |
3 | HG02145.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3827-7940G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980049 | |||||||
chr19:46980464 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3827-7525C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980464 | |||||||
chr19:46980631 | C | T | 4 | a0001c0001t0002g0054 a0001c0001t0015g0040 a0001c0001t0015g0227 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3827-7358C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980631 | |||||||
chr19:46980665 | G | A | 7 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-7324G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980665 | |||||||
chr19:46980738 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0095 |
2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3827-7251G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980738 | |||||||
chr19:46980746 | T | G | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-7243T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46980746 | |||||||
chr19:46981247 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3827-6742G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981247 | |||||||
chr19:46981317 | A | T | 1 | a0001c0001t0002g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3827-6672A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981317 | |||||||
chr19:46981408 | TAAGC | T | 3 | a0001c0001t0013g0087 a0001c0001t0013g0247 a0001c0001t0013g0248 |
3 | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3827-6577_3827-657 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981408 | ||||||
chr19:46981545 | G | A | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3827-6444G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981545 | |||||||
chr19:46981723 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-6266C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981723 | |||||||
chr19:46981824 | G | T | 1 | a0001c0002t0005g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3827-6165G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981824 | |||||||
chr19:46981825 | G | GTGTTT | 39 | a0001c0001t0001g0118 a0001c0001t0001g0143 a0001c0001t0001g0270 others(36): Show |
39 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.3827-6121_3827-611 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | ||||||
chr19:46981825 | G | GTGTTTTG others(3): Show |
11 | a0001c0001t0009g0111 a0001c0001t0017g0254 a0001c0001t0045g0229 others(8): Show |
11 | HG02027.hp2 HG02055.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.3827-6126_3827-611 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | ||||||
chr19:46981825 | G | GTGTTTTG others(8): Show |
1 | a0001c0005t0005g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3827-6131_3827-611 others(19): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | ||||||
chr19:46981825 | G | T | 1 | a0001c0002t0005g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3827-6164G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981825 | |||||||
chr19:46981825 | GTGTTT | G | 86 | a0001c0001t0001g0068 a0001c0001t0001g0130 a0001c0001t0001g0131 others(83): Show |
86 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.3827-6121_3827-611 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | ||||||
chr19:46981825 | GTGTTTTG others(3): Show |
G | 118 | a0001c0001t0001g0077 a0001c0001t0001g0134 a0001c0001t0001g0204 others(115): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.3827-6126_3827-611 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | ||||||
chr19:46981825 | GTGTTTTG others(13): Show |
G | 1 | a0001c0001t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3827-6136_3827-611 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46981825 | ||||||
chr19:46981875 | A | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA19004.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3827-6114A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981875 | |||||||
chr19:46981999 | A | T | 6 | a0001c0001t0002g0042 a0001c0001t0002g0046 a0001c0001t0002g0060 others(3): Show |
6 | HG02071.hp2 NA18943.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.3827-5990A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46981999 | |||||||
chr19:46982070 | C | T | 50 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(47): Show |
50 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.3827-5919C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982070 | |||||||
chr19:46982095 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3827-5894G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982095 | |||||||
chr19:46982114 | C | A | 11 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(8): Show |
11 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.3827-5875C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982114 | |||||||
chr19:46982152 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0022g0187 a0001c0001t0022g0288 |
3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.3827-5837A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982152 | |||||||
chr19:46982203 | G | A | 1 | a0001c0001t0045g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3827-5786G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982203 | |||||||
chr19:46982281 | A | C | 1 | a0001c0001t0017g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3827-5708A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982281 | |||||||
chr19:46982524 | T | TAAAAAGC others(1): Show |
5 | a0001c0001t0002g0013 a0001c0001t0002g0016 a0001c0001t0002g0017 others(2): Show |
5 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3827-5464_3827-545 others(12): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46982524 | ||||||
chr19:46982936 | C | T | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-5053C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46982936 | |||||||
chr19:46983054 | C | CA | 44 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3827-4905dupA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | C | CAA | 30 | a0001c0001t0001g0068 a0001c0001t0001g0173 a0001c0001t0001g0177 others(27): Show |
30 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3827-4906_3827-490 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | C | CAAA | 25 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0181 others(22): Show |
25 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3827-4907_3827-490 others(7): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | C | CAAAA | 19 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0045 others(16): Show |
19 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.3827-4908_3827-490 others(8): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | C | CAAAAA | 17 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(14): Show |
17 | HG00408.hp2 HG00642.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.3827-4909_3827-490 others(9): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | C | CAAAAAAA others(6): Show |
1 | a0002c0004t0002g0003 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3827-4917_3827-490 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | C | CAAAAAAA others(7): Show |
1 | a0002c0004t0002g0008 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3827-4918_3827-490 others(18): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | CA | C | 41 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.3827-4905delA | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | CAA | C | 43 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(40): Show |
43 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.3827-4906_3827-490 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3827-4916_3827-490 others(16): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983054 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-4917_3827-490 others(17): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983054 | ||||||
chr19:46983151 | G | A | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3827-4838G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983151 | |||||||
chr19:46983240 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3827-4749C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983240 | |||||||
chr19:46983483 | C | A | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3827-4506C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983483 | |||||||
chr19:46983606 | C | CT | 102 | a0001c0001t0001g0077 a0001c0001t0001g0141 a0001c0001t0001g0154 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3827-4358dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | ||||||
chr19:46983606 | C | CTT | 22 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0002g0046 others(19): Show |
22 | HG01243.hp2 HG01928.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.3827-4359_3827-435 others(6): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | ||||||
chr19:46983606 | CT | C | 6 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0218 others(3): Show |
6 | HG01070.hp1 HG01516.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.3827-4358delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | ||||||
chr19:46983606 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0020g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3827-4368_3827-435 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46983606 | ||||||
chr19:46983706 | C | G | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-4283C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983706 | |||||||
chr19:46983861 | C | T | 1 | a0006c0008t0011g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3827-4128C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983861 | |||||||
chr19:46983882 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3827-4107G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983882 | |||||||
chr19:46983912 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4077G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983912 | |||||||
chr19:46983947 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4042C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983947 | |||||||
chr19:46983950 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4039T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983950 | |||||||
chr19:46983954 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4035A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983954 | |||||||
chr19:46983960 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4029G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983960 | |||||||
chr19:46983963 | A | G | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3827-4026A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983963 | |||||||
chr19:46983968 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4021A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983968 | |||||||
chr19:46983971 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4018T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983971 | |||||||
chr19:46983980 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4009G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983980 | |||||||
chr19:46983982 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-4007C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983982 | |||||||
chr19:46983998 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3991G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46983998 | |||||||
chr19:46984017 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3972G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984017 | |||||||
chr19:46984032 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3957T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984032 | |||||||
chr19:46984092 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3897T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984092 | |||||||
chr19:46984146 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3843G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984146 | |||||||
chr19:46984147 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3842T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984147 | |||||||
chr19:46984153 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3836G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984153 | |||||||
chr19:46984155 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3834G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984155 | |||||||
chr19:46984157 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3832C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984157 | |||||||
chr19:46984165 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3824A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984165 | |||||||
chr19:46984183 | T | G | 1 | a0001c0001t0002g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3827-3806T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984183 | |||||||
chr19:46984195 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3794T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984195 | |||||||
chr19:46984217 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3772G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984217 | |||||||
chr19:46984225 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3764G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984225 | |||||||
chr19:46984231 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3758G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984231 | |||||||
chr19:46984245 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3744G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984245 | |||||||
chr19:46984249 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3740G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984249 | |||||||
chr19:46984252 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3737G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984252 | |||||||
chr19:46984289 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3700C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984289 | |||||||
chr19:46984290 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3699G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984290 | |||||||
chr19:46984292 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3697G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984292 | |||||||
chr19:46984296 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3693G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984296 | |||||||
chr19:46984301 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3688A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984301 | |||||||
chr19:46984428 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3561G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984428 | |||||||
chr19:46984452 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3537T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984452 | |||||||
chr19:46984469 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3520C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984469 | |||||||
chr19:46984478 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3511G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984478 | |||||||
chr19:46984479 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3510T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984479 | |||||||
chr19:46984491 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3498T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984491 | |||||||
chr19:46984493 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3496C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984493 | |||||||
chr19:46984501 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3827-3488G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984501 | |||||||
chr19:46984524 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3465G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984524 | |||||||
chr19:46984525 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3464T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984525 | |||||||
chr19:46984539 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3450T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984539 | |||||||
chr19:46984548 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3441A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984548 | |||||||
chr19:46984552 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3437C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984552 | |||||||
chr19:46984553 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3436T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984553 | |||||||
chr19:46984554 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3435A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984554 | |||||||
chr19:46984563 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3426T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984563 | |||||||
chr19:46984597 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3392C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984597 | |||||||
chr19:46984636 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3353C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984636 | |||||||
chr19:46984658 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3331G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984658 | |||||||
chr19:46984691 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3298G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984691 | |||||||
chr19:46984715 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3274T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984715 | |||||||
chr19:46984717 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3272A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984717 | |||||||
chr19:46984718 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3271T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984718 | |||||||
chr19:46984737 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3252G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984737 | |||||||
chr19:46984751 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3238C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984751 | |||||||
chr19:46984764 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3225G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984764 | |||||||
chr19:46984766 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3223T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984766 | |||||||
chr19:46984768 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3221C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984768 | |||||||
chr19:46984780 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3827-3209T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984780 | |||||||
chr19:46984793 | A | G | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3827-3196A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984793 | |||||||
chr19:46984814 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3175T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984814 | |||||||
chr19:46984815 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3174C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984815 | |||||||
chr19:46984816 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3173G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984816 | |||||||
chr19:46984823 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3166T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984823 | |||||||
chr19:46984824 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3165G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984824 | |||||||
chr19:46984828 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3827-3161T>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984828 | |||||||
chr19:46984831 | G | A | 1 | a0001c0001t0014g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3827-3158G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984831 | |||||||
chr19:46984848 | G | T | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3827-3141G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984848 | |||||||
chr19:46984972 | C | T | 29 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(26): Show |
29 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.3827-3017C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46984972 | |||||||
chr19:46985088 | G | A | 1 | a0001c0001t0012g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-2901G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985088 | |||||||
chr19:46985305 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0286 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3827-2684A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985305 | |||||||
chr19:46985327 | G | A | 1 | a0001c0001t0018g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3827-2662G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985327 | |||||||
chr19:46985380 | T | C | 64 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.3827-2609T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985380 | |||||||
chr19:46985573 | A | G | 50 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(47): Show |
50 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.3827-2416A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985573 | |||||||
chr19:46985634 | A | G | 186 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3827-2355A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985634 | |||||||
chr19:46985674 | C | T | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-2315C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985674 | |||||||
chr19:46985707 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3827-2282C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985707 | |||||||
chr19:46985709 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3827-2280C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985709 | |||||||
chr19:46985723 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3827-2266C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985723 | |||||||
chr19:46985789 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3827-2200C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985789 | |||||||
chr19:46985821 | C | G | 31 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(28): Show |
31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.3827-2168C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985821 | |||||||
chr19:46985858 | T | C | 4 | a0001c0001t0013g0069 a0001c0001t0013g0087 a0001c0001t0013g0247 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-2131T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46985858 | |||||||
chr19:46986076 | T | C | 2 | a0001c0001t0014g0093 a0001c0001t0014g0094 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3827-1913T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986076 | |||||||
chr19:46986245 | T | G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0016 others(3): Show |
6 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3827-1744T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986245 | |||||||
chr19:46986301 | C | T | 115 | a0001c0001t0001g0077 a0001c0001t0001g0130 a0001c0001t0002g0001 others(112): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.3827-1688C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986301 | |||||||
chr19:46986633 | A | G | 1 | a0001c0001t0012g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-1356A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986633 | |||||||
chr19:46986635 | G | A | 1 | a0001c0001t0012g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-1354G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986635 | |||||||
chr19:46986799 | A | G | 5 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(2): Show |
5 | HG02027.hp2 NA18961.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3827-1190A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986799 | |||||||
chr19:46986866 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3827-1123T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986866 | |||||||
chr19:46986887 | G | A | 4 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3827-1102G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46986887 | |||||||
chr19:46987036 | C | T | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3827-953C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987036 | |||||||
chr19:46987080 | G | A | 1 | a0003c0013t0003g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3827-909G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987080 | |||||||
chr19:46987162 | T | C | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3827-827T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987162 | |||||||
chr19:46987188 | C | A | 1 | a0001c0001t0012g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3827-801C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987188 | |||||||
chr19:46987218 | C | CT | 23 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(20): Show |
23 | HG01069.hp2 HG01261.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.3827-753dupT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46987218 | ||||||
chr19:46987218 | CT | C | 40 | a0001c0001t0001g0118 a0001c0001t0001g0169 a0001c0001t0001g0184 others(37): Show |
40 | HG00597.hp1 HG01070.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.3827-753delT | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 46987218 | ||||||
chr19:46987362 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3827-627C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987362 | |||||||
chr19:46987515 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3827-474A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987515 | |||||||
chr19:46987681 | T | C | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3827-308T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987681 | |||||||
chr19:46987823 | G | C | 1 | a0001c0001t0004g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3827-166G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | chr19 | 46987823 | |||||||
chr19:46988443 | G | T | 8 | a0001c0001t0004g0117 a0001c0001t0004g0120 a0001c0001t0004g0121 others(5): Show |
8 | NA18972.hp1 NA18973.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.3904+377G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46988443 | |||||||
chr19:46988460 | A | G | 94 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(91): Show |
94 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.3904+394A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46988460 | |||||||
chr19:46989218 | G | A | 174 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(171): Show |
174 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3905-326G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989218 | |||||||
chr19:46989255 | T | C | 1 | a0001c0001t0008g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3905-289T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989255 | |||||||
chr19:46989473 | AG | A | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3905-70delG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989473 | |||||||
chr19:46989478 | C | T | 1 | a0001c0001t0043g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3905-66C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4/6 | chr19 | 46989478 | |||||||
chr19:46989934 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4036+259C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46989934 | |||||||
chr19:46990021 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4036+346G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990021 | |||||||
chr19:46990192 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4036+517A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990192 | |||||||
chr19:46990376 | C | G | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4036+701C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990376 | |||||||
chr19:46990420 | C | T | 29 | a0001c0001t0001g0077 a0001c0001t0003g0022 a0001c0001t0003g0070 others(26): Show |
29 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.4036+745C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990420 | |||||||
chr19:46990567 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.4036+892T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46990567 | |||||||
chr19:46991414 | T | G | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4036+1739T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991414 | |||||||
chr19:46991481 | G | C | 1 | a0001c0001t0003g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4036+1806G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991481 | |||||||
chr19:46991485 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4036+1810T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991485 | |||||||
chr19:46991596 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0279 |
2 | HG02056.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.4036+1921G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991596 | |||||||
chr19:46991599 | G | A | 6 | a0001c0001t0016g0024 a0001c0001t0016g0219 a0001c0001t0024g0025 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4036+1924G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991599 | |||||||
chr19:46991626 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4036+1951G>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991626 | |||||||
chr19:46991683 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4036+2008G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991683 | |||||||
chr19:46991688 | T | G | 186 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.4036+2013T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991688 | |||||||
chr19:46991790 | T | C | 1 | a0001c0001t0014g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4036+2115T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46991790 | |||||||
chr19:46992166 | C | T | 4 | a0001c0001t0003g0072 a0001c0001t0003g0240 a0001c0001t0003g0242 others(1): Show |
4 | HG00558.hp1 NA18978.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.4036+2491C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992166 | |||||||
chr19:46992167 | G | A | 11 | a0001c0001t0008g0088 a0001c0001t0008g0091 a0001c0001t0008g0246 others(8): Show |
11 | HG00597.hp1 HG02080.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.4036+2492G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992167 | |||||||
chr19:46992320 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4036+2645C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992320 | |||||||
chr19:46992642 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4036+2967G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992642 | |||||||
chr19:46992679 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4036+3004C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992679 | |||||||
chr19:46992690 | G | T | 21 | a0001c0001t0001g0118 a0001c0001t0004g0117 a0001c0001t0004g0120 others(18): Show |
21 | HG01070.hp2 HG01192.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.4036+3015G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992690 | |||||||
chr19:46992831 | G | A | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4036+3156G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46992831 | |||||||
chr19:46993289 | G | A | 1 | a0001c0002t0005g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4036+3614G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993289 | |||||||
chr19:46993497 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0152 |
3 | NA19004.hp1 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.4036+3822C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993497 | |||||||
chr19:46993498 | C | T | 1 | a0001c0001t0037g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4036+3823C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993498 | |||||||
chr19:46993656 | T | G | 1 | a0001c0001t0002g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4036+3981T>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46993656 | |||||||
chr19:46994015 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4036+4340C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994015 | |||||||
chr19:46994155 | C | T | 1 | a0001c0001t0021g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4036+4480C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994155 | |||||||
chr19:46994219 | G | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4036+4544G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994219 | |||||||
chr19:46994220 | A | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4036+4545A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994220 | |||||||
chr19:46994347 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4036+4672G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994347 | |||||||
chr19:46994408 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0293 |
2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4036+4733G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994408 | |||||||
chr19:46994573 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4037-4731C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994573 | |||||||
chr19:46994585 | G | A | 1 | a0001c0001t0002g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4037-4719G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994585 | |||||||
chr19:46994590 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4037-4714G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994590 | |||||||
chr19:46994614 | G | A | 14 | a0001c0002t0005g0207 a0001c0002t0005g0209 a0001c0002t0005g0210 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.4037-4690G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994614 | |||||||
chr19:46994621 | A | G | 186 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0001g0130 others(183): Show |
186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.4037-4683A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994621 | |||||||
chr19:46994783 | C | T | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-4521C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994783 | |||||||
chr19:46994904 | C | T | 1 | a0001c0001t0003g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4037-4400C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994904 | |||||||
chr19:46994973 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4037-4331G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46994973 | |||||||
chr19:46995114 | A | C | 1 | a0001c0001t0003g0022 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4037-4190A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995114 | |||||||
chr19:46995154 | T | C | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-4150T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995154 | |||||||
chr19:46995155 | A | G | 2 | a0001c0001t0023g0034 a0001c0001t0023g0221 |
2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-4149A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995155 | |||||||
chr19:46995641 | C | A | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4037-3663C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995641 | |||||||
chr19:46995774 | T | C | 185 | a0001c0001t0001g0077 a0001c0001t0001g0118 a0001c0001t0002g0001 others(182): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.4037-3530T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995774 | |||||||
chr19:46995877 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4037-3427G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46995877 | |||||||
chr19:46996058 | G | T | 1 | a0001c0001t0013g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4037-3246G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996058 | |||||||
chr19:46996076 | G | T | 1 | a0001c0001t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4037-3228G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996076 | |||||||
chr19:46996166 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4037-3138C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996166 | |||||||
chr19:46996167 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0195 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4037-3137G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996167 | |||||||
chr19:46996221 | A | G | 1 | a0001c0001t0044g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4037-3083A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996221 | |||||||
chr19:46996252 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4037-3052C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996252 | |||||||
chr19:46996417 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0269 |
2 | HG02293.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.4037-2887A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996417 | |||||||
chr19:46996470 | C | T | 1 | a0001c0001t0008g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4037-2834C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996470 | |||||||
chr19:46996529 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4037-2775C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996529 | |||||||
chr19:46996591 | T | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0021 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4037-2713T>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996591 | |||||||
chr19:46996929 | G | A | 5 | a0001c0001t0007g0056 a0001c0001t0007g0057 a0001c0001t0007g0058 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4037-2375G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996929 | |||||||
chr19:46996934 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4037-2370G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46996934 | |||||||
chr19:46997093 | G | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.4037-2211G>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997093 | |||||||
chr19:46997285 | A | T | 2 | a0001c0003t0001g0073 a0001c0003t0003g0234 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4037-2019A>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997285 | |||||||
chr19:46997431 | C | G | 3 | a0001c0001t0001g0205 a0001c0001t0022g0187 a0001c0001t0022g0288 |
3 | HG00558.hp2 HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.4037-1873C>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997431 | |||||||
chr19:46997505 | G | A | 49 | a0001c0001t0001g0118 a0001c0001t0004g0102 a0001c0001t0004g0106 others(46): Show |
49 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.4037-1799G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997505 | |||||||
chr19:46997603 | A | G | 1 | a0005c0010t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4037-1701A>G | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997603 | |||||||
chr19:46997801 | C | A | 2 | a0001c0001t0019g0039 a0001c0001t0019g0055 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4037-1503C>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997801 | |||||||
chr19:46997831 | G | A | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4037-1473G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997831 | |||||||
chr19:46997963 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4037-1341G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46997963 | |||||||
chr19:46998034 | G | A | 1 | a0001c0001t0034g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4037-1270G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998034 | |||||||
chr19:46998057 | G | A | 1 | a0001c0002t0047g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4037-1247G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998057 | |||||||
chr19:46998245 | C | T | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4037-1059C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998245 | |||||||
chr19:46998445 | G | A | 1 | a0001c0001t0003g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4037-859G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998445 | |||||||
chr19:46998594 | T | TG | 5 | a0001c0001t0001g0158 a0001c0001t0001g0166 a0001c0001t0006g0052 others(2): Show |
5 | HG01243.hp2 HG01928.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4037-706dupG | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 46998594 | ||||||
chr19:46998629 | G | A | 1 | a0001c0001t0025g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4037-675G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998629 | |||||||
chr19:46998920 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4037-384G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998920 | |||||||
chr19:46998924 | G | A | 3 | a0001c0001t0023g0034 a0001c0001t0023g0221 a0001c0003t0003g0234 |
3 | HG02258.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4037-380G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46998924 | |||||||
chr19:46999179 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0040g0053 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.4037-125G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46999179 | |||||||
chr19:46999226 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4037-78G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46999226 | |||||||
chr19:46999228 | C | CCAT | 7 | a0001c0001t0011g0029 a0001c0001t0011g0036 a0001c0001t0019g0039 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.4037-73_4037-71dup others(3): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 46999228 | ||||||
chr19:46999241 | C | T | 1 | a0001c0002t0005g0212 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4037-63C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 5/6 | chr19 | 46999241 | |||||||
chr19:46999416 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02015.hp1 | splice_region_variant&intron_variant | LOW | c.4142+7C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999416 | |||||||
chr19:46999530 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4142+121G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999530 | |||||||
chr19:46999635 | G | A | 1 | a0001c0001t0046g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4142+226G>A | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999635 | |||||||
chr19:46999642 | C | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG00733.hp2 HG00738.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4142+233C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999642 | |||||||
chr19:46999798 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4142+389A>C | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999798 | |||||||
chr19:46999853 | C | T | 1 | a0001c0001t0004g0262 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4142+444C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999853 | |||||||
chr19:46999937 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4143-394C>T | ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 6/6 | chr19 | 46999937 |