Item | Value |
---|---|
geneid | 9938 |
ensemblid | ENSG00000163219.12 |
hgncid | 28951 |
symbol | ARHGAP25 |
name | Rho GTPase activating protein 25 |
refseq_nuc | NM_001007231.3 |
refseq_prot | NP_001007232.2 |
ensembl_nuc | ENST00000409202.8 |
ensembl_prot | ENSP00000386911.3 |
mane_status | MANE Select |
chr | chr2 |
start | 68734811 |
end | 68826833 |
strand | + |
ver | v1.2 |
region | chr2:68734811-68826833 |
region5000 | chr2:68729811-68831833 |
regionname0 | ARHGAP25_chr2_68734811_68826833 |
regionname5000 | ARHGAP25_chr2_68729811_68831833 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 646 | 138 | 38 | 22 | 63 | 6 | 9 | 50 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0002 | 1/1 | 646 | 123 | 39 | 28 | 22 | 7 | 25 | 17 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0003 | 0/0 | 646 | 93 | 10 | 19 | 53 | 5 | 6 | 41 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0004 | 0/0 | 646 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0005 | 0/0 | 646 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0006 | 0/0 | 646 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0007 | 0/0 | 646 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0008 | 0/0 | 646 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0009 | 0/0 | 646 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0010 | 0/0 | 646 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0011 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
a0012 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | MSLKL others(641): Show |
chr2 | 68729811 | 68831833 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1938 | 138 | 38 | 22 | 63 | 6 | 9 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0002 | 1/1 | 1938 | 98 | 20 | 24 | 22 | 6 | 24 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0004 | 0/0 | 1938 | 10 | 9 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0005 | 0/0 | 1938 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0007 | 0/0 | 1938 | 4 | 2 | 2 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0008 | 0/0 | 1938 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0012 | 0/0 | 1938 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0002c0020 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0003c0003 | 0/0 | 1938 | 88 | 10 | 19 | 48 | 5 | 6 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0003c0006 | 0/0 | 1938 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0003c0014 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0004c0009 | 0/0 | 1938 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0005c0011 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0006c0010 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0007c0013 | 0/0 | 1938 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0008c0017 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0009c0019 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0010c0018 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0011c0016 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 | ||
a0012c0015 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | ATGTC others(1933): Show |
chr2 | 68729811 | 68831833 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2969 | 80 | 13 | 10 | 50 | 2 | 5 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0002 | 0/0 | 2969 | 14 | 11 | 2 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0003 | 0/0 | 2969 | 28 | 7 | 7 | 10 | 0 | 4 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0004 | 0/0 | 2969 | 6 | 2 | 2 | 0 | 2 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0005 | 0/0 | 2969 | 4 | 1 | 0 | 2 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0008 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0013 | 0/0 | 2970 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0018 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0001c0001t0022 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0001 | 0/0 | 2969 | 13 | 5 | 5 | 1 | 0 | 2 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0002 | 1/1 | 2969 | 51 | 4 | 13 | 15 | 5 | 12 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0003 | 0/0 | 2969 | 6 | 4 | 0 | 0 | 1 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0004 | 0/0 | 2969 | 8 | 3 | 0 | 3 | 0 | 2 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0005 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0006 | 0/0 | 2969 | 4 | 0 | 2 | 0 | 0 | 2 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0010 | 0/0 | 2969 | 4 | 1 | 0 | 0 | 0 | 3 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0011 | 0/0 | 2969 | 4 | 0 | 2 | 1 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0014 | 0/0 | 2969 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0017 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0019 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0002t0023 | 0/0 | 2969 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0001 | 0/0 | 2969 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0002 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0003 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0005 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0008 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0013 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0002c0004t0020 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0005t0002 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0005t0012 | 0/0 | 2970 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0002c0007t0007 | 0/0 | 2969 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0007t0016 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0008t0008 | 0/0 | 2970 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0002c0012t0001 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0012t0002 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0002c0020t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0001 | 0/0 | 2969 | 68 | 8 | 11 | 40 | 4 | 5 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0003 | 0/0 | 2969 | 5 | 2 | 0 | 2 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0005 | 0/0 | 2969 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0006 | 0/0 | 2969 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0009 | 0/0 | 2969 | 5 | 0 | 4 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0010 | 0/0 | 2969 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0003t0015 | 0/0 | 2969 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0006t0003 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0006t0005 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0003c0006t0021 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2965): Show |
chr2 | 68729811 | 68831833 |
a0003c0014t0001 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0004c0009t0002 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0004c0009t0007 | 0/0 | 2969 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0005c0011t0001 | 0/0 | 2969 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0006c0010t0007 | 0/0 | 2969 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0007c0013t0001 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0008c0017t0016 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0009c0019t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0010c0018t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0011c0016t0001 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
a0012c0015t0003 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | AGTTG others(2964): Show |
chr2 | 68729811 | 68831833 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0013g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0013g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0001c0001t0022g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0006g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0006g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0006g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0010g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0010g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0010g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0011g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0011g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0011g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0014g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0014g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0014g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0017g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0017g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0019g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0002t0023g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0004t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0005t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0005t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0005t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0005t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0005t0012g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0007t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0007t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0007t0007g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0007t0016g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0008t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0008t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0012t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0012t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0002c0020t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0009g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0009g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0010g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0015g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0015g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0003t0015g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0006t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0006t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0006t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0006t0021g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0003c0014t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0004c0009t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0004c0009t0007g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0004c0009t0007g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0005c0011t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0005c0011t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0006c0010t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0007c0013t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0007c0013t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0008c0017t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0009c0019t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0010c0018t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0011c0016t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
a0012c0015t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0005 | g0042 | EUR | GBR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00099 | hp2 | a0002 | c0012 | t0002 | g0073 | EUR | GBR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00140 | hp1 | a0001 | c0001 | t0018 | g0164 | EUR | GBR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0256 | EUR | GBR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0029 | EUR | FIN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0171 | EUR | FIN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0070 | EUR | FIN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00323 | hp2 | a0002 | c0002 | t0003 | g0062 | EUR | FIN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00408 | hp1 | a0002 | c0002 | t0014 | g0037 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0315 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00544 | hp1 | a0003 | c0003 | t0001 | g0227 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00544 | hp2 | a0003 | c0003 | t0015 | g0305 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0329 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0299 | EAS | CHS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00639 | hp2 | a0003 | c0003 | t0010 | g0038 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00735 | hp2 | a0001 | c0001 | t0013 | g0340 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0301 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01074 | hp1 | a0002 | c0002 | t0006 | g0310 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0074 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01099 | hp2 | a0003 | c0003 | t0005 | g0026 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0322 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01167 | hp1 | a0004 | c0009 | t0007 | g0330 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01167 | hp2 | a0002 | c0007 | t0007 | g0264 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01168 | hp1 | a0002 | c0002 | t0011 | g0153 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01169 | hp2 | a0002 | c0007 | t0007 | g0265 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01243 | hp2 | a0002 | c0004 | t0001 | g0348 | AMR | PUR | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01256 | hp1 | a0002 | c0002 | t0023 | g0066 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01257 | hp1 | a0003 | c0003 | t0009 | g0033 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01258 | hp1 | a0003 | c0003 | t0009 | g0004 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01261 | hp1 | a0002 | c0002 | t0006 | g0188 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01261 | hp2 | a0002 | c0002 | t0014 | g0043 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0241 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0112 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01361 | hp1 | a0003 | c0003 | t0009 | g0034 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0249 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0259 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0194 | EUR | IBS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0215 | EUR | IBS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0152 | EUR | IBS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0077 | EUR | IBS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0216 | EUR | IBS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0234 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01884 | hp2 | a0003 | c0003 | t0003 | g0335 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0053 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01891 | hp2 | a0002 | c0004 | t0013 | g0343 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01928 | hp2 | a0003 | c0003 | t0015 | g0248 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0191 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0058 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01975 | hp2 | a0002 | c0002 | t0011 | g0141 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0245 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0252 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0064 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0284 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0247 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02055 | hp2 | a0002 | c0007 | t0016 | g0059 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0219 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02074 | hp2 | a0003 | c0014 | t0001 | g0246 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02135 | hp1 | a0003 | c0003 | t0006 | g0300 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02135 | hp2 | a0002 | c0002 | t0004 | g0168 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | CDX | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02257 | hp1 | a0002 | c0004 | t0003 | g0346 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0229 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0334 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02273 | hp1 | a0003 | c0003 | t0009 | g0035 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0269 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02280 | hp1 | a0002 | c0005 | t0012 | g0347 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02280 | hp2 | a0001 | c0001 | t0022 | g0333 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02293 | hp2 | a0003 | c0003 | t0015 | g0097 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02451 | hp1 | a0002 | c0002 | t0004 | g0051 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02451 | hp2 | a0002 | c0005 | t0002 | g0274 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0228 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02572 | hp2 | a0002 | c0005 | t0012 | g0185 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02615 | hp1 | a0008 | c0017 | t0016 | g0061 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02615 | hp2 | a0009 | c0019 | t0001 | g0008 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02622 | hp1 | a0002 | c0002 | t0003 | g0338 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02622 | hp2 | a0005 | c0011 | t0001 | g0275 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02630 | hp2 | a0002 | c0020 | t0001 | g0261 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0349 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0288 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0344 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02723 | hp2 | a0002 | c0005 | t0012 | g0210 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0226 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02738 | hp2 | a0002 | c0002 | t0006 | g0321 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02818 | hp1 | a0002 | c0004 | t0020 | g0052 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02818 | hp2 | a0002 | c0004 | t0001 | g0323 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02886 | hp1 | a0010 | c0018 | t0001 | g0277 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02886 | hp2 | a0002 | c0004 | t0001 | g0332 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0196 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02895 | hp2 | a0002 | c0002 | t0017 | g0308 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02897 | hp2 | a0002 | c0002 | t0017 | g0309 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0336 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02922 | hp2 | a0002 | c0002 | t0005 | g0044 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02970 | hp1 | a0002 | c0002 | t0010 | g0045 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0136 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02976 | hp2 | a0002 | c0004 | t0005 | g0060 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03041 | hp1 | a0003 | c0003 | t0003 | g0342 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03098 | hp1 | a0006 | c0010 | t0007 | g0011 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03098 | hp2 | a0002 | c0008 | t0008 | g0006 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0278 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03195 | hp1 | a0002 | c0002 | t0004 | g0047 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03209 | hp2 | a0002 | c0004 | t0002 | g0024 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0258 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0156 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0239 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03453 | hp1 | a0002 | c0004 | t0008 | g0291 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03486 | hp1 | a0005 | c0011 | t0001 | g0273 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03486 | hp2 | a0006 | c0010 | t0007 | g0011 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03491 | hp1 | a0002 | c0002 | t0010 | g0027 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0068 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03492 | hp1 | a0002 | c0002 | t0010 | g0028 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0212 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0075 | AFR | GWD | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03579 | hp1 | a0002 | c0002 | t0003 | g0339 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03579 | hp2 | a0002 | c0007 | t0007 | g0016 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0195 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03688 | hp1 | a0002 | c0002 | t0004 | g0057 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03688 | hp2 | a0002 | c0002 | t0011 | g0173 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0145 | SAS | PJL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0098 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0134 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03927 | hp1 | a0003 | c0003 | t0003 | g0166 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0209 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0250 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0267 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04115 | hp1 | a0002 | c0012 | t0001 | g0086 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04115 | hp2 | a0002 | c0002 | t0006 | g0320 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0217 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | BEB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0307 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0282 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04204 | hp1 | a0002 | c0002 | t0010 | g0041 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | CHB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18906 | hp1 | a0002 | c0004 | t0001 | g0290 | AFR | YRI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0337 | AFR | YRI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18939 | hp2 | a0003 | c0003 | t0006 | g0272 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18943 | hp2 | a0003 | c0003 | t0003 | g0155 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18945 | hp1 | a0003 | c0003 | t0001 | g0302 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0324 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0325 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18962 | hp2 | a0003 | c0003 | t0001 | g0198 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18969 | hp1 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18973 | hp1 | a0003 | c0006 | t0005 | g0031 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18977 | hp1 | a0007 | c0013 | t0001 | g0092 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0197 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18982 | hp1 | a0003 | c0003 | t0001 | g0238 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18982 | hp2 | a0003 | c0003 | t0003 | g0161 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18986 | hp2 | a0011 | c0016 | t0001 | g0351 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18987 | hp2 | a0003 | c0003 | t0001 | g0102 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18989 | hp2 | a0003 | c0003 | t0001 | g0218 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18997 | hp2 | a0003 | c0003 | t0001 | g0314 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18999 | hp2 | a0003 | c0003 | t0006 | g0105 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19000 | hp1 | a0003 | c0003 | t0001 | g0318 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19000 | hp2 | a0002 | c0002 | t0004 | g0142 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0313 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0211 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19005 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19006 | hp1 | a0003 | c0003 | t0001 | g0326 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19006 | hp2 | a0002 | c0002 | t0014 | g0036 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0201 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0231 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19011 | hp2 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0056 | AFR | LWK | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19057 | hp1 | a0003 | c0006 | t0021 | g0030 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0221 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19062 | hp2 | a0002 | c0002 | t0011 | g0144 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19064 | hp1 | a0007 | c0013 | t0001 | g0117 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19064 | hp2 | a0012 | c0015 | t0003 | g0160 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19065 | hp1 | a0003 | c0003 | t0009 | g0004 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0317 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19067 | hp1 | a0003 | c0003 | t0006 | g0289 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19067 | hp2 | a0003 | c0006 | t0005 | g0032 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19081 | hp1 | a0003 | c0003 | t0001 | g0319 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19083 | hp1 | a0003 | c0006 | t0003 | g0165 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19240 | hp1 | a0002 | c0005 | t0012 | g0019 | AFR | YRI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA19240 | hp2 | a0004 | c0009 | t0007 | g0350 | AFR | YRI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0279 | AFR | ASW | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20129 | hp2 | a0003 | c0003 | t0001 | g0079 | AFR | ASW | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0270 | EUR | TSI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0295 | EUR | TSI | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20905 | hp1 | a0002 | c0002 | t0019 | g0104 | SAS | GIH | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0078 | SAS | GIH | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG01123 | hp2 | a0002 | c0008 | t0008 | g0076 | AMR | CLM | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02109 | hp1 | a0004 | c0009 | t0002 | g0331 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0235 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | ACB | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
HG03471 | hp2 | a0002 | c0008 | t0008 | g0006 | AFR | MSL | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0316 | AFR | USA | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | USA | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0065 | REF | REF | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0106 | REF | REF | ARHGAP25_chr2_68729811_68831833 | ARHGAP25 | chr2 | 68729811 | 68831833 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68807287 | C | A | 1 | a0012 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.481C>A | p.Arg161Ser | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/11 | 870/2969 | 481/1941 | 161/646 | chr2 | 68807287 | |||
chr2:68807327 | C | G | 1 | a0009 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.521C>G | p.Pro174Arg | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/11 | 910/2969 | 521/1941 | 174/646 | chr2 | 68807327 | |||
chr2:68807383 | C | T | 1 | a0007 | 2 | NA18977.hp1 NA19064.hp1 |
missense_variant | MODERATE | c.577C>T | p.Arg193Trp | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/11 | 966/2969 | 577/1941 | 193/646 | chr2 | 68807383 | |||
chr2:68816331 | G | A | 1 | a0008 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.850G>A | p.Asp284Asn | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/11 | 1239/2969 | 850/1941 | 284/646 | chr2 | 68816331 | |||
chr2:68822671 | G | C | 1 | a0004 | 3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1532G>C | p.Gly511Ala | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 1921/2969 | 1532/1941 | 511/646 | chr2 | 68822671 | |||
chr2:68822710 | C | A | 1 | a0010 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1571C>A | p.Ala524Asp | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 1960/2969 | 1571/1941 | 524/646 | chr2 | 68822710 | |||
chr2:68822807 | G | T | 2 | a0003 a0011 |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
missense_variant | MODERATE | c.1668G>T | p.Arg556Ser | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 2057/2969 | 1668/1941 | 556/646 | chr2 | 68822807 | |||
chr2:68822809 | T | C | 4 | a0001 a0007 a0010 others(1): Show |
142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
missense_variant | MODERATE | c.1670T>C | p.Met557Thr | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 2059/2969 | 1670/1941 | 557/646 | chr2 | 68822809 | |||
chr2:68826034 | A | G | 1 | a0011 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.1781A>G | p.Asn594Ser | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 2170/2969 | 1781/1941 | 594/646 | chr2 | 68826034 | |||
chr2:68826186 | G | A | 1 | a0005 | 2 | HG02622.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1933G>A | p.Glu645Lys | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 2322/2969 | 1933/1941 | 645/646 | chr2 | 68826186 | |||
chr2:68826189 | G | A | 1 | a0006 | 2 | HG03098.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.1936G>A | p.Ala646Thr | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 2325/2969 | 1936/1941 | 646/646 | chr2 | 68826189 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68787901 | G | A | 1 | a0003c0014 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.411G>A | p.Ala137Ala | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/11 | 800/2969 | 411/1941 | 137/646 | chr2 | 68787901 | |||
chr2:68807322 | C | T | 1 | a0002c0020 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.516C>T | p.Phe172Phe | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/11 | 905/2969 | 516/1941 | 172/646 | chr2 | 68807322 | |||
chr2:68813368 | G | A | 6 | a0002c0004 a0002c0008 a0003c0003 others(3): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
synonymous_variant | LOW | c.756G>A | p.Gln252Gln | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/11 | 1145/2969 | 756/1941 | 252/646 | chr2 | 68813368 | |||
chr2:68819184 | C | G | 1 | a0002c0012 | 2 | HG00099.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.1065C>G | p.Pro355Pro | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/11 | 1454/2969 | 1065/1941 | 355/646 | chr2 | 68819184 | |||
chr2:68822390 | G | A | 3 | a0002c0007 a0006c0010 a0008c0017 |
7 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(4): Show |
synonymous_variant | LOW | c.1251G>A | p.Ala417Ala | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 1640/2969 | 1251/1941 | 417/646 | chr2 | 68822390 | |||
chr2:68822570 | T | C | 2 | a0002c0005 a0002c0020 |
6 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.1431T>C | p.Ala477Ala | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 1820/2969 | 1431/1941 | 477/646 | chr2 | 68822570 | |||
chr2:68822633 | A | G | 1 | a0003c0006 | 4 | NA18973.hp1 NA19057.hp1 NA19067.hp2 others(1): Show |
synonymous_variant | LOW | c.1494A>G | p.Gln498Gln | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 1883/2969 | 1494/1941 | 498/646 | chr2 | 68822633 | |||
chr2:68822654 | C | T | 1 | a0002c0008 | 3 | HG01123.hp2 HG03098.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.1515C>T | p.Asn505Asn | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/11 | 1904/2969 | 1515/1941 | 505/646 | chr2 | 68822654 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68734856 | G | A | 1 | a0001c0001t0018 | 1 | HG00140.hp1 | 5_prime_UTR_variant | MODIFIER | c.-344G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/11 | 344 | chr2 | 68734856 | ||||||
chr2:68735004 | T | C | 1 | a0002c0002t0019 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-196T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/11 | 196 | chr2 | 68735004 | ||||||
chr2:68735005 | G | A | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0013 others(10): Show |
65 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-195G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/11 | 195 | chr2 | 68735005 | ||||||
chr2:68735127 | T | C | 12 | a0001c0001t0005 a0002c0002t0005 a0002c0002t0010 others(9): Show |
26 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-73T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/11 | 73 | chr2 | 68735127 | ||||||
chr2:68826226 | G | C | 1 | a0002c0004t0020 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 32 | chr2 | 68826226 | ||||||
chr2:68826365 | G | A | 4 | a0002c0002t0006 a0002c0002t0011 a0002c0002t0014 others(1): Show |
15 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 171 | chr2 | 68826365 | ||||||
chr2:68826425 | T | C | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*231T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 231 | chr2 | 68826425 | ||||||
chr2:68826479 | C | T | 1 | a0002c0005t0012 | 4 | HG02280.hp1 HG02572.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 285 | chr2 | 68826479 | ||||||
chr2:68826617 | A | T | 2 | a0003c0003t0009 a0003c0003t0015 |
8 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*423A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 423 | chr2 | 68826617 | ||||||
chr2:68826622 | C | T | 4 | a0002c0002t0006 a0002c0002t0011 a0002c0002t0014 others(1): Show |
15 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*428C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 428 | chr2 | 68826622 | ||||||
chr2:68826706 | G | A | 1 | a0001c0001t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 512 | chr2 | 68826706 | ||||||
chr2:68826823 | T | TA | 9 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0022 others(6): Show |
17 | HG00735.hp2 HG01123.hp2 HG01891.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*628_*629insA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 629 | INFO_REALIGN_3_PRIME | chr2 | 68826823 | |||||
chr2:68826824 | A | T | 6 | a0002c0002t0023 a0002c0007t0007 a0002c0007t0016 others(3): Show |
10 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*630A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 11/11 | 630 | chr2 | 68826824 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68735280 | G | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+20G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735280 | |||||||
chr2:68735296 | T | C | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.61+36T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735296 | |||||||
chr2:68735300 | G | A | 1 | a0002c0002t0002g0025 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.61+40G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735300 | |||||||
chr2:68735438 | G | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+178G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735438 | |||||||
chr2:68735583 | A | G | 1 | a0011c0016t0001g0351 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.61+323A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735583 | |||||||
chr2:68735693 | G | A | 3 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 |
3 | HG02922.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+433G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735693 | |||||||
chr2:68735779 | T | G | 3 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 |
3 | HG02922.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+519T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735779 | |||||||
chr2:68735988 | A | G | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+728A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68735988 | |||||||
chr2:68736027 | G | A | 3 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 |
3 | HG02922.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+767G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736027 | |||||||
chr2:68736041 | T | G | 1 | a0002c0002t0004g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.61+781T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736041 | |||||||
chr2:68736220 | G | C | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+960G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736220 | |||||||
chr2:68736310 | C | T | 3 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 |
3 | HG02922.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+1050C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736310 | |||||||
chr2:68736318 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+1058A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736318 | |||||||
chr2:68736414 | T | C | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.61+1154T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736414 | |||||||
chr2:68736491 | C | T | 1 | a0004c0009t0007g0350 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.61+1231C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736491 | |||||||
chr2:68736852 | C | G | 2 | a0002c0004t0001g0348 a0003c0003t0001g0349 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61+1592C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736852 | |||||||
chr2:68736939 | T | C | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | NA18986.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.61+1679T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736939 | |||||||
chr2:68736985 | T | C | 9 | a0001c0001t0003g0005 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
10 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+1725T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68736985 | |||||||
chr2:68737026 | G | T | 1 | a0002c0005t0012g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.61+1766G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737026 | |||||||
chr2:68737091 | C | T | 13 | a0001c0001t0003g0341 a0001c0001t0003g0344 a0001c0001t0003g0345 others(10): Show |
13 | HG00735.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+1831C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737091 | |||||||
chr2:68737172 | TGAACTA | T | 3 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 |
3 | HG02922.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+1916_61+1921del others(6): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68737172 | ||||||
chr2:68737483 | A | G | 1 | a0001c0001t0022g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.61+2223A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737483 | |||||||
chr2:68737500 | A | G | 4 | a0002c0004t0001g0332 a0004c0009t0002g0331 a0004c0009t0007g0330 others(1): Show |
4 | HG01167.hp1 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+2240A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737500 | |||||||
chr2:68737668 | A | G | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+2408A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737668 | |||||||
chr2:68737781 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+2521T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737781 | |||||||
chr2:68737807 | C | A | 1 | a0003c0003t0001g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.61+2547C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737807 | |||||||
chr2:68737901 | G | A | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+2641G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737901 | |||||||
chr2:68737946 | G | T | 63 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0001t0001g0281 others(60): Show |
64 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.61+2686G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68737946 | |||||||
chr2:68738037 | A | C | 25 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(22): Show |
26 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.61+2777A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738037 | |||||||
chr2:68738085 | A | G | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+2825A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738085 | |||||||
chr2:68738197 | G | A | 1 | a0002c0002t0003g0062 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.61+2937G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738197 | |||||||
chr2:68738214 | T | TTGCTCGT others(9): Show |
6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+2957_61+2958ins others(16): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68738214 | ||||||
chr2:68738246 | G | A | 1 | a0003c0003t0006g0272 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61+2986G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738246 | |||||||
chr2:68738306 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.61+3046C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738306 | |||||||
chr2:68738343 | C | T | 1 | a0002c0002t0002g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61+3083C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738343 | |||||||
chr2:68738367 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.61+3107G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738367 | |||||||
chr2:68738565 | A | G | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+3305A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738565 | |||||||
chr2:68738654 | T | G | 3 | a0002c0005t0002g0274 a0005c0011t0001g0273 a0005c0011t0001g0275 |
3 | HG02451.hp2 HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.61+3394T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738654 | |||||||
chr2:68738724 | G | C | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+3464G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738724 | |||||||
chr2:68738730 | A | T | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61+3470A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738730 | |||||||
chr2:68738745 | C | T | 53 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(50): Show |
54 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.61+3485C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738745 | |||||||
chr2:68738771 | C | T | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+3511C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68738771 | |||||||
chr2:68738823 | G | GA | 29 | a0001c0001t0001g0063 a0001c0001t0005g0029 a0001c0001t0005g0039 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.61+3579dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68738823 | ||||||
chr2:68738823 | GA | G | 13 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0002c0002t0001g0266 others(10): Show |
13 | HG00597.hp2 HG02273.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+3579delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68738823 | ||||||
chr2:68739014 | C | T | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+3754C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739014 | |||||||
chr2:68739084 | C | G | 2 | a0002c0007t0007g0264 a0002c0007t0007g0265 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.61+3824C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739084 | |||||||
chr2:68739180 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+3920C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739180 | |||||||
chr2:68739270 | A | G | 10 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+4010A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739270 | |||||||
chr2:68739382 | T | A | 10 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(7): Show |
10 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+4122T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739382 | |||||||
chr2:68739431 | C | G | 16 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(13): Show |
17 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+4171C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739431 | |||||||
chr2:68739433 | G | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+4173G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739433 | |||||||
chr2:68739459 | A | T | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+4199A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739459 | |||||||
chr2:68739481 | A | T | 67 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0001t0001g0281 others(64): Show |
69 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.61+4221A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739481 | |||||||
chr2:68739507 | C | A | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+4247C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739507 | |||||||
chr2:68739658 | C | A | 1 | a0001c0001t0001g0281 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.61+4398C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739658 | |||||||
chr2:68739899 | C | A | 12 | a0001c0001t0003g0341 a0001c0001t0003g0344 a0001c0001t0003g0345 others(9): Show |
12 | HG00735.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+4639C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68739899 | |||||||
chr2:68739910 | GA | G | 5 | a0002c0004t0001g0332 a0002c0004t0003g0346 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+4660delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68739910 | ||||||
chr2:68740113 | G | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+4853G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740113 | |||||||
chr2:68740129 | C | T | 2 | a0001c0001t0001g0280 a0003c0003t0001g0279 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61+4869C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740129 | |||||||
chr2:68740249 | G | T | 1 | a0002c0020t0001g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61+4989G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740249 | |||||||
chr2:68740357 | G | T | 100 | a0001c0001t0001g0010 a0001c0001t0001g0180 a0001c0001t0001g0184 others(97): Show |
101 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.61+5097G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740357 | |||||||
chr2:68740624 | G | T | 2 | a0002c0004t0001g0323 a0003c0003t0001g0322 |
2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61+5364G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740624 | |||||||
chr2:68740772 | T | C | 1 | a0002c0012t0002g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61+5512T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740772 | |||||||
chr2:68740916 | G | A | 1 | a0003c0003t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.61+5656G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740916 | |||||||
chr2:68740996 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+5736C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68740996 | |||||||
chr2:68741055 | A | G | 11 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+5795A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741055 | |||||||
chr2:68741129 | C | T | 10 | a0001c0001t0001g0276 a0001c0001t0002g0262 a0001c0001t0008g0278 others(7): Show |
11 | HG02451.hp2 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+5869C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741129 | |||||||
chr2:68741178 | G | T | 1 | a0001c0001t0002g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.61+5918G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741178 | |||||||
chr2:68741286 | C | T | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+6026C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741286 | |||||||
chr2:68741287 | G | C | 1 | a0001c0001t0001g0283 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.61+6027G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741287 | |||||||
chr2:68741540 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0023 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.61+6280A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741540 | |||||||
chr2:68741635 | G | T | 8 | a0001c0001t0003g0005 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
9 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+6375G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741635 | |||||||
chr2:68741665 | C | A | 5 | a0002c0002t0001g0266 a0002c0008t0008g0006 a0002c0008t0008g0076 others(2): Show |
6 | HG01099.hp1 HG01123.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+6405C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741665 | |||||||
chr2:68741711 | T | A | 1 | a0003c0003t0001g0064 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.61+6451T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741711 | |||||||
chr2:68741839 | T | C | 11 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+6579T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68741839 | |||||||
chr2:68742054 | C | T | 1 | a0002c0004t0001g0323 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.61+6794C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742054 | |||||||
chr2:68742308 | A | G | 61 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0283 others(58): Show |
62 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.61+7048A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742308 | |||||||
chr2:68742396 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.61+7136T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742396 | |||||||
chr2:68742470 | G | A | 12 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
12 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+7210G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742470 | |||||||
chr2:68742475 | A | T | 11 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+7215A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742475 | |||||||
chr2:68742481 | G | C | 2 | a0001c0001t0001g0283 a0003c0003t0001g0284 |
2 | HG02015.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.61+7221G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742481 | |||||||
chr2:68742744 | T | A | 1 | a0001c0001t0002g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.61+7484T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742744 | |||||||
chr2:68742772 | A | G | 249 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(246): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.61+7512A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68742772 | |||||||
chr2:68743049 | A | C | 103 | a0001c0001t0001g0010 a0001c0001t0001g0172 a0001c0001t0001g0180 others(100): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.61+7789A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743049 | |||||||
chr2:68743209 | C | T | 70 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0001t0001g0281 others(67): Show |
72 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.61+7949C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743209 | |||||||
chr2:68743329 | A | ACAAGTGG others(13): Show |
248 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(245): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.61+8069_61+8070ins others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743329 | |||||||
chr2:68743344 | A | G | 11 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+8084A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743344 | |||||||
chr2:68743371 | C | G | 11 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+8111C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743371 | |||||||
chr2:68743421 | G | A | 9 | a0001c0001t0003g0005 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
10 | HG01891.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+8161G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743421 | |||||||
chr2:68743465 | C | T | 6 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+8205C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743465 | |||||||
chr2:68743507 | C | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+8247C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743507 | |||||||
chr2:68743565 | T | G | 2 | a0001c0001t0001g0280 a0003c0003t0001g0279 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61+8305T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743565 | |||||||
chr2:68743579 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.61+8319G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743579 | |||||||
chr2:68743592 | T | C | 4 | a0001c0001t0001g0271 a0001c0001t0002g0088 a0002c0007t0007g0264 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+8332T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743592 | |||||||
chr2:68743773 | T | A | 1 | a0004c0009t0007g0350 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.61+8513T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743773 | |||||||
chr2:68743815 | C | T | 11 | a0001c0001t0005g0046 a0002c0002t0005g0044 a0002c0002t0010g0045 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+8555C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68743815 | |||||||
chr2:68744068 | G | GTCATGCT others(60): Show |
1 | a0002c0002t0003g0136 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.61+8811_61+8877dup others(67): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68744068 | ||||||
chr2:68744137 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.61+8877C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744137 | |||||||
chr2:68744216 | A | G | 1 | a0003c0003t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61+8956A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744216 | |||||||
chr2:68744239 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+8979C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744239 | |||||||
chr2:68744260 | A | T | 2 | a0002c0004t0001g0323 a0003c0003t0001g0322 |
2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61+9000A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744260 | |||||||
chr2:68744306 | C | G | 14 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0005g0046 others(11): Show |
14 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+9046C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744306 | |||||||
chr2:68744433 | A | G | 57 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(54): Show |
58 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+9173A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744433 | |||||||
chr2:68744485 | A | G | 57 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(54): Show |
58 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+9225A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744485 | |||||||
chr2:68744552 | T | A | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+9292T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744552 | |||||||
chr2:68744552 | T | G | 244 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(241): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.61+9292T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744552 | |||||||
chr2:68744941 | T | C | 251 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(248): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.61+9681T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68744941 | |||||||
chr2:68745020 | T | A | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61+9760T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745020 | |||||||
chr2:68745080 | A | G | 2 | a0001c0001t0002g0179 a0002c0002t0002g0258 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.61+9820A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745080 | |||||||
chr2:68745436 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.61+10176A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745436 | |||||||
chr2:68745492 | C | T | 1 | a0001c0001t0008g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61+10232C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745492 | |||||||
chr2:68745531 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.61+10271C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745531 | |||||||
chr2:68745578 | T | C | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+10318T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745578 | |||||||
chr2:68745594 | G | A | 268 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(265): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.61+10334G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745594 | |||||||
chr2:68745906 | G | A | 1 | a0002c0002t0002g0077 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61+10646G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745906 | |||||||
chr2:68745926 | T | G | 17 | a0001c0001t0002g0262 a0001c0001t0003g0054 a0001c0001t0003g0055 others(14): Show |
18 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+10666T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68745926 | |||||||
chr2:68746012 | A | G | 3 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0010c0018t0001g0277 |
3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.61+10752A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746012 | |||||||
chr2:68746048 | T | A | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+10788T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746048 | |||||||
chr2:68746090 | G | A | 290 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(287): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.61+10830G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746090 | |||||||
chr2:68746174 | C | A | 1 | a0003c0003t0001g0324 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.61+10914C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746174 | |||||||
chr2:68746202 | G | A | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+10942G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746202 | |||||||
chr2:68746206 | C | G | 2 | a0002c0004t0001g0348 a0003c0003t0001g0349 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61+10946C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746206 | |||||||
chr2:68746225 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+10965T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746225 | |||||||
chr2:68746524 | G | A | 3 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0010c0018t0001g0277 |
3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.61+11264G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746524 | |||||||
chr2:68746590 | C | T | 2 | a0001c0001t0002g0179 a0002c0002t0002g0258 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.61+11330C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746590 | |||||||
chr2:68746703 | A | AC | 28 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0090 others(25): Show |
28 | HG00140.hp1 HG01261.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.61+11449dupC | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68746703 | ||||||
chr2:68746703 | A | ACC | 83 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0294 others(80): Show |
87 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+11448_61+11449d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68746703 | ||||||
chr2:68746708 | C | CCG | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+11449_61+11450i others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68746708 | ||||||
chr2:68746708 | C | CG | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+11448_61+11449i others(3): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746708 | |||||||
chr2:68746709 | C | T | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.61+11449C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746709 | |||||||
chr2:68746709 | CT | C | 7 | a0001c0001t0003g0137 a0002c0002t0001g0182 a0002c0002t0002g0181 others(4): Show |
7 | HG01243.hp2 HG02145.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+11450delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746709 | |||||||
chr2:68746710 | T | C | 236 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(233): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.61+11450T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746710 | |||||||
chr2:68746716 | T | A | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+11456T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746716 | |||||||
chr2:68746734 | C | T | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+11474C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746734 | |||||||
chr2:68746801 | G | A | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61+11541G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746801 | |||||||
chr2:68746835 | C | G | 1 | a0001c0001t0003g0345 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.61+11575C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746835 | |||||||
chr2:68746863 | C | A | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+11603C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746863 | |||||||
chr2:68746867 | G | T | 1 | a0002c0002t0006g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.61+11607G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746867 | |||||||
chr2:68746900 | C | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0003c0006t0003g0165 |
5 | NA18960.hp1 NA19068.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+11640C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68746900 | |||||||
chr2:68747008 | CA | C | 266 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(263): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.61+11768delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68747008 | ||||||
chr2:68747130 | G | C | 52 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(49): Show |
53 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.61+11870G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747130 | |||||||
chr2:68747132 | C | G | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61+11872C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747132 | |||||||
chr2:68747175 | C | G | 1 | a0003c0003t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.61+11915C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747175 | |||||||
chr2:68747189 | A | T | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+11929A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747189 | |||||||
chr2:68747192 | T | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+11932T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747192 | |||||||
chr2:68747225 | T | C | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+11965T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747225 | |||||||
chr2:68747250 | C | T | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+11990C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747250 | |||||||
chr2:68747318 | C | A | 1 | a0007c0013t0001g0092 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.61+12058C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747318 | |||||||
chr2:68747333 | G | T | 1 | a0003c0003t0001g0329 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.61+12073G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747333 | |||||||
chr2:68747346 | C | T | 16 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(13): Show |
17 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+12086C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747346 | |||||||
chr2:68747405 | G | A | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+12145G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747405 | |||||||
chr2:68747416 | C | A | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12156C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747416 | |||||||
chr2:68747448 | G | T | 21 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
22 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.61+12188G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747448 | |||||||
chr2:68747457 | G | C | 289 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.61+12197G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747457 | |||||||
chr2:68747516 | C | T | 1 | a0002c0002t0011g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.61+12256C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747516 | |||||||
chr2:68747535 | C | T | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12275C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747535 | |||||||
chr2:68747595 | G | T | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12335G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747595 | |||||||
chr2:68747888 | C | CT | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+12629dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68747888 | ||||||
chr2:68747996 | G | C | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61+12736G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68747996 | |||||||
chr2:68748023 | G | A | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+12763G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748023 | |||||||
chr2:68748112 | G | C | 295 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(292): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.61+12852G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748112 | |||||||
chr2:68748334 | A | G | 1 | a0002c0002t0014g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.61+13074A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748334 | |||||||
chr2:68748357 | C | A | 2 | a0002c0002t0017g0308 a0002c0002t0017g0309 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.61+13097C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748357 | |||||||
chr2:68748574 | T | C | 216 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(213): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.61+13314T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748574 | |||||||
chr2:68748575 | G | A | 1 | a0002c0002t0002g0267 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.61+13315G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748575 | |||||||
chr2:68748633 | A | AT | 14 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(11): Show |
14 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+13382dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68748633 | ||||||
chr2:68748722 | C | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+13462C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748722 | |||||||
chr2:68748770 | T | C | 239 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(236): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.61+13510T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748770 | |||||||
chr2:68748787 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0023 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.61+13527G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68748787 | |||||||
chr2:68749083 | T | C | 5 | a0001c0001t0003g0005 a0002c0002t0004g0051 a0002c0002t0004g0053 others(2): Show |
6 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+13823T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749083 | |||||||
chr2:68749216 | T | A | 289 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.61+13956T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749216 | |||||||
chr2:68749472 | G | T | 100 | a0001c0001t0001g0010 a0001c0001t0001g0180 a0001c0001t0001g0184 others(97): Show |
101 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.61+14212G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749472 | |||||||
chr2:68749503 | G | A | 1 | a0002c0002t0004g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+14243G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749503 | |||||||
chr2:68749564 | C | T | 4 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0005c0011t0001g0273 others(1): Show |
4 | HG02886.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+14304C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749564 | |||||||
chr2:68749599 | C | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+14339C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749599 | |||||||
chr2:68749773 | C | T | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+14513C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749773 | |||||||
chr2:68749865 | G | A | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+14605G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749865 | |||||||
chr2:68749894 | T | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+14634T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68749894 | |||||||
chr2:68750033 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | NA18984.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.61+14773G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750033 | |||||||
chr2:68750046 | G | A | 259 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(256): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.61+14786G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750046 | |||||||
chr2:68750069 | T | C | 1 | a0002c0002t0002g0194 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.61+14809T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750069 | |||||||
chr2:68750080 | C | T | 2 | a0001c0001t0001g0280 a0003c0003t0001g0279 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61+14820C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750080 | |||||||
chr2:68750122 | C | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(52): Show |
58 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+14862C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750122 | |||||||
chr2:68750145 | C | T | 225 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(222): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.61+14885C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750145 | |||||||
chr2:68750154 | G | A | 3 | a0002c0004t0005g0060 a0002c0007t0016g0059 a0008c0017t0016g0061 |
3 | HG02055.hp2 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+14894G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750154 | |||||||
chr2:68750173 | A | AT | 260 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(257): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.61+14926dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68750173 | ||||||
chr2:68750225 | G | A | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+14965G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750225 | |||||||
chr2:68750322 | CTT | C | 255 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(252): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.61+15078_61+15079d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68750322 | ||||||
chr2:68750447 | C | T | 2 | a0002c0004t0001g0348 a0003c0003t0001g0349 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61+15187C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750447 | |||||||
chr2:68750448 | A | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15188A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750448 | |||||||
chr2:68750476 | C | A | 3 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0010c0018t0001g0277 |
3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.61+15216C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750476 | |||||||
chr2:68750496 | T | C | 1 | a0003c0003t0001g0093 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.61+15236T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750496 | |||||||
chr2:68750513 | G | A | 260 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(257): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.61+15253G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750513 | |||||||
chr2:68750602 | C | A | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15342C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750602 | |||||||
chr2:68750610 | C | T | 2 | a0001c0001t0001g0280 a0003c0003t0001g0279 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61+15350C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750610 | |||||||
chr2:68750621 | G | A | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+15361G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750621 | |||||||
chr2:68750668 | G | A | 1 | a0002c0002t0002g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61+15408G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750668 | |||||||
chr2:68750725 | T | C | 2 | a0002c0002t0001g0182 a0002c0002t0002g0181 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.61+15465T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750725 | |||||||
chr2:68750747 | G | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15487G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750747 | |||||||
chr2:68750804 | C | T | 2 | a0001c0001t0001g0280 a0003c0003t0001g0279 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61+15544C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750804 | |||||||
chr2:68750822 | A | G | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+15562A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750822 | |||||||
chr2:68750834 | A | T | 6 | a0001c0001t0003g0005 a0002c0002t0004g0047 a0002c0002t0004g0051 others(3): Show |
7 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+15574A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750834 | |||||||
chr2:68750837 | G | C | 3 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0010c0018t0001g0277 |
3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.61+15577G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68750837 | |||||||
chr2:68751027 | C | T | 2 | a0002c0004t0001g0332 a0002c0004t0003g0346 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.61+15767C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751027 | |||||||
chr2:68751047 | C | T | 1 | a0003c0003t0001g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.61+15787C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751047 | |||||||
chr2:68751056 | C | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15796C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751056 | |||||||
chr2:68751098 | C | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15838C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751098 | |||||||
chr2:68751099 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(261): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.61+15839A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751099 | |||||||
chr2:68751115 | A | G | 7 | a0001c0001t0001g0253 a0001c0001t0003g0139 a0001c0001t0003g0158 others(4): Show |
7 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+15855A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751115 | |||||||
chr2:68751180 | C | T | 6 | a0001c0001t0003g0345 a0001c0001t0005g0046 a0002c0002t0010g0045 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+15920C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751180 | |||||||
chr2:68751181 | G | A | 1 | a0002c0002t0002g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.61+15921G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751181 | |||||||
chr2:68751428 | G | A | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+16168G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751428 | |||||||
chr2:68751477 | G | A | 3 | a0001c0001t0002g0262 a0002c0002t0001g0263 a0006c0010t0007g0011 |
4 | HG02809.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+16217G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751477 | |||||||
chr2:68751645 | C | T | 1 | a0001c0001t0005g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61+16385C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751645 | |||||||
chr2:68751799 | C | A | 1 | a0002c0002t0010g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61+16539C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751799 | |||||||
chr2:68751802 | T | A | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+16542T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751802 | |||||||
chr2:68751808 | A | G | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.61+16548A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68751808 | |||||||
chr2:68752009 | A | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(53): Show |
59 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+16749A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752009 | |||||||
chr2:68752036 | A | G | 2 | a0001c0001t0001g0280 a0003c0003t0001g0279 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.61+16776A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752036 | |||||||
chr2:68752044 | T | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+16784T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752044 | |||||||
chr2:68752054 | G | T | 156 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(153): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.61+16794G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752054 | |||||||
chr2:68752154 | C | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0311 a0002c0004t0001g0290 others(1): Show |
5 | HG02647.hp2 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+16894C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752154 | |||||||
chr2:68752170 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(52): Show |
58 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+16910G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752170 | |||||||
chr2:68752191 | T | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.61+16931T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752191 | |||||||
chr2:68752199 | G | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(53): Show |
59 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+16939G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752199 | |||||||
chr2:68752255 | T | A | 2 | a0002c0002t0001g0182 a0002c0002t0002g0181 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.61+16995T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752255 | |||||||
chr2:68752301 | AATGAAAT others(43): Show |
A | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+17044_61+17093d others(52): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68752301 | ||||||
chr2:68752437 | A | G | 267 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.61+17177A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752437 | |||||||
chr2:68752452 | A | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+17192A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752452 | |||||||
chr2:68752472 | A | G | 267 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.61+17212A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752472 | |||||||
chr2:68752524 | C | G | 12 | a0001c0001t0001g0276 a0001c0001t0002g0262 a0001c0001t0003g0054 others(9): Show |
13 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+17264C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752524 | |||||||
chr2:68752577 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.61+17317G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752577 | |||||||
chr2:68752594 | C | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.61+17334C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752594 | |||||||
chr2:68752747 | G | GC | 267 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.61+17488dupC | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68752747 | ||||||
chr2:68752872 | A | C | 250 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0081 others(247): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.61+17612A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752872 | |||||||
chr2:68752969 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0002c0007t0007g0016 |
3 | HG02965.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.61+17709C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68752969 | |||||||
chr2:68753057 | A | C | 267 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.61+17797A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753057 | |||||||
chr2:68753077 | A | AT | 5 | a0002c0002t0002g0251 a0002c0002t0002g0252 a0002c0002t0002g0255 others(2): Show |
5 | HG01928.hp1 HG01978.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+17818dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68753077 | ||||||
chr2:68753078 | T | TG | 98 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0180 others(95): Show |
100 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.61+17826dupG | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68753078 | ||||||
chr2:68753101 | C | A | 1 | a0001c0001t0002g0262 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.61+17841C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753101 | |||||||
chr2:68753221 | C | T | 11 | a0001c0001t0003g0005 a0001c0001t0008g0278 a0002c0002t0004g0047 others(8): Show |
12 | HG01891.hp1 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+17961C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753221 | |||||||
chr2:68753258 | A | G | 1 | a0002c0002t0006g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.61+17998A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753258 | |||||||
chr2:68753328 | T | C | 2 | a0001c0001t0001g0184 a0003c0003t0001g0196 |
2 | HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.61+18068T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753328 | |||||||
chr2:68753414 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+18154A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753414 | |||||||
chr2:68753498 | G | T | 2 | a0002c0002t0001g0268 a0002c0002t0003g0136 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.61+18238G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753498 | |||||||
chr2:68753585 | G | C | 7 | a0003c0003t0009g0004 a0003c0003t0009g0033 a0003c0003t0009g0034 others(4): Show |
8 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+18325G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753585 | |||||||
chr2:68753601 | T | A | 296 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(293): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.61+18341T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753601 | |||||||
chr2:68753606 | T | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+18346T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753606 | |||||||
chr2:68753637 | G | A | 249 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0081 others(246): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.61+18377G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753637 | |||||||
chr2:68753664 | G | T | 1 | a0003c0003t0001g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.61+18404G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753664 | |||||||
chr2:68753729 | G | T | 1 | a0003c0003t0001g0249 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.61+18469G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753729 | |||||||
chr2:68753830 | G | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.61+18570G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753830 | |||||||
chr2:68753904 | A | AT | 70 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(67): Show |
73 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.61+18660dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68753904 | ||||||
chr2:68753904 | AT | A | 27 | a0001c0001t0001g0017 a0001c0001t0001g0081 a0001c0001t0001g0082 others(24): Show |
28 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.61+18660delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68753904 | ||||||
chr2:68753933 | C | T | 1 | a0001c0001t0003g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.61+18673C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68753933 | |||||||
chr2:68754125 | G | C | 160 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(157): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.61+18865G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754125 | |||||||
chr2:68754238 | T | C | 3 | a0002c0004t0005g0060 a0002c0007t0016g0059 a0008c0017t0016g0061 |
3 | HG02055.hp2 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+18978T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754238 | |||||||
chr2:68754239 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+18979C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754239 | |||||||
chr2:68754241 | A | G | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.61+18981A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754241 | |||||||
chr2:68754306 | ATGCTTT | A | 270 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(267): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.61+19054_61+19059d others(8): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68754306 | ||||||
chr2:68754465 | A | G | 292 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(289): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.61+19205A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754465 | |||||||
chr2:68754526 | G | A | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+19266G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754526 | |||||||
chr2:68754593 | A | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+19333A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754593 | |||||||
chr2:68754601 | G | A | 1 | a0003c0003t0001g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.61+19341G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754601 | |||||||
chr2:68754670 | G | A | 266 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0081 others(263): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.61+19410G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754670 | |||||||
chr2:68754768 | T | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+19508T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68754768 | |||||||
chr2:68754932 | CT | C | 91 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(88): Show |
94 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.61+19677delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68754932 | ||||||
chr2:68755227 | C | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+19967C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755227 | |||||||
chr2:68755434 | T | C | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.62-19787T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755434 | |||||||
chr2:68755467 | A | G | 263 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(260): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.62-19754A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755467 | |||||||
chr2:68755506 | C | T | 10 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0002c0002t0006g0188 others(7): Show |
10 | HG00735.hp1 HG01109.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-19715C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755506 | |||||||
chr2:68755519 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-19702A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755519 | |||||||
chr2:68755521 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.62-19700C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755521 | |||||||
chr2:68755601 | C | T | 263 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(260): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.62-19620C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755601 | |||||||
chr2:68755632 | G | A | 7 | a0001c0001t0001g0253 a0001c0001t0003g0139 a0001c0001t0003g0158 others(4): Show |
7 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-19589G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755632 | |||||||
chr2:68755651 | CT | C | 263 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(260): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.62-19564delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68755651 | ||||||
chr2:68755728 | T | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-19493T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755728 | |||||||
chr2:68755744 | T | C | 292 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(289): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.62-19477T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755744 | |||||||
chr2:68755914 | G | A | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-19307G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755914 | |||||||
chr2:68755952 | A | G | 10 | a0001c0001t0001g0280 a0001c0001t0002g0262 a0001c0001t0008g0278 others(7): Show |
11 | HG02622.hp2 HG02809.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-19269A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755952 | |||||||
chr2:68755991 | T | C | 1 | a0001c0001t0002g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.62-19230T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68755991 | |||||||
chr2:68756024 | C | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-19197C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756024 | |||||||
chr2:68756069 | C | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-19152C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756069 | |||||||
chr2:68756085 | G | A | 159 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(156): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.62-19136G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756085 | |||||||
chr2:68756194 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.62-19027C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756194 | |||||||
chr2:68756253 | G | C | 29 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.62-18968G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756253 | |||||||
chr2:68756263 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-18958C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756263 | |||||||
chr2:68756308 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.62-18913T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756308 | |||||||
chr2:68756336 | A | T | 263 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(260): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.62-18885A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756336 | |||||||
chr2:68756519 | C | G | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-18702C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756519 | |||||||
chr2:68756743 | G | T | 200 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(197): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.62-18478G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756743 | |||||||
chr2:68756894 | A | C | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-18327A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756894 | |||||||
chr2:68756935 | T | C | 6 | a0001c0001t0003g0005 a0002c0002t0004g0047 a0002c0002t0004g0051 others(3): Show |
7 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-18286T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756935 | |||||||
chr2:68756985 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-18236T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68756985 | |||||||
chr2:68757267 | G | A | 1 | a0002c0002t0023g0066 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.62-17954G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757267 | |||||||
chr2:68757388 | G | T | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-17833G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757388 | |||||||
chr2:68757466 | G | A | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-17755G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757466 | |||||||
chr2:68757516 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-17705A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757516 | |||||||
chr2:68757573 | A | C | 6 | a0001c0001t0003g0005 a0002c0002t0004g0047 a0002c0002t0004g0051 others(3): Show |
7 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-17648A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757573 | |||||||
chr2:68757695 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.62-17526T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757695 | |||||||
chr2:68757741 | C | G | 3 | a0002c0002t0001g0094 a0002c0002t0001g0126 a0002c0002t0001g0127 |
3 | HG01070.hp2 HG01071.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.62-17480C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757741 | |||||||
chr2:68757749 | T | A | 292 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(289): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.62-17472T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757749 | |||||||
chr2:68757764 | G | A | 263 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(260): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.62-17457G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757764 | |||||||
chr2:68757992 | C | A | 5 | a0002c0004t0001g0332 a0002c0004t0003g0346 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-17229C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68757992 | |||||||
chr2:68758012 | AAAGTT | A | 3 | a0002c0002t0005g0044 a0002c0002t0017g0308 a0002c0002t0017g0309 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.62-17203_62-17199d others(7): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68758012 | ||||||
chr2:68758017 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.62-17204T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758017 | |||||||
chr2:68758152 | A | C | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-17069A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758152 | |||||||
chr2:68758752 | A | G | 1 | a0002c0002t0002g0241 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.62-16469A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758752 | |||||||
chr2:68758781 | C | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62-16440C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758781 | |||||||
chr2:68758790 | A | G | 3 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0010c0018t0001g0277 |
3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-16431A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758790 | |||||||
chr2:68758894 | G | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62-16327G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758894 | |||||||
chr2:68758943 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-16278A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758943 | |||||||
chr2:68758953 | T | G | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-16268T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68758953 | |||||||
chr2:68759071 | A | G | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02523.hp2 NA18955.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-16150A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759071 | |||||||
chr2:68759287 | A | T | 1 | a0003c0003t0003g0161 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.62-15934A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759287 | |||||||
chr2:68759289 | A | C | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-15932A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759289 | |||||||
chr2:68759329 | C | G | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-15892C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759329 | |||||||
chr2:68759336 | G | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62-15885G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759336 | |||||||
chr2:68759340 | A | C | 15 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(12): Show |
16 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.62-15881A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759340 | |||||||
chr2:68759413 | C | G | 101 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(98): Show |
104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.62-15808C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759413 | |||||||
chr2:68759431 | A | T | 291 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(288): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.62-15790A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759431 | |||||||
chr2:68759480 | A | C | 101 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(98): Show |
104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.62-15741A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759480 | |||||||
chr2:68759595 | A | G | 101 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(98): Show |
104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.62-15626A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759595 | |||||||
chr2:68759621 | AAG | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-15598_62-15597d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68759621 | ||||||
chr2:68759625 | C | T | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-15596C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759625 | |||||||
chr2:68759626 | C | T | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-15595C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759626 | |||||||
chr2:68759627 | T | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-15594T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759627 | |||||||
chr2:68759629 | A | G | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-15592A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759629 | |||||||
chr2:68759630 | T | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-15591T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759630 | |||||||
chr2:68759771 | A | T | 101 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(98): Show |
104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.62-15450A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759771 | |||||||
chr2:68759960 | C | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-15261C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759960 | |||||||
chr2:68759961 | G | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62-15260G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68759961 | |||||||
chr2:68760013 | A | G | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-15208A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760013 | |||||||
chr2:68760153 | A | G | 2 | a0002c0012t0001g0086 a0002c0012t0002g0073 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.62-15068A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760153 | |||||||
chr2:68760335 | C | G | 3 | a0002c0002t0002g0251 a0002c0002t0002g0252 a0002c0002t0002g0269 |
3 | HG01928.hp1 HG01978.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.62-14886C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760335 | |||||||
chr2:68760335 | C | T | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.62-14886C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760335 | |||||||
chr2:68760419 | A | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0063 others(9): Show |
18 | HG00597.hp1 HG02129.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-14802A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760419 | |||||||
chr2:68760564 | A | G | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62-14657A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760564 | |||||||
chr2:68760689 | A | G | 1 | a0002c0002t0002g0240 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.62-14532A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760689 | |||||||
chr2:68760863 | CA | C | 20 | a0001c0001t0001g0271 a0001c0001t0002g0088 a0001c0001t0005g0029 others(17): Show |
21 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.62-14340delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68760863 | ||||||
chr2:68760880 | AAT | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(64): Show |
70 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.62-14340_62-14339d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760880 | |||||||
chr2:68760881 | AT | A | 173 | a0001c0001t0001g0010 a0001c0001t0001g0089 a0001c0001t0001g0135 others(170): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.62-14335delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68760881 | ||||||
chr2:68760882 | T | A | 32 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(29): Show |
32 | HG00099.hp2 HG01167.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.62-14339T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68760882 | |||||||
chr2:68761414 | C | T | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-13807C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761414 | |||||||
chr2:68761422 | A | G | 159 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(156): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.62-13799A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761422 | |||||||
chr2:68761440 | T | TA | 15 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(12): Show |
16 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.62-13775dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68761440 | ||||||
chr2:68761491 | G | C | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.62-13730G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761491 | |||||||
chr2:68761532 | CA | C | 157 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(154): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.62-13680delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68761532 | ||||||
chr2:68761541 | A | C | 1 | a0002c0002t0003g0156 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-13680A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761541 | |||||||
chr2:68761581 | A | G | 171 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62-13640A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761581 | |||||||
chr2:68761780 | T | C | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-13441T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761780 | |||||||
chr2:68761874 | C | T | 16 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(13): Show |
17 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-13347C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761874 | |||||||
chr2:68761958 | A | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-13263A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68761958 | |||||||
chr2:68762065 | A | T | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-13156A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762065 | |||||||
chr2:68762066 | T | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-13155T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762066 | |||||||
chr2:68762080 | A | G | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-13141A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762080 | |||||||
chr2:68762083 | G | A | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-13138G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762083 | |||||||
chr2:68762174 | A | C | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-13047A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762174 | |||||||
chr2:68762262 | T | C | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-12959T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762262 | |||||||
chr2:68762319 | T | C | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-12902T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762319 | |||||||
chr2:68762330 | G | T | 2 | a0002c0002t0001g0008 a0009c0019t0001g0008 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.62-12891G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762330 | |||||||
chr2:68762393 | T | TA | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-12827dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68762393 | ||||||
chr2:68762487 | T | A | 1 | a0002c0002t0011g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.62-12734T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762487 | |||||||
chr2:68762556 | T | G | 3 | a0001c0001t0001g0096 a0002c0002t0001g0128 a0002c0002t0001g0129 |
3 | HG01074.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.62-12665T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762556 | |||||||
chr2:68762559 | C | T | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-12662C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762559 | |||||||
chr2:68762586 | C | G | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.62-12635C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762586 | |||||||
chr2:68762788 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.62-12433G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762788 | |||||||
chr2:68762839 | T | A | 1 | a0002c0020t0001g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.62-12382T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68762839 | |||||||
chr2:68763084 | A | G | 1 | a0002c0002t0002g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-12137A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763084 | |||||||
chr2:68763186 | C | A | 1 | a0001c0001t0002g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.62-12035C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763186 | |||||||
chr2:68763297 | A | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-11924A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763297 | |||||||
chr2:68763482 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.62-11739C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763482 | |||||||
chr2:68763720 | C | T | 5 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0005c0011t0001g0273 others(2): Show |
5 | HG02622.hp2 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-11501C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763720 | |||||||
chr2:68763888 | T | A | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-11333T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763888 | |||||||
chr2:68763923 | A | G | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-11298A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763923 | |||||||
chr2:68763954 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.62-11267G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763954 | |||||||
chr2:68763974 | T | C | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62-11247T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68763974 | |||||||
chr2:68764304 | A | G | 7 | a0001c0001t0001g0253 a0001c0001t0003g0139 a0001c0001t0003g0158 others(4): Show |
7 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-10917A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68764304 | |||||||
chr2:68764350 | C | T | 260 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0081 others(257): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.62-10871C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68764350 | |||||||
chr2:68764434 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-10787G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68764434 | |||||||
chr2:68764482 | G | A | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-10739G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68764482 | |||||||
chr2:68764750 | A | G | 11 | a0001c0001t0001g0280 a0001c0001t0002g0262 a0001c0001t0008g0278 others(8): Show |
12 | HG02451.hp2 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-10471A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68764750 | |||||||
chr2:68764833 | T | G | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-10388T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68764833 | |||||||
chr2:68765006 | C | T | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-10215C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68765006 | |||||||
chr2:68765056 | T | G | 15 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(12): Show |
16 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.62-10165T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68765056 | |||||||
chr2:68765245 | C | T | 1 | a0003c0003t0005g0026 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.62-9976C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68765245 | |||||||
chr2:68765360 | T | TA | 167 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(164): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.62-9848dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68765360 | ||||||
chr2:68765486 | C | T | 1 | a0003c0003t0001g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.62-9735C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68765486 | |||||||
chr2:68765515 | G | A | 2 | a0002c0002t0001g0008 a0009c0019t0001g0008 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.62-9706G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68765515 | |||||||
chr2:68765666 | C | T | 100 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(97): Show |
103 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.62-9555C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68765666 | |||||||
chr2:68766186 | C | T | 1 | a0002c0008t0008g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.62-9035C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68766186 | |||||||
chr2:68766270 | C | A | 78 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0283 others(75): Show |
81 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.62-8951C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68766270 | |||||||
chr2:68766301 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.62-8920T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68766301 | |||||||
chr2:68766714 | T | TTCTC | 4 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0002c0004t0001g0348 others(1): Show |
4 | HG01243.hp2 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-8491_62-8488dup others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68766714 | ||||||
chr2:68766714 | T | TTCTCTCT others(1): Show |
8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-8495_62-8488dup others(8): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68766714 | ||||||
chr2:68766732 | CTT | C | 6 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0003c0003t0003g0161 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-8488_62-8487del others(2): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68766732 | |||||||
chr2:68766767 | T | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG00099.hp2 HG01255.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-8454T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68766767 | |||||||
chr2:68766945 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-8276G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68766945 | |||||||
chr2:68767025 | G | A | 1 | a0012c0015t0003g0160 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.62-8196G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767025 | |||||||
chr2:68767122 | G | A | 5 | a0001c0001t0005g0046 a0002c0002t0010g0045 a0002c0004t0005g0060 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-8099G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767122 | |||||||
chr2:68767222 | T | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0002c0002t0001g0260 others(7): Show |
11 | HG00423.hp2 NA18747.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-7999T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767222 | |||||||
chr2:68767330 | A | C | 58 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(55): Show |
59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.62-7891A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767330 | |||||||
chr2:68767359 | G | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0203 a0001c0001t0001g0257 others(4): Show |
7 | HG00621.hp1 HG02015.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-7862G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767359 | |||||||
chr2:68767366 | A | G | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-7855A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767366 | |||||||
chr2:68767374 | G | A | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.62-7847G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767374 | |||||||
chr2:68767456 | C | T | 11 | a0001c0001t0003g0005 a0001c0001t0005g0046 a0002c0002t0004g0047 others(8): Show |
12 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-7765C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767456 | |||||||
chr2:68767466 | G | A | 160 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(157): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.62-7755G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767466 | |||||||
chr2:68767765 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.62-7456G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767765 | |||||||
chr2:68767791 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.62-7430C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767791 | |||||||
chr2:68767937 | A | G | 272 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(269): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.62-7284A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68767937 | |||||||
chr2:68768257 | C | T | 53 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(50): Show |
54 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.62-6964C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768257 | |||||||
chr2:68768320 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.62-6901A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768320 | |||||||
chr2:68768421 | A | G | 1 | a0003c0003t0005g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.62-6800A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768421 | |||||||
chr2:68768531 | A | G | 160 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0089 others(157): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.62-6690A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768531 | |||||||
chr2:68768641 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-6580G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768641 | |||||||
chr2:68768771 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.62-6450C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768771 | |||||||
chr2:68768879 | T | A | 2 | a0003c0003t0001g0292 a0003c0003t0001g0293 |
2 | NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.62-6342T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68768879 | |||||||
chr2:68769006 | C | T | 1 | a0002c0002t0003g0156 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-6215C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769006 | |||||||
chr2:68769092 | T | G | 1 | a0001c0001t0001g0237 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.62-6129T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769092 | |||||||
chr2:68769093 | A | G | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-6128A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769093 | |||||||
chr2:68769282 | G | A | 1 | a0002c0002t0002g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.62-5939G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769282 | |||||||
chr2:68769329 | C | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(168): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62-5892C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769329 | |||||||
chr2:68769536 | A | G | 204 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(201): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.62-5685A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769536 | |||||||
chr2:68769583 | T | A | 1 | a0001c0001t0003g0050 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.62-5638T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769583 | |||||||
chr2:68769617 | A | G | 60 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0294 others(57): Show |
61 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.62-5604A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769617 | |||||||
chr2:68769657 | G | T | 244 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(241): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.62-5564G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769657 | |||||||
chr2:68769705 | C | A | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-5516C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769705 | |||||||
chr2:68769758 | A | G | 1 | a0002c0002t0006g0321 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.62-5463A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769758 | |||||||
chr2:68769901 | C | T | 5 | a0001c0001t0003g0005 a0002c0002t0004g0047 a0002c0002t0004g0051 others(2): Show |
6 | HG01891.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5320C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68769901 | |||||||
chr2:68770012 | A | C | 121 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(118): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.62-5209A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770012 | |||||||
chr2:68770021 | A | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0089 others(73): Show |
78 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.62-5200A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770021 | |||||||
chr2:68770022 | C | T | 7 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0003c0003t0001g0171 others(4): Show |
7 | HG00280.hp2 HG00597.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-5199C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770022 | |||||||
chr2:68770050 | T | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG01255.hp1 HG01496.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5171T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770050 | |||||||
chr2:68770118 | G | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0089 others(75): Show |
81 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.62-5103G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770118 | |||||||
chr2:68770138 | G | A | 2 | a0002c0004t0002g0024 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-5083G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770138 | |||||||
chr2:68770288 | G | A | 240 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(237): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.62-4933G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770288 | |||||||
chr2:68770539 | G | A | 1 | a0002c0002t0002g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.62-4682G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770539 | |||||||
chr2:68770631 | C | A | 6 | a0002c0002t0005g0044 a0002c0002t0017g0308 a0002c0002t0017g0309 others(3): Show |
6 | HG01109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-4590C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770631 | |||||||
chr2:68770684 | A | G | 28 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(25): Show |
29 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.62-4537A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770684 | |||||||
chr2:68770912 | C | T | 2 | a0001c0001t0008g0278 a0002c0004t0001g0348 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.62-4309C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68770912 | |||||||
chr2:68771009 | CCACGAAA | C | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-4208_62-4202del others(7): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 68771009 | ||||||
chr2:68771058 | G | A | 2 | a0001c0001t0004g0336 a0001c0001t0013g0337 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.62-4163G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771058 | |||||||
chr2:68771236 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62-3985A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771236 | |||||||
chr2:68771278 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-3943C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771278 | |||||||
chr2:68771351 | T | G | 1 | a0002c0002t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.62-3870T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771351 | |||||||
chr2:68771555 | T | C | 41 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(38): Show |
41 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.62-3666T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771555 | |||||||
chr2:68771639 | T | G | 28 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(25): Show |
29 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.62-3582T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771639 | |||||||
chr2:68771654 | C | G | 2 | a0002c0004t0002g0024 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-3567C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771654 | |||||||
chr2:68771787 | T | C | 243 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.62-3434T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771787 | |||||||
chr2:68771823 | C | T | 2 | a0002c0004t0002g0024 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-3398C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771823 | |||||||
chr2:68771874 | T | C | 105 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.62-3347T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771874 | |||||||
chr2:68771905 | T | C | 2 | a0001c0001t0001g0180 a0003c0003t0001g0201 |
2 | HG02015.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.62-3316T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68771905 | |||||||
chr2:68772021 | C | T | 242 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.62-3200C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772021 | |||||||
chr2:68772042 | G | A | 2 | a0002c0004t0002g0024 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62-3179G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772042 | |||||||
chr2:68772508 | G | A | 17 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
18 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-2713G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772508 | |||||||
chr2:68772636 | G | A | 9 | a0001c0001t0001g0276 a0001c0001t0003g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-2585G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772636 | |||||||
chr2:68772721 | G | T | 242 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.62-2500G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772721 | |||||||
chr2:68772801 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.62-2420T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772801 | |||||||
chr2:68772999 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(11): Show |
14 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.62-2222G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68772999 | |||||||
chr2:68773168 | A | G | 242 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.62-2053A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773168 | |||||||
chr2:68773364 | T | G | 1 | a0003c0003t0001g0238 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.62-1857T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773364 | |||||||
chr2:68773604 | G | T | 242 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.62-1617G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773604 | |||||||
chr2:68773607 | G | C | 1 | a0002c0002t0011g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.62-1614G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773607 | |||||||
chr2:68773609 | T | C | 1 | a0003c0003t0005g0026 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.62-1612T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773609 | |||||||
chr2:68773615 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-1606C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773615 | |||||||
chr2:68773634 | T | A | 1 | a0002c0002t0002g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-1587T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773634 | |||||||
chr2:68773719 | A | C | 1 | a0002c0002t0005g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-1502A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773719 | |||||||
chr2:68773769 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.62-1452T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773769 | |||||||
chr2:68773879 | G | A | 197 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(194): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.62-1342G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68773879 | |||||||
chr2:68774039 | C | T | 51 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(48): Show |
51 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.62-1182C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68774039 | |||||||
chr2:68774074 | A | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.62-1147A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68774074 | |||||||
chr2:68774333 | G | T | 3 | a0001c0001t0001g0184 a0001c0001t0008g0229 a0003c0003t0001g0196 |
3 | HG02257.hp2 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.62-888G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68774333 | |||||||
chr2:68774435 | A | G | 2 | a0003c0003t0001g0227 a0003c0003t0001g0228 |
2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.62-786A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68774435 | |||||||
chr2:68774495 | T | C | 2 | a0001c0001t0003g0146 a0002c0002t0004g0145 |
2 | HG02040.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.62-726T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68774495 | |||||||
chr2:68774741 | C | T | 6 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(3): Show |
7 | HG01891.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-480C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68774741 | |||||||
chr2:68775130 | C | A | 1 | a0002c0002t0002g0287 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.62-91C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68775130 | |||||||
chr2:68775149 | C | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(60): Show |
64 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.62-72C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | 68775149 | |||||||
chr2:68775485 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.261+65A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775485 | |||||||
chr2:68775570 | C | T | 1 | a0003c0003t0001g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.261+150C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775570 | |||||||
chr2:68775628 | C | T | 97 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.261+208C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775628 | |||||||
chr2:68775850 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0225 |
2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.261+430A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775850 | |||||||
chr2:68775934 | A | G | 1 | a0003c0003t0005g0026 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.261+514A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775934 | |||||||
chr2:68775966 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.261+546G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775966 | |||||||
chr2:68775982 | C | A | 97 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.261+562C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68775982 | |||||||
chr2:68776116 | G | A | 1 | a0003c0003t0001g0009 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.261+696G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776116 | |||||||
chr2:68776149 | G | A | 91 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.261+729G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776149 | |||||||
chr2:68776252 | GGGTCAGG others(24): Show |
G | 22 | a0001c0001t0001g0280 a0001c0001t0005g0029 a0001c0001t0005g0039 others(19): Show |
23 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.261+835_261+865del others(31): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 68776252 | ||||||
chr2:68776325 | G | A | 1 | a0003c0003t0001g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.261+905G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776325 | |||||||
chr2:68776425 | G | A | 1 | a0003c0003t0001g0211 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.261+1005G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776425 | |||||||
chr2:68776486 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0002c0005t0012g0185 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1066G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776486 | |||||||
chr2:68776572 | A | C | 1 | a0002c0002t0002g0072 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.261+1152A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776572 | |||||||
chr2:68776669 | G | C | 28 | a0001c0001t0001g0280 a0001c0001t0005g0029 a0001c0001t0005g0039 others(25): Show |
29 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+1249G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776669 | |||||||
chr2:68776684 | G | A | 6 | a0001c0001t0003g0140 a0001c0001t0003g0147 a0001c0001t0003g0148 others(3): Show |
6 | HG01975.hp2 HG01981.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+1264G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776684 | |||||||
chr2:68776695 | G | A | 1 | a0003c0003t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.261+1275G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776695 | |||||||
chr2:68776744 | G | A | 1 | a0003c0003t0001g0324 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.261+1324G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776744 | |||||||
chr2:68776760 | G | A | 2 | a0001c0001t0001g0130 a0002c0002t0001g0098 |
2 | HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.261+1340G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776760 | |||||||
chr2:68776838 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | NA18956.hp1 NA18959.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+1418G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68776838 | |||||||
chr2:68777061 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(115): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.261+1641A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777061 | |||||||
chr2:68777137 | C | A | 2 | a0002c0002t0002g0230 a0003c0003t0001g0231 |
2 | NA18981.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.261+1717C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777137 | |||||||
chr2:68777163 | C | T | 17 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
18 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.261+1743C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777163 | |||||||
chr2:68777204 | G | A | 17 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
18 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.261+1784G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777204 | |||||||
chr2:68777205 | G | C | 2 | a0002c0002t0010g0027 a0002c0002t0010g0028 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.261+1785G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777205 | |||||||
chr2:68777223 | C | T | 1 | a0003c0003t0005g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.261+1803C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777223 | |||||||
chr2:68777325 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(115): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.261+1905A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777325 | |||||||
chr2:68777354 | G | A | 1 | a0002c0002t0002g0212 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.261+1934G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777354 | |||||||
chr2:68777358 | C | T | 11 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(8): Show |
12 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+1938C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777358 | |||||||
chr2:68777360 | C | T | 3 | a0001c0001t0001g0253 a0001c0001t0001g0306 a0001c0001t0003g0139 |
3 | HG01081.hp1 HG02300.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.261+1940C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777360 | |||||||
chr2:68777515 | A | C | 1 | a0003c0003t0001g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.261+2095A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777515 | |||||||
chr2:68777565 | G | A | 5 | a0001c0001t0001g0280 a0001c0001t0008g0278 a0001c0001t0022g0333 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+2145G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777565 | |||||||
chr2:68777575 | T | A | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.261+2155T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777575 | |||||||
chr2:68777659 | A | G | 88 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(85): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.261+2239A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777659 | |||||||
chr2:68777850 | T | C | 138 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(135): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.261+2430T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68777850 | |||||||
chr2:68778028 | G | C | 32 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(29): Show |
32 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.261+2608G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778028 | |||||||
chr2:68778190 | G | C | 1 | a0003c0003t0001g0235 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.261+2770G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778190 | |||||||
chr2:68778216 | A | T | 90 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.261+2796A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778216 | |||||||
chr2:68778332 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.261+2912G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778332 | |||||||
chr2:68778500 | G | A | 1 | a0002c0002t0011g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.261+3080G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778500 | |||||||
chr2:68778534 | A | G | 11 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(8): Show |
12 | HG01167.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+3114A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778534 | |||||||
chr2:68778724 | G | T | 118 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(115): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.261+3304G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778724 | |||||||
chr2:68778728 | T | C | 1 | a0002c0002t0002g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.261+3308T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778728 | |||||||
chr2:68778746 | G | T | 3 | a0001c0001t0001g0312 a0003c0003t0001g0304 a0003c0003t0015g0305 |
3 | HG00544.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.261+3326G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778746 | |||||||
chr2:68778791 | C | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(104): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.261+3371C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778791 | |||||||
chr2:68778845 | A | G | 6 | a0002c0002t0005g0044 a0002c0002t0017g0308 a0002c0002t0017g0309 others(3): Show |
6 | HG01109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-3388A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778845 | |||||||
chr2:68778955 | A | G | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG01255.hp1 HG01496.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-3278A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778955 | |||||||
chr2:68778991 | T | C | 94 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.262-3242T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68778991 | |||||||
chr2:68779204 | G | A | 6 | a0001c0001t0003g0140 a0001c0001t0003g0147 a0001c0001t0003g0148 others(3): Show |
6 | HG01975.hp2 HG01981.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-3029G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779204 | |||||||
chr2:68779363 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0089 others(87): Show |
92 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.262-2870A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779363 | |||||||
chr2:68779589 | A | C | 90 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.262-2644A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779589 | |||||||
chr2:68779606 | T | C | 88 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(85): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.262-2627T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779606 | |||||||
chr2:68779802 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.262-2431C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779802 | |||||||
chr2:68779881 | A | C | 1 | a0002c0002t0002g0252 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.262-2352A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779881 | |||||||
chr2:68779976 | G | A | 33 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(30): Show |
33 | HG00099.hp2 HG00621.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.262-2257G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68779976 | |||||||
chr2:68780175 | T | A | 10 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(7): Show |
11 | HG01891.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.262-2058T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780175 | |||||||
chr2:68780279 | T | G | 2 | a0001c0001t0003g0146 a0002c0002t0004g0145 |
2 | HG02040.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.262-1954T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780279 | |||||||
chr2:68780317 | G | A | 2 | a0002c0004t0002g0024 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.262-1916G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780317 | |||||||
chr2:68780413 | C | T | 2 | a0002c0004t0002g0024 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.262-1820C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780413 | |||||||
chr2:68780450 | A | G | 1 | a0003c0003t0003g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.262-1783A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780450 | |||||||
chr2:68780518 | A | G | 1 | a0003c0003t0003g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.262-1715A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780518 | |||||||
chr2:68780586 | TCTC | T | 90 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.262-1641_262-1639d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 68780586 | ||||||
chr2:68780630 | C | A | 2 | a0001c0001t0003g0137 a0001c0001t0003g0167 |
2 | HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.262-1603C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780630 | |||||||
chr2:68780737 | G | A | 2 | a0001c0001t0003g0137 a0001c0001t0003g0167 |
2 | HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.262-1496G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780737 | |||||||
chr2:68780886 | C | A | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.262-1347C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780886 | |||||||
chr2:68780888 | C | T | 1 | a0003c0003t0001g0319 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.262-1345C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780888 | |||||||
chr2:68780937 | G | A | 4 | a0002c0004t0002g0024 a0002c0007t0016g0059 a0008c0017t0016g0061 others(1): Show |
4 | HG02055.hp2 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1296G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780937 | |||||||
chr2:68780943 | T | C | 1 | a0003c0003t0005g0026 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.262-1290T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68780943 | |||||||
chr2:68781067 | A | G | 1 | a0003c0003t0001g0232 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.262-1166A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781067 | |||||||
chr2:68781073 | T | C | 249 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.262-1160T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781073 | |||||||
chr2:68781118 | T | C | 5 | a0001c0001t0001g0276 a0001c0001t0003g0005 a0001c0001t0003g0054 others(2): Show |
6 | HG02451.hp2 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-1115T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781118 | |||||||
chr2:68781366 | G | A | 17 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
18 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-867G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781366 | |||||||
chr2:68781371 | C | G | 17 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
18 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-862C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781371 | |||||||
chr2:68781377 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.262-856G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781377 | |||||||
chr2:68781427 | C | T | 16 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(13): Show |
17 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.262-806C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781427 | |||||||
chr2:68781484 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.262-749A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781484 | |||||||
chr2:68781606 | G | A | 1 | a0002c0002t0003g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.262-627G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781606 | |||||||
chr2:68781719 | C | T | 2 | a0002c0002t0002g0224 a0003c0003t0001g0009 |
3 | HG00639.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.262-514C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781719 | |||||||
chr2:68781728 | G | A | 99 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.262-505G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781728 | |||||||
chr2:68781912 | A | T | 1 | a0002c0005t0012g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.262-321A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781912 | |||||||
chr2:68781973 | G | A | 3 | a0003c0003t0001g0102 a0003c0003t0001g0103 a0003c0003t0006g0272 |
3 | NA18939.hp2 NA18987.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.262-260G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781973 | |||||||
chr2:68781985 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0276 a0001c0001t0001g0280 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.262-248T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68781985 | |||||||
chr2:68782040 | G | C | 3 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0010c0018t0001g0277 |
3 | HG02886.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.262-193G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68782040 | |||||||
chr2:68782062 | C | T | 5 | a0001c0001t0008g0278 a0002c0004t0002g0024 a0002c0007t0016g0059 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-171C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68782062 | |||||||
chr2:68782074 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.262-159T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68782074 | |||||||
chr2:68782162 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0276 a0001c0001t0001g0280 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.262-71T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68782162 | |||||||
chr2:68782172 | C | T | 99 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.262-61C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | chr2 | 68782172 | |||||||
chr2:68782407 | G | A | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.349+87G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782407 | |||||||
chr2:68782574 | G | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.349+254G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782574 | |||||||
chr2:68782651 | A | G | 5 | a0002c0002t0006g0310 a0002c0002t0006g0320 a0002c0002t0006g0321 others(2): Show |
5 | HG01074.hp1 HG01168.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+331A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782651 | |||||||
chr2:68782657 | T | A | 1 | a0002c0005t0002g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.349+337T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782657 | |||||||
chr2:68782657 | T | G | 248 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(245): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.349+337T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782657 | |||||||
chr2:68782698 | A | G | 7 | a0001c0001t0002g0179 a0002c0002t0002g0077 a0002c0002t0002g0251 others(4): Show |
7 | HG01516.hp2 HG01928.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+378A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782698 | |||||||
chr2:68782815 | G | A | 1 | a0002c0002t0002g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.349+495G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68782815 | |||||||
chr2:68783123 | C | A | 1 | a0003c0003t0005g0026 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.349+803C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783123 | |||||||
chr2:68783176 | G | T | 97 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0081 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.349+856G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783176 | |||||||
chr2:68783249 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0276 a0001c0001t0001g0280 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+929A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783249 | |||||||
chr2:68783352 | A | G | 4 | a0001c0001t0001g0135 a0002c0002t0002g0133 a0002c0002t0002g0176 others(1): Show |
4 | NA18747.hp1 NA18956.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1032A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783352 | |||||||
chr2:68783414 | A | T | 6 | a0001c0001t0001g0163 a0002c0004t0001g0332 a0002c0004t0003g0346 others(3): Show |
6 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1094A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783414 | |||||||
chr2:68783425 | T | C | 122 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.349+1105T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783425 | |||||||
chr2:68783459 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0280 a0001c0001t0022g0333 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1139T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783459 | |||||||
chr2:68783500 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349+1180T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783500 | |||||||
chr2:68783640 | T | A | 1 | a0002c0002t0010g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.349+1320T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783640 | |||||||
chr2:68783859 | T | G | 1 | a0001c0001t0001g0294 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.349+1539T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783859 | |||||||
chr2:68783926 | C | T | 4 | a0001c0001t0001g0135 a0002c0002t0002g0133 a0002c0002t0002g0176 others(1): Show |
4 | NA18747.hp1 NA18956.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1606C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783926 | |||||||
chr2:68783929 | C | A | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.349+1609C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68783929 | |||||||
chr2:68784022 | C | T | 100 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(97): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.349+1702C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784022 | |||||||
chr2:68784054 | A | G | 5 | a0002c0004t0001g0332 a0002c0004t0003g0346 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1734A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784054 | |||||||
chr2:68784090 | C | T | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.349+1770C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784090 | |||||||
chr2:68784095 | G | A | 1 | a0002c0002t0003g0156 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.349+1775G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784095 | |||||||
chr2:68784145 | T | C | 22 | a0001c0001t0001g0163 a0001c0001t0005g0029 a0001c0001t0005g0039 others(19): Show |
23 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.349+1825T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784145 | |||||||
chr2:68784175 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349+1855T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784175 | |||||||
chr2:68784178 | TCTCTCTC others(9): Show |
T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349+1860_349+1875d others(18): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 68784178 | ||||||
chr2:68784179 | C | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.349+1859C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784179 | |||||||
chr2:68784190 | T | A | 1 | a0001c0001t0003g0170 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.349+1870T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784190 | |||||||
chr2:68784190 | T | TCA | 8 | a0002c0004t0001g0332 a0002c0004t0003g0346 a0003c0003t0001g0178 others(5): Show |
8 | HG01167.hp1 HG02109.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+1888_349+1889d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 68784190 | ||||||
chr2:68784192 | A | T | 4 | a0001c0001t0001g0081 a0002c0007t0016g0059 a0003c0003t0003g0155 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1872A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784192 | |||||||
chr2:68784208 | A | C | 97 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0081 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.349+1888A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784208 | |||||||
chr2:68784218 | A | G | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.349+1898A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784218 | |||||||
chr2:68784266 | A | T | 5 | a0002c0004t0001g0332 a0002c0004t0003g0346 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1946A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784266 | |||||||
chr2:68784384 | C | G | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.349+2064C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784384 | |||||||
chr2:68784386 | G | A | 1 | a0003c0003t0001g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.349+2066G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784386 | |||||||
chr2:68784438 | T | G | 1 | a0002c0002t0002g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.349+2118T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784438 | |||||||
chr2:68784497 | G | GT | 17 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
18 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+2187dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 68784497 | ||||||
chr2:68784602 | G | C | 1 | a0002c0005t0012g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.349+2282G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784602 | |||||||
chr2:68784691 | G | A | 19 | a0001c0001t0005g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
20 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.349+2371G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784691 | |||||||
chr2:68784783 | C | T | 1 | a0002c0004t0020g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+2463C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784783 | |||||||
chr2:68784793 | G | A | 99 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0081 others(96): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.349+2473G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784793 | |||||||
chr2:68784885 | G | A | 1 | a0002c0002t0019g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.349+2565G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784885 | |||||||
chr2:68784906 | A | G | 16 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0010g0041 others(13): Show |
17 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+2586A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784906 | |||||||
chr2:68784907 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+2587T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68784907 | |||||||
chr2:68785026 | G | A | 16 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0010g0041 others(13): Show |
17 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+2706G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785026 | |||||||
chr2:68785186 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.350-2654T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785186 | |||||||
chr2:68785390 | G | A | 243 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0013 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.350-2450G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785390 | |||||||
chr2:68785544 | C | T | 1 | a0002c0002t0005g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.350-2296C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785544 | |||||||
chr2:68785565 | A | G | 1 | a0002c0002t0001g0260 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.350-2275A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785565 | |||||||
chr2:68785691 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.350-2149C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785691 | |||||||
chr2:68785707 | T | C | 33 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(30): Show |
36 | HG00438.hp1 HG00621.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.350-2133T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785707 | |||||||
chr2:68785714 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(122): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.350-2126A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785714 | |||||||
chr2:68785831 | G | A | 2 | a0002c0004t0001g0332 a0002c0004t0003g0346 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.350-2009G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785831 | |||||||
chr2:68785875 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(139): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.350-1965T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785875 | |||||||
chr2:68785901 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.350-1939G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785901 | |||||||
chr2:68785963 | A | T | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.350-1877A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68785963 | |||||||
chr2:68786034 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(138): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.350-1806C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786034 | |||||||
chr2:68786119 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.350-1721C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786119 | |||||||
chr2:68786182 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(74): Show |
84 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.350-1658T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786182 | |||||||
chr2:68786319 | A | C | 15 | a0001c0001t0002g0179 a0001c0001t0008g0278 a0002c0002t0002g0258 others(12): Show |
16 | HG01123.hp2 HG01167.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.350-1521A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786319 | |||||||
chr2:68786386 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.350-1454C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786386 | |||||||
chr2:68786482 | A | T | 3 | a0001c0001t0002g0179 a0002c0002t0002g0258 a0003c0003t0001g0349 |
3 | HG02647.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.350-1358A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786482 | |||||||
chr2:68786788 | A | G | 2 | a0002c0004t0001g0323 a0002c0004t0001g0348 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.350-1052A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68786788 | |||||||
chr2:68787094 | T | A | 160 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(157): Show |
168 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.350-746T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787094 | |||||||
chr2:68787148 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(159): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.350-692T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787148 | |||||||
chr2:68787148 | T | G | 8 | a0001c0001t0001g0017 a0001c0001t0002g0018 a0001c0001t0002g0021 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-692T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787148 | |||||||
chr2:68787179 | G | A | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.350-661G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787179 | |||||||
chr2:68787215 | C | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(137): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.350-625C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787215 | |||||||
chr2:68787247 | G | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0002c0005t0012g0347 |
3 | HG02280.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-593G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787247 | |||||||
chr2:68787312 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(135): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.350-528G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787312 | |||||||
chr2:68787388 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(137): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.350-452G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787388 | |||||||
chr2:68787397 | A | C | 2 | a0001c0001t0003g0138 a0003c0003t0003g0166 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.350-443A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787397 | |||||||
chr2:68787464 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(134): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.350-376C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787464 | |||||||
chr2:68787471 | C | T | 2 | a0001c0001t0008g0278 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.350-369C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787471 | |||||||
chr2:68787678 | T | A | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.350-162T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787678 | |||||||
chr2:68787697 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.350-143T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787697 | |||||||
chr2:68787718 | T | C | 5 | a0002c0002t0006g0310 a0002c0002t0006g0320 a0002c0002t0006g0321 others(2): Show |
5 | HG01074.hp1 HG01168.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-122T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787718 | |||||||
chr2:68787756 | A | G | 3 | a0003c0003t0001g0317 a0003c0003t0001g0318 a0003c0003t0001g0319 |
3 | NA19000.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.350-84A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787756 | |||||||
chr2:68787767 | G | A | 1 | a0002c0005t0012g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350-73G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | chr2 | 68787767 | |||||||
chr2:68787978 | C | A | 1 | a0002c0002t0002g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.466+22C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68787978 | |||||||
chr2:68787993 | A | G | 4 | a0003c0003t0001g0221 a0003c0003t0001g0238 a0003c0003t0001g0303 others(1): Show |
4 | NA18943.hp2 NA18962.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+37A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68787993 | |||||||
chr2:68788259 | T | C | 1 | a0002c0002t0002g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.466+303T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788259 | |||||||
chr2:68788336 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(254): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.466+380T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788336 | |||||||
chr2:68788548 | A | T | 1 | a0003c0003t0001g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.466+592A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788548 | |||||||
chr2:68788612 | C | T | 3 | a0001c0001t0001g0023 a0002c0008t0008g0006 a0002c0008t0008g0076 |
4 | HG01123.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+656C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788612 | |||||||
chr2:68788666 | G | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(313): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.466+710G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788666 | |||||||
chr2:68788874 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.466+918T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788874 | |||||||
chr2:68788964 | C | G | 11 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0187 others(8): Show |
11 | HG00621.hp1 HG02015.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+1008C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68788964 | |||||||
chr2:68789035 | T | C | 22 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0271 others(19): Show |
24 | HG01123.hp2 HG01167.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.466+1079T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789035 | |||||||
chr2:68789177 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0172 others(2): Show |
5 | HG00408.hp2 HG02129.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+1221C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789177 | |||||||
chr2:68789240 | A | G | 10 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(7): Show |
11 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+1284A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789240 | |||||||
chr2:68789331 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.466+1375C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789331 | |||||||
chr2:68789406 | A | G | 2 | a0001c0001t0008g0278 a0010c0018t0001g0277 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.466+1450A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789406 | |||||||
chr2:68789510 | A | G | 19 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0002g0025 others(16): Show |
20 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.466+1554A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789510 | |||||||
chr2:68789615 | C | G | 1 | a0002c0002t0002g0241 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.466+1659C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789615 | |||||||
chr2:68789705 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.466+1749T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789705 | |||||||
chr2:68789845 | C | T | 29 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(26): Show |
32 | HG00438.hp1 HG00621.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.466+1889C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789845 | |||||||
chr2:68789913 | G | C | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.466+1957G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68789913 | |||||||
chr2:68790074 | C | T | 17 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0014g0036 others(14): Show |
18 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+2118C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790074 | |||||||
chr2:68790119 | G | T | 5 | a0001c0001t0001g0013 a0001c0001t0004g0334 a0002c0004t0002g0024 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+2163G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790119 | |||||||
chr2:68790242 | G | A | 1 | a0002c0002t0010g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.466+2286G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790242 | |||||||
chr2:68790242 | G | C | 1 | a0002c0002t0002g0208 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.466+2286G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790242 | |||||||
chr2:68790382 | C | G | 2 | a0001c0001t0005g0039 a0001c0001t0005g0040 |
2 | HG00438.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.466+2426C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790382 | |||||||
chr2:68790386 | C | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(259): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.466+2430C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790386 | |||||||
chr2:68790462 | G | T | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+2506G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790462 | |||||||
chr2:68790520 | T | G | 1 | a0003c0003t0001g0293 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.466+2564T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790520 | |||||||
chr2:68790545 | G | T | 3 | a0001c0001t0001g0013 a0002c0007t0016g0059 a0008c0017t0016g0061 |
3 | HG02055.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.466+2589G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790545 | |||||||
chr2:68790555 | C | A | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+2599C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790555 | |||||||
chr2:68790615 | C | T | 1 | a0002c0004t0001g0332 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.466+2659C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790615 | |||||||
chr2:68790632 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.466+2676G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790632 | |||||||
chr2:68790668 | C | A | 3 | a0001c0001t0001g0013 a0002c0007t0016g0059 a0008c0017t0016g0061 |
3 | HG02055.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.466+2712C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790668 | |||||||
chr2:68790668 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.466+2712C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790668 | |||||||
chr2:68790677 | A | G | 1 | a0002c0002t0019g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.466+2721A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790677 | |||||||
chr2:68790692 | T | C | 29 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(26): Show |
32 | HG00438.hp1 HG00621.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.466+2736T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790692 | |||||||
chr2:68790772 | G | T | 101 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0081 others(98): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.466+2816G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68790772 | |||||||
chr2:68791025 | C | T | 101 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0081 others(98): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.466+3069C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791025 | |||||||
chr2:68791073 | C | T | 17 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0014g0036 others(14): Show |
18 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+3117C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791073 | |||||||
chr2:68791121 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0002g0262 a0002c0002t0001g0263 others(1): Show |
5 | HG01192.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+3165G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791121 | |||||||
chr2:68791224 | T | G | 4 | a0001c0001t0001g0163 a0001c0001t0002g0014 a0005c0011t0001g0273 others(1): Show |
4 | HG02622.hp2 HG03486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+3268T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791224 | |||||||
chr2:68791356 | G | A | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+3400G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791356 | |||||||
chr2:68791396 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.466+3440T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791396 | |||||||
chr2:68791429 | T | A | 3 | a0001c0001t0001g0013 a0002c0007t0016g0059 a0008c0017t0016g0061 |
3 | HG02055.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.466+3473T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791429 | |||||||
chr2:68791655 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.466+3699G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791655 | |||||||
chr2:68791658 | T | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0271 others(16): Show |
21 | HG01123.hp2 HG01167.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.466+3702T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791658 | |||||||
chr2:68791675 | G | A | 3 | a0002c0002t0002g0258 a0002c0007t0007g0016 a0003c0003t0001g0349 |
3 | HG02647.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.466+3719G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791675 | |||||||
chr2:68791711 | A | T | 10 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(7): Show |
11 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+3755A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791711 | |||||||
chr2:68791871 | T | C | 1 | a0004c0009t0007g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.466+3915T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791871 | |||||||
chr2:68791944 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0002g0014 a0005c0011t0001g0273 others(1): Show |
4 | HG02622.hp2 HG03486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+3988C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68791944 | |||||||
chr2:68792025 | T | G | 30 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(27): Show |
33 | HG00438.hp1 HG00621.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.466+4069T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792025 | |||||||
chr2:68792106 | ACT | A | 3 | a0001c0001t0002g0014 a0005c0011t0001g0273 a0005c0011t0001g0275 |
3 | HG02622.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.466+4153_466+4154d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68792106 | ||||||
chr2:68792140 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(306): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.466+4184A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792140 | |||||||
chr2:68792145 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.466+4189T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792145 | |||||||
chr2:68792298 | A | G | 104 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0081 others(101): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.466+4342A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792298 | |||||||
chr2:68792360 | A | G | 1 | a0002c0002t0004g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466+4404A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792360 | |||||||
chr2:68792367 | A | G | 3 | a0001c0001t0001g0023 a0002c0008t0008g0006 a0002c0008t0008g0076 |
4 | HG01123.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+4411A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792367 | |||||||
chr2:68792417 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(132): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.466+4461C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792417 | |||||||
chr2:68792472 | G | A | 2 | a0002c0002t0003g0338 a0002c0020t0001g0261 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.466+4516G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792472 | |||||||
chr2:68792484 | C | G | 4 | a0001c0001t0001g0013 a0002c0004t0002g0024 a0002c0007t0016g0059 others(1): Show |
4 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+4528C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792484 | |||||||
chr2:68792634 | C | A | 1 | a0001c0001t0003g0162 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.466+4678C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792634 | |||||||
chr2:68792636 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0271 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.466+4680A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792636 | |||||||
chr2:68792667 | G | A | 4 | a0002c0002t0002g0258 a0002c0007t0007g0016 a0003c0003t0001g0349 others(1): Show |
4 | HG01167.hp1 HG02647.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+4711G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792667 | |||||||
chr2:68792702 | A | G | 11 | a0001c0001t0003g0341 a0001c0001t0003g0345 a0001c0001t0004g0336 others(8): Show |
11 | HG00735.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.466+4746A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792702 | |||||||
chr2:68792815 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.466+4859G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792815 | |||||||
chr2:68792858 | T | C | 3 | a0001c0001t0001g0013 a0002c0007t0016g0059 a0008c0017t0016g0061 |
3 | HG02055.hp2 HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.466+4902T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792858 | |||||||
chr2:68792934 | T | C | 3 | a0001c0001t0002g0014 a0005c0011t0001g0273 a0005c0011t0001g0275 |
3 | HG02622.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.466+4978T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792934 | |||||||
chr2:68792980 | G | A | 29 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(26): Show |
32 | HG00438.hp1 HG00621.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.466+5024G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792980 | |||||||
chr2:68792985 | A | T | 3 | a0001c0001t0001g0096 a0002c0002t0001g0128 a0002c0002t0001g0129 |
3 | HG01074.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.466+5029A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68792985 | |||||||
chr2:68793029 | G | A | 18 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0271 others(15): Show |
20 | HG01123.hp2 HG01167.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.466+5073G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793029 | |||||||
chr2:68793035 | G | A | 3 | a0002c0002t0002g0258 a0002c0007t0007g0016 a0003c0003t0001g0349 |
3 | HG02647.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.466+5079G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793035 | |||||||
chr2:68793037 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.466+5081T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793037 | |||||||
chr2:68793046 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.466+5090T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793046 | |||||||
chr2:68793189 | G | A | 1 | a0003c0003t0001g0326 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.466+5233G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793189 | |||||||
chr2:68793416 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.466+5460C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793416 | |||||||
chr2:68793439 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0004g0334 a0002c0008t0008g0006 others(1): Show |
5 | HG01123.hp2 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+5483C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793439 | |||||||
chr2:68793467 | G | A | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+5511G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793467 | |||||||
chr2:68793531 | T | C | 99 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(96): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.466+5575T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793531 | |||||||
chr2:68793680 | T | A | 2 | a0003c0003t0001g0196 a0003c0003t0001g0235 |
2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.466+5724T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793680 | |||||||
chr2:68793789 | T | A | 1 | a0001c0001t0003g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.466+5833T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793789 | |||||||
chr2:68793817 | G | A | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+5861G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793817 | |||||||
chr2:68793972 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.466+6016C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68793972 | |||||||
chr2:68794033 | G | A | 1 | a0001c0001t0003g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.466+6077G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68794033 | |||||||
chr2:68794094 | C | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(117): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.466+6138C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68794094 | |||||||
chr2:68794401 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.466+6445G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68794401 | |||||||
chr2:68794438 | G | A | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+6482G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68794438 | |||||||
chr2:68794710 | G | A | 1 | a0002c0002t0002g0209 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.466+6754G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68794710 | |||||||
chr2:68794908 | T | G | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+6952T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68794908 | |||||||
chr2:68795265 | A | G | 1 | a0002c0002t0002g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.466+7309A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795265 | |||||||
chr2:68795380 | T | C | 1 | a0003c0003t0001g0067 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.466+7424T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795380 | |||||||
chr2:68795520 | C | T | 2 | a0002c0002t0003g0338 a0002c0020t0001g0261 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.466+7564C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795520 | |||||||
chr2:68795545 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(313): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.466+7589A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795545 | |||||||
chr2:68795822 | T | G | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+7866T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795822 | |||||||
chr2:68795862 | G | A | 5 | a0001c0001t0001g0013 a0002c0004t0002g0024 a0002c0004t0013g0343 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+7906G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795862 | |||||||
chr2:68795946 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(97): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.466+7990T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795946 | |||||||
chr2:68795986 | T | C | 65 | a0001c0001t0001g0017 a0001c0001t0001g0180 a0001c0001t0001g0186 others(62): Show |
65 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.466+8030T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68795986 | |||||||
chr2:68796123 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.466+8167G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796123 | |||||||
chr2:68796126 | T | G | 10 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(7): Show |
11 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+8170T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796126 | |||||||
chr2:68796285 | A | G | 20 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(17): Show |
20 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.466+8329A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796285 | |||||||
chr2:68796301 | A | G | 3 | a0001c0001t0003g0137 a0001c0001t0003g0167 a0001c0001t0003g0169 |
3 | HG03669.hp2 HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.466+8345A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796301 | |||||||
chr2:68796548 | A | G | 5 | a0001c0001t0001g0013 a0002c0004t0002g0024 a0002c0004t0013g0343 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+8592A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796548 | |||||||
chr2:68796572 | G | A | 66 | a0001c0001t0001g0017 a0001c0001t0001g0180 a0001c0001t0001g0186 others(63): Show |
66 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.466+8616G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796572 | |||||||
chr2:68796601 | T | C | 5 | a0002c0004t0001g0332 a0002c0004t0003g0346 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+8645T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796601 | |||||||
chr2:68796862 | A | T | 98 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.466+8906A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796862 | |||||||
chr2:68796911 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.466+8955C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796911 | |||||||
chr2:68796957 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(97): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.466+9001G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796957 | |||||||
chr2:68796978 | G | T | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+9022G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68796978 | |||||||
chr2:68797040 | G | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0002c0002t0001g0268 others(1): Show |
4 | HG02559.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+9084G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797040 | |||||||
chr2:68797051 | C | T | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.466+9095C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797051 | |||||||
chr2:68797196 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.466+9240A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797196 | |||||||
chr2:68797198 | G | A | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+9242G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797198 | |||||||
chr2:68797330 | G | T | 2 | a0002c0012t0001g0086 a0002c0012t0002g0073 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.466+9374G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797330 | |||||||
chr2:68797355 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0005g0039 a0001c0001t0005g0040 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.466+9399C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797355 | |||||||
chr2:68797362 | C | T | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+9406C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797362 | |||||||
chr2:68797411 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.466+9455A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797411 | |||||||
chr2:68797477 | A | G | 3 | a0002c0002t0001g0266 a0003c0003t0001g0074 a0003c0003t0001g0075 |
3 | HG01099.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.466+9521A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797477 | |||||||
chr2:68797587 | G | T | 1 | a0001c0001t0005g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.466+9631G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797587 | |||||||
chr2:68797603 | C | T | 2 | a0001c0001t0005g0046 a0002c0005t0012g0347 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.466+9647C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797603 | |||||||
chr2:68797657 | T | C | 188 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(185): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.467-9616T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797657 | |||||||
chr2:68797682 | C | T | 3 | a0003c0003t0001g0302 a0003c0003t0001g0316 a0003c0003t0006g0289 |
3 | NA18945.hp1 NA19067.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.467-9591C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797682 | |||||||
chr2:68797989 | G | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
7 | NA18973.hp2 NA18983.hp2 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-9284G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68797989 | |||||||
chr2:68798100 | G | C | 97 | a0001c0001t0001g0010 a0001c0001t0001g0081 a0001c0001t0001g0082 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.467-9173G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798100 | |||||||
chr2:68798106 | A | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0271 others(18): Show |
23 | HG01123.hp2 HG01167.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.467-9167A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798106 | |||||||
chr2:68798280 | G | A | 10 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(7): Show |
11 | HG02451.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.467-8993G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798280 | |||||||
chr2:68798396 | A | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG01255.hp1 HG01496.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-8877A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798396 | |||||||
chr2:68798502 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.467-8771G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798502 | |||||||
chr2:68798517 | G | GA | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(268): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.467-8745dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68798517 | ||||||
chr2:68798517 | G | GAA | 10 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(7): Show |
11 | HG02572.hp1 HG02886.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.467-8746_467-8745d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68798517 | ||||||
chr2:68798517 | G | GAAA | 10 | a0001c0001t0001g0023 a0001c0001t0003g0341 a0001c0001t0004g0336 others(7): Show |
11 | HG00735.hp2 HG01123.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.467-8747_467-8745d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68798517 | ||||||
chr2:68798544 | C | G | 102 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0081 others(99): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.467-8729C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798544 | |||||||
chr2:68798594 | C | T | 9 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(6): Show |
10 | HG02572.hp1 HG02886.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-8679C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798594 | |||||||
chr2:68798617 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(284): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.467-8656T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798617 | |||||||
chr2:68798796 | G | T | 2 | a0002c0002t0001g0266 a0003c0003t0001g0075 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.467-8477G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798796 | |||||||
chr2:68798832 | G | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0311 a0002c0020t0001g0261 |
4 | HG02630.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-8441G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798832 | |||||||
chr2:68798847 | G | T | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.467-8426G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68798847 | |||||||
chr2:68798956 | A | AT | 4 | a0001c0001t0001g0111 a0002c0002t0011g0144 a0003c0003t0001g0103 others(1): Show |
4 | HG00423.hp1 HG02523.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-8314dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68798956 | ||||||
chr2:68799271 | G | A | 5 | a0002c0002t0001g0263 a0002c0002t0003g0338 a0002c0007t0007g0264 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-8002G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799271 | |||||||
chr2:68799318 | C | T | 1 | a0002c0002t0003g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.467-7955C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799318 | |||||||
chr2:68799412 | A | G | 1 | a0003c0003t0001g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.467-7861A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799412 | |||||||
chr2:68799427 | T | A | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.467-7846T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799427 | |||||||
chr2:68799547 | A | G | 1 | a0002c0002t0002g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.467-7726A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799547 | |||||||
chr2:68799572 | C | T | 4 | a0002c0005t0002g0274 a0002c0005t0012g0019 a0002c0005t0012g0185 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-7701C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799572 | |||||||
chr2:68799757 | C | A | 11 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.467-7516C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799757 | |||||||
chr2:68799895 | A | T | 11 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.467-7378A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799895 | |||||||
chr2:68799920 | C | G | 42 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.467-7353C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799920 | |||||||
chr2:68799923 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0206 a0001c0001t0002g0015 others(1): Show |
4 | HG01192.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-7350C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799923 | |||||||
chr2:68799958 | G | A | 1 | a0001c0001t0022g0333 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.467-7315G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68799958 | |||||||
chr2:68800036 | G | A | 1 | a0003c0003t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.467-7237G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800036 | |||||||
chr2:68800065 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.467-7208A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800065 | |||||||
chr2:68800091 | G | A | 1 | a0002c0005t0012g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.467-7182G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800091 | |||||||
chr2:68800176 | C | T | 8 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(5): Show |
9 | HG02572.hp1 HG02896.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-7097C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800176 | |||||||
chr2:68800219 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.467-7054G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800219 | |||||||
chr2:68800282 | T | G | 1 | a0003c0003t0001g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.467-6991T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800282 | |||||||
chr2:68800339 | A | C | 1 | a0007c0013t0001g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.467-6934A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800339 | |||||||
chr2:68800377 | CAA | C | 12 | a0002c0002t0011g0141 a0003c0003t0009g0004 a0003c0003t0009g0033 others(9): Show |
13 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-6894_467-6893d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68800377 | ||||||
chr2:68800380 | A | C | 12 | a0002c0002t0011g0141 a0003c0003t0009g0004 a0003c0003t0009g0033 others(9): Show |
13 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-6893A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800380 | |||||||
chr2:68800381 | T | C | 12 | a0002c0002t0011g0141 a0003c0003t0009g0004 a0003c0003t0009g0033 others(9): Show |
13 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-6892T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800381 | |||||||
chr2:68800530 | A | T | 1 | a0003c0003t0001g0067 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.467-6743A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800530 | |||||||
chr2:68800607 | T | C | 6 | a0001c0001t0001g0013 a0002c0002t0017g0308 a0002c0002t0017g0309 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-6666T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800607 | |||||||
chr2:68800619 | T | C | 1 | a0002c0002t0002g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.467-6654T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800619 | |||||||
chr2:68800655 | C | G | 46 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(43): Show |
48 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.467-6618C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800655 | |||||||
chr2:68800688 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0206 a0001c0001t0001g0243 others(10): Show |
13 | HG01109.hp2 HG01175.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-6585G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800688 | |||||||
chr2:68800860 | T | A | 5 | a0002c0002t0001g0263 a0002c0002t0003g0338 a0002c0007t0007g0264 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-6413T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800860 | |||||||
chr2:68800871 | A | G | 1 | a0001c0001t0008g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.467-6402A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800871 | |||||||
chr2:68800873 | A | G | 109 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(106): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.467-6400A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800873 | |||||||
chr2:68800906 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.467-6367T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800906 | |||||||
chr2:68800933 | T | G | 11 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.467-6340T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68800933 | |||||||
chr2:68801109 | T | TA | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(137): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.467-6155dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68801109 | ||||||
chr2:68801334 | G | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.467-5939G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801334 | |||||||
chr2:68801403 | C | A | 23 | a0001c0001t0002g0012 a0001c0001t0002g0311 a0001c0001t0003g0003 others(20): Show |
26 | HG00438.hp1 HG00621.hp2 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.467-5870C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801403 | |||||||
chr2:68801421 | C | G | 9 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-5852C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801421 | |||||||
chr2:68801436 | G | C | 1 | a0002c0005t0012g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.467-5837G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801436 | |||||||
chr2:68801453 | A | G | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-5820A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801453 | |||||||
chr2:68801457 | A | G | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-5816A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801457 | |||||||
chr2:68801469 | G | C | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.467-5804G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801469 | |||||||
chr2:68801498 | G | C | 1 | a0002c0002t0004g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.467-5775G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801498 | |||||||
chr2:68801555 | G | C | 17 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0022 others(14): Show |
18 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-5718G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801555 | |||||||
chr2:68801584 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(342): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.467-5689T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801584 | |||||||
chr2:68801689 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-5584G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801689 | |||||||
chr2:68801696 | T | A | 3 | a0002c0002t0002g0020 a0002c0002t0002g0258 a0003c0003t0001g0349 |
3 | HG02055.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.467-5577T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68801696 | |||||||
chr2:68802083 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-5190G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802083 | |||||||
chr2:68802226 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.467-5047G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802226 | |||||||
chr2:68802228 | GAAACCCC others(10): Show |
G | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-5041_467-5025d others(19): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802228 | ||||||
chr2:68802278 | C | T | 3 | a0001c0001t0002g0014 a0005c0011t0001g0273 a0005c0011t0001g0275 |
3 | HG02622.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.467-4995C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802278 | |||||||
chr2:68802407 | C | CA | 67 | a0001c0001t0001g0013 a0001c0001t0001g0081 a0001c0001t0001g0082 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.467-4844dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802407 | ||||||
chr2:68802407 | C | CAA | 100 | a0001c0001t0001g0010 a0001c0001t0001g0190 a0001c0001t0001g0192 others(97): Show |
105 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.467-4845_467-4844d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802407 | ||||||
chr2:68802407 | CA | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(86): Show |
97 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.467-4844delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802407 | ||||||
chr2:68802407 | CAA | C | 8 | a0001c0001t0001g0063 a0001c0001t0003g0148 a0001c0001t0004g0159 others(5): Show |
8 | HG01256.hp2 HG02258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-4845_467-4844d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802407 | ||||||
chr2:68802441 | C | A | 1 | a0002c0002t0011g0141 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.467-4832C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802441 | |||||||
chr2:68802446 | T | C | 1 | a0001c0001t0005g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467-4827T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802446 | |||||||
chr2:68802558 | G | C | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-4715G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802558 | |||||||
chr2:68802575 | T | C | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-4698T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802575 | |||||||
chr2:68802621 | G | C | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.467-4652G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802621 | |||||||
chr2:68802638 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(255): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.467-4635T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802638 | |||||||
chr2:68802707 | A | AAG | 61 | a0001c0001t0001g0023 a0001c0001t0001g0081 a0001c0001t0001g0082 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.467-4542_467-4541d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802707 | ||||||
chr2:68802707 | AAG | A | 123 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0135 others(120): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.467-4542_467-4541d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802707 | ||||||
chr2:68802707 | AAGAGAG | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(5): Show |
9 | HG02572.hp1 HG02896.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-4546_467-4541d others(8): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802707 | ||||||
chr2:68802707 | AAGAGAGA others(1): Show |
A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(66): Show |
76 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.467-4548_467-4541d others(10): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802707 | ||||||
chr2:68802707 | AAGAGAGA others(5): Show |
A | 17 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0022 others(14): Show |
18 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-4552_467-4541d others(14): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802707 | ||||||
chr2:68802715 | G | A | 4 | a0002c0005t0002g0274 a0002c0005t0012g0019 a0002c0005t0012g0185 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-4558G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802715 | |||||||
chr2:68802883 | C | T | 1 | a0002c0002t0002g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.467-4390C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802883 | |||||||
chr2:68802898 | CACACATA others(11): Show |
C | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG01255.hp1 HG02258.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-4348_467-4331d others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802898 | ||||||
chr2:68802915 | A | T | 1 | a0002c0002t0002g0121 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.467-4358A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802915 | |||||||
chr2:68802927 | CCATATAT others(31): Show |
C | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.467-4330_467-4293d others(40): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802927 | ||||||
chr2:68802951 | A | G | 17 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(14): Show |
17 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.467-4322A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68802951 | |||||||
chr2:68802966 | CATATATA others(5): Show |
C | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-4295_467-4284d others(14): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 68802966 | ||||||
chr2:68803014 | T | G | 4 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0002c0002t0014g0036 others(1): Show |
4 | HG00408.hp1 HG00438.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-4259T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803014 | |||||||
chr2:68803016 | T | G | 110 | a0001c0001t0001g0017 a0001c0001t0001g0081 a0001c0001t0001g0082 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.467-4257T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803016 | |||||||
chr2:68803018 | T | G | 214 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.467-4255T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803018 | |||||||
chr2:68803050 | T | C | 23 | a0001c0001t0002g0012 a0001c0001t0002g0311 a0001c0001t0003g0003 others(20): Show |
26 | HG00438.hp1 HG00621.hp2 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.467-4223T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803050 | |||||||
chr2:68803191 | A | C | 2 | a0005c0011t0001g0273 a0005c0011t0001g0275 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.467-4082A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803191 | |||||||
chr2:68803195 | C | T | 1 | a0002c0002t0002g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.467-4078C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803195 | |||||||
chr2:68803246 | A | G | 52 | a0001c0001t0001g0184 a0001c0001t0001g0243 a0001c0001t0001g0271 others(49): Show |
54 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.467-4027A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803246 | |||||||
chr2:68803460 | G | A | 4 | a0002c0002t0001g0260 a0002c0002t0002g0199 a0002c0002t0002g0240 others(1): Show |
4 | NA19010.hp2 NA19058.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-3813G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803460 | |||||||
chr2:68803558 | A | T | 17 | a0001c0001t0002g0018 a0001c0001t0002g0021 a0001c0001t0002g0022 others(14): Show |
18 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-3715A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803558 | |||||||
chr2:68803718 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0100 a0001c0001t0001g0283 others(2): Show |
5 | NA18956.hp1 NA18959.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-3555C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803718 | |||||||
chr2:68803928 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
5 | HG01081.hp2 HG01952.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-3345G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803928 | |||||||
chr2:68803932 | G | A | 1 | a0002c0002t0002g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.467-3341G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803932 | |||||||
chr2:68803978 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(238): Show |
256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.467-3295G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803978 | |||||||
chr2:68803982 | C | T | 1 | a0002c0002t0002g0269 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.467-3291C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803982 | |||||||
chr2:68803995 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0002g0014 |
2 | HG01255.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.467-3278C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803995 | |||||||
chr2:68803996 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0190 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-3277G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68803996 | |||||||
chr2:68804057 | A | T | 1 | a0001c0001t0001g0327 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.467-3216A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804057 | |||||||
chr2:68804168 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(194): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.467-3105C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804168 | |||||||
chr2:68804430 | C | T | 18 | a0001c0001t0001g0243 a0001c0001t0001g0294 a0001c0001t0001g0296 others(15): Show |
18 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.467-2843C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804430 | |||||||
chr2:68804463 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(77): Show |
87 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.467-2810G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804463 | |||||||
chr2:68804646 | C | G | 121 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0023 others(118): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.467-2627C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804646 | |||||||
chr2:68804737 | A | C | 1 | a0001c0001t0008g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.467-2536A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804737 | |||||||
chr2:68804792 | G | T | 4 | a0001c0001t0001g0163 a0002c0004t0002g0024 a0002c0008t0008g0006 others(1): Show |
5 | HG01123.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-2481G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804792 | |||||||
chr2:68804817 | T | A | 1 | a0002c0002t0003g0338 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.467-2456T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804817 | |||||||
chr2:68804888 | G | A | 1 | a0003c0003t0001g0211 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.467-2385G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804888 | |||||||
chr2:68804922 | A | G | 2 | a0001c0001t0002g0018 a0001c0001t0002g0088 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.467-2351A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68804922 | |||||||
chr2:68805028 | G | A | 1 | a0002c0002t0011g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.467-2245G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805028 | |||||||
chr2:68805031 | G | C | 1 | a0003c0006t0021g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.467-2242G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805031 | |||||||
chr2:68805103 | G | T | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.467-2170G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805103 | |||||||
chr2:68805148 | G | C | 12 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0187 others(9): Show |
12 | HG00735.hp2 HG01167.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.467-2125G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805148 | |||||||
chr2:68805203 | C | T | 1 | a0001c0001t0005g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467-2070C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805203 | |||||||
chr2:68805336 | A | C | 4 | a0003c0003t0001g0102 a0003c0003t0001g0103 a0003c0003t0006g0105 others(1): Show |
4 | NA18939.hp2 NA18987.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-1937A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805336 | |||||||
chr2:68805345 | G | A | 1 | a0003c0003t0001g0349 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.467-1928G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805345 | |||||||
chr2:68805595 | G | A | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.467-1678G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805595 | |||||||
chr2:68805698 | G | A | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.467-1575G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805698 | |||||||
chr2:68805721 | G | A | 1 | a0003c0003t0001g0349 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.467-1552G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805721 | |||||||
chr2:68805764 | G | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(314): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.467-1509G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805764 | |||||||
chr2:68805878 | G | A | 5 | a0003c0003t0003g0335 a0003c0003t0003g0342 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-1395G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68805878 | |||||||
chr2:68806267 | G | C | 1 | a0001c0001t0003g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.467-1006G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806267 | |||||||
chr2:68806338 | C | T | 6 | a0003c0003t0001g0349 a0003c0003t0003g0335 a0003c0003t0003g0342 others(3): Show |
6 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-935C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806338 | |||||||
chr2:68806554 | T | C | 4 | a0002c0002t0002g0080 a0002c0002t0003g0062 a0002c0012t0001g0086 others(1): Show |
4 | HG00099.hp2 HG00323.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-719T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806554 | |||||||
chr2:68806579 | A | C | 2 | a0002c0002t0002g0020 a0002c0002t0002g0258 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.467-694A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806579 | |||||||
chr2:68806585 | C | T | 21 | a0003c0003t0001g0093 a0003c0003t0001g0110 a0003c0003t0001g0178 others(18): Show |
21 | HG00438.hp1 HG00621.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.467-688C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806585 | |||||||
chr2:68806642 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0063 others(9): Show |
18 | HG00597.hp1 HG02165.hp2 NA18957.hp2 others(15): Show |
intron_variant | MODIFIER | c.467-631C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806642 | |||||||
chr2:68806665 | A | G | 11 | a0002c0002t0006g0188 a0002c0002t0006g0310 a0002c0002t0006g0320 others(8): Show |
11 | HG00408.hp1 HG00639.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.467-608A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806665 | |||||||
chr2:68806694 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(304): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.467-579C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806694 | |||||||
chr2:68806743 | C | T | 17 | a0001c0001t0003g0344 a0001c0001t0008g0229 a0001c0001t0008g0278 others(14): Show |
17 | HG00735.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.467-530C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806743 | |||||||
chr2:68806842 | G | A | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.467-431G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806842 | |||||||
chr2:68806896 | C | G | 6 | a0003c0003t0001g0349 a0003c0003t0003g0335 a0003c0003t0003g0342 others(3): Show |
6 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-377C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806896 | |||||||
chr2:68806910 | T | G | 69 | a0001c0001t0001g0135 a0001c0001t0005g0046 a0002c0002t0001g0182 others(66): Show |
69 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.467-363T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806910 | |||||||
chr2:68806943 | C | T | 12 | a0002c0002t0002g0020 a0002c0002t0002g0258 a0002c0004t0001g0290 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.467-330C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68806943 | |||||||
chr2:68807025 | T | C | 158 | a0001c0001t0001g0017 a0001c0001t0001g0135 a0001c0001t0002g0015 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.467-248T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68807025 | |||||||
chr2:68807117 | T | C | 89 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0002c0002t0001g0268 others(86): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.467-156T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68807117 | |||||||
chr2:68807126 | G | A | 2 | a0003c0003t0003g0166 a0003c0003t0005g0042 |
2 | HG00099.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.467-147G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | chr2 | 68807126 | |||||||
chr2:68807598 | G | C | 3 | a0003c0003t0001g0196 a0003c0003t0001g0235 a0003c0003t0001g0322 |
3 | HG01109.hp1 HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.674+118G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807598 | |||||||
chr2:68807664 | G | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0297 others(2): Show |
5 | NA18950.hp2 NA18966.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+184G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807664 | |||||||
chr2:68807715 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
123 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.674+235C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807715 | |||||||
chr2:68807733 | G | A | 5 | a0003c0003t0003g0335 a0003c0003t0003g0342 a0004c0009t0002g0331 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+253G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807733 | |||||||
chr2:68807854 | A | G | 92 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0002c0002t0001g0268 others(89): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.674+374A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807854 | |||||||
chr2:68807888 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(109): Show |
123 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.674+408G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807888 | |||||||
chr2:68807897 | C | T | 92 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0002c0002t0001g0268 others(89): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.674+417C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807897 | |||||||
chr2:68807961 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.674+481G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807961 | |||||||
chr2:68807965 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.674+485T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807965 | |||||||
chr2:68807972 | T | C | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.674+492T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807972 | |||||||
chr2:68807998 | C | T | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674+518C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68807998 | |||||||
chr2:68808013 | A | G | 1 | a0003c0003t0001g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.674+533A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808013 | |||||||
chr2:68808023 | C | T | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674+543C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808023 | |||||||
chr2:68808179 | G | A | 6 | a0003c0003t0001g0349 a0003c0003t0003g0335 a0003c0003t0003g0342 others(3): Show |
6 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.674+699G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808179 | |||||||
chr2:68808285 | T | C | 2 | a0002c0002t0002g0020 a0002c0002t0002g0258 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.674+805T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808285 | |||||||
chr2:68808291 | T | G | 73 | a0001c0001t0001g0135 a0001c0001t0005g0046 a0002c0002t0001g0182 others(70): Show |
73 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.674+811T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808291 | |||||||
chr2:68808429 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(117): Show |
131 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.674+949C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808429 | |||||||
chr2:68808430 | G | A | 1 | a0001c0001t0005g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.674+950G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808430 | |||||||
chr2:68808477 | T | G | 2 | a0003c0003t0003g0335 a0003c0003t0003g0342 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.674+997T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808477 | |||||||
chr2:68808492 | A | T | 7 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(4): Show |
8 | HG02572.hp1 HG02896.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.674+1012A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808492 | |||||||
chr2:68808720 | T | C | 1 | a0002c0002t0002g0287 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.674+1240T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808720 | |||||||
chr2:68808881 | G | A | 87 | a0001c0001t0002g0015 a0002c0002t0001g0268 a0002c0002t0002g0224 others(84): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.674+1401G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808881 | |||||||
chr2:68808922 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.674+1442A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808922 | |||||||
chr2:68808967 | G | T | 1 | a0003c0003t0001g0349 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.674+1487G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68808967 | |||||||
chr2:68809069 | A | G | 98 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0015 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.674+1589A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809069 | |||||||
chr2:68809202 | T | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0225 |
2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.674+1722T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809202 | |||||||
chr2:68809279 | C | T | 2 | a0002c0008t0008g0006 a0002c0008t0008g0076 |
3 | HG01123.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.674+1799C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809279 | |||||||
chr2:68809310 | A | G | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674+1830A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809310 | |||||||
chr2:68809330 | G | A | 67 | a0001c0001t0001g0135 a0001c0001t0005g0046 a0002c0002t0001g0182 others(64): Show |
67 | HG00099.hp2 HG00323.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.674+1850G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809330 | |||||||
chr2:68809606 | A | T | 195 | a0001c0001t0002g0015 a0001c0001t0005g0046 a0002c0002t0001g0182 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.674+2126A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809606 | |||||||
chr2:68809634 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.674+2154T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809634 | |||||||
chr2:68809708 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.674+2228A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809708 | |||||||
chr2:68809733 | C | A | 11 | a0002c0002t0003g0156 a0002c0002t0006g0188 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.674+2253C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809733 | |||||||
chr2:68809794 | A | C | 92 | a0002c0002t0001g0182 a0002c0002t0001g0233 a0002c0002t0001g0260 others(89): Show |
93 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.674+2314A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68809794 | |||||||
chr2:68810128 | TA | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(193): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.674+2667delA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810128 | ||||||
chr2:68810128 | TAA | T | 21 | a0001c0001t0001g0253 a0001c0001t0001g0257 a0001c0001t0003g0170 others(18): Show |
22 | HG01123.hp2 HG01243.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.674+2666_674+2667d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810128 | ||||||
chr2:68810149 | A | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(11): Show |
15 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.674+2669A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810149 | |||||||
chr2:68810355 | G | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(111): Show |
125 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.674+2875G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810355 | |||||||
chr2:68810420 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.675-2867C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810420 | |||||||
chr2:68810529 | A | G | 1 | a0003c0003t0001g0211 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.675-2758A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810529 | |||||||
chr2:68810538 | A | G | 2 | a0003c0003t0006g0105 a0003c0003t0006g0272 |
2 | NA18939.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.675-2749A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810538 | |||||||
chr2:68810623 | A | G | 2 | a0001c0001t0003g0137 a0001c0001t0003g0167 |
2 | HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.675-2664A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810623 | |||||||
chr2:68810715 | TC | T | 11 | a0003c0003t0009g0004 a0003c0003t0009g0033 a0003c0003t0009g0034 others(8): Show |
12 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.675-2571delC | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810715 | |||||||
chr2:68810717 | T | A | 11 | a0003c0003t0009g0004 a0003c0003t0009g0033 a0003c0003t0009g0034 others(8): Show |
12 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.675-2570T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810717 | |||||||
chr2:68810724 | TTCTTC | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0084 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.675-2558_675-2554d others(7): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810724 | ||||||
chr2:68810726 | CTTCTCT | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(220): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.675-2558_675-2553d others(8): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810726 | ||||||
chr2:68810728 | TCTC | T | 21 | a0002c0002t0002g0020 a0002c0002t0002g0071 a0002c0002t0003g0156 others(18): Show |
21 | HG00408.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.675-2558_675-2556d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810728 | |||||||
chr2:68810729 | C | T | 76 | a0002c0002t0001g0182 a0002c0002t0001g0233 a0002c0002t0001g0260 others(73): Show |
77 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.675-2558C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810729 | |||||||
chr2:68810731 | CT | C | 10 | a0002c0002t0001g0128 a0002c0002t0002g0077 a0002c0002t0002g0251 others(7): Show |
10 | HG01169.hp1 HG01516.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.675-2535delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810731 | ||||||
chr2:68810731 | CTT | C | 66 | a0002c0002t0001g0182 a0002c0002t0001g0233 a0002c0002t0001g0260 others(63): Show |
67 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.675-2536_675-2535d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810731 | ||||||
chr2:68810731 | CTTT | C | 6 | a0002c0005t0002g0274 a0002c0005t0012g0019 a0002c0005t0012g0185 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-2537_675-2535d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68810731 | ||||||
chr2:68810734 | T | C | 21 | a0002c0002t0002g0020 a0002c0002t0002g0071 a0002c0002t0003g0156 others(18): Show |
21 | HG00408.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.675-2553T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810734 | |||||||
chr2:68810735 | T | C | 1 | a0002c0002t0002g0258 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.675-2552T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810735 | |||||||
chr2:68810736 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0084 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.675-2551T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810736 | |||||||
chr2:68810737 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(221): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.675-2550T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810737 | |||||||
chr2:68810739 | T | C | 11 | a0002c0002t0003g0156 a0002c0002t0006g0188 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.675-2548T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810739 | |||||||
chr2:68810742 | T | C | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-2545T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810742 | |||||||
chr2:68810795 | T | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-2492T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810795 | |||||||
chr2:68810940 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-2347T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810940 | |||||||
chr2:68810942 | C | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-2345C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68810942 | |||||||
chr2:68811143 | C | T | 1 | a0003c0003t0001g0217 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.675-2144C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811143 | |||||||
chr2:68811153 | G | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(111): Show |
125 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.675-2134G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811153 | |||||||
chr2:68811156 | G | C | 1 | a0001c0001t0003g0162 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.675-2131G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811156 | |||||||
chr2:68811237 | T | A | 1 | a0001c0001t0003g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.675-2050T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811237 | |||||||
chr2:68811314 | G | A | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-1973G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811314 | |||||||
chr2:68811315 | A | T | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-1972A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811315 | |||||||
chr2:68811316 | G | A | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-1971G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811316 | |||||||
chr2:68811426 | G | A | 8 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.675-1861G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811426 | |||||||
chr2:68811464 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-1823T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811464 | |||||||
chr2:68811609 | G | A | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.675-1678G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811609 | |||||||
chr2:68811643 | A | G | 11 | a0002c0002t0002g0181 a0002c0002t0002g0208 a0002c0002t0002g0209 others(8): Show |
11 | HG00639.hp1 HG00741.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.675-1644A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68811643 | |||||||
chr2:68811659 | G | GA | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(327): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.675-1627dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68811659 | ||||||
chr2:68812016 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-1271T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812016 | |||||||
chr2:68812122 | G | T | 71 | a0002c0002t0001g0182 a0002c0002t0001g0233 a0002c0002t0001g0260 others(68): Show |
71 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.675-1165G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812122 | |||||||
chr2:68812169 | T | A | 1 | a0001c0001t0003g0149 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.675-1118T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812169 | |||||||
chr2:68812197 | A | T | 4 | a0001c0001t0001g0237 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
4 | NA18939.hp1 NA18943.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.675-1090A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812197 | |||||||
chr2:68812246 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-1041C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812246 | |||||||
chr2:68812253 | CTCT | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-1026_675-1024d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 68812253 | ||||||
chr2:68812285 | T | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(91): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.675-1002T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812285 | |||||||
chr2:68812285 | T | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(136): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.675-1002T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812285 | |||||||
chr2:68812410 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.675-877C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812410 | |||||||
chr2:68812482 | C | T | 1 | a0003c0003t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.675-805C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812482 | |||||||
chr2:68812610 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.675-677G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812610 | |||||||
chr2:68812636 | T | G | 1 | a0002c0002t0002g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.675-651T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812636 | |||||||
chr2:68812642 | G | A | 11 | a0002c0002t0003g0156 a0002c0002t0006g0188 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.675-645G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812642 | |||||||
chr2:68812642 | G | T | 6 | a0002c0002t0002g0020 a0002c0002t0002g0258 a0002c0002t0017g0308 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-645G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812642 | |||||||
chr2:68812753 | A | G | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.675-534A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812753 | |||||||
chr2:68812811 | T | C | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(327): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.675-476T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812811 | |||||||
chr2:68812835 | A | T | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-452A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812835 | |||||||
chr2:68812867 | A | G | 1 | a0002c0004t0001g0332 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.675-420A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812867 | |||||||
chr2:68812967 | G | C | 2 | a0002c0002t0002g0288 a0002c0002t0002g0301 |
2 | HG01069.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.675-320G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812967 | |||||||
chr2:68812984 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.675-303A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68812984 | |||||||
chr2:68813065 | T | C | 5 | a0003c0003t0001g0102 a0003c0003t0001g0103 a0003c0003t0001g0326 others(2): Show |
5 | HG00597.hp2 NA18982.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-222T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68813065 | |||||||
chr2:68813084 | G | T | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-203G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68813084 | |||||||
chr2:68813279 | T | C | 6 | a0002c0007t0007g0016 a0002c0007t0007g0264 a0002c0007t0007g0265 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.675-8T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | 68813279 | |||||||
chr2:68813478 | C | G | 2 | a0002c0008t0008g0006 a0002c0008t0008g0076 |
3 | HG01123.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.807+59C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68813478 | |||||||
chr2:68813577 | A | C | 1 | a0002c0002t0003g0062 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.807+158A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68813577 | |||||||
chr2:68813627 | T | C | 11 | a0001c0001t0001g0017 a0001c0001t0002g0015 a0001c0001t0002g0018 others(8): Show |
11 | HG01243.hp1 HG02258.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.807+208T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68813627 | |||||||
chr2:68813672 | A | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(11): Show |
15 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.807+253A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68813672 | |||||||
chr2:68813797 | G | A | 2 | a0002c0002t0017g0308 a0002c0002t0017g0309 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.807+378G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68813797 | |||||||
chr2:68814005 | C | T | 104 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(101): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.807+586C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814005 | |||||||
chr2:68814135 | T | C | 9 | a0002c0002t0003g0156 a0002c0002t0006g0310 a0002c0002t0006g0320 others(6): Show |
9 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.807+716T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814135 | |||||||
chr2:68814321 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0014 a0001c0001t0002g0311 |
4 | HG02647.hp2 HG02723.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+902C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814321 | |||||||
chr2:68814483 | A | G | 1 | a0010c0018t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.807+1064A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814483 | |||||||
chr2:68814546 | G | C | 2 | a0002c0002t0002g0209 a0002c0002t0004g0145 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.807+1127G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814546 | |||||||
chr2:68814576 | A | C | 16 | a0003c0003t0001g0075 a0003c0003t0001g0134 a0003c0003t0001g0197 others(13): Show |
17 | HG00544.hp2 HG01257.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.807+1157A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814576 | |||||||
chr2:68814612 | A | G | 1 | a0005c0011t0001g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.807+1193A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814612 | |||||||
chr2:68814651 | G | A | 106 | a0002c0002t0001g0268 a0002c0002t0003g0136 a0002c0004t0001g0290 others(103): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.807+1232G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814651 | |||||||
chr2:68814691 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.807+1272C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814691 | |||||||
chr2:68814749 | C | T | 2 | a0002c0002t0017g0308 a0002c0002t0017g0309 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.807+1330C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814749 | |||||||
chr2:68814872 | T | A | 1 | a0003c0003t0001g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.808-1417T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814872 | |||||||
chr2:68814961 | T | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(232): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.808-1328T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68814961 | |||||||
chr2:68815010 | G | A | 69 | a0002c0002t0001g0182 a0002c0002t0001g0233 a0002c0002t0001g0260 others(66): Show |
69 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.808-1279G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815010 | |||||||
chr2:68815019 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-1270C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815019 | |||||||
chr2:68815164 | G | T | 1 | a0002c0002t0002g0071 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.808-1125G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815164 | |||||||
chr2:68815223 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.808-1066G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815223 | |||||||
chr2:68815280 | A | G | 3 | a0002c0002t0002g0181 a0002c0002t0003g0056 a0002c0002t0004g0053 |
3 | HG01891.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.808-1009A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815280 | |||||||
chr2:68815316 | G | A | 7 | a0001c0001t0001g0087 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
7 | NA18950.hp2 NA18956.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.808-973G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815316 | |||||||
chr2:68815317 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-972C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815317 | |||||||
chr2:68815329 | A | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(224): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.808-960A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815329 | |||||||
chr2:68815363 | G | A | 94 | a0002c0002t0001g0268 a0002c0002t0003g0136 a0003c0003t0001g0009 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.808-926G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815363 | |||||||
chr2:68815389 | G | C | 95 | a0002c0002t0001g0268 a0002c0002t0003g0136 a0002c0004t0001g0348 others(92): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.808-900G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815389 | |||||||
chr2:68815416 | C | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.808-873C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815416 | |||||||
chr2:68815421 | CG | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.808-866delG | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815421 | ||||||
chr2:68815443 | C | CT | 6 | a0002c0002t0011g0144 a0002c0004t0008g0291 a0003c0003t0001g0110 others(3): Show |
6 | HG01257.hp1 HG03453.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-821dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | C | CTT | 70 | a0003c0003t0001g0009 a0003c0003t0001g0058 a0003c0003t0001g0064 others(67): Show |
72 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.808-822_808-821dup others(2): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | C | CTTT | 18 | a0002c0002t0011g0141 a0002c0002t0011g0153 a0003c0003t0001g0103 others(15): Show |
18 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.808-823_808-821dup others(3): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | C | CTTTT | 8 | a0002c0002t0006g0188 a0002c0002t0006g0310 a0002c0002t0006g0320 others(5): Show |
8 | HG00408.hp1 HG01074.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.808-824_808-821dup others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | CT | C | 71 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0001g0111 others(68): Show |
71 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.808-821delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | CTT | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(125): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.808-822_808-821del others(2): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | CTTTT | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.808-824_808-821del others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815443 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0268 a0002c0002t0003g0136 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.808-831_808-821del others(11): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815443 | ||||||
chr2:68815481 | G | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(220): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.808-808G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815481 | |||||||
chr2:68815493 | C | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0311 |
3 | HG02647.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.808-796C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815493 | |||||||
chr2:68815496 | G | T | 1 | a0010c0018t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.808-793G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815496 | |||||||
chr2:68815506 | A | G | 1 | a0002c0002t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.808-783A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815506 | |||||||
chr2:68815514 | G | A | 11 | a0002c0002t0003g0156 a0002c0002t0006g0188 a0002c0002t0006g0310 others(8): Show |
11 | HG00408.hp1 HG01074.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.808-775G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815514 | |||||||
chr2:68815544 | G | T | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.808-745G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815544 | |||||||
chr2:68815576 | G | A | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.808-713G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815576 | |||||||
chr2:68815578 | G | A | 1 | a0003c0003t0003g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.808-711G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815578 | |||||||
chr2:68815596 | G | A | 95 | a0002c0002t0001g0268 a0002c0002t0003g0136 a0002c0004t0001g0348 others(92): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.808-693G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815596 | |||||||
chr2:68815674 | G | C | 1 | a0002c0002t0002g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.808-615G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815674 | |||||||
chr2:68815708 | C | G | 1 | a0001c0001t0003g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.808-581C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815708 | |||||||
chr2:68815802 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-487C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815802 | |||||||
chr2:68815804 | T | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-485T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815804 | |||||||
chr2:68815806 | C | CT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-482dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68815806 | ||||||
chr2:68815808 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-481C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815808 | |||||||
chr2:68815811 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.808-478G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815811 | |||||||
chr2:68815989 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(91): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.808-300G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68815989 | |||||||
chr2:68816068 | A | G | 1 | a0002c0002t0002g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.808-221A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68816068 | |||||||
chr2:68816132 | CT | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(221): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.808-146delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 68816132 | ||||||
chr2:68816134 | T | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(221): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.808-155T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68816134 | |||||||
chr2:68816188 | T | C | 6 | a0002c0002t0002g0020 a0002c0002t0002g0258 a0002c0002t0017g0308 others(3): Show |
6 | HG02055.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-101T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | chr2 | 68816188 | |||||||
chr2:68816407 | G | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.881+45G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816407 | |||||||
chr2:68816501 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0005g0046 |
2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.881+139C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816501 | |||||||
chr2:68816517 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.881+155T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816517 | |||||||
chr2:68816549 | A | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(333): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.881+187A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816549 | |||||||
chr2:68816563 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.881+201G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816563 | |||||||
chr2:68816871 | T | C | 2 | a0003c0003t0001g0074 a0003c0003t0001g0075 |
2 | HG01099.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.881+509T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816871 | |||||||
chr2:68816932 | A | C | 106 | a0002c0002t0001g0268 a0002c0002t0002g0020 a0002c0002t0002g0258 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.881+570A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68816932 | |||||||
chr2:68817111 | T | TG | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(127): Show |
142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.881+749_881+750ins others(1): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68817111 | |||||||
chr2:68817396 | A | T | 172 | a0002c0002t0001g0182 a0002c0002t0001g0233 a0002c0002t0001g0260 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.882-477A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68817396 | |||||||
chr2:68817497 | G | T | 59 | a0003c0003t0001g0009 a0003c0003t0001g0058 a0003c0003t0001g0064 others(56): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.882-376G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68817497 | |||||||
chr2:68817520 | G | C | 1 | a0003c0003t0005g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882-353G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68817520 | |||||||
chr2:68817819 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0213 a0001c0001t0003g0137 others(3): Show |
6 | HG03654.hp1 HG03654.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.882-54C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68817819 | |||||||
chr2:68817839 | G | A | 5 | a0001c0001t0003g0140 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
5 | HG01943.hp2 HG01981.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.882-34G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 7/10 | chr2 | 68817839 | |||||||
chr2:68818026 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(112): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1003+32C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818026 | |||||||
chr2:68818124 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(112): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1003+130C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818124 | |||||||
chr2:68818178 | A | G | 5 | a0002c0005t0002g0274 a0002c0005t0012g0019 a0002c0005t0012g0185 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003+184A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818178 | |||||||
chr2:68818256 | G | A | 1 | a0002c0004t0005g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1003+262G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818256 | |||||||
chr2:68818391 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1003+397A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818391 | |||||||
chr2:68818423 | G | T | 1 | a0002c0002t0002g0068 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1003+429G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818423 | |||||||
chr2:68818459 | C | A | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1003+465C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818459 | |||||||
chr2:68818524 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(183): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1003+530T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818524 | |||||||
chr2:68818563 | A | G | 3 | a0002c0004t0001g0290 a0002c0004t0008g0291 a0002c0004t0013g0343 |
3 | HG01891.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1004-560A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818563 | |||||||
chr2:68818641 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(183): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1004-482C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818641 | |||||||
chr2:68818659 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(11): Show |
15 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1004-464G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818659 | |||||||
chr2:68818713 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1004-410G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818713 | |||||||
chr2:68818821 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1004-302A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68818821 | |||||||
chr2:68819032 | C | A | 22 | a0002c0002t0002g0077 a0002c0002t0002g0078 a0002c0002t0002g0080 others(19): Show |
22 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004-91C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 8/10 | chr2 | 68819032 | |||||||
chr2:68819424 | T | G | 4 | a0002c0002t0002g0202 a0002c0002t0002g0204 a0002c0002t0002g0214 others(1): Show |
4 | NA18952.hp2 NA18959.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+105T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68819424 | |||||||
chr2:68819587 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(112): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1200+268G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68819587 | |||||||
chr2:68819738 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(112): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1200+419G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68819738 | |||||||
chr2:68819775 | C | T | 1 | a0002c0002t0019g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1200+456C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68819775 | |||||||
chr2:68819878 | G | A | 1 | a0001c0001t0003g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1200+559G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68819878 | |||||||
chr2:68820205 | T | A | 1 | a0003c0003t0001g0102 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1200+886T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820205 | |||||||
chr2:68820234 | A | G | 1 | a0004c0009t0007g0330 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1200+915A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820234 | |||||||
chr2:68820329 | A | G | 2 | a0001c0001t0003g0158 a0001c0001t0005g0029 |
2 | HG00280.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1200+1010A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820329 | |||||||
chr2:68820377 | G | A | 2 | a0002c0002t0002g0209 a0002c0002t0004g0145 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1200+1058G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820377 | |||||||
chr2:68820703 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(113): Show |
127 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1200+1384C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820703 | |||||||
chr2:68820762 | T | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(11): Show |
15 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200+1443T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820762 | |||||||
chr2:68820849 | G | C | 6 | a0002c0007t0007g0016 a0002c0007t0007g0264 a0002c0007t0007g0265 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-1491G>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820849 | |||||||
chr2:68820869 | A | G | 7 | a0001c0001t0001g0184 a0001c0001t0001g0271 a0001c0001t0001g0276 others(4): Show |
8 | HG02572.hp1 HG02896.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-1471A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820869 | |||||||
chr2:68820916 | A | T | 1 | a0010c0018t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1201-1424A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820916 | |||||||
chr2:68820919 | A | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(198): Show |
213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1201-1421A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820919 | |||||||
chr2:68820977 | A | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(11): Show |
15 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-1363A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820977 | |||||||
chr2:68820998 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1201-1342C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68820998 | |||||||
chr2:68821042 | A | G | 1 | a0003c0003t0001g0183 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1201-1298A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821042 | |||||||
chr2:68821092 | C | CT | 21 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0099 others(18): Show |
21 | HG01243.hp2 HG01257.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.1201-1226dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821092 | ||||||
chr2:68821092 | C | CTT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
101 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1201-1227_1201-122 others(6): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821092 | ||||||
chr2:68821092 | C | CTTT | 17 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0203 others(14): Show |
18 | HG00621.hp1 HG02647.hp2 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.1201-1228_1201-122 others(7): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821092 | ||||||
chr2:68821092 | CT | C | 116 | a0002c0002t0001g0129 a0002c0002t0002g0072 a0002c0002t0003g0156 others(113): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1201-1226delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821092 | ||||||
chr2:68821092 | CTT | C | 6 | a0003c0003t0001g0110 a0003c0003t0001g0215 a0003c0003t0001g0325 others(3): Show |
6 | HG00099.hp1 HG01515.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-1227_1201-122 others(6): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821092 | ||||||
chr2:68821130 | T | C | 8 | a0002c0004t0001g0290 a0002c0004t0001g0323 a0002c0004t0001g0332 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-1210T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821130 | |||||||
chr2:68821151 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(113): Show |
127 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1201-1189C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821151 | |||||||
chr2:68821163 | C | T | 1 | a0002c0020t0001g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1201-1177C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821163 | |||||||
chr2:68821194 | A | T | 25 | a0002c0002t0001g0233 a0002c0002t0001g0260 a0002c0002t0002g0121 others(22): Show |
25 | HG01928.hp1 HG01978.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.1201-1146A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821194 | |||||||
chr2:68821375 | C | T | 3 | a0002c0005t0012g0019 a0002c0005t0012g0185 a0002c0005t0012g0210 |
3 | HG02572.hp2 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1201-965C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821375 | |||||||
chr2:68821486 | A | T | 1 | a0002c0002t0010g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1201-854A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68821486 | |||||||
chr2:68821906 | G | GT | 102 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0186 others(99): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1201-412dupT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821906 | ||||||
chr2:68821906 | G | GTT | 15 | a0001c0001t0001g0163 a0002c0005t0002g0274 a0002c0005t0012g0019 others(12): Show |
15 | HG00597.hp2 HG01943.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-413_1201-412d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821906 | ||||||
chr2:68821906 | GT | G | 16 | a0002c0002t0002g0077 a0002c0002t0002g0133 a0002c0002t0002g0224 others(13): Show |
17 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1201-412delT | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821906 | ||||||
chr2:68821906 | GTTT | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(108): Show |
123 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1201-414_1201-412d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 68821906 | ||||||
chr2:68822026 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(113): Show |
127 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1201-314C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68822026 | |||||||
chr2:68822266 | C | G | 92 | a0003c0003t0001g0009 a0003c0003t0001g0058 a0003c0003t0001g0064 others(89): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1201-74C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | chr2 | 68822266 | |||||||
chr2:68822884 | A | G | 1 | a0003c0003t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1733+12A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68822884 | |||||||
chr2:68822899 | G | A | 1 | a0002c0004t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1733+27G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68822899 | |||||||
chr2:68822957 | A | G | 1 | a0001c0001t0004g0334 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1733+85A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68822957 | |||||||
chr2:68823176 | TTA | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(11): Show |
15 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1733+306_1733+307d others(4): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 68823176 | ||||||
chr2:68823254 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(127): Show |
142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1733+382G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823254 | |||||||
chr2:68823296 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1733+424G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823296 | |||||||
chr2:68823298 | A | ACTT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(127): Show |
142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1733+429_1733+431d others(5): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 68823298 | ||||||
chr2:68823508 | G | T | 5 | a0002c0008t0008g0006 a0002c0008t0008g0076 a0004c0009t0002g0331 others(2): Show |
6 | HG01123.hp2 HG01167.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1733+636G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823508 | |||||||
chr2:68823510 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1733+638G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823510 | |||||||
chr2:68823656 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(127): Show |
142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1733+784G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823656 | |||||||
chr2:68823782 | G | T | 2 | a0002c0002t0001g0263 a0002c0002t0003g0338 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1733+910G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823782 | |||||||
chr2:68823805 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(214): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1733+933G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823805 | |||||||
chr2:68823843 | A | T | 1 | a0010c0018t0001g0277 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1733+971A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823843 | |||||||
chr2:68823988 | G | A | 6 | a0002c0007t0007g0016 a0002c0007t0007g0264 a0002c0007t0007g0265 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1733+1116G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823988 | |||||||
chr2:68823990 | G | A | 1 | a0002c0002t0011g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1733+1118G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68823990 | |||||||
chr2:68824056 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1733+1184T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824056 | |||||||
chr2:68824134 | C | A | 9 | a0002c0002t0001g0182 a0002c0004t0001g0290 a0002c0004t0001g0323 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1733+1262C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824134 | |||||||
chr2:68824188 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(215): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1733+1316G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824188 | |||||||
chr2:68824265 | TGTCAGA | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(215): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1733+1397_1733+140 others(10): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 68824265 | ||||||
chr2:68824288 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(242): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1733+1416A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824288 | |||||||
chr2:68824290 | T | C | 3 | a0004c0009t0002g0331 a0004c0009t0007g0330 a0004c0009t0007g0350 |
3 | HG01167.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1733+1418T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824290 | |||||||
chr2:68824370 | A | G | 1 | a0003c0003t0001g0238 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1733+1498A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824370 | |||||||
chr2:68824470 | T | C | 131 | a0001c0001t0001g0017 a0001c0001t0001g0131 a0001c0001t0001g0190 others(128): Show |
134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1734-1517T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824470 | |||||||
chr2:68824483 | T | C | 1 | a0003c0003t0001g0174 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1734-1504T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824483 | |||||||
chr2:68824506 | G | A | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1734-1481G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824506 | |||||||
chr2:68824525 | G | A | 3 | a0002c0002t0006g0188 a0002c0002t0011g0141 a0002c0002t0011g0144 |
3 | HG01261.hp1 HG01975.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1734-1462G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824525 | |||||||
chr2:68824538 | C | G | 3 | a0001c0001t0001g0328 a0002c0002t0001g0128 a0002c0002t0001g0129 |
3 | HG01168.hp2 HG01169.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1734-1449C>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824538 | |||||||
chr2:68824546 | T | G | 2 | a0003c0003t0003g0335 a0003c0003t0003g0342 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1734-1441T>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824546 | |||||||
chr2:68824553 | T | C | 1 | a0002c0002t0002g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1734-1434T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824553 | |||||||
chr2:68824559 | G | A | 3 | a0002c0002t0001g0263 a0002c0002t0003g0156 a0002c0004t0001g0348 |
3 | HG01243.hp2 HG02809.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1734-1428G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824559 | |||||||
chr2:68824568 | A | C | 1 | a0003c0003t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1734-1419A>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824568 | |||||||
chr2:68824569 | T | C | 1 | a0003c0003t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1734-1418T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824569 | |||||||
chr2:68824576 | C | A | 1 | a0003c0003t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1734-1411C>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824576 | |||||||
chr2:68824612 | G | A | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1734-1375G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824612 | |||||||
chr2:68824614 | T | C | 1 | a0002c0002t0014g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1734-1373T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824614 | |||||||
chr2:68824674 | G | A | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1734-1313G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824674 | |||||||
chr2:68824678 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1734-1309C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824678 | |||||||
chr2:68824691 | G | A | 1 | a0002c0004t0001g0290 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1734-1296G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824691 | |||||||
chr2:68824697 | A | G | 1 | a0003c0003t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1734-1290A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824697 | |||||||
chr2:68824698 | T | C | 6 | a0001c0001t0001g0131 a0001c0001t0001g0190 a0001c0001t0001g0192 others(3): Show |
6 | HG00140.hp2 NA18955.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1734-1289T>C | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824698 | |||||||
chr2:68824721 | A | G | 71 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(68): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1734-1266A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824721 | |||||||
chr2:68824722 | A | G | 39 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0163 others(36): Show |
39 | HG00438.hp1 HG00621.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1734-1265A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824722 | |||||||
chr2:68824737 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1734-1250G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824737 | |||||||
chr2:68824741 | C | CA | 7 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0002g0070 others(4): Show |
7 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1734-1238dupA | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 68824741 | ||||||
chr2:68824766 | A | G | 2 | a0002c0008t0008g0006 a0002c0008t0008g0076 |
3 | HG01123.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1734-1221A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824766 | |||||||
chr2:68824804 | G | A | 5 | a0002c0005t0002g0274 a0002c0005t0012g0019 a0002c0005t0012g0185 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734-1183G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824804 | |||||||
chr2:68824898 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1734-1089C>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824898 | |||||||
chr2:68824998 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(124): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1734-989A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68824998 | |||||||
chr2:68825161 | G | A | 3 | a0002c0002t0002g0069 a0002c0002t0002g0070 a0003c0003t0010g0038 |
3 | HG00323.hp1 HG00639.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1734-826G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825161 | |||||||
chr2:68825220 | T | A | 1 | a0003c0003t0001g0198 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1734-767T>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825220 | |||||||
chr2:68825266 | A | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0184 a0001c0001t0001g0271 others(6): Show |
10 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1734-721A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825266 | |||||||
chr2:68825391 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(87): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1734-596G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825391 | |||||||
chr2:68825417 | A | G | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0294 others(1): Show |
4 | HG00735.hp1 HG01109.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734-570A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825417 | |||||||
chr2:68825707 | G | A | 1 | a0004c0009t0007g0350 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1734-280G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825707 | |||||||
chr2:68825745 | A | T | 1 | a0002c0004t0001g0323 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1734-242A>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825745 | |||||||
chr2:68825818 | G | A | 1 | a0002c0004t0001g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1734-169G>A | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825818 | |||||||
chr2:68825859 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(200): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1734-128A>G | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825859 | |||||||
chr2:68825983 | G | T | 21 | a0002c0002t0001g0008 a0002c0002t0001g0094 a0002c0002t0001g0098 others(18): Show |
21 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1734-4G>T | ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | chr2 | 68825983 |