Item | Value |
---|---|
geneid | 57584 |
ensemblid | ENSG00000107863.20 |
hgncid | 23725 |
symbol | ARHGAP21 |
name | Rho GTPase activating protein 21 |
refseq_nuc | NM_020824.4 |
refseq_prot | NP_065875.3 |
ensembl_nuc | ENST00000396432.7 |
ensembl_prot | ENSP00000379709.2 |
mane_status | MANE Select |
chr | chr10 |
start | 24583614 |
end | 24723887 |
strand | - |
ver | v1.2 |
region | chr10:24583614-24723887 |
region5000 | chr10:24578614-24728887 |
regionname0 | ARHGAP21_chr10_24583614_24723887 |
regionname5000 | ARHGAP21_chr10_24578614_24728887 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1958 | 139 | 43 | 24 | 46 | 7 | 18 | 38 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0002 | 0/0 | 1958 | 126 | 21 | 30 | 58 | 7 | 10 | 43 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0003 | 0/0 | 1958 | 42 | 0 | 5 | 34 | 0 | 3 | 26 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0004 | 0/0 | 1958 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0005 | 0/0 | 1958 | 8 | 7 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0006 | 0/0 | 1976 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1971): Show |
chr10 | 24578614 | 24728887 |
a0007 | 0/0 | 1958 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0008 | 0/0 | 1958 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0009 | 0/0 | 1958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0010 | 0/0 | 1958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0011 | 0/0 | 1958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0012 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0013 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0014 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0015 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0016 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0017 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0018 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0019 | 0/0 | 1958 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0020 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1971): Show |
chr10 | 24578614 | 24728887 |
a0021 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
a0022 | 0/1 | 1958 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | MMATR others(1953): Show |
chr10 | 24578614 | 24728887 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5874 | 138 | 42 | 24 | 46 | 7 | 18 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0001c0014 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0002c0002 | 0/0 | 5874 | 121 | 20 | 29 | 55 | 7 | 10 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0002c0015 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0002c0017 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0002c0018 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0002c0021 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0002c0030 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0003c0003 | 0/0 | 5874 | 37 | 0 | 5 | 29 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0003c0006 | 0/0 | 5874 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0004c0004 | 0/0 | 5874 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0005c0005 | 0/0 | 5874 | 8 | 7 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0006c0007 | 0/0 | 5928 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5923): Show |
chr10 | 24578614 | 24728887 | ||
a0006c0029 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5923): Show |
chr10 | 24578614 | 24728887 | ||
a0007c0008 | 0/0 | 5874 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0008c0009 | 0/0 | 5874 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0009c0010 | 0/0 | 5874 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0010c0012 | 0/0 | 5874 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0011c0011 | 0/0 | 5874 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0012c0019 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0013c0026 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0014c0022 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0015c0020 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0016c0016 | 0/0 | 5874 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0017c0013 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0018c0027 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0019c0023 | 0/0 | 5874 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0020c0028 | 0/0 | 5928 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5923): Show |
chr10 | 24578614 | 24728887 | ||
a0021c0024 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 | ||
a0022c0025 | 0/1 | 5874 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | ATGAT others(5869): Show |
chr10 | 24578614 | 24728887 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7379 | 78 | 32 | 12 | 19 | 3 | 12 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0002 | 0/0 | 7378 | 42 | 3 | 9 | 24 | 1 | 5 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7373): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0003 | 1/0 | 7381 | 4 | 2 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0004 | 0/0 | 7376 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7371): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0005 | 0/0 | 7385 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7380): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0008 | 0/0 | 7380 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7375): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0009 | 0/0 | 7383 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7378): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0013 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0001c0001t0016 | 0/0 | 7378 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7373): Show |
chr10 | 24578614 | 24728887 |
a0001c0014t0004 | 0/0 | 7376 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7371): Show |
chr10 | 24578614 | 24728887 |
a0002c0002t0001 | 0/0 | 7379 | 115 | 19 | 29 | 54 | 5 | 8 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0002c0002t0004 | 0/0 | 7376 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7371): Show |
chr10 | 24578614 | 24728887 |
a0002c0002t0007 | 0/0 | 7382 | 3 | 0 | 0 | 0 | 1 | 2 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7377): Show |
chr10 | 24578614 | 24728887 |
a0002c0002t0014 | 0/0 | 7379 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0002c0015t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0002c0017t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0002c0018t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0002c0021t0001 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0002c0030t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0003c0003t0001 | 0/0 | 7379 | 36 | 0 | 5 | 28 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0003c0003t0012 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0003c0006t0002 | 0/0 | 7378 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7373): Show |
chr10 | 24578614 | 24728887 |
a0003c0006t0003 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0004c0004t0001 | 0/0 | 7379 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0005c0005t0001 | 0/0 | 7379 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0005c0005t0003 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0005c0005t0004 | 0/0 | 7376 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7371): Show |
chr10 | 24578614 | 24728887 |
a0006c0007t0006 | 0/0 | 7434 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7429): Show |
chr10 | 24578614 | 24728887 |
a0006c0007t0015 | 0/0 | 7432 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7427): Show |
chr10 | 24578614 | 24728887 |
a0006c0029t0006 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7429): Show |
chr10 | 24578614 | 24728887 |
a0007c0008t0001 | 0/0 | 7379 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0007c0008t0004 | 0/0 | 7376 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7371): Show |
chr10 | 24578614 | 24728887 |
a0008c0009t0005 | 0/0 | 7385 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7380): Show |
chr10 | 24578614 | 24728887 |
a0009c0010t0001 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0010c0012t0010 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0011c0011t0001 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0012c0019t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0013c0026t0003 | 0/0 | 7381 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0014c0022t0002 | 0/0 | 7378 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7373): Show |
chr10 | 24578614 | 24728887 |
a0015c0020t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0016c0016t0003 | 0/0 | 7381 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0017c0013t0002 | 0/0 | 7378 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7373): Show |
chr10 | 24578614 | 24728887 |
a0018c0027t0001 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0019c0023t0001 | 0/0 | 7379 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7374): Show |
chr10 | 24578614 | 24728887 |
a0020c0028t0006 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7429): Show |
chr10 | 24578614 | 24728887 |
a0021c0024t0011 | 0/0 | 7381 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
a0022c0025t0003 | 0/1 | 7381 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | GCTTC others(7376): Show |
chr10 | 24578614 | 24728887 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0003g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0008g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0001t0016g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0001c0014t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0007g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0007g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0002t0014g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0015t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0017t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0018t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0021t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0002c0030t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0003t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0006t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0006t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0006t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0006t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0003c0006t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0004c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0005c0005t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0006c0007t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0006c0007t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0006c0007t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0006c0007t0015g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0006c0029t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0007c0008t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0007c0008t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0007c0008t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0008c0009t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0008c0009t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0008c0009t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0009c0010t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0009c0010t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0010c0012t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0010c0012t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0011c0011t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0011c0011t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0012c0019t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0013c0026t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0014c0022t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0015c0020t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0016c0016t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0017c0013t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0018c0027t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0019c0023t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0020c0028t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0021c0024t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
a0022c0025t0003g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0280 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0279 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00280 | hp1 | a0002 | c0002 | t0007 | g0009 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0156 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0220 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0231 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0180 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00609 | hp2 | a0005 | c0005 | t0003 | g0147 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00642 | hp2 | a0012 | c0019 | t0001 | g0037 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00735 | hp2 | a0002 | c0018 | t0001 | g0099 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01081 | hp1 | a0013 | c0026 | t0003 | g0157 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0328 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01109 | hp1 | a0014 | c0022 | t0002 | g0338 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0325 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01261 | hp2 | a0015 | c0020 | t0001 | g0113 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01433 | hp1 | a0016 | c0016 | t0003 | g0028 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0159 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01516 | hp2 | a0002 | c0002 | t0014 | g0106 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01517 | hp1 | a0001 | c0001 | t0009 | g0160 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0124 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01884 | hp1 | a0002 | c0002 | t0004 | g0296 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0213 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0266 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0200 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0248 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02055 | hp1 | a0005 | c0005 | t0001 | g0105 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02074 | hp2 | a0002 | c0017 | t0001 | g0048 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02083 | hp1 | a0002 | c0015 | t0001 | g0162 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0211 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0237 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02129 | hp2 | a0006 | c0007 | t0006 | g0292 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02145 | hp1 | a0004 | c0004 | t0001 | g0087 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0202 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0214 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02451 | hp1 | a0005 | c0005 | t0001 | g0104 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02523 | hp1 | a0017 | c0013 | t0002 | g0316 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02523 | hp2 | a0006 | c0007 | t0006 | g0294 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0031 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02647 | hp2 | a0018 | c0027 | t0001 | g0036 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02723 | hp1 | a0010 | c0012 | t0010 | g0017 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02738 | hp2 | a0019 | c0023 | t0001 | g0091 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02809 | hp2 | a0004 | c0004 | t0001 | g0098 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02818 | hp2 | a0011 | c0011 | t0001 | g0259 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02896 | hp1 | a0010 | c0012 | t0010 | g0016 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02970 | hp1 | a0004 | c0004 | t0001 | g0032 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02976 | hp1 | a0002 | c0021 | t0001 | g0084 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02976 | hp2 | a0004 | c0004 | t0001 | g0092 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03017 | hp2 | a0002 | c0002 | t0007 | g0010 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03130 | hp1 | a0001 | c0001 | t0013 | g0255 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03130 | hp2 | a0005 | c0005 | t0001 | g0168 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03139 | hp2 | a0004 | c0004 | t0001 | g0041 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03195 | hp1 | a0009 | c0010 | t0001 | g0267 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03209 | hp1 | a0005 | c0005 | t0004 | g0288 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03209 | hp2 | a0005 | c0005 | t0001 | g0103 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0107 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03486 | hp2 | a0011 | c0011 | t0001 | g0260 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0345 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03540 | hp2 | a0004 | c0004 | t0001 | g0040 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03579 | hp2 | a0004 | c0004 | t0001 | g0038 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03688 | hp1 | a0002 | c0002 | t0007 | g0008 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0277 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0212 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG04228 | hp2 | a0003 | c0003 | t0001 | g0117 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18522 | hp1 | a0005 | c0005 | t0001 | g0285 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18747 | hp1 | a0006 | c0007 | t0015 | g0289 | EAS | CHB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | CHB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18906 | hp1 | a0001 | c0014 | t0004 | g0287 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18941 | hp2 | a0007 | c0008 | t0001 | g0262 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18945 | hp1 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18947 | hp1 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18957 | hp1 | a0003 | c0006 | t0002 | g0347 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18961 | hp2 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18963 | hp1 | a0003 | c0003 | t0001 | g0278 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18974 | hp2 | a0007 | c0008 | t0001 | g0263 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0302 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18982 | hp2 | a0003 | c0003 | t0001 | g0203 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18986 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18987 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18989 | hp1 | a0006 | c0029 | t0006 | g0291 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18989 | hp2 | a0001 | c0001 | t0016 | g0351 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18992 | hp1 | a0003 | c0006 | t0002 | g0349 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18995 | hp2 | a0008 | c0009 | t0005 | g0005 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0225 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19004 | hp1 | a0008 | c0009 | t0005 | g0003 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19005 | hp2 | a0003 | c0006 | t0002 | g0350 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19011 | hp1 | a0008 | c0009 | t0005 | g0004 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19011 | hp2 | a0020 | c0028 | t0006 | g0290 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19030 | hp1 | a0005 | c0005 | t0001 | g0138 | AFR | LWK | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19030 | hp2 | a0021 | c0024 | t0011 | g0033 | AFR | LWK | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19056 | hp1 | a0003 | c0003 | t0012 | g0173 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19056 | hp2 | a0006 | c0007 | t0006 | g0293 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19057 | hp2 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19060 | hp1 | a0003 | c0006 | t0002 | g0348 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19066 | hp2 | a0007 | c0008 | t0004 | g0346 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19072 | hp1 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19078 | hp1 | a0003 | c0003 | t0001 | g0217 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19081 | hp1 | a0003 | c0006 | t0003 | g0216 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19085 | hp2 | a0003 | c0003 | t0001 | g0205 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19087 | hp2 | a0002 | c0030 | t0001 | g0090 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0222 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ASW | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0324 | EUR | TSI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0201 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02109 | hp1 | a0009 | c0010 | t0001 | g0268 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG02559 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | USA | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | USA | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
homoSapiens | chm13v2 | a0022 | c0025 | t0003 | g0029 | REF | REF | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0158 | REF | REF | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:24584440 | C | G | 10 | a0002 a0003 a0004 others(7): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
missense_variant | MODERATE | c.5849G>C | p.Ser1950Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6555/7381 | 5849/5877 | 1950/1958 | chr10 | 24584440 | |||
chr10:24584440 | C | T | 1 | a0003 | 5 | NA18957.hp1 NA18992.hp1 NA19005.hp2 others(2): Show |
missense_variant | MODERATE | c.5849G>A | p.Ser1950Asn | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6555/7381 | 5849/5877 | 1950/1958 | chr10 | 24584440 | |||
chr10:24584635 | G | A | 1 | a0017 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.5654C>T | p.Thr1885Met | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6360/7381 | 5654/5877 | 1885/1958 | chr10 | 24584635 | |||
chr10:24584959 | G | A | 1 | a0012 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.5330C>T | p.Ala1777Val | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6036/7381 | 5330/5877 | 1777/1958 | chr10 | 24584959 | |||
chr10:24585182 | G | A | 1 | a0015 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.5107C>T | p.Leu1703Phe | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5813/7381 | 5107/5877 | 1703/1958 | chr10 | 24585182 | |||
chr10:24585335 | T | C | 1 | a0006 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.4954A>G | p.Arg1652Gly | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5660/7381 | 4954/5877 | 1652/1958 | chr10 | 24585335 | |||
chr10:24594993 | G | GAAAGGAA others(47): Show |
2 | a0006 a0020 |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
conservative_inframe_insertion | MODERATE | c.3787-8_3832dupTGTT others(50): Show |
p.Leu1277_Ser1278ins others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/26 | 4538/7381 | 3832/5877 | 1278/1958 | chr10 | 24594993 | |||
chr10:24596856 | C | T | 2 | a0004 a0021 |
10 | HG02145.hp1 HG02559.hp2 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.3361G>A | p.Gly1121Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/26 | 4067/7381 | 3361/5877 | 1121/1958 | chr10 | 24596856 | |||
chr10:24600731 | C | G | 1 | a0011 | 2 | HG02818.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.3047G>C | p.Cys1016Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/26 | 3753/7381 | 3047/5877 | 1016/1958 | chr10 | 24600731 | |||
chr10:24619599 | C | T | 1 | a0016 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.2296G>A | p.Gly766Arg | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 3002/7381 | 2296/5877 | 766/1958 | chr10 | 24619599 | |||
chr10:24619757 | T | C | 10 | a0002 a0004 a0005 others(7): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
missense_variant | MODERATE | c.2138A>G | p.Asn713Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2844/7381 | 2138/5877 | 713/1958 | chr10 | 24619757 | |||
chr10:24619844 | G | C | 1 | a0010 | 2 | HG02723.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.2051C>G | p.Ser684Cys | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2757/7381 | 2051/5877 | 684/1958 | chr10 | 24619844 | |||
chr10:24620069 | C | T | 1 | a0007 | 3 | NA18941.hp2 NA18974.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.1826G>A | p.Arg609Gln | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2532/7381 | 1826/5877 | 609/1958 | chr10 | 24620069 | |||
chr10:24620159 | G | T | 1 | a0020 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1736C>A | p.Ser579Tyr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2442/7381 | 1736/5877 | 579/1958 | chr10 | 24620159 | |||
chr10:24620286 | T | C | 1 | a0014 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1609A>G | p.Arg537Gly | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2315/7381 | 1609/5877 | 537/1958 | chr10 | 24620286 | |||
chr10:24620421 | T | C | 1 | a0019 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1474A>G | p.Arg492Gly | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2180/7381 | 1474/5877 | 492/1958 | chr10 | 24620421 | |||
chr10:24620630 | G | A | 1 | a0021 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1265C>T | p.Thr422Met | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1971/7381 | 1265/5877 | 422/1958 | chr10 | 24620630 | |||
chr10:24620709 | T | C | 1 | a0013 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1186A>G | p.Ile396Val | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1892/7381 | 1186/5877 | 396/1958 | chr10 | 24620709 | |||
chr10:24620916 | T | C | 1 | a0018 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.979A>G | p.Thr327Ala | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1685/7381 | 979/5877 | 327/1958 | chr10 | 24620916 | |||
chr10:24621258 | C | T | 1 | a0009 | 2 | HG02109.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.637G>A | p.Ala213Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1343/7381 | 637/5877 | 213/1958 | chr10 | 24621258 | |||
chr10:24670388 | T | C | 1 | a0008 | 3 | NA18995.hp2 NA19004.hp1 NA19011.hp1 |
missense_variant | MODERATE | c.73A>G | p.Asn25Asp | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/26 | 779/7381 | 73/5877 | 25/1958 | chr10 | 24670388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:24584478 | C | G | 1 | a0002c0018 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.5811G>C | p.Ala1937Ala | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6517/7381 | 5811/5877 | 1937/1958 | chr10 | 24584478 | |||
chr10:24585882 | C | T | 1 | a0002c0017 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.4407G>A | p.Gln1469Gln | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5113/7381 | 4407/5877 | 1469/1958 | chr10 | 24585882 | |||
chr10:24595900 | A | G | 3 | a0006c0007 a0006c0029 a0020c0028 |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
synonymous_variant | LOW | c.3621T>C | p.Asp1207Asp | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 18/26 | 4327/7381 | 3621/5877 | 1207/1958 | chr10 | 24595900 | |||
chr10:24619600 | G | A | 1 | a0001c0014 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2295C>T | p.Thr765Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 3001/7381 | 2295/5877 | 765/1958 | chr10 | 24619600 | |||
chr10:24619651 | C | T | 1 | a0002c0015 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.2244G>A | p.Pro748Pro | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2950/7381 | 2244/5877 | 748/1958 | chr10 | 24619651 | |||
chr10:24620152 | C | A | 1 | a0002c0021 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1743G>T | p.Ser581Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2449/7381 | 1743/5877 | 581/1958 | chr10 | 24620152 | |||
chr10:24620941 | T | G | 3 | a0006c0007 a0006c0029 a0020c0028 |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
synonymous_variant | LOW | c.954A>C | p.Thr318Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1660/7381 | 954/5877 | 318/1958 | chr10 | 24620941 | |||
chr10:24621280 | G | A | 1 | a0002c0030 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.615C>T | p.Pro205Pro | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1321/7381 | 615/5877 | 205/1958 | chr10 | 24621280 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:24583825 | G | A | 1 | a0002c0002t0014 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 587 | chr10 | 24583825 | ||||||
chr10:24583830 | G | A | 1 | a0003c0003t0012 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 582 | chr10 | 24583830 | ||||||
chr10:24584031 | T | A | 4 | a0006c0007t0006 a0006c0007t0015 a0006c0029t0006 others(1): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 381 | chr10 | 24584031 | ||||||
chr10:24584053 | C | T | 1 | a0010c0012t0010 | 2 | HG02723.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*359G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 359 | chr10 | 24584053 | ||||||
chr10:24584181 | T | C | 1 | a0010c0012t0010 | 2 | HG02723.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*231A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 231 | chr10 | 24584181 | ||||||
chr10:24584208 | C | G | 1 | a0001c0001t0013 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 204 | chr10 | 24584208 | ||||||
chr10:24584221 | A | AAT | 5 | a0001c0001t0008 a0001c0001t0009 a0006c0007t0006 others(2): Show |
10 | HG01099.hp2 HG01255.hp2 HG01516.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*189_*190dupAT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 190 | chr10 | 24584221 | ||||||
chr10:24584221 | AAT | A | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(25): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*189_*190delAT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 189 | chr10 | 24584221 | ||||||
chr10:24584240 | A | G | 1 | a0021c0024t0011 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 172 | chr10 | 24584240 | ||||||
chr10:24723673 | C | CCCG | 1 | a0002c0002t0007 | 3 | HG00280.hp1 HG03017.hp2 HG03688.hp1 |
5_prime_UTR_variant | MODIFIER | c.-495_-493dupCGG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | 24723673 | ||||||
chr10:24723673 | C | CCCGCCG | 2 | a0001c0001t0005 a0008c0009t0005 |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-498_-493dupCGGCGG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | 24723673 | ||||||
chr10:24723673 | CCCG | C | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(12): Show |
67 | HG00673.hp2 HG00733.hp1 HG01099.hp2 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-495_-493delCGG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | 24723673 | ||||||
chr10:24723846 | G | A | 1 | a0001c0001t0016 | 1 | NA18989.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-665C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | chr10 | 24723846 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:24586167 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4183-61T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586167 | |||||||
chr10:24586501 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4183-395C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586501 | |||||||
chr10:24586523 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4183-417A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586523 | |||||||
chr10:24586917 | G | A | 1 | a0001c0001t0004g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4183-811C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586917 | |||||||
chr10:24587244 | A | G | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4183-1138T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587244 | |||||||
chr10:24587285 | A | G | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4183-1179T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587285 | |||||||
chr10:24587466 | AAATTTAG others(6): Show |
A | 34 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0177 others(31): Show |
34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.4183-1373_4183-136 others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587466 | |||||||
chr10:24587620 | T | G | 1 | a0001c0001t0002g0321 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4183-1514A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587620 | |||||||
chr10:24587690 | T | C | 43 | a0002c0002t0001g0018 a0002c0002t0001g0020 a0002c0002t0001g0063 others(40): Show |
43 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.4182+1581A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587690 | |||||||
chr10:24587734 | G | A | 168 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.4182+1537C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587734 | |||||||
chr10:24587827 | TTACTC | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG02145.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4182+1439_4182+144 others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587827 | |||||||
chr10:24587840 | C | G | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.4182+1431G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587840 | |||||||
chr10:24588347 | C | CTAGGGTA others(31): Show |
40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
40 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.4182+886_4182+923d others(40): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588347 | |||||||
chr10:24588570 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4182+701A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588570 | |||||||
chr10:24588915 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0060 |
2 | HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4182+356G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588915 | |||||||
chr10:24588925 | C | T | 1 | a0001c0001t0008g0325 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4182+346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588925 | |||||||
chr10:24588954 | T | A | 1 | a0001c0001t0001g0273 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4182+317A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588954 | |||||||
chr10:24588997 | T | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.4182+274A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588997 | |||||||
chr10:24589093 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.4182+178G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589093 | |||||||
chr10:24589113 | C | A | 144 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.4182+158G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589113 | |||||||
chr10:24589173 | A | G | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4182+98T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589173 | |||||||
chr10:24589179 | C | T | 3 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0283 |
3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4182+92G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589179 | |||||||
chr10:24589200 | G | A | 290 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(287): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.4182+71C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589200 | |||||||
chr10:24589673 | T | A | 1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4151-371A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24589673 | |||||||
chr10:24589905 | G | A | 143 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.4151-603C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24589905 | |||||||
chr10:24589907 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4151-605C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24589907 | |||||||
chr10:24590855 | ATAC | A | 24 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(21): Show |
24 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.4150+367_4150+369d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590855 | |||||||
chr10:24590940 | T | TA | 6 | a0001c0001t0001g0177 a0001c0001t0001g0258 a0001c0001t0002g0322 others(3): Show |
6 | HG01261.hp1 HG02083.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4150+284dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590940 | |||||||
chr10:24590940 | TA | T | 25 | a0001c0001t0001g0175 a0001c0001t0001g0219 a0001c0001t0001g0221 others(22): Show |
25 | HG00323.hp1 HG00609.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.4150+284delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590940 | |||||||
chr10:24591447 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.4045-117A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 23/25 | chr10 | 24591447 | |||||||
chr10:24591484 | C | T | 7 | a0001c0001t0002g0303 a0001c0001t0002g0315 a0001c0001t0002g0320 others(4): Show |
7 | HG00673.hp2 HG01109.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-154G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 23/25 | chr10 | 24591484 | |||||||
chr10:24591572 | T | C | 1 | a0002c0002t0001g0042 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4044+70A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 23/25 | chr10 | 24591572 | |||||||
chr10:24591783 | G | A | 155 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.4003-100C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 22/25 | chr10 | 24591783 | |||||||
chr10:24592156 | A | AT | 17 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0164 others(14): Show |
17 | HG01258.hp2 HG01934.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3877-145dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | |||||||
chr10:24592156 | AT | A | 188 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0161 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.3877-145delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | |||||||
chr10:24592156 | ATT | A | 38 | a0001c0001t0001g0014 a0002c0002t0001g0018 a0002c0002t0001g0020 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.3877-146_3877-145d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | |||||||
chr10:24592156 | ATTTTTT | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877-150_3877-145d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | |||||||
chr10:24592636 | T | C | 169 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.3877-624A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592636 | |||||||
chr10:24592643 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3877-631G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592643 | |||||||
chr10:24592714 | C | T | 159 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.3877-702G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592714 | |||||||
chr10:24592720 | A | AGTAAGAT others(11): Show |
3 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0112 |
3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3877-726_3877-709d others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592720 | |||||||
chr10:24592746 | G | GA | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877-735dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592746 | |||||||
chr10:24592922 | A | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0250 |
3 | HG00621.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3877-910T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592922 | |||||||
chr10:24592952 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3877-940A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592952 | |||||||
chr10:24593080 | CA | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877-1069delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593080 | |||||||
chr10:24593172 | T | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877-1160A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593172 | |||||||
chr10:24593258 | A | AGAAAGAA others(7): Show |
1 | a0001c0001t0001g0272 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3877-1260_3877-124 others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593258 | |||||||
chr10:24593267 | CTA | C | 4 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3877-1257_3877-125 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593267 | |||||||
chr10:24593303 | C | T | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3877-1291G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593303 | |||||||
chr10:24593492 | G | GTAATATT others(30): Show |
1 | a0002c0002t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3876+1421_3876+145 others(41): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593492 | |||||||
chr10:24593590 | T | TGAAAGAT others(14): Show |
133 | a0001c0001t0008g0325 a0001c0014t0004g0287 a0002c0002t0001g0011 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.3876+1339_3876+135 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593590 | |||||||
chr10:24593590 | T | TGAAAGAT others(14): Show |
4 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0002t0001g0080 others(1): Show |
4 | HG00741.hp1 HG01975.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.3876+1359_3876+136 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593590 | |||||||
chr10:24593629 | A | G | 9 | a0002c0002t0001g0064 a0002c0002t0001g0065 a0002c0002t0001g0066 others(6): Show |
9 | HG00639.hp1 HG01069.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.3876+1321T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593629 | |||||||
chr10:24593832 | G | A | 137 | a0001c0001t0008g0325 a0001c0014t0004g0287 a0002c0002t0001g0011 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3876+1118C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593832 | |||||||
chr10:24593969 | A | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3876+981T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593969 | |||||||
chr10:24594171 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3876+779T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594171 | |||||||
chr10:24594203 | T | TTAAAATC others(10): Show |
1 | a0002c0002t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3876+730_3876+746d others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594203 | |||||||
chr10:24594329 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3876+621G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594329 | |||||||
chr10:24594617 | G | GTATTCT | 152 | a0001c0001t0008g0325 a0001c0014t0004g0287 a0002c0002t0001g0011 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3876+327_3876+332d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594617 | |||||||
chr10:24594844 | T | G | 167 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.3876+106A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594844 | |||||||
chr10:24595102 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3786+15A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 20/25 | chr10 | 24595102 | |||||||
chr10:24595227 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3713-37A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595227 | |||||||
chr10:24595294 | T | C | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3713-104A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595294 | |||||||
chr10:24595375 | C | T | 1 | a0002c0002t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3713-185G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595375 | |||||||
chr10:24595390 | A | C | 167 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.3713-200T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595390 | |||||||
chr10:24595581 | A | G | 21 | a0001c0001t0002g0303 a0001c0001t0002g0311 a0001c0001t0002g0312 others(18): Show |
21 | HG00673.hp2 HG00733.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3712+136T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595581 | |||||||
chr10:24595585 | G | A | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3712+132C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595585 | |||||||
chr10:24595850 | GA | G | 108 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(105): Show |
108 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.3633+37delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 18/25 | chr10 | 24595850 | |||||||
chr10:24596101 | T | C | 3 | a0001c0001t0002g0336 a0001c0001t0002g0337 a0014c0022t0002g0338 |
3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3478-58A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596101 | |||||||
chr10:24596134 | G | A | 1 | a0019c0023t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3478-91C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596134 | |||||||
chr10:24596242 | TGAAA | T | 84 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0021 others(81): Show |
84 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.3478-203_3478-200d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596242 | |||||||
chr10:24596490 | C | T | 6 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0002t0001g0080 others(3): Show |
6 | HG00741.hp1 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.3477+250G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596490 | |||||||
chr10:24596563 | T | C | 1 | a0015c0020t0001g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3477+177A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596563 | |||||||
chr10:24596570 | A | G | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3477+170T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596570 | |||||||
chr10:24596628 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3477+112T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596628 | |||||||
chr10:24596673 | T | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3477+67A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596673 | |||||||
chr10:24596681 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3477+59G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596681 | |||||||
chr10:24596716 | A | G | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3477+24T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596716 | |||||||
chr10:24596718 | C | T | 2 | a0003c0003t0001g0199 a0003c0003t0001g0249 |
2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.3477+22G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596718 | |||||||
chr10:24597066 | G | A | 1 | a0002c0002t0014g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3335-184C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597066 | |||||||
chr10:24597075 | TTTTC | T | 147 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.3335-197_3335-194d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597075 | |||||||
chr10:24597090 | C | CA | 164 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.3335-209dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597090 | |||||||
chr10:24597372 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3334+75T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597372 | |||||||
chr10:24597395 | G | A | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3334+52C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597395 | |||||||
chr10:24597605 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3198-22C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 15/25 | chr10 | 24597605 | |||||||
chr10:24597846 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3197+99T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 15/25 | chr10 | 24597846 | |||||||
chr10:24598199 | T | C | 1 | a0002c0030t0001g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3133-190A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598199 | |||||||
chr10:24598264 | T | C | 174 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.3133-255A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598264 | |||||||
chr10:24598528 | TAAGAG | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG00642.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3133-524_3133-520d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598528 | |||||||
chr10:24598741 | A | AGTCT | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-736_3133-733d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598741 | |||||||
chr10:24598779 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3133-770A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598779 | |||||||
chr10:24598987 | T | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-978A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598987 | |||||||
chr10:24598990 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3133-981C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598990 | |||||||
chr10:24599003 | T | C | 46 | a0002c0002t0001g0018 a0002c0002t0001g0020 a0002c0002t0001g0063 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.3133-994A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599003 | |||||||
chr10:24599012 | T | C | 1 | a0002c0002t0001g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3133-1003A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599012 | |||||||
chr10:24599033 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-1024A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599033 | |||||||
chr10:24599102 | A | C | 1 | a0003c0003t0001g0181 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3133-1093T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599102 | |||||||
chr10:24599113 | T | C | 42 | a0002c0002t0001g0018 a0002c0002t0001g0020 a0002c0002t0001g0063 others(39): Show |
42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.3133-1104A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599113 | |||||||
chr10:24599161 | C | T | 77 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0182 others(74): Show |
77 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.3133-1152G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599161 | |||||||
chr10:24599319 | A | C | 1 | a0002c0002t0001g0052 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3133-1310T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599319 | |||||||
chr10:24599337 | T | C | 4 | a0005c0005t0001g0104 a0005c0005t0001g0105 a0005c0005t0001g0138 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3132+1309A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599337 | |||||||
chr10:24599470 | G | A | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3132+1176C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599470 | |||||||
chr10:24599579 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3132+1067T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599579 | |||||||
chr10:24599616 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3132+1030A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599616 | |||||||
chr10:24599696 | TTCA | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+947_3132+949d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599696 | |||||||
chr10:24599718 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+928C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599718 | |||||||
chr10:24599791 | T | C | 5 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3132+855A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599791 | |||||||
chr10:24599900 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3132+746C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599900 | |||||||
chr10:24599916 | A | G | 3 | a0001c0001t0001g0172 a0001c0001t0004g0298 a0001c0001t0004g0299 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3132+730T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599916 | |||||||
chr10:24600014 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3132+632A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600014 | |||||||
chr10:24600128 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+518C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600128 | |||||||
chr10:24600132 | C | CAAAA | 13 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0163 others(10): Show |
13 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.3132+510_3132+513d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | |||||||
chr10:24600132 | C | CAAAAA | 7 | a0001c0001t0001g0144 a0006c0007t0006g0292 a0006c0007t0006g0293 others(4): Show |
7 | HG02129.hp2 HG02523.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3132+509_3132+513d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | |||||||
chr10:24600132 | C | CAAAAAA | 17 | a0001c0014t0004g0287 a0002c0002t0001g0067 a0002c0002t0001g0076 others(14): Show |
17 | HG00099.hp1 HG01069.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3132+508_3132+513d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | |||||||
chr10:24600132 | C | CAAAAAAA | 113 | a0001c0001t0008g0325 a0002c0002t0001g0011 a0002c0002t0001g0018 others(110): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.3132+507_3132+513d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | |||||||
chr10:24600132 | C | CAAAAAAA others(1): Show |
23 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0061 others(20): Show |
23 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.3132+506_3132+513d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | |||||||
chr10:24600132 | CA | C | 7 | a0001c0001t0001g0195 a0001c0001t0002g0321 a0001c0001t0003g0155 others(4): Show |
7 | HG01081.hp1 HG01099.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3132+513delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | |||||||
chr10:24600454 | G | C | 76 | a0001c0001t0008g0325 a0002c0002t0001g0011 a0002c0002t0001g0019 others(73): Show |
76 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.3132+192C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600454 | |||||||
chr10:24600543 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+103G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600543 | |||||||
chr10:24600972 | T | G | 153 | a0001c0001t0001g0253 a0001c0001t0008g0325 a0001c0014t0004g0287 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2848-42A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24600972 | |||||||
chr10:24601232 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2848-302G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601232 | |||||||
chr10:24601401 | T | C | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2848-471A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601401 | |||||||
chr10:24601573 | GAAAC | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2847+401_2847+404d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601573 | |||||||
chr10:24601603 | A | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2847+375T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601603 | |||||||
chr10:24601637 | T | A | 171 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2847+341A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601637 | |||||||
chr10:24601742 | C | T | 1 | a0003c0003t0001g0202 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2847+236G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601742 | |||||||
chr10:24601823 | G | A | 7 | a0002c0002t0001g0020 a0002c0002t0001g0114 a0002c0002t0001g0115 others(4): Show |
7 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2847+155C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601823 | |||||||
chr10:24601863 | T | C | 2 | a0002c0002t0001g0108 a0002c0002t0001g0112 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2847+115A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601863 | |||||||
chr10:24601899 | T | C | 102 | a0001c0001t0008g0325 a0002c0002t0001g0011 a0002c0002t0001g0019 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2847+79A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601899 | |||||||
chr10:24602164 | A | G | 1 | a0002c0002t0001g0049 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2722-61T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602164 | |||||||
chr10:24602235 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2722-132A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602235 | |||||||
chr10:24602332 | G | T | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-229C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602332 | |||||||
chr10:24602398 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2722-295G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602398 | |||||||
chr10:24602423 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2722-320C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602423 | |||||||
chr10:24602438 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2722-335G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602438 | |||||||
chr10:24602708 | C | T | 1 | a0005c0005t0001g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2722-605G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602708 | |||||||
chr10:24602931 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2722-828C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602931 | |||||||
chr10:24602977 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2722-874T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602977 | |||||||
chr10:24603470 | A | C | 1 | a0002c0002t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2721+842T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603470 | |||||||
chr10:24603560 | A | C | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2721+752T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603560 | |||||||
chr10:24603822 | A | C | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2721+490T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603822 | |||||||
chr10:24603921 | G | A | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+391C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603921 | |||||||
chr10:24604064 | G | C | 3 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0112 |
3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2721+248C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24604064 | |||||||
chr10:24604131 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2721+181G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24604131 | |||||||
chr10:24604453 | C | T | 1 | a0002c0002t0001g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2685-105G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24604453 | |||||||
chr10:24604590 | G | A | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2685-242C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24604590 | |||||||
chr10:24604747 | C | T | 1 | a0011c0011t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2685-399G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24604747 | |||||||
chr10:24605008 | T | TA | 4 | a0005c0005t0001g0104 a0005c0005t0001g0105 a0005c0005t0001g0138 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685-661dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605008 | |||||||
chr10:24605132 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2685-784G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605132 | |||||||
chr10:24605191 | G | A | 5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0015g0289 others(2): Show |
5 | HG02129.hp2 NA18747.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685-843C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605191 | |||||||
chr10:24605365 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2685-1017A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605365 | |||||||
chr10:24605371 | C | T | 2 | a0001c0001t0002g0323 a0001c0001t0002g0334 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2685-1023G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605371 | |||||||
chr10:24605417 | T | C | 2 | a0001c0001t0002g0315 a0001c0001t0002g0344 |
2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2685-1069A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605417 | |||||||
chr10:24605481 | C | T | 10 | a0002c0002t0001g0020 a0002c0002t0001g0114 a0002c0002t0001g0115 others(7): Show |
10 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.2685-1133G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605481 | |||||||
chr10:24605502 | C | T | 60 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(57): Show |
60 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2685-1154G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605502 | |||||||
chr10:24605514 | TCCTGCTA others(14): Show |
T | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2685-1187_2685-116 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605514 | |||||||
chr10:24605519 | C | T | 3 | a0001c0001t0002g0336 a0001c0001t0002g0337 a0014c0022t0002g0338 |
3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2685-1171G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605519 | |||||||
chr10:24605731 | T | C | 1 | a0002c0002t0001g0154 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2685-1383A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605731 | |||||||
chr10:24605807 | T | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2685-1459A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605807 | |||||||
chr10:24605811 | CAGG | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
44 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2685-1466_2685-146 others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605811 | |||||||
chr10:24605894 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2685-1546C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605894 | |||||||
chr10:24605992 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+1507G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605992 | |||||||
chr10:24606108 | C | A | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2684+1391G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606108 | |||||||
chr10:24606115 | AT | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2684+1383delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606115 | |||||||
chr10:24606229 | A | C | 1 | a0002c0002t0001g0100 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2684+1270T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606229 | |||||||
chr10:24606479 | A | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+1020T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606479 | |||||||
chr10:24606487 | G | A | 1 | a0001c0001t0008g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2684+1012C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606487 | |||||||
chr10:24606510 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2684+989C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606510 | |||||||
chr10:24606540 | T | G | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+959A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606540 | |||||||
chr10:24606568 | T | G | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+931A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606568 | |||||||
chr10:24606831 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+668T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606831 | |||||||
chr10:24606937 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+562G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606937 | |||||||
chr10:24607138 | G | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+361C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607138 | |||||||
chr10:24607139 | T | G | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+360A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607139 | |||||||
chr10:24607140 | A | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+359T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607140 | |||||||
chr10:24607219 | T | C | 2 | a0002c0002t0001g0045 a0002c0002t0001g0093 |
2 | NA18747.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2684+280A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607219 | |||||||
chr10:24607231 | AAAG | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+265_2684+267d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607231 | |||||||
chr10:24607259 | A | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+240T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607259 | |||||||
chr10:24608065 | C | CAGTT | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-166_2423-163d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608065 | |||||||
chr10:24608108 | G | A | 145 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2423-205C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608108 | |||||||
chr10:24608117 | T | TAAA | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2423-217_2423-215d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608117 | |||||||
chr10:24608435 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2423-532G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608435 | |||||||
chr10:24608571 | T | C | 1 | a0002c0002t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2423-668A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608571 | |||||||
chr10:24608648 | C | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-745G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608648 | |||||||
chr10:24608778 | TA | T | 123 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.2423-876delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608778 | |||||||
chr10:24608854 | C | T | 1 | a0001c0001t0008g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2423-951G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608854 | |||||||
chr10:24608861 | T | TTACTATT others(18): Show |
6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-983_2423-959d others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608861 | |||||||
chr10:24609108 | A | C | 1 | a0002c0002t0001g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2423-1205T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609108 | |||||||
chr10:24609161 | A | G | 1 | a0002c0002t0007g0009 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2423-1258T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609161 | |||||||
chr10:24609180 | T | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1277A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609180 | |||||||
chr10:24609419 | T | C | 1 | a0002c0002t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2423-1516A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609419 | |||||||
chr10:24609651 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1748C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609651 | |||||||
chr10:24609662 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1759G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609662 | |||||||
chr10:24609663 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2423-1760C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609663 | |||||||
chr10:24609679 | G | GT | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1777dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609679 | |||||||
chr10:24609806 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2423-1903T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609806 | |||||||
chr10:24610104 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2423-2201C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610104 | |||||||
chr10:24610152 | G | C | 1 | a0002c0002t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2423-2249C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610152 | |||||||
chr10:24610180 | C | G | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2423-2277G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610180 | |||||||
chr10:24610185 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2423-2282A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610185 | |||||||
chr10:24610249 | C | T | 3 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0112 |
3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2423-2346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610249 | |||||||
chr10:24610372 | C | CA | 9 | a0001c0001t0001g0172 a0001c0001t0001g0190 a0001c0001t0002g0320 others(6): Show |
9 | HG00673.hp2 HG00741.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.2423-2470dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610372 | |||||||
chr10:24610372 | C | CAA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-2471_2423-247 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610372 | |||||||
chr10:24610372 | CA | C | 111 | a0001c0001t0002g0317 a0002c0002t0001g0011 a0002c0002t0001g0018 others(108): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.2423-2470delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610372 | |||||||
chr10:24610374 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2423-2471T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610374 | |||||||
chr10:24610375 | A | C | 3 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0285 |
3 | HG02451.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2423-2472T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610375 | |||||||
chr10:24610377 | A | C | 2 | a0005c0005t0001g0103 a0005c0005t0001g0104 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2423-2474T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610377 | |||||||
chr10:24610877 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2423-2974G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610877 | |||||||
chr10:24611067 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0223 a0001c0001t0003g0218 |
3 | HG01069.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2423-3164A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611067 | |||||||
chr10:24611177 | C | T | 2 | a0002c0002t0001g0078 a0002c0002t0001g0079 |
2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2423-3274G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611177 | |||||||
chr10:24611211 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-3308C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611211 | |||||||
chr10:24611246 | T | A | 1 | a0015c0020t0001g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2423-3343A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611246 | |||||||
chr10:24611341 | T | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2423-3438A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611341 | |||||||
chr10:24611450 | T | C | 1 | a0001c0001t0002g0311 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2423-3547A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611450 | |||||||
chr10:24611556 | T | C | 1 | a0017c0013t0002g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2423-3653A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611556 | |||||||
chr10:24611660 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-3757G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611660 | |||||||
chr10:24611671 | G | A | 64 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(61): Show |
64 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2423-3768C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611671 | |||||||
chr10:24611833 | A | T | 1 | a0005c0005t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2423-3930T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611833 | |||||||
chr10:24612022 | G | C | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2423-4119C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612022 | |||||||
chr10:24612057 | C | G | 4 | a0003c0003t0001g0211 a0003c0003t0001g0214 a0003c0003t0001g0220 others(1): Show |
4 | HG00423.hp1 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.2423-4154G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612057 | |||||||
chr10:24612218 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-4315G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612218 | |||||||
chr10:24612311 | T | C | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2423-4408A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612311 | |||||||
chr10:24612408 | T | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2423-4505A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612408 | |||||||
chr10:24612453 | A | T | 1 | a0017c0013t0002g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2423-4550T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612453 | |||||||
chr10:24612625 | C | T | 34 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0177 others(31): Show |
34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.2423-4722G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612625 | |||||||
chr10:24612856 | A | AAAAT | 141 | a0001c0001t0001g0161 a0001c0001t0001g0170 a0001c0001t0001g0171 others(138): Show |
141 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2423-4957_2423-495 others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612856 | |||||||
chr10:24612856 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG02818.hp2 HG02965.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.2423-4961_2423-495 others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612856 | |||||||
chr10:24612959 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2423-5056G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612959 | |||||||
chr10:24613021 | T | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2423-5118A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613021 | |||||||
chr10:24613579 | T | C | 1 | a0001c0001t0002g0320 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2423-5676A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613579 | |||||||
chr10:24613609 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0236 |
2 | NA18975.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2423-5706C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613609 | |||||||
chr10:24613682 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2423-5779A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613682 | |||||||
chr10:24613709 | T | G | 5 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0002g0334 others(2): Show |
5 | HG01099.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2422+5764A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613709 | |||||||
chr10:24613817 | G | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+5656C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613817 | |||||||
chr10:24613826 | C | G | 1 | a0001c0001t0016g0351 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2422+5647G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613826 | |||||||
chr10:24613873 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+5600C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613873 | |||||||
chr10:24613880 | A | AGGTTACA others(3): Show |
15 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2422+5583_2422+559 others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613880 | |||||||
chr10:24613992 | G | A | 23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2422+5481C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613992 | |||||||
chr10:24614398 | T | G | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+5075A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614398 | |||||||
chr10:24614399 | G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+5074C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614399 | |||||||
chr10:24614411 | T | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0188 |
2 | NA18988.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2422+5062A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614411 | |||||||
chr10:24614462 | A | G | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2422+5011T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614462 | |||||||
chr10:24614641 | G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4832C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614641 | |||||||
chr10:24614691 | G | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4782C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614691 | |||||||
chr10:24614692 | A | G | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4781T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614692 | |||||||
chr10:24614693 | G | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4780C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614693 | |||||||
chr10:24614740 | G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4733C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614740 | |||||||
chr10:24614782 | C | CA | 25 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(22): Show |
25 | HG00642.hp1 HG01109.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2422+4690dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614782 | |||||||
chr10:24614782 | C | CAA | 136 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2422+4689_2422+469 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614782 | |||||||
chr10:24614782 | C | CAAA | 14 | a0002c0002t0001g0046 a0002c0002t0001g0088 a0002c0002t0001g0095 others(11): Show |
14 | HG00438.hp1 HG01175.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2422+4688_2422+469 others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614782 | |||||||
chr10:24614845 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2422+4628A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614845 | |||||||
chr10:24614915 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+4558C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614915 | |||||||
chr10:24615017 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2422+4456G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615017 | |||||||
chr10:24615047 | G | C | 3 | a0003c0003t0001g0222 a0003c0003t0001g0229 a0003c0003t0001g0269 |
3 | HG00408.hp2 NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2422+4426C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615047 | |||||||
chr10:24615058 | T | C | 339 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(336): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.2422+4415A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615058 | |||||||
chr10:24615105 | A | T | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2422+4368T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615105 | |||||||
chr10:24615122 | G | A | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2422+4351C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615122 | |||||||
chr10:24615186 | G | A | 15 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2422+4287C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615186 | |||||||
chr10:24615388 | T | G | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2422+4085A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615388 | |||||||
chr10:24615421 | T | C | 1 | a0002c0002t0001g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2422+4052A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615421 | |||||||
chr10:24615457 | C | T | 1 | a0001c0001t0004g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2422+4016G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615457 | |||||||
chr10:24615484 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2422+3989C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615484 | |||||||
chr10:24615491 | A | C | 23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2422+3982T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615491 | |||||||
chr10:24615534 | C | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+3939G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615534 | |||||||
chr10:24615569 | T | C | 15 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2422+3904A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615569 | |||||||
chr10:24615771 | ATTATT | A | 134 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.2422+3697_2422+370 others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615771 | |||||||
chr10:24616073 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+3400G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616073 | |||||||
chr10:24616221 | C | A | 1 | a0001c0001t0001g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2422+3252G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616221 | |||||||
chr10:24616345 | T | A | 1 | a0001c0001t0003g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2422+3128A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616345 | |||||||
chr10:24616441 | C | T | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2422+3032G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616441 | |||||||
chr10:24616507 | T | G | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2422+2966A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616507 | |||||||
chr10:24616631 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2842A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616631 | |||||||
chr10:24616668 | G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+2805C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616668 | |||||||
chr10:24616678 | G | A | 6 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0002t0001g0080 others(3): Show |
6 | HG00741.hp1 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2795C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616678 | |||||||
chr10:24616904 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2422+2569T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616904 | |||||||
chr10:24617034 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2439C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617034 | |||||||
chr10:24617214 | C | T | 111 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0020 others(108): Show |
111 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2422+2259G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617214 | |||||||
chr10:24617244 | T | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2229A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617244 | |||||||
chr10:24617439 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2422+2034A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617439 | |||||||
chr10:24617535 | G | C | 1 | a0004c0004t0001g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2422+1938C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617535 | |||||||
chr10:24617595 | G | A | 1 | a0002c0002t0001g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2422+1878C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617595 | |||||||
chr10:24617611 | T | TA | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2422+1861dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617611 | |||||||
chr10:24617643 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2422+1830T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617643 | |||||||
chr10:24617724 | T | TAGCTTTA others(37): Show |
23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2422+1705_2422+174 others(48): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617724 | |||||||
chr10:24617740 | T | TCCGTAGA others(37): Show |
1 | a0002c0002t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2422+1732_2422+173 others(48): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617740 | |||||||
chr10:24618012 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+1461C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618012 | |||||||
chr10:24618046 | CT | C | 155 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2422+1426delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618046 | |||||||
chr10:24618136 | A | G | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2422+1337T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618136 | |||||||
chr10:24618195 | T | TA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+1277dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618195 | |||||||
chr10:24618328 | A | C | 1 | a0005c0005t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2422+1145T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618328 | |||||||
chr10:24618348 | T | C | 1 | a0002c0002t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2422+1125A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618348 | |||||||
chr10:24618649 | G | C | 1 | a0011c0011t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2422+824C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618649 | |||||||
chr10:24618864 | A | T | 1 | a0003c0003t0001g0232 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2422+609T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618864 | |||||||
chr10:24618922 | G | T | 3 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0112 |
3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2422+551C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618922 | |||||||
chr10:24619054 | GTTAAATT others(3): Show |
G | 1 | a0001c0001t0002g0305 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2422+409_2422+418d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619054 | |||||||
chr10:24619251 | T | C | 1 | a0002c0002t0001g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2422+222A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619251 | |||||||
chr10:24619261 | G | GT | 135 | a0001c0001t0001g0261 a0002c0002t0001g0011 a0002c0002t0001g0018 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.2422+211dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619261 | |||||||
chr10:24619261 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2422+212C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619261 | |||||||
chr10:24619271 | T | A | 4 | a0003c0003t0001g0211 a0003c0003t0001g0214 a0003c0003t0001g0220 others(1): Show |
4 | HG00423.hp1 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.2422+202A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619271 | |||||||
chr10:24619271 | T | TA | 14 | a0002c0002t0001g0071 a0002c0002t0001g0086 a0002c0002t0001g0151 others(11): Show |
14 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422+201dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619271 | |||||||
chr10:24619272 | A | T | 3 | a0003c0003t0001g0232 a0003c0003t0001g0278 a0008c0009t0005g0005 |
3 | NA18963.hp1 NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2422+201T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619272 | |||||||
chr10:24619290 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2422+183T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619290 | |||||||
chr10:24619356 | G | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+117C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619356 | |||||||
chr10:24621826 | G | A | 157 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.526-457C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24621826 | |||||||
chr10:24621830 | A | AATTT | 80 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0182 others(77): Show |
80 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.526-465_526-462dup others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24621830 | |||||||
chr10:24621986 | G | C | 292 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.526-617C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24621986 | |||||||
chr10:24622013 | G | A | 2 | a0002c0002t0001g0089 a0018c0027t0001g0036 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.526-644C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622013 | |||||||
chr10:24622083 | C | T | 157 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.525+650G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622083 | |||||||
chr10:24622119 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.525+614T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622119 | |||||||
chr10:24622433 | C | CAT | 7 | a0001c0001t0001g0171 a0001c0001t0001g0239 a0001c0001t0001g0241 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+298_525+299dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | C | CATAT | 5 | a0001c0001t0001g0170 a0001c0001t0001g0191 a0001c0001t0001g0275 others(2): Show |
5 | HG00423.hp2 HG00673.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+296_525+299dup others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | C | CATATAT | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0242 others(1): Show |
4 | HG00140.hp1 HG03710.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+294_525+299dup others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0276 |
3 | HG02965.hp1 HG03225.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.525+292_525+299dup others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.525+288_525+299dup others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CAT | C | 14 | a0001c0001t0001g0143 a0001c0001t0001g0179 a0001c0001t0002g0303 others(11): Show |
14 | HG01099.hp2 HG01168.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.525+298_525+299del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATAT | C | 22 | a0001c0001t0001g0144 a0001c0001t0001g0177 a0001c0001t0001g0190 others(19): Show |
22 | HG00408.hp2 HG00733.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.525+296_525+299del others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATAT | C | 20 | a0001c0001t0001g0240 a0001c0001t0002g0001 a0001c0001t0002g0301 others(17): Show |
21 | HG00639.hp2 HG01109.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.525+294_525+299del others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(1): Show |
C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0196 a0001c0001t0001g0198 others(12): Show |
15 | HG01517.hp2 HG01928.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.525+292_525+299del others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(3): Show |
C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0194 a0001c0001t0002g0327 others(7): Show |
10 | HG00597.hp2 HG01891.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+290_525+299del others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(5): Show |
C | 12 | a0001c0001t0001g0193 a0001c0001t0001g0254 a0001c0001t0002g0295 others(9): Show |
12 | HG02257.hp1 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.525+288_525+299del others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(7): Show |
C | 21 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0215 others(18): Show |
21 | HG00099.hp2 HG01192.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.525+286_525+299del others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(9): Show |
C | 43 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0184 others(40): Show |
43 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.525+284_525+299del others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(11): Show |
C | 13 | a0001c0001t0001g0219 a0001c0001t0001g0253 a0001c0001t0005g0006 others(10): Show |
13 | HG00642.hp1 HG01069.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+282_525+299del others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(13): Show |
C | 30 | a0001c0001t0005g0002 a0001c0001t0005g0007 a0001c0014t0004g0287 others(27): Show |
30 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.525+280_525+299del others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(15): Show |
C | 13 | a0002c0002t0001g0075 a0002c0002t0001g0076 a0002c0002t0001g0107 others(10): Show |
13 | HG01261.hp2 HG02027.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+278_525+299del others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(17): Show |
C | 86 | a0001c0001t0001g0270 a0002c0002t0001g0011 a0002c0002t0001g0019 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.525+276_525+299del others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(19): Show |
C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+274_525+299del others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(21): Show |
C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0006c0007t0006g0293 |
3 | HG02280.hp1 HG02486.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.525+272_525+299del others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(23): Show |
C | 7 | a0001c0001t0001g0273 a0003c0003t0001g0266 a0006c0007t0006g0292 others(4): Show |
7 | HG01993.hp1 HG02129.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+270_525+299del others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622433 | CATATATA others(31): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.525+262_525+299del others(38): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | |||||||
chr10:24622441 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.525+292A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622441 | |||||||
chr10:24622443 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.525+290A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622443 | |||||||
chr10:24622455 | T | A | 3 | a0001c0001t0004g0297 a0001c0001t0004g0298 a0001c0001t0004g0299 |
3 | HG02895.hp1 HG02897.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.525+278A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622455 | |||||||
chr10:24622485 | T | C | 89 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0021 others(86): Show |
89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.525+248A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622485 | |||||||
chr10:24622506 | C | T | 4 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0001g0109 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+227G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622506 | |||||||
chr10:24622607 | G | T | 2 | a0001c0001t0002g0336 a0001c0001t0002g0337 |
2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.525+126C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622607 | |||||||
chr10:24622611 | G | C | 1 | a0005c0005t0004g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.525+122C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622611 | |||||||
chr10:24622894 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.496-132C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24622894 | |||||||
chr10:24623118 | C | G | 17 | a0002c0002t0001g0020 a0002c0002t0001g0107 a0002c0002t0001g0108 others(14): Show |
17 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.496-356G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623118 | |||||||
chr10:24623430 | G | T | 1 | a0002c0002t0001g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.496-668C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623430 | |||||||
chr10:24623507 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.496-745G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623507 | |||||||
chr10:24623681 | T | C | 1 | a0007c0008t0001g0263 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.496-919A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623681 | |||||||
chr10:24623704 | G | A | 138 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(135): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.496-942C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623704 | |||||||
chr10:24624337 | C | CT | 32 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0182 others(29): Show |
32 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.496-1576dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | |||||||
chr10:24624337 | C | CTTTTTTT | 87 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.496-1582_496-1576d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | |||||||
chr10:24624337 | C | CTTTTTTT others(1): Show |
58 | a0002c0002t0001g0025 a0002c0002t0001g0035 a0002c0002t0001g0042 others(55): Show |
58 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.496-1583_496-1576d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | |||||||
chr10:24624337 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
16 | HG01433.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-1584_496-1576d others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | |||||||
chr10:24624337 | C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0145 a0001c0001t0001g0163 a0001c0001t0001g0165 others(5): Show |
8 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-1585_496-1576d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | |||||||
chr10:24624337 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.496-1586_496-1576d others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | |||||||
chr10:24624457 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.496-1695T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624457 | |||||||
chr10:24624557 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.496-1795G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624557 | |||||||
chr10:24624581 | C | A | 1 | a0001c0001t0002g0321 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.496-1819G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624581 | |||||||
chr10:24624756 | C | T | 159 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.496-1994G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624756 | |||||||
chr10:24624901 | T | C | 1 | a0015c0020t0001g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.496-2139A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624901 | |||||||
chr10:24624993 | C | T | 9 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0163 others(6): Show |
9 | HG02280.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-2231G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624993 | |||||||
chr10:24625050 | T | A | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496-2288A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625050 | T | TG | 53 | a0001c0001t0002g0001 a0001c0001t0002g0295 a0001c0001t0002g0311 others(50): Show |
53 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.496-2289dupC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625050 | T | TGG | 45 | a0001c0001t0001g0192 a0001c0001t0002g0001 a0001c0001t0002g0304 others(42): Show |
45 | HG00733.hp1 HG01168.hp2 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.496-2290_496-2289d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625050 | T | TGGG | 21 | a0001c0001t0002g0301 a0001c0001t0002g0303 a0001c0001t0002g0320 others(18): Show |
21 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.496-2291_496-2289d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625050 | T | TGGGGG | 19 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0188 others(16): Show |
19 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.496-2293_496-2289d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625050 | T | TGGGGGGG others(3): Show |
4 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0196 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-2298_496-2289d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625050 | T | TGGGGGGG others(4): Show |
1 | a0001c0001t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.496-2299_496-2289d others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | |||||||
chr10:24625051 | G | A | 2 | a0006c0029t0006g0291 a0020c0028t0006g0290 |
2 | NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.496-2289C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625051 | |||||||
chr10:24625052 | G | A | 3 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0015g0289 |
3 | HG02129.hp2 NA18747.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.496-2290C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625052 | |||||||
chr10:24625062 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.496-2300C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496-2300C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(4): Show |
3 | a0003c0003t0001g0199 a0003c0003t0001g0225 a0008c0009t0005g0003 |
3 | NA18959.hp1 NA19002.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.496-2301_496-2300i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(5): Show |
10 | a0001c0001t0001g0198 a0003c0003t0001g0174 a0003c0003t0001g0181 others(7): Show |
10 | HG01952.hp1 HG02040.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(7): Show |
1 | a0003c0003t0001g0232 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.496-2301_496-2300i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(6): Show |
11 | a0001c0001t0001g0219 a0001c0001t0001g0227 a0001c0001t0001g0250 others(8): Show |
11 | HG00621.hp1 HG01069.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(7): Show |
13 | a0001c0001t0001g0215 a0001c0001t0001g0224 a0001c0001t0001g0226 others(10): Show |
13 | HG00423.hp1 HG00597.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(8): Show |
10 | a0001c0001t0001g0221 a0001c0001t0001g0234 a0001c0001t0001g0235 others(7): Show |
10 | HG00408.hp2 HG01192.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(9): Show |
6 | a0001c0001t0001g0175 a0001c0001t0001g0236 a0003c0003t0001g0012 others(3): Show |
6 | HG01123.hp1 HG02004.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(10): Show |
3 | a0001c0001t0001g0223 a0001c0001t0001g0233 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG03453.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.496-2301_496-2300i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(11): Show |
1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.496-2301_496-2300i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(12): Show |
2 | a0001c0001t0001g0228 a0003c0003t0001g0202 |
2 | HG02148.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.496-2301_496-2300i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625062 | G | GGGGGGGG others(10): Show |
1 | a0003c0003t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.496-2301_496-2300i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | |||||||
chr10:24625063 | GGA | G | 18 | a0002c0002t0001g0018 a0002c0002t0001g0022 a0002c0002t0001g0023 others(15): Show |
18 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.496-2303_496-2302d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625063 | |||||||
chr10:24625064 | GA | G | 12 | a0002c0002t0001g0045 a0002c0002t0001g0110 a0002c0002t0001g0114 others(9): Show |
12 | HG01256.hp2 HG02027.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.496-2303delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625064 | |||||||
chr10:24625065 | A | G | 97 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0020 others(94): Show |
97 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.496-2303T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625065 | |||||||
chr10:24625068 | A | G | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.496-2306T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625068 | |||||||
chr10:24625071 | A | G | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.496-2309T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625071 | |||||||
chr10:24625075 | G | A | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.496-2313C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625075 | |||||||
chr10:24625114 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496-2352A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625114 | |||||||
chr10:24625282 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.496-2520T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625282 | |||||||
chr10:24625299 | G | GC | 77 | a0001c0001t0001g0144 a0001c0001t0001g0172 a0001c0001t0001g0175 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.496-2538_496-2537i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625299 | G | GCA | 83 | a0001c0001t0001g0184 a0001c0001t0004g0298 a0001c0001t0016g0351 others(80): Show |
83 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.496-2538_496-2537i others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625299 | G | GCAA | 16 | a0002c0002t0001g0034 a0002c0002t0001g0060 a0002c0002t0001g0082 others(13): Show |
16 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.496-2538_496-2537i others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625299 | G | GCAAA | 3 | a0002c0002t0001g0052 a0002c0002t0001g0059 a0002c0002t0001g0135 |
3 | HG02257.hp2 NA18970.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.496-2538_496-2537i others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625299 | GA | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0194 a0001c0001t0001g0235 others(4): Show |
7 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-2538delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625299 | GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.496-2549_496-2538d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625299 | GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.496-2550_496-2538d others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | |||||||
chr10:24625300 | A | C | 160 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0142 others(157): Show |
161 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.496-2538T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625300 | |||||||
chr10:24625301 | A | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0194 a0001c0001t0001g0235 others(2): Show |
5 | HG01169.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-2539T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625301 | |||||||
chr10:24625312 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.496-2550T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625312 | |||||||
chr10:24625313 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.496-2551T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625313 | |||||||
chr10:24625412 | T | A | 1 | a0003c0003t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496-2650A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625412 | |||||||
chr10:24625435 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-2673A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625435 | |||||||
chr10:24625457 | C | A | 23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.496-2695G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625457 | |||||||
chr10:24625486 | T | A | 1 | a0003c0003t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.496-2724A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625486 | |||||||
chr10:24625530 | AT | A | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(124): Show |
127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.496-2769delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625530 | |||||||
chr10:24625563 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.496-2801A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625563 | |||||||
chr10:24625932 | T | C | 1 | a0011c0011t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.496-3170A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625932 | |||||||
chr10:24626073 | T | C | 1 | a0002c0002t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.496-3311A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626073 | |||||||
chr10:24626267 | G | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-3505C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626267 | |||||||
chr10:24626292 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-3530G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626292 | |||||||
chr10:24626392 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0221 a0001c0001t0001g0224 |
3 | HG01192.hp1 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.495+3604C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626392 | |||||||
chr10:24626513 | C | T | 6 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG00423.hp2 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3483G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626513 | |||||||
chr10:24626637 | T | G | 2 | a0002c0002t0001g0020 a0002c0002t0014g0106 |
2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.495+3359A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626637 | |||||||
chr10:24626701 | T | C | 1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.495+3295A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626701 | |||||||
chr10:24626774 | A | T | 1 | a0001c0001t0002g0311 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.495+3222T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626774 | |||||||
chr10:24626882 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+3114A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626882 | |||||||
chr10:24627125 | T | C | 5 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG00621.hp2 HG02155.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+2871A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627125 | |||||||
chr10:24627176 | T | G | 1 | a0003c0003t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.495+2820A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627176 | |||||||
chr10:24627177 | G | C | 1 | a0003c0003t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.495+2819C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627177 | |||||||
chr10:24627230 | C | A | 1 | a0002c0002t0001g0050 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.495+2766G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627230 | |||||||
chr10:24627282 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.495+2714A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627282 | |||||||
chr10:24627365 | A | C | 1 | a0002c0002t0001g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.495+2631T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627365 | |||||||
chr10:24627411 | A | T | 1 | a0003c0003t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.495+2585T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627411 | |||||||
chr10:24627417 | T | C | 34 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0177 others(31): Show |
34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.495+2579A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627417 | |||||||
chr10:24627464 | A | AAGGAT | 215 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.495+2531_495+2532i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627464 | |||||||
chr10:24627589 | C | T | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.495+2407G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627589 | |||||||
chr10:24627596 | G | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.495+2400C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627596 | |||||||
chr10:24627607 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+2389G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627607 | |||||||
chr10:24627655 | T | TACTTTAT others(24): Show |
1 | a0003c0003t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.495+2340_495+2341i others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627655 | |||||||
chr10:24627764 | C | T | 1 | a0002c0002t0001g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.495+2232G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627764 | |||||||
chr10:24627767 | C | T | 1 | a0002c0002t0001g0050 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.495+2229G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627767 | |||||||
chr10:24627805 | C | T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+2191G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627805 | |||||||
chr10:24628072 | A | G | 1 | a0011c0011t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+1924T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628072 | |||||||
chr10:24628135 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.495+1861C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628135 | |||||||
chr10:24628219 | A | C | 1 | a0002c0002t0014g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.495+1777T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628219 | |||||||
chr10:24628333 | T | A | 3 | a0002c0002t0001g0035 a0002c0002t0001g0097 a0002c0002t0001g0146 |
3 | NA18988.hp2 NA18992.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.495+1663A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628333 | |||||||
chr10:24628349 | G | A | 1 | a0003c0003t0001g0204 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.495+1647C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628349 | |||||||
chr10:24628361 | T | C | 3 | a0003c0003t0001g0211 a0003c0003t0001g0214 a0003c0003t0001g0220 |
3 | HG00423.hp1 HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.495+1635A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628361 | |||||||
chr10:24628412 | G | A | 162 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.495+1584C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628412 | |||||||
chr10:24628422 | AT | A | 168 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.495+1573delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628422 | |||||||
chr10:24628603 | T | C | 24 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(21): Show |
24 | HG01891.hp2 HG02129.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.495+1393A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628603 | |||||||
chr10:24628753 | A | ATG | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(124): Show |
127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.495+1241_495+1242d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628753 | |||||||
chr10:24628753 | ATG | A | 3 | a0001c0001t0001g0194 a0009c0010t0001g0267 a0009c0010t0001g0268 |
3 | HG02109.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.495+1241_495+1242d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628753 | |||||||
chr10:24628753 | ATGTGTG | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+1237_495+1242d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628753 | |||||||
chr10:24628766 | T | C | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1230A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628766 | |||||||
chr10:24628767 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1229C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628767 | |||||||
chr10:24628768 | TGTGC | T | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1224_495+1227d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628768 | |||||||
chr10:24628770 | T | C | 3 | a0002c0002t0001g0108 a0002c0002t0001g0112 a0002c0002t0001g0148 |
3 | HG02258.hp1 HG02630.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.495+1226A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628770 | |||||||
chr10:24628771 | G | A | 3 | a0002c0002t0001g0108 a0002c0002t0001g0112 a0002c0002t0001g0148 |
3 | HG02258.hp1 HG02630.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.495+1225C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628771 | |||||||
chr10:24628771 | G | GTGCA | 4 | a0002c0002t0001g0042 a0002c0002t0001g0107 a0010c0012t0010g0016 others(1): Show |
4 | HG02723.hp1 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1224_495+1225i others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628771 | |||||||
chr10:24628772 | C | CAT | 131 | a0001c0014t0004g0287 a0002c0002t0001g0011 a0002c0002t0001g0018 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.495+1222_495+1223d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628772 | |||||||
chr10:24628772 | C | T | 7 | a0002c0002t0001g0042 a0002c0002t0001g0107 a0002c0002t0001g0108 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1224G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628772 | |||||||
chr10:24628782 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.495+1214A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628782 | |||||||
chr10:24628798 | C | CAT | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1196_495+1197d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628798 | |||||||
chr10:24628808 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+1188A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628808 | |||||||
chr10:24628808 | T | TATATATA others(27): Show |
2 | a0005c0005t0001g0138 a0005c0005t0001g0285 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.495+1187_495+1188i others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628808 | |||||||
chr10:24628810 | T | TATATATA others(23): Show |
10 | a0002c0002t0001g0020 a0002c0002t0001g0114 a0002c0002t0001g0115 others(7): Show |
10 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.495+1185_495+1186i others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628810 | |||||||
chr10:24628810 | T | TATATATA others(25): Show |
1 | a0005c0005t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495+1185_495+1186i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628810 | |||||||
chr10:24628810 | TATATAC | T | 3 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0002t0001g0111 |
3 | HG02148.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.495+1180_495+1185d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628810 | |||||||
chr10:24628812 | TATAC | T | 26 | a0002c0002t0001g0018 a0002c0002t0001g0107 a0002c0002t0001g0108 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.495+1180_495+1183d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628812 | |||||||
chr10:24628814 | T | C | 3 | a0002c0002t0001g0065 a0002c0002t0001g0067 a0002c0002t0001g0078 |
3 | HG01257.hp2 HG01258.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.495+1182A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628814 | |||||||
chr10:24628816 | C | CAT | 113 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0163 others(110): Show |
113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.495+1178_495+1179d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628816 | |||||||
chr10:24628816 | C | CATATATA others(25): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.495+1179_495+1180i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628816 | |||||||
chr10:24628816 | C | T | 16 | a0002c0002t0001g0020 a0002c0002t0001g0065 a0002c0002t0001g0067 others(13): Show |
16 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+1180G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628816 | |||||||
chr10:24628820 | T | C | 65 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(62): Show |
65 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.495+1176A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628820 | |||||||
chr10:24628833 | GTACATAT others(7): Show |
G | 2 | a0001c0001t0009g0159 a0001c0001t0009g0160 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.495+1149_495+1162d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628833 | |||||||
chr10:24628850 | CAT | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0172 a0001c0001t0001g0228 others(9): Show |
12 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+1144_495+1145d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628850 | |||||||
chr10:24628872 | T | TACATATA others(27): Show |
1 | a0001c0001t0001g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.495+1090_495+1123d others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628872 | |||||||
chr10:24628874 | C | CAT | 48 | a0002c0002t0001g0018 a0002c0002t0001g0020 a0002c0002t0001g0107 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.495+1120_495+1121d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628874 | |||||||
chr10:24628882 | C | T | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1114G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628882 | |||||||
chr10:24628884 | CAT | C | 11 | a0001c0001t0001g0172 a0001c0001t0002g0303 a0001c0001t0004g0297 others(8): Show |
11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1110_495+1111d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628884 | |||||||
chr10:24628886 | T | C | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1110A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628886 | |||||||
chr10:24628896 | TACATATA others(3): Show |
T | 1 | a0003c0003t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+1090_495+1099d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628896 | |||||||
chr10:24628898 | C | CAT | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1096_495+1097d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628898 | |||||||
chr10:24628916 | C | CATATATA others(7): Show |
5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0015g0289 others(2): Show |
5 | HG02129.hp2 NA18747.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1079_495+1080i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628916 | |||||||
chr10:24628916 | C | CATATATA others(1): Show |
149 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.495+1079_495+1080i others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628916 | |||||||
chr10:24628918 | C | T | 3 | a0006c0007t0006g0294 a0010c0012t0010g0016 a0010c0012t0010g0017 |
3 | HG02523.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.495+1078G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628918 | |||||||
chr10:24628924 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1072A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628924 | |||||||
chr10:24628928 | C | T | 3 | a0002c0002t0001g0131 a0002c0002t0001g0132 a0006c0007t0006g0294 |
3 | HG00323.hp2 HG00733.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.495+1068G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628928 | |||||||
chr10:24628940 | T | C | 1 | a0002c0002t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.495+1056A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628940 | |||||||
chr10:24628942 | C | T | 2 | a0002c0002t0001g0151 a0002c0002t0001g0152 |
2 | NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.495+1054G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628942 | |||||||
chr10:24628944 | C | T | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1052G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628944 | |||||||
chr10:24628952 | C | CACTATAT others(3): Show |
1 | a0010c0012t0010g0016 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.495+1043_495+1044i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTA | 18 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0307 others(15): Show |
18 | HG01168.hp2 HG01175.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1042_495+1043d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATA | 8 | a0002c0002t0001g0024 a0002c0002t0001g0035 a0002c0002t0001g0042 others(5): Show |
8 | HG00621.hp2 HG02738.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1040_495+1043d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATA | 5 | a0001c0001t0008g0306 a0002c0002t0001g0064 a0002c0002t0001g0072 others(2): Show |
5 | HG00639.hp1 NA18943.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1038_495+1043d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATAT others(1): Show |
5 | a0001c0001t0001g0250 a0002c0002t0001g0011 a0002c0002t0001g0128 others(2): Show |
5 | HG02071.hp2 HG02074.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1036_495+1043d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATAT others(3): Show |
6 | a0001c0001t0001g0270 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG00597.hp1 HG00673.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1034_495+1043d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATAT others(5): Show |
4 | a0002c0002t0001g0045 a0002c0002t0001g0093 a0002c0002t0001g0286 others(1): Show |
4 | NA18747.hp2 NA18972.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1032_495+1043d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0194 a0002c0002t0001g0053 a0009c0010t0001g0267 |
3 | HG03195.hp1 HG03195.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.495+1030_495+1043d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATAT others(9): Show |
1 | a0009c0010t0001g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.495+1028_495+1043d others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | C | CTATATAT others(11): Show |
1 | a0002c0002t0001g0257 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.495+1026_495+1043d others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTA | C | 6 | a0001c0001t0003g0155 a0003c0003t0001g0204 a0003c0003t0001g0205 others(3): Show |
6 | HG01081.hp1 HG02818.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+1042_495+1043d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTATATA | C | 3 | a0001c0001t0001g0274 a0001c0001t0002g0318 a0001c0001t0002g0327 |
3 | HG02155.hp1 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.495+1038_495+1043d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0015c0020t0001g0113 |
3 | HG01169.hp2 HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.495+1036_495+1043d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTATATAT others(3): Show |
C | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.495+1034_495+1043d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTATATAT others(5): Show |
C | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.495+1032_495+1043d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTATATAT others(7): Show |
C | 2 | a0002c0002t0014g0106 a0005c0005t0001g0285 |
2 | HG01516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.495+1030_495+1043d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628952 | CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+1028_495+1043d others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | |||||||
chr10:24628953 | T | A | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1043A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628953 | |||||||
chr10:24628954 | A | C | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1042T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628954 | |||||||
chr10:24628961 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1035A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628961 | |||||||
chr10:24628963 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1033A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628963 | |||||||
chr10:24628965 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1031A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628965 | |||||||
chr10:24628967 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1029A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628967 | |||||||
chr10:24628968 | ATATATAT others(10): Show |
A | 1 | a0002c0002t0004g0302 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.495+1011_495+1027d others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628968 | |||||||
chr10:24628969 | T | C | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1027A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628969 | |||||||
chr10:24628972 | ATATATAT others(12): Show |
A | 4 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0015g0289 others(1): Show |
4 | HG02129.hp2 NA18747.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1005_495+1023d others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628972 | |||||||
chr10:24628974 | ATATATAT others(12): Show |
A | 1 | a0006c0029t0006g0291 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.495+1003_495+1021d others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628974 | |||||||
chr10:24628976 | A | T | 2 | a0003c0003t0001g0206 a0003c0003t0001g0209 |
2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.495+1020T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628976 | |||||||
chr10:24628978 | A | T | 6 | a0001c0001t0001g0171 a0001c0001t0001g0186 a0001c0001t0001g0189 others(3): Show |
6 | HG01169.hp2 HG03942.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1018T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628978 | |||||||
chr10:24628980 | A | T | 16 | a0001c0001t0001g0171 a0001c0001t0001g0185 a0001c0001t0001g0186 others(13): Show |
16 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+1016T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628980 | |||||||
chr10:24628982 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0258 |
2 | HG02738.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(6): Show |
1 | a0003c0003t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0264 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(23): Show |
1 | a0002c0002t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(29): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(24): Show |
1 | a0004c0004t0001g0098 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(25): Show |
1 | a0002c0002t0001g0121 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(18): Show |
1 | a0002c0002t0001g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0163 a0004c0004t0001g0041 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0164 a0004c0004t0001g0040 a0005c0005t0001g0168 |
3 | HG02572.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(14): Show |
1 | a0002c0002t0001g0124 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(23): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(15): Show |
2 | a0002c0002t0001g0111 a0002c0002t0001g0132 |
2 | HG00323.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0240 |
2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(17): Show |
3 | a0001c0001t0001g0015 a0004c0004t0001g0039 a0004c0004t0001g0092 |
3 | HG02559.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(18): Show |
1 | a0002c0002t0001g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(11): Show |
7 | a0001c0001t0001g0144 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01256.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0169 a0001c0001t0001g0276 a0002c0002t0001g0071 others(1): Show |
4 | HG00642.hp2 HG01123.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(14): Show |
4 | a0001c0001t0001g0184 a0001c0001t0001g0239 a0001c0001t0001g0241 others(1): Show |
4 | HG01884.hp2 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(23): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(15): Show |
1 | a0004c0004t0001g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0129 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(10): Show |
2 | a0002c0002t0007g0010 a0003c0003t0001g0202 |
2 | HG02148.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(11): Show |
2 | a0002c0002t0001g0116 a0002c0002t0001g0125 |
2 | HG01099.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(16): Show |
1 | a0002c0002t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0273 a0001c0001t0001g0275 |
2 | HG00423.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0226 a0002c0002t0001g0126 a0002c0002t0004g0296 |
3 | HG01433.hp2 HG01884.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0238 a0002c0002t0001g0118 a0007c0008t0001g0263 |
3 | HG02723.hp2 HG03471.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(10): Show |
4 | a0002c0002t0001g0282 a0002c0002t0001g0284 a0002c0002t0007g0008 others(1): Show |
4 | HG02027.hp2 HG02970.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(11): Show |
3 | a0002c0002t0001g0281 a0002c0002t0001g0283 a0004c0004t0001g0031 |
3 | HG02647.hp1 NA18953.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(12): Show |
2 | a0002c0002t0001g0115 a0002c0002t0001g0131 |
2 | HG00733.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(20): Show |
1 | a0002c0002t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(29): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0313 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(7): Show |
3 | a0002c0002t0001g0110 a0002c0002t0001g0127 a0002c0002t0001g0154 |
3 | HG00735.hp1 HG02148.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0143 a0001c0001t0001g0261 a0003c0003t0001g0201 others(1): Show |
4 | HG01123.hp1 HG01978.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0242 a0002c0017t0001g0048 a0007c0008t0001g0262 |
3 | HG00140.hp1 HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0254 a0002c0002t0001g0114 a0004c0004t0001g0038 |
3 | HG02630.hp2 HG03579.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(3): Show |
4 | a0003c0003t0001g0213 a0003c0003t0001g0217 a0003c0003t0001g0266 others(1): Show |
4 | HG01952.hp1 HG01993.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0170 a0001c0001t0001g0230 a0001c0001t0001g0245 others(2): Show |
5 | HG04199.hp1 HG04228.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0178 a0001c0001t0001g0223 a0001c0001t0001g0236 others(1): Show |
4 | HG01081.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0253 a0001c0001t0002g0312 a0003c0003t0001g0176 |
3 | HG00642.hp1 NA18994.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(7): Show |
3 | a0003c0003t0001g0174 a0003c0003t0012g0173 a0021c0024t0011g0033 |
3 | NA19004.hp2 NA19030.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(8): Show |
1 | a0003c0003t0001g0200 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0188 a0002c0002t0001g0021 a0002c0002t0001g0139 |
3 | HG02922.hp1 HG03041.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0179 a0001c0001t0001g0224 a0001c0001t0001g0243 others(1): Show |
4 | HG01109.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(5): Show |
2 | a0002c0002t0001g0141 a0003c0003t0001g0117 |
2 | HG04228.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0272 |
2 | HG01069.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0190 a0002c0002t0007g0009 a0003c0003t0001g0180 |
3 | HG00280.hp1 HG00609.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATAT others(8): Show |
1 | a0003c0003t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0246 a0003c0003t0001g0214 |
2 | HG00323.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0233 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATTTTT others(3): Show |
2 | a0001c0001t0001g0244 a0003c0003t0001g0248 |
2 | HG01361.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATATTTTT others(4): Show |
2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | ATT | 8 | a0001c0001t0002g0001 a0001c0001t0002g0310 a0001c0001t0002g0315 others(5): Show |
8 | HG01891.hp1 NA18954.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1012_495+1013d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628982 | A | T | 31 | a0001c0001t0001g0171 a0001c0001t0001g0185 a0001c0001t0001g0186 others(28): Show |
31 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.495+1014T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | |||||||
chr10:24628983 | T | TA | 5 | a0001c0001t0002g0309 a0002c0002t0001g0062 a0002c0002t0001g0081 others(2): Show |
5 | HG00099.hp1 HG00140.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATA | 15 | a0001c0001t0009g0159 a0001c0001t0009g0160 a0002c0002t0001g0034 others(12): Show |
15 | HG01516.hp1 HG01517.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATA | 14 | a0001c0001t0002g0324 a0002c0002t0001g0019 a0002c0002t0001g0030 others(11): Show |
14 | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATATA | 5 | a0001c0001t0001g0271 a0002c0002t0001g0023 a0002c0002t0001g0068 others(2): Show |
5 | HG01255.hp1 HG02083.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATATA others(2): Show |
7 | a0002c0002t0001g0043 a0002c0002t0001g0050 a0002c0002t0001g0054 others(4): Show |
7 | HG00408.hp1 HG00735.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATATA others(4): Show |
5 | a0001c0001t0001g0145 a0001c0001t0001g0177 a0002c0002t0001g0051 others(2): Show |
5 | HG01261.hp1 HG02080.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATATA others(6): Show |
3 | a0001c0001t0001g0142 a0001c0001t0005g0002 a0002c0002t0001g0058 |
3 | HG02280.hp1 HG03927.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.495+1012_495+1013i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATATA others(8): Show |
1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.495+1012_495+1013i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628983 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.495+1012_495+1013i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | |||||||
chr10:24628984 | T | A | 36 | a0001c0001t0001g0270 a0001c0001t0002g0340 a0001c0001t0005g0006 others(33): Show |
36 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.495+1012A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628984 | |||||||
chr10:24628985 | T | A | 27 | a0001c0001t0001g0271 a0002c0002t0001g0019 a0002c0002t0001g0034 others(24): Show |
27 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.495+1011A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628985 | |||||||
chr10:24628986 | T | A | 22 | a0001c0001t0001g0270 a0001c0001t0013g0255 a0001c0014t0004g0287 others(19): Show |
22 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.495+1010A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628986 | |||||||
chr10:24628987 | T | A | 5 | a0002c0002t0001g0052 a0002c0002t0001g0056 a0002c0002t0001g0060 others(2): Show |
5 | HG00408.hp1 HG01952.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1009A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628987 | |||||||
chr10:24628988 | T | A | 4 | a0001c0001t0001g0270 a0001c0001t0013g0255 a0002c0002t0001g0097 others(1): Show |
4 | HG00597.hp1 HG02523.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1008A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628988 | |||||||
chr10:24628989 | T | A | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1007A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628989 | |||||||
chr10:24628990 | T | A | 4 | a0001c0001t0001g0270 a0001c0001t0013g0255 a0002c0002t0001g0077 others(1): Show |
4 | HG00597.hp1 HG02523.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1006A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628990 | |||||||
chr10:24628991 | T | A | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1005A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628991 | |||||||
chr10:24628992 | T | A | 3 | a0001c0001t0013g0255 a0002c0002t0001g0077 a0003c0003t0001g0208 |
3 | HG03130.hp1 HG04199.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.495+1004A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628992 | |||||||
chr10:24628993 | T | A | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1003A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628993 | |||||||
chr10:24628994 | T | A | 3 | a0001c0001t0013g0255 a0002c0002t0001g0077 a0003c0003t0001g0208 |
3 | HG03130.hp1 HG04199.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.495+1002A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628994 | |||||||
chr10:24628995 | T | A | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1001A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628995 | |||||||
chr10:24628996 | T | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495+1000A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628996 | |||||||
chr10:24628997 | T | A | 1 | a0010c0012t0010g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+999A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628997 | |||||||
chr10:24628998 | T | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495+998A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628998 | |||||||
chr10:24629000 | T | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495+996A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629000 | |||||||
chr10:24629043 | TGGAGTGC others(12): Show |
T | 9 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+934_495+952del others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629043 | |||||||
chr10:24629057 | G | A | 6 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(3): Show |
6 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+939C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629057 | |||||||
chr10:24629360 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+636A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629360 | |||||||
chr10:24629392 | A | C | 1 | a0002c0002t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.495+604T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629392 | |||||||
chr10:24629494 | C | T | 2 | a0001c0001t0002g0341 a0001c0001t0002g0345 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.495+502G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629494 | |||||||
chr10:24629607 | AT | A | 7 | a0001c0001t0001g0272 a0006c0007t0006g0292 a0006c0007t0006g0293 others(4): Show |
7 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+388delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629607 | |||||||
chr10:24629898 | AT | A | 16 | a0002c0002t0001g0020 a0002c0002t0001g0043 a0002c0002t0001g0114 others(13): Show |
16 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+97delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629898 | |||||||
chr10:24630153 | G | A | 10 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.441-103C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24630153 | |||||||
chr10:24630392 | T | G | 10 | a0002c0002t0001g0019 a0002c0002t0001g0049 a0002c0002t0001g0056 others(7): Show |
10 | HG00735.hp2 HG01934.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-342A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24630392 | |||||||
chr10:24630882 | C | T | 2 | a0003c0003t0001g0199 a0003c0003t0001g0249 |
2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.441-832G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24630882 | |||||||
chr10:24631063 | C | T | 2 | a0002c0002t0001g0065 a0002c0002t0001g0067 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.441-1013G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631063 | |||||||
chr10:24631103 | G | A | 1 | a0002c0002t0001g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.441-1053C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631103 | |||||||
chr10:24631180 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-1130T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631180 | |||||||
chr10:24631195 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.441-1145G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631195 | |||||||
chr10:24631293 | G | C | 1 | a0007c0008t0001g0263 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.441-1243C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631293 | |||||||
chr10:24631418 | A | ACTATT | 151 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.441-1369_441-1368i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631418 | |||||||
chr10:24631445 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.441-1395A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631445 | |||||||
chr10:24631465 | T | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-1415A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631465 | |||||||
chr10:24631699 | T | C | 151 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.441-1649A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631699 | |||||||
chr10:24631700 | G | A | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.441-1650C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631700 | |||||||
chr10:24631729 | T | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+1673A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631729 | |||||||
chr10:24631803 | C | G | 14 | a0002c0002t0001g0020 a0002c0002t0001g0110 a0002c0002t0001g0111 others(11): Show |
14 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.440+1599G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631803 | |||||||
chr10:24631828 | A | G | 13 | a0002c0002t0001g0071 a0002c0002t0001g0086 a0004c0004t0001g0031 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.440+1574T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631828 | |||||||
chr10:24631869 | C | A | 2 | a0003c0003t0001g0199 a0003c0003t0001g0249 |
2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.440+1533G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631869 | |||||||
chr10:24631984 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1418T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631984 | |||||||
chr10:24632062 | G | C | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.440+1340C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632062 | |||||||
chr10:24632139 | T | G | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.440+1263A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632139 | |||||||
chr10:24632281 | T | C | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.440+1121A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632281 | |||||||
chr10:24632359 | A | T | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.440+1043T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632359 | |||||||
chr10:24632468 | T | C | 1 | a0001c0001t0002g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.440+934A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632468 | |||||||
chr10:24633248 | T | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.440+154A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633248 | |||||||
chr10:24633290 | C | T | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.440+112G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633290 | |||||||
chr10:24633316 | T | G | 1 | a0001c0001t0002g0317 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.440+86A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633316 | |||||||
chr10:24633372 | C | A | 1 | a0003c0003t0001g0181 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.440+30G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633372 | |||||||
chr10:24633394 | A | G | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.440+8T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633394 | |||||||
chr10:24633558 | T | TA | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-79dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633558 | |||||||
chr10:24633819 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.362-339A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633819 | |||||||
chr10:24633883 | C | CT | 112 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0175 others(109): Show |
112 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.362-404dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | |||||||
chr10:24633883 | C | CTT | 61 | a0001c0001t0001g0254 a0002c0002t0001g0011 a0002c0002t0001g0018 others(58): Show |
61 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.362-405_362-404dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | |||||||
chr10:24633883 | C | CTTT | 16 | a0002c0002t0001g0035 a0002c0002t0001g0094 a0002c0002t0001g0107 others(13): Show |
16 | HG00099.hp2 HG00673.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.362-406_362-404dup others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | |||||||
chr10:24633883 | CT | C | 8 | a0001c0001t0001g0195 a0001c0001t0002g0334 a0001c0014t0004g0287 others(5): Show |
8 | HG01081.hp1 HG01256.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-404delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | |||||||
chr10:24633883 | CTTTTTTT | C | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.362-410_362-404del others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | |||||||
chr10:24633943 | G | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-463C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633943 | |||||||
chr10:24634016 | G | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-536C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634016 | |||||||
chr10:24634389 | A | T | 1 | a0003c0003t0001g0174 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.361+622T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634389 | |||||||
chr10:24634415 | A | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+596T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634415 | |||||||
chr10:24634691 | T | A | 1 | a0002c0002t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+320A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634691 | |||||||
chr10:24634911 | T | C | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+100A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634911 | |||||||
chr10:24635138 | C | T | 1 | a0002c0002t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.269-35G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635138 | |||||||
chr10:24635175 | ATT | A | 3 | a0001c0001t0001g0191 a0002c0002t0001g0125 a0002c0002t0001g0127 |
3 | HG00735.hp1 HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.269-74_269-73delAA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635175 | |||||||
chr10:24635255 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-152C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635255 | |||||||
chr10:24635288 | C | A | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.269-185G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635288 | |||||||
chr10:24635640 | G | A | 1 | a0002c0002t0001g0043 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.269-537C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635640 | |||||||
chr10:24635790 | C | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0146 |
2 | NA18988.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.269-687G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635790 | |||||||
chr10:24635911 | T | G | 2 | a0001c0001t0003g0155 a0013c0026t0003g0157 |
2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.269-808A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635911 | |||||||
chr10:24636001 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-898C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636001 | |||||||
chr10:24636033 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.269-930C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636033 | |||||||
chr10:24636279 | G | A | 1 | a0002c0002t0001g0124 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.269-1176C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636279 | |||||||
chr10:24636316 | G | A | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.269-1213C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636316 | |||||||
chr10:24636680 | C | T | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.269-1577G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636680 | |||||||
chr10:24636942 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0221 a0001c0001t0001g0224 |
3 | HG01192.hp1 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.269-1839G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636942 | |||||||
chr10:24636979 | T | A | 1 | a0002c0002t0001g0076 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.269-1876A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636979 | |||||||
chr10:24637172 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-2069G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637172 | |||||||
chr10:24637254 | A | G | 77 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0022 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.269-2151T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637254 | |||||||
chr10:24637795 | T | G | 21 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(18): Show |
21 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.269-2692A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637795 | |||||||
chr10:24637866 | A | AT | 8 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0242 others(5): Show |
8 | HG00140.hp1 HG01099.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-2764dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637866 | |||||||
chr10:24637866 | AT | A | 27 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(24): Show |
27 | HG00735.hp1 HG01517.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.269-2764delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637866 | |||||||
chr10:24637972 | C | T | 1 | a0002c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.269-2869G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637972 | |||||||
chr10:24638051 | G | A | 136 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.269-2948C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638051 | |||||||
chr10:24638117 | G | A | 9 | a0002c0002t0001g0064 a0002c0002t0001g0065 a0002c0002t0001g0066 others(6): Show |
9 | HG00639.hp1 HG01069.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-3014C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638117 | |||||||
chr10:24638236 | TAGAG | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.269-3137_269-3134d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638236 | |||||||
chr10:24638396 | C | T | 3 | a0001c0001t0002g0301 a0001c0001t0002g0339 a0001c0001t0002g0340 |
3 | HG01169.hp1 HG01934.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.269-3293G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638396 | |||||||
chr10:24638518 | C | A | 86 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0021 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.269-3415G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638518 | |||||||
chr10:24638522 | A | T | 10 | a0002c0002t0001g0019 a0002c0002t0001g0049 a0002c0002t0001g0056 others(7): Show |
10 | HG00735.hp2 HG01934.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.269-3419T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638522 | |||||||
chr10:24638570 | T | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.269-3467A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638570 | |||||||
chr10:24638683 | A | T | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.269-3580T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638683 | |||||||
chr10:24638708 | A | C | 1 | a0002c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.269-3605T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638708 | |||||||
chr10:24638756 | T | C | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-3653A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638756 | |||||||
chr10:24638787 | A | C | 1 | a0003c0003t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.269-3684T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638787 | |||||||
chr10:24638929 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.269-3826G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638929 | |||||||
chr10:24639330 | C | T | 23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.269-4227G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639330 | |||||||
chr10:24639636 | G | A | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.269-4533C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639636 | |||||||
chr10:24639747 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-4644A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639747 | |||||||
chr10:24639755 | C | CA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-4653dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639755 | |||||||
chr10:24639815 | T | C | 1 | a0001c0001t0004g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.269-4712A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639815 | |||||||
chr10:24639833 | GAGAAAGC others(3): Show |
G | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.269-4740_269-4731d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639833 | |||||||
chr10:24639919 | C | CA | 143 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
143 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-4817dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639919 | |||||||
chr10:24639919 | C | CAA | 13 | a0001c0001t0001g0190 a0003c0003t0001g0117 a0003c0003t0001g0181 others(10): Show |
13 | HG00423.hp1 HG00597.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.269-4818_269-4817d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639919 | |||||||
chr10:24640212 | G | A | 291 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.269-5109C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640212 | |||||||
chr10:24640289 | A | AAT | 7 | a0001c0001t0001g0265 a0002c0002t0001g0065 a0002c0002t0001g0067 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-5188_269-5187d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640289 | |||||||
chr10:24640307 | T | TATATATA others(1): Show |
6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-5205_269-5204i others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640307 | |||||||
chr10:24640447 | T | C | 1 | a0002c0002t0001g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-5344A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640447 | |||||||
chr10:24640583 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-5480T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640583 | |||||||
chr10:24640631 | C | T | 333 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(330): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.269-5528G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640631 | |||||||
chr10:24640869 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.269-5766T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640869 | |||||||
chr10:24640971 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.269-5868C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640971 | |||||||
chr10:24641264 | G | A | 154 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.269-6161C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641264 | |||||||
chr10:24641354 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.269-6251T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641354 | |||||||
chr10:24641557 | T | C | 2 | a0002c0002t0001g0063 a0002c0002t0001g0286 |
2 | HG00408.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.269-6454A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641557 | |||||||
chr10:24641562 | T | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0060 |
2 | HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.269-6459A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641562 | |||||||
chr10:24641734 | G | A | 1 | a0005c0005t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.269-6631C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641734 | |||||||
chr10:24641747 | G | A | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.269-6644C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641747 | |||||||
chr10:24641780 | G | A | 1 | a0002c0002t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.269-6677C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641780 | |||||||
chr10:24641872 | C | T | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-6769G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641872 | |||||||
chr10:24641890 | G | C | 1 | a0001c0001t0005g0002 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.269-6787C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641890 | |||||||
chr10:24641920 | C | T | 1 | a0002c0002t0001g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.269-6817G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641920 | |||||||
chr10:24641952 | C | T | 1 | a0003c0003t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.269-6849G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641952 | |||||||
chr10:24641953 | G | A | 77 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0022 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.269-6850C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641953 | |||||||
chr10:24641997 | G | GA | 82 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0182 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.269-6895dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641997 | |||||||
chr10:24642080 | T | A | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-6977A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642080 | |||||||
chr10:24642246 | G | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-7143C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642246 | |||||||
chr10:24642342 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
38 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.269-7239G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642342 | |||||||
chr10:24642376 | G | A | 1 | a0003c0003t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.269-7273C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642376 | |||||||
chr10:24642514 | C | CA | 37 | a0001c0001t0001g0215 a0001c0001t0001g0265 a0001c0001t0002g0310 others(34): Show |
37 | HG00323.hp2 HG00642.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.269-7412dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642514 | |||||||
chr10:24642514 | CA | C | 10 | a0001c0001t0001g0145 a0001c0001t0001g0179 a0001c0001t0001g0273 others(7): Show |
10 | HG01069.hp1 HG01975.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-7412delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642514 | |||||||
chr10:24642830 | C | T | 1 | a0002c0002t0001g0024 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.269-7727G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642830 | |||||||
chr10:24642933 | T | C | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-7830A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642933 | |||||||
chr10:24643119 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-8016G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643119 | |||||||
chr10:24643243 | A | G | 1 | a0005c0005t0003g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.269-8140T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643243 | |||||||
chr10:24643294 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-8191C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643294 | |||||||
chr10:24643303 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-8200A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643303 | |||||||
chr10:24643480 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-8377A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643480 | |||||||
chr10:24643754 | G | T | 291 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.269-8651C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643754 | |||||||
chr10:24644032 | T | C | 1 | a0001c0001t0002g0327 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.269-8929A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644032 | |||||||
chr10:24644200 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.269-9097G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644200 | |||||||
chr10:24644465 | G | A | 4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0136 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-9362C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644465 | |||||||
chr10:24644543 | G | C | 1 | a0002c0002t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.269-9440C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644543 | |||||||
chr10:24644559 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.269-9456G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644559 | |||||||
chr10:24644608 | A | C | 1 | a0003c0003t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.269-9505T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644608 | |||||||
chr10:24644771 | G | T | 202 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(199): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.269-9668C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644771 | |||||||
chr10:24644871 | A | G | 1 | a0002c0002t0001g0150 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.269-9768T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644871 | |||||||
chr10:24644883 | C | A | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-9780G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644883 | |||||||
chr10:24644973 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-9870A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644973 | |||||||
chr10:24644980 | C | A | 3 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0322 |
3 | HG02080.hp2 NA18939.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.269-9877G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644980 | |||||||
chr10:24645003 | T | G | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-9900A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645003 | |||||||
chr10:24645027 | G | A | 153 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.269-9924C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645027 | |||||||
chr10:24645142 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.269-10039T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645142 | |||||||
chr10:24645317 | A | G | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-10214T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645317 | |||||||
chr10:24645379 | G | C | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-10276C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645379 | |||||||
chr10:24645517 | T | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0250 |
3 | HG00621.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.269-10414A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645517 | |||||||
chr10:24645585 | GA | G | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.269-10483delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645585 | |||||||
chr10:24645666 | C | T | 291 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(288): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.269-10563G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645666 | |||||||
chr10:24645674 | T | C | 149 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.269-10571A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645674 | |||||||
chr10:24645749 | T | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.269-10646A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645749 | |||||||
chr10:24646100 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-10997G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646100 | |||||||
chr10:24646270 | A | G | 166 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.269-11167T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646270 | |||||||
chr10:24646339 | A | T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-11236T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646339 | |||||||
chr10:24646497 | G | A | 2 | a0005c0005t0001g0103 a0005c0005t0001g0104 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.269-11394C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646497 | |||||||
chr10:24646516 | T | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-11413A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646516 | |||||||
chr10:24646637 | T | C | 2 | a0004c0004t0001g0039 a0004c0004t0001g0040 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.269-11534A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646637 | |||||||
chr10:24646767 | G | A | 2 | a0001c0001t0002g0315 a0001c0001t0002g0344 |
2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.269-11664C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646767 | |||||||
chr10:24646796 | T | C | 1 | a0003c0003t0001g0181 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.269-11693A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646796 | |||||||
chr10:24647003 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-11900A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647003 | |||||||
chr10:24647021 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.269-11918C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647021 | |||||||
chr10:24647030 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-11927T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647030 | |||||||
chr10:24647085 | G | A | 1 | a0001c0001t0002g0321 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.269-11982C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647085 | |||||||
chr10:24647216 | G | T | 1 | a0002c0002t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.269-12113C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647216 | |||||||
chr10:24647612 | C | T | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-12509G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647612 | |||||||
chr10:24647760 | G | C | 1 | a0006c0007t0015g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.269-12657C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647760 | |||||||
chr10:24647900 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-12797G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647900 | |||||||
chr10:24648169 | C | T | 1 | a0002c0002t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.269-13066G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648169 | |||||||
chr10:24648170 | G | A | 2 | a0002c0002t0001g0043 a0003c0006t0003g0216 |
2 | NA18980.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.269-13067C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648170 | |||||||
chr10:24648501 | C | T | 151 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.269-13398G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648501 | |||||||
chr10:24648546 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-13443C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648546 | |||||||
chr10:24648641 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.269-13538C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648641 | |||||||
chr10:24648702 | C | T | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-13599G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648702 | |||||||
chr10:24648709 | G | A | 1 | a0003c0003t0001g0181 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.269-13606C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648709 | |||||||
chr10:24648728 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.269-13625C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648728 | |||||||
chr10:24648732 | T | C | 1 | a0002c0002t0001g0011 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.269-13629A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648732 | |||||||
chr10:24648779 | C | CA | 86 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(83): Show |
86 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.269-13677dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648779 | |||||||
chr10:24648779 | C | CAA | 77 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0023 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.269-13678_269-1367 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648779 | |||||||
chr10:24648814 | T | C | 2 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.269-13711A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648814 | |||||||
chr10:24648961 | T | C | 151 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.269-13858A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648961 | |||||||
chr10:24649314 | T | C | 14 | a0002c0002t0001g0020 a0002c0002t0001g0107 a0002c0002t0001g0108 others(11): Show |
14 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.269-14211A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649314 | |||||||
chr10:24649629 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.269-14526C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649629 | |||||||
chr10:24649705 | T | TAA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-14604_269-1460 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649705 | |||||||
chr10:24649751 | TAGAAAAC others(7): Show |
T | 1 | a0002c0002t0001g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.269-14662_269-1464 others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649751 | |||||||
chr10:24649946 | T | C | 1 | a0001c0001t0002g0311 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.269-14843A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649946 | |||||||
chr10:24649962 | AAACTT | A | 17 | a0002c0002t0001g0020 a0002c0002t0001g0107 a0002c0002t0001g0108 others(14): Show |
17 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.269-14864_269-1486 others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649962 | |||||||
chr10:24650179 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-15076T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650179 | |||||||
chr10:24650181 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02965.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.269-15078T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650181 | |||||||
chr10:24650591 | A | G | 1 | a0002c0002t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.269-15488T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650591 | |||||||
chr10:24650622 | A | G | 40 | a0002c0002t0001g0018 a0002c0002t0001g0020 a0002c0002t0001g0107 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.269-15519T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650622 | |||||||
chr10:24650736 | T | C | 168 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.269-15633A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650736 | |||||||
chr10:24650834 | T | G | 1 | a0003c0003t0001g0176 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.269-15731A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650834 | |||||||
chr10:24650965 | CA | C | 7 | a0001c0001t0002g0301 a0006c0007t0006g0292 a0006c0007t0006g0293 others(4): Show |
7 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-15863delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650965 | |||||||
chr10:24650981 | C | T | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0250 others(2): Show |
5 | HG00621.hp1 HG01496.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-15878G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650981 | |||||||
chr10:24651088 | T | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.268+15897A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651088 | |||||||
chr10:24651191 | T | A | 10 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+15794A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651191 | |||||||
chr10:24651321 | G | C | 14 | a0001c0001t0002g0303 a0001c0001t0002g0315 a0001c0001t0002g0320 others(11): Show |
14 | HG00673.hp2 HG01109.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.268+15664C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651321 | |||||||
chr10:24651446 | A | G | 1 | a0001c0001t0003g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.268+15539T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651446 | |||||||
chr10:24651492 | T | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.268+15493A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651492 | |||||||
chr10:24651774 | G | A | 1 | a0003c0006t0002g0349 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.268+15211C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651774 | |||||||
chr10:24651830 | T | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+15155A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651830 | |||||||
chr10:24651885 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+15100T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651885 | |||||||
chr10:24652024 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+14961C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652024 | |||||||
chr10:24652076 | C | T | 3 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0283 |
3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.268+14909G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652076 | |||||||
chr10:24652118 | G | A | 1 | a0003c0003t0001g0207 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.268+14867C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652118 | |||||||
chr10:24652123 | A | G | 5 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0105 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+14862T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652123 | |||||||
chr10:24652210 | A | G | 7 | a0003c0003t0001g0213 a0003c0003t0001g0217 a0003c0003t0001g0222 others(4): Show |
7 | HG00408.hp2 HG01952.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+14775T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652210 | |||||||
chr10:24652479 | A | T | 1 | a0003c0003t0001g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.268+14506T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652479 | |||||||
chr10:24652569 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0219 a0001c0001t0001g0221 others(3): Show |
6 | HG01069.hp2 HG01192.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+14416A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652569 | |||||||
chr10:24652728 | C | A | 1 | a0002c0002t0001g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.268+14257G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652728 | |||||||
chr10:24653087 | C | G | 3 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0285 |
3 | HG02451.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268+13898G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653087 | |||||||
chr10:24653122 | T | A | 2 | a0002c0002t0001g0065 a0002c0002t0001g0067 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268+13863A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653122 | |||||||
chr10:24653222 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+13763T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653222 | |||||||
chr10:24653346 | G | A | 1 | a0002c0002t0014g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.268+13639C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653346 | |||||||
chr10:24653453 | A | G | 1 | a0003c0003t0001g0213 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268+13532T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653453 | |||||||
chr10:24653551 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.268+13434G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653551 | |||||||
chr10:24653552 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.268+13433C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653552 | |||||||
chr10:24653662 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268+13323A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653662 | |||||||
chr10:24653696 | C | T | 28 | a0003c0003t0001g0012 a0003c0003t0001g0174 a0003c0003t0001g0176 others(25): Show |
28 | HG00408.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.268+13289G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653696 | |||||||
chr10:24653724 | G | T | 2 | a0002c0002t0001g0078 a0002c0002t0001g0079 |
2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.268+13261C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653724 | |||||||
chr10:24653996 | C | T | 2 | a0002c0002t0001g0065 a0002c0002t0001g0067 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268+12989G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653996 | |||||||
chr10:24654265 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+12720G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654265 | |||||||
chr10:24654340 | CCT | C | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+12643_268+1264 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654340 | |||||||
chr10:24654371 | GA | G | 60 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(57): Show |
60 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.268+12613delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654371 | |||||||
chr10:24654459 | C | G | 1 | a0002c0002t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.268+12526G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654459 | |||||||
chr10:24654464 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.268+12521C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654464 | |||||||
chr10:24654490 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.268+12495C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654490 | |||||||
chr10:24654523 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268+12462A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654523 | |||||||
chr10:24654609 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+12376C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654609 | |||||||
chr10:24654647 | A | G | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+12338T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654647 | |||||||
chr10:24654649 | G | A | 1 | a0003c0003t0001g0203 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.268+12336C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654649 | |||||||
chr10:24654698 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+12287T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654698 | |||||||
chr10:24654728 | C | G | 1 | a0002c0002t0001g0023 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.268+12257G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654728 | |||||||
chr10:24654790 | A | G | 2 | a0003c0003t0001g0199 a0003c0003t0001g0249 |
2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.268+12195T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654790 | |||||||
chr10:24654841 | G | GA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+12143dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654841 | |||||||
chr10:24654851 | A | G | 2 | a0002c0002t0001g0071 a0012c0019t0001g0037 |
2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.268+12134T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654851 | |||||||
chr10:24655040 | A | C | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.268+11945T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655040 | |||||||
chr10:24655097 | T | C | 1 | a0003c0003t0001g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.268+11888A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655097 | |||||||
chr10:24655124 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.268+11861T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655124 | |||||||
chr10:24655210 | G | A | 1 | a0003c0003t0001g0248 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.268+11775C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655210 | |||||||
chr10:24655272 | G | T | 2 | a0001c0001t0002g0323 a0001c0001t0002g0334 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.268+11713C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655272 | |||||||
chr10:24655330 | G | C | 3 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0053 |
3 | NA18975.hp2 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.268+11655C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655330 | |||||||
chr10:24655375 | A | G | 3 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0053 |
3 | NA18975.hp2 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.268+11610T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655375 | |||||||
chr10:24655546 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.268+11439C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655546 | |||||||
chr10:24655557 | G | A | 1 | a0005c0005t0004g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.268+11428C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655557 | |||||||
chr10:24655583 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.268+11402C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655583 | |||||||
chr10:24655618 | C | T | 2 | a0002c0002t0001g0027 a0016c0016t0003g0028 |
2 | HG01433.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.268+11367G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655618 | |||||||
chr10:24655743 | G | A | 1 | a0002c0002t0001g0282 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.268+11242C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655743 | |||||||
chr10:24655787 | G | A | 1 | a0003c0003t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.268+11198C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655787 | |||||||
chr10:24655809 | G | A | 10 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(7): Show |
10 | HG02129.hp2 HG02523.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+11176C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655809 | |||||||
chr10:24655814 | TCTCTGCC others(69): Show |
T | 1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.268+11095_268+1117 others(80): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655814 | |||||||
chr10:24655925 | G | C | 3 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0285 |
3 | HG02451.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268+11060C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655925 | |||||||
chr10:24655929 | G | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+11056C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655929 | |||||||
chr10:24655943 | A | G | 292 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.268+11042T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655943 | |||||||
chr10:24655948 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+11037C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655948 | |||||||
chr10:24655992 | GAGAAGTG others(73): Show |
G | 4 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+10913_268+1099 others(84): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655992 | |||||||
chr10:24655998 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+10987A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655998 | |||||||
chr10:24656065 | C | A | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+10920G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656065 | |||||||
chr10:24656067 | C | T | 8 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+10918G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656067 | |||||||
chr10:24656072 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10913T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656072 | |||||||
chr10:24656112 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10873C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656112 | |||||||
chr10:24656162 | T | TG | 98 | a0001c0001t0001g0270 a0002c0002t0001g0011 a0002c0002t0001g0019 others(95): Show |
98 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.268+10822dupC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656162 | |||||||
chr10:24656168 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.268+10817C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656168 | |||||||
chr10:24656198 | A | G | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+10787T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656198 | |||||||
chr10:24656201 | C | T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+10784G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656201 | |||||||
chr10:24656213 | GGGGGGGT others(718): Show |
G | 6 | a0001c0001t0001g0145 a0001c0001t0001g0163 a0001c0001t0001g0165 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10047_268+1077 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656213 | |||||||
chr10:24656214 | GGGGGGTC others(717): Show |
G | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+10047_268+1077 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656214 | |||||||
chr10:24656250 | CGGGAGGT others(979): Show |
C | 1 | a0002c0002t0001g0023 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.268+9749_268+10734 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656250 | |||||||
chr10:24656251 | G | A | 1 | a0004c0004t0001g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.268+10734C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656251 | |||||||
chr10:24656301 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+10684G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656301 | |||||||
chr10:24656308 | GCCTGGCC others(43): Show |
G | 1 | a0003c0006t0003g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.268+10627_268+1067 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656308 | |||||||
chr10:24656311 | T | C | 336 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(333): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.268+10674A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656311 | |||||||
chr10:24656312 | G | A | 1 | a0003c0003t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.268+10673C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656312 | |||||||
chr10:24656370 | G | A | 1 | a0003c0006t0003g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.268+10615C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656370 | |||||||
chr10:24656375 | G | A | 1 | a0002c0002t0001g0150 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.268+10610C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656375 | |||||||
chr10:24656389 | T | TG | 16 | a0001c0001t0001g0221 a0001c0001t0001g0253 a0001c0001t0002g0344 others(13): Show |
16 | HG00642.hp1 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.268+10595dupC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656389 | |||||||
chr10:24656391 | G | A | 2 | a0001c0001t0002g0317 a0001c0001t0002g0326 |
2 | HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.268+10594C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656391 | |||||||
chr10:24656400 | G | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10585C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656400 | |||||||
chr10:24656404 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG02129.hp2 HG02523.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+10581A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656404 | |||||||
chr10:24656411 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.268+10574C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656411 | |||||||
chr10:24656427 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10558A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656427 | |||||||
chr10:24656432 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10553C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656432 | |||||||
chr10:24656438 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10547C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656438 | |||||||
chr10:24656442 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10543C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656442 | |||||||
chr10:24656456 | A | G | 156 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.268+10529T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656456 | |||||||
chr10:24656464 | TGTGAAGT others(866): Show |
T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9648_268+10520 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656464 | |||||||
chr10:24656466 | T | G | 157 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.268+10519A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656466 | |||||||
chr10:24656467 | GAAGTGAG others(546): Show |
G | 1 | a0001c0001t0002g0322 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.268+9965_268+10517 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656467 | |||||||
chr10:24656502 | G | A | 3 | a0001c0001t0001g0265 a0002c0002t0001g0151 a0002c0002t0001g0152 |
3 | HG02145.hp2 NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.268+10483C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656502 | |||||||
chr10:24656506 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0250 |
3 | HG00621.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.268+10479C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656506 | |||||||
chr10:24656534 | G | A | 4 | a0002c0002t0001g0049 a0002c0002t0001g0056 a0002c0002t0001g0057 others(1): Show |
4 | HG01934.hp1 HG01952.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10451C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656534 | |||||||
chr10:24656550 | T | C | 119 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(116): Show |
119 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.268+10435A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656550 | |||||||
chr10:24656581 | T | TCCGCCCA others(5): Show |
1 | a0002c0002t0001g0121 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.268+10392_268+1040 others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656581 | |||||||
chr10:24656595 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.268+10390G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656595 | |||||||
chr10:24656596 | G | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+10389C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656596 | |||||||
chr10:24656597 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268+10388G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656597 | |||||||
chr10:24656619 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(1): Show |
4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10366C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656619 | |||||||
chr10:24656661 | T | TGCCCGGC others(42): Show |
11 | a0001c0001t0002g0001 a0001c0001t0002g0304 a0001c0001t0002g0305 others(8): Show |
12 | HG01168.hp2 HG01975.hp2 NA18906.hp1 others(9): Show |
intron_variant | MODIFIER | c.268+10275_268+1032 others(53): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656661 | |||||||
chr10:24656661 | TGCCCGGC others(42): Show |
T | 2 | a0001c0001t0002g0344 a0001c0001t0004g0297 |
2 | NA19058.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.268+10275_268+1032 others(53): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656661 | |||||||
chr10:24656661 | TGCCCGGC others(91): Show |
T | 34 | a0001c0001t0003g0156 a0002c0002t0001g0018 a0002c0002t0001g0020 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.268+10226_268+1032 others(102): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656661 | |||||||
chr10:24656673 | C | CGCCCCGT others(42): Show |
1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.268+10311_268+1031 others(53): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656673 | |||||||
chr10:24656683 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0224 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.268+10302C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656683 | |||||||
chr10:24656694 | GGGGGGGT others(90): Show |
G | 3 | a0002c0002t0001g0057 a0002c0002t0007g0008 a0019c0023t0001g0091 |
3 | HG01934.hp1 HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.268+10194_268+1029 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656694 | |||||||
chr10:24656704 | G | GCCCCCCG others(43): Show |
1 | a0005c0005t0004g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.268+10231_268+1028 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656704 | |||||||
chr10:24656705 | CCCCCCGC others(90): Show |
C | 3 | a0002c0002t0001g0055 a0002c0002t0001g0064 a0002c0002t0001g0129 |
3 | HG00639.hp1 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.268+10183_268+1027 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656705 | |||||||
chr10:24656722 | C | T | 53 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0182 others(50): Show |
53 | HG00423.hp1 HG00597.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.268+10263G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656722 | |||||||
chr10:24656742 | T | TGGGGGGG others(43): Show |
1 | a0001c0001t0002g0310 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.268+10242_268+1024 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656742 | |||||||
chr10:24656750 | T | A | 112 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0247 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.268+10235A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656750 | |||||||
chr10:24656753 | G | GC | 9 | a0001c0001t0001g0177 a0001c0001t0001g0230 a0001c0001t0001g0258 others(6): Show |
9 | HG01261.hp1 HG02071.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+10231dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656753 | |||||||
chr10:24656753 | G | GCCCCCCG others(44): Show |
1 | a0001c0001t0001g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.268+10231_268+1023 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656753 | |||||||
chr10:24656754 | CCCCCCGC others(90): Show |
C | 2 | a0005c0005t0001g0103 a0015c0020t0001g0113 |
2 | HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.268+10134_268+1023 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656754 | |||||||
chr10:24656766 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.268+10219G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656766 | |||||||
chr10:24656792 | GGGGGGGT others(90): Show |
G | 2 | a0002c0002t0001g0121 a0002c0002t0001g0128 |
2 | HG00438.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.268+10096_268+1019 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656792 | |||||||
chr10:24656793 | GGGGGGTC others(138): Show |
G | 1 | a0003c0003t0001g0249 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.268+10047_268+1019 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656793 | |||||||
chr10:24656794 | GGGGGTCG others(137): Show |
G | 1 | a0003c0003t0001g0199 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.268+10047_268+1019 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656794 | |||||||
chr10:24656799 | T | A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0258 others(2): Show |
5 | HG00597.hp1 HG01261.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+10186A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656799 | |||||||
chr10:24656801 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.268+10184C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656801 | |||||||
chr10:24656801 | GGCCCCCC others(449): Show |
G | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.268+9728_268+10183 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656801 | |||||||
chr10:24656802 | G | GC | 9 | a0001c0001t0001g0245 a0001c0001t0001g0253 a0001c0001t0002g0336 others(6): Show |
9 | HG00642.hp1 HG01934.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+10182dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656802 | |||||||
chr10:24656841 | GGGGGGGT others(90): Show |
G | 15 | a0002c0002t0001g0050 a0002c0002t0001g0053 a0002c0002t0001g0058 others(12): Show |
15 | HG00099.hp2 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656841 | |||||||
chr10:24656842 | GGGGGGTC others(89): Show |
G | 40 | a0002c0002t0001g0011 a0002c0002t0001g0022 a0002c0002t0001g0025 others(37): Show |
40 | HG00099.hp1 HG00642.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(100): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656842 | |||||||
chr10:24656843 | GGGGGTCG others(88): Show |
G | 44 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0247 others(41): Show |
44 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(99): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656843 | |||||||
chr10:24656844 | GGGGTCGG others(87): Show |
G | 6 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0095 others(3): Show |
6 | HG00438.hp1 HG01255.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(98): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656844 | |||||||
chr10:24656845 | GGGTCGGC others(86): Show |
G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0279 |
2 | HG00140.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.268+10047_268+1013 others(97): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656845 | |||||||
chr10:24656848 | T | A | 47 | a0001c0001t0001g0179 a0001c0001t0001g0253 a0001c0001t0001g0264 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.268+10137A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | |||||||
chr10:24656848 | T | TCGGCCCC others(43): Show |
3 | a0001c0001t0001g0243 a0001c0001t0001g0271 a0003c0003t0001g0117 |
3 | HG01109.hp2 HG04228.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.268+10136_268+1013 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | |||||||
chr10:24656848 | T | TCGGCCCC others(44): Show |
1 | a0001c0001t0001g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268+10136_268+1013 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | |||||||
chr10:24656848 | T | TCGGCCCC others(43): Show |
2 | a0001c0001t0001g0221 a0003c0003t0001g0207 |
2 | HG01192.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.268+10136_268+1013 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | |||||||
chr10:24656848 | TCGGCCCC others(90): Show |
T | 1 | a0002c0002t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.268+10040_268+1013 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | |||||||
chr10:24656851 | G | GC | 8 | a0001c0001t0001g0177 a0001c0001t0002g0303 a0001c0001t0002g0340 others(5): Show |
8 | HG00639.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+10133dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656851 | |||||||
chr10:24656851 | G | GCCCCCCG others(43): Show |
1 | a0001c0001t0001g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.268+10133_268+1013 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656851 | |||||||
chr10:24656889 | TGGGGGGG others(43): Show |
T | 2 | a0001c0001t0002g0341 a0001c0001t0002g0345 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.268+10046_268+1009 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656889 | |||||||
chr10:24656890 | GGGGGGGT others(41): Show |
G | 1 | a0001c0001t0002g0315 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.268+10047_268+1009 others(52): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656890 | |||||||
chr10:24656892 | GGGGGTCG others(39): Show |
G | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0258 others(1): Show |
4 | HG00597.hp1 HG01261.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10047_268+1009 others(50): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656892 | |||||||
chr10:24656893 | GGGGTCGG others(38): Show |
G | 1 | a0003c0003t0001g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.268+10047_268+1009 others(49): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656893 | |||||||
chr10:24656897 | T | A | 94 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(91): Show |
94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.268+10088A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656897 | |||||||
chr10:24656938 | T | TCGGGGGG others(44): Show |
1 | a0001c0001t0001g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268+10046_268+1004 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656938 | T | TGGGGGGG others(47): Show |
1 | a0001c0001t0001g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.268+10046_268+1004 others(58): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656938 | T | TGGGGGGG others(46): Show |
1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.268+10046_268+1004 others(57): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656938 | T | TGGGGGGG others(43): Show |
4 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0241 others(1): Show |
4 | HG00741.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656938 | T | TGGGGGGG others(44): Show |
24 | a0001c0001t0001g0013 a0001c0001t0001g0170 a0001c0001t0001g0186 others(21): Show |
24 | HG00323.hp1 HG00639.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656938 | T | TGGGGGGG others(45): Show |
49 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0161 others(46): Show |
49 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(56): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656938 | T | TGGGGGGG others(46): Show |
4 | a0001c0001t0001g0223 a0001c0001t0003g0218 a0003c0003t0001g0222 others(1): Show |
4 | HG03225.hp1 HG03453.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(57): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | |||||||
chr10:24656940 | G | GGGGGGGT others(41): Show |
1 | a0001c0001t0005g0002 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+10044_268+1004 others(52): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656940 | |||||||
chr10:24656944 | GGGGGTCA others(124): Show |
G | 6 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0003c0003t0001g0201 others(3): Show |
6 | HG01123.hp1 HG01981.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+9910_268+10040 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656944 | |||||||
chr10:24656951 | A | G | 108 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(105): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.268+10034T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656951 | |||||||
chr10:24656954 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.268+10031G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656954 | |||||||
chr10:24656958 | CTGCCCGG others(72): Show |
C | 1 | a0001c0001t0001g0276 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.268+9948_268+10026 others(82): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656958 | |||||||
chr10:24656960 | G | A | 2 | a0005c0005t0001g0103 a0005c0005t0001g0104 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.268+10025C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656960 | |||||||
chr10:24656963 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.268+10022G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656963 | |||||||
chr10:24656995 | G | A | 147 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.268+9990C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656995 | |||||||
chr10:24657020 | A | G | 1 | a0001c0001t0005g0002 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+9965T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657020 | |||||||
chr10:24657049 | C | T | 112 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(109): Show |
112 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.268+9936G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657049 | |||||||
chr10:24657069 | TGGGGGTG others(43): Show |
T | 1 | a0002c0002t0001g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.268+9866_268+9915d others(52): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657069 | |||||||
chr10:24657075 | T | G | 1 | a0001c0001t0005g0002 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+9910A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657075 | |||||||
chr10:24657079 | A | G | 6 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0003c0003t0001g0201 others(3): Show |
6 | HG01123.hp1 HG01981.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+9906T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657079 | |||||||
chr10:24657080 | G | GCCCCCGG others(603): Show |
1 | a0001c0001t0005g0002 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+9904_268+9905i others(612): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657080 | |||||||
chr10:24657086 | C | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+9899G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657086 | |||||||
chr10:24657087 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.268+9898C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657087 | |||||||
chr10:24657090 | C | T | 1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.268+9895G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657090 | |||||||
chr10:24657099 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01516.hp1 HG01517.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+9886C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657099 | |||||||
chr10:24657118 | TG | T | 24 | a0001c0001t0001g0172 a0001c0001t0004g0298 a0001c0001t0004g0299 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+9866delC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657118 | |||||||
chr10:24657132 | C | T | 1 | a0002c0002t0001g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.268+9853G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657132 | |||||||
chr10:24657137 | T | C | 1 | a0002c0002t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.268+9848A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657137 | |||||||
chr10:24657142 | G | A | 1 | a0003c0003t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.268+9843C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657142 | |||||||
chr10:24657155 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.268+9830C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657155 | |||||||
chr10:24657173 | GCCTCTGC others(30): Show |
G | 101 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0021 others(98): Show |
101 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.268+9775_268+9811d others(39): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657173 | |||||||
chr10:24657182 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.268+9803G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657182 | |||||||
chr10:24657184 | G | A | 1 | a0003c0003t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.268+9801C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657184 | |||||||
chr10:24657187 | A | G | 183 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.268+9798T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657187 | |||||||
chr10:24657198 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.268+9787C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657198 | |||||||
chr10:24657210 | C | G | 1 | a0011c0011t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.268+9775G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657210 | |||||||
chr10:24657236 | A | C | 285 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.268+9749T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657236 | |||||||
chr10:24657248 | G | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268+9737C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657248 | |||||||
chr10:24657265 | GCCGGCCA others(124): Show |
G | 1 | a0003c0003t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.268+9589_268+9719d others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657265 | |||||||
chr10:24657276 | G | A | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+9709C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657276 | |||||||
chr10:24657295 | TG | T | 264 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.268+9689delC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657295 | |||||||
chr10:24657297 | G | T | 3 | a0002c0002t0001g0119 a0002c0002t0001g0120 a0002c0002t0001g0128 |
3 | HG00673.hp1 HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.268+9688C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657297 | |||||||
chr10:24657301 | G | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+9684C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657301 | |||||||
chr10:24657310 | CCCCCTCG others(120): Show |
C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG02559.hp1 HG03130.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9548_268+9674d others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657310 | |||||||
chr10:24657315 | T | C | 279 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.268+9670A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657315 | |||||||
chr10:24657328 | C | T | 1 | a0015c0020t0001g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.268+9657G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657328 | |||||||
chr10:24657329 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.268+9656C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657329 | |||||||
chr10:24657342 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9643C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657342 | |||||||
chr10:24657351 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9634A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657351 | |||||||
chr10:24657362 | G | A | 4 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+9623C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657362 | |||||||
chr10:24657397 | C | T | 1 | a0003c0003t0001g0204 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.268+9588G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657397 | |||||||
chr10:24657399 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0241 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.268+9586C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657399 | |||||||
chr10:24657416 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.268+9569C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657416 | |||||||
chr10:24657427 | T | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.268+9558A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657427 | |||||||
chr10:24657465 | G | A | 4 | a0002c0002t0001g0131 a0002c0002t0001g0132 a0002c0002t0001g0153 others(1): Show |
4 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+9520C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657465 | |||||||
chr10:24657478 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9507G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657478 | |||||||
chr10:24657478 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(5): Show |
8 | HG01099.hp2 HG01255.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+9507G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657478 | |||||||
chr10:24657591 | T | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9394A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657591 | |||||||
chr10:24657598 | T | A | 2 | a0002c0002t0001g0045 a0002c0002t0001g0093 |
2 | NA18747.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.268+9387A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657598 | |||||||
chr10:24657611 | C | T | 2 | a0002c0002t0001g0121 a0002c0002t0001g0133 |
2 | HG00438.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.268+9374G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657611 | |||||||
chr10:24657626 | A | G | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+9359T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657626 | |||||||
chr10:24657639 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657639 | |||||||
chr10:24657640 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268+9345G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657640 | |||||||
chr10:24657652 | G | A | 3 | a0001c0014t0004g0287 a0002c0002t0001g0050 a0005c0005t0004g0288 |
3 | HG03209.hp1 NA18906.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.268+9333C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657652 | |||||||
chr10:24657693 | T | G | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0189 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+9292A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657693 | |||||||
chr10:24657700 | A | G | 287 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.268+9285T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657700 | |||||||
chr10:24657859 | C | T | 1 | a0002c0002t0001g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.268+9126G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657859 | |||||||
chr10:24657883 | A | G | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268+9102T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657883 | |||||||
chr10:24658033 | C | T | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.268+8952G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658033 | |||||||
chr10:24658060 | T | TA | 61 | a0001c0001t0002g0001 a0001c0001t0002g0295 a0001c0001t0002g0301 others(58): Show |
62 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.268+8924dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | |||||||
chr10:24658060 | T | TAA | 14 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0145 others(11): Show |
14 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.268+8923_268+8924d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | |||||||
chr10:24658060 | T | TAAA | 9 | a0001c0001t0001g0144 a0001c0001t0001g0163 a0001c0001t0001g0164 others(6): Show |
9 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+8922_268+8924d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | |||||||
chr10:24658060 | T | TTA | 256 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.268+8924_268+8925i others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | |||||||
chr10:24658060 | T | TTAA | 4 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(1): Show |
4 | NA18978.hp2 NA19058.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+8924_268+8925i others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | |||||||
chr10:24658116 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.268+8869G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658116 | |||||||
chr10:24658261 | G | A | 1 | a0001c0001t0004g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.268+8724C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658261 | |||||||
chr10:24658379 | CAT | C | 15 | a0001c0001t0001g0187 a0002c0002t0001g0020 a0002c0002t0001g0107 others(12): Show |
15 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+8604_268+8605d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658379 | |||||||
chr10:24658389 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+8596A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658389 | |||||||
chr10:24658392 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.268+8593G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658392 | |||||||
chr10:24658571 | C | T | 1 | a0003c0003t0012g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.268+8414G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658571 | |||||||
chr10:24658734 | G | A | 1 | a0002c0030t0001g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.268+8251C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658734 | |||||||
chr10:24658741 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.268+8244G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658741 | |||||||
chr10:24658797 | T | C | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.268+8188A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658797 | |||||||
chr10:24658809 | C | CTAGAACT | 288 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.268+8175_268+8176i others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658809 | |||||||
chr10:24658902 | A | G | 1 | a0002c0002t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.268+8083T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658902 | |||||||
chr10:24659143 | T | C | 147 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.268+7842A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659143 | |||||||
chr10:24659401 | C | T | 1 | a0002c0015t0001g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.268+7584G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659401 | |||||||
chr10:24659408 | C | T | 1 | a0004c0004t0001g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268+7577G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659408 | |||||||
chr10:24659454 | T | C | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+7531A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659454 | |||||||
chr10:24659503 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.268+7482A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659503 | |||||||
chr10:24659539 | T | C | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.268+7446A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659539 | |||||||
chr10:24659680 | T | G | 1 | a0002c0002t0001g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.268+7305A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659680 | |||||||
chr10:24659689 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.268+7296C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659689 | |||||||
chr10:24659718 | G | C | 1 | a0001c0001t0002g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.268+7267C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659718 | |||||||
chr10:24659747 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.268+7238A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659747 | |||||||
chr10:24659794 | A | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+7191T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659794 | |||||||
chr10:24659907 | A | G | 2 | a0001c0001t0003g0155 a0013c0026t0003g0157 |
2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.268+7078T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659907 | |||||||
chr10:24659981 | T | TC | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+7003dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659981 | |||||||
chr10:24660053 | T | C | 147 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.268+6932A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660053 | |||||||
chr10:24660262 | T | C | 1 | a0002c0002t0001g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.268+6723A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660262 | |||||||
chr10:24660309 | AT | A | 105 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(102): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.268+6675delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660309 | |||||||
chr10:24660386 | T | TAA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+6597_268+6598d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | T | TAAA | 17 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0044 others(14): Show |
17 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.268+6596_268+6598d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | T | TAAAA | 74 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0020 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.268+6595_268+6598d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | T | TAAAAA | 108 | a0001c0001t0001g0161 a0001c0001t0001g0186 a0001c0001t0001g0187 others(105): Show |
108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.268+6594_268+6598d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | T | TAAAAAA | 47 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
47 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.268+6593_268+6598d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | T | TAAAAAAA | 15 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0183 others(12): Show |
15 | HG00642.hp1 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.268+6592_268+6598d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | T | TAAAAAAA others(3): Show |
2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+6589_268+6598d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | TA | T | 7 | a0001c0001t0002g0304 a0001c0001t0002g0319 a0001c0001t0002g0322 others(4): Show |
7 | HG00280.hp2 HG01099.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+6598delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660386 | TAAAAAAA others(2): Show |
T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+6590_268+6598d others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | |||||||
chr10:24660433 | G | T | 149 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.268+6552C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660433 | |||||||
chr10:24660507 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+6478G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660507 | |||||||
chr10:24660566 | C | G | 1 | a0014c0022t0002g0338 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.268+6419G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660566 | |||||||
chr10:24660786 | A | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0146 |
2 | NA18988.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.268+6199T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660786 | |||||||
chr10:24660814 | G | C | 104 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0021 others(101): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.268+6171C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660814 | |||||||
chr10:24660836 | T | A | 1 | a0002c0002t0001g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.268+6149A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660836 | |||||||
chr10:24661046 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+5939A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661046 | |||||||
chr10:24661200 | G | A | 8 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0239 others(5): Show |
8 | HG00639.hp2 HG01257.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+5785C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661200 | |||||||
chr10:24661266 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+5719G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661266 | |||||||
chr10:24661305 | T | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+5680A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661305 | |||||||
chr10:24661423 | C | T | 7 | a0002c0002t0001g0020 a0002c0002t0001g0281 a0002c0002t0001g0282 others(4): Show |
7 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+5562G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661423 | |||||||
chr10:24661738 | T | C | 1 | a0001c0001t0004g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.268+5247A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661738 | |||||||
chr10:24661775 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.268+5210A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661775 | |||||||
chr10:24662049 | T | C | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+4936A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662049 | |||||||
chr10:24662113 | G | A | 2 | a0001c0001t0002g0318 a0001c0001t0002g0327 |
2 | HG02155.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.268+4872C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662113 | |||||||
chr10:24662118 | G | A | 1 | a0001c0001t0002g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.268+4867C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662118 | |||||||
chr10:24662489 | G | T | 1 | a0002c0002t0001g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.268+4496C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662489 | |||||||
chr10:24662549 | C | T | 2 | a0002c0002t0001g0071 a0012c0019t0001g0037 |
2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.268+4436G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662549 | |||||||
chr10:24662846 | T | G | 1 | a0002c0002t0001g0100 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.268+4139A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662846 | |||||||
chr10:24662877 | C | T | 170 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.268+4108G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662877 | |||||||
chr10:24662964 | A | AT | 246 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.268+4020dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662964 | |||||||
chr10:24662964 | A | ATT | 10 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(7): Show |
10 | HG00423.hp1 HG01175.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+4019_268+4020d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662964 | |||||||
chr10:24662964 | AT | A | 7 | a0001c0001t0001g0172 a0001c0001t0002g0342 a0001c0001t0004g0297 others(4): Show |
7 | HG01891.hp2 HG02723.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+4020delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662964 | |||||||
chr10:24663007 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.268+3978G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663007 | |||||||
chr10:24663099 | C | T | 2 | a0002c0002t0001g0078 a0002c0002t0001g0079 |
2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.268+3886G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663099 | |||||||
chr10:24663360 | C | T | 1 | a0005c0005t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268+3625G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663360 | |||||||
chr10:24663482 | A | G | 287 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.268+3503T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663482 | |||||||
chr10:24663531 | CTAT | C | 3 | a0001c0001t0001g0172 a0001c0001t0004g0298 a0001c0001t0004g0299 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.268+3451_268+3453d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663531 | |||||||
chr10:24663604 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3381G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663604 | |||||||
chr10:24663615 | G | C | 2 | a0002c0002t0001g0063 a0002c0002t0001g0286 |
2 | HG00408.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.268+3370C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663615 | |||||||
chr10:24663822 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3163G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663822 | |||||||
chr10:24664219 | C | T | 1 | a0002c0015t0001g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.268+2766G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664219 | |||||||
chr10:24664259 | A | G | 1 | a0003c0003t0001g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.268+2726T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664259 | |||||||
chr10:24664328 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+2657T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664328 | |||||||
chr10:24664419 | G | T | 1 | a0001c0001t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.268+2566C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664419 | |||||||
chr10:24664445 | C | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0047 |
2 | NA19003.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.268+2540G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664445 | |||||||
chr10:24664518 | T | C | 1 | a0003c0003t0001g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.268+2467A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664518 | |||||||
chr10:24664554 | C | CA | 7 | a0003c0006t0002g0348 a0006c0007t0006g0292 a0006c0007t0006g0293 others(4): Show |
7 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+2430dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664554 | |||||||
chr10:24664566 | AT | A | 5 | a0001c0001t0002g0343 a0004c0004t0001g0092 a0005c0005t0001g0138 others(2): Show |
5 | HG02109.hp1 HG02896.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+2418delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664566 | |||||||
chr10:24664567 | T | A | 166 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(163): Show |
166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.268+2418A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664567 | |||||||
chr10:24664570 | T | A | 16 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0215 others(13): Show |
16 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.268+2415A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664570 | |||||||
chr10:24664573 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.268+2412A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664573 | |||||||
chr10:24664609 | G | A | 287 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.268+2376C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664609 | |||||||
chr10:24664646 | T | A | 1 | a0002c0002t0001g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.268+2339A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664646 | |||||||
chr10:24664723 | C | CTTTT | 294 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.268+2261_268+2262i others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664723 | |||||||
chr10:24664758 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268+2227A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664758 | |||||||
chr10:24665164 | T | C | 1 | a0002c0002t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.268+1821A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665164 | |||||||
chr10:24665500 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.268+1485T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665500 | |||||||
chr10:24665690 | G | A | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.268+1295C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665690 | |||||||
chr10:24665726 | C | T | 1 | a0005c0005t0003g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.268+1259G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665726 | |||||||
chr10:24665984 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.268+1001T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665984 | |||||||
chr10:24666030 | T | G | 1 | a0003c0003t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.268+955A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666030 | |||||||
chr10:24666042 | T | G | 1 | a0002c0002t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.268+943A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666042 | |||||||
chr10:24666189 | C | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.268+796G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666189 | |||||||
chr10:24666277 | G | A | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.268+708C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666277 | |||||||
chr10:24666322 | G | A | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+663C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666322 | |||||||
chr10:24666325 | C | T | 169 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.268+660G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666325 | |||||||
chr10:24666343 | G | A | 1 | a0003c0003t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.268+642C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666343 | |||||||
chr10:24666535 | T | C | 1 | a0015c0020t0001g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.268+450A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666535 | |||||||
chr10:24666544 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268+441A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666544 | |||||||
chr10:24666547 | G | A | 2 | a0001c0001t0002g0305 a0001c0001t0002g0309 |
2 | NA18959.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.268+438C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666547 | |||||||
chr10:24667095 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-86G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667095 | |||||||
chr10:24667112 | G | A | 3 | a0004c0004t0001g0039 a0004c0004t0001g0040 a0004c0004t0001g0098 |
3 | HG02559.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.244-103C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667112 | |||||||
chr10:24667188 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.244-179G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667188 | |||||||
chr10:24667352 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244-343T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667352 | |||||||
chr10:24667427 | CTT | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-420_244-419del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667427 | |||||||
chr10:24667484 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-475C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667484 | |||||||
chr10:24667585 | G | T | 1 | a0003c0003t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.244-576C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667585 | |||||||
chr10:24667713 | A | G | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.244-704T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667713 | |||||||
chr10:24668217 | G | A | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.244-1208C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668217 | |||||||
chr10:24668969 | T | C | 1 | a0002c0002t0001g0149 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.243+1249A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668969 | |||||||
chr10:24668977 | G | C | 17 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(14): Show |
17 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.243+1241C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668977 | |||||||
chr10:24668999 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0013g0255 |
2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.243+1219T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668999 | |||||||
chr10:24669105 | T | C | 2 | a0001c0001t0002g0341 a0001c0001t0002g0345 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.243+1113A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669105 | |||||||
chr10:24669230 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+988G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669230 | |||||||
chr10:24669389 | A | G | 6 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG00423.hp2 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+829T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669389 | |||||||
chr10:24669528 | T | C | 1 | a0019c0023t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243+690A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669528 | |||||||
chr10:24669587 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.243+631A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669587 | |||||||
chr10:24669779 | T | C | 4 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+439A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669779 | |||||||
chr10:24670145 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.243+73T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24670145 | |||||||
chr10:24670199 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+19G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24670199 | |||||||
chr10:24670536 | T | C | 1 | a0002c0002t0001g0284 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64-139A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24670536 | |||||||
chr10:24670807 | T | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-410A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24670807 | |||||||
chr10:24671140 | C | G | 1 | a0006c0007t0006g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.64-743G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671140 | |||||||
chr10:24671254 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
38 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.64-857G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671254 | |||||||
chr10:24671372 | T | C | 23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.64-975A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671372 | |||||||
chr10:24671723 | A | AT | 15 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(12): Show |
15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-1327dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671723 | |||||||
chr10:24671723 | AT | A | 20 | a0001c0001t0001g0186 a0001c0001t0001g0251 a0001c0001t0001g0252 others(17): Show |
20 | HG01081.hp1 HG01169.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-1327delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671723 | |||||||
chr10:24671775 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.64-1378A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671775 | |||||||
chr10:24671798 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1401G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671798 | |||||||
chr10:24671805 | C | T | 5 | a0001c0001t0001g0190 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
5 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-1408G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671805 | |||||||
chr10:24671884 | A | AT | 34 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0167 others(31): Show |
34 | HG00423.hp2 HG00621.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-1488dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671884 | |||||||
chr10:24671884 | AT | A | 124 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0171 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.64-1488delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671884 | |||||||
chr10:24671884 | ATT | A | 6 | a0002c0002t0001g0019 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02523.hp2 NA18747.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1489_64-1488del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671884 | |||||||
chr10:24671915 | A | C | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.64-1518T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671915 | |||||||
chr10:24671987 | C | T | 1 | a0002c0002t0001g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64-1590G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671987 | |||||||
chr10:24672055 | C | A | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1658G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672055 | |||||||
chr10:24672244 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.64-1847T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672244 | |||||||
chr10:24672359 | C | T | 2 | a0002c0002t0001g0089 a0018c0027t0001g0036 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.64-1962G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672359 | |||||||
chr10:24672371 | T | C | 4 | a0003c0006t0002g0347 a0003c0006t0002g0348 a0003c0006t0002g0349 others(1): Show |
4 | NA18957.hp1 NA18992.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1974A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672371 | |||||||
chr10:24672474 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-2077A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672474 | |||||||
chr10:24672522 | T | C | 1 | a0002c0002t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-2125A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672522 | |||||||
chr10:24672577 | T | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-2180A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672577 | |||||||
chr10:24672739 | A | G | 1 | a0001c0001t0008g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.64-2342T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672739 | |||||||
chr10:24672845 | G | A | 1 | a0002c0002t0001g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.64-2448C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672845 | |||||||
chr10:24673096 | T | G | 17 | a0002c0002t0001g0020 a0002c0002t0001g0107 a0002c0002t0001g0108 others(14): Show |
17 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-2699A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673096 | |||||||
chr10:24673319 | G | A | 4 | a0001c0001t0001g0163 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2922C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673319 | |||||||
chr10:24673477 | C | T | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-3080G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673477 | |||||||
chr10:24673495 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0247 |
2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.64-3098A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673495 | |||||||
chr10:24673519 | A | G | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-3122T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673519 | |||||||
chr10:24673589 | T | C | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3192A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673589 | |||||||
chr10:24673721 | G | T | 1 | a0002c0002t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64-3324C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673721 | |||||||
chr10:24673831 | C | T | 34 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0177 others(31): Show |
34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-3434G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673831 | |||||||
chr10:24674012 | C | A | 1 | a0002c0002t0001g0281 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64-3615G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674012 | |||||||
chr10:24674053 | A | T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-3656T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674053 | |||||||
chr10:24674057 | A | G | 1 | a0006c0007t0015g0289 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.64-3660T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674057 | |||||||
chr10:24674252 | A | G | 105 | a0002c0002t0001g0011 a0002c0002t0001g0019 a0002c0002t0001g0021 others(102): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.64-3855T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674252 | |||||||
chr10:24674296 | G | A | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3899C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674296 | |||||||
chr10:24674336 | C | T | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-3939G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674336 | |||||||
chr10:24674380 | A | G | 2 | a0005c0005t0001g0103 a0005c0005t0001g0104 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.64-3983T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674380 | |||||||
chr10:24674424 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4027G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674424 | |||||||
chr10:24674531 | A | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4134T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674531 | |||||||
chr10:24674615 | G | T | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-4218C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674615 | |||||||
chr10:24674701 | T | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4304A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674701 | |||||||
chr10:24674714 | T | TAC | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4319_64-4318dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674714 | |||||||
chr10:24674724 | C | T | 2 | a0001c0001t0002g0336 a0001c0001t0002g0337 |
2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.64-4327G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674724 | |||||||
chr10:24674907 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64-4510A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674907 | |||||||
chr10:24674979 | C | T | 149 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-4582G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674979 | |||||||
chr10:24675123 | T | G | 3 | a0001c0001t0002g0335 a0001c0001t0002g0341 a0001c0001t0002g0345 |
3 | HG03490.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.64-4726A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675123 | |||||||
chr10:24675124 | G | T | 3 | a0001c0001t0002g0335 a0001c0001t0002g0341 a0001c0001t0002g0345 |
3 | HG03490.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.64-4727C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675124 | |||||||
chr10:24675139 | A | G | 287 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.64-4742T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675139 | |||||||
chr10:24675147 | C | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4750G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675147 | |||||||
chr10:24675148 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4751T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675148 | |||||||
chr10:24675456 | T | G | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-5059A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675456 | |||||||
chr10:24675524 | T | C | 1 | a0003c0003t0001g0266 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.64-5127A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675524 | |||||||
chr10:24675542 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-5145G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675542 | |||||||
chr10:24675637 | A | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-5240T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675637 | |||||||
chr10:24675715 | T | G | 120 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
120 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.64-5318A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675715 | |||||||
chr10:24676108 | G | A | 13 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(10): Show |
13 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-5711C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676108 | |||||||
chr10:24676150 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.64-5753C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676150 | |||||||
chr10:24676246 | C | A | 3 | a0001c0001t0002g0301 a0001c0001t0002g0339 a0001c0001t0002g0340 |
3 | HG01169.hp1 HG01934.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.64-5849G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676246 | |||||||
chr10:24676281 | C | G | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.64-5884G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676281 | |||||||
chr10:24676445 | A | G | 1 | a0003c0006t0002g0347 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.64-6048T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676445 | |||||||
chr10:24676481 | C | A | 1 | a0004c0004t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-6084G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676481 | |||||||
chr10:24676538 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6141C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676538 | |||||||
chr10:24676792 | G | A | 2 | a0001c0001t0002g0317 a0001c0001t0002g0326 |
2 | HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.64-6395C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676792 | |||||||
chr10:24676892 | T | C | 78 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0182 others(75): Show |
78 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.64-6495A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676892 | |||||||
chr10:24677107 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-6710G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677107 | |||||||
chr10:24677265 | T | C | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.64-6868A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677265 | |||||||
chr10:24677384 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64-6987A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677384 | |||||||
chr10:24677584 | A | G | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-7187T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677584 | |||||||
chr10:24677658 | C | T | 1 | a0002c0015t0001g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.64-7261G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677658 | |||||||
chr10:24677876 | C | A | 1 | a0003c0003t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.64-7479G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677876 | |||||||
chr10:24678059 | C | T | 2 | a0001c0001t0002g0315 a0001c0001t0002g0344 |
2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.64-7662G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678059 | |||||||
chr10:24678163 | C | T | 168 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.64-7766G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678163 | |||||||
chr10:24678247 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-7850C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678247 | |||||||
chr10:24678297 | G | A | 166 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.64-7900C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678297 | |||||||
chr10:24678360 | C | T | 2 | a0002c0002t0001g0108 a0002c0002t0001g0112 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.64-7963G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678360 | |||||||
chr10:24678964 | T | A | 1 | a0003c0003t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64-8567A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678964 | |||||||
chr10:24679131 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8734C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679131 | |||||||
chr10:24679267 | C | T | 13 | a0002c0002t0001g0071 a0002c0002t0001g0086 a0004c0004t0001g0031 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-8870G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679267 | |||||||
chr10:24679357 | C | A | 2 | a0002c0002t0001g0148 a0002c0002t0001g0149 |
2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.64-8960G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679357 | |||||||
chr10:24679642 | A | AT | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9246dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679642 | |||||||
chr10:24679681 | G | T | 15 | a0002c0002t0001g0035 a0002c0002t0001g0042 a0002c0002t0001g0043 others(12): Show |
15 | HG00609.hp2 HG02083.hp1 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-9284C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679681 | |||||||
chr10:24680032 | A | T | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9635T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680032 | |||||||
chr10:24680086 | C | T | 170 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-9689G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680086 | |||||||
chr10:24680199 | T | C | 1 | a0003c0003t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-9802A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680199 | |||||||
chr10:24680242 | T | TAG | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9846_64-9845ins others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680242 | |||||||
chr10:24680357 | T | C | 1 | a0001c0014t0004g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-9960A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680357 | |||||||
chr10:24680829 | T | A | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.64-10432A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680829 | |||||||
chr10:24680837 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-10440G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680837 | |||||||
chr10:24680864 | G | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-10467C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680864 | |||||||
chr10:24680975 | G | T | 1 | a0011c0011t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-10578C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680975 | |||||||
chr10:24681272 | G | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-10875C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681272 | |||||||
chr10:24681279 | T | C | 1 | a0002c0002t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.64-10882A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681279 | |||||||
chr10:24681522 | T | C | 1 | a0001c0001t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-11125A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681522 | |||||||
chr10:24681597 | G | C | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-11200C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681597 | |||||||
chr10:24681640 | C | CT | 9 | a0001c0001t0003g0218 a0001c0014t0004g0287 a0005c0005t0004g0288 others(6): Show |
9 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-11244dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681640 | |||||||
chr10:24681802 | G | A | 1 | a0003c0003t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-11405C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681802 | |||||||
chr10:24681872 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-11475A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681872 | |||||||
chr10:24681887 | T | C | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-11490A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681887 | |||||||
chr10:24682067 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-11670C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682067 | |||||||
chr10:24682166 | C | T | 1 | a0006c0007t0006g0293 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-11769G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682166 | |||||||
chr10:24682292 | G | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-11895C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682292 | |||||||
chr10:24682669 | A | T | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12272T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682669 | |||||||
chr10:24682698 | T | C | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12301A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682698 | |||||||
chr10:24682862 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64-12465C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682862 | |||||||
chr10:24683095 | C | CA | 6 | a0001c0001t0001g0172 a0001c0001t0001g0186 a0001c0001t0002g0312 others(3): Show |
6 | HG00733.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12699dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683095 | |||||||
chr10:24683095 | CAAAAA | C | 65 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-12703_64-12699d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683095 | |||||||
chr10:24683457 | T | C | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.64-13060A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683457 | |||||||
chr10:24683620 | T | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-13223A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683620 | |||||||
chr10:24683657 | T | C | 1 | a0001c0001t0002g0326 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.64-13260A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683657 | |||||||
chr10:24683743 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-13346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683743 | |||||||
chr10:24683795 | C | T | 1 | a0001c0001t0002g0330 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-13398G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683795 | |||||||
chr10:24683799 | T | A | 1 | a0011c0011t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-13402A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683799 | |||||||
chr10:24684243 | T | C | 285 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(282): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.64-13846A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684243 | |||||||
chr10:24684302 | C | A | 1 | a0011c0011t0001g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-13905G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684302 | |||||||
chr10:24684416 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64-14019G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684416 | |||||||
chr10:24684498 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-14101A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684498 | |||||||
chr10:24684586 | G | C | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-14189C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684586 | |||||||
chr10:24684604 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0246 |
2 | HG00323.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.64-14207G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684604 | |||||||
chr10:24684799 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.64-14402G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684799 | |||||||
chr10:24684840 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-14443G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684840 | |||||||
chr10:24685281 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-14884C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685281 | |||||||
chr10:24685342 | T | C | 1 | a0002c0002t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.64-14945A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685342 | |||||||
chr10:24685471 | C | A | 1 | a0002c0002t0001g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-15074G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685471 | |||||||
chr10:24685487 | T | C | 1 | a0003c0003t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.64-15090A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685487 | |||||||
chr10:24685608 | G | A | 3 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0112 |
3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64-15211C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685608 | |||||||
chr10:24685650 | C | T | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-15253G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685650 | |||||||
chr10:24685704 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-15307G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685704 | |||||||
chr10:24685886 | A | G | 5 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0002g0334 others(2): Show |
5 | HG01099.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-15489T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685886 | |||||||
chr10:24686013 | C | T | 1 | a0003c0003t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-15616G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686013 | |||||||
chr10:24686096 | G | T | 8 | a0001c0014t0004g0287 a0005c0005t0004g0288 a0006c0007t0006g0292 others(5): Show |
8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-15699C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686096 | |||||||
chr10:24686153 | G | A | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-15756C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686153 | |||||||
chr10:24686223 | G | A | 163 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.64-15826C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686223 | |||||||
chr10:24686531 | C | G | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.64-16134G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686531 | |||||||
chr10:24686688 | G | A | 61 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(58): Show |
61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.64-16291C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686688 | |||||||
chr10:24686718 | C | T | 1 | a0002c0002t0001g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.64-16321G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686718 | |||||||
chr10:24687127 | G | GATCGC | 292 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.64-16731_64-16730i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687127 | |||||||
chr10:24687128 | G | T | 292 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.64-16731C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687128 | |||||||
chr10:24687371 | C | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-16974G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687371 | |||||||
chr10:24687371 | C | T | 1 | a0003c0003t0001g0200 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.64-16974G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687371 | |||||||
chr10:24687735 | G | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-17338C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687735 | |||||||
chr10:24687744 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02965.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.64-17347A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687744 | |||||||
chr10:24687923 | A | C | 1 | a0001c0001t0004g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64-17526T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687923 | |||||||
chr10:24687934 | T | C | 3 | a0003c0003t0001g0209 a0003c0003t0001g0210 a0003c0003t0001g0232 |
3 | NA18947.hp1 NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.64-17537A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687934 | |||||||
chr10:24688030 | G | C | 1 | a0001c0001t0002g0322 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.64-17633C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688030 | |||||||
chr10:24688117 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-17720C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688117 | |||||||
chr10:24688221 | T | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-17824A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688221 | |||||||
chr10:24688260 | G | A | 11 | a0001c0001t0001g0270 a0002c0002t0001g0064 a0002c0002t0001g0065 others(8): Show |
11 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-17863C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688260 | |||||||
chr10:24688275 | C | T | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-17878G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688275 | |||||||
chr10:24688368 | G | A | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-17971C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688368 | |||||||
chr10:24688500 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64-18103G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688500 | |||||||
chr10:24688543 | G | C | 1 | a0003c0003t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-18146C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688543 | |||||||
chr10:24688703 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-18306C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688703 | |||||||
chr10:24688855 | C | G | 168 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.64-18458G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688855 | |||||||
chr10:24688991 | G | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-18594C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688991 | |||||||
chr10:24689488 | C | A | 149 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-19091G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689488 | |||||||
chr10:24689697 | C | T | 1 | a0018c0027t0001g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-19300G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689697 | |||||||
chr10:24689758 | C | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-19361G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689758 | |||||||
chr10:24689841 | TATATGTA others(27): Show |
T | 2 | a0002c0002t0001g0071 a0015c0020t0001g0113 |
2 | HG01123.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.64-19478_64-19445d others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689841 | |||||||
chr10:24689843 | TATGTATA others(25): Show |
T | 137 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.64-19478_64-19447d others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689843 | |||||||
chr10:24689889 | T | C | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-19492A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689889 | |||||||
chr10:24689894 | ATGTGTAT others(33): Show |
A | 10 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-19537_64-19498d others(42): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689894 | |||||||
chr10:24689898 | G | A | 16 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(13): Show |
16 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-19501C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689898 | |||||||
chr10:24689902 | A | G | 16 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(13): Show |
16 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-19505T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689902 | |||||||
chr10:24689904 | ATACATGT others(23): Show |
A | 16 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(13): Show |
16 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-19537_64-19508d others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689904 | |||||||
chr10:24689933 | T | A | 5 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0105 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-19536A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689933 | |||||||
chr10:24689942 | G | A | 261 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.64-19545C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689942 | |||||||
chr10:24689944 | A | G | 261 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.64-19547T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689944 | |||||||
chr10:24689946 | A | G | 2 | a0001c0001t0001g0230 a0011c0011t0001g0259 |
2 | HG02818.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64-19549T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689946 | |||||||
chr10:24689946 | ATG | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00733.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-19551_64-19550d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689946 | |||||||
chr10:24689946 | ATGTG | A | 22 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(19): Show |
22 | HG02129.hp2 HG02145.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-19553_64-19550d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689946 | |||||||
chr10:24689948 | G | A | 263 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.64-19551C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689948 | |||||||
chr10:24689950 | G | A | 2 | a0001c0001t0001g0230 a0011c0011t0001g0259 |
2 | HG02818.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64-19553C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689950 | |||||||
chr10:24689964 | G | A | 176 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.64-19567C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689964 | |||||||
chr10:24690252 | T | C | 2 | a0002c0002t0001g0151 a0002c0002t0001g0152 |
2 | NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.64-19855A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690252 | |||||||
chr10:24690421 | T | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.64-20024A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690421 | |||||||
chr10:24690604 | A | G | 292 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(289): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.64-20207T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690604 | |||||||
chr10:24690609 | A | T | 2 | a0002c0002t0001g0131 a0002c0002t0001g0132 |
2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.64-20212T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690609 | |||||||
chr10:24690705 | G | A | 1 | a0003c0006t0002g0349 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.64-20308C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690705 | |||||||
chr10:24690827 | C | CA | 9 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(6): Show |
9 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-20431dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690827 | |||||||
chr10:24690827 | CA | C | 145 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.64-20431delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690827 | |||||||
chr10:24690835 | A | T | 1 | a0003c0003t0001g0248 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.64-20438T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690835 | |||||||
chr10:24690837 | A | AT | 6 | a0001c0001t0002g0304 a0001c0001t0002g0305 a0001c0001t0002g0307 others(3): Show |
6 | HG01168.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-20441_64-20440i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690837 | |||||||
chr10:24690837 | A | T | 19 | a0001c0001t0001g0161 a0001c0001t0001g0265 a0001c0001t0001g0271 others(16): Show |
19 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-20440T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690837 | |||||||
chr10:24690838 | AT | A | 5 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(2): Show |
5 | NA18957.hp2 NA18978.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-20442delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690838 | |||||||
chr10:24690839 | T | A | 15 | a0001c0001t0001g0163 a0001c0001t0001g0182 a0001c0001t0001g0183 others(12): Show |
15 | HG00639.hp2 HG01257.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-20442A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690839 | |||||||
chr10:24690841 | T | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-20444A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690841 | |||||||
chr10:24690855 | C | T | 2 | a0001c0001t0003g0155 a0013c0026t0003g0157 |
2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-20458G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690855 | |||||||
chr10:24690859 | T | C | 1 | a0002c0002t0001g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-20462A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690859 | |||||||
chr10:24691081 | C | A | 3 | a0001c0001t0002g0336 a0001c0001t0002g0337 a0014c0022t0002g0338 |
3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.64-20684G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691081 | |||||||
chr10:24691116 | G | C | 1 | a0002c0002t0001g0282 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.64-20719C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691116 | |||||||
chr10:24691154 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-20757A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691154 | |||||||
chr10:24691235 | C | T | 1 | a0001c0001t0002g0312 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.64-20838G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691235 | |||||||
chr10:24691335 | A | G | 3 | a0003c0003t0001g0200 a0003c0003t0001g0201 a0003c0003t0001g0202 |
3 | HG01123.hp1 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.64-20938T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691335 | |||||||
chr10:24691355 | T | C | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-20958A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691355 | |||||||
chr10:24691472 | TA | T | 7 | a0002c0002t0001g0119 a0002c0002t0001g0120 a0002c0002t0001g0121 others(4): Show |
7 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-21076delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691472 | |||||||
chr10:24691563 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-21166C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691563 | |||||||
chr10:24691655 | T | G | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(112): Show |
115 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.64-21258A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691655 | |||||||
chr10:24691739 | TAAATGTT others(11): Show |
T | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-21360_64-21343d others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691739 | |||||||
chr10:24692249 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.64-21852G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692249 | |||||||
chr10:24692279 | T | C | 1 | a0003c0003t0001g0181 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.64-21882A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692279 | |||||||
chr10:24692314 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-21917C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692314 | |||||||
chr10:24692491 | A | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-22094T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692491 | |||||||
chr10:24692544 | T | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-22147A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692544 | |||||||
chr10:24692548 | T | C | 4 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-22151A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692548 | |||||||
chr10:24692554 | A | G | 1 | a0005c0005t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-22157T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692554 | |||||||
chr10:24692843 | AT | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
5 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-22447delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692843 | |||||||
chr10:24692845 | A | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-22448T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692845 | |||||||
chr10:24692854 | A | T | 2 | a0001c0001t0002g0321 a0002c0030t0001g0090 |
2 | HG02071.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.64-22457T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692854 | |||||||
chr10:24693047 | T | C | 5 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0105 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-22650A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693047 | |||||||
chr10:24693125 | C | T | 1 | a0011c0011t0001g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-22728G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693125 | |||||||
chr10:24693126 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-22729C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693126 | |||||||
chr10:24693253 | C | G | 1 | a0002c0002t0001g0279 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64-22856G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693253 | |||||||
chr10:24693278 | C | T | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-22881G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693278 | |||||||
chr10:24693317 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-22920G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693317 | |||||||
chr10:24693325 | A | C | 269 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(266): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.64-22928T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693325 | |||||||
chr10:24693338 | C | CT | 10 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(7): Show |
10 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-22942dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693338 | |||||||
chr10:24693454 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23057T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693454 | |||||||
chr10:24693512 | G | A | 2 | a0002c0002t0007g0008 a0002c0002t0007g0009 |
2 | HG00280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.64-23115C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693512 | |||||||
chr10:24693596 | G | A | 51 | a0002c0002t0001g0019 a0002c0002t0001g0022 a0002c0002t0001g0027 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.64-23199C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693596 | |||||||
chr10:24693684 | C | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23287G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693684 | |||||||
chr10:24693763 | C | T | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-23366G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693763 | |||||||
chr10:24693891 | T | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-23494A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693891 | |||||||
chr10:24693929 | A | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23532T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693929 | |||||||
chr10:24694146 | A | G | 21 | a0001c0001t0001g0233 a0001c0001t0002g0303 a0001c0001t0002g0311 others(18): Show |
21 | HG00673.hp2 HG00733.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-23749T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694146 | |||||||
chr10:24694174 | C | G | 3 | a0007c0008t0001g0262 a0007c0008t0001g0263 a0007c0008t0004g0346 |
3 | NA18941.hp2 NA18974.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.64-23777G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694174 | |||||||
chr10:24694370 | G | A | 8 | a0001c0001t0001g0198 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG00621.hp1 HG02040.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-23973C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694370 | |||||||
chr10:24694461 | G | A | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-24064C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694461 | |||||||
chr10:24694612 | C | T | 1 | a0002c0002t0001g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-24215G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694612 | |||||||
chr10:24694649 | C | A | 1 | a0002c0002t0001g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-24252G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694649 | |||||||
chr10:24694790 | G | A | 1 | a0003c0003t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64-24393C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694790 | |||||||
chr10:24694901 | A | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-24504T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694901 | |||||||
chr10:24695044 | C | T | 1 | a0003c0003t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.64-24647G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695044 | |||||||
chr10:24695050 | CAAAAA | C | 13 | a0001c0001t0002g0001 a0001c0001t0002g0308 a0001c0001t0002g0309 others(10): Show |
14 | HG01081.hp1 HG01258.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-24658_64-24654d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAA | C | 14 | a0001c0001t0001g0233 a0001c0001t0002g0304 a0001c0001t0002g0305 others(11): Show |
14 | HG01109.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-24659_64-24654d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA | C | 10 | a0001c0001t0002g0303 a0001c0001t0002g0312 a0001c0001t0002g0319 others(7): Show |
10 | HG00673.hp2 HG01169.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-24660_64-24654d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0009c0010t0001g0268 |
3 | HG02109.hp1 NA19065.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.64-24663_64-24654d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(4): Show |
C | 14 | a0001c0001t0001g0175 a0001c0001t0001g0223 a0001c0001t0001g0224 others(11): Show |
14 | HG00621.hp1 HG01981.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-24664_64-24654d others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(5): Show |
C | 19 | a0001c0001t0001g0198 a0001c0001t0001g0219 a0001c0001t0001g0221 others(16): Show |
19 | HG00423.hp1 HG01069.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-24665_64-24654d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(6): Show |
C | 16 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0215 others(13): Show |
16 | HG00408.hp2 HG01952.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-24666_64-24654d others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(7): Show |
C | 1 | a0003c0003t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.64-24667_64-24654d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(8): Show |
C | 7 | a0001c0001t0001g0245 a0006c0007t0006g0293 a0006c0007t0015g0289 others(4): Show |
7 | HG02818.hp2 HG03486.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-24668_64-24654d others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0001g0172 a0001c0014t0004g0287 a0005c0005t0004g0288 others(1): Show |
4 | HG01891.hp2 HG02523.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-24669_64-24654d others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(10): Show |
C | 4 | a0001c0001t0002g0311 a0001c0001t0004g0298 a0001c0001t0004g0299 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-24670_64-24654d others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0002g0336 a0001c0001t0002g0337 |
2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.64-24672_64-24654d others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0002g0301 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.64-24673_64-24654d others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(14): Show |
C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-24674_64-24654d others(23): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(16): Show |
C | 1 | a0003c0003t0001g0210 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.64-24676_64-24654d others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(17): Show |
C | 20 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0004g0297 others(17): Show |
20 | HG00609.hp1 HG01123.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-24677_64-24654d others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(18): Show |
C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
36 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.64-24678_64-24654d others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(22): Show |
C | 3 | a0002c0002t0001g0082 a0002c0002t0001g0125 a0002c0002t0001g0153 |
3 | HG00099.hp2 HG01099.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.64-24682_64-24654d others(31): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(23): Show |
C | 157 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(154): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.64-24683_64-24654d others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695050 | CAAAAAAA others(24): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-24684_64-24654d others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | |||||||
chr10:24695098 | G | A | 2 | a0001c0001t0001g0275 a0002c0002t0001g0257 |
2 | HG00423.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.64-24701C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695098 | |||||||
chr10:24695335 | G | A | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-24938C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695335 | |||||||
chr10:24695398 | G | A | 6 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG00423.hp2 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-25001C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695398 | |||||||
chr10:24695405 | C | A | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-25008G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695405 | |||||||
chr10:24695477 | G | A | 1 | a0001c0001t0002g0319 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-25080C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695477 | |||||||
chr10:24695564 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.64-25167C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695564 | |||||||
chr10:24695566 | C | CA | 86 | a0001c0001t0001g0145 a0001c0001t0002g0321 a0001c0001t0002g0339 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.64-25170dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695566 | |||||||
chr10:24695566 | C | CAAA | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-25172_64-25170d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695566 | |||||||
chr10:24695585 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02280.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.64-25188A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695585 | |||||||
chr10:24695962 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-25565A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695962 | |||||||
chr10:24696061 | T | A | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25664A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696061 | |||||||
chr10:24696063 | T | G | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25666A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696063 | |||||||
chr10:24696066 | C | G | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25669G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696066 | |||||||
chr10:24696068 | C | G | 273 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(270): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.64-25671G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696068 | |||||||
chr10:24696068 | C | T | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25671G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696068 | |||||||
chr10:24696069 | C | G | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25672G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696069 | |||||||
chr10:24696070 | A | T | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25673T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696070 | |||||||
chr10:24696071 | A | T | 1 | a0001c0001t0002g0339 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25674T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696071 | |||||||
chr10:24696237 | G | A | 10 | a0002c0002t0001g0011 a0002c0002t0001g0020 a0002c0002t0001g0114 others(7): Show |
10 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+25600C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696237 | |||||||
chr10:24696277 | T | C | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+25560A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696277 | |||||||
chr10:24696426 | G | C | 5 | a0002c0002t0001g0011 a0002c0002t0001g0114 a0002c0002t0001g0115 others(2): Show |
5 | HG02027.hp2 HG02074.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+25411C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696426 | |||||||
chr10:24696472 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+25365T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696472 | |||||||
chr10:24696511 | C | T | 1 | a0001c0001t0008g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.63+25326G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696511 | |||||||
chr10:24696764 | G | A | 102 | a0001c0001t0001g0145 a0002c0002t0001g0019 a0002c0002t0001g0021 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.63+25073C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696764 | |||||||
chr10:24696861 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+24976G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696861 | |||||||
chr10:24696974 | T | A | 3 | a0008c0009t0005g0003 a0008c0009t0005g0004 a0008c0009t0005g0005 |
3 | NA18995.hp2 NA19004.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.63+24863A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696974 | |||||||
chr10:24697210 | C | T | 12 | a0001c0001t0002g0001 a0001c0001t0002g0304 a0001c0001t0002g0305 others(9): Show |
13 | HG01168.hp2 HG01928.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+24627G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697210 | |||||||
chr10:24697217 | A | G | 281 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.63+24620T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697217 | |||||||
chr10:24697455 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+24382G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697455 | |||||||
chr10:24697457 | T | C | 281 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.63+24380A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697457 | |||||||
chr10:24697673 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+24164T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697673 | |||||||
chr10:24697768 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+24069C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697768 | |||||||
chr10:24697833 | C | T | 1 | a0002c0002t0001g0035 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.63+24004G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697833 | |||||||
chr10:24697834 | T | C | 1 | a0002c0002t0001g0035 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.63+24003A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697834 | |||||||
chr10:24697839 | G | A | 5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(2): Show |
5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+23998C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697839 | |||||||
chr10:24697949 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.63+23888A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697949 | |||||||
chr10:24698001 | T | C | 4 | a0002c0002t0001g0011 a0002c0002t0001g0114 a0002c0002t0001g0115 others(1): Show |
4 | HG02074.hp1 NA18995.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+23836A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698001 | |||||||
chr10:24698213 | C | T | 3 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0112 |
3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.63+23624G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698213 | |||||||
chr10:24698483 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+23354T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698483 | |||||||
chr10:24698738 | T | C | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+23099A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698738 | |||||||
chr10:24698783 | A | G | 3 | a0002c0002t0001g0035 a0002c0002t0001g0097 a0002c0002t0001g0146 |
3 | NA18988.hp2 NA18992.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.63+23054T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698783 | |||||||
chr10:24699336 | A | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | NA18970.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.63+22501T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699336 | |||||||
chr10:24699339 | T | A | 2 | a0001c0001t0002g0301 a0007c0008t0001g0263 |
2 | NA18974.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.63+22498A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699339 | |||||||
chr10:24699388 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+22449C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699388 | |||||||
chr10:24699580 | C | A | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+22257G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699580 | |||||||
chr10:24699802 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.63+22035C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699802 | |||||||
chr10:24700203 | G | A | 6 | a0001c0001t0005g0002 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+21634C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700203 | |||||||
chr10:24700516 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+21321C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700516 | |||||||
chr10:24700522 | G | A | 5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(2): Show |
5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21315C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700522 | |||||||
chr10:24700589 | G | A | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+21248C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700589 | |||||||
chr10:24700742 | A | C | 2 | a0003c0003t0001g0199 a0003c0003t0001g0249 |
2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.63+21095T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700742 | |||||||
chr10:24700756 | T | A | 5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(2): Show |
5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21081A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700756 | |||||||
chr10:24700954 | T | A | 1 | a0002c0002t0001g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.63+20883A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700954 | |||||||
chr10:24701183 | A | T | 4 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(1): Show |
4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+20654T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701183 | |||||||
chr10:24701240 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.63+20597C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701240 | |||||||
chr10:24701413 | T | C | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+20424A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701413 | |||||||
chr10:24701505 | G | A | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+20332C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701505 | |||||||
chr10:24701610 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+20227A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701610 | |||||||
chr10:24701840 | T | C | 1 | a0002c0002t0001g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.63+19997A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701840 | |||||||
chr10:24702126 | TC | T | 7 | a0002c0002t0001g0011 a0002c0002t0001g0114 a0002c0002t0001g0115 others(4): Show |
7 | HG02027.hp2 HG02074.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+19710delG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702126 | |||||||
chr10:24702127 | C | CT | 24 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(21): Show |
24 | HG00733.hp2 HG01496.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+19709dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | |||||||
chr10:24702127 | C | CTT | 218 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.63+19708_63+19709d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | |||||||
chr10:24702127 | C | CTTT | 20 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0192 others(17): Show |
20 | HG00438.hp1 HG00621.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+19707_63+19709d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | |||||||
chr10:24702127 | C | T | 1 | a0002c0002t0014g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.63+19710G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | |||||||
chr10:24702127 | CT | C | 11 | a0001c0001t0001g0172 a0001c0001t0002g0315 a0001c0001t0004g0297 others(8): Show |
11 | HG01891.hp2 HG02129.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+19709delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | |||||||
chr10:24702127 | CTTTTT | C | 13 | a0002c0002t0001g0071 a0002c0002t0001g0086 a0002c0002t0001g0137 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+19705_63+19709d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | |||||||
chr10:24702223 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+19614G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702223 | |||||||
chr10:24702278 | C | T | 3 | a0002c0002t0007g0008 a0002c0002t0007g0009 a0002c0002t0007g0010 |
3 | HG00280.hp1 HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.63+19559G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702278 | |||||||
chr10:24702297 | A | AT | 7 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(4): Show |
7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+19539dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702297 | |||||||
chr10:24702477 | T | C | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(112): Show |
115 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+19360A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702477 | |||||||
chr10:24702583 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.63+19254C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702583 | |||||||
chr10:24702955 | A | C | 1 | a0001c0001t0005g0006 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.63+18882T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702955 | |||||||
chr10:24702980 | T | TAC | 5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(2): Show |
5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+18855_63+18856d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702980 | |||||||
chr10:24703091 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63+18746T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703091 | |||||||
chr10:24703408 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+18429C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703408 | |||||||
chr10:24703960 | T | C | 5 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(2): Show |
5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17877A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703960 | |||||||
chr10:24703994 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+17843C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703994 | |||||||
chr10:24704069 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+17768G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704069 | |||||||
chr10:24704193 | G | C | 5 | a0002c0002t0001g0019 a0002c0002t0001g0073 a0002c0002t0001g0074 others(2): Show |
5 | NA18957.hp2 NA18978.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17644C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704193 | |||||||
chr10:24704217 | T | A | 1 | a0003c0003t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.63+17620A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704217 | |||||||
chr10:24704289 | C | CT | 29 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(26): Show |
29 | HG00621.hp2 HG00735.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.63+17547dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704289 | |||||||
chr10:24704289 | CT | C | 9 | a0001c0001t0001g0197 a0001c0001t0002g0303 a0001c0001t0002g0322 others(6): Show |
9 | HG01517.hp1 HG02109.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+17547delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704289 | |||||||
chr10:24704294 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.63+17543A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704294 | |||||||
chr10:24704416 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+17421C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704416 | |||||||
chr10:24704465 | A | AT | 331 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(328): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.63+17371dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704465 | |||||||
chr10:24704683 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.63+17154C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704683 | |||||||
chr10:24704796 | G | T | 1 | a0002c0002t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+17041C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704796 | |||||||
chr10:24704993 | G | C | 1 | a0005c0005t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+16844C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704993 | |||||||
chr10:24705226 | G | A | 6 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0002t0001g0080 others(3): Show |
6 | HG00741.hp1 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+16611C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705226 | |||||||
chr10:24705380 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63+16457C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705380 | |||||||
chr10:24705651 | C | T | 1 | a0001c0001t0003g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+16186G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705651 | |||||||
chr10:24705862 | CAAT | C | 5 | a0001c0001t0016g0351 a0003c0006t0002g0347 a0003c0006t0002g0348 others(2): Show |
5 | NA18957.hp1 NA18989.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+15972_63+15974d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705862 | |||||||
chr10:24705998 | A | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+15839T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705998 | |||||||
chr10:24706220 | T | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+15617A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706220 | |||||||
chr10:24706309 | T | A | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.63+15528A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706309 | |||||||
chr10:24706423 | T | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.63+15414A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706423 | |||||||
chr10:24706512 | C | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+15325G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706512 | |||||||
chr10:24706655 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+15182C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706655 | |||||||
chr10:24706706 | C | G | 1 | a0003c0003t0001g0174 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.63+15131G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706706 | |||||||
chr10:24706728 | T | C | 1 | a0005c0005t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+15109A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706728 | |||||||
chr10:24706769 | C | T | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+15068G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706769 | |||||||
chr10:24706834 | T | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15003A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706834 | |||||||
chr10:24707044 | G | A | 2 | a0002c0002t0001g0126 a0015c0020t0001g0113 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.63+14793C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707044 | |||||||
chr10:24707286 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+14551G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707286 | |||||||
chr10:24707291 | A | C | 1 | a0001c0001t0002g0305 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.63+14546T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707291 | |||||||
chr10:24707504 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+14333G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707504 | |||||||
chr10:24707596 | T | C | 3 | a0001c0001t0002g0336 a0001c0001t0002g0337 a0014c0022t0002g0338 |
3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.63+14241A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707596 | |||||||
chr10:24707781 | C | T | 147 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.63+14056G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707781 | |||||||
chr10:24707902 | A | G | 280 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.63+13935T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707902 | |||||||
chr10:24707991 | C | CA | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+13845dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707991 | |||||||
chr10:24708008 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+13829C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708008 | |||||||
chr10:24708159 | G | A | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+13678C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708159 | |||||||
chr10:24708504 | T | C | 286 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+13333A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708504 | |||||||
chr10:24708513 | G | A | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+13324C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708513 | |||||||
chr10:24708701 | G | T | 1 | a0002c0002t0014g0106 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.63+13136C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708701 | |||||||
chr10:24708771 | T | C | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.63+13066A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708771 | |||||||
chr10:24708854 | G | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12983C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708854 | |||||||
chr10:24708938 | T | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+12899A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708938 | |||||||
chr10:24709012 | T | C | 1 | a0006c0007t0006g0293 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+12825A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709012 | |||||||
chr10:24709032 | A | G | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
38 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.63+12805T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709032 | |||||||
chr10:24709104 | C | T | 3 | a0004c0004t0001g0031 a0004c0004t0001g0032 a0021c0024t0011g0033 |
3 | HG02647.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.63+12733G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709104 | |||||||
chr10:24709721 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+12116T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709721 | |||||||
chr10:24709738 | TA | T | 27 | a0001c0001t0001g0193 a0001c0001t0002g0304 a0002c0002t0001g0018 others(24): Show |
27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.63+12098delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709738 | |||||||
chr10:24709770 | CACAACA | C | 61 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(58): Show |
61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.63+12061_63+12066d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709770 | |||||||
chr10:24709871 | C | A | 166 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.63+11966G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709871 | |||||||
chr10:24710102 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63+11735G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710102 | |||||||
chr10:24710182 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+11655G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710182 | |||||||
chr10:24710532 | C | T | 149 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.63+11305G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710532 | |||||||
chr10:24710597 | C | CT | 293 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.63+11239_63+11240i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710597 | |||||||
chr10:24710664 | G | A | 40 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0020 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.63+11173C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710664 | |||||||
chr10:24710739 | T | G | 269 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(266): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.63+11098A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710739 | |||||||
chr10:24710824 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.63+11013C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710824 | |||||||
chr10:24710888 | G | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10949C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710888 | |||||||
chr10:24710993 | C | T | 1 | a0002c0002t0001g0146 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.63+10844G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710993 | |||||||
chr10:24711034 | C | G | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+10803G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711034 | |||||||
chr10:24711050 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+10787G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711050 | |||||||
chr10:24711093 | CA | C | 202 | a0001c0001t0001g0172 a0001c0001t0001g0182 a0001c0001t0001g0183 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.63+10743delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711093 | |||||||
chr10:24711113 | A | AGG | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10723_63+10724i others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711113 | |||||||
chr10:24711114 | A | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10723T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711114 | |||||||
chr10:24711116 | G | A | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10721C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711116 | |||||||
chr10:24711168 | AAGAAAGA others(1): Show |
A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10661_63+10668d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711168 | |||||||
chr10:24711231 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+10606T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711231 | |||||||
chr10:24711269 | T | C | 5 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0105 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+10568A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711269 | |||||||
chr10:24711411 | T | C | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10426A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711411 | |||||||
chr10:24711460 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63+10377C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711460 | |||||||
chr10:24711840 | C | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
6 | NA18945.hp2 NA18961.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9997G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711840 | |||||||
chr10:24711910 | G | A | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.63+9927C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711910 | |||||||
chr10:24711999 | C | G | 3 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0283 |
3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.63+9838G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711999 | |||||||
chr10:24712103 | A | T | 2 | a0002c0002t0001g0027 a0016c0016t0003g0028 |
2 | HG01433.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.63+9734T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712103 | |||||||
chr10:24712151 | A | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9686T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712151 | |||||||
chr10:24712153 | T | A | 1 | a0001c0001t0002g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+9684A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712153 | |||||||
chr10:24712218 | G | A | 148 | a0001c0001t0001g0145 a0002c0002t0001g0011 a0002c0002t0001g0018 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.63+9619C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712218 | |||||||
chr10:24712269 | G | T | 1 | a0002c0002t0001g0024 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.63+9568C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712269 | |||||||
chr10:24712295 | C | A | 1 | a0002c0002t0001g0154 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+9542G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712295 | |||||||
chr10:24712299 | G | A | 176 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.63+9538C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712299 | |||||||
chr10:24712492 | G | A | 1 | a0002c0002t0001g0102 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.63+9345C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712492 | |||||||
chr10:24712579 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+9258G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712579 | |||||||
chr10:24712980 | T | TA | 20 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(17): Show |
20 | HG01891.hp2 HG01981.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+8856dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712980 | |||||||
chr10:24713007 | C | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0247 |
2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.63+8830G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713007 | |||||||
chr10:24713169 | T | C | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+8668A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713169 | |||||||
chr10:24713199 | G | C | 1 | a0005c0005t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+8638C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713199 | |||||||
chr10:24713221 | A | G | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.63+8616T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713221 | |||||||
chr10:24713335 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0179 |
2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.63+8502C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713335 | |||||||
chr10:24713428 | T | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+8409A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713428 | |||||||
chr10:24713638 | CT | C | 6 | a0001c0001t0001g0246 a0001c0001t0002g0333 a0001c0001t0002g0334 others(3): Show |
6 | HG00323.hp1 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8198delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713638 | |||||||
chr10:24713797 | G | A | 1 | a0002c0002t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.63+8040C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713797 | |||||||
chr10:24713889 | T | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7948A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713889 | |||||||
chr10:24713942 | C | A | 1 | a0001c0001t0002g0335 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.63+7895G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713942 | |||||||
chr10:24714228 | C | G | 1 | a0003c0003t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.63+7609G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714228 | |||||||
chr10:24714431 | G | C | 2 | a0010c0012t0010g0016 a0010c0012t0010g0017 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+7406C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714431 | |||||||
chr10:24714604 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.63+7233C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714604 | |||||||
chr10:24714772 | C | T | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+7065G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714772 | |||||||
chr10:24714818 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+7019T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714818 | |||||||
chr10:24714862 | C | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6975G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714862 | |||||||
chr10:24714949 | G | A | 3 | a0001c0001t0002g0336 a0001c0001t0002g0337 a0014c0022t0002g0338 |
3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.63+6888C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714949 | |||||||
chr10:24714955 | G | A | 1 | a0001c0014t0004g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+6882C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714955 | |||||||
chr10:24714969 | T | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6868A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714969 | |||||||
chr10:24715007 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02280.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6830C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715007 | |||||||
chr10:24715029 | C | CA | 283 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.63+6807dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715029 | |||||||
chr10:24715029 | C | CAA | 10 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+6806_63+6807dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715029 | |||||||
chr10:24715088 | T | C | 1 | a0001c0001t0016g0351 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.63+6749A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715088 | |||||||
chr10:24715137 | C | G | 9 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6700G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715137 | |||||||
chr10:24715235 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02280.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6602T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715235 | |||||||
chr10:24715375 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0004g0297 a0001c0001t0004g0298 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6462C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715375 | |||||||
chr10:24715511 | T | C | 1 | a0003c0003t0001g0248 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.63+6326A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715511 | |||||||
chr10:24715512 | G | A | 139 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(136): Show |
139 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.63+6325C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715512 | |||||||
chr10:24715541 | A | T | 3 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 |
3 | HG00621.hp2 HG02165.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.63+6296T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715541 | |||||||
chr10:24715547 | T | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+6290A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715547 | |||||||
chr10:24715573 | T | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
4 | NA18970.hp1 NA18975.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6264A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715573 | |||||||
chr10:24715733 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6104G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715733 | |||||||
chr10:24715749 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+6088A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715749 | |||||||
chr10:24715767 | G | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6070C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715767 | |||||||
chr10:24715782 | T | C | 293 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.63+6055A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715782 | |||||||
chr10:24715958 | C | G | 10 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+5879G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715958 | |||||||
chr10:24716000 | C | T | 3 | a0001c0014t0004g0287 a0002c0002t0001g0023 a0005c0005t0004g0288 |
3 | HG03209.hp1 NA18906.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.63+5837G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716000 | |||||||
chr10:24716208 | G | A | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+5629C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716208 | |||||||
chr10:24716254 | C | A | 1 | a0002c0002t0001g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+5583G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716254 | |||||||
chr10:24716693 | T | C | 3 | a0001c0001t0002g0301 a0001c0001t0002g0339 a0001c0001t0002g0340 |
3 | HG01169.hp1 HG01934.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.63+5144A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716693 | |||||||
chr10:24716772 | A | G | 5 | a0005c0005t0001g0103 a0005c0005t0001g0104 a0005c0005t0001g0105 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+5065T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716772 | |||||||
chr10:24716980 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.63+4857A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716980 | |||||||
chr10:24717003 | C | T | 100 | a0002c0002t0001g0019 a0002c0002t0001g0021 a0002c0002t0001g0022 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.63+4834G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717003 | |||||||
chr10:24717035 | T | C | 286 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(283): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.63+4802A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717035 | |||||||
chr10:24717205 | A | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4632T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717205 | |||||||
chr10:24717221 | G | A | 1 | a0003c0003t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.63+4616C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717221 | |||||||
chr10:24717300 | T | C | 1 | a0003c0003t0001g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+4537A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717300 | |||||||
chr10:24717418 | T | A | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4419A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717418 | |||||||
chr10:24717573 | AG | A | 3 | a0002c0002t0001g0114 a0002c0002t0001g0115 a0002c0002t0001g0116 |
3 | NA18995.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.63+4263delC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717573 | |||||||
chr10:24717618 | A | G | 293 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.63+4219T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717618 | |||||||
chr10:24717772 | TCAGCTGG others(4): Show |
T | 2 | a0011c0011t0001g0259 a0011c0011t0001g0260 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.63+4054_63+4064del others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717772 | |||||||
chr10:24717858 | GT | G | 140 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(137): Show |
140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.63+3978delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717858 | |||||||
chr10:24717915 | A | AC | 3 | a0001c0001t0001g0163 a0001c0001t0002g0303 a0003c0003t0001g0248 |
3 | HG02027.hp1 NA18906.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.63+3921dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717915 | |||||||
chr10:24717952 | T | C | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+3885A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717952 | |||||||
chr10:24718015 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+3822C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718015 | |||||||
chr10:24718037 | T | C | 1 | a0001c0001t0004g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+3800A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718037 | |||||||
chr10:24718071 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0247 |
2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.63+3766A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718071 | |||||||
chr10:24718154 | GGAATGAC others(2): Show |
G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3674_63+3682del others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718154 | |||||||
chr10:24718166 | C | T | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3671G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718166 | |||||||
chr10:24718377 | T | C | 71 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0001g0198 others(68): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+3460A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718377 | |||||||
chr10:24718463 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+3374C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718463 | |||||||
chr10:24718483 | C | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3354G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718483 | |||||||
chr10:24718822 | T | A | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+3015A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718822 | |||||||
chr10:24718822 | T | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+3015A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718822 | |||||||
chr10:24718916 | T | C | 23 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+2921A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718916 | |||||||
chr10:24719094 | G | A | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.63+2743C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719094 | |||||||
chr10:24719098 | T | TAC | 48 | a0001c0001t0001g0175 a0001c0001t0002g0341 a0001c0001t0002g0342 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.63+2737_63+2738dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACAC | 13 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0171 others(10): Show |
13 | HG00597.hp1 HG00609.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+2735_63+2738dup others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACACAC | 86 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0161 others(83): Show |
86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.63+2733_63+2738dup others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACACACA others(1): Show |
27 | a0001c0001t0001g0170 a0001c0001t0001g0238 a0001c0001t0001g0239 others(24): Show |
27 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.63+2731_63+2738dup others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0265 others(3): Show |
6 | HG00642.hp1 HG01993.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2729_63+2738dup others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACACACA others(5): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02622.hp1 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2727_63+2738dup others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACACACA others(7): Show |
6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2725_63+2738dup others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0169 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+2723_63+2738dup others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719098 | TAC | T | 94 | a0001c0001t0016g0351 a0002c0002t0001g0019 a0002c0002t0001g0021 others(91): Show |
94 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.63+2737_63+2738del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | |||||||
chr10:24719129 | A | C | 1 | a0002c0030t0001g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.63+2708T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719129 | |||||||
chr10:24719133 | C | A | 1 | a0002c0015t0001g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+2704G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719133 | |||||||
chr10:24719214 | G | A | 4 | a0002c0002t0001g0021 a0002c0002t0001g0139 a0002c0002t0001g0140 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+2623C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719214 | |||||||
chr10:24719434 | C | T | 148 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0019 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.63+2403G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719434 | |||||||
chr10:24719805 | A | G | 1 | a0002c0002t0004g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+2032T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719805 | |||||||
chr10:24719983 | T | C | 269 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(266): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.63+1854A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719983 | |||||||
chr10:24719989 | T | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+1848A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719989 | |||||||
chr10:24720083 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.63+1754T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720083 | |||||||
chr10:24720212 | G | T | 1 | a0002c0002t0001g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+1625C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720212 | |||||||
chr10:24720244 | C | G | 1 | a0003c0003t0001g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.63+1593G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720244 | |||||||
chr10:24720254 | C | CA | 123 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.63+1582dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720254 | |||||||
chr10:24720254 | C | CAA | 158 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.63+1581_63+1582dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720254 | |||||||
chr10:24720254 | C | CAAA | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG00609.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+1580_63+1582dup others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720254 | |||||||
chr10:24720288 | C | A | 2 | a0002c0002t0001g0151 a0002c0002t0001g0152 |
2 | NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.63+1549G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720288 | |||||||
chr10:24720382 | T | G | 2 | a0009c0010t0001g0267 a0009c0010t0001g0268 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.63+1455A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720382 | |||||||
chr10:24720429 | A | T | 1 | a0002c0015t0001g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+1408T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720429 | |||||||
chr10:24720449 | G | A | 1 | a0003c0003t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.63+1388C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720449 | |||||||
chr10:24720569 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0001g0154 |
2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.63+1268C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720569 | |||||||
chr10:24720574 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG00423.hp2 HG00597.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1263C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720574 | |||||||
chr10:24720657 | C | T | 166 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.63+1180G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720657 | |||||||
chr10:24720770 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.63+1067G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720770 | |||||||
chr10:24720994 | G | GA | 141 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.63+842dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720994 | |||||||
chr10:24720997 | A | G | 1 | a0001c0001t0002g0301 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+840T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720997 | |||||||
chr10:24721606 | G | A | 1 | a0003c0003t0001g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+231C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24721606 | |||||||
chr10:24721729 | C | A | 5 | a0001c0001t0016g0351 a0003c0006t0002g0347 a0003c0006t0002g0348 others(2): Show |
5 | NA18957.hp1 NA18989.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+108G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24721729 | |||||||
chr10:24722388 | A | C | 1 | a0002c0002t0001g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-380-109T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722388 | |||||||
chr10:24722477 | C | T | 13 | a0001c0001t0004g0297 a0001c0001t0004g0298 a0001c0001t0004g0299 others(10): Show |
13 | HG01884.hp1 HG02129.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-380-198G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722477 | |||||||
chr10:24722586 | T | C | 1 | a0003c0003t0001g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-380-307A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722586 | |||||||
chr10:24722617 | G | C | 1 | a0003c0003t0001g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-380-338C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722617 | |||||||
chr10:24722758 | G | GCCGCCCC others(1): Show |
3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 |
3 | HG02965.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-380-487_-380-480d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722758 | |||||||
chr10:24722842 | G | A | 2 | a0002c0002t0001g0279 a0002c0002t0001g0280 |
2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.-380-563C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722842 | |||||||
chr10:24722846 | G | C | 3 | a0002c0002t0001g0281 a0002c0002t0001g0282 a0002c0002t0001g0283 |
3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-380-567C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722846 | |||||||
chr10:24722908 | G | A | 1 | a0002c0002t0001g0284 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-380-629C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722908 | |||||||
chr10:24723067 | G | C | 1 | a0005c0005t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-381+495C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723067 | |||||||
chr10:24723073 | C | G | 1 | a0003c0003t0001g0012 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-381+489G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723073 | |||||||
chr10:24723111 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-381+451G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723111 | |||||||
chr10:24723137 | G | A | 1 | a0002c0002t0001g0286 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-381+425C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723137 | |||||||
chr10:24723242 | C | G | 6 | a0006c0007t0006g0292 a0006c0007t0006g0293 a0006c0007t0006g0294 others(3): Show |
6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-381+320G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723242 | |||||||
chr10:24723272 | A | C | 1 | a0002c0002t0001g0011 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-381+290T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723272 | |||||||
chr10:24723454 | C | T | 2 | a0001c0014t0004g0287 a0005c0005t0004g0288 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-381+108G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723454 |