Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9826 |
| ensemblid | ENSG00000132694.19 |
| hgncid | 14580 |
| symbol | ARHGEF11 |
| name | Rho guanine nucleotide exchange factor 11 |
| refseq_nuc | NM_198236.3 |
| refseq_prot | NP_937879.1 |
| ensembl_nuc | ENST00000368194.8 |
| ensembl_prot | ENSP00000357177.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 156934840 |
| end | 157045742 |
| strand | - |
| ver | v1.2 |
| region | chr1:156934840-157045742 |
| region5000 | chr1:156929840-157050742 |
| regionname0 | ARHGEF11_chr1_156934840_157045742 |
| regionname5000 | ARHGEF11_chr1_156929840_157050742 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1562 | 150 | 23 | 39 | 62 | 6 | 20 | 49 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0002 | 0/0 | 1562 | 144 | 48 | 18 | 62 | 3 | 13 | 48 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0003 | 1/1 | 1562 | 59 | 12 | 10 | 22 | 5 | 8 | 17 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0004 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0005 | 0/0 | 1562 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0006 | 0/0 | 1562 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0007 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0008 | 0/0 | 1562 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0009 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| a0010 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | MSVRL others(1557): Show |
chr1 | 156929840 | 157050742 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4686 | 146 | 23 | 36 | 61 | 6 | 20 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0001c0005 | 0/0 | 4686 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0001c0011 | 0/0 | 4686 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0002c0002 | 0/0 | 4686 | 86 | 13 | 12 | 51 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0002c0004 | 0/0 | 4686 | 57 | 35 | 6 | 11 | 0 | 5 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0002c0008 | 0/0 | 4686 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0003c0003 | 1/1 | 4686 | 59 | 12 | 10 | 22 | 5 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0004c0006 | 0/0 | 4686 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0005c0007 | 0/0 | 4686 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0006c0009 | 0/0 | 4686 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0007c0014 | 0/0 | 4686 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0008c0013 | 0/0 | 4686 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0009c0012 | 0/0 | 4686 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 | ||
| a0010c0010 | 0/0 | 4686 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | ATGAG others(4681): Show |
chr1 | 156929840 | 157050742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7261 | 73 | 3 | 16 | 43 | 3 | 8 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0003 | 0/0 | 7261 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0004 | 0/0 | 7261 | 37 | 5 | 16 | 7 | 3 | 6 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0006 | 0/0 | 7261 | 7 | 5 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0007 | 0/0 | 7261 | 8 | 0 | 1 | 1 | 0 | 6 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0010 | 0/0 | 7261 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0015 | 0/0 | 7262 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0020 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0028 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0030 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0032 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0034 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0035 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0001c0001t0036 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0005t0001 | 0/0 | 7261 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0001c0011t0004 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0002 | 0/0 | 7261 | 67 | 11 | 12 | 34 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0011 | 0/0 | 7261 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0012 | 0/0 | 7262 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0016 | 0/0 | 7261 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0017 | 0/0 | 7261 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0023 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0024 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0002t0029 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0005 | 0/0 | 7261 | 26 | 12 | 2 | 9 | 0 | 3 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0008 | 0/0 | 7262 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0009 | 0/0 | 7261 | 6 | 0 | 4 | 0 | 0 | 2 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0013 | 0/0 | 7262 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0014 | 0/0 | 7262 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0018 | 0/0 | 7261 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0021 | 0/0 | 7263 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7258): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0022 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0025 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0026 | 0/0 | 7263 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7258): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0027 | 0/0 | 7261 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0004t0033 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0002c0008t0002 | 0/0 | 7261 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0003c0003t0003 | 0/0 | 7261 | 45 | 6 | 7 | 22 | 3 | 7 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0003c0003t0006 | 1/1 | 7261 | 10 | 3 | 2 | 0 | 2 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0003c0003t0019 | 0/0 | 7260 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7255): Show |
chr1 | 156929840 | 157050742 |
| a0003c0003t0031 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0004c0006t0005 | 0/0 | 7261 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0005c0007t0003 | 0/0 | 7261 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0006c0009t0003 | 0/0 | 7261 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0007c0014t0014 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7257): Show |
chr1 | 156929840 | 157050742 |
| a0008c0013t0007 | 0/0 | 7261 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0009c0012t0003 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| a0010c0010t0003 | 0/0 | 7261 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | AGTCG others(7256): Show |
chr1 | 156929840 | 157050742 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0010g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0015g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0020g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0028g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0030g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0032g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0034g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0035g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0001t0036g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0005t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0005t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0001c0011t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0012g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0016g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0017g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0017g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0017g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0023g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0024g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0002t0029g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0009g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0018g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0018g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0022g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0022g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0025g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0004t0033g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0002c0008t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0006g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0019g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0019g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0019g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0003c0003t0031g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0004c0006t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0004c0006t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0005c0007t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0005c0007t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0006c0009t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0007c0014t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0008c0013t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0009c0012t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| a0010c0010t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0006 | g0027 | EUR | GBR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | GBR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0092 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0226 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00323 | hp1 | a0003 | c0003 | t0003 | g0227 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0152 | EUR | FIN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00408 | hp2 | a0002 | c0004 | t0005 | g0131 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00438 | hp2 | a0003 | c0003 | t0003 | g0215 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00597 | hp1 | a0003 | c0003 | t0003 | g0230 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00609 | hp2 | a0002 | c0002 | t0012 | g0192 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00621 | hp2 | a0002 | c0004 | t0033 | g0283 | EAS | CHS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00639 | hp2 | a0003 | c0003 | t0003 | g0240 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00642 | hp1 | a0002 | c0004 | t0009 | g0119 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00741 | hp1 | a0002 | c0004 | t0005 | g0015 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01071 | hp1 | a0003 | c0003 | t0003 | g0228 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01167 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01169 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01192 | hp2 | a0003 | c0003 | t0031 | g0222 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0148 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01257 | hp1 | a0003 | c0003 | t0006 | g0019 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01257 | hp2 | a0002 | c0004 | t0009 | g0004 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01258 | hp1 | a0002 | c0004 | t0009 | g0004 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01346 | hp2 | a0002 | c0004 | t0009 | g0117 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01433 | hp2 | a0002 | c0004 | t0005 | g0025 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01496 | hp2 | a0003 | c0003 | t0006 | g0021 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0157 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01515 | hp2 | a0003 | c0003 | t0006 | g0020 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0158 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0213 | EUR | IBS | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0211 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01891 | hp1 | a0002 | c0004 | t0005 | g0112 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01928 | hp1 | a0001 | c0001 | t0028 | g0183 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0281 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01934 | hp2 | a0003 | c0003 | t0003 | g0268 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01943 | hp1 | a0001 | c0005 | t0001 | g0287 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01975 | hp2 | a0003 | c0003 | t0003 | g0223 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01978 | hp1 | a0003 | c0003 | t0003 | g0266 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02004 | hp1 | a0001 | c0001 | t0032 | g0255 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02015 | hp1 | a0002 | c0004 | t0005 | g0059 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02055 | hp1 | a0004 | c0006 | t0005 | g0029 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02055 | hp2 | a0003 | c0003 | t0003 | g0265 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0149 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02083 | hp1 | a0001 | c0001 | t0036 | g0350 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02132 | hp1 | a0003 | c0003 | t0003 | g0250 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0249 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02145 | hp1 | a0002 | c0004 | t0027 | g0172 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02145 | hp2 | a0002 | c0004 | t0013 | g0189 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02257 | hp1 | a0002 | c0004 | t0018 | g0247 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02257 | hp2 | a0004 | c0006 | t0005 | g0030 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02258 | hp2 | a0002 | c0004 | t0008 | g0195 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02280 | hp1 | a0002 | c0004 | t0008 | g0197 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02280 | hp2 | a0002 | c0004 | t0005 | g0022 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02300 | hp1 | a0001 | c0011 | t0004 | g0163 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02300 | hp2 | a0006 | c0009 | t0003 | g0261 | AMR | PEL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0248 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0219 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02572 | hp1 | a0002 | c0004 | t0021 | g0174 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02572 | hp2 | a0003 | c0003 | t0019 | g0352 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0165 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02615 | hp2 | a0001 | c0001 | t0030 | g0208 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02622 | hp1 | a0002 | c0002 | t0024 | g0011 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02622 | hp2 | a0003 | c0003 | t0019 | g0351 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02630 | hp1 | a0002 | c0004 | t0008 | g0198 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02630 | hp2 | a0002 | c0004 | t0005 | g0014 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02647 | hp2 | a0002 | c0004 | t0008 | g0199 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02683 | hp1 | a0003 | c0003 | t0003 | g0221 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02683 | hp2 | a0002 | c0004 | t0005 | g0024 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02723 | hp1 | a0003 | c0003 | t0003 | g0243 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0220 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02735 | hp2 | a0002 | c0008 | t0002 | g0072 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02738 | hp1 | a0002 | c0004 | t0005 | g0129 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0146 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0169 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0168 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02895 | hp1 | a0002 | c0004 | t0005 | g0031 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0202 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02896 | hp2 | a0002 | c0004 | t0022 | g0135 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0201 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02897 | hp2 | a0002 | c0004 | t0005 | g0032 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02922 | hp2 | a0002 | c0004 | t0014 | g0205 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02965 | hp2 | a0003 | c0003 | t0003 | g0245 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02976 | hp1 | a0002 | c0004 | t0005 | g0016 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02976 | hp2 | a0002 | c0004 | t0013 | g0184 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03041 | hp1 | a0003 | c0003 | t0006 | g0034 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03098 | hp1 | a0007 | c0014 | t0014 | g0200 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03130 | hp2 | a0002 | c0004 | t0005 | g0017 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03139 | hp1 | a0002 | c0004 | t0005 | g0013 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03139 | hp2 | a0002 | c0004 | t0021 | g0173 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03195 | hp1 | a0002 | c0004 | t0013 | g0185 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ESN | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03209 | hp2 | a0002 | c0004 | t0005 | g0108 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03225 | hp1 | a0003 | c0003 | t0006 | g0033 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03225 | hp2 | a0002 | c0004 | t0008 | g0196 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0224 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03453 | hp2 | a0002 | c0004 | t0008 | g0193 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0204 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0225 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0155 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03540 | hp1 | a0002 | c0004 | t0013 | g0188 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0207 | AFR | GWD | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03654 | hp1 | a0003 | c0003 | t0003 | g0242 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03669 | hp2 | a0008 | c0013 | t0007 | g0147 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03704 | hp2 | a0002 | c0004 | t0009 | g0121 | SAS | PJL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0100 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0150 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03942 | hp1 | a0003 | c0003 | t0003 | g0238 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0145 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04184 | hp1 | a0002 | c0004 | t0009 | g0118 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0151 | SAS | BEB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04199 | hp2 | a0003 | c0003 | t0006 | g0076 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04204 | hp2 | a0002 | c0004 | t0005 | g0122 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0063 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0143 | SAS | STU | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18522 | hp2 | a0002 | c0004 | t0005 | g0109 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | CHB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18906 | hp1 | a0002 | c0004 | t0014 | g0206 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18943 | hp1 | a0002 | c0004 | t0005 | g0114 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18943 | hp2 | a0002 | c0002 | t0012 | g0190 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18944 | hp2 | a0002 | c0002 | t0016 | g0253 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18948 | hp1 | a0002 | c0002 | t0012 | g0186 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18948 | hp2 | a0003 | c0003 | t0003 | g0267 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18952 | hp2 | a0002 | c0002 | t0017 | g0048 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18960 | hp1 | a0003 | c0003 | t0003 | g0257 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18960 | hp2 | a0002 | c0002 | t0011 | g0080 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18963 | hp2 | a0003 | c0003 | t0003 | g0217 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18964 | hp2 | a0002 | c0004 | t0005 | g0116 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0346 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18966 | hp2 | a0002 | c0002 | t0023 | g0010 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18967 | hp2 | a0009 | c0012 | t0003 | g0239 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18968 | hp1 | a0002 | c0002 | t0017 | g0058 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0214 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18979 | hp1 | a0003 | c0003 | t0003 | g0216 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18981 | hp2 | a0003 | c0003 | t0003 | g0263 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18987 | hp1 | a0002 | c0004 | t0005 | g0123 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18987 | hp2 | a0001 | c0001 | t0034 | g0342 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18988 | hp2 | a0002 | c0002 | t0016 | g0232 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18994 | hp2 | a0001 | c0001 | t0010 | g0343 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18995 | hp2 | a0005 | c0007 | t0003 | g0251 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18997 | hp1 | a0005 | c0007 | t0003 | g0252 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18997 | hp2 | a0001 | c0001 | t0010 | g0348 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18998 | hp1 | a0003 | c0003 | t0003 | g0258 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18998 | hp2 | a0002 | c0002 | t0011 | g0079 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19000 | hp2 | a0001 | c0001 | t0010 | g0347 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19002 | hp1 | a0002 | c0002 | t0011 | g0083 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19002 | hp2 | a0002 | c0004 | t0025 | g0124 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19004 | hp1 | a0003 | c0003 | t0003 | g0260 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19004 | hp2 | a0002 | c0002 | t0017 | g0057 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19005 | hp2 | a0003 | c0003 | t0003 | g0236 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0256 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19010 | hp2 | a0002 | c0002 | t0012 | g0191 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19011 | hp1 | a0003 | c0003 | t0003 | g0234 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19011 | hp2 | a0001 | c0001 | t0010 | g0345 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19030 | hp1 | a0002 | c0004 | t0022 | g0134 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19030 | hp2 | a0003 | c0003 | t0019 | g0353 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19043 | hp1 | a0002 | c0004 | t0008 | g0194 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | LWK | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19055 | hp2 | a0001 | c0005 | t0001 | g0278 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19056 | hp1 | a0002 | c0002 | t0011 | g0082 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19056 | hp2 | a0003 | c0003 | t0003 | g0235 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19060 | hp2 | a0002 | c0002 | t0016 | g0254 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19063 | hp1 | a0003 | c0003 | t0003 | g0262 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0237 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19068 | hp1 | a0002 | c0002 | t0011 | g0081 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19068 | hp2 | a0002 | c0004 | t0005 | g0120 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19070 | hp2 | a0002 | c0002 | t0016 | g0233 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19074 | hp2 | a0003 | c0003 | t0003 | g0218 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19078 | hp1 | a0003 | c0003 | t0003 | g0264 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0344 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19083 | hp2 | a0002 | c0004 | t0005 | g0132 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19084 | hp1 | a0002 | c0004 | t0005 | g0061 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19085 | hp1 | a0010 | c0010 | t0003 | g0231 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19087 | hp1 | a0002 | c0004 | t0005 | g0130 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19090 | hp1 | a0003 | c0003 | t0003 | g0259 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19240 | hp1 | a0001 | c0001 | t0035 | g0349 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA19240 | hp2 | a0002 | c0004 | t0005 | g0026 | AFR | YRI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20129 | hp1 | a0003 | c0003 | t0006 | g0018 | AFR | ASW | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20129 | hp2 | a0002 | c0004 | t0026 | g0110 | AFR | ASW | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0107 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0052 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0241 | SAS | GIH | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0144 | SAS | GIH | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02109 | hp1 | a0003 | c0003 | t0003 | g0229 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02109 | hp2 | a0002 | c0004 | t0005 | g0028 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02486 | hp1 | a0002 | c0004 | t0018 | g0246 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG02486 | hp2 | a0002 | c0002 | t0029 | g0187 | AFR | ACB | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03471 | hp1 | a0002 | c0004 | t0014 | g0203 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | MSL | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG06807 | hp1 | a0002 | c0004 | t0018 | g0244 | AFR | USA | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | USA | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0006 | g0023 | REF | REF | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0006 | g0111 | REF | REF | ARHGEF11_chr1_156929840_157050742 | ARHGEF11 | chr1 | 156929840 | 157050742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156937289 | T | C | 5 | a0001 a0002 a0004 others(2): Show |
298 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(295): Show |
missense_variant | MODERATE | c.4400A>G | p.His1467Arg | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/41 | 5812/7261 | 4400/4689 | 1467/1562 | chr1 | 156937289 | |||
| chr1:156937323 | T | C | 2 | a0001 a0008 |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
missense_variant | MODERATE | c.4366A>G | p.Ser1456Gly | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/41 | 5778/7261 | 4366/4689 | 1456/1562 | chr1 | 156937323 | |||
| chr1:156937340 | G | A | 1 | a0009 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.4349C>T | p.Pro1450Leu | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/41 | 5761/7261 | 4349/4689 | 1450/1562 | chr1 | 156937340 | |||
| chr1:156939704 | G | A | 1 | a0008 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3940C>T | p.Arg1314Trp | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/41 | 5352/7261 | 3940/4689 | 1314/1562 | chr1 | 156939704 | |||
| chr1:156939892 | A | C | 1 | a0010 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.3752T>G | p.Leu1251Arg | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/41 | 5164/7261 | 3752/4689 | 1251/1562 | chr1 | 156939892 | |||
| chr1:156941907 | G | A | 1 | a0004 | 2 | HG02055.hp1 HG02257.hp2 |
missense_variant | MODERATE | c.3409C>T | p.Pro1137Ser | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/41 | 4821/7261 | 3409/4689 | 1137/1562 | chr1 | 156941907 | |||
| chr1:156941926 | C | T | 1 | a0006 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.3390G>A | p.Met1130Ile | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/41 | 4802/7261 | 3390/4689 | 1130/1562 | chr1 | 156941926 | |||
| chr1:156948185 | G | A | 1 | a0005 | 2 | NA18995.hp2 NA18997.hp1 |
missense_variant | MODERATE | c.2149C>T | p.Arg717Cys | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 24/41 | 3561/7261 | 2149/4689 | 717/1562 | chr1 | 156948185 | |||
| chr1:156969356 | G | A | 1 | a0007 | 1 | HG03098.hp1 | missense_variant&splice_region_variant | MODERATE | c.751C>T | p.Arg251Trp | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/41 | 2163/7261 | 751/4689 | 251/1562 | chr1 | 156969356 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156936940 | C | T | 1 | a0001c0011 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.4506G>A | p.Thr1502Thr | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/41 | 5918/7261 | 4506/4689 | 1502/1562 | chr1 | 156936940 | |||
| chr1:156939903 | G | A | 2 | a0002c0002 a0002c0008 |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
synonymous_variant | LOW | c.3741C>T | p.Asn1247Asn | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/41 | 5153/7261 | 3741/4689 | 1247/1562 | chr1 | 156939903 | |||
| chr1:156968104 | C | T | 1 | a0002c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.846G>A | p.Ser282Ser | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/41 | 2258/7261 | 846/4689 | 282/1562 | chr1 | 156968104 | |||
| chr1:156984427 | T | C | 1 | a0001c0005 | 3 | HG01928.hp2 HG01943.hp1 NA19055.hp2 |
synonymous_variant | LOW | c.135A>G | p.Gln45Gln | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/41 | 1547/7261 | 135/4689 | 45/1562 | chr1 | 156984427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156934852 | A | G | 10 | a0002c0002t0002 a0002c0002t0011 a0002c0002t0012 others(7): Show |
89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1148T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 1148 | chr1 | 156934852 | ||||||
| chr1:156934967 | T | TTA | 2 | a0002c0004t0021 a0002c0004t0026 |
3 | HG02572.hp1 HG03139.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031_*1032dupTA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 1032 | chr1 | 156934967 | ||||||
| chr1:156934982 | T | G | 1 | a0002c0002t0011 | 5 | NA18960.hp2 NA18998.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1018A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 1018 | chr1 | 156934982 | ||||||
| chr1:156935026 | G | A | 10 | a0002c0002t0002 a0002c0002t0011 a0002c0002t0012 others(7): Show |
89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 974 | chr1 | 156935026 | ||||||
| chr1:156935045 | G | T | 3 | a0001c0001t0007 a0001c0001t0032 a0008c0013t0007 |
10 | HG01243.hp1 HG02004.hp1 HG02071.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*955C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 955 | chr1 | 156935045 | ||||||
| chr1:156935103 | C | T | 2 | a0002c0002t0029 a0002c0004t0021 |
3 | HG02486.hp2 HG02572.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*897G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 897 | chr1 | 156935103 | ||||||
| chr1:156935172 | C | T | 1 | a0003c0003t0031 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*828G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 828 | chr1 | 156935172 | ||||||
| chr1:156935525 | C | T | 1 | a0002c0004t0009 | 6 | HG00642.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 475 | chr1 | 156935525 | ||||||
| chr1:156935594 | G | T | 1 | a0002c0004t0025 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 406 | chr1 | 156935594 | ||||||
| chr1:156935743 | G | A | 1 | a0002c0002t0017 | 3 | NA18952.hp2 NA18968.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*257C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 257 | chr1 | 156935743 | ||||||
| chr1:156935792 | A | G | 21 | a0002c0002t0002 a0002c0002t0011 a0002c0002t0012 others(18): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*208T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 208 | chr1 | 156935792 | ||||||
| chr1:156935860 | C | G | 1 | a0002c0004t0021 | 2 | HG02572.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 140 | chr1 | 156935860 | ||||||
| chr1:156935890 | C | G | 1 | a0001c0001t0020 | 2 | HG02809.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*110G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 41/41 | 110 | chr1 | 156935890 | ||||||
| chr1:157044443 | T | C | 1 | a0001c0001t0034 | 1 | NA18987.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-113A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | chr1 | 157044443 | |||||||
| chr1:157044500 | C | T | 1 | a0002c0002t0024 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-170G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 170 | chr1 | 157044500 | ||||||
| chr1:157044799 | G | T | 2 | a0001c0001t0035 a0002c0004t0008 |
8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-469C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 469 | chr1 | 157044799 | ||||||
| chr1:157044910 | G | A | 25 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(22): Show |
134 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-580C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | chr1 | 157044910 | |||||||
| chr1:157044975 | C | A | 1 | a0001c0001t0028 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-645G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 645 | chr1 | 157044975 | ||||||
| chr1:157045078 | C | CA | 8 | a0001c0001t0015 a0001c0001t0035 a0002c0002t0012 others(5): Show |
25 | HG00609.hp2 HG02145.hp2 HG02258.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-749dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 749 | chr1 | 157045078 | ||||||
| chr1:157045085 | A | T | 7 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0030 others(4): Show |
86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
5_prime_UTR_variant | MODIFIER | c.-755T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 755 | chr1 | 157045085 | ||||||
| chr1:157045172 | T | A | 11 | a0001c0001t0003 a0001c0001t0030 a0001c0001t0032 others(8): Show |
63 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-842A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 842 | chr1 | 157045172 | ||||||
| chr1:157045233 | G | C | 1 | a0001c0001t0010 | 6 | NA18966.hp1 NA18994.hp2 NA18997.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-903C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 903 | chr1 | 157045233 | ||||||
| chr1:157045234 | C | A | 6 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0034 others(3): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-904G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 904 | chr1 | 157045234 | ||||||
| chr1:157045424 | T | C | 1 | a0001c0001t0035 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1094A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 1094 | chr1 | 157045424 | ||||||
| chr1:157045571 | G | A | 1 | a0001c0001t0036 | 1 | HG02083.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1241C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | chr1 | 157045571 | |||||||
| chr1:157045641 | G | T | 1 | a0002c0002t0023 | 1 | NA18966.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1311C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 1311 | chr1 | 157045641 | ||||||
| chr1:157045642 | AC | A | 1 | a0003c0003t0019 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1313delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/41 | 1313 | chr1 | 157045642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:156936301 | C | T | 1 | a0003c0003t0003g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4631-243G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936301 | |||||||
| chr1:156936320 | G | A | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4631-262C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936320 | |||||||
| chr1:156936354 | C | T | 1 | a0003c0003t0003g0238 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4631-296G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936354 | |||||||
| chr1:156936355 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4631-297C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936355 | |||||||
| chr1:156936378 | T | C | 9 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(6): Show |
9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.4631-320A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936378 | |||||||
| chr1:156936480 | GA | G | 6 | a0003c0003t0003g0248 a0003c0003t0003g0262 a0003c0003t0003g0265 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4630+335delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936480 | |||||||
| chr1:156936493 | A | AATATAT | 6 | a0001c0001t0001g0272 a0001c0001t0001g0292 a0001c0001t0001g0293 others(3): Show |
6 | HG02015.hp2 HG02258.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.4630+322_4630+323i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | AATATATA others(3): Show |
3 | a0001c0001t0001g0322 a0001c0001t0001g0324 a0001c0001t0007g0145 |
3 | HG01123.hp2 HG01256.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4630+322_4630+323i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | AATATATA others(5): Show |
2 | a0001c0001t0001g0008 a0002c0002t0002g0039 |
2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.4630+322_4630+323i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | AATATATA others(13): Show |
2 | a0001c0001t0001g0273 a0001c0005t0001g0278 |
2 | HG00558.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.4630+322_4630+323i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | AATATATA others(23): Show |
1 | a0001c0001t0001g0285 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4630+322_4630+323i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | ATATATAT others(12): Show |
1 | a0002c0002t0002g0092 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4630+322_4630+323i others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0286 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4630+322_4630+323i others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936493 | A | T | 3 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 |
3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4630+323T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936493 | |||||||
| chr1:156936495 | A | AATAT | 7 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0288 others(4): Show |
7 | HG01167.hp1 HG02074.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATAT | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0276 others(23): Show |
27 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(1): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0310 a0001c0001t0001g0330 others(11): Show |
14 | HG01106.hp1 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(3): Show |
10 | a0001c0001t0001g0316 a0001c0001t0001g0321 a0001c0001t0001g0323 others(7): Show |
10 | HG01433.hp1 HG01934.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(5): Show |
3 | a0001c0001t0007g0146 a0001c0001t0007g0149 a0001c0001t0010g0343 |
3 | HG02071.hp2 HG02738.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.4630+320_4630+321i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0326 a0001c0001t0007g0150 |
2 | HG03927.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.4630+320_4630+321i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(9): Show |
1 | a0001c0001t0006g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(11): Show |
1 | a0001c0005t0001g0281 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(15): Show |
1 | a0002c0002t0002g0087 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0313 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4630+320_4630+321i others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(23): Show |
1 | a0002c0004t0008g0198 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4630+320_4630+321i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | AATATATA others(25): Show |
1 | a0002c0004t0008g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | ATATAT | 12 | a0001c0001t0001g0271 a0001c0001t0001g0303 a0001c0001t0001g0307 others(9): Show |
12 | HG00323.hp2 HG01099.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | ATATATAT | 12 | a0001c0001t0001g0275 a0001c0001t0001g0308 a0001c0001t0004g0006 others(9): Show |
13 | HG01070.hp2 HG01346.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(9): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | ATATATAT others(2): Show |
8 | a0001c0001t0001g0277 a0001c0001t0001g0304 a0001c0001t0004g0177 others(5): Show |
8 | HG01192.hp1 HG01255.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | ATATATAT others(4): Show |
4 | a0001c0001t0004g0158 a0002c0002t0002g0002 a0002c0002t0002g0050 others(1): Show |
4 | HG01517.hp1 NA18955.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.4630+320_4630+321i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | ATATATAT others(6): Show |
2 | a0001c0001t0004g0157 a0008c0013t0007g0147 |
2 | HG01515.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.4630+320_4630+321i others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0295 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4630+320_4630+321i others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | A | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0272 a0001c0001t0001g0273 others(23): Show |
26 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.4630+321T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936495 | AAAATATA others(3): Show |
A | 1 | a0002c0004t0008g0197 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4630+311_4630+320d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936495 | |||||||
| chr1:156936497 | A | AAAAAAAA others(23): Show |
1 | a0002c0004t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAA others(27): Show |
1 | a0002c0004t0026g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(36): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAA others(29): Show |
1 | a0002c0004t0005g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(38): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAA others(17): Show |
1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAA others(4): Show |
2 | a0002c0004t0005g0114 a0002c0004t0009g0004 |
3 | HG01257.hp2 HG01258.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAA others(3): Show |
3 | a0002c0004t0005g0131 a0002c0004t0005g0132 a0002c0004t0025g0124 |
3 | HG00408.hp2 NA19002.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAA others(5): Show |
1 | a0002c0004t0009g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAAAT others(4): Show |
1 | a0002c0004t0009g0121 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAATA others(3): Show |
1 | a0002c0004t0033g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAAATA others(5): Show |
1 | a0002c0002t0002g0070 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAATAT others(22): Show |
1 | a0002c0004t0008g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAAATAT others(24): Show |
1 | a0002c0004t0013g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAATAT | 8 | a0001c0001t0001g0312 a0002c0002t0002g0035 a0002c0002t0002g0051 others(5): Show |
8 | HG00642.hp2 HG02451.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAATATA others(3): Show |
3 | a0002c0002t0002g0062 a0002c0002t0002g0069 a0002c0002t0029g0187 |
3 | HG02486.hp2 HG02698.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAATATA others(5): Show |
1 | a0002c0002t0002g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAAATATA others(25): Show |
2 | a0002c0004t0013g0185 a0002c0004t0013g0189 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AAATATAT others(4): Show |
3 | a0001c0001t0004g0154 a0001c0001t0010g0345 a0002c0002t0002g0093 |
3 | HG01169.hp1 HG02071.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATAT | 28 | a0001c0001t0001g0284 a0001c0001t0001g0301 a0001c0001t0001g0309 others(25): Show |
28 | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.4630+313_4630+318d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATATA others(3): Show |
3 | a0001c0001t0001g0320 a0001c0001t0006g0113 a0002c0002t0002g0086 |
3 | NA18947.hp1 NA18951.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.4630+309_4630+318d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATATA others(5): Show |
2 | a0001c0001t0007g0143 a0002c0002t0002g0073 |
2 | HG04228.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.4630+307_4630+318d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATATA others(7): Show |
1 | a0002c0002t0002g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4630+305_4630+318d others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATATA others(13): Show |
1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4630+299_4630+318d others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATATA others(21): Show |
1 | a0002c0004t0008g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4630+291_4630+318d others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | AATATATA others(23): Show |
1 | a0002c0004t0008g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATAT | 6 | a0001c0001t0004g0167 a0002c0002t0002g0001 a0002c0002t0002g0040 others(3): Show |
6 | HG01243.hp2 HG02818.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT | 11 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0004g0153 others(8): Show |
11 | HG01099.hp2 HG01175.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(9): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(2): Show |
4 | a0001c0001t0001g0311 a0001c0001t0004g0005 a0002c0002t0002g0043 others(1): Show |
4 | HG01496.hp1 HG02965.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.4630+318_4630+319i others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(4): Show |
2 | a0002c0002t0002g0078 a0002c0002t0016g0254 |
2 | NA19009.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.4630+318_4630+319i others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(10): Show |
1 | a0001c0001t0004g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(12): Show |
1 | a0001c0005t0001g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(14): Show |
1 | a0002c0004t0013g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0274 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4630+318_4630+319i others(25): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | ATATATAT others(20): Show |
1 | a0001c0001t0036g0350 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4630+318_4630+319i others(29): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936497 | A | T | 149 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(146): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.4630+319T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936497 | |||||||
| chr1:156936498 | AT | A | 5 | a0002c0004t0022g0135 a0003c0003t0006g0019 a0003c0003t0031g0222 others(2): Show |
5 | HG01192.hp2 HG01257.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4630+317delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936498 | |||||||
| chr1:156936499 | T | A | 18 | a0001c0001t0020g0168 a0001c0001t0020g0169 a0002c0004t0005g0013 others(15): Show |
18 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.4630+317A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936499 | |||||||
| chr1:156936501 | T | A | 5 | a0002c0004t0005g0014 a0002c0004t0022g0135 a0005c0007t0003g0251 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4630+315A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936501 | |||||||
| chr1:156936527 | A | T | 1 | a0001c0001t0006g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4630+289T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936527 | |||||||
| chr1:156936532 | A | T | 1 | a0002c0002t0002g0069 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4630+284T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936532 | |||||||
| chr1:156936565 | C | T | 4 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0030g0208 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4630+251G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936565 | |||||||
| chr1:156936647 | G | A | 1 | a0003c0003t0003g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4630+169C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936647 | |||||||
| chr1:156936658 | A | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(83): Show |
88 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.4630+158T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936658 | |||||||
| chr1:156936781 | A | G | 19 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0112 others(16): Show |
20 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.4630+35T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | 156936781 | |||||||
| chr1:156937016 | C | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4441-11G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937016 | |||||||
| chr1:156937089 | G | A | 84 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.4441-84C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937089 | |||||||
| chr1:156937118 | C | T | 132 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(129): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.4441-113G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937118 | |||||||
| chr1:156937234 | C | G | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+15G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937234 | |||||||
| chr1:156937235 | C | G | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+14G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937235 | |||||||
| chr1:156937236 | C | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+13G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937236 | |||||||
| chr1:156937237 | T | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+12A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937237 | |||||||
| chr1:156937238 | G | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4440+11C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937238 | |||||||
| chr1:156937239 | C | T | 98 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.4440+10G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 39/40 | chr1 | 156937239 | |||||||
| chr1:156937627 | C | T | 2 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4193-131G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937627 | |||||||
| chr1:156937656 | C | T | 3 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0030g0208 |
3 | HG01884.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4193-160G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937656 | |||||||
| chr1:156937674 | G | A | 1 | a0001c0001t0006g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4193-178C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937674 | |||||||
| chr1:156937717 | G | A | 1 | a0001c0001t0007g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4193-221C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937717 | |||||||
| chr1:156937758 | C | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(83): Show |
89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4193-262G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937758 | |||||||
| chr1:156937774 | G | A | 1 | a0002c0002t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4193-278C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937774 | |||||||
| chr1:156937843 | G | A | 13 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(10): Show |
13 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.4193-347C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156937843 | |||||||
| chr1:156938374 | C | T | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.4192+44G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 38/40 | chr1 | 156938374 | |||||||
| chr1:156938534 | C | T | 1 | a0001c0001t0004g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4097-21G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938534 | |||||||
| chr1:156938797 | G | A | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.4097-284C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938797 | |||||||
| chr1:156938835 | C | A | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4097-322G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938835 | |||||||
| chr1:156938943 | C | T | 1 | a0002c0002t0002g0088 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4097-430G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156938943 | |||||||
| chr1:156939122 | T | A | 4 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4096+426A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939122 | |||||||
| chr1:156939194 | T | C | 111 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(108): Show |
114 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4096+354A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939194 | |||||||
| chr1:156939453 | CAGGGGGA others(4): Show |
C | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4096+84_4096+94del others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939453 | |||||||
| chr1:156939511 | T | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(83): Show |
89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.4096+37A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | 156939511 | |||||||
| chr1:156940104 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3733+103G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 36/40 | chr1 | 156940104 | |||||||
| chr1:156940157 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3733+50C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 36/40 | chr1 | 156940157 | |||||||
| chr1:156940470 | G | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3515-45C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940470 | |||||||
| chr1:156940473 | C | T | 1 | a0002c0002t0002g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3515-48G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940473 | |||||||
| chr1:156940695 | C | T | 1 | a0002c0002t0002g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3515-270G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940695 | |||||||
| chr1:156940696 | A | G | 116 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(113): Show |
120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.3515-271T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940696 | |||||||
| chr1:156940702 | T | C | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3515-277A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940702 | |||||||
| chr1:156940704 | C | A | 9 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(6): Show |
9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3515-279G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940704 | |||||||
| chr1:156940757 | C | T | 84 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.3515-332G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940757 | |||||||
| chr1:156940806 | C | T | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.3515-381G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940806 | |||||||
| chr1:156940921 | C | T | 1 | a0003c0003t0003g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3514+451G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156940921 | |||||||
| chr1:156941004 | C | T | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3514+368G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941004 | |||||||
| chr1:156941051 | A | G | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3514+321T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941051 | |||||||
| chr1:156941085 | G | A | 2 | a0002c0004t0005g0059 a0002c0004t0005g0061 |
2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3514+287C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941085 | |||||||
| chr1:156941100 | GCTCGTCT others(1): Show |
G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(83): Show |
89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.3514+264_3514+271d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941100 | |||||||
| chr1:156941116 | A | G | 142 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(139): Show |
146 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.3514+256T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941116 | |||||||
| chr1:156941158 | T | C | 1 | a0003c0003t0006g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3514+214A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941158 | |||||||
| chr1:156941229 | C | G | 1 | a0003c0003t0003g0007 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3514+143G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941229 | |||||||
| chr1:156941336 | T | A | 5 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0330 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3514+36A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 35/40 | chr1 | 156941336 | |||||||
| chr1:156941496 | G | A | 11 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0030g0208 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3453-63C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941496 | |||||||
| chr1:156941516 | TC | T | 13 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(10): Show |
13 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3453-84delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941516 | |||||||
| chr1:156941579 | G | A | 1 | a0007c0014t0014g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3453-146C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941579 | |||||||
| chr1:156941587 | A | G | 100 | a0001c0001t0001g0314 a0001c0001t0004g0152 a0002c0002t0002g0001 others(97): Show |
103 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.3453-154T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941587 | |||||||
| chr1:156941670 | G | A | 1 | a0003c0003t0003g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3452+194C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 34/40 | chr1 | 156941670 | |||||||
| chr1:156942277 | A | T | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3327-288T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 33/40 | chr1 | 156942277 | |||||||
| chr1:156942904 | C | T | 1 | a0002c0004t0005g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3236-124G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156942904 | |||||||
| chr1:156942991 | C | T | 2 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3236-211G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156942991 | |||||||
| chr1:156943065 | C | CTTTTTT | 17 | a0002c0004t0005g0061 a0002c0004t0005g0114 a0002c0004t0005g0116 others(14): Show |
18 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.3236-291_3236-286d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943065 | |||||||
| chr1:156943065 | C | CTTTTTTT | 32 | a0002c0002t0002g0035 a0002c0002t0002g0063 a0002c0002t0002g0078 others(29): Show |
32 | HG01070.hp1 HG01433.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.3236-292_3236-286d others(9): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943065 | |||||||
| chr1:156943065 | C | CTTTTTTT others(1): Show |
89 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(86): Show |
92 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.3236-293_3236-286d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943065 | |||||||
| chr1:156943079 | G | T | 1 | a0001c0001t0004g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3236-299C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943079 | |||||||
| chr1:156943183 | C | T | 3 | a0002c0002t0002g0046 a0002c0004t0021g0173 a0002c0004t0021g0174 |
3 | HG02572.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3236-403G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943183 | |||||||
| chr1:156943357 | G | C | 1 | a0001c0001t0004g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3236-577C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943357 | |||||||
| chr1:156943657 | C | T | 100 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(97): Show |
103 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.3235+278G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943657 | |||||||
| chr1:156943659 | C | A | 1 | a0001c0001t0001g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3235+276G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943659 | |||||||
| chr1:156943786 | C | T | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3235+149G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 32/40 | chr1 | 156943786 | |||||||
| chr1:156944278 | C | A | 116 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(113): Show |
120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.3067+80G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 31/40 | chr1 | 156944278 | |||||||
| chr1:156944310 | G | A | 2 | a0002c0004t0005g0059 a0002c0004t0005g0061 |
2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3067+48C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 31/40 | chr1 | 156944310 | |||||||
| chr1:156944448 | C | A | 1 | a0002c0004t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2992-15G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944448 | |||||||
| chr1:156944448 | CCATT | C | 165 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(162): Show |
169 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.2992-19_2992-16del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944448 | |||||||
| chr1:156944448 | CCATTCAT others(1): Show |
C | 121 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0002c0002t0002g0001 others(118): Show |
125 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.2992-23_2992-16del others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944448 | |||||||
| chr1:156944644 | C | T | 1 | a0002c0004t0014g0205 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2992-211G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944644 | |||||||
| chr1:156944671 | T | C | 1 | a0001c0001t0036g0350 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2992-238A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944671 | |||||||
| chr1:156944676 | C | A | 1 | a0003c0003t0003g0007 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2992-243G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944676 | |||||||
| chr1:156944676 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2992-243G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944676 | |||||||
| chr1:156944832 | C | T | 1 | a0001c0001t0007g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2991+187G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944832 | |||||||
| chr1:156944915 | C | G | 3 | a0001c0001t0006g0126 a0001c0001t0006g0127 a0001c0001t0006g0128 |
3 | HG02723.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2991+104G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944915 | |||||||
| chr1:156944927 | C | T | 1 | a0007c0014t0014g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2991+92G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944927 | |||||||
| chr1:156944931 | T | G | 1 | a0002c0002t0002g0099 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2991+88A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | 156944931 | |||||||
| chr1:156945220 | T | C | 4 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2813-23A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945220 | |||||||
| chr1:156945246 | C | T | 143 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(140): Show |
147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2813-49G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945246 | |||||||
| chr1:156945417 | C | A | 6 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.2813-220G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945417 | |||||||
| chr1:156945454 | A | T | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2813-257T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945454 | |||||||
| chr1:156945457 | T | G | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2813-260A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945457 | |||||||
| chr1:156945530 | T | C | 1 | a0002c0002t0002g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2813-333A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945530 | |||||||
| chr1:156945746 | C | A | 14 | a0002c0002t0002g0062 a0002c0002t0002g0063 a0002c0002t0002g0064 others(11): Show |
14 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2812+299G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945746 | |||||||
| chr1:156945787 | G | A | 3 | a0003c0003t0003g0234 a0003c0003t0003g0235 a0003c0003t0003g0236 |
3 | NA19005.hp2 NA19011.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2812+258C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 29/40 | chr1 | 156945787 | |||||||
| chr1:156946848 | G | GCCTATCC others(3): Show |
143 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(140): Show |
147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.2569-62_2569-61ins others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 27/40 | chr1 | 156946848 | |||||||
| chr1:156947133 | T | C | 1 | a0001c0001t0007g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2489-118A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 26/40 | chr1 | 156947133 | |||||||
| chr1:156947248 | G | T | 1 | a0001c0001t0004g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2488+56C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 26/40 | chr1 | 156947248 | |||||||
| chr1:156947738 | C | T | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2341+31G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 25/40 | chr1 | 156947738 | |||||||
| chr1:156948556 | T | C | 23 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(20): Show |
23 | HG00741.hp1 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1926-58A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156948556 | |||||||
| chr1:156948652 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0036g0350 |
3 | HG00558.hp2 HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1926-154T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156948652 | |||||||
| chr1:156948800 | T | C | 1 | a0006c0009t0003g0261 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1926-302A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156948800 | |||||||
| chr1:156949124 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1926-626T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949124 | |||||||
| chr1:156949188 | C | T | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1926-690G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949188 | |||||||
| chr1:156949276 | G | A | 3 | a0002c0004t0018g0246 a0002c0004t0018g0247 a0002c0004t0027g0172 |
3 | HG02145.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1926-778C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949276 | |||||||
| chr1:156949298 | C | T | 4 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1926-800G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949298 | |||||||
| chr1:156949332 | T | C | 132 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(129): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1926-834A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949332 | |||||||
| chr1:156949388 | A | G | 95 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(92): Show |
98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1926-890T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949388 | |||||||
| chr1:156949607 | T | C | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1926-1109A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949607 | |||||||
| chr1:156949659 | C | A | 9 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(6): Show |
9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1926-1161G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949659 | |||||||
| chr1:156949823 | A | G | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1926-1325T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949823 | |||||||
| chr1:156949990 | A | G | 143 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(140): Show |
147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1926-1492T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156949990 | |||||||
| chr1:156950119 | C | A | 1 | a0001c0001t0004g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1925+1454G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950119 | |||||||
| chr1:156950433 | C | T | 2 | a0002c0004t0008g0196 a0002c0004t0008g0197 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1925+1140G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950433 | |||||||
| chr1:156950677 | AAACAAAC others(1): Show |
A | 4 | a0002c0004t0005g0022 a0002c0004t0005g0108 a0002c0004t0005g0109 others(1): Show |
4 | HG02280.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1925+888_1925+895d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950677 | |||||||
| chr1:156950685 | G | A | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1925+888C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156950685 | |||||||
| chr1:156951166 | A | G | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1925+407T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951166 | |||||||
| chr1:156951370 | G | A | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1925+203C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951370 | |||||||
| chr1:156951418 | T | C | 1 | a0002c0004t0005g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1925+155A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951418 | |||||||
| chr1:156951428 | A | G | 44 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(41): Show |
46 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.1925+145T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951428 | |||||||
| chr1:156951484 | G | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1925+89C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 22/40 | chr1 | 156951484 | |||||||
| chr1:156951808 | G | C | 1 | a0001c0001t0001g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1799-109C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156951808 | |||||||
| chr1:156951884 | G | A | 1 | a0003c0003t0006g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1799-185C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156951884 | |||||||
| chr1:156952604 | C | T | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1799-905G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156952604 | |||||||
| chr1:156952784 | G | T | 132 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(129): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1799-1085C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156952784 | |||||||
| chr1:156953112 | CAG | C | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1799-1415_1799-141 others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953112 | |||||||
| chr1:156953117 | G | C | 8 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(5): Show |
8 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1799-1418C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953117 | |||||||
| chr1:156953295 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1799-1596G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953295 | |||||||
| chr1:156953424 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1798+1468G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953424 | |||||||
| chr1:156953432 | T | C | 1 | a0008c0013t0007g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1798+1460A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953432 | |||||||
| chr1:156953445 | A | G | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+1447T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953445 | |||||||
| chr1:156953514 | AC | A | 3 | a0003c0003t0019g0351 a0003c0003t0019g0352 a0003c0003t0019g0353 |
3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1798+1377delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953514 | |||||||
| chr1:156953523 | C | A | 3 | a0003c0003t0019g0351 a0003c0003t0019g0352 a0003c0003t0019g0353 |
3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1798+1369G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953523 | |||||||
| chr1:156953684 | C | A | 1 | a0001c0001t0004g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1798+1208G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953684 | |||||||
| chr1:156953686 | C | A | 90 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0270 others(87): Show |
92 | HG00438.hp1 HG00609.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.1798+1206G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953686 | |||||||
| chr1:156953688 | C | A | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(120): Show |
126 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.1798+1204G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953688 | |||||||
| chr1:156953690 | C | A | 341 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(338): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1798+1202G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953690 | |||||||
| chr1:156953841 | A | G | 13 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(10): Show |
13 | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1798+1051T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953841 | |||||||
| chr1:156953934 | G | A | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1798+958C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156953934 | |||||||
| chr1:156954027 | C | T | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+865G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954027 | |||||||
| chr1:156954102 | G | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+790C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954102 | |||||||
| chr1:156954164 | G | A | 1 | a0002c0004t0005g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1798+728C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954164 | |||||||
| chr1:156954287 | C | T | 1 | a0002c0004t0025g0124 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1798+605G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954287 | |||||||
| chr1:156954336 | C | T | 2 | a0003c0003t0003g0228 a0003c0003t0031g0222 |
2 | HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1798+556G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954336 | |||||||
| chr1:156954380 | C | CA | 18 | a0003c0003t0003g0007 a0003c0003t0003g0220 a0003c0003t0003g0225 others(15): Show |
18 | HG00597.hp1 HG00639.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1798+511dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | C | CAA | 7 | a0003c0003t0003g0007 a0003c0003t0003g0211 a0003c0003t0003g0234 others(4): Show |
7 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1798+510_1798+511d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | C | CAAAAAAA others(6): Show |
1 | a0003c0003t0003g0218 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1798+499_1798+511d others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CA | C | 12 | a0003c0003t0003g0221 a0003c0003t0003g0245 a0003c0003t0003g0248 others(9): Show |
12 | HG00099.hp1 HG01515.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1798+511delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0274 a0001c0001t0001g0306 a0001c0001t0004g0139 others(7): Show |
10 | HG02135.hp2 HG03669.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1798+504_1798+511d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(2): Show |
C | 81 | a0001c0001t0001g0009 a0001c0001t0001g0272 a0001c0001t0001g0275 others(78): Show |
81 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1798+503_1798+511d others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(3): Show |
C | 141 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0279 others(138): Show |
145 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.1798+502_1798+511d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0001g0273 a0001c0001t0004g0159 a0001c0001t0015g0202 others(6): Show |
9 | HG00558.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1798+501_1798+511d others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0015g0201 a0002c0004t0005g0026 a0002c0004t0022g0134 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1798+500_1798+511d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(7): Show |
C | 6 | a0002c0004t0005g0022 a0002c0004t0005g0108 a0002c0004t0005g0109 others(3): Show |
6 | HG02280.hp2 HG03041.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1798+498_1798+511d others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(8): Show |
C | 26 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(23): Show |
27 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1798+497_1798+511d others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(9): Show |
C | 2 | a0002c0004t0005g0116 a0002c0004t0005g0132 |
2 | NA18964.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1798+496_1798+511d others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(10): Show |
C | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1798+495_1798+511d others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(12): Show |
C | 1 | a0003c0003t0003g0213 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1798+493_1798+511d others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(17): Show |
C | 1 | a0003c0003t0003g0266 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1798+488_1798+511d others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954380 | CAAAAAAA others(19): Show |
C | 13 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(10): Show |
13 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1798+486_1798+511d others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954380 | |||||||
| chr1:156954456 | G | C | 3 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0207 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1798+436C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954456 | |||||||
| chr1:156954467 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1798+425G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954467 | |||||||
| chr1:156954532 | AG | A | 6 | a0002c0002t0002g0037 a0002c0002t0002g0040 a0002c0002t0002g0041 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1798+359delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954532 | |||||||
| chr1:156954616 | C | A | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1798+276G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954616 | |||||||
| chr1:156954680 | G | C | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1798+212C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | 156954680 | |||||||
| chr1:156955091 | G | A | 1 | a0002c0004t0005g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1769-170C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955091 | |||||||
| chr1:156955215 | T | C | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1769-294A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955215 | |||||||
| chr1:156955297 | CT | C | 115 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(112): Show |
119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1769-377delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955297 | |||||||
| chr1:156955327 | G | A | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1768+376C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955327 | |||||||
| chr1:156955621 | C | A | 4 | a0003c0003t0003g0214 a0003c0003t0003g0217 a0003c0003t0003g0218 others(1): Show |
4 | HG02523.hp1 NA18963.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1768+82G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955621 | |||||||
| chr1:156955643 | T | C | 95 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(92): Show |
98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1768+60A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955643 | |||||||
| chr1:156955684 | T | C | 1 | a0003c0003t0003g0223 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1768+19A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 20/40 | chr1 | 156955684 | |||||||
| chr1:156955849 | C | T | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1672-50G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156955849 | |||||||
| chr1:156955877 | C | A | 1 | a0002c0002t0002g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1672-78G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156955877 | |||||||
| chr1:156956307 | GGTTTCAC others(3): Show |
G | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1671+103_1671+112d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156956307 | |||||||
| chr1:156956317 | T | C | 1 | a0003c0003t0003g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1671+103A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 19/40 | chr1 | 156956317 | |||||||
| chr1:156956641 | C | T | 4 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0030g0208 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527-77G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156956641 | |||||||
| chr1:156956849 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1527-285A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156956849 | |||||||
| chr1:156956901 | G | T | 1 | a0003c0003t0003g0216 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1527-337C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156956901 | |||||||
| chr1:156957532 | G | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1526+260C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156957532 | |||||||
| chr1:156957772 | C | T | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG02129.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1526+20G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 18/40 | chr1 | 156957772 | |||||||
| chr1:156957959 | T | C | 117 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0207 others(114): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1503-144A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156957959 | |||||||
| chr1:156958234 | C | T | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1503-419G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958234 | |||||||
| chr1:156958348 | A | G | 3 | a0002c0004t0018g0244 a0004c0006t0005g0029 a0004c0006t0005g0030 |
3 | HG02055.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1502+394T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958348 | |||||||
| chr1:156958423 | A | G | 2 | a0002c0004t0005g0017 a0002c0004t0005g0025 |
2 | HG01433.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1502+319T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958423 | |||||||
| chr1:156958530 | T | C | 1 | a0002c0002t0011g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1502+212A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958530 | |||||||
| chr1:156958700 | C | T | 9 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(6): Show |
9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1502+42G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 17/40 | chr1 | 156958700 | |||||||
| chr1:156958984 | A | T | 98 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1379+62T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 16/40 | chr1 | 156958984 | |||||||
| chr1:156958992 | C | A | 2 | a0003c0003t0003g0214 a0003c0003t0003g0217 |
2 | NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1379+54G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 16/40 | chr1 | 156958992 | |||||||
| chr1:156959231 | C | T | 13 | a0001c0001t0001g0337 a0001c0001t0004g0133 a0001c0001t0004g0136 others(10): Show |
13 | HG01243.hp1 HG02004.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1283-89G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959231 | |||||||
| chr1:156959471 | T | C | 2 | a0002c0004t0008g0196 a0002c0004t0008g0197 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1283-329A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959471 | |||||||
| chr1:156959530 | A | G | 1 | a0001c0001t0006g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1283-388T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959530 | |||||||
| chr1:156959788 | C | G | 1 | a0002c0004t0025g0124 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1282+630G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959788 | |||||||
| chr1:156959802 | T | C | 98 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282+616A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959802 | |||||||
| chr1:156959843 | G | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1282+575C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959843 | |||||||
| chr1:156959924 | A | AC | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1282+493dupG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959924 | |||||||
| chr1:156959927 | CCCCCT | C | 83 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(80): Show |
86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1282+486_1282+490d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959927 | |||||||
| chr1:156959932 | T | C | 44 | a0002c0004t0005g0016 a0002c0004t0005g0017 a0002c0004t0005g0022 others(41): Show |
45 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1282+486A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959932 | |||||||
| chr1:156959932 | TC | T | 66 | a0001c0001t0001g0275 a0001c0001t0001g0337 a0001c0001t0003g0209 others(63): Show |
68 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1282+485delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959932 | |||||||
| chr1:156959933 | C | T | 42 | a0002c0004t0005g0016 a0002c0004t0005g0017 a0002c0004t0005g0022 others(39): Show |
43 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1282+485G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959933 | |||||||
| chr1:156959936 | C | G | 4 | a0003c0003t0003g0257 a0003c0003t0003g0259 a0003c0003t0003g0264 others(1): Show |
4 | NA18948.hp2 NA18960.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+482G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959936 | |||||||
| chr1:156959939 | C | A | 1 | a0001c0001t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1282+479G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959939 | |||||||
| chr1:156959940 | C | A | 5 | a0002c0002t0002g0002 a0002c0002t0002g0039 a0002c0002t0002g0050 others(2): Show |
6 | HG00597.hp2 NA18955.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+478G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959940 | |||||||
| chr1:156959941 | C | A | 87 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(84): Show |
90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282+477G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959941 | |||||||
| chr1:156959941 | C | CA | 3 | a0001c0001t0001g0274 a0001c0001t0001g0312 a0001c0001t0001g0320 |
3 | NA18963.hp1 NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1282+476_1282+477i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959941 | |||||||
| chr1:156959942 | C | A | 178 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0270 others(175): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1282+476G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959942 | |||||||
| chr1:156959942 | C | CA | 28 | a0001c0001t0001g0269 a0001c0001t0001g0272 a0001c0001t0001g0273 others(25): Show |
28 | HG00438.hp1 HG00558.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1282+475_1282+476i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959942 | |||||||
| chr1:156959943 | C | A | 274 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(271): Show |
282 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.1282+475G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959943 | |||||||
| chr1:156959943 | C | CA | 6 | a0001c0001t0001g0288 a0001c0001t0015g0201 a0001c0001t0015g0207 others(3): Show |
6 | HG00741.hp1 HG02602.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282+474dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156959943 | |||||||
| chr1:156960073 | A | G | 144 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(141): Show |
148 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1282+345T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960073 | |||||||
| chr1:156960109 | C | T | 13 | a0001c0001t0004g0151 a0002c0004t0005g0013 a0002c0004t0005g0014 others(10): Show |
13 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282+309G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960109 | |||||||
| chr1:156960188 | G | A | 6 | a0002c0002t0002g0037 a0002c0002t0002g0040 a0002c0002t0002g0041 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+230C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960188 | |||||||
| chr1:156960261 | C | T | 98 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(95): Show |
101 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282+157G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960261 | |||||||
| chr1:156960351 | A | G | 1 | a0002c0002t0002g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1282+67T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960351 | |||||||
| chr1:156960361 | G | A | 3 | a0002c0004t0008g0193 a0002c0004t0008g0194 a0002c0004t0008g0195 |
3 | HG02258.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1282+57C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 15/40 | chr1 | 156960361 | |||||||
| chr1:156960495 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1240-35C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960495 | |||||||
| chr1:156960503 | A | G | 1 | a0003c0003t0003g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1240-43T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960503 | |||||||
| chr1:156960531 | C | T | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-71G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960531 | |||||||
| chr1:156960611 | C | A | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1240-151G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960611 | |||||||
| chr1:156960668 | T | C | 1 | a0006c0009t0003g0261 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1240-208A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960668 | |||||||
| chr1:156960687 | C | T | 1 | a0002c0002t0002g0099 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1240-227G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960687 | |||||||
| chr1:156960744 | A | C | 3 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 |
3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240-284T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960744 | |||||||
| chr1:156960849 | A | C | 2 | a0001c0001t0020g0168 a0001c0001t0020g0169 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1240-389T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156960849 | |||||||
| chr1:156961437 | T | G | 2 | a0002c0004t0005g0016 a0002c0004t0005g0022 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1239+240A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156961437 | |||||||
| chr1:156961586 | T | C | 2 | a0002c0002t0002g0049 a0002c0002t0002g0056 |
2 | NA18952.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1239+91A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 14/40 | chr1 | 156961586 | |||||||
| chr1:156962235 | A | G | 1 | a0001c0001t0004g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1141-460T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962235 | |||||||
| chr1:156962290 | C | T | 4 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-515G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962290 | |||||||
| chr1:156962312 | C | A | 4 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-537G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962312 | |||||||
| chr1:156962460 | C | T | 1 | a0003c0003t0003g0221 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1141-685G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962460 | |||||||
| chr1:156962772 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0272 a0001c0001t0001g0277 others(9): Show |
13 | HG01255.hp1 HG02040.hp1 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.1140+431C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962772 | |||||||
| chr1:156962842 | G | A | 1 | a0001c0001t0006g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1140+361C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962842 | |||||||
| chr1:156962862 | G | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1140+341C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962862 | |||||||
| chr1:156962878 | C | CA | 91 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0284 others(88): Show |
91 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.1140+324dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | |||||||
| chr1:156962878 | C | CAA | 20 | a0001c0001t0001g0297 a0001c0001t0001g0306 a0001c0001t0001g0309 others(17): Show |
20 | HG00438.hp1 HG00741.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.1140+323_1140+324d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | |||||||
| chr1:156962878 | CA | C | 32 | a0001c0001t0015g0207 a0002c0002t0002g0012 a0002c0002t0002g0036 others(29): Show |
32 | HG00621.hp1 HG01123.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1140+324delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | |||||||
| chr1:156962878 | CAA | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(52): Show |
58 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1140+323_1140+324d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | |||||||
| chr1:156962878 | CAAAAAAA others(6): Show |
C | 2 | a0003c0003t0003g0249 a0003c0003t0003g0250 |
2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1140+312_1140+324d others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962878 | |||||||
| chr1:156962908 | A | T | 1 | a0001c0001t0001g0275 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1140+295T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156962908 | |||||||
| chr1:156963000 | T | A | 1 | a0003c0003t0003g0258 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1140+203A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | 156963000 | |||||||
| chr1:156963355 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1039-51G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 12/40 | chr1 | 156963355 | |||||||
| chr1:156963509 | G | C | 9 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(6): Show |
9 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+11C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 12/40 | chr1 | 156963509 | |||||||
| chr1:156963775 | G | A | 2 | a0002c0004t0005g0059 a0002c0004t0005g0061 |
2 | HG02015.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.964-181C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156963775 | |||||||
| chr1:156963821 | G | T | 147 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(144): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.964-227C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156963821 | |||||||
| chr1:156964075 | C | T | 1 | a0001c0001t0003g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.964-481G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964075 | |||||||
| chr1:156964170 | A | G | 96 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(93): Show |
99 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.964-576T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964170 | |||||||
| chr1:156964356 | A | G | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.964-762T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964356 | |||||||
| chr1:156964637 | G | A | 1 | a0002c0002t0002g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.964-1043C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964637 | |||||||
| chr1:156964767 | T | C | 9 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-1173A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156964767 | |||||||
| chr1:156965101 | T | C | 147 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(144): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.964-1507A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965101 | |||||||
| chr1:156965256 | A | G | 8 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(5): Show |
8 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-1662T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965256 | |||||||
| chr1:156965310 | C | T | 3 | a0002c0002t0002g0062 a0002c0002t0002g0063 a0002c0002t0002g0064 |
3 | HG02698.hp2 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.964-1716G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965310 | |||||||
| chr1:156965340 | G | C | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.964-1746C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965340 | |||||||
| chr1:156965437 | C | A | 1 | a0002c0002t0002g0069 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.964-1843G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965437 | |||||||
| chr1:156965576 | T | C | 1 | a0002c0002t0002g0069 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.964-1982A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965576 | |||||||
| chr1:156965650 | G | A | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.964-2056C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965650 | |||||||
| chr1:156965697 | G | C | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.964-2103C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965697 | |||||||
| chr1:156965717 | G | C | 1 | a0001c0001t0015g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.964-2123C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156965717 | |||||||
| chr1:156966201 | T | C | 1 | a0001c0001t0007g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.963+1786A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966201 | |||||||
| chr1:156966252 | A | C | 3 | a0001c0005t0001g0278 a0001c0005t0001g0281 a0001c0005t0001g0287 |
3 | HG01928.hp2 HG01943.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.963+1735T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966252 | |||||||
| chr1:156966490 | T | C | 116 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(113): Show |
120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.963+1497A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966490 | |||||||
| chr1:156966624 | A | C | 1 | a0001c0001t0007g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.963+1363T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966624 | |||||||
| chr1:156966868 | T | C | 18 | a0002c0004t0005g0059 a0002c0004t0005g0061 a0002c0004t0005g0114 others(15): Show |
19 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+1119A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966868 | |||||||
| chr1:156966904 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.963+1083C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156966904 | |||||||
| chr1:156967139 | A | G | 11 | a0002c0004t0008g0193 a0002c0004t0008g0194 a0002c0004t0008g0195 others(8): Show |
11 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+848T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967139 | |||||||
| chr1:156967184 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+803T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967184 | |||||||
| chr1:156967322 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+665C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967322 | |||||||
| chr1:156967399 | T | C | 2 | a0002c0004t0014g0205 a0002c0004t0014g0206 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.963+588A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967399 | |||||||
| chr1:156967500 | C | T | 3 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 |
3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.963+487G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967500 | |||||||
| chr1:156967653 | C | T | 2 | a0002c0004t0005g0016 a0002c0004t0005g0022 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.963+334G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967653 | |||||||
| chr1:156967781 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.963+206A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 11/40 | chr1 | 156967781 | |||||||
| chr1:156968243 | C | T | 1 | a0003c0003t0003g0226 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.826-119G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968243 | |||||||
| chr1:156968548 | AT | A | 95 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(92): Show |
98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.826-425delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968548 | |||||||
| chr1:156968775 | C | T | 3 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 |
3 | HG00741.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.825+507G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968775 | |||||||
| chr1:156968918 | C | T | 7 | a0001c0001t0001g0304 a0002c0004t0005g0017 a0002c0004t0005g0028 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.825+364G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968918 | |||||||
| chr1:156968969 | T | C | 1 | a0001c0001t0001g0334 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.825+313A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156968969 | |||||||
| chr1:156969039 | C | T | 2 | a0002c0004t0005g0016 a0002c0004t0005g0022 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.825+243G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156969039 | |||||||
| chr1:156969085 | G | T | 1 | a0002c0002t0002g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.825+197C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156969085 | |||||||
| chr1:156969275 | G | A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(77): Show |
83 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(80): Show |
splice_region_variant&intron_variant | LOW | c.825+7C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 10/40 | chr1 | 156969275 | |||||||
| chr1:156969379 | A | G | 23 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(20): Show |
24 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.749-21T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969379 | |||||||
| chr1:156969383 | C | T | 275 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(272): Show |
283 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.749-25G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969383 | |||||||
| chr1:156969516 | C | T | 1 | a0002c0004t0033g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.749-158G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969516 | |||||||
| chr1:156969929 | G | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.748+69C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969929 | |||||||
| chr1:156969991 | G | T | 1 | a0003c0003t0003g0007 | 2 | HG01167.hp2 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.748+7C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 9/40 | chr1 | 156969991 | |||||||
| chr1:156970385 | G | A | 1 | a0002c0004t0005g0131 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.703-342C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970385 | |||||||
| chr1:156970454 | T | C | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-411A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970454 | |||||||
| chr1:156970533 | A | G | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.703-490T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970533 | |||||||
| chr1:156970602 | A | G | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703-559T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970602 | |||||||
| chr1:156970785 | A | G | 8 | a0002c0004t0018g0244 a0002c0004t0018g0246 a0002c0004t0018g0247 others(5): Show |
8 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-742T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156970785 | |||||||
| chr1:156971304 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.702+393C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156971304 | |||||||
| chr1:156971620 | T | G | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.702+77A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 8/40 | chr1 | 156971620 | |||||||
| chr1:156971920 | C | T | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-104G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156971920 | |||||||
| chr1:156972232 | G | A | 1 | a0001c0001t0007g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.583-416C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972232 | |||||||
| chr1:156972244 | C | T | 5 | a0002c0004t0005g0016 a0002c0004t0005g0022 a0003c0003t0019g0351 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.583-428G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972244 | |||||||
| chr1:156972344 | T | C | 1 | a0002c0008t0002g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.583-528A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972344 | |||||||
| chr1:156972363 | C | T | 1 | a0003c0003t0003g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.583-547G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972363 | |||||||
| chr1:156972436 | C | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(85): Show |
90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.583-620G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972436 | |||||||
| chr1:156972835 | A | AC | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.583-1020dupG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156972835 | |||||||
| chr1:156973181 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.583-1365C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973181 | |||||||
| chr1:156973330 | C | T | 1 | a0001c0001t0015g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.583-1514G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973330 | |||||||
| chr1:156973395 | T | C | 2 | a0003c0003t0003g0228 a0003c0003t0031g0222 |
2 | HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.583-1579A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973395 | |||||||
| chr1:156973509 | C | T | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1693G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973509 | |||||||
| chr1:156973512 | A | T | 9 | a0001c0001t0007g0143 a0001c0001t0007g0144 a0001c0001t0007g0145 others(6): Show |
9 | HG01243.hp1 HG02004.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.583-1696T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973512 | |||||||
| chr1:156973620 | C | T | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.583-1804G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973620 | |||||||
| chr1:156973778 | T | C | 1 | a0002c0004t0033g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.583-1962A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973778 | |||||||
| chr1:156973884 | C | A | 1 | a0001c0001t0001g0339 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.583-2068G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973884 | |||||||
| chr1:156973890 | G | A | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-2074C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973890 | |||||||
| chr1:156973933 | T | C | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.583-2117A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156973933 | |||||||
| chr1:156974027 | A | G | 5 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(2): Show |
5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.583-2211T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974027 | |||||||
| chr1:156974090 | G | A | 1 | a0002c0002t0012g0191 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.583-2274C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974090 | |||||||
| chr1:156974385 | G | A | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-2569C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974385 | |||||||
| chr1:156974407 | T | C | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.582+2576A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974407 | |||||||
| chr1:156974578 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0304 |
2 | HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.582+2405G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974578 | |||||||
| chr1:156974590 | G | C | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.582+2393C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974590 | |||||||
| chr1:156974650 | G | A | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.582+2333C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974650 | |||||||
| chr1:156974668 | T | C | 9 | a0001c0001t0001g0275 a0001c0001t0004g0006 a0001c0001t0004g0160 others(6): Show |
10 | HG01070.hp2 HG01346.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.582+2315A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974668 | |||||||
| chr1:156974760 | G | A | 4 | a0002c0004t0005g0016 a0003c0003t0019g0351 a0003c0003t0019g0352 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+2223C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974760 | |||||||
| chr1:156974885 | G | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.582+2098C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974885 | |||||||
| chr1:156974991 | T | G | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.582+1992A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156974991 | |||||||
| chr1:156975211 | C | T | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+1772G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975211 | |||||||
| chr1:156975290 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.582+1693A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975290 | |||||||
| chr1:156975302 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0276 a0001c0001t0001g0315 others(1): Show |
5 | NA18949.hp2 NA18973.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+1681A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975302 | |||||||
| chr1:156975570 | A | T | 1 | a0002c0002t0002g0074 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.582+1413T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975570 | |||||||
| chr1:156975578 | G | T | 15 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(12): Show |
15 | HG00408.hp2 HG02723.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.582+1405C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975578 | |||||||
| chr1:156975642 | T | C | 5 | a0002c0004t0005g0016 a0002c0004t0005g0022 a0003c0003t0019g0351 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.582+1341A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975642 | |||||||
| chr1:156975701 | C | T | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.582+1282G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975701 | |||||||
| chr1:156975892 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.582+1091G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975892 | |||||||
| chr1:156975916 | C | G | 213 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(210): Show |
219 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.582+1067G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156975916 | |||||||
| chr1:156976134 | C | T | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.582+849G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976134 | |||||||
| chr1:156976197 | T | G | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.582+786A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976197 | |||||||
| chr1:156976258 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.582+725T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976258 | |||||||
| chr1:156976307 | T | C | 287 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(284): Show |
295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.582+676A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976307 | |||||||
| chr1:156976754 | T | A | 1 | a0001c0001t0004g0161 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.582+229A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976754 | |||||||
| chr1:156976797 | G | A | 1 | a0002c0002t0024g0011 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.582+186C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976797 | |||||||
| chr1:156976848 | C | A | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.582+135G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 7/40 | chr1 | 156976848 | |||||||
| chr1:156977106 | T | G | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.511-52A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977106 | |||||||
| chr1:156977203 | T | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.511-149A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977203 | |||||||
| chr1:156977499 | A | G | 214 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(211): Show |
220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.511-445T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977499 | |||||||
| chr1:156977566 | C | A | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.511-512G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977566 | |||||||
| chr1:156977717 | A | G | 2 | a0002c0002t0002g0049 a0002c0002t0002g0056 |
2 | NA18952.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.510+487T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977717 | |||||||
| chr1:156977756 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510+448A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156977756 | |||||||
| chr1:156978110 | C | T | 2 | a0002c0004t0005g0017 a0002c0004t0005g0025 |
2 | HG01433.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+94G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978110 | |||||||
| chr1:156978136 | T | C | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.510+68A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978136 | |||||||
| chr1:156978161 | A | T | 87 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(84): Show |
90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.510+43T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978161 | |||||||
| chr1:156978164 | G | C | 5 | a0002c0004t0005g0016 a0002c0004t0005g0022 a0003c0003t0019g0351 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+40C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 6/40 | chr1 | 156978164 | |||||||
| chr1:156978448 | G | A | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-66C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978448 | |||||||
| chr1:156978450 | A | G | 5 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 others(2): Show |
5 | HG03041.hp1 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-68T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978450 | |||||||
| chr1:156978465 | C | T | 1 | a0007c0014t0014g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.332-83G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978465 | |||||||
| chr1:156978700 | T | C | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.332-318A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978700 | |||||||
| chr1:156978716 | A | G | 1 | a0002c0004t0009g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.332-334T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978716 | |||||||
| chr1:156978838 | C | T | 1 | a0001c0001t0003g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.331+391G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156978838 | |||||||
| chr1:156979088 | C | A | 113 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0115 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.331+141G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156979088 | |||||||
| chr1:156979164 | CCCT | C | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.331+62_331+64delAG others(1): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 5/40 | chr1 | 156979164 | |||||||
| chr1:156979361 | C | CT | 95 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(92): Show |
98 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.274-76dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | |||||||
| chr1:156979361 | C | CTT | 72 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0004g0005 others(69): Show |
74 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.274-77_274-76dupAA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | |||||||
| chr1:156979361 | C | CTTT | 8 | a0001c0001t0001g0275 a0001c0001t0004g0153 a0001c0001t0004g0178 others(5): Show |
8 | HG01175.hp2 HG02148.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-78_274-76dupAA others(1): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | |||||||
| chr1:156979361 | CT | C | 84 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0270 others(81): Show |
86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.274-76delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | |||||||
| chr1:156979361 | CTTTT | C | 14 | a0002c0004t0005g0114 a0002c0004t0005g0116 a0002c0004t0005g0120 others(11): Show |
15 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-79_274-76delAA others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979361 | |||||||
| chr1:156979406 | C | T | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-120G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979406 | |||||||
| chr1:156979555 | G | A | 4 | a0002c0004t0013g0184 a0002c0004t0013g0185 a0002c0004t0013g0188 others(1): Show |
4 | HG02145.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-269C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979555 | |||||||
| chr1:156979606 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.274-320G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979606 | |||||||
| chr1:156979610 | C | T | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-324G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979610 | |||||||
| chr1:156979655 | C | T | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(95): Show |
100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.274-369G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979655 | |||||||
| chr1:156979921 | T | C | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.273+516A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979921 | |||||||
| chr1:156979946 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.273+491G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | 156979946 | |||||||
| chr1:156980603 | A | G | 1 | a0002c0002t0011g0081 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.224-117T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980603 | |||||||
| chr1:156980603 | A | T | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-117T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980603 | |||||||
| chr1:156980791 | G | A | 36 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(33): Show |
38 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.224-305C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980791 | |||||||
| chr1:156980833 | C | CG | 34 | a0001c0001t0004g0005 a0001c0001t0004g0137 a0001c0001t0004g0141 others(31): Show |
35 | HG01071.hp1 HG01192.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.224-348dupC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | |||||||
| chr1:156980833 | C | CGG | 20 | a0001c0001t0004g0179 a0001c0001t0004g0180 a0001c0001t0007g0144 others(17): Show |
20 | HG01099.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.224-349_224-348dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | |||||||
| chr1:156980833 | C | CGGGGGGG others(4): Show |
2 | a0001c0001t0004g0133 a0002c0004t0022g0134 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.224-358_224-348dup others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | |||||||
| chr1:156980833 | CG | C | 20 | a0001c0001t0001g0282 a0001c0001t0001g0292 a0001c0001t0001g0296 others(17): Show |
20 | HG00639.hp1 HG01255.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-348delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | |||||||
| chr1:156980833 | CGG | C | 85 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(82): Show |
87 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.224-349_224-348del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | |||||||
| chr1:156980833 | CGGGG | C | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-351_224-348del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980833 | |||||||
| chr1:156980847 | GA | G | 11 | a0002c0002t0002g0035 a0002c0002t0002g0036 a0002c0002t0002g0038 others(8): Show |
11 | HG00642.hp2 HG02071.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-362delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980847 | |||||||
| chr1:156980847 | GAA | G | 68 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.224-363_224-362del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980847 | |||||||
| chr1:156980848 | A | G | 9 | a0001c0001t0004g0133 a0002c0002t0002g0047 a0002c0002t0002g0066 others(6): Show |
9 | HG00621.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-362T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980848 | |||||||
| chr1:156980849 | A | G | 18 | a0001c0001t0004g0133 a0002c0002t0002g0035 a0002c0002t0002g0036 others(15): Show |
18 | HG00621.hp1 HG00642.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.224-363T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980849 | |||||||
| chr1:156980864 | T | G | 5 | a0002c0002t0002g0103 a0002c0002t0002g0104 a0002c0002t0002g0105 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-378A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980864 | |||||||
| chr1:156980991 | C | A | 214 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(211): Show |
220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.224-505G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156980991 | |||||||
| chr1:156981003 | A | G | 83 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(80): Show |
86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.224-517T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981003 | |||||||
| chr1:156981121 | T | G | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-635A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981121 | |||||||
| chr1:156981200 | TA | T | 21 | a0001c0001t0001g0294 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.224-715delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981200 | |||||||
| chr1:156981212 | A | T | 1 | a0002c0004t0014g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-726T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981212 | |||||||
| chr1:156981212 | AT | A | 90 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(87): Show |
93 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.224-727delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981212 | |||||||
| chr1:156981213 | T | A | 3 | a0002c0002t0002g0064 a0002c0002t0002g0068 a0002c0002t0002g0099 |
3 | HG02129.hp2 HG03927.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.224-727A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981213 | |||||||
| chr1:156981214 | T | A | 92 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(89): Show |
95 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.224-728A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981214 | |||||||
| chr1:156981270 | T | C | 5 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(2): Show |
5 | HG02723.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-784A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981270 | |||||||
| chr1:156981366 | C | A | 2 | a0001c0001t0004g0179 a0001c0001t0004g0180 |
2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.224-880G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981366 | |||||||
| chr1:156981535 | G | A | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-1049C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981535 | |||||||
| chr1:156981579 | T | C | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.224-1093A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981579 | |||||||
| chr1:156981583 | C | CCTCCCAT others(8): Show |
1 | a0002c0002t0002g0099 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.224-1112_224-1098d others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981583 | |||||||
| chr1:156981944 | A | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.224-1458T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156981944 | |||||||
| chr1:156982050 | TA | T | 3 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 |
3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.224-1565delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982050 | |||||||
| chr1:156982172 | G | A | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-1686C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982172 | |||||||
| chr1:156982262 | C | A | 113 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0115 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.224-1776G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982262 | |||||||
| chr1:156982334 | C | T | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-1848G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982334 | |||||||
| chr1:156982350 | A | G | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.224-1864T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982350 | |||||||
| chr1:156982455 | T | A | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.223+1884A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982455 | |||||||
| chr1:156982625 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.223+1714G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156982625 | |||||||
| chr1:156983267 | G | A | 1 | a0009c0012t0003g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.223+1072C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983267 | |||||||
| chr1:156983282 | G | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.223+1057C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983282 | |||||||
| chr1:156983700 | G | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+639C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983700 | |||||||
| chr1:156983777 | A | G | 1 | a0002c0002t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.223+562T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983777 | |||||||
| chr1:156983928 | A | G | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.223+411T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156983928 | |||||||
| chr1:156984051 | G | A | 1 | a0002c0002t0002g0099 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.223+288C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156984051 | |||||||
| chr1:156984088 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.223+251G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | 156984088 | |||||||
| chr1:156984475 | C | T | 225 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(222): Show |
231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.125-38G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984475 | |||||||
| chr1:156984571 | C | A | 1 | a0002c0002t0002g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125-134G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984571 | |||||||
| chr1:156984576 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.125-139G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984576 | |||||||
| chr1:156984592 | T | C | 214 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(211): Show |
220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.125-155A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984592 | |||||||
| chr1:156984611 | T | C | 1 | a0002c0004t0005g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.125-174A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984611 | |||||||
| chr1:156984641 | T | C | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.125-204A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984641 | |||||||
| chr1:156984689 | T | C | 15 | a0002c0004t0005g0114 a0002c0004t0005g0116 a0002c0004t0005g0120 others(12): Show |
16 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-252A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984689 | |||||||
| chr1:156984764 | C | T | 1 | a0002c0004t0033g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.125-327G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984764 | |||||||
| chr1:156984799 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.125-362G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156984799 | |||||||
| chr1:156985289 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.124+793A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985289 | |||||||
| chr1:156985487 | G | A | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.124+595C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985487 | |||||||
| chr1:156985492 | C | T | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.124+590G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985492 | |||||||
| chr1:156985515 | C | G | 7 | a0001c0001t0007g0143 a0001c0001t0007g0144 a0001c0001t0007g0145 others(4): Show |
7 | HG01243.hp1 HG02071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+567G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985515 | |||||||
| chr1:156985545 | T | A | 1 | a0001c0001t0004g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124+537A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985545 | |||||||
| chr1:156985730 | C | CT | 168 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(165): Show |
173 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.124+351dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985730 | |||||||
| chr1:156985748 | T | A | 3 | a0003c0003t0003g0257 a0003c0003t0003g0264 a0003c0003t0003g0267 |
3 | NA18948.hp2 NA18960.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.124+334A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985748 | |||||||
| chr1:156985749 | A | T | 1 | a0001c0001t0001g0331 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+333T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156985749 | |||||||
| chr1:156986001 | T | C | 5 | a0002c0002t0011g0079 a0002c0002t0011g0080 a0002c0002t0011g0081 others(2): Show |
5 | NA18960.hp2 NA18998.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+81A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156986001 | |||||||
| chr1:156986077 | G | T | 1 | a0001c0001t0001g0337 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.124+5C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 2/40 | chr1 | 156986077 | |||||||
| chr1:156986197 | T | C | 1 | a0001c0001t0007g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-24A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986197 | |||||||
| chr1:156986265 | T | C | 85 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(82): Show |
87 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.33-92A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986265 | |||||||
| chr1:156986326 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-153A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986326 | |||||||
| chr1:156986469 | G | A | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-296C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986469 | |||||||
| chr1:156986554 | G | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0020g0168 others(1): Show |
4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-381C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986554 | |||||||
| chr1:156986566 | G | A | 113 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0115 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-393C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986566 | |||||||
| chr1:156986736 | C | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-563G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986736 | |||||||
| chr1:156986839 | T | C | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-666A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986839 | |||||||
| chr1:156986889 | T | C | 4 | a0002c0004t0005g0016 a0003c0003t0019g0351 a0003c0003t0019g0352 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-716A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986889 | |||||||
| chr1:156986946 | C | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-773G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156986946 | |||||||
| chr1:156987240 | T | C | 33 | a0001c0001t0001g0275 a0001c0001t0004g0005 a0001c0001t0004g0006 others(30): Show |
35 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-1067A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987240 | |||||||
| chr1:156987450 | A | T | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-1277T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987450 | |||||||
| chr1:156987559 | G | T | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-1386C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987559 | |||||||
| chr1:156987613 | T | G | 1 | a0001c0001t0020g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.33-1440A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156987613 | |||||||
| chr1:156988272 | C | T | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-2099G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988272 | |||||||
| chr1:156988306 | C | T | 3 | a0002c0002t0002g0097 a0002c0002t0002g0100 a0002c0008t0002g0072 |
3 | HG02735.hp2 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.33-2133G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988306 | |||||||
| chr1:156988555 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-2382A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988555 | |||||||
| chr1:156988680 | G | A | 14 | a0001c0001t0004g0005 a0001c0001t0004g0153 a0001c0001t0004g0154 others(11): Show |
15 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.33-2507C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988680 | |||||||
| chr1:156988718 | T | G | 1 | a0002c0002t0002g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-2545A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988718 | |||||||
| chr1:156988833 | G | A | 20 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(17): Show |
21 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-2660C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156988833 | |||||||
| chr1:156989015 | G | C | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-2842C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989015 | |||||||
| chr1:156989129 | G | C | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(95): Show |
100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.33-2956C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989129 | |||||||
| chr1:156989132 | G | A | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-2959C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989132 | |||||||
| chr1:156989141 | C | T | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-2968G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989141 | |||||||
| chr1:156989330 | T | G | 1 | a0002c0004t0014g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.33-3157A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989330 | |||||||
| chr1:156989656 | T | C | 2 | a0002c0004t0005g0123 a0002c0004t0025g0124 |
2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.33-3483A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989656 | |||||||
| chr1:156989727 | C | T | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-3554G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989727 | |||||||
| chr1:156989735 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-3562T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989735 | |||||||
| chr1:156989804 | G | A | 2 | a0002c0004t0005g0109 a0002c0004t0026g0110 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33-3631C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989804 | |||||||
| chr1:156989888 | T | C | 2 | a0002c0002t0011g0081 a0002c0002t0011g0082 |
2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.33-3715A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156989888 | |||||||
| chr1:156990121 | G | A | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-3948C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990121 | |||||||
| chr1:156990123 | C | A | 2 | a0002c0002t0002g0085 a0002c0002t0002g0086 |
2 | HG02040.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.33-3950G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990123 | |||||||
| chr1:156990277 | T | A | 1 | a0002c0002t0012g0190 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.33-4104A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990277 | |||||||
| chr1:156990340 | T | C | 1 | a0002c0002t0016g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33-4167A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990340 | |||||||
| chr1:156990472 | A | G | 1 | a0003c0003t0003g0238 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.33-4299T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990472 | |||||||
| chr1:156990476 | C | T | 1 | a0002c0002t0002g0065 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.33-4303G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990476 | |||||||
| chr1:156990497 | C | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(85): Show |
90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-4324G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990497 | |||||||
| chr1:156990613 | T | C | 2 | a0002c0002t0002g0040 a0002c0002t0002g0045 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.33-4440A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990613 | |||||||
| chr1:156990631 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG02129.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.33-4458C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990631 | |||||||
| chr1:156990699 | T | TA | 113 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-4527dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990699 | |||||||
| chr1:156990942 | T | C | 3 | a0002c0002t0017g0048 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | NA18952.hp2 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.33-4769A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156990942 | |||||||
| chr1:156991091 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-4918A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991091 | |||||||
| chr1:156991111 | G | A | 3 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0030g0208 |
3 | HG01884.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.33-4938C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991111 | |||||||
| chr1:156991350 | C | T | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-5177G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991350 | |||||||
| chr1:156991362 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0020g0168 others(1): Show |
4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-5189G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991362 | |||||||
| chr1:156991438 | G | C | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-5265C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991438 | |||||||
| chr1:156991476 | C | T | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-5303G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991476 | |||||||
| chr1:156991707 | CTTATTT | C | 11 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(8): Show |
11 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-5540_33-5535del others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991707 | |||||||
| chr1:156991710 | A | AT | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(74): Show |
79 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-5538dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | ATT | 21 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0001g0276 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-5539_33-5538dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | ATTTTTTT | 10 | a0001c0001t0006g0113 a0002c0004t0005g0116 a0002c0004t0005g0122 others(7): Show |
10 | HG00408.hp2 HG01346.hp2 HG03704.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-5544_33-5538dup others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0006g0115 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.33-5547_33-5538dup others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0006g0125 a0001c0001t0006g0128 |
2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.33-5548_33-5538dup others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0006g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.33-5549_33-5538dup others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0006g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-5550_33-5538dup others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | A | T | 1 | a0002c0004t0009g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.33-5537T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | ATTTTTTT others(3): Show |
A | 3 | a0002c0002t0017g0048 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | NA18952.hp2 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.33-5547_33-5538del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991710 | ATTTTTTT others(4): Show |
A | 90 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(87): Show |
93 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-5548_33-5538del others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991710 | |||||||
| chr1:156991715 | T | A | 3 | a0002c0004t0005g0016 a0003c0003t0019g0351 a0003c0003t0019g0352 |
3 | HG02572.hp2 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.33-5542A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991715 | |||||||
| chr1:156991719 | T | A | 1 | a0003c0003t0019g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-5546A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991719 | |||||||
| chr1:156991720 | T | A | 3 | a0002c0004t0005g0016 a0003c0003t0019g0351 a0003c0003t0019g0352 |
3 | HG02572.hp2 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.33-5547A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991720 | |||||||
| chr1:156991740 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.33-5567C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991740 | |||||||
| chr1:156991777 | C | T | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-5604G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991777 | |||||||
| chr1:156991938 | G | A | 1 | a0002c0002t0002g0099 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.33-5765C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156991938 | |||||||
| chr1:156992023 | T | C | 1 | a0002c0004t0008g0197 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-5850A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992023 | |||||||
| chr1:156992148 | G | T | 1 | a0001c0001t0001g0314 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.33-5975C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992148 | |||||||
| chr1:156992379 | T | TCCTG | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-6210_33-6207dup others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992379 | |||||||
| chr1:156992389 | T | C | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-6216A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992389 | |||||||
| chr1:156992399 | G | T | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-6226C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992399 | |||||||
| chr1:156992414 | T | G | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-6241A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992414 | |||||||
| chr1:156992509 | G | A | 5 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 others(2): Show |
5 | HG03041.hp1 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-6336C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992509 | |||||||
| chr1:156992603 | ATG | A | 126 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(123): Show |
130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.33-6432_33-6431del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992603 | |||||||
| chr1:156992615 | GTA | G | 88 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(85): Show |
90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-6444_33-6443del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992615 | |||||||
| chr1:156992927 | C | T | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-6754G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992927 | |||||||
| chr1:156992943 | C | T | 2 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.33-6770G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156992943 | |||||||
| chr1:156993304 | A | G | 5 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(2): Show |
5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-7131T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993304 | |||||||
| chr1:156993470 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.33-7297G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993470 | |||||||
| chr1:156993564 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.33-7391T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993564 | |||||||
| chr1:156993619 | G | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0020g0168 others(1): Show |
4 | HG02809.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-7446C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993619 | |||||||
| chr1:156993685 | T | C | 1 | a0002c0002t0002g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.33-7512A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993685 | |||||||
| chr1:156993722 | G | C | 1 | a0001c0001t0004g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.33-7549C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993722 | |||||||
| chr1:156993868 | T | C | 5 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(2): Show |
5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-7695A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993868 | |||||||
| chr1:156993932 | T | C | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-7759A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156993932 | |||||||
| chr1:156994082 | T | C | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-7909A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994082 | |||||||
| chr1:156994183 | G | A | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8010C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994183 | |||||||
| chr1:156994207 | A | T | 3 | a0002c0002t0002g0036 a0002c0002t0002g0043 a0002c0002t0002g0044 |
3 | HG02647.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.33-8034T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994207 | |||||||
| chr1:156994260 | C | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(97): Show |
102 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.33-8087G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994260 | |||||||
| chr1:156994386 | T | TTG | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-8215_33-8214dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994386 | |||||||
| chr1:156994392 | G | GT | 132 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0004g0005 others(129): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.33-8220dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | |||||||
| chr1:156994392 | G | GTGT | 83 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(80): Show |
86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.33-8220_33-8219ins others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | |||||||
| chr1:156994392 | G | GTT | 22 | a0001c0001t0001g0298 a0001c0001t0001g0304 a0001c0001t0004g0181 others(19): Show |
22 | HG00597.hp1 HG01255.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-8221_33-8220dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | |||||||
| chr1:156994392 | G | GTTT | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(74): Show |
79 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-8222_33-8220dup others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994392 | |||||||
| chr1:156994675 | C | A | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-8502G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994675 | |||||||
| chr1:156994784 | C | G | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-8611G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994784 | |||||||
| chr1:156994836 | AGGTAATA others(15): Show |
A | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8685_33-8664del others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994836 | |||||||
| chr1:156994859 | G | A | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8686C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994859 | |||||||
| chr1:156994990 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.33-8817G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156994990 | |||||||
| chr1:156995010 | CTT | C | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-8839_33-8838del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995010 | |||||||
| chr1:156995559 | C | CT | 23 | a0001c0001t0001g0314 a0001c0001t0006g0115 a0001c0001t0006g0125 others(20): Show |
24 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-9387dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995559 | |||||||
| chr1:156995596 | C | T | 1 | a0002c0004t0005g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33-9423G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995596 | |||||||
| chr1:156995704 | G | GT | 89 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(86): Show |
91 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.33-9532dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995704 | |||||||
| chr1:156995722 | T | TA | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0333 |
3 | NA18995.hp1 NA19062.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.33-9550dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156995722 | |||||||
| chr1:156996153 | C | A | 1 | a0002c0002t0002g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.33-9980G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996153 | |||||||
| chr1:156996156 | A | G | 113 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0115 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-9983T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996156 | |||||||
| chr1:156996634 | G | A | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-10461C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996634 | |||||||
| chr1:156996645 | C | T | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-10472G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996645 | |||||||
| chr1:156996653 | G | A | 6 | a0002c0002t0002g0037 a0002c0002t0002g0040 a0002c0002t0002g0041 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-10480C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996653 | |||||||
| chr1:156996689 | C | T | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.33-10516G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996689 | |||||||
| chr1:156996705 | G | A | 4 | a0002c0004t0005g0016 a0003c0003t0019g0351 a0003c0003t0019g0352 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-10532C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996705 | |||||||
| chr1:156996766 | C | T | 5 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-10593G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996766 | |||||||
| chr1:156996772 | C | CA | 57 | a0001c0001t0001g0009 a0001c0001t0001g0274 a0001c0001t0001g0276 others(54): Show |
58 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.33-10600dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996772 | C | CAA | 9 | a0001c0001t0001g0272 a0001c0001t0001g0277 a0001c0001t0001g0282 others(6): Show |
9 | HG02040.hp1 HG02132.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-10601_33-10600d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996772 | C | CAAA | 64 | a0001c0001t0001g0008 a0001c0001t0004g0133 a0001c0001t0006g0094 others(61): Show |
68 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-10602_33-10600d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996772 | C | CAAAA | 23 | a0001c0001t0001g0340 a0002c0002t0002g0041 a0002c0002t0002g0042 others(20): Show |
23 | HG00642.hp2 HG01175.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-10603_33-10600d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996772 | C | CAAAAA | 9 | a0001c0001t0001g0341 a0002c0002t0002g0053 a0002c0002t0002g0074 others(6): Show |
9 | HG00741.hp2 HG01433.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-10604_33-10600d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996772 | CA | C | 6 | a0001c0001t0004g0171 a0002c0004t0005g0013 a0002c0004t0005g0014 others(3): Show |
6 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-10600delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996772 | CAAAAA | C | 19 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(16): Show |
20 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-10604_33-10600d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996772 | |||||||
| chr1:156996794 | AG | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0295 a0001c0001t0001g0338 |
3 | HG02273.hp1 HG02523.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.33-10622delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996794 | |||||||
| chr1:156996795 | G | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(77): Show |
82 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.33-10622C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996795 | |||||||
| chr1:156996797 | C | A | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.33-10624G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996797 | |||||||
| chr1:156996808 | A | G | 113 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0115 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-10635T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996808 | |||||||
| chr1:156996859 | A | ATT | 21 | a0001c0001t0001g0269 a0001c0001t0001g0302 a0001c0001t0001g0320 others(18): Show |
22 | HG00408.hp2 HG01167.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-10688_33-10687d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | |||||||
| chr1:156996859 | A | ATTT | 84 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0270 others(81): Show |
86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.33-10689_33-10687d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | |||||||
| chr1:156996859 | A | ATTTT | 12 | a0001c0001t0001g0276 a0001c0001t0001g0307 a0001c0001t0001g0309 others(9): Show |
12 | HG00621.hp2 HG01361.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-10690_33-10687d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | |||||||
| chr1:156996859 | AT | A | 85 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.33-10687delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996859 | |||||||
| chr1:156996948 | A | G | 1 | a0003c0003t0003g0221 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33-10775T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996948 | |||||||
| chr1:156996973 | C | T | 8 | a0002c0002t0016g0232 a0002c0002t0016g0233 a0002c0002t0016g0253 others(5): Show |
8 | HG02523.hp1 NA18944.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-10800G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996973 | |||||||
| chr1:156996984 | C | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-10811G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156996984 | |||||||
| chr1:156997038 | A | T | 19 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(16): Show |
20 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-10865T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997038 | |||||||
| chr1:156997039 | T | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0272 a0001c0001t0001g0277 others(7): Show |
11 | HG02040.hp1 HG03704.hp1 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-10866A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997039 | |||||||
| chr1:156997313 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-11140A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997313 | |||||||
| chr1:156997544 | C | A | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-11371G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997544 | |||||||
| chr1:156997550 | G | A | 1 | a0001c0001t0020g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-11377C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997550 | |||||||
| chr1:156997609 | C | T | 1 | a0002c0002t0002g0055 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.33-11436G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997609 | |||||||
| chr1:156997685 | A | T | 4 | a0001c0001t0007g0143 a0001c0001t0007g0146 a0001c0001t0007g0149 others(1): Show |
4 | HG02071.hp2 HG02738.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-11512T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997685 | |||||||
| chr1:156997747 | G | GA | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11575dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997747 | |||||||
| chr1:156997852 | AT | A | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11680delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997852 | |||||||
| chr1:156997892 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.33-11719G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156997892 | |||||||
| chr1:156998031 | C | CAG | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-11860_33-11859d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998031 | |||||||
| chr1:156998123 | G | A | 3 | a0001c0001t0004g0138 a0001c0001t0004g0140 a0001c0001t0004g0181 |
3 | NA18977.hp1 NA19000.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.33-11950C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998123 | |||||||
| chr1:156998151 | G | A | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(95): Show |
100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.33-11978C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998151 | |||||||
| chr1:156998330 | T | C | 4 | a0002c0004t0013g0184 a0002c0004t0013g0185 a0002c0004t0013g0188 others(1): Show |
4 | HG02145.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-12157A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998330 | |||||||
| chr1:156998488 | C | T | 8 | a0002c0002t0016g0232 a0002c0002t0016g0233 a0002c0002t0016g0253 others(5): Show |
8 | HG02523.hp1 NA18944.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-12315G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998488 | |||||||
| chr1:156998506 | T | A | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-12333A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998506 | |||||||
| chr1:156998776 | C | T | 87 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(84): Show |
90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.33-12603G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998776 | |||||||
| chr1:156998908 | G | A | 3 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 |
3 | HG00741.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.33-12735C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998908 | |||||||
| chr1:156998953 | A | T | 87 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(84): Show |
90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.33-12780T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156998953 | |||||||
| chr1:156999055 | G | A | 1 | a0002c0002t0002g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.33-12882C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999055 | |||||||
| chr1:156999058 | C | A | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-12885G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999058 | |||||||
| chr1:156999101 | A | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-12928T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999101 | |||||||
| chr1:156999266 | T | A | 59 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(56): Show |
61 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-13093A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999266 | |||||||
| chr1:156999274 | A | G | 3 | a0002c0004t0005g0108 a0002c0004t0005g0109 a0002c0004t0026g0110 |
3 | HG03209.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.33-13101T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999274 | |||||||
| chr1:156999281 | G | A | 1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-13108C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999281 | |||||||
| chr1:156999302 | A | G | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-13129T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999302 | |||||||
| chr1:156999710 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0334 |
2 | NA18947.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.33-13537C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999710 | |||||||
| chr1:156999718 | T | C | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13545A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999718 | |||||||
| chr1:156999811 | A | G | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-13638T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999811 | |||||||
| chr1:156999815 | C | A | 1 | a0001c0001t0003g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-13642G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999815 | |||||||
| chr1:156999967 | C | T | 5 | a0002c0004t0009g0004 a0002c0004t0009g0117 a0002c0004t0009g0118 others(2): Show |
6 | HG00642.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-13794G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 156999967 | |||||||
| chr1:157000076 | A | G | 214 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(211): Show |
220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.33-13903T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000076 | |||||||
| chr1:157000104 | G | T | 338 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(335): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.33-13931C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000104 | |||||||
| chr1:157000108 | G | A | 6 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0300 others(3): Show |
6 | HG01361.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-13935C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000108 | |||||||
| chr1:157000154 | C | G | 214 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(211): Show |
220 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.33-13981G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000154 | |||||||
| chr1:157000252 | C | T | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(95): Show |
100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.33-14079G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000252 | |||||||
| chr1:157000253 | G | A | 1 | a0003c0003t0003g0221 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33-14080C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000253 | |||||||
| chr1:157000335 | T | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(94): Show |
99 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.33-14162A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000335 | |||||||
| chr1:157000343 | A | G | 1 | a0001c0001t0006g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-14170T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000343 | |||||||
| chr1:157000545 | A | G | 2 | a0002c0004t0005g0024 a0002c0004t0005g0026 |
2 | HG02683.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.33-14372T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000545 | |||||||
| chr1:157000648 | G | A | 3 | a0002c0002t0002g0052 a0002c0002t0002g0053 a0002c0002t0002g0054 |
3 | HG00741.hp2 HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.33-14475C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000648 | |||||||
| chr1:157000803 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-14630G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000803 | |||||||
| chr1:157000961 | G | A | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-14788C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157000961 | |||||||
| chr1:157001183 | G | A | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-15010C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001183 | |||||||
| chr1:157001368 | T | C | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-15195A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001368 | |||||||
| chr1:157001485 | C | T | 1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-15312G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001485 | |||||||
| chr1:157001551 | T | A | 1 | a0002c0002t0016g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33-15378A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001551 | |||||||
| chr1:157001815 | G | T | 93 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(90): Show |
96 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.33-15642C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001815 | |||||||
| chr1:157001875 | G | A | 10 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(7): Show |
10 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-15702C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001875 | |||||||
| chr1:157001995 | C | T | 1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-15822G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157001995 | |||||||
| chr1:157002189 | T | C | 287 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(284): Show |
295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.33-16016A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002189 | |||||||
| chr1:157002269 | G | C | 1 | a0002c0004t0009g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.33-16096C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002269 | |||||||
| chr1:157002295 | A | G | 2 | a0001c0001t0001g0313 a0001c0001t0034g0342 |
2 | HG00438.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.33-16122T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002295 | |||||||
| chr1:157002354 | C | G | 4 | a0001c0001t0001g0286 a0001c0005t0001g0278 a0001c0005t0001g0281 others(1): Show |
4 | HG00609.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-16181G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002354 | |||||||
| chr1:157002588 | T | C | 10 | a0001c0001t0004g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(7): Show |
10 | HG01243.hp1 HG02004.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-16415A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002588 | |||||||
| chr1:157002613 | T | G | 1 | a0002c0002t0002g0001 | 2 | NA18970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.33-16440A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002613 | |||||||
| chr1:157002626 | C | G | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-16453G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002626 | |||||||
| chr1:157002675 | T | C | 287 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(284): Show |
295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.33-16502A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002675 | |||||||
| chr1:157002686 | A | G | 287 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(284): Show |
295 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.33-16513T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002686 | |||||||
| chr1:157002693 | C | T | 59 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(56): Show |
61 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-16520G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002693 | |||||||
| chr1:157002745 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-16572A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002745 | |||||||
| chr1:157002766 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-16593A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002766 | |||||||
| chr1:157002942 | A | G | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02698.hp1 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.33-16769T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157002942 | |||||||
| chr1:157003068 | T | G | 1 | a0002c0002t0002g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.33-16895A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003068 | |||||||
| chr1:157003104 | A | G | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-16931T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003104 | |||||||
| chr1:157003372 | C | G | 1 | a0002c0004t0005g0130 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.33-17199G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003372 | |||||||
| chr1:157003485 | T | C | 1 | a0003c0003t0003g0211 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.33-17312A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003485 | |||||||
| chr1:157003704 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.33-17531G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003704 | |||||||
| chr1:157003974 | G | A | 1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-17801C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157003974 | |||||||
| chr1:157004153 | C | T | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.33-17980G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004153 | |||||||
| chr1:157004234 | G | A | 2 | a0002c0002t0002g0001 a0002c0002t0023g0010 |
3 | NA18966.hp2 NA18970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.33-18061C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004234 | |||||||
| chr1:157004530 | C | T | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-18357G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004530 | |||||||
| chr1:157004613 | C | T | 4 | a0002c0004t0005g0013 a0002c0004t0005g0015 a0002c0004t0005g0031 others(1): Show |
4 | HG00741.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-18440G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004613 | |||||||
| chr1:157004625 | C | G | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.33-18452G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004625 | |||||||
| chr1:157004824 | C | A | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.33-18651G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004824 | |||||||
| chr1:157004829 | C | A | 1 | a0002c0002t0012g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.33-18656G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004829 | |||||||
| chr1:157004831 | A | G | 88 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(85): Show |
90 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-18658T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004831 | |||||||
| chr1:157004940 | G | T | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.33-18767C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157004940 | |||||||
| chr1:157005204 | C | G | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.33-19031G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005204 | |||||||
| chr1:157005209 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.33-19036G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005209 | |||||||
| chr1:157005230 | T | A | 64 | a0001c0001t0032g0255 a0002c0002t0016g0232 a0002c0002t0016g0233 others(61): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.33-19057A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005230 | |||||||
| chr1:157005838 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.33-19665G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005838 | |||||||
| chr1:157005918 | C | G | 3 | a0003c0003t0019g0351 a0003c0003t0019g0352 a0003c0003t0019g0353 |
3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.33-19745G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157005918 | |||||||
| chr1:157006015 | C | T | 252 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(249): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.33-19842G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006015 | |||||||
| chr1:157006157 | T | A | 1 | a0002c0002t0002g0069 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.33-19984A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006157 | |||||||
| chr1:157006277 | A | G | 232 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(229): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.33-20104T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006277 | |||||||
| chr1:157006433 | C | T | 252 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(249): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.33-20260G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006433 | |||||||
| chr1:157006440 | G | A | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-20267C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006440 | |||||||
| chr1:157006472 | C | T | 10 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(7): Show |
10 | NA18966.hp1 NA18979.hp2 NA18994.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-20299G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006472 | |||||||
| chr1:157006483 | C | CT | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-20311_33-20310i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006483 | |||||||
| chr1:157006484 | C | CG | 337 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(334): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.33-20312_33-20311i others(3): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006484 | |||||||
| chr1:157006484 | C | G | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-20311G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006484 | |||||||
| chr1:157006601 | A | C | 64 | a0001c0001t0032g0255 a0002c0002t0016g0232 a0002c0002t0016g0233 others(61): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.33-20428T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006601 | |||||||
| chr1:157006695 | A | G | 1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-20522T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006695 | |||||||
| chr1:157006772 | C | T | 1 | a0002c0002t0002g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-20599G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006772 | |||||||
| chr1:157006820 | G | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-20647C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157006820 | |||||||
| chr1:157007026 | G | A | 1 | a0003c0003t0003g0214 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.33-20853C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007026 | |||||||
| chr1:157007384 | C | T | 345 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(342): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.33-21211G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007384 | |||||||
| chr1:157007389 | T | C | 346 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(343): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.33-21216A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007389 | |||||||
| chr1:157007469 | C | A | 1 | a0002c0002t0002g0087 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.33-21296G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007469 | |||||||
| chr1:157007662 | C | T | 1 | a0006c0009t0003g0261 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.33-21489G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007662 | |||||||
| chr1:157007756 | C | T | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-21583G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007756 | |||||||
| chr1:157007899 | GT | G | 85 | a0001c0001t0001g0334 a0001c0001t0004g0133 a0001c0001t0006g0094 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.33-21727delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007899 | |||||||
| chr1:157007906 | T | G | 4 | a0002c0004t0014g0203 a0002c0004t0014g0205 a0002c0004t0014g0206 others(1): Show |
4 | HG02922.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-21733A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007906 | |||||||
| chr1:157007910 | T | G | 3 | a0003c0003t0003g0257 a0003c0003t0003g0259 a0003c0003t0003g0267 |
3 | NA18948.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.33-21737A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007910 | |||||||
| chr1:157007911 | T | G | 2 | a0002c0002t0012g0186 a0003c0003t0003g0264 |
2 | NA18948.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.33-21738A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007911 | |||||||
| chr1:157007911 | TTG | T | 164 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(161): Show |
168 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.33-21740_33-21739d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007911 | |||||||
| chr1:157007912 | T | G | 8 | a0002c0002t0002g0056 a0002c0002t0002g0074 a0002c0002t0002g0075 others(5): Show |
8 | HG00558.hp1 HG02132.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-21739A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007912 | |||||||
| chr1:157007912 | TG | T | 5 | a0002c0002t0002g0062 a0002c0002t0002g0063 a0002c0002t0002g0064 others(2): Show |
5 | HG02698.hp2 HG03927.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-21740delC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007912 | |||||||
| chr1:157007913 | G | T | 10 | a0002c0002t0002g0056 a0002c0002t0002g0074 a0002c0002t0002g0075 others(7): Show |
10 | HG00558.hp1 HG02132.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-21740C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007913 | |||||||
| chr1:157007913 | GT | G | 78 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(75): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.33-21741delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007913 | |||||||
| chr1:157007914 | T | G | 169 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(166): Show |
173 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.33-21741A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007914 | |||||||
| chr1:157007919 | T | G | 1 | a0003c0003t0003g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.33-21746A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007919 | |||||||
| chr1:157007920 | T | G | 60 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(57): Show |
62 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.33-21747A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007920 | |||||||
| chr1:157007963 | CA | C | 348 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(345): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.33-21791delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007963 | |||||||
| chr1:157007989 | T | C | 1 | a0002c0004t0005g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.33-21816A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157007989 | |||||||
| chr1:157008098 | C | T | 4 | a0001c0001t0001g0286 a0001c0005t0001g0278 a0001c0005t0001g0281 others(1): Show |
4 | HG00609.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-21925G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008098 | |||||||
| chr1:157008113 | A | G | 232 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(229): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.33-21940T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008113 | |||||||
| chr1:157008216 | C | T | 5 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(2): Show |
5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-22043G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008216 | |||||||
| chr1:157008226 | T | A | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-22053A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008226 | |||||||
| chr1:157008233 | T | G | 5 | a0002c0004t0005g0016 a0002c0004t0005g0022 a0003c0003t0019g0351 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-22060A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008233 | |||||||
| chr1:157008406 | G | GCA | 13 | a0001c0001t0004g0133 a0002c0002t0002g0045 a0002c0002t0002g0046 others(10): Show |
13 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-22235_33-22234d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | |||||||
| chr1:157008406 | G | GCACA | 67 | a0001c0001t0006g0094 a0002c0002t0002g0002 a0002c0002t0002g0003 others(64): Show |
69 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.33-22237_33-22234d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | |||||||
| chr1:157008406 | G | GCACACA | 9 | a0002c0002t0002g0038 a0002c0002t0002g0056 a0002c0002t0002g0070 others(6): Show |
9 | HG00558.hp1 HG02630.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-22239_33-22234d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | |||||||
| chr1:157008406 | G | GCACACAC others(7): Show |
1 | a0002c0002t0029g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.33-22247_33-22234d others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | |||||||
| chr1:157008406 | GCA | G | 95 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(92): Show |
98 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.33-22235_33-22234d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | |||||||
| chr1:157008406 | GCACA | G | 157 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(154): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.33-22237_33-22234d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008406 | |||||||
| chr1:157008523 | C | T | 2 | a0003c0003t0003g0258 a0003c0003t0003g0260 |
2 | NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.33-22350G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008523 | |||||||
| chr1:157008727 | A | C | 1 | a0002c0002t0002g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.33-22554T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157008727 | |||||||
| chr1:157009073 | C | T | 1 | a0003c0003t0003g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.33-22900G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157009073 | |||||||
| chr1:157009554 | A | G | 1 | a0002c0004t0005g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.33-23381T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157009554 | |||||||
| chr1:157009903 | C | T | 2 | a0003c0003t0003g0259 a0003c0003t0003g0267 |
2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.33-23730G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157009903 | |||||||
| chr1:157010009 | G | C | 9 | a0003c0003t0003g0230 a0003c0003t0003g0234 a0003c0003t0003g0235 others(6): Show |
9 | HG00597.hp1 NA18967.hp2 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-23836C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010009 | |||||||
| chr1:157010029 | C | G | 1 | a0001c0001t0001g0315 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.33-23856G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010029 | |||||||
| chr1:157010058 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0338 |
2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.33-23885C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010058 | |||||||
| chr1:157010080 | C | A | 4 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0140 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-23907G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010080 | |||||||
| chr1:157010094 | G | T | 1 | a0002c0002t0002g0073 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.33-23921C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010094 | |||||||
| chr1:157010197 | C | A | 1 | a0007c0014t0014g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.33-24024G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010197 | |||||||
| chr1:157010237 | T | C | 1 | a0003c0003t0003g0257 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.33-24064A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010237 | |||||||
| chr1:157010369 | C | CA | 232 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(229): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.33-24197dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010369 | |||||||
| chr1:157010488 | C | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-24315G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010488 | |||||||
| chr1:157010595 | G | C | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-24422C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010595 | |||||||
| chr1:157010597 | T | TG | 346 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(343): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.33-24425dupC | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010597 | |||||||
| chr1:157010901 | A | G | 1 | a0002c0004t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33-24728T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157010901 | |||||||
| chr1:157011045 | C | T | 253 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(250): Show |
260 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.33-24872G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011045 | |||||||
| chr1:157011193 | T | G | 1 | a0001c0001t0020g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-25020A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011193 | |||||||
| chr1:157011240 | T | C | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-25067A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011240 | |||||||
| chr1:157011359 | C | T | 346 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(343): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.33-25186G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011359 | |||||||
| chr1:157011456 | C | A | 348 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(345): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.33-25283G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011456 | |||||||
| chr1:157011493 | T | C | 3 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0207 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.33-25320A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011493 | |||||||
| chr1:157011556 | G | A | 114 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0001c0001t0006g0113 others(111): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-25383C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011556 | |||||||
| chr1:157011856 | T | C | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-25683A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011856 | |||||||
| chr1:157011857 | G | A | 2 | a0002c0002t0002g0097 a0002c0002t0002g0100 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.33-25684C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157011857 | |||||||
| chr1:157012036 | T | C | 5 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(2): Show |
5 | HG01433.hp2 HG02109.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-25863A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012036 | |||||||
| chr1:157012127 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.33-25954G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012127 | |||||||
| chr1:157012400 | G | C | 1 | a0002c0004t0005g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-26227C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012400 | |||||||
| chr1:157012838 | T | C | 6 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(3): Show |
6 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-26665A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157012838 | |||||||
| chr1:157013104 | G | A | 248 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.33-26931C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013104 | |||||||
| chr1:157013144 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.33-26971G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013144 | |||||||
| chr1:157013145 | C | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-26972G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013145 | |||||||
| chr1:157013170 | T | C | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-26997A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013170 | |||||||
| chr1:157013259 | T | TCA | 3 | a0001c0001t0001g0276 a0001c0001t0001g0282 a0002c0004t0027g0172 |
3 | HG02145.hp1 HG03831.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.33-27088_33-27087d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACA | 50 | a0001c0001t0001g0008 a0001c0001t0001g0272 a0001c0001t0001g0273 others(47): Show |
51 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACA | 19 | a0001c0001t0001g0270 a0001c0001t0001g0289 a0001c0001t0001g0290 others(16): Show |
19 | HG01074.hp1 HG01361.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0302 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
8 | HG01106.hp1 HG02074.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0269 a0001c0001t0001g0271 a0003c0003t0003g0265 |
3 | HG01099.hp1 HG01167.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(5): Show |
6 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0002c0004t0014g0203 others(3): Show |
6 | HG02723.hp1 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(7): Show |
5 | a0002c0004t0008g0198 a0002c0004t0008g0199 a0002c0004t0014g0205 others(2): Show |
5 | HG02451.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(9): Show |
11 | a0001c0001t0004g0140 a0001c0001t0004g0142 a0001c0001t0007g0165 others(8): Show |
11 | HG02004.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(11): Show |
16 | a0001c0001t0001g0335 a0001c0001t0004g0138 a0001c0001t0007g0143 others(13): Show |
16 | HG01257.hp1 HG02004.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(13): Show |
13 | a0001c0001t0004g0139 a0001c0001t0004g0181 a0001c0001t0007g0144 others(10): Show |
13 | HG01192.hp2 HG01517.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(15): Show |
6 | a0001c0001t0007g0145 a0003c0003t0003g0224 a0003c0003t0003g0250 others(3): Show |
6 | HG00099.hp1 HG02132.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(17): Show |
22 | a0001c0001t0007g0146 a0001c0001t0020g0169 a0002c0004t0008g0196 others(19): Show |
23 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(19): Show |
6 | a0002c0002t0016g0232 a0002c0002t0016g0254 a0002c0004t0013g0188 others(3): Show |
6 | HG03139.hp2 HG03540.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(21): Show |
9 | a0001c0001t0004g0170 a0002c0004t0008g0197 a0002c0004t0013g0184 others(6): Show |
9 | HG00639.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(23): Show |
5 | a0001c0001t0004g0171 a0002c0002t0016g0233 a0003c0003t0003g0234 others(2): Show |
5 | NA18906.hp2 NA19011.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(32): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(25): Show |
2 | a0003c0003t0003g0236 a0003c0003t0003g0256 |
2 | NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(34): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(31): Show |
2 | a0002c0002t0016g0253 a0003c0003t0003g0237 |
2 | NA18944.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(40): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCACACAC others(33): Show |
1 | a0003c0003t0003g0263 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.33-27087_33-27086i others(42): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(3): Show |
2 | a0001c0001t0003g0209 a0001c0001t0004g0152 |
2 | HG00323.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(5): Show |
2 | a0001c0001t0001g0275 a0001c0001t0004g0160 |
2 | NA19055.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(7): Show |
6 | a0001c0001t0004g0151 a0001c0001t0004g0153 a0001c0001t0004g0154 others(3): Show |
6 | HG01169.hp1 HG01192.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(9): Show |
3 | a0001c0001t0004g0005 a0001c0001t0004g0167 a0001c0001t0004g0176 |
4 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(11): Show |
9 | a0001c0001t0003g0210 a0001c0001t0004g0006 a0001c0001t0004g0137 others(6): Show |
10 | HG01070.hp2 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(13): Show |
4 | a0001c0001t0004g0141 a0001c0001t0004g0178 a0001c0001t0028g0183 others(1): Show |
4 | HG01928.hp1 HG02148.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-27087_33-27086i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(15): Show |
2 | a0001c0001t0004g0159 a0001c0001t0004g0164 |
2 | HG01255.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.33-27087_33-27086i others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013259 | T | TCTCACAC others(17): Show |
1 | a0001c0001t0030g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.33-27087_33-27086i others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013259 | |||||||
| chr1:157013261 | A | T | 1 | a0001c0001t0004g0166 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.33-27088T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013261 | |||||||
| chr1:157013263 | T | A | 247 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(244): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.33-27090A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | |||||||
| chr1:157013263 | T | TCACA | 49 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(46): Show |
51 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.33-27094_33-27091d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | |||||||
| chr1:157013263 | T | TCACACA | 10 | a0002c0002t0002g0003 a0002c0002t0002g0036 a0002c0002t0002g0044 others(7): Show |
11 | HG00280.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-27096_33-27091d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | |||||||
| chr1:157013263 | T | TCACACAC others(1): Show |
5 | a0002c0002t0002g0093 a0002c0002t0023g0010 a0002c0004t0005g0026 others(2): Show |
5 | HG02071.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27098_33-27091d others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | |||||||
| chr1:157013263 | T | TCACACAC others(3): Show |
4 | a0002c0002t0002g0035 a0002c0004t0005g0017 a0002c0004t0005g0024 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-27100_33-27091d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | |||||||
| chr1:157013263 | TCACACA | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-27096_33-27091d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013263 | |||||||
| chr1:157013299 | A | ACACACAC others(21): Show |
1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.33-27127_33-27126i others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(13): Show |
5 | a0002c0004t0005g0116 a0002c0004t0005g0120 a0002c0004t0005g0122 others(2): Show |
5 | HG00642.hp1 HG04204.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(22): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(11): Show |
2 | a0002c0004t0005g0130 a0002c0004t0005g0131 |
2 | HG00408.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.33-27127_33-27126i others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(9): Show |
5 | a0002c0002t0012g0191 a0002c0004t0005g0114 a0002c0004t0005g0123 others(2): Show |
5 | HG02738.hp1 NA18943.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(7): Show |
1 | a0002c0004t0009g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.33-27127_33-27126i others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(5): Show |
1 | a0002c0004t0009g0121 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-27127_33-27126i others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(3): Show |
4 | a0002c0002t0012g0190 a0002c0002t0012g0192 a0002c0004t0009g0004 others(1): Show |
5 | HG00609.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACAC others(1): Show |
4 | a0001c0001t0006g0126 a0001c0001t0006g0127 a0002c0002t0012g0186 others(1): Show |
4 | HG02735.hp2 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACACC | 3 | a0002c0002t0002g0071 a0002c0002t0002g0097 a0002c0002t0002g0100 |
3 | HG00408.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.33-27127_33-27126i others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | ACACC | 21 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0128 others(18): Show |
21 | HG00741.hp2 HG01175.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-27127_33-27126i others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013299 | A | C | 1 | a0002c0002t0002g0060 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.33-27126T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013299 | |||||||
| chr1:157013300 | C | CACACACA others(6): Show |
1 | a0001c0001t0007g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-27128_33-27127i others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | |||||||
| chr1:157013300 | C | CACACACA others(10): Show |
1 | a0001c0001t0004g0166 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.33-27128_33-27127i others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | |||||||
| chr1:157013300 | C | CACACACA others(16): Show |
1 | a0001c0001t0007g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.33-27128_33-27127i others(25): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | |||||||
| chr1:157013300 | C | CACACACA others(18): Show |
1 | a0001c0001t0007g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.33-27128_33-27127i others(27): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013300 | |||||||
| chr1:157013387 | C | T | 8 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(5): Show |
8 | HG01433.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-27214G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013387 | |||||||
| chr1:157013536 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.33-27363A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013536 | |||||||
| chr1:157013545 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-27372A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013545 | |||||||
| chr1:157013701 | G | GA | 86 | a0001c0001t0004g0133 a0001c0001t0006g0094 a0002c0002t0002g0001 others(83): Show |
89 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.33-27529dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013701 | |||||||
| chr1:157013859 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.33-27686A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013859 | |||||||
| chr1:157013913 | C | T | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(91): Show |
96 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.33-27740G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157013913 | |||||||
| chr1:157014004 | A | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(96): Show |
101 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.33-27831T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014004 | |||||||
| chr1:157014090 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.33-27917G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014090 | |||||||
| chr1:157014247 | T | G | 223 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(220): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.33-28074A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014247 | |||||||
| chr1:157014309 | A | G | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-28136T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014309 | |||||||
| chr1:157014330 | T | C | 348 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(345): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.33-28157A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014330 | |||||||
| chr1:157014658 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18955.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.33-28485G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014658 | |||||||
| chr1:157014741 | C | T | 3 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0207 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.33-28568G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014741 | |||||||
| chr1:157014934 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-28761G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157014934 | |||||||
| chr1:157015058 | G | A | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.33-28885C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015058 | |||||||
| chr1:157015125 | T | C | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-28952A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015125 | |||||||
| chr1:157015150 | A | T | 59 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(56): Show |
61 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-28977T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015150 | |||||||
| chr1:157015219 | T | C | 1 | a0002c0004t0005g0130 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.33-29046A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015219 | |||||||
| chr1:157015535 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.32+28764G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015535 | |||||||
| chr1:157015638 | G | C | 83 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(80): Show |
86 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.32+28661C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015638 | |||||||
| chr1:157015739 | C | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0304 |
2 | HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.32+28560G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157015739 | |||||||
| chr1:157016103 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+28196A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016103 | |||||||
| chr1:157016235 | T | C | 26 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(23): Show |
27 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+28064A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016235 | |||||||
| chr1:157016344 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+27955G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016344 | |||||||
| chr1:157016354 | GGATTATA others(2): Show |
G | 12 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(9): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+27936_32+27944d others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016354 | |||||||
| chr1:157016711 | T | C | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+27588A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016711 | |||||||
| chr1:157016798 | A | ATTAT | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+27497_32+27500d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016798 | |||||||
| chr1:157016798 | ATTAT | A | 310 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(307): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.32+27497_32+27500d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016798 | |||||||
| chr1:157016798 | ATTATTTA others(5): Show |
A | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+27489_32+27500d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016798 | |||||||
| chr1:157016906 | G | C | 1 | a0002c0002t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+27393C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157016906 | |||||||
| chr1:157017080 | G | A | 344 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(341): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.32+27219C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017080 | |||||||
| chr1:157017089 | A | G | 3 | a0002c0002t0002g0056 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | NA18952.hp1 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.32+27210T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017089 | |||||||
| chr1:157017121 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+27178G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017121 | |||||||
| chr1:157017306 | C | A | 1 | a0001c0001t0001g0318 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.32+26993G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017306 | |||||||
| chr1:157017492 | G | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+26807C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017492 | |||||||
| chr1:157017570 | G | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+26729C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017570 | |||||||
| chr1:157017577 | C | T | 1 | a0001c0001t0004g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.32+26722G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017577 | |||||||
| chr1:157017662 | G | A | 4 | a0002c0004t0013g0184 a0002c0004t0013g0185 a0002c0004t0013g0188 others(1): Show |
4 | HG02145.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+26637C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017662 | |||||||
| chr1:157017701 | C | T | 1 | a0002c0004t0005g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+26598G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017701 | |||||||
| chr1:157017702 | G | A | 11 | a0001c0001t0004g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02004.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+26597C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017702 | |||||||
| chr1:157017706 | C | CA | 105 | a0001c0001t0001g0275 a0001c0001t0001g0305 a0001c0001t0001g0306 others(102): Show |
108 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.32+26592dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017706 | |||||||
| chr1:157017706 | CA | C | 9 | a0001c0001t0004g0161 a0001c0001t0004g0179 a0001c0001t0006g0115 others(6): Show |
9 | HG00741.hp1 HG01099.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+26592delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017706 | |||||||
| chr1:157017706 | CAAAAAAA others(3): Show |
C | 3 | a0002c0002t0002g0055 a0002c0002t0002g0101 a0002c0002t0002g0102 |
3 | NA18973.hp1 NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.32+26583_32+26592d others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017706 | |||||||
| chr1:157017725 | A | G | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0285 others(4): Show |
7 | HG00558.hp2 HG00609.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+26574T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017725 | |||||||
| chr1:157017745 | G | C | 4 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0004g0140 others(1): Show |
4 | NA18977.hp1 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+26554C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017745 | |||||||
| chr1:157017905 | C | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+26394G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157017905 | |||||||
| chr1:157018204 | A | T | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+26095T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018204 | |||||||
| chr1:157018257 | T | C | 2 | a0001c0001t0001g0275 a0001c0001t0004g0160 |
2 | NA19055.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.32+26042A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018257 | |||||||
| chr1:157018370 | G | A | 1 | a0001c0001t0004g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32+25929C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018370 | |||||||
| chr1:157018371 | C | T | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+25928G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018371 | |||||||
| chr1:157018469 | C | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+25830G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018469 | |||||||
| chr1:157018506 | G | A | 85 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(82): Show |
87 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.32+25793C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018506 | |||||||
| chr1:157018513 | C | T | 6 | a0003c0003t0003g0257 a0003c0003t0003g0258 a0003c0003t0003g0259 others(3): Show |
6 | NA18948.hp2 NA18960.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+25786G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018513 | |||||||
| chr1:157018540 | G | A | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.32+25759C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018540 | |||||||
| chr1:157018561 | C | T | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+25738G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018561 | |||||||
| chr1:157018712 | C | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+25587G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018712 | |||||||
| chr1:157018780 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.32+25519A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018780 | |||||||
| chr1:157018829 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+25470G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018829 | |||||||
| chr1:157018830 | G | A | 1 | a0001c0001t0006g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.32+25469C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018830 | |||||||
| chr1:157018931 | C | T | 346 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(343): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.32+25368G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018931 | |||||||
| chr1:157018981 | C | T | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+25318G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157018981 | |||||||
| chr1:157019000 | T | C | 219 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(216): Show |
225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.32+25299A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019000 | |||||||
| chr1:157019006 | G | C | 2 | a0003c0003t0003g0007 a0003c0003t0003g0241 |
3 | HG01167.hp2 HG01169.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.32+25293C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019006 | |||||||
| chr1:157019502 | C | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+24797G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019502 | |||||||
| chr1:157019505 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+24794A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019505 | |||||||
| chr1:157019995 | C | T | 1 | a0001c0001t0007g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32+24304G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157019995 | |||||||
| chr1:157020019 | C | T | 40 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(37): Show |
42 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.32+24280G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020019 | |||||||
| chr1:157020080 | C | T | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+24219G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020080 | |||||||
| chr1:157020111 | G | A | 3 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0176 |
3 | HG00639.hp1 HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.32+24188C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020111 | |||||||
| chr1:157020125 | G | GA | 132 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(129): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+24173dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020125 | |||||||
| chr1:157020154 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.32+24145G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020154 | |||||||
| chr1:157020383 | T | G | 1 | a0003c0003t0003g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32+23916A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020383 | |||||||
| chr1:157020444 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+23855T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020444 | |||||||
| chr1:157020499 | G | A | 1 | a0002c0002t0002g0088 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.32+23800C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020499 | |||||||
| chr1:157020570 | A | G | 1 | a0003c0003t0003g0257 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.32+23729T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020570 | |||||||
| chr1:157020652 | A | G | 1 | a0003c0003t0003g0218 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.32+23647T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020652 | |||||||
| chr1:157020844 | C | G | 1 | a0003c0003t0006g0033 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32+23455G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020844 | |||||||
| chr1:157020845 | G | A | 1 | a0001c0001t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.32+23454C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020845 | |||||||
| chr1:157020865 | T | C | 1 | a0007c0014t0014g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.32+23434A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020865 | |||||||
| chr1:157020894 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.32+23405A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157020894 | |||||||
| chr1:157021018 | T | C | 1 | a0003c0003t0003g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.32+23281A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021018 | |||||||
| chr1:157021047 | G | A | 1 | a0002c0002t0002g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.32+23252C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021047 | |||||||
| chr1:157021168 | G | A | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+23131C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021168 | |||||||
| chr1:157021517 | A | C | 84 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(81): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.32+22782T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021517 | |||||||
| chr1:157021661 | CA | C | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+22637delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021661 | |||||||
| chr1:157021736 | A | G | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+22563T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021736 | |||||||
| chr1:157021779 | C | T | 132 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(129): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+22520G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021779 | |||||||
| chr1:157021896 | T | C | 11 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(8): Show |
11 | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+22403A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157021896 | |||||||
| chr1:157022317 | AAGTC | A | 7 | a0002c0004t0018g0244 a0002c0004t0018g0246 a0002c0004t0018g0247 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+21978_32+21981d others(6): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022317 | |||||||
| chr1:157022329 | T | G | 1 | a0001c0001t0020g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+21970A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022329 | |||||||
| chr1:157022428 | A | G | 2 | a0001c0001t0020g0168 a0001c0001t0020g0169 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.32+21871T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022428 | |||||||
| chr1:157022495 | A | C | 1 | a0002c0004t0005g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+21804T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022495 | |||||||
| chr1:157022840 | T | C | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.32+21459A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022840 | |||||||
| chr1:157022947 | C | T | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.32+21352G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022947 | |||||||
| chr1:157022961 | C | T | 209 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(206): Show |
215 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.32+21338G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022961 | |||||||
| chr1:157022973 | C | T | 1 | a0002c0002t0002g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32+21326G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022973 | |||||||
| chr1:157022991 | T | C | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+21308A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157022991 | |||||||
| chr1:157023207 | A | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+21092T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023207 | |||||||
| chr1:157023495 | GTGGCTCA others(4): Show |
G | 1 | a0001c0001t0035g0349 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32+20793_32+20803d others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023495 | |||||||
| chr1:157023626 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.32+20673G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023626 | |||||||
| chr1:157023697 | G | A | 1 | a0002c0002t0002g0090 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.32+20602C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023697 | |||||||
| chr1:157023747 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+20552G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023747 | |||||||
| chr1:157023765 | C | CA | 142 | a0001c0001t0001g0275 a0001c0001t0001g0309 a0001c0001t0001g0326 others(139): Show |
145 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.32+20533dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023765 | |||||||
| chr1:157023787 | TAAC | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+20509_32+20511d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023787 | |||||||
| chr1:157023789 | A | C | 2 | a0003c0003t0003g0218 a0003c0003t0003g0219 |
2 | HG02523.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.32+20510T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023789 | |||||||
| chr1:157023891 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+20408T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023891 | |||||||
| chr1:157023912 | T | A | 5 | a0002c0004t0005g0013 a0002c0004t0005g0014 a0002c0004t0005g0015 others(2): Show |
5 | HG00741.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+20387A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157023912 | |||||||
| chr1:157024068 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.32+20231G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024068 | |||||||
| chr1:157024101 | T | TA | 344 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(341): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.32+20197dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024101 | |||||||
| chr1:157024365 | G | T | 1 | a0001c0001t0001g0270 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+19934C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024365 | |||||||
| chr1:157024463 | C | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19836G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024463 | |||||||
| chr1:157024519 | T | C | 1 | a0002c0002t0002g0054 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+19780A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024519 | |||||||
| chr1:157024687 | T | C | 3 | a0003c0003t0019g0351 a0003c0003t0019g0352 a0003c0003t0019g0353 |
3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.32+19612A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024687 | |||||||
| chr1:157024732 | GCA | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19565_32+19566d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024732 | |||||||
| chr1:157024827 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19472A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024827 | |||||||
| chr1:157024849 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19450G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157024849 | |||||||
| chr1:157025004 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+19295A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025004 | |||||||
| chr1:157025082 | A | G | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+19217T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025082 | |||||||
| chr1:157025156 | A | G | 3 | a0002c0004t0005g0017 a0002c0004t0005g0025 a0002c0004t0005g0028 |
3 | HG01433.hp2 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.32+19143T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025156 | |||||||
| chr1:157025335 | C | T | 1 | a0002c0004t0005g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+18964G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025335 | |||||||
| chr1:157025360 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+18939T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025360 | |||||||
| chr1:157025620 | G | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+18679C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025620 | |||||||
| chr1:157025866 | T | C | 3 | a0002c0002t0002g0052 a0002c0002t0002g0053 a0002c0002t0002g0054 |
3 | HG00741.hp2 HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.32+18433A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025866 | |||||||
| chr1:157025991 | T | C | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+18308A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157025991 | |||||||
| chr1:157026398 | G | A | 2 | a0002c0004t0005g0123 a0002c0004t0025g0124 |
2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.32+17901C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026398 | |||||||
| chr1:157026452 | T | C | 4 | a0003c0003t0003g0249 a0003c0003t0003g0250 a0005c0007t0003g0251 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17847A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026452 | |||||||
| chr1:157026463 | C | T | 8 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0285 others(5): Show |
8 | HG00558.hp2 HG00609.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+17836G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026463 | |||||||
| chr1:157026586 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18955.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.32+17713C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026586 | |||||||
| chr1:157026656 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.32+17643G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026656 | |||||||
| chr1:157026811 | T | C | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32+17488A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026811 | |||||||
| chr1:157026855 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+17444T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157026855 | |||||||
| chr1:157027092 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+17207A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027092 | |||||||
| chr1:157027359 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.32+16940C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027359 | |||||||
| chr1:157027389 | A | C | 1 | a0002c0004t0005g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.32+16910T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027389 | |||||||
| chr1:157027683 | G | A | 1 | a0002c0004t0005g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+16616C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027683 | |||||||
| chr1:157027706 | C | T | 5 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+16593G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027706 | |||||||
| chr1:157027852 | C | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+16447G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157027852 | |||||||
| chr1:157028158 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.32+16141T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028158 | |||||||
| chr1:157028252 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+16047A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028252 | |||||||
| chr1:157028304 | T | C | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0036g0350 |
3 | HG00558.hp2 HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.32+15995A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028304 | |||||||
| chr1:157028435 | G | C | 1 | a0002c0002t0002g0091 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.32+15864C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028435 | |||||||
| chr1:157028555 | A | G | 3 | a0002c0002t0002g0052 a0002c0002t0002g0053 a0002c0002t0002g0054 |
3 | HG00741.hp2 HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.32+15744T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028555 | |||||||
| chr1:157028734 | CAAAGA | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+15560_32+15564d others(7): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028734 | |||||||
| chr1:157028932 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.32+15367A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157028932 | |||||||
| chr1:157029128 | T | C | 1 | a0002c0002t0016g0253 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.32+15171A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029128 | |||||||
| chr1:157029167 | C | CA | 15 | a0001c0001t0001g0275 a0001c0001t0001g0313 a0001c0001t0004g0140 others(12): Show |
15 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.32+15131dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029167 | |||||||
| chr1:157029261 | T | TTTG | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+15035_32+15037d others(5): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | |||||||
| chr1:157029261 | T | TTTGTTG | 166 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(163): Show |
170 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.32+15032_32+15037d others(8): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | |||||||
| chr1:157029261 | T | TTTGTTGT others(2): Show |
87 | a0001c0001t0006g0094 a0001c0001t0015g0204 a0001c0001t0032g0255 others(84): Show |
90 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.32+15029_32+15037d others(11): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | |||||||
| chr1:157029261 | T | TTTGTTGT others(5): Show |
3 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0024g0011 |
3 | HG02622.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+15026_32+15037d others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029261 | |||||||
| chr1:157029331 | G | A | 6 | a0002c0002t0002g0093 a0002c0004t0005g0016 a0002c0004t0005g0022 others(3): Show |
6 | HG02071.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+14968C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029331 | |||||||
| chr1:157029519 | GC | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+14779delG | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029519 | |||||||
| chr1:157029842 | A | C | 1 | a0002c0004t0014g0205 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.32+14457T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029842 | |||||||
| chr1:157029845 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+14454G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029845 | |||||||
| chr1:157029981 | G | T | 1 | a0002c0004t0005g0116 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.32+14318C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157029981 | |||||||
| chr1:157030325 | T | C | 1 | a0001c0001t0006g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.32+13974A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030325 | |||||||
| chr1:157030562 | T | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(83): Show |
89 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.32+13737A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030562 | |||||||
| chr1:157030659 | C | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+13640G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030659 | |||||||
| chr1:157030830 | C | A | 2 | a0001c0001t0004g0140 a0001c0001t0004g0181 |
2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.32+13469G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030830 | |||||||
| chr1:157030924 | G | A | 133 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(130): Show |
136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.32+13375C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030924 | |||||||
| chr1:157030925 | C | T | 2 | a0003c0003t0003g0214 a0003c0003t0003g0217 |
2 | NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.32+13374G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157030925 | |||||||
| chr1:157031025 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.32+13274G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031025 | |||||||
| chr1:157031090 | A | T | 1 | a0002c0004t0033g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.32+13209T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031090 | |||||||
| chr1:157031163 | G | A | 2 | a0002c0004t0008g0198 a0002c0004t0008g0199 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.32+13136C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031163 | |||||||
| chr1:157031183 | A | G | 2 | a0002c0002t0002g0049 a0002c0002t0017g0048 |
2 | NA18952.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.32+13116T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031183 | |||||||
| chr1:157031235 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+13064G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031235 | |||||||
| chr1:157031483 | A | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+12816T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031483 | |||||||
| chr1:157031484 | T | C | 1 | a0001c0001t0006g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32+12815A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031484 | |||||||
| chr1:157031529 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.32+12770G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031529 | |||||||
| chr1:157031537 | C | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01099.hp1 HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.32+12762G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031537 | |||||||
| chr1:157031805 | G | C | 11 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(8): Show |
11 | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+12494C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031805 | |||||||
| chr1:157031813 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32+12486T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031813 | |||||||
| chr1:157031816 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.32+12483G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031816 | |||||||
| chr1:157031869 | C | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+12430G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031869 | |||||||
| chr1:157031873 | G | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+12426C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031873 | |||||||
| chr1:157031927 | T | C | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.32+12372A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157031927 | |||||||
| chr1:157032141 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.32+12158T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032141 | |||||||
| chr1:157032147 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+12152G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032147 | |||||||
| chr1:157032345 | TAA | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+11952_32+11953d others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032345 | |||||||
| chr1:157032431 | G | C | 1 | a0002c0002t0024g0011 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32+11868C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032431 | |||||||
| chr1:157032651 | T | C | 132 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(129): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+11648A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032651 | |||||||
| chr1:157032707 | A | G | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+11592T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032707 | |||||||
| chr1:157032849 | A | G | 1 | a0001c0005t0001g0281 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.32+11450T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032849 | |||||||
| chr1:157032972 | T | C | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+11327A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032972 | |||||||
| chr1:157032996 | G | T | 2 | a0002c0002t0002g0105 a0002c0002t0002g0106 |
2 | HG01123.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.32+11303C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157032996 | |||||||
| chr1:157033074 | T | C | 1 | a0002c0002t0012g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.32+11225A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033074 | |||||||
| chr1:157033391 | T | C | 1 | a0003c0003t0003g0267 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.32+10908A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033391 | |||||||
| chr1:157033480 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+10819G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033480 | |||||||
| chr1:157033572 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0276 a0001c0001t0001g0279 others(5): Show |
9 | HG02129.hp1 NA18949.hp2 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+10727A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033572 | |||||||
| chr1:157033632 | G | C | 1 | a0001c0001t0001g0337 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+10667C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033632 | |||||||
| chr1:157033735 | C | A | 348 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(345): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.32+10564G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033735 | |||||||
| chr1:157033944 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+10355T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157033944 | |||||||
| chr1:157034072 | T | C | 7 | a0002c0004t0005g0024 a0002c0004t0005g0026 a0003c0003t0006g0018 others(4): Show |
7 | HG00099.hp1 HG01257.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+10227A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034072 | |||||||
| chr1:157034107 | C | A | 6 | a0003c0003t0003g0257 a0003c0003t0003g0258 a0003c0003t0003g0259 others(3): Show |
6 | NA18948.hp2 NA18960.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+10192G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034107 | |||||||
| chr1:157034330 | C | T | 5 | a0001c0001t0006g0115 a0001c0001t0006g0125 a0001c0001t0006g0126 others(2): Show |
5 | HG02723.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+9969G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034330 | |||||||
| chr1:157034477 | T | C | 1 | a0002c0004t0005g0130 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.32+9822A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034477 | |||||||
| chr1:157034629 | A | G | 8 | a0001c0001t0035g0349 a0002c0004t0008g0193 a0002c0004t0008g0194 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+9670T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034629 | |||||||
| chr1:157034738 | A | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+9561T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157034738 | |||||||
| chr1:157035035 | C | T | 8 | a0001c0001t0015g0201 a0001c0001t0015g0202 a0001c0001t0015g0204 others(5): Show |
8 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+9264G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035035 | |||||||
| chr1:157035076 | G | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+9223C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035076 | |||||||
| chr1:157035362 | C | A | 62 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(59): Show |
63 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.32+8937G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035362 | |||||||
| chr1:157035401 | C | CT | 7 | a0001c0001t0001g0279 a0001c0005t0001g0278 a0002c0004t0005g0114 others(4): Show |
7 | HG00438.hp2 HG03098.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+8897dupA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035401 | |||||||
| chr1:157035401 | CT | C | 21 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(18): Show |
22 | HG01070.hp2 HG01123.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.32+8897delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035401 | |||||||
| chr1:157035437 | C | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8862G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035437 | |||||||
| chr1:157035474 | C | T | 1 | a0003c0003t0003g0211 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32+8825G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035474 | |||||||
| chr1:157035530 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.32+8769G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035530 | |||||||
| chr1:157035550 | A | C | 346 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(343): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.32+8749T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035550 | |||||||
| chr1:157035566 | C | T | 88 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(85): Show |
91 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.32+8733G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035566 | |||||||
| chr1:157035759 | A | AAT | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+8538_32+8539dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035759 | |||||||
| chr1:157035773 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8526G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035773 | |||||||
| chr1:157035773 | CAGGAATA others(9): Show |
C | 11 | a0002c0004t0005g0017 a0002c0004t0005g0024 a0002c0004t0005g0025 others(8): Show |
11 | HG00099.hp1 HG01257.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+8510_32+8525del others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035773 | |||||||
| chr1:157035775 | G | T | 2 | a0001c0001t0004g0133 a0002c0004t0022g0135 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.32+8524C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035775 | |||||||
| chr1:157035776 | G | A | 2 | a0001c0001t0004g0133 a0002c0004t0022g0135 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.32+8523C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035776 | |||||||
| chr1:157035777 | A | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8522T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035777 | |||||||
| chr1:157035791 | G | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8508C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035791 | |||||||
| chr1:157035792 | G | A | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8507C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035792 | |||||||
| chr1:157035793 | A | T | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8506T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035793 | |||||||
| chr1:157035803 | C | T | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8496G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035803 | |||||||
| chr1:157035805 | G | T | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8494C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035805 | |||||||
| chr1:157035817 | T | C | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8482A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035817 | |||||||
| chr1:157035818 | AGGAATAT others(6): Show |
A | 166 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.32+8468_32+8480del others(13): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035818 | |||||||
| chr1:157035820 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.32+8479C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035820 | |||||||
| chr1:157035831 | T | A | 2 | a0001c0001t0004g0133 a0002c0004t0005g0016 |
2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.32+8468A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035831 | |||||||
| chr1:157035831 | T | TA | 181 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(178): Show |
186 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.32+8467_32+8468ins others(1): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035831 | |||||||
| chr1:157035833 | G | A | 4 | a0002c0002t0012g0186 a0002c0002t0012g0190 a0002c0002t0012g0191 others(1): Show |
4 | HG00609.hp2 NA18943.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8466C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035833 | |||||||
| chr1:157035843 | ATGTATAT others(3): Show |
A | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8446_32+8455del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035843 | |||||||
| chr1:157035846 | T | A | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8453A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035846 | |||||||
| chr1:157035853 | T | A | 2 | a0001c0001t0004g0142 a0002c0004t0005g0016 |
2 | HG02004.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.32+8446A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035853 | |||||||
| chr1:157035854 | T | C | 2 | a0002c0004t0022g0134 a0002c0004t0022g0135 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8445A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035854 | |||||||
| chr1:157035856 | G | T | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8443C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035856 | |||||||
| chr1:157035858 | A | T | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8441T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035858 | |||||||
| chr1:157035860 | TATATATA others(3): Show |
T | 9 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(6): Show |
9 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+8429_32+8438del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035860 | |||||||
| chr1:157035862 | T | C | 2 | a0001c0001t0004g0136 a0001c0001t0007g0165 |
2 | HG02602.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.32+8437A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035862 | |||||||
| chr1:157035865 | A | T | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8434T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035865 | |||||||
| chr1:157035868 | G | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8431C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035868 | |||||||
| chr1:157035870 | A | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8429T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035870 | |||||||
| chr1:157035871 | ATATATAT others(33): Show |
A | 2 | a0002c0002t0002g0097 a0002c0002t0002g0100 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.32+8388_32+8427del others(40): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035871 | |||||||
| chr1:157035871 | ATATATAT others(61): Show |
A | 1 | a0006c0009t0003g0261 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.32+8360_32+8427del others(68): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035871 | |||||||
| chr1:157035874 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8425A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035874 | |||||||
| chr1:157035877 | A | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+8422T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035877 | |||||||
| chr1:157035883 | ATATATAT others(21): Show |
A | 257 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(254): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.32+8388_32+8415del others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035883 | |||||||
| chr1:157035883 | ATATATAT others(49): Show |
A | 64 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(61): Show |
65 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.32+8360_32+8415del others(56): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035883 | |||||||
| chr1:157035886 | T | C | 11 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(8): Show |
11 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+8413A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035886 | |||||||
| chr1:157035892 | G | T | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8407C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035892 | |||||||
| chr1:157035893 | GAA | G | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8404_32+8405del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035893 | |||||||
| chr1:157035894 | AATATATA others(23): Show |
A | 1 | a0007c0014t0014g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.32+8375_32+8404del others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035894 | |||||||
| chr1:157035895 | ATATATAT others(37): Show |
A | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.32+8360_32+8403del others(44): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035895 | |||||||
| chr1:157035903 | A | T | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8396T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035903 | |||||||
| chr1:157035906 | T | G | 12 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(9): Show |
12 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+8393A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035906 | |||||||
| chr1:157035909 | ATC | A | 12 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(9): Show |
12 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+8388_32+8389del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035909 | |||||||
| chr1:157035914 | T | C | 268 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(265): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.32+8385A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035914 | |||||||
| chr1:157035922 | AAT | A | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8375_32+8376del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035922 | |||||||
| chr1:157035934 | T | G | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8365A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035934 | |||||||
| chr1:157035937 | ATC | A | 11 | a0001c0001t0004g0133 a0001c0001t0007g0143 a0001c0001t0007g0144 others(8): Show |
11 | HG01243.hp1 HG02071.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+8360_32+8361del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035937 | |||||||
| chr1:157035942 | T | C | 77 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(74): Show |
78 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.32+8357A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035942 | |||||||
| chr1:157035950 | AATATATA others(23): Show |
A | 1 | a0002c0004t0005g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32+8319_32+8348del others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035950 | |||||||
| chr1:157035952 | TATATATA others(47): Show |
T | 2 | a0002c0004t0021g0173 a0002c0004t0021g0174 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+8293_32+8346del others(54): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035952 | |||||||
| chr1:157035978 | AAT | A | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8319_32+8320del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157035978 | |||||||
| chr1:157036006 | AATATATA others(23): Show |
A | 4 | a0001c0001t0006g0125 a0001c0001t0006g0126 a0001c0001t0006g0127 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+8263_32+8292del others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036006 | |||||||
| chr1:157036032 | AAT | A | 88 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(85): Show |
91 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.32+8265_32+8266del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036032 | |||||||
| chr1:157036078 | AAT | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0020g0168 others(2): Show |
5 | HG02145.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+8219_32+8220del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036078 | |||||||
| chr1:157036099 | A | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8200T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036099 | |||||||
| chr1:157036107 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.32+8192T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036107 | |||||||
| chr1:157036126 | AAAAT | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8169_32+8172del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036126 | |||||||
| chr1:157036140 | AATATATG others(5): Show |
A | 2 | a0002c0004t0008g0198 a0002c0004t0008g0199 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.32+8147_32+8158del others(12): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036140 | |||||||
| chr1:157036148 | AATAC | A | 3 | a0002c0002t0002g0056 a0002c0002t0017g0057 a0002c0002t0017g0058 |
3 | NA18952.hp1 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.32+8147_32+8150del others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036148 | |||||||
| chr1:157036164 | T | TATATATG others(17): Show |
2 | a0001c0001t0004g0166 a0001c0001t0004g0167 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.32+8111_32+8134dup others(24): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036164 | |||||||
| chr1:157036186 | TACATATA others(3): Show |
T | 9 | a0001c0001t0004g0142 a0001c0001t0007g0143 a0001c0001t0007g0144 others(6): Show |
9 | HG01243.hp1 HG02004.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+8103_32+8112del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036186 | |||||||
| chr1:157036196 | A | AAT | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(94): Show |
99 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.32+8101_32+8102dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036196 | |||||||
| chr1:157036196 | AATATATA others(3): Show |
A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+8093_32+8102del others(10): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036196 | |||||||
| chr1:157036204 | TAC | T | 37 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0006g0113 others(34): Show |
38 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.32+8093_32+8094del others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036204 | |||||||
| chr1:157036206 | C | T | 306 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(303): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.32+8093G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036206 | |||||||
| chr1:157036308 | CT | C | 7 | a0002c0004t0005g0016 a0002c0004t0005g0022 a0003c0003t0019g0351 others(4): Show |
7 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+7990delA | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036308 | |||||||
| chr1:157036385 | G | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0020g0168 others(2): Show |
5 | HG02145.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+7914C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036385 | |||||||
| chr1:157036943 | T | C | 2 | a0002c0004t0014g0205 a0002c0004t0014g0206 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.32+7356A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036943 | |||||||
| chr1:157036997 | A | G | 132 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(129): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+7302T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157036997 | |||||||
| chr1:157037082 | C | T | 1 | a0002c0004t0005g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+7217G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037082 | |||||||
| chr1:157037116 | A | G | 346 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(343): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.32+7183T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037116 | |||||||
| chr1:157037184 | T | C | 129 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(126): Show |
132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.32+7115A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037184 | |||||||
| chr1:157037256 | G | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+7043C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037256 | |||||||
| chr1:157037352 | C | T | 49 | a0001c0001t0001g0275 a0001c0001t0004g0005 a0001c0001t0004g0006 others(46): Show |
51 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+6947G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037352 | |||||||
| chr1:157037416 | T | C | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.32+6883A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037416 | |||||||
| chr1:157037710 | C | T | 132 | a0001c0001t0001g0275 a0001c0001t0003g0209 a0001c0001t0003g0210 others(129): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.32+6589G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037710 | |||||||
| chr1:157037736 | C | A | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+6563G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037736 | |||||||
| chr1:157037873 | A | C | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32+6426T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037873 | |||||||
| chr1:157037967 | G | A | 2 | a0003c0003t0003g0262 a0003c0003t0003g0263 |
2 | NA18981.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.32+6332C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037967 | |||||||
| chr1:157037988 | C | T | 26 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(23): Show |
27 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+6311G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157037988 | |||||||
| chr1:157038009 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.32+6290C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038009 | |||||||
| chr1:157038029 | C | CA | 154 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0270 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.32+6269dupT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038029 | |||||||
| chr1:157038029 | C | CAA | 21 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(18): Show |
22 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+6268_32+6269dup others(2): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038029 | |||||||
| chr1:157038029 | CA | C | 23 | a0001c0001t0004g0133 a0001c0001t0004g0136 a0001c0001t0006g0113 others(20): Show |
23 | HG00741.hp1 HG01891.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+6269delT | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038029 | |||||||
| chr1:157038146 | G | A | 1 | a0003c0003t0003g0268 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.32+6153C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038146 | |||||||
| chr1:157038153 | G | A | 1 | a0001c0001t0015g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+6146C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038153 | |||||||
| chr1:157038194 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.32+6105C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038194 | |||||||
| chr1:157038222 | T | C | 1 | a0001c0001t0001g0336 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.32+6077A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038222 | |||||||
| chr1:157038240 | C | T | 2 | a0001c0001t0003g0212 a0003c0003t0003g0213 |
2 | HG00735.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.32+6059G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038240 | |||||||
| chr1:157038252 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+6047G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038252 | |||||||
| chr1:157038278 | G | GGAGA | 348 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(345): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.32+6020_32+6021ins others(4): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038278 | |||||||
| chr1:157038447 | C | T | 349 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(346): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.32+5852G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038447 | |||||||
| chr1:157038718 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+5581T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157038718 | |||||||
| chr1:157039063 | C | A | 2 | a0004c0006t0005g0029 a0004c0006t0005g0030 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.32+5236G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039063 | |||||||
| chr1:157039384 | C | T | 6 | a0001c0001t0004g0137 a0001c0001t0004g0138 a0001c0001t0004g0139 others(3): Show |
6 | HG02074.hp1 NA18977.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+4915G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039384 | |||||||
| chr1:157039508 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+4791A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039508 | |||||||
| chr1:157039508 | T | TTTTTTCT others(39): Show |
1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4745_32+4790dup others(46): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039508 | |||||||
| chr1:157039654 | A | C | 1 | a0003c0003t0003g0211 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32+4645T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039654 | |||||||
| chr1:157039880 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+4419A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157039880 | |||||||
| chr1:157040236 | C | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0036g0350 |
3 | HG00558.hp2 HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.32+4063G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040236 | |||||||
| chr1:157040245 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+4054A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040245 | |||||||
| chr1:157040268 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4031A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040268 | |||||||
| chr1:157040270 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4029A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040270 | |||||||
| chr1:157040274 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4025A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040274 | |||||||
| chr1:157040278 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4021C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040278 | |||||||
| chr1:157040282 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4017C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040282 | |||||||
| chr1:157040290 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+4009A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040290 | |||||||
| chr1:157040300 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3999C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040300 | |||||||
| chr1:157040310 | CAGCTAAA others(7): Show |
C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3975_32+3988del others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040310 | |||||||
| chr1:157040325 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3974C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040325 | |||||||
| chr1:157040332 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3967A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040332 | |||||||
| chr1:157040334 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3965C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040334 | |||||||
| chr1:157040348 | A | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3951T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040348 | |||||||
| chr1:157040358 | G | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3941C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040358 | |||||||
| chr1:157040359 | A | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3940T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040359 | |||||||
| chr1:157040406 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+3893T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040406 | |||||||
| chr1:157040479 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3820A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040479 | |||||||
| chr1:157040487 | C | G | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3812G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040487 | |||||||
| chr1:157040503 | TTAAGGTG others(14): Show |
T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3775_32+3795del others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040503 | |||||||
| chr1:157040530 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3769A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040530 | |||||||
| chr1:157040531 | C | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3768G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040531 | |||||||
| chr1:157040533 | C | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3766G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040533 | |||||||
| chr1:157040618 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3681A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040618 | |||||||
| chr1:157040619 | C | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3680G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040619 | |||||||
| chr1:157040624 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32+3675G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040624 | |||||||
| chr1:157040697 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3602A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040697 | |||||||
| chr1:157040710 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3589C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040710 | |||||||
| chr1:157040711 | T | G | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3588A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040711 | |||||||
| chr1:157040712 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3587A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040712 | |||||||
| chr1:157040713 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3586A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040713 | |||||||
| chr1:157040714 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3585A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040714 | |||||||
| chr1:157040716 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3583A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040716 | |||||||
| chr1:157040717 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3582A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040717 | |||||||
| chr1:157040718 | T | G | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3581A>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040718 | |||||||
| chr1:157040719 | T | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3580A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040719 | |||||||
| chr1:157040720 | G | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3579C>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040720 | |||||||
| chr1:157040721 | G | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3578C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040721 | |||||||
| chr1:157040722 | G | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3577C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040722 | |||||||
| chr1:157040727 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3572A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040727 | |||||||
| chr1:157040728 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3571A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040728 | |||||||
| chr1:157040732 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3567A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040732 | |||||||
| chr1:157040751 | G | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3548C>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040751 | |||||||
| chr1:157040752 | C | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3547G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040752 | |||||||
| chr1:157040759 | A | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3540T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040759 | |||||||
| chr1:157040772 | T | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3527A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040772 | |||||||
| chr1:157040787 | A | T | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3512T>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040787 | |||||||
| chr1:157040902 | C | A | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3397G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040902 | |||||||
| chr1:157040903 | A | C | 1 | a0001c0001t0006g0113 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.32+3396T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157040903 | |||||||
| chr1:157041353 | T | C | 2 | a0002c0004t0005g0031 a0002c0004t0005g0032 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+2946A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041353 | |||||||
| chr1:157041502 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.32+2797G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041502 | |||||||
| chr1:157041533 | A | G | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.32+2766T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041533 | |||||||
| chr1:157041635 | G | A | 1 | a0002c0004t0005g0131 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.32+2664C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041635 | |||||||
| chr1:157041699 | C | A | 1 | a0002c0004t0005g0132 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.32+2600G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041699 | |||||||
| chr1:157041768 | C | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01099.hp1 HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.32+2531G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041768 | |||||||
| chr1:157041814 | T | C | 1 | a0001c0001t0004g0181 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.32+2485A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041814 | |||||||
| chr1:157041822 | C | G | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+2477G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041822 | |||||||
| chr1:157041827 | G | A | 2 | a0003c0003t0006g0033 a0003c0003t0006g0034 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+2472C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157041827 | |||||||
| chr1:157042224 | T | C | 1 | a0003c0003t0003g0007 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.32+2075A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042224 | |||||||
| chr1:157042391 | C | T | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1908G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042391 | |||||||
| chr1:157042429 | T | C | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1870A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042429 | |||||||
| chr1:157042454 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.32+1845A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042454 | |||||||
| chr1:157042666 | T | C | 3 | a0001c0001t0001g0339 a0001c0001t0001g0340 a0001c0001t0001g0341 |
3 | NA19009.hp2 NA19064.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.32+1633A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042666 | |||||||
| chr1:157042783 | A | C | 83 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(80): Show |
85 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.32+1516T>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042783 | |||||||
| chr1:157042802 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1497T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042802 | |||||||
| chr1:157042989 | G | A | 2 | a0002c0002t0002g0101 a0002c0002t0002g0102 |
2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.32+1310C>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157042989 | |||||||
| chr1:157043183 | A | G | 3 | a0001c0001t0004g0133 a0002c0004t0022g0134 a0002c0004t0022g0135 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+1116T>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043183 | |||||||
| chr1:157043273 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+1026G>A | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043273 | |||||||
| chr1:157043357 | T | A | 5 | a0002c0002t0002g0103 a0002c0002t0002g0104 a0002c0002t0002g0105 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+942A>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043357 | |||||||
| chr1:157043369 | T | C | 88 | a0001c0001t0006g0094 a0002c0002t0002g0001 a0002c0002t0002g0002 others(85): Show |
91 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.32+930A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043369 | |||||||
| chr1:157043498 | C | G | 348 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(345): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.32+801G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043498 | |||||||
| chr1:157043579 | T | C | 1 | a0002c0004t0005g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+720A>G | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043579 | |||||||
| chr1:157043669 | C | G | 3 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0030g0208 |
3 | HG01884.hp2 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.32+630G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043669 | |||||||
| chr1:157043962 | C | A | 1 | a0001c0001t0004g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+337G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043962 | |||||||
| chr1:157043981 | C | G | 1 | a0002c0002t0002g0012 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.32+318G>C | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157043981 | |||||||
| chr1:157044157 | C | A | 21 | a0001c0001t0006g0113 a0001c0001t0006g0115 a0001c0001t0006g0125 others(18): Show |
22 | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+142G>T | ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | 157044157 |